Tag | Content |
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EnhancerAtlas ID | HS133-13643 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:78679520-78681640 |
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) |
Foxa2 | MA0047.2 | chr17:78680317-78680329 | ACTATGTAAACA | - | 6.22 | NKX2-5 | MA0063.2 | chr17:78679566-78679576 | CTCAAGTGGT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 78680230 | 78680782 | chr17 | 78680951 | 78681148 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I080705 | chr17 | 78679646 | 78681125 |
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Enhancer Sequence | ACGAGGGATC TGACTATGTT GCCCAGGCTG GTCTTGAACT CCTGGCCTCA AGTGGTCCTT 60 CCACCGTGGC CTCCGAAATG CTGGGATTCC AGGTGTGAGC CCCCGTGTCC GGCAGGGGAA 120 CCTTTCTTAA GCATGAATGG TGTGCCCTCC TCAGGGTGTG TCCTCTCTGC TTCCTTTCTC 180 AGTCACATCA GCAGGTGCTT CGTGTGCATC TGTGTGCCCA GCCTGGGCAC AGCGGGAGCC 240 CAGGCCTTCC TTCAAACGCA GCCTCCCCTG CACGTTCCAA ACACTTACTG GCATTTTTCT 300 TCAAGTGATG ATCATGGCAT TGGCCTTACT TATTTTAGTT GTTTTTAAAA GAAAGTTTTA 360 AAAGTTTATC AAAGTGATGA ACATACACAT CACTTTTTAA AAACATAATC CCCACCCAGA 420 GGCAAACCCT TTTAGCTATT TGTTCTAGTG GCATATGTTG GTGCTGCTTT GCACTGACTC 480 ATCAACTCAG GGCATCTTCC CTGACTGCCT GGTGTGGCCC CAGCACTTTC ACACCCGTTG 540 TTCCCCTCCC CAACCCCAGA AGGTCGTAGA TTTACTCTGT CGGTTCTTCT TTGTTGGGAG 600 TTCACCATGA AAAGTACTTT GCAGGAAAAG AGCAATGATA GAACTGGAGT AGCTCCTCGC 660 ATGACCCACC TGTGCCCGTT TTCCAGCATC CTGCCACCCA GCCAGGTCTG TCTCCTCCTT 720 GGCCCGTTCT CCTCACTCAG GTTCTCTGGA AGTTGGCACA GTTTTACTAA AATAAAATCA 780 GCATTCATAG CATTAGGACT ATGTAAACAC TGTTCTCAAG CAAGCCAAGT CATGTGTACT 840 TGGGTCTGAT TCTGGACTTT GTGTGTGAGT TCCCTGGGCT GCTGGTCTCC GTGCCCCCAG 900 CCTCGCTGTC TTAATGAGAG GCCCTAGGGG AGCCTGCAGT GTCTGGCAAG GCCAGGTTGC 960 CCTCAGGGCT TTCTGCTGCC ATGATTTTCT GGCCCTTCGT CCCTGTTTGT TTTTCCCTGT 1020 GACCTTCAGT AGCAGCTTAG CTCCTTGGGG TATTTACTGG GAATGCATTG AATATGTGAA 1080 TTAAACGAGC GAGAGCTGAC ATCTTAAGAA TGTTGACTCA GCCCACCCAA GCAGGGAGCA 1140 TCTTCCCATT TGTTCACGTC TTCTGTGTTT TCCAGGAGAG CTTTGAAAAT CTTCCATGTC 1200 TGTGTTTTGC ACATTTCATG TTAAACTTAT TCCTATGCAT TCAGTCTGCT CTGTGGCTTT 1260 CGAGATGGGG TTTTCTTTGC CATGATGTTC CTTTGTTTAT TATTTGTGTA TATCAAGGCT 1320 ATTGATTGTT CTCTGTCAGT TTTAGATTCT GCTCATTCAG GGTTAAGGGC CCAGGCAGGA 1380 GGCGGAGGGA GGAGCTTTCA GCAGGGCGAT TCCTTACTCG GTCTCTTCAC TCTTCTGCCA 1440 TTGCTGCCAT GTGTACATTG CAGGCTCCTT CATTTGAGCA AATTCTCTCT TCCATGCTCC 1500 AGATGTTTTC AGAAGGACCG CGTACTTCTG AGAAACACTT GGTACCCCAG TGGCAGCTGC 1560 GTTTGCCTTG GTGTTGCCAT GTGACAGGCA TTACTTGTTT ATCTCATTGT TGTTCCTAGT 1620 AGTTCTCAAT GTTTGTTGAA TGAATATTTA TAACCATCAT GTGTGGCAGT TCTTATGTAG 1680 TGTTTTGATT TGTTTTTTTG AGACCATCTC ACTCTGTCAC TCAGGCTGGA GTACAGTGTT 1740 GTGATCATGG TTCACTGCAA CCTCAACCTC CTGGGCTTAA GTGATCCTTC CACCTCAGCT 1800 GGGACTACAG GTGTGTGCCA CCACACCTGG CTAATTTTTT TTTTTTTTAA TTGTAGAGAT 1860 GGGGTCTCAT TCTGCTGCCC AGGCTGATCT TGAGCTCCCG GGCTCAACCA GTTCTCCCAC 1920 CTTGGCCTCC TAAGCTGCTG GGATTTTCGG CATGAGCCAG GGTGCCTGGC ATTACCTGGT 1980 TTTATAGATG GAGAAACTCA GAGCCATGTG TCCAGGACCA CACAGCTATT AACTGCAAAC 2040 CCAGAGGAAA GGGTAGGGGA TGAGTTCCAA GCATTCCCTG GAGTCCGTGG TAAATTTCTT 2100 CATTTCTTCT CCTGCAACAG 2120
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