Tag | Content |
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EnhancerAtlas ID | HS182-19700 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:32551040-32552380 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr7:32551397-32551418 | GGAGGAAGAAGGGCTGGAAGA | + | 6.93 | ZNF263 | MA0528.1 | chr7:32551160-32551181 | TGAGGAGGGCGAGGGGGAAAG | + | 7.01 | ZNF263 | MA0528.1 | chr7:32551385-32551406 | TGAGGAGTAAGGGGAGGAAGA | + | 7.31 |
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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 |
GH07I032511 | chr7 | 32551548 | 32551619 |
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Enhancer Sequence | GTCCACAGTC CTGGAAATTC TGAACTGCCC CAGTAGGAGG GAAGCCATCT CTCTAGGATA 60 AGATGCAGGG GTGTACTAGG TTGTGGGGAT TAGAGTACAG GGGACTAGCA AGAGGGTCTA 120 TGAGGAGGGC GAGGGGGAAA GATAGGAGGA CACTTGGAAA GGGGTGCCTG ACGAGCAGGG 180 CGGTGGCATA CGGACGCTCT GGAATTAACA GAGGAAGAGC TGGGCAGGGA GTTCCGGGAG 240 GTAGGGTGCT GGGAAGGGGC GACATTAGTC AGCTGGGGGA AACAGGTACG CTGGAAAACT 300 GAACAGCTTG GACGGTCCTG GAGAGGAGGC TGAGGGCAGG AAGTTTGAGG AGTAAGGGGA 360 GGAAGAAGGG CTGGAAGACG AGAGCCAGAA GGAACAGAAA GAAATGGAGG CCAGGGTTGA 420 GGCCGAGAAA TTGGAGGTAG CTTTCTGGTC ATTTTTCCAA ATGAGTGCTG TAGTAACTCA 480 CTTGTCCAAA CGAGTCAGAA TGAATAACTG AGATGTGCTG AGACCGACTC CAGCATTTAT 540 CTCCTCAGGA CATTCCATCA CAGAATGCCT ATTATGAAAC ATACATTTAT CTCCTTAGGA 600 CATTTCTTGA TGGAATGCCC ATTATGAAAC ATACATGCTC CCTTTTATTC TAGTGAGGAG 660 GCCCCATCAA TCAGGGAAAT GGTCCCAGTT TCTCAGTTTA AGAGTGGTCA TGGGAAGTAG 720 CAAAGAAAAT AAATGGATCT GTAATTATTG GTCCTTGTTC TTGGGATACC ATGTAGTTTT 780 GCCCCTCCAT AGGCAAAGAT TGATCAAGGG GCTAACAGAG GCAGGGGCTT GGGGCCTAGG 840 AGAGCAGTTC TGAAGCAGGA ATTGGGAAAA TGGGAAGTCA GTATCCTAGT CTCTTTTCCT 900 TACTACATTG TTCAAAGCCC TTTCACATCA TTTACCTCAC TGTGTGAATG CACATGATTA 960 GAGATGTTAC GTTATTTTAT CGATGAGGAC ACTAAAGACC AGAAAACGAA CTACCAGTAG 1020 GCACAAAGCA GGTGGGACTA GAACTTGGCC AGAAAGAGGG CTGGTGGGAG GGAGCACAGA 1080 ATGGCACAAA GTGCTTACCA GCATCTTTGC CTCCTCCTGT GTCTCTGGAC AGGATCTTGT 1140 AGGAGGAGCT TAAGAGCAGA ACTGTACTTT TCGTAGCTTA CCTCGTAGTT CCTGTGGTCC 1200 CTTGGTTTGA TGCCTTTCTG TTCACTGGAA CCAGAAACAA AAGGCCAAAG CTGGTACACT 1260 CTCTGCCCAT TGAAACTGTG CCCCAAAGAG CTGAAGAAAG CAGTAACAGA AATCTTCGAG 1320 CTTGCAGGAT GGCAGATAAG 1340
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