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- rs150957191[chr17:7887957]
Enhancers that have rs150957191[chr17:7887957]
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Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
chr17 |
7882325 |
7888250 |
enh32072 |
|
|
Transcript factors that have rs150957191[chr17:7887957]
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Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
chr17
|
7884760
|
7890121
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741477
|
|
chr17
|
7885181
|
7888709
|
STAT3
|
GTRD
|
no
|
Blood (OCI-LY7)
|
21741480
|
|
chr17
|
7885352
|
7888638
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741482
|
|
chr17
|
7885360
|
7889805
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741483
|
|
chr17
|
7885565
|
7888174
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741491
|
|
chr17
|
7885572
|
7888089
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741492
|
|
chr17
|
7886137
|
7889563
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741500
|
|
chr17
|
7886194
|
7888044
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741501
|
|
chr17
|
7886661
|
7888075
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741503
|
|
chr17
|
7886883
|
7888215
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741504
|
|
chr17
|
7886966
|
7888239
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741505
|
|
chr17
|
7887041
|
7888146
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741506
|
|
chr17
|
7887087
|
7888924
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741507
|
|
chr17
|
7887095
|
7888590
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741508
|
|
chr17
|
7887107
|
7888356
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741509
|
|
chr17
|
7887145
|
7888225
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741510
|
|
chr17
|
7887172
|
7888170
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741511
|
|
chr17
|
7887265
|
7888347
|
ZNF274
|
GTRD
|
no
|
Cervix (HeLa-S3)
|
21741514
|
|
chr17
|
7887280
|
7888908
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741515
|
|
chr17
|
7887406
|
7888884
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741516
|
|
chr17
|
7887409
|
7888918
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741517
|
|
chr17
|
7887413
|
7888732
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741518
|
|
chr17
|
7887452
|
7888588
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741519
|
|
chr17
|
7887590
|
7888544
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21741520
|
|
chr17
|
7887956
|
7887964
|
HOXA5
|
JASPAR
|
yes
|
|
52960995
|
|
chr17
|
7887956
|
7887966
|
POU6F2
|
JASPAR
|
yes
|
|
52960996
|
|
chr17
|
7887957
|
7887967
|
ALX3
|
JASPAR
|
yes
|
|
52960997
|
|
chr17
|
7887957
|
7887967
|
EMX1
|
JASPAR
|
yes
|
|
52960998
|
|
chr17
|
7887957
|
7887967
|
EMX2
|
JASPAR
|
yes
|
|
52960999
|
|
chr17
|
7887957
|
7887967
|
ESX1
|
JASPAR
|
yes
|
|
52961000
|
|
chr17
|
7887957
|
7887967
|
GBX2
|
JASPAR
|
yes
|
|
52961001
|
|
chr17
|
7887957
|
7887967
|
GSX1
|
JASPAR
|
yes
|
|
52961002
|
|
chr17
|
7887957
|
7887967
|
GSX2
|
JASPAR
|
yes
|
|
52961003
|
|
chr17
|
7887957
|
7887967
|
HESX1
|
JASPAR
|
yes
|
|
52961004
|
|
chr17
|
7887957
|
7887967
|
HOXB2
|
JASPAR
|
yes
|
|
52961005
|
|
chr17
|
7887957
|
7887967
|
HOXB3
|
JASPAR
|
yes
|
|
52961006
|
|
chr17
|
7887957
|
7887967
|
LBX2
|
JASPAR
|
yes
|
|
52961007
|
|
chr17
|
7887957
|
7887967
|
LHX2
|
JASPAR
|
yes
|
|
52961008
|
|
chr17
|
7887957
|
7887967
|
LHX6
|
JASPAR
|
yes
|
|
52961009
|
|
chr17
|
7887957
|
7887967
|
MEOX1
|
JASPAR
|
yes
|
|
52961010
|
|
chr17
|
7887957
|
7887967
|
MEOX2
|
JASPAR
|
yes
|
|
52961011
|
|
chr17
|
7887957
|
7887967
|
MIXL1
|
JASPAR
|
yes
|
|
52961012
|
|
chr17
|
7887957
|
7887967
|
MNX1
|
JASPAR
|
yes
|
|
52961013
|
|
chr17
|
7887957
|
7887967
|
NOTO
|
JASPAR
|
yes
|
|
52961014
|
|
chr17
|
7887957
|
7887967
|
RAX
|
JASPAR
|
yes
|
|
52961015
|
|
chr17
|
7887957
|
7887969
|
MEF2B
|
JASPAR
|
yes
|
|
52961016
|
|
Genes associated with rs150957191[chr17:7887957], comfirmed by eQTL
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Blank TSI value indicates lack of sufficient expression for calculation
Chrom. |
Start |
End |
Strand |
Gene name |
Ensembl ID |
TSS of gene |
Distance between TSS and SNP |
Tissue |
q Value |
id |
More |