Tag | Content |
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EnhancerAtlas ID | HS184-05898 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr11:70079180-70080520 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:70079305-70079323 | CCTTTATTCCTTCCTTCT | - | 6.47 |
| | 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 |
GH11I070232 | chr11 | 70079005 | 70080718 |
| Enhancer Sequence | ATTTCCCAAC CTCCCCTGCA GCCAGGTGTG GCCCTTTGAC TAAGTTCTGC ATATGTGCAG 60 AAATGGAGTG TGGAACTTCC TAAAAACAGC CTTAAAGGAG GGAGAGGATT GTGCCCTTCA 120 GCATCCCTTT ATTCCTTCCT TCTGCCTGGA ATGCAAGCAT GATAGCTGGA GCACAGGCAG 180 CTATATTGGG TCATGAGGAA GCAATGCAGC AGGATAGAAG GATCCTGGGT TCTTAAAGAT 240 TACAGAGCCT CCCTGCTAGC CCTAGAAAGC TTACATCAGG GTTGCCTTTG TATGAGAAAA 300 ATAAACCCTC ATTGAAGTCA CTGTGATTTG GAGACTTCAG ACACTTACAC AAAGCTAACC 360 TTGATTGAAA CACAGTATCA CTTGGAATAA TCAGGAGGTG GCTATGAAAA GGAATGCAAT 420 AAAAAAGTGA CATTCTGAAA CTCGTCATAC ACTCCACTGC CTTCCAGGCT CTGAAACTGA 480 GGGCTACTCA CTTTGTTTAA GAAGACATTA GTCATCACTA GCCCGAGATG AAATCTCACT 540 TTGTTCAGAG GGACTGACCG ATTGTTGAAA AGGGAAAGAC GTTCTCACCG TGTGACTCAA 600 CACTGTTCAG TGCCAAGTTC CTCACCTCAC CATTAACTGG AGTCATTGAC TGTCTACACC 660 TGCAGGCTGA ACGCACCGCC CCAGGATGAA GTGTGAGTCC TCGGCATCCC AGGGAGGTTA 720 GTGTCCTCCT GCGAAGCTCC AGCCTTGGGG AGTGCCTCCA CGTCCAGGCT GGAGCCACCT 780 CCCTACTCCC TCTCCCCAGG GCCTGGCACG GTCAGCCATC ATGAGTGTCC CAGCTAGAGT 840 CAACCAGCAG ATGATGTTTA GTGCCTCTCT GTGCCTTCAG AAATGCTTCC CACCCTCAGG 900 AATTCCAATG CCTGCTTCTC TCTCCTGCTA CACTCCTACT CATTGCCCAT CTCTGCGTAG 960 ATGCCCCAGC GGATCACCGT TCAGTCGACA TTTACCAGGC ACTCCCTGTT CGGGGGTGAG 1020 TGTTGGCTAT GGAGTTAGCC GCCAGGAGCC TGCCTCCTGC TGACTGGGCG ATCTGGGCAA 1080 GTTATTTAGC TTCTCCGCCT CAGTCCTTCC TATCTGTAAA ATGGGGATAG GAATGGCACC 1140 TTCCTCAAGG GTGTTGGTGA GGGTTAGACC AGTCGATATG CTAAGTGCTT AGAACACATT 1200 AACCCCCTGG GACATCTCAG GTGCTGCTGT TGTCTGTCAG GCTAGGAGGC TAAGGGATCT 1260 GCTTTCATGG GGGGGATGGA GTGACCTTCT AGAACCTGCT GCAGATAGAG CTTCAGCTTC 1320 ACCCTCTGTA TTAAGCATGC 1340
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