Tag | Content |
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EnhancerAtlas ID | HS069-02247 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr12:124520630-124522250 |
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 | chr12:124521319-124521338 | CAGCCACAAGGGGGCACCT | + | 6.51 | HSF1 | MA0486.2 | chr12:124521713-124521726 | GAAGGTTCTGGAA | - | 6.3 | HSF1 | MA0486.2 | chr12:124521995-124522008 | GAACATTCTGGAA | - | 6.54 | HSF1 | MA0486.2 | chr12:124522082-124522095 | GAACATTCTGGAA | - | 6.54 | HSF1 | MA0486.2 | chr12:124522087-124522100 | TTCTGGAATGTTC | + | 6.59 | LHX2 | MA0700.1 | chr12:124521242-124521252 | ACTAATTAAC | + | 6.02 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH12I124036 | chr12 | 124521019 | 124521548 |
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Enhancer Sequence | CCCACTCCAC ACAACCCCTG ATTTGACTTT TTCCTATCAC TGCATCTTCT GGAAGTTCAT 60 ATAAATAGCA TGGTGCCCTT GTGTAAGGCT GCTTTCACAT GGCATAATGC TTTTGTTATG 120 TACCCATGTC GTGTGTGTCA CAATAGCCTG TGATTTTTAT TGTTATGGAG TAGCCTGTCA 180 CATGATGTGT CCACCATTTA CTCATCCATC ACTTGTTGAG GGACATTTAG GCTGAATCTT 240 CCATTTGGCG ATGATGAGTA AAGCTGCTAT GAACATTTTC ATGTACAGGT TTTTTTGTGG 300 ACTCTCGCAA ACGTCTCCTA CTGCTGGTTT ATTTTAACCA TGATGCAATC AAGGTCCCAC 360 CCTGCAGCCG ATTGTTGTGC TTCTGACGTT TCCTTTAATT AAGTTGAAGG GGCCCAGTCA 420 AACCCCCTGT TGTAGCCACA GCTCCGGTTA CCTGCCAGGC ATACAAAGGA GCTGAGTTCT 480 CAGAGTAACA ACAGCTACTG AGCTGCTTGT GTAGACCTTA GGCTTGTGAT TGGAATGGTT 540 TCGTTGTACA CCCGCCGGTT GTTACAGGGA AGAAAGACTC CAGGCTGGAC ATCTCAGAAC 600 TAAACTAATT GAACTAATTA ACCTAATCTC TCCCTCTTTC TCATACTCTG GGAGTCAGCC 660 ATTTTTGTTG GTGATGCTGC ACTGTTTCGC AGCCACAAGG GGGCACCTGT GTGCTTTGTA 720 TGATTTAAAA TTTTCATTTG GCAATTAAAA AAAGTTCTCC CAGAAAATCA GTATTTTAAG 780 ATGCTTTCCC TGTTTCCCAG TCTATTGAAT TCAATGGTGA CTTTTGTTCA ATTGTTCAAT 840 ACGTATTTAC CGAATACCCA CCATGACTAA TGCATTGTGC TACGCACTGT GGGTGGTGAA 900 GAAATAAAAT AGTTCCTACC CTTGGGACTC TTCTGACCCA CAGGGAGGAG AGAGAACCAC 960 AGTACAGCTC GGCATGTGTT TGAAGTCAGA AGAATGGGGC GAAACTGTGG AGATTCAGGT 1020 GGGTGGGAGC TGGCATCGCG ATATTCCGGG AGGCCATGAT GTCAAGAGCA AGTGAAGAGA 1080 CCAGAAGGTT CTGGAACCCA GGATCTGTTA GGGATGCTGG AAGGGATTCG ATGGTCCAGA 1140 GCTAGGGAAT TTGGAACTTA TTCATGATGT TGAATGACAC GGGGGAGTTT TCAGTGGGGA 1200 AGTGACTGGT AGTATTGAAT TGGAGAGGAA AGAGAAGAGG CAGGAAACTC TCTGTGGGGG 1260 CAGTTTGGGG GTGATGGGGC CCATGCTGGG GTGACCCTGG GAGAATGGCT GAGAATCATC 1320 TCTGAGTGCT GTAGGAATGA ATGAGACCAA TGGAGAGGAG AGAGAGAACA TTCTGGAATC 1380 CTTCTGGAAT GACTGAAAAT CATCTCTGAG TGTTGTAGGA ATGAAGGAGA CCACTTGGGG 1440 AGAGGAGAGA GAGAACATTC TGGAATGTTC TGAGAATCAT TCCAGAATTA CTGCAGACCA 1500 CTTGGGGAGA GGAGAGAAAG ACAATATCCT GGAATGTTCT TGGAGCAGTC TTATTTTGAA 1560 GTTTGGTTTT CAAAGTCAAG TAGCTTTGCA TTATATGAAA ACTTTCACTA AGATACTTCC 1620
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