Tag | Content |
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EnhancerAtlas ID | HS095-32584 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chrX:128756490-128757640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chrX:128756720-128756738 | GGAAGGAAGCAAGGAGTA | + | 6.44 | EWSR1-FLI1 | MA0149.1 | chrX:128756716-128756734 | AGAGGGAAGGAAGCAAGG | + | 6.84 |
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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 |
GH0XI129621 | chrX | 128755831 | 128758281 |
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Enhancer Sequence | GGAGGCTGAG GCAGGAGGAT TGCTTGAACC AGGAGGTCGA GGCTGCAGTG AGCCATGATC 60 GCACTACTGC ATTCCATTCT GGGTGACAGA GAGAGACCCT GTCTGTAAAA ACAAAAACAG 120 AAAAAAAGAC AATGGCCTTA ATCTCCCCCT GCTTTCCCTA GGCCTAAAAG GTACCCTGCC 180 TTTTAGGCAG GGTGAATCGG GTGGGGGCTG CCTGCCTTCC TCAGAGAGAG GGAAGGAAGC 240 AAGGAGTAGG GGGTCTGACT GGGGCCCTAC AGCTCCCAAC CTCAAGACCT GCCTTTTGAG 300 GCCATAGAGA AGCTGCAGCT TTGCTTTTGC AGCTGCAGCG GCAGTGAAGA AAGCAGGAGG 360 GCATCCTGAG GCGGGAAATG CCTGTCAGTG TCATCCCCAG CTGCTTCCGG CTTCCTCCTT 420 CAAGGATTCC AGGGGCTCCT CTGTAACCTT GCCAACCCCT CTCCCCTGCC CCAGGTTCTG 480 GCAGGCAGCT GTGCGCCCCC CCTCAGGGCC CACGTCACAA GTCCTCAGAG GGGCTGTCAA 540 CTCCCCATTG TTCTCGGGGC TTCTGGGGCT TCTCCGGCAT TCCTTTGGCT CATGAGGGGA 600 AATGCCTGAA GCTTCGTCTT CACCTCTTCA GATGCTTGAC CTAATAGTCA CCCGGCCCTC 660 CTGGCCCCTC AAGGGATGCT GTGGTGCGTG GGAGAATCTG GCTAGGCTAG CACTACAAGT 720 ACACTTACCT CAGGTCAAAG ATGAAATCTG AGGGGGTACC TAGGCCTCTG TGTCTTGAAC 780 TCACCTTGAA GGCCCCAGCC AAGTATTTCC CCCTCTCCCT CCTGAGTATT GCACACAGCT 840 ACCCGCAGAG TTACATAAAC ACAGCCATAC TCCTCCATTC CAAATTCTAC CCATTCCACA 900 CAGTTCTGTA CATGCTCTCA CATGCACACT CCCACCCAAC CCATCTTTCC AGGGGAGCCA 960 TCAGGTGTGT CAGGGCCAGA AGCTACTTTT GCTGTGGGTA CAGGACTGAC ATTCTTCCAG 1020 GAAGCCTCCC CTGACTGACA GGCAAAACTT CCTGGGTAGA AGCTGACCCC AGTCCCCATC 1080 TACTATTTAA AATATGGTGG GTAGGGAAGG TTTTACTGGA GAAGGTGATG TTTAAAGCAA 1140 ATACTAAAGG 1150
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