Tag | Content |
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EnhancerAtlas ID | HS044-07925 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:242485990-242487220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SP2 | MA0516.2 | chr2:242486148-242486165 | TCAAGTCCCGCCCCCAG | + | 6.32 | ZNF263 | MA0528.1 | chr2:242486557-242486578 | GGAGGAGGAGGAGGGGGAGAG | + | 10.22 | ZNF263 | MA0528.1 | chr2:242486550-242486571 | GAGGGAGGGAGGAGGAGGAGG | + | 6.92 | ZNF263 | MA0528.1 | chr2:242486563-242486584 | GGAGGAGGGGGAGAGGAAGGC | + | 7.56 | ZNF263 | MA0528.1 | chr2:242486560-242486581 | GGAGGAGGAGGGGGAGAGGAA | + | 9.36 | ZNF263 | MA0528.1 | chr2:242486554-242486575 | GAGGGAGGAGGAGGAGGGGGA | + | 9.3 |
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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 |
GH02I241543 | chr2 | 242483409 | 242487823 |
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Enhancer Sequence | GGAAAAATTT CCCCAAATTG AAGAGAAATG TAAGTTTTCA GGTGAAAAGG GGAAAACAAA 60 ATGTTGACCT GACACATGAT AGTTAGTTTT GAAAACTTTA ATGATAAAGA CAAATCTTAA 120 AACCTGAGAG GGGAATTGTG TCCCCACAAA AAATATGTTC AAGTCCCGCC CCCAGCAGCT 180 GGGAGTGTGG CTTGACTTGG AAATAGTCTT TGCAGATGTG ATGAGGTTAA TACGAGGTCA 240 CCCTGGATTA GGATGGGTCC CATGACCAGT GACTGTTATC CTTAGACAGA GCGGGAGATT 300 TGGACACAGA GACACCAGGA GGAGGCCACA TGGTGGGAGA GGCGGACGTT GGAGCCATGC 360 AGCAATGAGC CGGGGACCGC CGGGGACCGC TGGCAGGTGC CCAAGCGAGG AGACGGGCAT 420 GCGGCTGGCC CTGCCCTGGA GGCTTCAGAA GAGCACGTCC TGCCAGCACC CCGACTTCTG 480 GACTTCCAGC CTCAGGAACT GTGAGAGAGT AAGTGTGTGT TGTCCTAAGC CGCCAGGTTC 540 GTGTCAGGAA ACTAATGCGG GAGGGAGGGA GGAGGAGGAG GGGGAGAGGA AGGCTATGAG 600 GTAAAGAAGG AACACAAATC AGATTGACAC GTACAACTGG AGTATAAAGA CCAATGGGTG 660 ACAGCTTCAA ATCTATCCGC AGTCATCATC TTTCAAGCAT GAGAGGAATT CCAGGCATTT 720 GCAAACCCAC CCGGACTCAG GGAGTTTGCC CCCACAAGCC TGCTTAAGGG AAGGAATGAC 780 GGGACAACAC TGTCCACGAG AAAACAAAAG GCCCTGGAAT GAAGCCACAC AGCAGGCAGA 840 GGCCAGCAAA GCATGCACTG GAGTCCACAG GCGCTGATCG TAAACCAAAG AGCGCAGGGC 900 AGCCACGATC CCTGTTATCT GTGTCTCCTT AGCCCTCTCT CCCTCCCAAA CCCTCCTACA 960 ATAACAGGAA AGGAATTTTA AAAACTTCCC TCTAAAGGAG AAAAGCCCAC AAGAAAAAGA 1020 AAAAAAGCTG GGGAGGAGAC AACAGTAGAT GAGAGATTTT TTTTTTTTTT TTTTGGTGGG 1080 AGATCGAGTC TCTCTCTGTT GCCCAGGCCG GGCAAACCTT TGCCTCCTGG GTTCAAGTGA 1140 TTCTCCTGCC TAAGCCTCCT GAGTAGCTGG GATGACAGGT GTGTGCCACC ATGCCCAGCT 1200 AATTTTTGTA TTTTTAGTAG AGATGGGATT 1230
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