Tag | Content |
---|
EnhancerAtlas ID | HS133-01387 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr1:38189040-38190520 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr1:38189314-38189325 | CCCAATCCACA | + | 6.14 | REST | MA0138.2 | chr1:38190181-38190202 | GGAAGCACCAAGGACAGTACA | + | 6.37 | RUNX1 | MA0002.2 | chr1:38189193-38189204 | CTCTGTGGTTT | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 38189548 | 38189624 | chr1 | 38189109 | 38189500 |
| Enhancer Sequence | GGGCCTGGCA GGGAGTTCAG GGTCATTCTT TCAGCCAGGC CACCCCGGCC CTTCCCATTA 60 CAGAGCACTG AGGGCAGCAC CTCTTTGTCC CTTCAAAAGA CAAGGCCTGT GCCCTGGGGG 120 AGGGAACTTC TTGTCCAGCT GGTTTAAAAG CTTCTCTGTG GTTTGACGAC CTCCCCATGG 180 CACAGATACA ACCGTAGCCC TAGACCAAAC CGTCACCACC ACCACCATCC CTAGCTACTT 240 TCACATGGTG AAAATTATTG CAACTCCAGA GGCACCCAAT CCACATCCTG GCTGCAGGCC 300 CCCAGCTGCC CCCGCATGCG GTTTTGTGAA AGTGTGAATA AGGCAAGCGG ATCCAGCACT 360 CGGGGGCAGC TTCTGGTCTG GTCAGGAAAA CAAACATGGA GAGTTAGCCA CAAGCCCACT 420 CACCAGTGCT GGCAAAGGAG AAAGGTGCTG TACTGTTGGG ACACGGGACA GACAGGCCTG 480 ACCTGATCCA AGGTCATTGT GGAGGGCTTC CTGAGACAGA GGCAGCCACG GGCCAAAGGA 540 CTGCATCACA GTCAACAAAG CCACAGGCCG GTACTTGGGG CCCCTAGGGG CAGGGCCTTG 600 CTGGCCAAGA TAAAGACTTT GGCTTTTATT CTGGGAGCAG AGGAGAGCCC CTGTGGGGTT 660 GAAGCAGAGG AGTGCAATGA TTTGATTTCT ACTTTAGAAA GAGCTCCAGT TGCAGAGTGG 720 AAGCTGCCAC GGGTGTCACC ACAGGAGAGG AGCTGGCAGT GGTTCTAGCT ATGGGGTCAA 780 CATGGGCATG GAGAGAGGCA GAGGACTCGA GTGACATGAA GGTGACAGGG GCCACAGGGC 840 TGAGAGGTTG TTGGATGGCA GAAAGGAAGA GGGAGAAGTT GCCCACAGTT TATGGTGGTG 900 CCATTTACTG GGATGAGGAG ACAAAAAGTT CACATTTAGA CATCTGAGTT TGCAGGCCTG 960 GGGGATAAGC AGGGAAGATA AGACGGGCGT TCGACGTGTG TGTGTGTGTC TGGAGCTTGG 1020 AAGAGAGGCC TGCTCTGCAG ATACAAATCA GGAGCAATGA GCATGGCCCA GGGAGAGGAT 1080 GGAGTCTGAG AAGAGGGACT AGGAATAAGT CTGAGAAACC CCAACATCTA GGCTAGCGGA 1140 AGGAAGCACC AAGGACAGTA CAAAAGAATC GCCAGAGGAA CAGAAGGAGA GCAGAGGGAA 1200 ACTGGGGCAG GGTATCACAG GGACCAAGGA CAGAGAAAGT AGAGGGGATG GTAGAGAGAA 1260 ATCACATAAA GGTACAAGGA TGAGAGACCA AGGGAGGAGT TTCCGAAGTT TTCACAACAG 1320 AGATGATCAC ATGTAGATAC AGATGGGAAG GAGGAGCTAG GCTGTCACAC AGGGGGAAGC 1380 GGCCACCGCA GGGTGTTGAC AGCCTGGGCT CGGAACCTGA CTGCAGGGAC CTGCTTCCCA 1440 GCATCTCCGC TCGGTAGCTG TGGGACTGGG TGGCTCCATT 1480
|
| |
|
|
|