Tag | Content |
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EnhancerAtlas ID | HS133-29116 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:99052840-99054050 |
Target genes | Number: 37 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr7:99053097-99053112 | CAGGTCACAAGGTCA | + | 6.49 |
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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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Enhancer Sequence | TGTCACCCCA TTAATGTCAG AGACACTTCA TGTAAGTCCT GGATTCCCCA GAGTCAGCTG 60 TGGGGTCCGA CAGACATGCC AGATGCCGTG AGCAGGGTGT GTGGTCCCTC CCCCAGCCAT 120 CATGTTAGCC CTACAGCCCA TCGGCAGCCT CTCCATACAG AGTCACACCT GCAGATCAGA 180 CAAAGTTGAA AACACAGGGA CAGCTGGGTG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT 240 TGGGAGGCCG AGGGGAGCAG GTCACAAGGT CAGGAGTTCG AGACCATCCT GGCCAACATA 300 GAAGAAAGAA AACAGGAATT GCAGAGCCAG GGAATAGAGC TGGCAAGAGT GTTGGGTGCC 360 AACTGGGCAG AGCCCCTCAG GGCAGCAGGG ACTCAGGGGT GGGTGTCAGT ACAGAGTCAG 420 TGCCCCCAGC TGCCTCCTGA CCCTTTTGTT CAGTGCTTGA GGCTGCCGTT TTAGGAGTCA 480 TAGAGTAAAG AGAAGCTATG GAAGGGCCTG GATAATCAGG ACTGGGATGA GGCAGGGTCA 540 GGGCTGGATT TGTCATGTGG CTCTGCAGGC TCCCCTTACC CAAGTCTAAG CATCGTCCCA 600 TCTCTCTGAT CCTGTAATCA AAACCTGTCC CCAAGGTAGC TTAGGTGTGT CACAGCCACG 660 AGGGAAAACG TTGGGTACAG CCCACCCTCT GTCCCCAGCA GTGGCTCCCC AAGGGAGGGG 720 AGGCTGGGAC ACTTCTGATG CTGTTCCCTC CCATCTCCTG CCAGGGAACC CCAGACCTTG 780 GCTCAGAGGT AAGTGACTGG CCTGTGGTGC AGAAGGGCTT GGTCCCCAGA CGGGGTGGCG 840 GAGCTCAGGT GCCACGGGCT TCTCTTTGTC CTGCTACCCA CTTGGGAGTC CCTCCCTGGG 900 CAGGCCATGT GTCCAGGTGG GAGAGTTGTG GGCCTGAAAG AGCAGGTCGC TAGCAGGTCG 960 CCTTCTGGCG GCCTTGTTCT CCCTTGCATC TGCGGAGTTG CTGGCTAGTT TCTGCACCAC 1020 TGCACTTTCC ATCCTGAGCT CCCTCACCCT CTAATTTGAA AGAAACTCTG TACCACTGAG 1080 AATTTCAGAG TCATGTCCCG ACTGGGGACT TGGTGGATGA TTTGGGATTT GGTGGGCACT 1140 CCCTTAGTTG AAAACTGCAT TTGAACAGTG TTGTTGTCTG TCTCTCCTCT TCCCCCACTT 1200 CCTGCTGTTC 1210
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