Tag | Content |
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EnhancerAtlas ID | HS184-26109 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:33784500-33785730 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:33784578-33784599 | CCTTTCTTTCTTTTTCTTTTT | + | 6.68 | ZNF263 | MA0528.1 | chr6:33785323-33785344 | TCCTCCTCAACCCCTTCCTTC | - | 6.71 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33656 | chr6:33784137-33785901 | H2171 |
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| 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 |
GH06I033816 | chr6 | 33784138 | 33785901 |
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Enhancer Sequence | TTCATATTCT AAGAAAGCCA CCCCCAGATC TGCCACCTCC ATCCCCACCT TTCCAGTCTC 60 TATCTTCAAC ATCCTTCTCC TTTCTTTCTT TTTCTTTTTT TTTTTTTTAT TTGCAGGGAA 120 TGGAAACGGG ACTTGTCAGA AACCTGCCTC CAGAATAAAG AGAAGAAGGG GAAATGTGAT 180 TAGGAGAGCT GTGAAGTGGT GATGACAGCA GCTGCTTAAT ATGGAAAAAG GAATCCTAAT 240 TATTGCTTGG ACAGGCAGGA AGTAAAAAGT CAATCAGAGC CAAGGTGGAG GGCAAACACG 300 CATGTCAGGG CGGGCTGCCC CTGCTAAGAA CCGCATGCCT TCTTGAGGTG GAGGAGCCTC 360 TGACTGAGAG GCAAGGAGAT GGTGAGCAAA GGAACTGGGC CAACCAGCCG CTCAGCCTGG 420 GGGAAACTGG TTCTCCTGAG GAACTGGCAG GGCTGAAGCA GAAGAGCTGC ATTCGTATTC 480 CAGCCAGAAG AGCAGGGGCT TTGGGAGAGT GTTAGGCAAT GCATCTGGCC TCAGGGGTCT 540 CAGTTTTCTC ATCGGTAGTG ACCCAGATGT GTCCGACTTC TCCGGTCTAT GGGGTCTGTG 600 ATTTTCAGGG CGACGATACT CTGAGCCCCT CCCATTCCCG CCATGTGGCA AGTCCAGTCT 660 TTTTCAGGTT TCCCTCCCAA GTAGTTCTAG GGATCCCTAA GGAATTCTTG CACATCTCCC 720 AAAATCCGTG GTGGCAGCTC TGCCAGCATC TCGCTCCCAC TGACAGCTGT TCCTGGTCTC 780 TGCCTGCCAT GTCTTCACTG TGGGCACTTT CAGGTCAATT CCTTCCTCCT CAACCCCTTC 840 CTTCCAAGCT GGGACACGGC CTAATTCCCT TAATTTGCAA AGTCTGGCAA AGACCAGGCT 900 CTGGGGTTTA AACAAGCTTT ACTTAGGGCT TAGCCAGTGT AAAGAAAAGT TGGCTGGCAG 960 GTGCCCTGAT CCTGCCTCCA CGGGCACCTC TCCAACCCTT CTCCCACTGG GTGGCTCTCA 1020 CTTTAGGTTG GACCGATACC AAGCGGCCAC TTACACCTTT AGTGAAAGCG CCTTTGGCCC 1080 TAACCCTGTG ACCCATGGTC CAGATCCCCA ACCTCTGCTG AGCTGAGAGA CAGAGAGAGA 1140 GAGGCCACAT TGCCTCCAAA ATCATGTGCT TCTCATCAAA TCCACTCTCT CCAGTCCAGA 1200 AGAGGAGTTT AGCTGCACTT TTACACAAAA 1230
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