| Tag | Content |
|---|
EnhancerAtlas ID | HS133-16257 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr19:59002870-59003990 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr19:59003241-59003254 | TTCCAGAAGGTTC | + | 6.15 | | Nr2f6(var.2) | MA0728.1 | chr19:59003955-59003970 | GAGGTCAAGAGATCG | + | 6 | | PRDM1 | MA0508.2 | chr19:59002919-59002929 | TCACTTTCAC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CCTACTACAG CAGATGCCAA AGGGCACTGG GCATGGTGTG GGGGTCAGTT CACTTTCACA 60
CAGGGCTTGT GTTTTCCGTG GTCTCGGCAA CACCAACAGT GTCTGAACAT GACTGCACAG 120
ACATTGGTGC CCGCCGCTGC TTGTGAGCTC CAAGACCATC TCTCCTTCTG TGGGTGCCCC 180
ACTTATCTCA CTTTTTGACC CCTCCCCAGG TCTCTGGAAC CCTCTCTTCA GTCTTGACTT 240
CCTGCTGGCC TGTCTGGACC AGGTCTGTCA GTCCTACTCC CCAGCACCAG ATGGGCCCTA 300
AGAATCCCCC TCCTGCCACA CCTGCTATTT CCTCATATCC AGCCTCTCAG GCTACGATCA 360
CCACGCCACC CTTCCAGAAG GTTCCTTCCA ACCGCCCTTC CGAAAAGGCC CTCTCCATGG 420
CCCTCTTGTC AATGACTCAC TCCCAGCATG GACAGCAGAG ACGTGACCCA CACCTCTAAC 480
CCATGAGGCT CTGCCCAGCC CTCCCTGGAC ATGTCAGAAA ACAGAGAGAC CCTAGTCACT 540
GTGGGTCCAG AGGCAGGACC AGCAGCCACG TCCATGCCTT TTCAGAGCAC CCTCACCAGG 600
GTAAGGCAAG TTCTAGCAAG GCAGAGAGGG ATCTGTGTGA GGAGGTACCT CTCATTACCA 660
CCACTGTTAA TCATCATTGA CTTATTCATT CATAGAGAAA AAGTCATCTT GAACCATCAA 720
ACCCGAGAGC ATAATGTCGG ATACGGAAAG TCGGTGGGAG AAGTCATCTG TCATTAGGGG 780
TGGGAGCGGG GAACTTAACA CGGGCATCCA GGAAAAGGCA GGATGAGAAG AAACCGTGGA 840
CTTGGTAAAG TCTGTAAGAA ACGTCACCAT CTGAGCCATC GCTACAGCAT CTGCCTGTAT 900
TTCTCACATG CTTACATGAA AGGCATTATT TATTCACTTG GACAACAAAG GCTGCTTTTC 960
GTGAGAGTCA CTGGTCCTCC CATGAGGGCA TCCACCGATA CTTCAAGAAT CCTTCCTGGG 1020
GCCGGGCACA GTGGCTCACG CCTGTAATCC CAGCACTCTG GGAGGCTAAG GGGGGGGCGG 1080
ATCACGAGGT CAAGAGATCG AGACCATCCT GGGTAACACG 1120
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