| Tag | Content |
|---|
EnhancerAtlas ID | HS098-50738 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr6:161351430-161352580 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:161351886-161351905 | AGGCCGGCAGGGGGCGGCA | + | 6.48 | | Crx | MA0467.1 | chr6:161351430-161351441 | AAGGGGATTAG | + | 6.32 | | TCF3 | MA0522.2 | chr6:161352563-161352573 | AACACCTGCT | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGGGGATTA GTTTTAGTTG CAAAGTGAAC AACAAGTAGG CAACAAATTA GCTCTTCCAA 60
CATTTTCTTC TCCTGAAAAG GCTCTTTGAA AGCCCTGTTT TGCAGAAACT TGCTCCTTTT 120
GCATGACGGG TAAATCGTAG GAGACCTGGT AGATTATGCT ACAAACTTAA TGTGGAAAGG 180
TTGCTTCATC CAAGATCCTG GAGTTTTCGT AGACATTGTC CTGATACTTC CCCTTGGGCA 240
ATACCAGCGC CTGCAGGCAA CAGCTCTGAC GCACTTAAGA CTTAAATACT ACCCACAGAA 300
GTGCTGGCTT GGCTGGGAAA ACCTTTTGCT AAATAGAAGA ACAACATTTT TTTTTCTTTT 360
CTGGAATTTG CAAACAGCAT TTATTCTCAG CCTTGCCTTC CAAACGTTCC AATTGGACAT 420
TGCTGGGCAG CGTGGAAGCA GAAGCGAACG TCACCCAGGC CGGCAGGGGG CGGCACACCC 480
CACACTTCGC TGCGCGCCCT CGCCTCCTTG GGAGGGAGTG TCCAGCTCCC AAAACCTGTC 540
GTGGGTTTTG TCCCAAGTGA CTTCAGCCAG CAGATGGTTC AAGTCCTGAG GCTGCAAAAT 600
TCGGGGTGGA AGGAGTGGGG CGTAAGGCTG AGAGTGGGGA GAGCAATCCA GGGGCGCCAG 660
GGTGGGAGCC GCAGCGGGCC CGCGGCCGCC CGGAGGACAC TGATGCTTCT GGAGCTCGCG 720
AAGGGTCCCC CGCGGGAGAG GAACAAGGCC GCTTGCGCTC CGCAGAGGCG CAGGCACGGG 780
GCTGGGGCCC GGGGCGGGGG CGCGGGTGGG CGGACCCCTC CCGCAAGCCC ATGATGGCCA 840
GGCCAAGGCC GCTGGGAAAG GCAGGACGCT CGCCCATGCG CTGCCAGCTG GGCTTTTCTC 900
CTTCGCCCGC CCTGTGTTCC AGGGCGCGAC CCCGTTCGGT CCAGCCGCTG GCTCCGGGGC 960
TGAACCCCAG GTAGGTGGGT CGGAGCCCCT GAGAGAACTG GGGCTTGAGG GCGTTTCTGC 1020
TTCCAAGCGC AAGCACGGGG AGCCCTGATG CTCCAGCCCC TGGACACTGG ATTGGAAACT 1080
GGCAAGGGTA GGAGATGTTT TGCAGGAGGC CGCCCTCTGT CTTCCTCTGT TCTAACACCT 1140
GCTGGACACA 1150
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