Enhancers that regulate HBM[ENSG00000206177.2]
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Chrom. Start End Enhancer ID TSS of gene Distance between enhancer and TSS Tissues that enhancer appears More
chr16 115405 125035 enh99305 203891 78856
chr16 121563 121849 vista21497 203891 82042
chr16 124533 124922 vista21498 203891 78969
chr16 127789 133393 enh102537 203891 70498
chr16 130955 131250 vista21499 203891 72641
chr16 145023 145249 vista21500 203891 58642
chr16 150045 161355 enh64930 203891 42536
chr16 151121 151408 vista21501 203891 52483
chr16 154913 155267 vista21502 203891 48624
chr16 163381 163878 vista21503 203891 40013
chr16 192865 197015 enh16485 203891 6876
chr16 193028 193281 vista21504 203891 10610
chr16 199321 199454 vista21505 203891 4437
chr16 261125 267095 enh16486 203891 57234
chr16 298325 302475 enh109694 203891 94434

Transcript facotrs that regulate HBM[ENSG00000206177.2]
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Chrom. Start End TF name Source Predicted site? Tissue TSS of gene Distance between TFBS and gene id More
chr16 199208 199684 ZZZ3 ENCODE Uniform TFBS no Cervix (HeLa-S3) 203891 4207 108170055
chr16 199215 199685 ZNF217 ENCODE Uniform TFBS no Epithelial (MCF-7) 203891 4206 108170056
chr16 199299 199514 ZNF143 GTRD no Epithelial (MCF-7) 203891 4377 108170057
chr16 199348 199354 ZNF354C JASPAR yes 203891 4537 49324442
chr16 199368 199383 STAT1 JASPAR yes 203891 4508 49324443
chr16 199370 199381 STAT1 JASPAR yes 203891 4510 49324444
chr16 199370 199381 STAT3 JASPAR yes 203891 4510 49324445
chr16 199386 199397 NFKB1 JASPAR yes 203891 4494 49324446
chr16 199387 199397 NFKB1 JASPAR yes 203891 4494 49324447
chr16 199393 199399 SP1 TRANSFAC yes 203891 4492 49324448
chr16 199393 199403 SP1 JASPAR yes 203891 4488 49324449
chr16 199409 199422 TFAP2A JASPAR yes 203891 4469 49324450
chr16 199409 199422 TFAP2B JASPAR yes 203891 4469 49324451
chr16 199409 199422 TFAP2C JASPAR yes 203891 4469 49324452
chr16 199409 199424 TFAP2A JASPAR yes 203891 4467 49324453
chr16 199410 199419 TFAP2A JASPAR yes 203891 4472 49324454
chr16 199417 199421 LFA1 TRANSFAC yes 203891 4470 49324455
chr16 199417 199431 TCF7L2 JASPAR yes 203891 4460 49324456
chr16 199417 199432 LEF1 JASPAR yes 203891 4459 49324457
chr16 199435 199444 THAP1 JASPAR yes 203891 4447 49324458
chr16 199442 199454 INSM1 JASPAR yes 203891 4437 49324459

Chrom. Position dbSNP ID Reference Allele Alternative Allele Distance between TSS and SNP Tissue q Value id More
chr16 1063457 rs73489811 T C 846690 Heart 0.26915 4251534
chr16 156313 rs750083495 C CAAAT 47578 Liver 0.272901 4244294

Genomic Location chr16:203891-216767[+]
TSS 203891
Gene Name HBM
Ensembl ID ENSG00000206177.2
ENTREZID 3042
Uniprot
Q6B0K9
A0A1K0FU50
Protein Name
Hemoglobin subunit mu