Tag | Content |
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EnhancerAtlas ID | HS197-05988 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr13:49921750-49923240 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr13:49922007-49922025 | CCTTCCTTCCTTCCCTCA | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr13:49922003-49922021 | TTTTCCTTCCTTCCTTCC | - | 9.07 | TFAP2A | MA0003.3 | chr13:49922301-49922312 | TGCCTGAGGCT | - | 6.32 | ZNF263 | MA0528.1 | chr13:49921982-49922003 | TTCCCAAGCCCTTCCTCCTTC | - | 6.28 | ZNF263 | MA0528.1 | chr13:49921995-49922016 | CCTCCTTCTTTTCCTTCCTTC | - | 6.3 | ZNF263 | MA0528.1 | chr13:49921991-49922012 | CCTTCCTCCTTCTTTTCCTTC | - | 6.67 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I049348 | chr13 | 49922693 | 49923230 |
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Enhancer Sequence | GAAATGGAAT CATCCTTTGT ATTTAATGTC ATTCTTCATG TTGGATGCAA CCGAGGCCTA 60 TCTCACCACT AGCTCTAGAT CCACCTTTTG AGGGGATCAT CTCTAGCCGC TGTACAATTT 120 TTGTCTTCCG GGGTGAGAAA CAGCCACTCC TGGGATTTCC AACACTCGGA GCCCGGAGCC 180 ATGCTGCCCT CACCGCCCCT CCCTTCACCC AGCAGTCACT TCCAGGAGTC TGTTCCCAAG 240 CCCTTCCTCC TTCTTTTCCT TCCTTCCTTC CCTCACTCGG CTGTTCTCCC GAGATTTCAG 300 TTTCCTTACT CCAAGCTTCC CATTCTTCAT ACTCCGCCTC TCGTTAACTC CCCTTCTTCC 360 CTTCCCCTTC TTTTCCTTGC CCTTTTCTGT CTACCCAGAC CTCCCCTGTG GGCTCCTCCT 420 CTCTTCCCTG TTTTCTTCAG GGAGACCATA GGACGCTGGC AGGCTGAATG GAGGCCTGTG 480 GACACCCGAG CAGGCTGCAA ACTCCTTCCC TTCAAACCCG GACGCTAGAG GCCTTGTGTT 540 TGTTGCAGTT TTGCCTGAGG CTTTGGGGAA ATGATGGCAT TGCGGTTCCT TTCCTCTGAT 600 GTCTCGGGCA ATTCAGTGCT TGTCCGAAAC CCGCACACCC TCCTGCTTAC GACAACAAAA 660 GTGCCACAGT GGCCGGGCGC AGTGACTCAC ACCTGTAATC CTGGCACTTT GCAGGGGCCA 720 AGGCAGGCGG ATGGCTTGAG GTCAGGAGTT CGAGACCAGC CTGGCCAACA TGGCAAAACC 780 CCCTCTCTAC TAAAAATGCA AAAATTAGCC GAGCATGGTG GTATGCGCCC GTGGTCCCAG 840 CTACCTGGGA GGCTGAGGTG GGAGGATCAC CTGAGCCTGG GAGGCTGAGG CTGCAATGAG 900 CTGAGATTGC ACCACTGCAC TCCAGCCTAG GTGAGGGAGT GAGACCTTGT CTCAAAAAGT 960 GCTGCAGTTA ACTGGGCTTA CCCTGCTCCT AGGCAGCTGT TAACAACCAG CTGCTGTTGC 1020 TTAAGCCTGC CCTGGAATCC ACCCCCAGCC CACCCCAAGT GGCTTCCAAA TATTCCCATC 1080 ATTCTCAAAC AGTATTCTCC CTCCAGAGTT CTTGTCAATT AAATTTTCCT TTGCATCCTG 1140 TATTTCCAGA GATGGCCTGG TTGCCTTTAT AGATCGTGTG CCAGGCAGCT GCCAGGACTT 1200 GCCTCCCGCT TAACCACCCA CCACTCTTTG GTCTTCTCCA TCACAACAAA TCTCTCTGAC 1260 GGCCCAGCCT GCAGGCTCCG CCTCCAGGGA GACCACGCCC CGTCCCTCAC CCTCCGCCAG 1320 GCATTCTTCT CCCTAAGTCC CAGCTTCCTT CTGCCCCACT GACATCTCCT ACCCTTTACC 1380 ACTCTCTGAC ACTCTCTCAC ACTTTGTGTC ACCATGTGAC CTAATATACC TTTCAACAGA 1440 TTTATGGCAC CTTCTCAGAA CAGGCTGGGT AACTTCCTAG TCTGCAGATA 1490
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