| Tag | Content |
|---|
EnhancerAtlas ID | HS041-05158 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr12:54042400-54043390 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr12:54043001-54043016 | AGAGTCCAAAGGCCA | + | 7.58 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 54042797 | 54043102 | | chr12 | 54042838 | 54043000 |
| Enhancer Sequence | AGTCAGGGTT CTCCAGAGGG ATAGAACCAA TAAGCCATAT GTATATATAA AAGAAGTTTA 60
TTGGCTGGGC ACGGTGGCTC ACAACTGTAA TCCTAGCACT TTGGGAGGCC AAAGCGGGCA 120
GATCACTTGA GATCAGGAGT TTGAAACCAG CCTGGACAAC ATGGTGAAAC CCCGTGTCTA 180
CTAAAAATAC AAAAAAGTAG ACAGGCGTGG TGGCGGGCGC CTGTAATCCC AGCTACTTGG 240
GAGGCTGAGG CAGGAGAGTT GCTTGAACCT GCGAGGTGGA GGTTGCAGTG AGCTGAGATC 300
TGGGAGGTGG AGGTTGCAGT GAGCCGAGAT CGTGCCTCTG CACTCCAGCC TGGGCAACAG 360
AGCTAGACTC TGCCTCAAAA AAAAAACAAA AAAAACAAAA AAAAAGTTTA TTAGGGAGAA 420
TTGGCTCACA TGATCACAAG GCAAAGTCCC ACAATGGGCC ATCTGCCAGC TGGGGAAAGA 480
GAAGCCGGTA GTGTGGCTCA GTCCAAGTCT GAAAGCCTCA AAACTAGGGA AGCCAACAGT 540
GCAGCCCTCA GTCTGAGGCC AAAGGCCCGA GAGCCCCCGG GAGGCCGCTG GTGCAAGTCC 600
CAGAGTCCAA AGGCCAAATA ACCTGCAGTC TGACATCCAA GGGCAGGAGG AGAGGAAGCA 660
AGTGTCCAAC ATAGGAAGAG AGAGACAGCC AGAAGACTCA GCAAGAGGCT GGGCATGGTG 720
GTTCATGCCT ATAATCCCAG CACTTTGGGA GGCTGAGGTG GGTGGATCAT TTGAGGTCAG 780
GAGGCTGAGA CCAGCCTAGC CAAGATGGTG AAACCCTGTC TCTACTAAAA ACATACAAAA 840
ATTAGCCGGG TGTGGTGGCA TGCACCTGTA GTCTCAGCTA CTGCGGAGAC TGAGGCAGGA 900
GAATCGGTTG AACCCAGGAG GCGGAGGTTG CAGTGAGCAG AGACTGCACC ACTGCACTCC 960
AGCCTGGGCA GTAGGGCAAG ACTCTTTCTC 990
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