Tag | Content |
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EnhancerAtlas ID | HS044-09642 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr4:24974860-24976180 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2A | MA0003.3 | chr4:24975154-24975165 | TGCCTGAGGCT | - | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 24975200 | 24975985 | chr4 | 24975738 | 24976056 |
| | Number: 1 | ID | Chromosome | Start | End |
GH04I024973 | chr4 | 24974653 | 24976822 |
| Enhancer Sequence | TAACCCAACC ACCTTGGGCA CATATTCTCA GCACCTCTTG GGACTGTGCC TCAGGCCTTA 60 GTCACTCATA TTTGGCTCAG AATAAACCTG TTTAAAAATT TTATGGAGTC TGACTCTTTG 120 TGTCGACATG GTGGTGGTCC CATGGGTGTA CACATATGTC AAAACTTATC CAATTGTACA 180 CTTTAAGTAT ATGGAGTTTA CTGTATATCA ACTGTACCTC AATAAAGTGC ATTTAAAAAA 240 AGTCTGGAGA AAAAGAAGTC CCCTTTTGTT TGCACTTGGA GCTGTGATTA AGCATGCCTG 300 AGGCTACTGG CAGCTATCTT GACATTGTGA GGAGAAAACA TGCTTGAGAG TGAGGCCAAC 360 CCAGAGGATA AAAAGAACTG AAAAAGGCCA GAGTTAGACC AGATTCCAGC CATCCATCGG 420 TACTGGATCC AGCTGTGCCT ACAGCAGTCT CTGGAATTTT TGCTCATTGA GACAATACGT 480 GTGTGTGAGT GTATGATTAA CCCGGTCTGA ACTGAGTTTT GTTGGTTACA ACTGAGGAGT 540 TCTGTGCAAC GTTATCCACA GTCCACCAGG CAGGCTGAGA GCTGCTTCTT AACCAGCAAG 600 TGCCTCATGG AGGGATTGGG TTTGGGGTTA TGGAAGTGAA CAGAGCTGCC TGCCTTAAGG 660 CAAGTAGGCC TTGCTCTGTT CCCCTTGCAG TCCCCGAGCC CGGGAAGCCC GAGAGGGAGC 720 CCTTCAGTGC TTGTGCACTC GGCTGTTTCG CAAGAGTCAC GGTCAGTTGC GCCTCTGCTT 780 CGGAAGAGTA TTTTTAGTGG CAAATAAAGT GGTGCGCAAA TAAACAAACG CCTGGAACAA 840 ATCCTGCAAA GGAGAGCGCC TGTGTGCGGC CCACTGTCTA ACTAGGTCAG CCTCGGGCAC 900 AGCTCCTTTT GACAGTTTGC TCCCCAGGGC GGAAGGTGAC CCGCAGGTGC CGGCTGCTTT 960 CCCCACCAAT CAGCCATCTG TGGTTTGAGA CTCACAAGCT TAGGAGAGAC TCGGGAGGCA 1020 TCAGTTCCGC ATCCCGCACT CCCACGTGAA TTTGCCCCCG CCCTGAGTCA GAACCCTAGA 1080 GGGGTGAAAT CCCTGAATTC TGCAGAGGAA ACCCATACTT CTTTGCTTTT TCAGCAATTC 1140 CAGGAGATGT CGTTTTTCAA GTGGCAAATG TGTGGCTCTA GAGGACAGAG TAACCACCTT 1200 GCAGCCAAGA AGCCCTGATG TCAACTCCCA GCTCTGCTGC AGCACCCAGA AATCACCGGA 1260 CCTTTCTGCA TCTTTCTGGG TGACTCTGTC ATGAGGATTT CATAATGTAA TTCCCTAGCA 1320
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