| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08502 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr22:28422960-28424290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr22:28423285-28423296 | GTCTTTGTTTT | - | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I028026 | chr22 | 28422486 | 28427373 |
| Enhancer Sequence | CTGTAGTCCA GGATCCAGGA TGCAGTCAAA AGCCTGTCCT GTTCTTCTTC GTCTTTTCTA 60
CAGCAAATGT GATCTGCTGA CTGACCCAGG TCCAGTCACA TACACACATA TCATATATAC 120
ATACCACACA CAAACACACA CACACAAATA CAACCCTGCA CATACAAATA CATACATACA 180
TTCCCACAGA ACCTCCCCTG ACACACACAC AGACACTTAC ATGCATGTGC TGGCCTACCA 240
GTCCTCCGCG TCACTCCCAA AGGGTAGGGC TGCTGCTCTG CCCTCTGGGG CTCACACCAA 300
GGTCAGGGTG CTGGCCAAGA GAAGGGTCTT TGTTTTTCAT TCAATAGCAG TGCCTACCCT 360
GGGTTCAAAA TGCACATGTG TTTTCTGCCA ATAGGCAAGA AGAAAAATAG TGATTGCCGA 420
GACCTCAAAA ATGACAGCAG AACAAAGAGC AATTCCTGAA GTGGCAAGGG AGAAAAACCT 480
AAAGCCAAGT CTCACTTGAC TCGCATTAGC TACAGAGGCC TCATTGCCAA ATCAGTCCAG 540
CAAACCACCA AGGAACAAAG GGGCCAAGGA ATCCATAAAA TCACTGAGCT GGAGAGCCCC 600
CGGAGAGGGA AGCCCTTACT GCTCCAGTAC ACAAGGCCCT ACACACATGG TTGCTTCCAT 660
ATCACCTCTG TTGGCTCCAG GCTACAAGGA CTCTGCAAAC GCTAGCCACT ATCAGCAATC 720
TGCAGAAAAG CCACTTCTAG CCGCTCTGTT CAGTCACAAG CCAGTGCACT CTTAGCCCAG 780
ATCCCTGGCC ATACATGGGA CAGAGAGGGA GGCCTGGGAC CCCACAGCAG GGCAGGGACA 840
GGCTGGCAGG GAAGCTGCGA GGCATGTTTT GGCACCTGTT CATGGGCAGA TCTCCCTCCT 900
CTCTGGCCTA TGTGTGCTCA GCTATAAGAC ATGAGGCTGC ACTGAAAGTG CCAGGGAAGT 960
TTGCACTGTT CTAGCAAGGA TACCTTTGCC TCTGTGGTTC CCTCAGCTGT AGCTCCACTC 1020
TCTTGTGGAT GAAGGCCAGA ACCCCCCTTC CTGGCTTGTG AGAGAGGCGC CAGAGAACAC 1080
GCAGTGTTGC AAACTTTCCT GGGCCTTAAG GGCTTACCAC ATTGAAGCGA GAAGAACGCC 1140
GGCTATTTCC CTCATCCAAA GGGTCGGGGT TGGAAGAGTC TGCAGAGACC CCTTCAATTT 1200
CTTTGCTTTT CTGAGGGTGG GACTGGATTG GGTCAGGCCT TGCCAAGGGA GCTGGGTGCA 1260
AGCTCCGGGG CTGTGGGCCT TGCTGCTCCC CACTCAGTCC CCAGGGCTGG GCACAATACT 1320
CAGCCTGGCT 1330
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