Tag | Content |
---|
EnhancerAtlas ID | HS184-06979 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:129730520-129732620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr11:129731420-129731430 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr11:129731420-129731430 | GGCACGTGCC | - | 6.02 | RREB1 | MA0073.1 | chr11:129732499-129732519 | CCCCTAACCACCCAACAACT | + | 6.32 | TBX20 | MA0689.1 | chr11:129731007-129731018 | AAGGTGTGAAG | + | 6.32 | TBX21 | MA0690.1 | chr11:129731007-129731017 | AAGGTGTGAA | + | 6.02 |
|
| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_27353 | chr11:129731037-129732709 | Esophagus | SE_27846 | chr11:129730398-129732763 | Fetal_Intestine | SE_35121 | chr11:129730409-129733029 | HeLa | SE_36539 | chr11:129730682-129732779 | HMEC | SE_57651 | chr11:129732057-129732417 | VACO_503 | SE_64293 | chr11:129730399-129732758 | NHEK |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 129731556 | 129732597 | chr11 | 129731747 | 129732130 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I129860 | chr11 | 129730176 | 129732734 |
|
Enhancer Sequence | GGTGGCAAAG CCAGTCTTAT GACTCCAAAA CCAGGCATCT GTCTCACCAT TCTAACCCTG 60 CTACGTCACA CAAATCCAGG AGAGAGAATT TACATAAAGC ACTGCATGCG CTTTGGAAGA 120 AATGCTGTAC TTAATTAAGT GAAGGTAACC TCCCAGAGTT AGCCAGCCTT TCAGAGTTGA 180 AGTCACAGCT TAGGGATTCA AAATGAGCTA CTAAAAACAC TAATTTAGTT ATTAGAGAAC 240 TCCGGGTTCC ACTTTCAGGA TCCACCTTGG TTGGCCAGTG GAAAAACACA AGTATTCTTC 300 ATTCAACAAG TACTGAAGGA CCTATTATTG GCAATGAACG TAACATGTGT TCTTTCCTTG 360 GGGACTGCAG GTGGGCAGAA GGACCTGTTC AGTTTTACTT TCAAAGAAAA GATCCACATT 420 TGAGGTTTCT TTAAGTGTAC CATATTTTAA GAAAGAAAAT GTACTATTTT CTCCAGAGTG 480 AGGGGCTAAG GTGTGAAGAA CAGATATAAA ATATTAAAAT GTATTCAGAT GCCCTTCACA 540 CAGCAAGGCT TGTGATGCCT TCATGGAAGT GATCAACCCT ATCATAAACA TTGTTAGATG 600 TGGTATTAAA GTATAAACTG ATGACAGTAC TATTCTCCAC ATCCTGTCTT AGATATGTTT 660 TCTGAATAAT TTTACCCATA TCTGTCAACC AGAGGCTCAA TGGTTGCCAC CAGAAGTCCT 720 TTTGAAATTG TTCCCTACAA AACACCCACC ATGGCTGGGT GCAGTGGCTC ACGCCTGTAA 780 TCCCAGCACT TTGGGAGGCT GAGGCAGACA GATCACCTGA GGTGACAAGT TGGAGACCAG 840 CCTAGCCAAA ATGGTGAAAC CCCATTTCTA CCAAAAATAC AAAAATTAGC AGGGCGTGGT 900 GGCACGTGCC TGTGATTGAT CCCAACTACT CAGGAGGCTG AGGCAGGAGA ATCACTTGAA 960 CCCAGGAGGC GGAGGTTGCA GTGAGCTGAG ATCTTGCCGC TGCACTCCAG CCTGGGCTAC 1020 AGAGTGAGAC TCCATCTCAA AAACAAAAAC AAAAACAAAA CACTCACCAT AGCTGTGCCA 1080 TTCATCTATC AGAAACCTGA AGCCAGCATA TGAAGGAAGC AAGTGTGGCA CAAATCCTGG 1140 GCTGTCACCG TAAACAGCTC CAGTAGGAAG TTCCCATTCT CCGCTATTGC CATTCCACCC 1200 ACAGGCTGGA TAGTGCCGAA GTTACACTTC TGAGGAGTCA GCATCCTGAC GCAGCCTAAA 1260 CTTTACACTC ACTCCCTGCT CTCCAGAATG CACACGTCTG CCTGTGCAAA AACGACAAGC 1320 AGAGTCAGGT GACCTCAGCT AACAGGAATG TGGGCAGGGC TGCGGCTGAA TGCCAGAGCT 1380 ACTTTTATTA AATTCCTTGT TAAGTAAATT CAAAAGGGGT TTGTTTGTAG CTGGCAGTAA 1440 ATACCTAAGA CAAGATCTCT GGAATTTCTA CCTTTTTTTT TTTTTAATTT AAAAACTGTC 1500 ACATGGCTTT CTATGTGAAA TGTGATTCTT GAAAATAACA GATACGCAAA TATCAAAGGA 1560 TTATCAAACG CAGACACACT CGCCTTTCTC AGGTGGAAAG GCCCATTTCC CCGCACTGCA 1620 TCCTACCTCT CCCCACTGCC AACCTCATCC CGTGCCAGTC TACTTGCCCA TCACAAGCTC 1680 AACCTGGGAG GCCCATTCAC CTCTGCTCTC TGCAATGCAG GCCTCCCACC TCCTAAGACT 1740 GGATCGCCCC CAGGCTCGCC AGGATACATC ACAGCCCTCC TGCCCGGAGG AAGGCAACAG 1800 AGAGAGACTT GACTTAGAAT CAGAAGCTTC TCTTTAACTT CAACTCAGAC TCATGTCTTC 1860 CAACGGTTAA AGGGGAATGA TGACACTGAT TTTACAAAAT TGCTCTAAGA ATTAAACAAA 1920 ATGTCTGTGA AACAGCTGTG GAGCCAACCA GCCTCCCAGA CCCTCCTCCG CTTCGCAACC 1980 CCCTAACCAC CCAACAACTA AGCCAGGCTG CCTCCATCCC ACATCCTTCA GCTCCACCTC 2040 TTCAACCCAC AAGAGCTTCA ATACACTCCA AAAATTAAAG ATACTTTTTT TTTTTGAGAC 2100
|