Tag | Content |
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EnhancerAtlas ID | HS133-17865 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:180208860-180210210 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr2:180210058-180210069 | AAGCAATAAAA | + | 6.32 | NFAT5 | MA0606.1 | chr2:180209138-180209148 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr2:180209138-180209148 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr2:180209138-180209148 | ATTTTCCATT | + | 6.02 | NFE2L1 | MA0089.2 | chr2:180209346-180209361 | CAGTGACTCAGCACT | + | 6.58 | Nfe2l2 | MA0150.2 | chr2:180209344-180209359 | TTCAGTGACTCAGCA | + | 6.02 | TFAP2C | MA0524.2 | chr2:180210004-180210016 | TGCCTCAGGGCA | + | 6.18 | ZNF263 | MA0528.1 | chr2:180210148-180210169 | TTCCTCCCTTCCTCCTTCTTC | - | 6.42 | ZNF263 | MA0528.1 | chr2:180210145-180210166 | TATTTCCTCCCTTCCTCCTTC | - | 6.53 |
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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 |
GH02I179344 | chr2 | 180208945 | 180209979 |
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Enhancer Sequence | TTTGGGAAAT TTAAAATGGA AAGTTTGAAT CCCAGACTTT GGTTTTGAAG CAATAGCTGT 60 TTGAAGATCA AGAGCTAAAT CAAGGCATTC AGAGGCTCAG AACTTCACAC ATTCATCCTT 120 TCAGTACCCT TCTATTACAG GAGGAGCAAA GGTCATCTTC CCATTTAACT GGTGAAAAAC 180 TCAAAGGTGG AGACCAGTAG GAAAGGATGA GAACAAACAG AACTCTCTGC AGTCCCAGCC 240 CAAGGCTGAT GAGCTACCTC CTTGCTGCTA AATAGGGAAT TTTCCATTCA TGCCATTTTA 300 ATTTATGAAA TATGATCTTC CTCAAACTCT GAAATAGACT TTGTGCTTTT TACCCTGCAT 360 GAACTTCTCA CCCTCTTTCC TGATCCTCCG GAGTTTGCTC TCTTAAAAGT AACCTTTTAA 420 ATCCTGGAAA ATGATTCTGT TTTCTCAATT GACTATGGCT GCTCACAGAG TGTCTGTAGC 480 TCTCTTCAGT GACTCAGCAC TTTACAGAGA AAAATTGTTC TGGAGGGAAT GTTAGGGCAG 540 TCCACATAGC CGCTTACAGG AAAGAAAGAG ATCAAATCCT GCCTACAGGG AAAGCTGAAA 600 CACCAAACTT AAATGCTAAA TGGAAACAAT AACAACAATA ACAACAACAA CAACAACAAC 660 AAACGACCAA CAGATGATGA AAACCCCGTG AAGCAAGGTA AAGAAGGGAA GAGCAGAAGT 720 TCTCCTAGGT ATGAACAGGG CAGGTTCTGA AAAGCTGTGT GTAAATCTCT CAGTATCCAT 780 GAGCAAAGAG GCCCTAATCA GGTGATCACA CTGCTGTGGC TGGTAGGTAG AGCCTACTCT 840 CCCTTGTTCT GATGCCTGCT TTATCCTCAC TTTTCTGAAG TTGGAAGTTT GTGTGTAAAG 900 ATGCAGTATA GAATTTGAAC TTAGAAAATT GCAAAGGAAC CAAGGAAAAA TCACTCTTCA 960 CTGCCTCTCT CACTTGTTCA TTTGGATCCA ATGCACCTGG CCTATTTCCT AAGAAAATAG 1020 TCTGTTTTAG GTTGTTTCTA TGGTCACAGT GGGTCTTGTC AGAGCTGTAT GTGTACTTGG 1080 GACTTGGACA CTGTCATTCT TCTTGAAGCC AAGTAGTAGA GAAAAATCTT CCATTTGTCA 1140 TGTTTGCCTC AGGGCAGCTC CTCCTGAATC ACTGTAGATT GTTCTAGAAA CACAGACAAA 1200 GCAATAAAAC CCTCTTTCAT ATTGCGTTGA CTTGAAATCA TAACCATAAG TTCCCACCAC 1260 AAATTTCTTT CTTCATTAAT TCATTTATTT CCTCCCTTCC TCCTTCTTCT TGTACAAAGG 1320 CTTTGAAGGA GCATAGTAAA ATCTTAAAGA 1350
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