| Tag | Content |
|---|
EnhancerAtlas ID | HS076-29050 | Organism | Homo sapiens | Tissue/cell | H1 | Coordinate | chr19:30348900-30350010 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:30349084-30349103 | TGGCCAGCAGGTGGCAGTT | + | 7.39 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I029858 | chr19 | 30349061 | 30349210 |
| Enhancer Sequence | GCTATGGTTT TTGTAACCTT GTTTTGGCAT TTTTTTTCTG ACTCGTCAAA GAATATTTCG 60
GCAACTTTGG AGTGGCCAGG CTTCCCTTTC CCATGCGCAG CAGGAAGTCC AGGTGGGAAT 120
GGGGAGAGGC TGGGAGATCC CTCAGGTCGG CGGCTTTCAG AGCTCTCCAG GCCACGCCTC 180
TCAGTGGCCA GCAGGTGGCA GTTCTGAGCC TTCCACCTGG CCACCCTCCT TCCTCCACCC 240
CCGGGGTGCC CGTCCCCCCA GTCCACATAC CACAGAGTCC CAGGTGGCTG GAGAGAGCTC 300
CTGGCTTCCA GGCCCTGGGC CATTCTGAGA AGCTGGATGA GGCAGCCTAG TGGCCATCCA 360
GCTGCCCCTG CCTGGGACTG CCTGCCTACC CCTTCCCATC CTTGGCTCCA TGCTAAAGGA 420
AGGTGGGCTT CCTGGAGGAG CTGACATCTT AAGTGAGACC TGCAGGACAA TAAAGGATTT 480
CAGGCAGAGG GAACGGAATA TGCCCAAATC CAGAGAATCC AGACCCTGTG CTTTCAGGAA 540
CTGGCAGGAG GCTGATGTGG CTAGAATGCA GACTGTTGGG CTTGGGAGAG GGACTAGGGA 600
GGCCAGGTAA TGCTTGGCAC TCTGGGAGCA GCAGGACCAG GGCAGCCCGA GTCTAGACAT 660
TATCTTGAGG GCAGTAAGGA GCCCTCAGCC CATTCTAACC CATCAGAGTT GGCCTCCGGA 720
AGGATCGCCA TGGCTGCAAA CTGCCTAGCC TCTCATCGCC CCTCACCCGC TGTCACTCAC 780
ACACCTGGGC CTCCTACCGT GCTGGCCAGG AAAGAGCTGC AAGTCCTCGG GCCCGAGGCT 840
CGGCAGGCAG CCGACCTACC TTGCAGTCCT CAGGAGAAGC TGTCCAGGAA CCCCACCCTC 900
CTGAGCTCCC GGGGCTTTGG TGGGGAAGGG AGCCTCCCAG GGTCCCGGAG CACTAAACAA 960
AAAGGAGCTG AAGGTCACCA CACTTTGGCC ATTTGCAGGG AGCCCTTCCC CACACAGGGG 1020
CGGCATGTTC CCTTGTGGCT GCCAGGGAGC CCCCAACACC CCTGGGAAGA TGGCAGGTCG 1080
AGGGGAGGGG ACATGGCCTG AAAACAAGGA 1110
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