| Tag | Content |
|---|
EnhancerAtlas ID | HS062-11233 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr3:47563050-47564600 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:47563757-47563776 | CACCCACCAGAGGGCAGCA | + | 6.56 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 47563624 | 47564338 | | chr3 | 47563747 | 47564357 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH03I047522 | chr3 | 47563492 | 47564091 |
| Enhancer Sequence | AAACAGCACG GGCCCTGCCA GCCCCAGTCC CCGCGCTGCT GCATGGACAC TATGGCTCCC 60
TGTGCCTCCC TGTCTCTCAG TTGATGACTT GCTGCCTCAT CAATAGGTTG TTGTCTGACA 120
CCTCTATCAT CTGTGACAAG AGGTTGTGTT TTTGTTTTGT TTTTTAATAA TAGAGATAAG 180
GGCCAGGTGT GGTGGCTCAC ACCTGTAATC CCAGCACTTG AGGAGGCTGA AGCAGGCGGA 240
TCACTTGAGG TCAGGAGTTC GAAACCAGCC TGGCCAACAT GGTGAAACCC CGTCTCTACT 300
AAAAATACAA AAATCAGCCA GGTGTGGTGG TGTGCGCCTG TAGTCCCAGC TACTCAAGAG 360
GCTAAGACAC GAGAATTGCT TGAACCTGGG GATTGAAGGT TGCAGTGAGC CAAAATCACG 420
CCACTGCACT CCAGCCTGGG CAACAGAGCA AGACTTCATC TCAAAAAAAA AAAATAATAA 480
TAATAATAAT AGTGATGGAG TTTTGCCATA TTGCCCAGGC TGGTCTCGAA CTCCTGGGCT 540
CAAGCGATCC TCCCATCTCA GCCTCCCAAA GTGCTGAGAT TACAGGTGTG AGCCACCACG 600
CCCAGTCTAG AGAGTTTTCA TACCACAAAG TTGAAGGTGA ACCTGTAGAA CCCATAAACT 660
GTTGACAAAA GAAAAAAGCG GGAAGCAGCC TTGGGTTATC TCCAGCACAC CCACCAGAGG 720
GCAGCAGACA CTGGCTAAAG CTCTTAGTCA TAAGTCCTGA GTGCTGGAAA CAGTTGCAAT 780
GGCCAGCACG TGGGCAGAGC TCACCGCAGA CAGTCCTCAG AGGTCGGAAT CTGCCGTGCA 840
TCTGGCAATC TCTCTGCTGC CCCTGCCCCA GCCTGCCCTT AGCTCATCTC TCTGGAGCCC 900
AGTGGTAGTC TTCATGGGCT CTCCTGCTTC AGGCTGTCCT GACTTAAGGA ATGTCCCCAC 960
TGCCCTCATC CCTTCACAGC TCCTCTGCAG ATCAGAGTGC AAGCCAGAGT CCTACAGTGG 1020
CCTCACAGCC CTGGCTGCTT GGAATCCTTA CCCGTTCCCC ACTCACTGTG GCACCACCAG 1080
GCTCCGCGCT GTTATTCCAG GCCTCAGAGA CGGGCACACT CAGGGGCCAT GTGCTTCTGT 1140
TCCCTTTGTT TATGAGCTAT TCCCCCAGGT GTCTGCAGAG CACGCTTCCT TGAACTCCTT 1200
CAGGCCTTCC CTGAGCACAC CCTTGTAAGT ACACACAGAC GGCACCACCA CATCCCTTTC 1260
AGCAGGACCC AGGGGAAGAG CAGTCACCAG ACACCCTCCA GCTCTCTGTT CCTGCAGGGC 1320
CCAGCACGGC TGCATACAGC CTCACCTGAG GTCACACCCT TCCTAAGGCA GCCTTCATCT 1380
GGTGACTGAG CAAAGCAGGG GCTATAAAGA ACTGGCCATT TCCATCTCAT GTGAGACTCT 1440
GTCCGACTGT CTAACTTCTC CAAGACTTTG TTGGGTGCCC ATCACTGTTC AAGTTCTCCT 1500
GCCCCATCCT GCTTCCGCCT CCTTCCTTCC ACAGGTGTTG GCCTCATATT 1550
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