Tag | Content |
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EnhancerAtlas ID | HS133-12139 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:1849170-1850990 |
Target genes | Number: 26 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HEY2 | MA0649.1 | chr17:1849619-1849629 | GGCACGTGTC | - | 6.02 | Npas2 | MA0626.1 | chr17:1849619-1849629 | GGCACGTGTC | + | 6.02 |
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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: 2 | ID | Chromosome | Start | End |
GH17I001945 | chr17 | 1849250 | 1849470 | GH17I001947 | chr17 | 1850841 | 1850990 |
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Enhancer Sequence | AGCAGGGGGA CTGAGAGATG CTGCTCAGGA AGCCCTAGGC CCAGGGCCTG GCTCCTAGCA 60 GGCGCTCCAT AAACAGAGGG GCGCTTACCC AAAGCGAGGA GACTCAGAGC CTCCAGGGTG 120 AGAGCAGAGA CTAGGCCCTG GCTCTATCTG GAGGCTTCCT GGTCAATCAC GGGGTGACCA 180 CACGGTGAGG AGAGCTCTGG GAAGGAGGAT CCAGCCCCAG GCCAGCCAGA GGCCCAGGGC 240 AGGGTGACCA GGGCAGGTTT GCCTGGGACA GAGGGGTTTT CCAGGATGTG TGGGACTTTC 300 AGTGCTAAAA CCAGGACAGT CCCAAACAAA CCAACCAACC AGGACAGGTC AGTCATCCAG 360 GTCATTCAGG TCAGGCAAAT CCAAGCCTGT GCCTCCCTCA ACAAAAACCT CTGAATGCAG 420 GAAGGGGAGG GGCACACAGG CAGGCACAAG GCACGTGTCT TCTCAAACAC CATGCGTCCC 480 GCTCAGTCCC TGCAGCCAGG AGGCCGGCCT GGGCCCAGAC TGAGCCTGTG CGTGGTGTGT 540 GTACCTGTGT GTCATGGGCA TGTGTACGTG TGTGCACAGG GTCTGTGTCC ATCTATGTTG 600 AATGTGTGTC TGTGGGTGCA CGGGGTCTGC GTGGATCTAT GTGTGATTGT GTGTCTGTGT 660 GTGCATGGCA AATGTGTGTG TCTCTGTGTG AATGTGTGTG TGTGCACGGG GTCTGTGTGC 720 ATCTATGTTG AATGTGTGTC TGTGTGCACG TGTGTCTGTG CATCTCTGTG TGAATATGTG 780 TGTGTGCATG TGTGTCTGTG TGCATCTCTG TGAATGTGTG TGTGCACGGG GTCTGTGTGT 840 GTCTCTGTGT GAATATGTGT GTGCACGGGG TCTGTGTGGA TCTATGTGTG ATTGTGTGTC 900 TGTGTGTGCA TGGCGAATGT GTGCGTCTCT GTGTGAATTG TGTGTGCACG GGGTCTGTGT 960 GCATCTATGT TGAATGTGTG TCTGTGTGCA CGTGTGTCTG TGTCTCTGTG TGTGCACGTG 1020 TGTCTGTGTA TGCACGTGTG TCTGTGTGCA TCTCTGTGTG AATGTGTGTG TGCACGGGGT 1080 CTGTGTGCGT CTCTGTGTGA ATGTGTGTGC ATGGGGCCTG TGTGCATCTC TGTGTGAATG 1140 TGTCTGTGTG TGCACATGTG TCTGTGTGCG TCTCTGTGAA TGTGTCTGTG TGTGCACGGG 1200 GTCTGTGCGT GTCTCTGTGT CAATGTGTGT GTGCGCACGG GGTCTGTGTG TGTCTATGTT 1260 GAATGTGTGT CTGTGTATGC ACGGGGTCTG TGTGCGTCTC TGTGTGACTG TGTGTCTGTG 1320 TGTGCACGTG TGTCTGCGCA CGCACGCTTG TGTGCTCATG TACCTGGGCG GGCCTGTGTT 1380 TACATGTGTG TGCACAGCTG AGTGCACGTG CAAAGCCGAT GCATGTGTGC AAATACACAG 1440 GTATGCACAC AGAAACACAT GCCTGTCTCG GGACTGTGGA TAGGGTGGCG GCCCGGCCCC 1500 CTTCACCCTG CAGCGTGCCT CGCTCACCCT CCTGAAAAGG GAGCGGGGCC CTGTTCTGGG 1560 CAGAGCCACC CATCCCAGGT CTTATCTCGG CACTGGCTCT GGTTTGCCTT CAACTCCCGC 1620 CCTCCTCCCG ACACGCTGAA TTATGTACCC ACTCCAGGTC CCTCCAGCAC GCCAGGATCG 1680 CTCTCAGCTG AGAAGTGGGC GGCCCCTTAT TGGAATAGCC TTTCAGCTTT CATCTGCCTC 1740 GCTGGGCCCC TGGAGCAGGC CTGGCTGGGA ATGCCGTGCT AATTAGGCCG CCACATTCTC 1800 AGGGGGCCTT GTCGGAGCCA 1820
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