Tag | Content |
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EnhancerAtlas ID | HS133-22815 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:122542690-122545620 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:122543510-122543528 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr3:122543522-122543540 | CCTTCCCTCCCTCCCTTC | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr3:122543523-122543541 | CTTCCCTCCCTCCCTTCC | - | 6.36 | EWSR1-FLI1 | MA0149.1 | chr3:122543485-122543503 | TTTTCCTTCCCTCCCTCC | - | 6.45 | EWSR1-FLI1 | MA0149.1 | chr3:122543506-122543524 | TCGTCTTTCCTTCCTTCC | - | 6.8 | EWSR1-FLI1 | MA0149.1 | chr3:122543527-122543545 | CCTCCCTCCCTTCCTTTC | - | 7.08 | EWSR1-FLI1 | MA0149.1 | chr3:122543531-122543549 | CCTCCCTTCCTTTCTTCC | - | 8.08 | EWSR1-FLI1 | MA0149.1 | chr3:122543518-122543536 | CCTTCCTTCCCTCCCTCC | - | 8.45 | EWSR1-FLI1 | MA0149.1 | chr3:122543535-122543553 | CCTTCCTTTCTTCCTTTC | - | 8 | EWSR1-FLI1 | MA0149.1 | chr3:122543514-122543532 | CCTTCCTTCCTTCCCTCC | - | 9.47 | Foxd3 | MA0041.1 | chr3:122543908-122543920 | GTTTGTTTGTTT | + | 6.32 | IRF1 | MA0050.2 | chr3:122543414-122543435 | TCTTTCTTTCTCTTTCTTTCT | + | 6.76 | IRF1 | MA0050.2 | chr3:122543456-122543477 | CTTTTCTTTCTCTTTCTTTCT | + | 6.95 | Nkx3-2 | MA0122.3 | chr3:122544103-122544116 | AAAACCACTTAAT | + | 7.22 | ZNF263 | MA0528.1 | chr3:122543481-122543502 | TTCTTTTTCCTTCCCTCCCTC | - | 6.03 | ZNF263 | MA0528.1 | chr3:122543523-122543544 | CTTCCCTCCCTCCCTTCCTTT | - | 6.11 | ZNF263 | MA0528.1 | chr3:122544581-122544602 | CCTTCCCTTTCCTCTACCTCC | - | 6.15 | ZNF263 | MA0528.1 | chr3:122543531-122543552 | CCTCCCTTCCTTTCTTCCTTT | - | 6.18 | ZNF263 | MA0528.1 | chr3:122543518-122543539 | CCTTCCTTCCCTCCCTCCCTT | - | 7.03 | ZNF263 | MA0528.1 | chr3:122543514-122543535 | CCTTCCTTCCTTCCCTCCCTC | - | 7.27 | ZNF263 | MA0528.1 | chr3:122543485-122543506 | TTTTCCTTCCCTCCCTCCCTC | - | 7.51 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 122543845 | 122544344 | chr3 | 122544874 | 122544924 | chr3 | 122544384 | 122544649 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I122825 | chr3 | 122544041 | 122544190 |
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Enhancer Sequence | TGGTAGGTGG TAGAAAATAG TGTCAGGCAA ACATGACAAT CTTAATATTA CAGATTACTG 60 TAACATCACA GTCCCCAGGA CAACAGTGCT TATGACCAGT TGTAACACAT TAGAAGCTGC 120 TGAACCCTGA GGGACGCTAG GATATAAGTG TCAGAAGGAG CAGGACTAAG TTCTGGAAAA 180 CTACAAAGTG CTGGGAGGAG TGGGACTGGG TTTCCCTGCC AGGTTTCTCA TGAATTCAGA 240 GGATAACTAG TTCTCCTACT GAGCTTGTTT ATGAAGAGTG TATGTATGAT GACTTTTAAT 300 ACAAAAGCAT GTAATTATCT AAAATTGGAG TAACTTTGCA ACACCACATA AGCTTATTTT 360 AATTCCTGAG ATGGTTTTTA ACTCTAACTT ATATGCCCTA GATTGGCCTC CCAAGTTCAA 420 GGACCTTTAA ACCAAGAACC CATCTGAAGT GTCCCTGGTG CTATTCCTTC TTTGGATACT 480 ACTTTAACAC GTACTGTATC GTAGTGAGAA ATGTTCTGGT CTAAGAGTCA AGTAAACTGG 540 ATTTGGATGG CCCTTAAATT ATCTGAAACT CACACATTCT CTGACTCTTA GGTCAGACTC 600 TGCTGCTTGG GTAATAGTCT ATTTGTGATT CCACTGAGAG GTGACAAAGA GTTAAGCCAT 660 GGCAATAATT TGAGTTTTAT ACCTTAACTA TGAGGAGCTT CACTTTGCTT CTCTTCTCTT 720 CTCTTCTTTC TTTCTCTTTC TTTCTTTCCT GTCTTTCCTT TCCTTTCTTT TCTTTCTCTT 780 TCTTTCTTTC TTTCTTTTTC CTTCCCTCCC TCCCTCTCGT CTTTCCTTCC TTCCTTCCCT 840 CCCTCCCTTC CTTTCTTCCT TTCCTTTCCT TTCTTTTTTT TTCCTTCTTT TTTTTTTTTT 900 TTTTTTTGAG ACAAAATCTT GCTCTGTCGC CCAGGCTGTA GTGCAGTGGC ACAATCTCTG 960 CTCACTGCAA CCTCTGCCTC CCAAGCTCAA GTGATTCTCG CGCCTCAGCC TTCTGAGTAG 1020 CTGGGATTAC AGGCATGCGT CACCATGCCC AGCTAATTTT TGTATTTTTA GAGGAGGTGG 1080 GGTTTTGTCA TGTTGGCCAG GCTGGTCTTG AACTCCTGGC CTCAAGTGAT CCACCCACCT 1140 CGGCCTCCCA AAGTGCTGGG GTTACAGGCA TGAGCCACTG TTCCCAGCCA GGAGTCCTGC 1200 TTTCTTATCA GTCTTTTTGT TTGTTTGTTT TTGATTTATT TCTTCCATGT TCTCCTTCTA 1260 CCCTTAACAT TTTTAGACAT AGTAAAGTTT ACTCATTCCA AGCCTTCTAG TTGACATGAG 1320 TCTAATACCT CATTAAAAGT ATCAAATATC AAAGCAGTTA CTTTATGGGT CATCACACAC 1380 TGTCTCATTG TTGTGCCATC ACATGCAATG ATTAAAACCA CTTAATGACG TTATTGCTGG 1440 AACATTTCTG TAATAAAATT GCTGTGGGAC AGCTTTGGTT CCACTGGCTT TTGGAGGACA 1500 TAAACAGTTT AAATTATTTC TGTCATCTGG AAAATAATTC CCCTTACACA GAGAGATTTT 1560 TAAATGTCTT GAGTTTTTTT AATTTAGTAA TATCAATATC AATGACACTT GGAGCTATGT 1620 TGCCTTCATA TAATTTTTCC AACATAACGA AGCTATGGGC AGCCCTAATT CACATATTTC 1680 ACTTCCCACT CACTTCTGTT TCTACATTAG GGCCCTTCCT CTCCCCACGT GCCTGTTTAT 1740 TTTTCTCTTC GGCATTCAGC AAACTTTTCT AACTGGCTTA AGATGGCAGT TTAAAAAAAA 1800 AAAGAGGATT TGAGACTCAC ATAGTGCTTA GAAAGCAAAA CAAGCAGAAG AAAAAGATGA 1860 GTTCATATCA TGAAATGTCA CATGTACTGT CCCTTCCCTT TCCTCTACCT CCAGGGCAAG 1920 AGAGGTCGAC ACATCTCCCT TTCTTGTCTA TGCTTTCTTT GGACTTCTGG CCTCTTTTCT 1980 ATTTCAAGGC AGCTCTTAAA TGTGAATGTG TATATTGGGG GTGAGGGAGT AATGGGAGAA 2040 AAGAGTTGGT CAACAAGGAA CAGGAGTGCT AAGGAGAATA TTGGGAAAAG GTCAGCAAGA 2100 GAACAAATGG AATGGAAAAA AGAAACTGCT TTTCATTAAC CCTTACAATT AAAGTCAGAA 2160 TTAGAGTATG AGAACTGGAA GGGACTTAGT GGTCCTGTCA TTACAGTACC CTAACCTAAC 2220 AGATGCTCCG TAAATGCATA TTCAACTTCA GCTGATCTCC TCATTTCACG AGGGAAGAAA 2280 TGGAACCCCA CAAAGTTAGG TATTGTTCAG GGCTAGCCCT GAGCTCAGCT GGAACCCAGG 2340 TCCTCCGGTT CCTCAACTAC CTTTTCTATT AGAAGATATT TTAATGAGTC TTTCATTTTT 2400 TGTATTTCCA CCATTTGGCA AAGAGTGGGT ATGAAATGTT GAGCTCAACT ATAAGGCTGG 2460 TGGCACTTAG TAGGTCTGTT AATGAGTGGC AGTCTAGTAG AAGGAGTATG GATTTTGGAA 2520 TCAGACCTGG ATCTAAACTT CAGCTCTGCC TGTCAGCGCT TGGGCAAGTT TCTTAATCTT 2580 TCCAAATCTA GGATTTTTCA TCTCAGTAAA TGGGGATCAT AATAGCTACC ACTTAGTGTT 2640 GTTATAACAA CTAAATGAAG CAAGGTTCTA AGTACTTACA GGAAGTACTT AGTTTGATGT 2700 GTGGCACAAA TCATAGGTCA CAGTAAATAT TTGTGAAATG AATAAATGGT AACTATTACT 2760 ATGTTTGATC CTCCCTCATA GGGAGTCAAC ATACCTGTTT TAGAAGGTAA ATCAACATGT 2820 CTTTTAGGCA TGTCATATTC TTTACAGATA TGTATACTTA TTGCCATAGT TAAAAACTGC 2880 TGTTTGGCTC ATTTCTTTTT GTCTTAGAAA ATGCCTGTTT CAAATACCTC 2930
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