Tag | Content |
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EnhancerAtlas ID | HS108-09187 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:28012280-28013760 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2F1 | MA0017.2 | chr12:28012478-28012491 | CTCATGACCTCTG | - | 6.04 | RARA(var.2) | MA0730.1 | chr12:28012471-28012488 | TGGCCTTCTCATGACCT | - | 6.34 | SOX10 | MA0442.2 | chr12:28013006-28013017 | TTCTTTGTTTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61017 | chr12:27959154-28076345 | HBL1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CAGCAGAGAA GTACAGACAA AAGGAGCCGA TTTGGGAGTC ATTATTGCAG TGTTGGGTGA 60 AGCCAAGAAT GTAGAGGAGA GTCTCAAGGA GAGGGAAAAG TAGGAACATT GGAACACAAA 120 TTGGAAGACC CTATACTGAC ATGGAGCACT TATTGGTTAG GACTTTGTAT ATGATGCTGT 180 GGATGCCTAC ATGGCCTTCT CATGACCTCT GTGGTCAATC CAATTGGCTC TGGATTTTCA 240 TACACCCCCT ACCTCTTGCC ACATCTCAAC AACATTCACT GTTCCACTAT GCACCTCCTT 300 CAAGCACCTG TGACTCTCTG CCTCTCGTTC CACAAGTAGG GCAGGCCAGA AATGTCAGGG 360 AGTGAATGTC TGTGGGAGCA GCCCTTGGGC AGGCAGGGTG AGCACTGGAG GATGGATATC 420 CTTCCTCATG TGGAATGACT TGGAGGCCTA TTCTACCCTC TCCAGAGTTA CTCAGCAGGA 480 TTGACTGTCG GTTGCTCACA GTGATAAACT ATTGTGGCTT TCTGGGCTTC CTGTTGTCTT 540 CCCATTCCCC CAGTGGTACT TCTTGGAATC ACCTCCCCAG TAAACAACTT ATACTTAAAT 600 CCCTGTCTCA GGATCTGCTT CCGGAAGAAT CTGAACTAAG ACAGCCTTCT TGTTCTCCCC 660 AGTCTCTTGA GGGTGAACGA TTTGAAATGT ATAAACTGCT TATATCCTTC TGCGTCTGCT 720 GCCATATTCT TTGTTTTACC TTCTGCCGTC TTCTCTCAAT GCTACCCTTC TATAATCTCT 780 CAAAACAAAC ATGGAATTAT AAGTGAGTCC CCTTAACTCA AGAGACACCA AGGGATAACA 840 GACACCTGGA TAGAAAGTCC CTCTTCTATT CTAGGAAGCA GATGTAATGA TAATCATATT 900 TTGTATTTAC TAAAAATCTT TCCTTCTGAG GAGTTCAAAG TGTTCCTTAT GTATCCCCTG 960 TGGGTAAGAG CAGGACTGAC TTCTAGCACA GCTGTCAATT ATGTAAAGTG TAAATGATAT 1020 GAAACTGGGA TTTAGAAACC ATCCTGTTTC CCCTTCAAGT GGCCTTCTCC CTGTTCCCTT 1080 GCACTGGGGC CCCTCCCTGC TGTTCCATTT CTGTTGTTAC CCCCACTGTG TTCCTTCCCA 1140 TAGTGACTTG CTCTTAACCA TCTTTCAACC AATCTCCACT TCCAGGGTGA CTATTGATAC 1200 TATTAACATG ACATTTTCCC CAGGAATATT GGCATTTCAA TAGGATACAC TTACAAACAG 1260 AACATTTTAA AAAATGAAAC TGAATAGAAA GATCATAGGC AAATAAGAAC TTTCATTCAT 1320 AGATGGTATT AAGCCTTTTG TAAATCTATA TGATTTCAAA TTGACTGATG GGGAACTTTC 1380 GAGAGGAAAA ATACACGTGT TTGGAGTTCC AGCCATTTGT TTCAGGGATG AGTTGAAAAA 1440 ACAAAAATGA AATGATAAGA TTCCATGGAA AAAGTTCTGT 1480
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