Tag | Content |
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EnhancerAtlas ID | HS041-14557 | Organism | Homo sapiens | Tissue/cell | EWS502 | Coordinate | chr3:41411800-41413070 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr3:41412496-41412512 | CACAGTGTAAACAAAG | + | 6 | RELA | MA0107.1 | chr3:41412161-41412171 | GGAAATTCCC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGAGACTAT CACTTTATGA TAAATAAGTG TTTAGTGGGG ATTACCAGGC AAGATGGCCA 60 AATAGGAGCA GCTCTGGTCT GCAGCTCCCA GCAAGACCAA CCCAGAAGGT GGGTGATTTC 120 TACATTTCCA ACTGAGGTAC TCAGCTCATC TCACTGGGAC TGGTTAACTG GTTAGACAGT 180 GCGTACAGCC CACGGAGCAC AAGCCAAAGC AGGGTGGGGC ATTGCCTCAC CCAGGAAGGG 240 CAAGGGGTTG GGGAACTTCC TACCCTAGCC AAGGGAAGCC ATGAGGGACT GTGCCACGAG 300 CGACGGAGCT ATTCGGCCCA GATACTATGC TTTCCCCATG GTCTTTGCAA CTTGCAGACC 360 AGGAAATTCC CGCAGGTGCC TACACCACAA AAGCCCTGGG TTTCATGCAC AAAACTGGGT 420 GGCCAAGCTA GCTGCAGGAG TATTTTTCCA AACCCCAGTG GCGCCTGGAA CGTCAGCATG 480 AAAGAACTGT TCACTACCCT GAAAAGGGGG CTGAAGCCAG GGAGCCAAGT GGTCTTGCTC 540 AGCGGATTCT ACCCCCATGG AGCCCAGCAA GCTAAGATCC ACTGGCTTGA AATTCTTACT 600 GACAGCACAG CAATCTGAAG CTGATCCTGG ATGCTCGAGC TTGGTGGGGG GAGGGGCGTA 660 CACCATTACT GAGGCTTGAG TAGGTGGTTT TCCCTTCACA GTGTAAACAA AGCTGCCTGG 720 AAGTTTGAAC TGGGCAGAGC CCACCGCAGC TCAGCAAGGC CACTGTGGTC AGACTGCCTC 780 TCTAGATTCC TCCACTCTGG GCAGGGCATC TCTGAAAGAA AGGCAGCAGC TCCAGTCAGG 840 GTACTGTAGA TCAAACTCCC ATCTCCCTAG GACAGAGCAA CTCGGGGAAG GGGCGGCTGT 900 GGGCACAGCT TCAGCAGACT TAAATGTTCC TGCTTGCTGG GTCTGAAGAG AGCAGCGGTT 960 CTCTCAGCAC AGTGCTCAAG CTCTGCTAAC AGATGGTCTG CCTCCTCAAG TGGGTCCCTG 1020 ACCCCCGTGC CTCCTGATGG GGAGATACCT CATGGCAGGA GTCGACAGAC ACCTCACACA 1080 GGAGAGCTCC AGCTGACATC TGGCAGCTGC CCCTCTGGGA AAAAGCTTCT GAGGAAGGAG 1140 CAGGCAGCAA TCTTTGCTGT TCTGCAGCCT CTGCTGGTGA TACCCAGGCA AACAGGGTCT 1200 GAAGTGGACC CCCAGCAAAC TCCTGCTGAC GAGCAGAAGA GAAGCCTGAC TGTTAAAAGA 1260 AAAACTAACA 1270
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