Tag | Content |
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EnhancerAtlas ID | HS182-21056 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:121873170-121874550 |
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 | CCAGAAATAC TGATTGATTT TTCTTTAAAA TATCTCTTTA TCTCGTTTAA TTTTTTTTTC 60 ATTCATATCC TCCATTTGTT CCCTTCTCCA AGACCCTTCA TGAGTGGGAG GGCTGCCTGA 120 CTGTCGGGGT AGATCTGAGA CTAGACTTTC CCCAGTGAGC CTAGCAGTGT GCCTATGCCT 180 CTGCTGAAAG AAACTGCCCA CAAGTGGAAA GCTCGGGGAC TCAGGGCTTG CAGCCTGATT 240 TCTTTTGTCT CATGGGATGC TCCCTTGAGA TGTCCCATGA GACATCCCAT CAGATGTCCA 300 TGGCGCATTC CCTCTACCCT AGGAGTAGCA GTCCCTGCGG GGGCAAGACT ACTGTGAATC 360 CTGCTGCTCC TCTGGGTCTA GCCACCCAGT GGGGCTGCTG TACTCCAGTC TGGTGCTGGG 420 GAATGTCTGC AGGGGATCCA GTGATGTGAT GTTCCTAGTA GTGGGTAACA GCATCATTCC 480 TGATGGGGGT CAGAGGGTAG TGCCATAGAC TCTGGGATTT CCTGGATATA AATAGGCTTG 540 TCATAGTAAT ATACTAAATA CGTGGATAGA CTCAAGGCCT CCTGGTTAGC CTGGATGATG 600 CAAGCAATTG TGATCGCTGA GGTTACATAA AAGTATTCTC CTTCCTGAGT GCTGTGTTAT 660 TGTGCCTGCA GATGTTGCAA TGGGCTGTGC CAGCTGGCCT CCAGCCAGGA GGTGGTGCTT 720 GCCAAAGAGC ACCAGCTGCA GTGGTAGCAG TGGAATTTGT GCTCGCCTTA TGTTACCCAC 780 TGCAGGTACT CTGGTATCTC AGGTGATGGG TAAGGCCATG GAGCTTCCAA ATATTCCTCT 840 CCATTGTGTT ACACTACCAG GGTAGGTGGA AGGGCAGAGC CTGGTAGGGC CTAGGTCAGG 900 CAAGTTTGTA CTCTGGCTTC CCAAGTGTGG ACACAAGCAG TGGCCCCACT GAAGATCAGA 960 CAGCTGTTCC CTGGCTGCTG GGAGGAGCAC AGCTGCCTCT GCTGCACAAA AAGATCCACG 1020 CAGGAAGCAG GGGATAGCAG GTGGCAATAA GCCCCACTCA GCTACTCAGC TCCTACTTAT 1080 CTGGCAATAC AGGTCTCACA CTTGGGTTCC AGGCAGCCTG TACTCAGAAC TCAAAACTGC 1140 CCCAGGCTCT AGGCCTACCC AACTGAGACA GAAACAGTGG CTTTCAGGTT ATACCCCTTC 1200 CAGTCCATCC ACAAAGCAGG CACCCAGCTC CTGTGCCCAT TTCTTAGCAC ACTTCCTGCT 1260 CTCCCCTTGG TTCTGGGCAT CAGGTTTCAT CCCCCTTGAG ATTATATCAC AAATATCAAT 1320 TCGGAGCTTC TGTCAACCTG TGACCACTGC CTGAGTTAGC TGGCAGACTT CTGTAAGGTC 1380
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