Tag | Content |
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EnhancerAtlas ID | HS133-17363 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:101196930-101198280 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr2:101197975-101197985 | GGGGATTAGC | - | 6.02 | IRF1 | MA0050.2 | chr2:101197849-101197870 | AAACACAAAGTGAAAGCAGAA | - | 6.9 |
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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: 1 | ID | Chromosome | Start | End |
GH02I100579 | chr2 | 101196443 | 101198651 |
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Enhancer Sequence | TCCTGCTTAC AGAAACCAGC TATTACTCAC AGATATAACC TTAGAGACAG GTGGCTGTCA 60 GTCTCAAGTG AAGATGTGCC TGTTTCCAAG TCCCCTCCCT CCCTCTCTGC TTTTGACCAC 120 ATTCTCTACC CCATTCTTTG CTTCAGTAAT CATCCGTCTT GATTTCCGCT TCTCCCTGGA 180 CATGGGGCCT TCAGGTAGTA ACAGTGTTAG GGTCCTGTGG CAGAGAGTGC TGGTTGCCCA 240 CCAGTATCCA GGATTCTCCC CCTCTACTCC AGTGGCAATG GGACCCGCTG GAAGAGTAAA 300 CCCCGGCCTC TCTTGAGCTG TGGGTGGTTG GCTGGGAGTT CAGTTCTGGG CAAGCTGCTA 360 CTAGGAGGAA CAGACAACTG TCATGTGCCC TTTGTGGGCT TAACCCCCTT CCTTCTACTT 420 TCTGACGGAA GTGTGCATGC GACTGCAGCC TGCGTGGGCC GTGAGGTATT TATACATAGA 480 GGCAAAGCAG TAAGGACAAT ATTCCCAAAG ATGCTGTGGA GCCACTATAT CCCAGCCCTT 540 GACTGTCCTC TCTGGACTTC TGTCATTAGG AAAGACGTAA CTTCCGTCTT GGTCTCTGTT 600 AGTAGCAGCT GATGCATTTC CTGATAAAAC CACCCGTCAA AGAAAACCTC AAACAAAACA 660 TTCATTCTAG CTTTCTACTG CCCGATGCTG AATTACTTGA CATAACACAA GAGTACTCTG 720 TATTCCCTGC CTCTAGCTGT CACCATTGCC TTTCAGTAAC TTCATGGGCC CGGCTTTTGG 780 ACTTCCATTT CCAGCACTTG AGGAACACTA AAAAACCCAC CTGATGATGA CTCAAGCTGT 840 TGGAGAAAAC TTATTTTTAA ATGTTATGTT CTTAACTGTT TCACTGAGTT GGTAAGAAAG 900 GAAAACATTC TGAGAGGCCA AACACAAAGT GAAAGCAGAA CTTCAGGAAG GTAAGGGGGC 960 ATTCAACTTT TCTCCCTAGG GATACAAACC AAATCTTAGT GATGCTGTGC TTCTATTAGG 1020 ATGGACTTGT GGGGCCCAGG TGACAGGGGA TTAGCGTGGG GAGTGCCTAA GTTGGGGGTC 1080 TGATTAGGAA GTCTCTGTGC AAACAGCTGG AATCCCAAAA GATTGCATTC AGTGTTAGGG 1140 GAAACTGGCA CTAGCTGGAA GAGAACATAG TTGTCTCTGA GATGCCAACT ACAAGCCTTC 1200 CCTCATGCAG GTTTGTAGTT CTAATTCTCA TGCTACATCA GGTCTAAAAT CCTCTCAAAC 1260 CAGGTTCTCA AAGAGGCCCT AGGCTGGGCG CGGTGGTTCA TGCCTGTAAT CCTAGCACTT 1320 TGGGAGGCCG AGGAGGGTGG ATCATCTGAG 1350
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