Tag | Content |
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EnhancerAtlas ID | HS184-06683 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:118145560-118146330 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:118145734-118145752 | AGTGCCTTCCTTCCCTCC | - | 6.14 | IRF1 | MA0050.2 | chr11:118146308-118146329 | ATTTTCTTTCTTTTTTTATTT | + | 6.15 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35154 | chr11:118143808-118149545 | HeLa |
|
| 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 |
GH11I118273 | chr11 | 118143774 | 118149113 |
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Enhancer Sequence | GTCACCAGGC TAGTGATATA GTCAGACTCA CAACAAGACC TGCCTAACTC ACAGGTCAAC 60 TCCAGAGACA ACTTCAACTC CTCCTTCAAC ATCAGTCTCC CTTCCTCATT AGAATCTACC 120 AAACACGTCA ACAGTCAACT CTCAGTTGTA TGTACCAACC ACTCTTTGAC CAGTAGTGCC 180 TTCCTTCCCT CCCCAGAACT GCACCTCCAC CATTCTGGAA GACTTTTGAA GCAAAAGCAA 240 ATGAAATAAA CAGTAGGCAT CCTTTTCTCA GCATCTCTCC TGAAAGAAAA AGTCGAAGGG 300 AAAATACTTG GAATTTTTGC CTACAATGAG GTTAGGACTG TGCAAAATCT CATTTTGTTC 360 CGTTTGCCTC CTATTACTTT AAAAAAATAG TTTTGAGCAA CTACCAAGTG TCAGGCACCA 420 TCCTCAGGAA TTCAAGGGTG AAAATGATAA GATCTTAGCC CTCAAGGAGC TCTCAGGTTA 480 AAGAAAAAGA AAATTAGTCA CAATACAGGG TGACGTCAAT AATAAAGGAA ATGCCAAGTT 540 CAAATGATAG CACAGGAAGA ACAAGCTCTG CCTGGAAGCA TGAGGGAAGC TGTCTCTGAA 600 AAGGCTAACC ATACATGGCA TCCTTTAGCC AAGACCCGAT GACAAAAGAA CAGGGGGGCT 660 GGGTTAGGGT GAAATAGCAT GGCTCACACA AGAGCTTCAA GTCAGAGGCC AGCTTGTGGG 720 AATCGCAATA ACTACCATTT GTTAAATAAT TTTCTTTCTT TTTTTATTTT 770
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