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- rs398099362[chr14:55766212]
Enhancers that have rs398099362[chr14:55766212]
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| Chrom. |
Start |
End |
Enhancer ID |
Tissues that enhancer appears |
More |
| chr14 |
55762685 |
55778955 |
enh3215 |
|
|
| chr14 |
55765939 |
55766288 |
vista17873 |
|
|
Transcript factors that have rs398099362[chr14:55766212]
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| Chrom. |
Start |
End |
TF name |
Source |
Predicted site? |
Tissue |
id |
More |
|
chr14
|
55765789
|
55766473
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104107
|
|
|
chr14
|
55766023
|
55766356
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104108
|
|
|
chr14
|
55766027
|
55766427
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104109
|
|
|
chr14
|
55766052
|
55766478
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104110
|
|
|
chr14
|
55766059
|
55766412
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104111
|
|
|
chr14
|
55766061
|
55766392
|
ZNF274
|
GTRD
|
no
|
Liver (HepG2)
|
108104112
|
|
|
chr14
|
55766068
|
55766402
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104113
|
|
|
chr14
|
55766097
|
55766348
|
ZNF274
|
GTRD
|
no
|
Liver (HepG2)
|
108104114
|
|
|
chr14
|
55766098
|
55766311
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104115
|
|
|
chr14
|
55766100
|
55766524
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21620471
|
|
|
chr14
|
55766100
|
55766524
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
108104116
|
|
|
chr14
|
55766108
|
55766960
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
21620472
|
|
|
chr14
|
55766108
|
55766960
|
ZNF143
|
GTRD
|
no
|
Epithelial (MCF-7)
|
108104117
|
|
|
chr14
|
55766127
|
55766501
|
ZNF274
|
GTRD
|
no
|
Bone Marrow (K562)
|
108104118
|
|
|
chr14
|
55766206
|
55766227
|
IRF1
|
JASPAR
|
yes
|
|
107553520
|
|
|
chr14
|
55766206
|
55766227
|
IRF1
|
JASPAR
|
yes
|
|
115540204
|
|
|
chr14
|
55766211
|
55766630
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
21620473
|
|
|
chr14
|
55766211
|
55766630
|
TCF7L2
|
GTRD
|
no
|
Colon (HCT116)
|
108104119
|
|
Genes associated with rs398099362[chr14:55766212], 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 |
|
chr14
|
55833110
|
55878576
|
-
|
ATG14
|
ENSG00000126775.8
|
55878576
|
66898
|
Esophagus
|
0.0483985
|
13338
|
|