Tag | Content |
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EnhancerAtlas ID | HS176-10289 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:102288290-102289060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr12:102288700-102288711 | GATGAGTCACC | - | 6.32 | JUND | MA0491.1 | chr12:102288700-102288711 | GATGAGTCACC | - | 6.62 |
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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 |
GH12I101894 | chr12 | 102288127 | 102289389 |
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Enhancer Sequence | AAATGCTGGG ATTACAGGTG TGAGCTACCG TGCCTGGCCT CCACCTGTAT GGTTTTAAAT 60 GTACAGATAA GCAAGAATAG AACACGACCC TGGAATTCCA AGTTTTCAGA TCACGTGTTT 120 GATGTCATGT GGACTCCACA CCTGGGCCTT TGACATAGTC TCAATTTGCC ATCAATAGAC 180 AGAGTCCCCA GGTCTGGTCT TCTCTTCAGT CAGAGCACCT AGAGCACCTT CATATCGCCA 240 CCTCCCTATC TTCCTAAATA TCCTCCTCAT TCTTTCATTG CCTTCCCTTT CTCCACAGAC 300 AGGCAAACAA CCTTCTTCCC AGCGCTTCTC CTCTGTGTTT GCTCCGATGC CTGGCATGTG 360 GCTGTCTGAG GTTCAGAATT ATTCTCAGAC CTGTGTAACA AGAACTCTAG GATGAGTCAC 420 CTGGTGCCTG CTTTTTTATA CCCTCAGGCC AAGGCAGGGA GGCCTGATTT CCCTGGCAGA 480 GTTAATTGTG TGGCAAAAGT GCTGCCCAAG GTTATGAGCT GTCTCTGCTT TTTTCCCCAT 540 TACTGGTTCC CATTCCTGTC TCTCTGCCCA TTCAGCATTG TGCTCAGAAG GGCATCCTCC 600 ACCTCAACAT TCCTGTAGTG TGAAAAATGG TTATTGTAGG AAAAGTGGTA ATGCTAAATT 660 CGAAACCCTT CAGGTTTTTT TTTTTTTTTT TTTTTTTTTT TTTTACCCAG GCTGGAGTGC 720 AGTGGCGTGA TCTCAGCTCA CTGCAAACTC TACCTCCTGG GTTCAAGTGA 770
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