Tag | Content |
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EnhancerAtlas ID | HS184-15722 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr19:49600270-49601510 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:49601242-49601261 | TGTCCAGTAGGTGGCAGTG | + | 7.37 |
| | 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 |
GH19I049097 | chr19 | 49600707 | 49601810 |
| Enhancer Sequence | CAGCTGCTTG AGAAGCTGAG GCAGGAGAAT TGCTTGAACC TCGGAGGCAG AGGTTGCAGT 60 GAGACGAGAT TGCGCCATTG CACTTTAAGC CTGGGCAACA GAGCAAGACT CTGTTTAAAA 120 AAAAAAAAAA TCTGAGACTT TATTTCTCTA GCTTCTGGCA ACACCCACAC TGTCTTCCTG 180 AAAAGGTAGC ACCCGAGGGT TCGGGGAAGG AGCCTGGTAG TTCAAGTGCC CGGGGTGAGA 240 GGTGAAGTCT GCCTTGGCCC TTCGCCACTT TAACACCTCC CTTTTTCTGT GTCTCGAGTT 300 TGTTCTGTTT TACTTCCATT TGCAAAATAG TAATAAATAA ATATCAGTGT CCAGCACTGT 360 GTCTGGGCCA TAGTACGTGT TCAGTAAATT ATATGTCTAA TGTTCCATTA TTGGAACGCT 420 AAGCATGTGG GAGTTATTTA TATCCTACTG CTCGGGTCAT CACCAGGGTC TGATTTTTCA 480 CACGTGTCTG CAATTCAAAA AATTGCAACC TCTGGCATAA ATGGGTTAAT GTTATTCCTT 540 TTCTCATGCT CTCCCAGAAT GTGACAGGGC TTCCGAGGGA AACACTATAC CATGGAAGAA 600 CCGGCAGAGT GTCCTTAAGG CCCCGGCAGG AGTCAGGGTC ATTATGTGCT GGAGCCACCA 660 TATTTGGTGA AAAGGACTTA TTCCCAGGCC TGACCCAGCA GGATCACCTA TGAAATTGGT 720 TTCTTAGGAG ATTCCTGGCT CTTTTCTTTG GAGATTGTTA TTCCTTAGTA GCCAGGTAGA 780 ACAGTTTGCC TCACAGTAGT GAGGCTGGAG TGAGAATCTG ATCTGACGCT AGTCAGTTCC 840 TGGGTTCCTT TTTAGAGACA CAGGGCACAG ACAGGAAAGC AGAGCTTACT TAGTGTTTGC 900 TTTCCTGGCT CTCATTCTTA GCCTTGGGGC AGCTTGGTCT CAGGTTTTCC TGTGGGCTGT 960 AGTTGCAGTC TGTGTCCAGT AGGTGGCAGT GTGGCCCTGC CTACAGGAGG GAGCTCAGAA 1020 CCTGGGGGCA TCAGCTGCAT CTCCAGGGAG GCCCAGTTGG GCTATTACTG TTTGGATCAC 1080 CTTGCATCTG GGAGCGATAG GGCCCTTAGG GTTTATGTAG GTCTGAAATG GCAGTTGGGC 1140 CTGCCCACAT CCTGTCAGCT TGAAGTCAGC CTTACCTCCT CTCCTCAGCA GCCTGGATTA 1200 TCTCTCAGCC ACTCTGATAA AGCCCACTGT GCCTCAGAGA 1240
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