Tag | Content |
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EnhancerAtlas ID | HS184-15892 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:9937650-9938620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:9937896-9937914 | CCTTTATTCCTTCCCTCC | - | 6.56 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26755 | chr2:9937112-9944172 | Esophagus |
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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 |
GH02I009797 | chr2 | 9937341 | 9944100 |
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Enhancer Sequence | GCTATATGAC TTGCAGATAT TTAGACTTAG AGTAGGTGGG CCTCCAATTC TACTCTTGCC 60 TCAGCACCTG GAAGTATTAG GGTAAGGTCT GCAAAGTACC CATTTCTCTG AAAACACCCA 120 GCTCAGGAAT TGGTACAGGG AGTCCCCTTT CTGGAAGGCC CTCCCCCACG TCTGCCTGGC 180 CTATCCGGTT CTTCCCTCAA GTTTCAGCCC AGATTCTGAC TCTTCCGAGC AGACAGGCCC 240 CCGTGGCCTT TATTCCTTCC CTCCCAGCAC TGTCTGGCCA GCATGTGCGG TCGCGTGAAG 300 ACCTGCTAAC AGCAGGAGCT GGGGACTCCC TGAAGGCGCT GACCTCGGCC GACTCCCCCA 360 AGAATTCCCA GACCCTGGCA CGGGTGCCGG CACATGTGCT GCCCAGGGCA GGCTCGGTGG 420 ACACATCTAC AGTTCATTCT CCCACTTTAG TCCATTTGCT TAAGACACCC TTCCCTGGCA 480 ATCGGTAAGG TGCACACATA CTGCCTGGGG CTCTCATTAA ACTGCAGATT CCAGTTCTGT 540 AGGTCTGGGA GGGGCCTATG ATTGTGCAGT TCTAACCAGC TCCCAGGTGA GGCCAATGCT 600 GCTGGCTCAG GGACCACACT TTTCACAGTG AAGCTTTAGA GCTCATTATC TTCCAGGAAG 660 ACAAATGCAA TACAGGTGTT GCCTGTAGCC AATGCTTCAG CAAATGCTAT GGATGCTGCG 720 ACTCTGAAAC TGGCTGCACC TGCCCAGCAG TCCTGTGAGA GAGTCTGTTA ATAAGTAGCA 780 AAGTAGACTC CTCACTGAGG AGGGCAGTTC AGGGACTCGG AAGTCAGGGA TGCCCAGAAG 840 GTACACAAGG GGGCTGGGAA TCCAGGCTGC AACCTCTAGG CCCAGAGGCC TGGGTGCCAG 900 GCTCAACACA GTTGCTGCTC GCCCAGTGAC CTCACGTGAG ACACCTCCTC TCTCTGGGCC 960 TCTGCACCTA 970
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