Tag | Content |
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EnhancerAtlas ID | HS007-16859 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr8:121873240-121874390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIL3 | MA0025.1 | chr8:121873789-121873800 | AGGTTACATAA | - | 6.14 | NR2C2 | MA0504.1 | chr8:121873654-121873669 | GGGGGTCAGAGGGTA | + | 6.05 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 121873306 | 121873367 | chr8 | 121873467 | 121874371 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I120860 | chr8 | 121873165 | 121874705 |
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Enhancer Sequence | TCCATTTGTT CCCTTCTCCA AGACCCTTCA TGAGTGGGAG GGCTGCCTGA CTGTCGGGGT 60 AGATCTGAGA CTAGACTTTC CCCAGTGAGC CTAGCAGTGT GCCTATGCCT CTGCTGAAAG 120 AAACTGCCCA CAAGTGGAAA GCTCGGGGAC TCAGGGCTTG CAGCCTGATT TCTTTTGTCT 180 CATGGGATGC TCCCTTGAGA TGTCCCATGA GACATCCCAT CAGATGTCCA TGGCGCATTC 240 CCTCTACCCT AGGAGTAGCA GTCCCTGCGG GGGCAAGACT ACTGTGAATC CTGCTGCTCC 300 TCTGGGTCTA GCCACCCAGT GGGGCTGCTG TACTCCAGTC TGGTGCTGGG GAATGTCTGC 360 AGGGGATCCA GTGATGTGAT GTTCCTAGTA GTGGGTAACA GCATCATTCC TGATGGGGGT 420 CAGAGGGTAG TGCCATAGAC TCTGGGATTT CCTGGATATA AATAGGCTTG TCATAGTAAT 480 ATACTAAATA CGTGGATAGA CTCAAGGCCT CCTGGTTAGC CTGGATGATG CAAGCAATTG 540 TGATCGCTGA GGTTACATAA AAGTATTCTC CTTCCTGAGT GCTGTGTTAT TGTGCCTGCA 600 GATGTTGCAA TGGGCTGTGC CAGCTGGCCT CCAGCCAGGA GGTGGTGCTT GCCAAAGAGC 660 ACCAGCTGCA GTGGTAGCAG TGGAATTTGT GCTCGCCTTA TGTTACCCAC TGCAGGTACT 720 CTGGTATCTC AGGTGATGGG TAAGGCCATG GAGCTTCCAA ATATTCCTCT CCATTGTGTT 780 ACACTACCAG GGTAGGTGGA AGGGCAGAGC CTGGTAGGGC CTAGGTCAGG CAAGTTTGTA 840 CTCTGGCTTC CCAAGTGTGG ACACAAGCAG TGGCCCCACT GAAGATCAGA CAGCTGTTCC 900 CTGGCTGCTG GGAGGAGCAC AGCTGCCTCT GCTGCACAAA AAGATCCACG CAGGAAGCAG 960 GGGATAGCAG GTGGCAATAA GCCCCACTCA GCTACTCAGC TCCTACTTAT CTGGCAATAC 1020 AGGTCTCACA CTTGGGTTCC AGGCAGCCTG TACTCAGAAC TCAAAACTGC CCCAGGCTCT 1080 AGGCCTACCC AACTGAGACA GAAACAGTGG CTTTCAGGTT ATACCCCTTC CAGTCCATCC 1140 ACAAAGCAGG 1150
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