| Tag | Content |
|---|
EnhancerAtlas ID | HS108-06725 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr11:1673720-1674860 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:1674092-1674111 | TGGCCACCAGGTGGCACTG | + | 9.43 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH11I001652 | chr11 | 1674021 | 1674190 | | GH11I001653 | chr11 | 1674261 | 1674430 |
| Enhancer Sequence | ACCGCCCAAA GCGTGCACTC TGTGGGCTGT TTAAAAAATT ATATGCGCAC AGACTCTAAA 60
GGAAAAACCA GAGACAAACC GCTCATATTC CATGAACCTT CCTTCTGCAT AAACCGCCAC 120
GTGTCGCTTG GCAAAGCCGT GGGCCTGGCA GTGGGGTTAG CCTTTCCCAC TCAGGAACCG 180
CGCTGGCCAC GTTTCTGCCG GCATCAGCGC CCCTGAGCTG CTTTCCAAAG CGCGGCGTCA 240
GGAACGTCAC TCTTCACTGT TGAATTCAAC GTGGGCACCT TTAATGGCTC AGTCATTTTT 300
TTAAAAAAAA TCAAAATTCC ACGCAGGGGC CTTGGTTCCA GAGCTCCCTT TCCAGGAGGC 360
TGTTGCGCGG GCTGGCCACC AGGTGGCACT GTTGCATAGC AAAAGGAACG CGGCTCCGCG 420
CTGGAGAACC GGGCCGGGCT GCGCGGAAGC CCTGGAGGGC CAGCCGGGTG GAGGGAGCTG 480
CAGGAGGGGG CGGCGTGCTT TCCGGGGGTG CAACTTGGTT TTCCCTGGAG GGATAAAGCT 540
CTCCTTTGGC AGGTGCCTGG GGGTGCCCTT TAAAGCAGGG AGCCCAGGGA AGACCCAGCT 600
CTCTTCCTGT GAGCTCATCC CTGGCATTCA GGGTGAAGGA CCTGCAGCCT GGTCTCGGAA 660
ACGGCCCTCC AAGGCCTCCT TGTCCCCTGA AGCACACAGG CAGACCGCGG GTCGGGGTGC 720
ACCGTGGCTG TCCCTTCCCT CCAATGCTGG GCGACCCGGG CGGGTGGCCA CCGCCTGACC 780
TGGGCCTCCT GGCTGCCAGC CTGCACGCCC TGGGTGCAGA GGCAGGCGAG CCTGGCCTGG 840
TCTGAACAGT CTTATGAGGA TTCTCTGGGC CCGTGTGCTC CCGCCTGCCC CTGAAGGGCG 900
TAGTGGAAGC ATCCGAACAT GCACTGGGTA CCCTCGTGGC CTGGGACAGC CCTTCCCTGC 960
TGGGCTCCTT GCTTTGTGTT AACCCTGAGG CCTGGGAGCC TGAGTTGGGG AAACGGGGGA 1020
CTCCAGACAA CACCCAGCTT GGATGCCGGC GTCCACTTCT GCTCAGAGAA TCCAGTCAAC 1080
TCAGGGCTTT GGGCTTTCCC ATGACCAAAG AAAAGAAGTC AGTGAATGAG AATCAAATAA 1140
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