Tag | Content |
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EnhancerAtlas ID | HS184-18068 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:34350300-34351050 |
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) |
EWSR1-FLI1 | MA0149.1 | chr20:34350572-34350590 | TCTTGCTTCCTTCATTTC | - | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 34350498 | 34350796 | chr20 | 34350494 | 34350600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I035762 | chr20 | 34350501 | 34350650 |
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Enhancer Sequence | AGCTATTTGG GATTCTCTTG GGATTAAGGA GAATCGCTCA AACTCGGGAG TTGGAGGTTG 60 CGGTGAGCTG AGATCACGCC ACTGCACTCC AGCCTAGGCA ACAAGAGCAA AACTCTATCT 120 CCAAAAAAAA AAAAAAAGAA GGAAAAGAAA TGTTGATAAT TAATGCTCTG CCACCCGGAC 180 CTCTGCGAAT CCCTTCTTGT CTGCTTACTG ACTCACCAAG ACCCTAAGGC TCTCTCTCCC 240 TTCACTGTCA CCCTACACTT ACAGATTTGA AATCTTGCTT CCTTCATTTC ACCCTCCCCA 300 GCCTAGTGCA TACTTCCCTT GGGCCTAAAA AGGTATCTGA AGTCCAATCT GAATTCCAAA 360 TTCCACACTC TAAATAGCAC CACTAAAGAA AGTCACTGGA GGAACAATTA TGGAAAAACA 420 GGCACTGACA GGTACTCTCA CGCCTTGTTC CATTTTCCCT GCTTTCCTTG ACTATGTCAT 480 TGTCCTATCC CCTCGCCCCA ACCCACGACT ACTTCACAAG CACCAAACTC TTTTCAGCCT 540 TTATTCTTTT TTTTTTTTTT TTTTTTTTTG GGGACAGAGT CTTGCCCTGT CGCTCAGGCT 600 GGAGTGCAAT GGCGACATCT CAGCTCACTG CAACCTCCGC CTCCCGGGTT CAAGCAGAGG 660 CTCCTGCCTT AGCCTCCCGA GTAGCTGGGA TTACAGGCGC GCACCACCAC CACCACACCC 720 GGCTAATTTT TTGTAACTTT AGTAGAGATG 750
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