Tag | Content |
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EnhancerAtlas ID | HS062-04277 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:121937320-121938720 |
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) |
CTCF | MA0139.1 | chr12:121937865-121937884 | CGGCCACCAGGGGGCGCCC | + | 9 | Nr2f6(var.2) | MA0728.1 | chr12:121937534-121937549 | GAGGTCAGGAGTTCA | + | 6.22 | Zfx | MA0146.2 | chr12:121938663-121938677 | GAGGCCGAGGCGGG | - | 6.01 | Znf423 | MA0116.1 | chr12:121938095-121938110 | GCCCCCTAAGGGTTA | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_60917 | chr12:121937595-121976920 | DHL6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr12 | 121938497 | 121938591 | chr12 | 121937989 | 121938382 | chr12 | 121937334 | 121937530 | chr12 | 121937606 | 121937741 | chr12 | 121937786 | 121938623 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121499 | chr12 | 121937601 | 121938803 |
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Enhancer Sequence | GTGTGCACCT GTAGTCCTAG CTTCTTGGGG AGATTGAGGT GGGAGGATTG CTTGAGCCCA 60 GGAGTTCGAG GCTGCAGTGA GCTATGATCA CACAACTACA CTCCAACCTG GGCAAAAGTA 120 GGAGACTCTG TCTCTAAATA ATAATAATGG CCAGGTGTGG TGGCTCACGC CTGTAATTCC 180 AGCACTTTGA GAGGCCAAGG TGGACAAATC ACCTGAGGTC AGGAGTTCAA GACAAGCCTG 240 TCCAACATAG TGAAACCCCA TCTCTATTAA AACTACAAAA AAATTAGCCA GGCATGGTGG 300 CACGCGTCTG TGGTCTTAGC TGCTCGGGAG ACTGAGGCAG GAGAATCACT TGAACCCGGA 360 GGCAGAGGTT ACAGTGAGCC AAGATCGCAC CACTGCACTC TAGCCTGGGT GACAGAATGG 420 GACTCTAACT CAAAAAAAAA TAATTATTTA ATAATAATTA AAAATAAAAA GAATTTTCCC 480 CAAGTGCCCT GAGCCCAGGA TCTCACACTC ATACCTCCCG TTTCCCTCTG TGTGTGGCCC 540 CCCTGCGGCC ACCAGGGGGC GCCCTGGGCT CTGTCCCTCA GGGAAGAATT TTCATTTGTG 600 TATGACAGGC TCCGGGAAAA GAAGATTATT CTAATTGGAG ATTTCATCTC TGAGAAATAG 660 GTTGTGCTGG AGGGAATCAT GTCACTGGCT TCCCTAGGCC CTGCTTGAAT TTATACACTC 720 CCTGGGGCTC TCGGCAGCAC AGATATAAGG AAGGCTGGGT GCCCTCACCA GCTCAGCCCC 780 CTAAGGGTTA CACCTTACAC GCCCGTCCCC TCCGAAAGTC CAGGGCAGGT TTTCGAAGAG 840 AAAGATCCAA CCGTGGGACC CTTTCTGCGG GAAACTGCCC CGTACTGGAC CTGACGAGAT 900 AACCACAGAC AAGGGATGGC TGGGCCTGGG CGGCCCTTTA TGCCAACTTC TCTCAAAGAG 960 ATAATTAGTT AACAATGGAT TCGGGTCCCA CTGCTTCCTA GGCTGGGGCT TTAATAATCA 1020 GAAACTCCCT CCATGCCATG ACTAAAAATA TCCCACTGTG AAAACAAGGC AGGCATCAGG 1080 GAAGAATCGC CATCCACAGG CCGGCAAAGG GAGGCGCAGC TTGGGGAACT CCTGCTCTGG 1140 GGAACCAGCA CCCTCCGGGG TGCCCCCTTC TATGGGGAAA GAGACCCACC AGGCATCAAC 1200 GCACCTGGGG TCTCTCAAGT ACCCTCCCTC CATCCCAGCC CCACCGTCTG TGAAAACCCA 1260 TCTGAAGTAG CTTGAATTGT GTCCCAAAAA ATATGTGTTC AGGCCAGGCA CAGTGGCTCC 1320 CGCCTGTAAT CCCAGCACTT TGGGAGGCCG AGGCGGGCGG ATCACTTGAG GCAAAGAGTT 1380 CGAGACCAGC CTGGTCAACA 1400
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