| Tag | Content |
|---|
EnhancerAtlas ID | HS133-32959 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chrX:152095930-152097110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chrX:152096143-152096164 | GCCTCTACCTCCTCCTCCTCC | - | 7.83 | | ZNF263 | MA0528.1 | chrX:152096146-152096167 | TCTACCTCCTCCTCCTCCCCC | - | 8.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGACAGAGA TGAGCAGCCC GCTGACCCAG CCCTCCATGG CTCATTCCTT GCTTTCACCT 60
TGGCCACTCC ATCCCCTACC CCTCCTGGGA CCCCTGAGTG GCCTCTTTAA AGTGCCAGTC 120
TGAACCTATA AACCCCCCAC CTCCACTTCA AGCCCATCCT GCATCTTCCC TTTGCCATAC 180
CAGATCTAGT CTGTACATTC AGGACCCCTG CCAGCCTCTA CCTCCTCCTC CTCCCCCGAT 240
CTCCCTTCAG CTGGCCTGGG TCGGGCTATG CCTCCATGAA GCTTGTCCAC TGCTCCCATG 300
GCTAAACCTG TTCTGGGCCC TGCAGCACAG CAAGGTCAGT TTCCATGCCT CTCTGCCCCT 360
GCCTGACCCT GCTGGGCCCA GAGCTTCACC AGGGCAGGCC TGGGGCTCAG GCTTGTCTGC 420
ACTTCCAGGG CCCAGGGACA AAGGCAGGAG TGACTGCAAT GTGGCTTGGA ATTAGGCTTT 480
GCTCCATGGA CCTAAGGAGG TCTGGTTTGG GGTGAAGGGT CCACCCCCAG AAAGCCTGGG 540
AGCTCTATAT TCTCTCTGGC CCTGGCCACA CCATGGCCAA GCCTGCTGGG CGTCATGCCT 600
TGCAGTACGG CCAGAGAATG CATCAGACTT GGAGGGATGT GTGTCCGGGG TGGCCTGTGG 660
TCATCTGGGG GAGGGCTCTG AGCGTGGCTG GCAAGAGGAA AGCTCAAAGG GGCCCTTTGT 720
CCTCATCCCC GAGTCTGCGA CATCCCCTCC CACTGGTTTT CATTCCATAT TTGGTCTGTG 780
GGTTTTCTCA GTCTCTCGTA CCCCTCAGTC CCCACCAGTC CATGAATGCA GAACTACCCC 840
TGGCCTCACA AATGGCCACT TTGGATACCC TGGTGGGGTC ACAGGCTGCG GTTGCCCCTG 900
CAAATGGTTG GTAGAAGCAC GGGTTGGGAG GTTTCATTTC TACCCAGAAG GGCCCTTGCT 960
GTGCCTGAGG GAGGGCTGGG CTCAGGTCAG GGGTGGGAGA CCGGGGAAGG GGCCTACAGG 1020
TCAGTGGCCC GAGCTCAGCT GCAGCACCAA CAAGGCTCAA GGCCAAGGAG GAGATGAGAG 1080
CACATCAAAA GGGGGCAGTG GGTCTGGGCG GCCCACCGCA CTCACCAGCC CAAGAAGGGG 1140
GAGACTTTTC TCACCTGCAA CCCACTGGGT CTCTCCTTTG 1180
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