Tag | Content |
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EnhancerAtlas ID | HS112-08564 | Organism | Homo sapiens | Tissue/cell | KELLY | Coordinate | chr20:5277260-5278900 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F4 | MA0470.2 | chr20:5277841-5277855 | AAAGGGCGCCAAAC | - | 6.26 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAGATTAAA TTGTGCTTGA AGGAAATAAA GACATTTACT ATGGGAATCC AGGCTGCCTT 60 GCTAATGAAT TGCTCCATGT AGCAGCGAGG TTTCTCCCAG CCGAGGGCTG AAAGTGAAGA 120 CCTTGCTTAG CAAAAGGTAT GTTGATTAAA TAAATGTGTT CCTCACATAG TAGTTCCGCC 180 ACTGGACACT CAGGGTTTCT GTATCCATGT CCTAGGGTAC AGCTATCCAA ACTTCTGCCA 240 GGAAAGAAAC AGATAAAAGT TGTGTTTGTG CTGCTATTTA GTGGGGCATG AGGCTGGGTG 300 TGGTGGCTCA TGCCTATAAT CCCAGCAATT TGGGAGGCCA AGGCAGGTGG ATCACTTGAG 360 GTCAGGAGTT TGAGACCAGC TTGGCCAACA TGGTGAAACC CCGCCTCTAC TAAAAATACA 420 AAAATTAGCT AGGCGTGATG GTGTATGCCT GTAATACCAG CTACTAGGAA GCCTGAGGCA 480 GGAGAATCTC TTGAACCCAG GAGGCTGAGG TTGCAGTGAG TCAAGATCGT GCCGCTGCAC 540 TCCAGCCCAG GTGACAGAGC GAGACTTCAT CTCAAAAAAA AAAAGGGCGC CAAACATCTA 600 CTGTGTACCC ACAAAAATTA AAATTATAAA AAGACGGCAT CAGCAATCCC AGGAGGTGAT 660 GTGTCCCTGG TTGGTGTACC TCAGGAGTTG CTGCATTTGC CTCACATCAC CATGTGAGAT 720 AAAGTAGCAA ATGTAAGAAG CCACGTGTGC TCATTTCTGT TTGCCAGCAA AATTTCACAA 780 AGCTTCTTGC CTGAGTCACT ATATTTCTCG AAAGATGAAT GATCCTAGCC CTTGCCTTTT 840 TCTGCACGTA AGATAACATC TGACAGGGTT AATGATTATG CTTCTGTAAT TATAACCAGA 900 TGTACTCTTG CACCCAAGCT TTGATGTGAT TGTACACGTG CTAAACCTTC ATCACCCGCA 960 TATAAACTGT GAACTAAAAC ATAGCTTTGG AGGTGTCTGA CAGAACCTCT CTGAAAGACT 1020 CCTCTTGGGC TATAGTCCTC AGTCAGACTT CTGAATAAAA CCAACTTGAA CTCTTTAAAA 1080 GTTTGATGTT TATTTCTTTA GAAGGCATTT GGCTGCTAGG AGACACAAAG CACAACCACA 1140 GCTAAGTCAG CCAGCAGTGG CTTGGGTGAA GACTGCACGT TGTGTTGTGG GTGGCCCTGT 1200 ACTTGCCTTG TTTTGGAGTG CGAGCAAACC CCCTCCCCTC CACCTGCTTT TCCTGGGGCC 1260 GGGTTACCTC TCAGCACAAC CTGCTTTCCC ATTTGGCTCC TGAATCACTT GCAAACAGCT 1320 CCATGTGCAT TCGAGTCTAA TGCGTTAAGA GCCCCTCCAC GCCCATTTAT CTCAATAGGA 1380 GAAAAGAAAG GCAGGAGCAC TAGGATGATT CTGGGGTGAT TCTCTCTGGT TTCCCTGGAA 1440 TCCTGGAGTC TCAATTATGG TCCCTTGGAT TGGATGTGCT CTTGGCCTGC CAGAGGGAGG 1500 AACAGTATCT TTTCTGCAGT TTAAGATTCT GCCGGGAGGC CAGAAACCAG CTGAGGGTCC 1560 ACTCCTTAGG AGTCAGGAGT GCAGTCCCCG AGTGCAGTTC GCTGCATCAG AGTGAAAATC 1620 TTGGGGCAAT ATCTTGGCTC 1640
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