Tag | Content |
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EnhancerAtlas ID | HS133-17032 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:65258640-65260030 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr2:65258724-65258735 | GTTTGTGGTTT | + | 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: 1 | ID | Chromosome | Start | End |
GH02I065030 | chr2 | 65257801 | 65260188 |
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Enhancer Sequence | CCCATGCCCA CCTTCCCAGC TGCAGCTTCT GAGTTTCACA CAGGTGCTCT GCTTGGCAGA 60 CCTGCAAGGA AGTCTGAAAA AGCAGTTTGT GGTTTTCCGT CTGTGCAGCT CAGGAAGGTA 120 CACCTGATGG GAGTTAGCTG GGCTTTGGCT AGCCAACCTG CAGGGTCTGG AACTGCTTCT 180 GTTTGCAGGA CGCATCCCCC TATTCCAGAC AAGCTCTGGA TTCCCCTAAG TGCCTATTAC 240 ATGACAAAGG CAGGCTTTGT GAATGAGCGA ATACATCAAA CCCTCTCATA GTGCTGCTGC 300 CTACCAGCCA GTGGGTCTGT TTCTGTGCTG CCACCAACTT TGTTGAGCAA TATTTGTCTT 360 ACAGCTATTT TGAGTATTTT ATTGCACTGC CTTTGTTCTT TTATTCCACC CCTCTTCCTC 420 TCTCTCTAAG TGAAAGAAGT GAAGTAACGA TATTTGTGAT AAGAAGTGTA GTCTCATACA 480 TTTTATGAAA CTGAAACAAT TAAAATTACC AGTAGTATCC GAAGCAGCCT ATCTATATCC 540 TCAATGAGAC CTCAGTGGGA AAAAAGATCT ACTGCCTCTT CACCTGTAAA TAACACGTGA 600 AACTGCTAAG ACCGTGTTAT TGAAGAATGT GGCTAGTGGG CAGAGTGCCA TTTGGAATTT 660 TATAGTCGTC ATTATCTTTC TGGGAGTGGA ACCTCCCTTA TAACGTGGAA GGCTATTTTC 720 AACTTTTGCA CTTTTTTACT TGGATGCCTT TTCCAGACTC TGTTAACGTT TGGAATTGGG 780 TTTCACTCTA CAGAGAAAGA GAAGCAGGAG GACAGGTGTA GAGGGGAGGA GAGGGAGGAC 840 CGTGGGTCGC AGATTGGGCC TATTCCCCTG CACTCACCAC TTTGTCTGTC ACTGCCAGCC 900 CGCTCCCCCC TTTTCAGATA CCAACACCAG GCCAGGGGTG ACAGCCCAGG AAGGTGGCAT 960 CCACAGCCCT CAGCCCTCTG TCCTTGTCAT TCACTCCTAC CAGTCCTCAG CCCTCTTATC 1020 TGTCTGGGAG TGAGATGAAG GGCAGCTGGA AGCGGGAGGA AAGGTCCTCT CCTCTCCACT 1080 ACAGTGACAA GAGGTTTGGA GGAGCTTCTG GGTGAGGCTT AGGGGGTGAC CCTCCTGTGC 1140 AGAGCGGCAT GGGCTACAAA AGAGTGGATG TTTGTCCTGT GTGTGGGTCC CTCCTGGGGG 1200 CTAAAATGAA ATCTCCTTTC ATTTTCTGAT ATCATGTGAT CTCTGACTTA CAAACCTACT 1260 TTCCTGTGCC ATTTCTGTCT AAGACAACAG TCGCTTCTAA CAGAGCCAGA GTCCTACATT 1320 ACTGAGGAAA CCACCACCAT ATCCCATGCA TGAAAGGGCC GGCCTGTTGT GAATAACAAA 1380 CTAGTGGCCT 1390
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