Tag | Content |
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EnhancerAtlas ID | HS133-26841 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:35159140-35160780 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Znf423 | MA0116.1 | chr6:35160329-35160344 | GGCCCCTAGGGTTCA | + | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr6 | 35159402 | 35159523 | chr6 | 35159657 | 35160035 | chr6 | 35159725 | 35159966 | chr6 | 35160212 | 35160470 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I035191 | chr6 | 35158917 | 35160429 |
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Enhancer Sequence | GGCACAAAAG CCATGGCCTC TGGCCTCTAT TTAGCTGGGC AGGTGGTATA GGGGCAGGGT 60 GTGTTTAGAA TCACAGAAAG GATAGAAAAC ACATACTTTT ACATTTCAGA AGGAGGAGAT 120 CCTGCCAAGC GCTACAGTAG TCCAGGGAGG CTCCCAGGAG GAGGCAAGAT GGGGGAACAA 180 GCCCTGGGAG AGTCTTCAGA ATTCAGACAG GTAGAAAGAA AGCAGAGGGT CCCATGACGG 240 GGGAGGTAGG AAATGATGAG GTGCCAAGCT GGCTGGAAGG ATGGAACATG AGGGAATAAA 300 CAGAAGTATT GGAGAGTGAG CTGAGGAGGC TGAGAGAAGA TGGAGAGGAA ACAGCTCTGG 360 GAGGACCAGG AGGGGCACGA GTCCACAGAG GACAGGCAAG GCCCAGAGTG TGGCCTGGGG 420 CCAAGGCATC ACTGGGGCGC CGAGGGTGTG TGGGGTGGAT TTCTCTCCCA CCCCCAAATG 480 TGCTGCAGAC CACCAGGCAC AGCGCCCCAA GAATGCCTCT CACCCCCTTC CCTCAGCTCC 540 GCCATGGCCT TCGTCCCCCT TAGGGCAGTG AGCGCTGGAG AAAGACAGGA AAACCCACAA 600 AAATCTTCCA AATAAGACAA ATATGTAGTG CAGACAAAGG CCGCTTTGGG TGGGATGAGG 660 TTTCGGTTGC TCCCCAGTGG GGCGGACCCG TCAAAGTGGC TTGTGGCCAC AGAAAAAATG 720 CGTCATCTCC TGCTCTGGGT GGGGGCTCGT TGTCTCAGCT ACCCCCAAAG AAAGCCCAGG 780 CTGGGGGTTC CCATGGCCGG GGAATTGGGT CCTCCAAGTC ACCCACATGG CCCTGCTCAC 840 CCTTCAGCAG GGCATCCAGG CCTTCTCGGG GAACTGGGAG ACCCACTTTG GGGTGTTGGT 900 GGGGCTGTTT TAAGCTGTCC CCTTGCTGCA GCTCCCGGCC TTCCTGGTGT GTGGTGAGTC 960 CCAGGGCATG GCTGGGGTGG GCGGCGCCTG TGCAGCCCCT TAGAACCTCA TGAGAGTGTG 1020 AAGGGCCGAG AGTCAAGTGG TGTTTGCAAT GGAAAAGTCA GGTGCCGCCA GAAGCACCTC 1080 ATTAGGGACA GGGGTATAGG GGGTGATGGG AGGAGGCGAG GGCAGGCGCT TTCCTCTGCC 1140 GCCTGTCTCC CCAATCCCCT CCCCACTCCT ACACCCCTCC AGGCTCCCAG GCCCCTAGGG 1200 TTCATTCCAT TTCTGCTCCA GTTCCATGCC TGTTAATGGC CATTGTTCTG TGGAGAAAGA 1260 CAAAAATGTT TTCAGTTTAG AGGCATTGTT TTGGACTTTC TCTCTGTGGG CCACGGGCCT 1320 GGATGGGAGG CCTCTTGGCA GAGTGGCCCC AGGCAAGGAG AGGTTGGTTG CACTGGGAGG 1380 TGGGGGTAGG GTAATGGGGG AGGAGGGCTG GATGAGAGGC TGAGTGGAGT CCTCCGTCTG 1440 TGCTGGGTGT GCATAGGGAC AGCCCCCAAG AGAGGTCAGT CCCCTCCTGT CTTTGGCCTC 1500 CTCCTGGCCT CCAGTCCCAT CCCAGCTATT TTGGCCCAGG CATAATTTTC TCTTTAGGCT 1560 CCCTGACTTT GGATGGGTGA GCAACTTTCT CTCTGTGGGC CTCAATTTCC TCATCTGTAA 1620 AATGAGAGGC TTCGAAGACT 1640
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