Tag | Content |
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EnhancerAtlas ID | HS051-21513 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr4:184328190-184328970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr4:184328781-184328802 | GATCTCTTTCTCTTTCTTTTC | + | 6.6 | IRF1 | MA0050.2 | chr4:184328851-184328872 | TCTTGCTTTCTCTTTTTCTTT | + | 7.44 | IRF1 | MA0050.2 | chr4:184328874-184328895 | TCTTGCTTTCTCTTTTTCTTT | + | 7.44 | ZNF263 | MA0528.1 | chr4:184328942-184328963 | CTTTCTTCTTTCTCCTCTTCC | - | 6.11 | ZNF263 | MA0528.1 | chr4:184328948-184328969 | TCTTTCTCCTCTTCCTTCTTT | - | 6.46 | ZNF263 | MA0528.1 | chr4:184328945-184328966 | TCTTCTTTCTCCTCTTCCTTC | - | 7.54 |
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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 |
GH04I183406 | chr4 | 184327841 | 184333385 |
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Enhancer Sequence | TAAATAAAAA AGAAAAAAAA AAAGATGTGC TCTATTCTTT CTTTATGTAA AAGAGAGCAA 60 ACCTGGCCTA TCCACGCTGC AAGTGGTTGT GGAGGGGCTG GCCCGCGCCC CTTCCGCGCA 120 GTCTCCTTCC GCGTCACCTC TGTGACCGCT GTGCCCAGTC GGGCCCCACA GAAGCGGCAA 180 GCGACGTCCT CAACCGCAAT CTCGGCTCCT CGGGCGCCAC CCAGTGGCCT CGGGGCGGAA 240 TCGCGGGCGA GCTCGGAGGG GCTCGGGGTG GCGGGGCGCA GCGCGGCGCC TGTAAAACAA 300 CCCTTTGTCT TCAGAAGGCG CTTGTCCTGC CAAAGCAAAG CACCGTGCTT TACAGCTACT 360 GGAAGAGCAG TCCTGAGAAA CAAAGCCCCG ATTTTTTATA GCCACCGGGG AAACCAGAGC 420 CCACTTCCTT CCTCCAGGAC CAGGGCTTTA TTGATGCGGA TCATCTTGTT TCAGGGCTGA 480 CCTGCTGCCA TCCCTCCAAG AGAGACAGGA GAAAGATTGA AGCTCTCTCA GGGAATTCAT 540 CAAAGGTTTT TCTGTTCAGG TTACCAAACT GTTACAAAGA ACTCTCTTAT GGATCTCTTT 600 CTCTTTCTTT TCTTTTCTTT TTCTCTTTCC TTTCTTTCTT TTCGTTCTTC CTTTCTTTTC 660 CTCTTGCTTT CTCTTTTTCT TTCTTCTTGC TTTCTCTTTT TCTTTCTTCC TTCTCTTTCT 720 TGCTTTCTCT CTTTTTTCTT TCTTCCTTCT TTCTTTCTTC TTTCTCCTCT TCCTTCTTTC 780
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