Tag | Content |
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EnhancerAtlas ID | HS099-21441 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr8:27153640-27155060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr8:27154523-27154533 | GGGGATTAGC | - | 6.02 | Mecom | MA0029.1 | chr8:27154456-27154470 | CATTATCTTATCTA | - | 6.32 |
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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 |
GH08I027295 | chr8 | 27153509 | 27155099 |
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Enhancer Sequence | ATTGGAGAGA GTAGAATCCA GGGTGATTCT CTTTTTTTTT TTTTTTTTTT ACATTTAAGT 60 TCCAGGATAC ATGTGCAGGA CATGCAGGTT TGTTACATAG GTAAATGTGC GCCATGGTGG 120 TCTGCTGCAC CTGTCAACCC ATCACCTAGG CATTAAGCCC CGCATGCATT AGCTATTTAT 180 CCTGATGCTC TCCCTCTCCC CAGTAATTCT TATCACACAA AAACATCAAG AACACAGCAT 240 GGCAGGAAAA ACCAGCAAGT GCAAGGTCAA CTCCTGCCCA CTCACCGTGG GCAATGACGG 300 CCTCACTGTA AAGGAACAAA CACCAGAACT TTCACTTTCC TCATCGACCT GATAACTGAA 360 TTTAATAGAA AAAGTACTAA TCAGGCTGGA ATTCTAGGGG CTTCCCATGT GACCTCATTA 420 CCCTTAGCCT CAGCAAAAAG CTCAGGACTC CTACACTCCC TGGGATGGGC AGGCAGTGCC 480 ACCACACAGA CAGACAGATA CTCCCTAAGT ATCCCCAACC CAGTCCTGTA CAAGGCAAGC 540 CAGTCATATG GCTTTAGCCA CAGAAGGAAA CCAAGTAAGA GAACAATGAT AAAGCTACAT 600 GACTCCACGA TGACTACTGG AAAAACAACT CAACAAACTC CAGCAACAGC AGGTTCGTAA 660 TCGCTATTTG GAGTTGGAAT TTCAACATGT ATTTATGGCT CTGACATCGG ATGACAAAAT 720 AATCTACTGA ACAAAGTGAA AACTCTCTCC CACCAGTTTG TTGGTCTATT AGACATCAGA 780 AATGTTAAGG ACTTGTCTCT GTTGGGCACT TGTATGCATT ATCTTATCTA AATTTTTTTT 840 TAAAAACCCT AGTAAAAGGG AATTGCCCTC TTTTTACAGA GGAGGGGATT AGCTTGGAGG 900 GGGTTGAGGG ATTTGCTGGG GAACTGGGCT TAGATTTGGA AATAGGTCTG CTTTGCGGTT 960 ACTGCCCTGG CACCCAGTGT GTCACATAAT CCTTTCTTCC ACACTGTTCC ACCAGCTCTG 1020 TGGCTCAGGG TAAACTCCAC AGCCAAATGT TAATGAGGCT CTTTCCTGGG ACTAATCCTC 1080 ACCTATGGAC ACATGGTGGA GGGGACCGCA GGCTCCTGAG GACAGCGCCC AGCAACCTGG 1140 ACCAGGCATG GCTCAGCTGT GGCTAAGATG AGTCTAACAG AGTGGTAATT ACTAGAAGCA 1200 ACCACTTCAG AAAGCCAAAG ACCAGAGCCA AGATCAACAG TCAGAAACAA GGTTGCCAAT 1260 CCACACAGGA CCTGGAGGAA GAGAGGGTGC CAGGCAGAAC AACCAGAATG GGGACAGAGG 1320 GAGCCCACTC ATTCATTTGA TTAACAGTTA TTGGTCACCT ACCCACTTCA CTCATTCAAT 1380 CAACAATTTT TATTGGTCAC CTATTGTGTG CCAAGAACTC 1420
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