Tag | Content |
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EnhancerAtlas ID | HS143-01920 | Organism | Homo sapiens | Tissue/cell | NGP | Coordinate | chr20:5277190-5278880 | 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 | GCAGTCATTT GCAGGATCAG GGTAGGGATC TTTGCCAATT AATGTGGTCA TATTCCTACC 60 ATTGGAGGAG TCAGATTAAA TTGTGCTTGA AGGAAATAAA GACATTTACT ATGGGAATCC 120 AGGCTGCCTT GCTAATGAAT TGCTCCATGT AGCAGCGAGG TTTCTCCCAG CCGAGGGCTG 180 AAAGTGAAGA CCTTGCTTAG CAAAAGGTAT GTTGATTAAA TAAATGTGTT CCTCACATAG 240 TAGTTCCGCC ACTGGACACT CAGGGTTTCT GTATCCATGT CCTAGGGTAC AGCTATCCAA 300 ACTTCTGCCA GGAAAGAAAC AGATAAAAGT TGTGTTTGTG CTGCTATTTA GTGGGGCATG 360 AGGCTGGGTG TGGTGGCTCA TGCCTATAAT CCCAGCAATT TGGGAGGCCA AGGCAGGTGG 420 ATCACTTGAG GTCAGGAGTT TGAGACCAGC TTGGCCAACA TGGTGAAACC CCGCCTCTAC 480 TAAAAATACA AAAATTAGCT AGGCGTGATG GTGTATGCCT GTAATACCAG CTACTAGGAA 540 GCCTGAGGCA GGAGAATCTC TTGAACCCAG GAGGCTGAGG TTGCAGTGAG TCAAGATCGT 600 GCCGCTGCAC TCCAGCCCAG GTGACAGAGC GAGACTTCAT CTCAAAAAAA AAAAGGGCGC 660 CAAACATCTA CTGTGTACCC ACAAAAATTA AAATTATAAA AAGACGGCAT CAGCAATCCC 720 AGGAGGTGAT GTGTCCCTGG TTGGTGTACC TCAGGAGTTG CTGCATTTGC CTCACATCAC 780 CATGTGAGAT AAAGTAGCAA ATGTAAGAAG CCACGTGTGC TCATTTCTGT TTGCCAGCAA 840 AATTTCACAA AGCTTCTTGC CTGAGTCACT ATATTTCTCG AAAGATGAAT GATCCTAGCC 900 CTTGCCTTTT TCTGCACGTA AGATAACATC TGACAGGGTT AATGATTATG CTTCTGTAAT 960 TATAACCAGA TGTACTCTTG CACCCAAGCT TTGATGTGAT TGTACACGTG CTAAACCTTC 1020 ATCACCCGCA TATAAACTGT GAACTAAAAC ATAGCTTTGG AGGTGTCTGA CAGAACCTCT 1080 CTGAAAGACT CCTCTTGGGC TATAGTCCTC AGTCAGACTT CTGAATAAAA CCAACTTGAA 1140 CTCTTTAAAA GTTTGATGTT TATTTCTTTA GAAGGCATTT GGCTGCTAGG AGACACAAAG 1200 CACAACCACA GCTAAGTCAG CCAGCAGTGG CTTGGGTGAA GACTGCACGT TGTGTTGTGG 1260 GTGGCCCTGT ACTTGCCTTG TTTTGGAGTG CGAGCAAACC CCCTCCCCTC CACCTGCTTT 1320 TCCTGGGGCC GGGTTACCTC TCAGCACAAC CTGCTTTCCC ATTTGGCTCC TGAATCACTT 1380 GCAAACAGCT CCATGTGCAT TCGAGTCTAA TGCGTTAAGA GCCCCTCCAC GCCCATTTAT 1440 CTCAATAGGA GAAAAGAAAG GCAGGAGCAC TAGGATGATT CTGGGGTGAT TCTCTCTGGT 1500 TTCCCTGGAA TCCTGGAGTC TCAATTATGG TCCCTTGGAT TGGATGTGCT CTTGGCCTGC 1560 CAGAGGGAGG AACAGTATCT TTTCTGCAGT TTAAGATTCT GCCGGGAGGC CAGAAACCAG 1620 CTGAGGGTCC ACTCCTTAGG AGTCAGGAGT GCAGTCCCCG AGTGCAGTTC GCTGCATCAG 1680 AGTGAAAATC 1690
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