Tag | Content |
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EnhancerAtlas ID | HS089-12067 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr8:9150260-9151030 |
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) |
ESR2 | MA0258.2 | chr8:9150859-9150874 | TGGACAAGGTGACCT | - | 6.08 | MEF2C | MA0497.1 | chr8:9150377-9150392 | TTCTATTTTTGACCC | - | 6.21 |
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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 | CAGGATCTTG AAGGGAGGTA GAGGTTAGAG ACTAACAACC ACCCTGCAAC CCCTGTACAT 60 GAAGAGGGGT CAGTTGGTGC TTGAAACATC TCTGTTCTCT ATTGGCCCCT GACTGTCTTC 120 TATTTTTGAC CCTGAGCCAT AAGAAAAATC ACTGCCAACT CTGACATCTT CTCTTCTTTC 180 CCATGGCTTA GCAAGCTGGA CCTGTTCTTC CATGTTCTGG ATCTGGCTTC CGGCTGCAAC 240 CCCCACCATC ATCTGAATAT TCAACCTCAT CTCATTAGCC TAGTCCCATC TCAGATTAAT 300 CCGACTGCCA TTCTCAGCAG GGAGAGCCTA AACTTCTTTT AATACACATA TAGAGCTCAC 360 ATACTTTAGA AAGATTTTTT TAATATCACA GGCATTTTAA AAGAATGAGT AAGGCACCGG 420 TGAAGCTTAA GATTAAATTA AACATAATCC TGCCACAAAG CATCTAGCTA ATTGAGATGA 480 TGGTCTCAAA AAAATTCAGG ATTCAGTAGG GCAGTTACTA AAGGAGTTTG TGGAGGACAG 540 AAGCTATGTA AGTTACTATC TAAAGGGATT GTTGAGGGAA TTTTTCAGGG GTAGGAGATT 600 GGACAAGGTG ACCTTCCAAC TGTGCATTTA ATGGTTGCAA TAGCCGTCAA GGTCAGAGTT 660 GATAGGAACA ATCCAAGTTA ATATCTAGAT CTGCCAGTTT TCAGTCCCAT GTGGATGGAG 720 AAAAAAATCA TGGAACCATT GCTGAGCCAC ACCGAAGATG AACAGGGCCA 770
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