Tag | Content |
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EnhancerAtlas ID | HS133-27625 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:161458260-161460400 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr6:161459044-161459062 | CCATCCTTCCTTTCATCC | - | 6.88 | EWSR1-FLI1 | MA0149.1 | chr6:161459028-161459046 | CTGTCTTTCCTTCCTTCC | - | 6.96 | EWSR1-FLI1 | MA0149.1 | chr6:161459040-161459058 | CCTTCCATCCTTCCTTTC | - | 7.95 | EWSR1-FLI1 | MA0149.1 | chr6:161459032-161459050 | CTTTCCTTCCTTCCATCC | - | 8.48 | EWSR1-FLI1 | MA0149.1 | chr6:161459036-161459054 | CCTTCCTTCCATCCTTCC | - | 9.35 | ZNF263 | MA0528.1 | chr6:161459113-161459134 | CCTTTTTTCCTTTCCTCCCTC | - | 6.3 | ZNF263 | MA0528.1 | chr6:161459032-161459053 | CTTTCCTTCCTTCCATCCTTC | - | 6.48 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 161458731 | 161458798 | chr6 | 161458878 | 161460315 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I161037 | chr6 | 161458571 | 161460690 |
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Enhancer Sequence | CAGCACAGCA TGGTGGACAA AAGCAGAATC TTGGTTGCTT GATCACCCGG ACTCCAGTCC 60 TGGTTCCGCT ATCTTCTGCG TATGCAGCCT CCATATCTCG TTTCTCTATC TGTAAAATCA 120 TCTGCCTTAT AGTGTTGTTA GGATTATGTA TTCAGTATTA GTTATCATCA TTATTATTGT 180 AAACTCAGGA TTTCTTTTAT TTTTTCTGAG ACGGAGTTTC ACTCTTGTTG CCCAGGCTGG 240 AGTGCAGTGG CGCGATCTCA GCTCACTGCA ACCTCCGCCT CCTGGGTTCA AGCAATTCTC 300 CTGCCTCACC CTCCCGAGTA GCTAGGACTA CAGGCATGCG CCACCATGCC CGACTAATTT 360 TGTATTTTTG GTAGAGACGA TGTTTCGCTA TGTTGGCCAG GCTGGTCTCG AACTGCTGAC 420 CTCAGGTGAT CCACCTGCCT CAGTCTCCCA AAGTGCTGGG ATTATAGGCA CGAGCAACCA 480 TGACCGGTTG TAAAGTCAGG ATTTCTTCCC AACACTTACT ACTTTTTTTC TTGACTTAAA 540 TCTTAAAGCA AAATTAAATA ATTACATTGT TGACATATCC TTATTAAATG GTGTGCCCAT 600 TTTTAGGACC CTGAGTCTTA GATTAAATGA TTGTCTCAAG TCGTGTAGCT ACTGTTCCTG 660 CTTCTGTCCT GCCTGGACTA CACATTTCCT TGTATGTCTT CCTAGTCCTT CGCTTTATCT 720 CACTACATAA TGCTGCTAGT ACATTTTTTT TGTTACTGTT GCTGTTGCCT GTCTTTCCTT 780 CCTTCCATCC TTCCTTTCAT CCTCTTCCTT TCTTTTCTTT CTTCTGCCTT TCTCACGCTT 840 TCTCTCCTCA CTTCCTTTTT TCCTTTCCTC CCTCTGTTCT TTCCTTATTT CTCCTCCATT 900 CTTTCCATTG AATCAGCATT TGAGTGACTC CATAGGCATG TGCTCTTTTG GAAGATGAAT 960 AAGACCTAGT TCCAGGTCAA GTAGGGAGTA CACAAATGAC CAACAGTACA GGCTCATCTG 1020 GATGCACACA GGAGGCAGTA TTGAGAAGAC CTGGGCTTGG GAAGACTTCT GGAACAAGTG 1080 ACATTTGTGC TGTGACCTCA AAGCTGAGTC AGGAAGACTA GTATTTCAGA CTAGCATGTG 1140 ACTCATAATA ATATATTGGC CCCCTCAGTA TTTTGAGGAG CTTTTTAGAA TTAATTAGAT 1200 TGGTCAGATT TATTTAAAAA GCTGTCCAAG GAAATGTGAA CTGTTACATT ATTTCTTTCT 1260 CACTGCAACA GACAAAGGAT CTCTGAGTCA TACTATTAAC TTTAGAACTG CGGTCAGAGT 1320 TGGACTCATC TTTTAAATAG TCACCAATAA CATTTGCATT TTTCAGATTA TCTATTGTTG 1380 TGTAACAAAC CACTGTGAAA CTTAATGGCA TGAAAGAGCA ATTATTTTAT TGCTCATGAT 1440 TCTGTGGTTC AGGTGTGTAG GCAGGGTACA GGTCATCCCT GTCCCAGGAT GTCTGGAGCC 1500 TTGGCTGGAA TAGCTCAGTT GGCTGGAAAC ATCCTGGCTT GGCTGGGGCC CTAAGTCTGA 1560 GCCCTCATTT TTTTTGTCTG CATAGTGTCT GCTGGATGTC AAACATCCAC GATGGCTCCC 1620 TCACTCACAT ATGTGTCTGT TCACTTGGGC TGAGAGAGCA GGAACAGCTG AGGGCTGCTG 1680 GCACAGTTTT CTTTCCATGT GATCTTCCTC ATGGCTAGCC CAGGGTGGTC CTTGGGTAAT 1740 TGGACTTCTT ACACGGCAGC TGTCTTTCCT CAGAGCCAGT GTTTTGAGAG ACTGAGGTGG 1800 AAATCGCAGG CCTTCTTAGG CCTTAGCTTC CGCGGTTGTG CAGTGTCACT TCTGTTGTGT 1860 TCTTTTAGTT CCATGAGGCT GGCCCAAATT CACTGTGGGA GGCGACTGCT CAAGGCAGCG 1920 GTACCAGGTC GGGTTTGTAG GTTACTTTGG GAAGTTAACT GCTACATGCA TTCATTGTAA 1980 AGCTTTGGGG AATTAGAATC TGGTCAGTCA TACTGTCTTT GCTTCCCCTA GCCCCGAACC 2040 CGCAAAAATG CAAAAAAAAA AAAAAAAAAA AACATCAAGT ACATCCCTGA AGGAATGTAA 2100 GGACTCAGAA AGGTAACTGA GGGGACTATT TAGAGGAAGA 2140
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