Tag | Content |
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EnhancerAtlas ID | HS110-04264 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr6:142290230-142291320 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:142290309-142290327 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr6:142290313-142290331 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr6:142290317-142290335 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr6:142290321-142290339 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr6:142290325-142290343 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr6:142290333-142290351 | GGAAGGAAGGGAGGGAAG | + | 7.46 | EWSR1-FLI1 | MA0149.1 | chr6:142290305-142290323 | AGATGGAAGGAAGGAAGG | + | 7.69 | EWSR1-FLI1 | MA0149.1 | chr6:142290301-142290319 | GGAAAGATGGAAGGAAGG | + | 7.91 | EWSR1-FLI1 | MA0149.1 | chr6:142290329-142290347 | GGAAGGAAGGAAGGGAGG | + | 9.42 | FOXA1 | MA0148.4 | chr6:142291126-142291142 | GCTTAGGTAAACAAAG | + | 6.31 | NR2F1 | MA0017.2 | chr6:142290372-142290385 | CAGAGGTCACAAG | + | 6 | ZNF263 | MA0528.1 | chr6:142290230-142290251 | GGGGGAGGACCAAGAGGTGGA | + | 6.06 | ZNF263 | MA0528.1 | chr6:142290335-142290356 | AAGGAAGGGAGGGAAGGAGGA | + | 6.12 | ZNF263 | MA0528.1 | chr6:142290233-142290254 | GGAGGACCAAGAGGTGGAGGA | + | 6.69 | ZNF263 | MA0528.1 | chr6:142290330-142290351 | GAAGGAAGGAAGGGAGGGAAG | + | 6.71 | ZNF263 | MA0528.1 | chr6:142290326-142290347 | GAAGGAAGGAAGGAAGGGAGG | + | 6.76 | ZNF263 | MA0528.1 | chr6:142290334-142290355 | GAAGGAAGGGAGGGAAGGAGG | + | 6.86 | ZNF263 | MA0528.1 | chr6:142290310-142290331 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr6:142290314-142290335 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr6:142290318-142290339 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr6:142290322-142290343 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 |
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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 |
GH06I141969 | chr6 | 142290502 | 142290595 |
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Enhancer Sequence | GGGGGAGGAC CAAGAGGTGG AGGAAAAGTA GGTGGCAGGG GAATGCAGCA ATGATTGAGG 60 AGAAAAAAAT GGGAAAGATG GAAGGAAGGA AGGAAGGAAG GAAGGAAGGA AGGGAGGGAA 120 GGAGGATTGC CAGCCATCAT TCCAGAGGTC ACAAGATACG CTACTTCCCC AATTACTCCG 180 GCAGAATACA TCACTATTAC AAAACCTAAA ATTGGCTTTT GAGATATCTT TTCAGATTTT 240 TTGCATGCCT GATACATATG ATGACTCAAC CTGGACCCAC CCGCTGCTTC TGAGGCCCCA 300 CCCAGGAGTA ATTCAGAGCA AAGGAGAATC ATTTCCCATA CTCCTATGAT TGCACCCCCC 360 AACCAAACAG CAACAAGCAT CCATTGTCTA GCCATCCCCA CCCCGTTCCA CAAACTACCT 420 TTGAAAAACC CCTTGAGGGT AGAGCCAAGA TAGCCGAATA GGAACAGCTC CAGTCTACAG 480 CTCCCAGCAT GAGCGATGCA GAAGTCGGGT ATTTCTGCAT TTCCATCTGA GGTACCGGGT 540 TCATCTCACT AGGGAGTGCC AGACAGTGGG CGCAGGACAG TGGGTGCAGC ACACCGTGCG 600 CGAGCCGAAG CAGGGCGAGG CATTGCCTCA CTCGGGAAGC GCAAGGGGTC AGGGAGTTCC 660 CTTTCCTAGT CAAATAAAGG GGTGACAGAC GGCACCTGGA AAATCGGGTC ACTCCCACCC 720 CAATACTGAG CTTTTCCAAC GGGCTTAAAA AACGGCGCAC CAGGAGATTA TACGCCACAC 780 ATGGCTCGGA GGGTCCTACG CCCACAGAGT CTCACTCATT GCTAGCACAG CAGTCTGAGA 840 TCAAACTGCA AGGCGGCAGC GAGCCTGGGG GAGGGGTGCC CGCCATTGCC CAGCTTGCTT 900 AGGTAAACAA AGCAGCCGGG AAGCTCCAAC TGGGTGGAGC CCACCACAGC TCAAGGAGGT 960 CTGCCTGCCT CTGTAGGCTC CACCTCTGGG GGCAGGGCAC AGACAAACAA AAAGACAGCA 1020 GTAACCTCTG CAGACTTAAA TGTCCCTGTC TGACAGCTTT GAAGAGAGCA GTGGTTCTCC 1080 CAGCACGCAG 1090
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