Tag | Content |
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EnhancerAtlas ID | HS133-07604 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:56477690-56478260 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:56478178-56478193 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr12:56477700-56477721 | CCTCCTTCCTCAACCTGCTCC | - | 6.01 | ZNF263 | MA0528.1 | chr12:56477703-56477724 | CCTTCCTCAACCTGCTCCTCT | - | 6.15 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_07629 | chr12:56472009-56479657 | Brain_Hippocampus_Middle_150 | SE_23624 | chr12:56472516-56478145 | Colon_Crypt_1 | SE_27988 | chr12:56472169-56478232 | Fetal_Intestine | SE_28993 | chr12:56472036-56478358 | Fetal_Intestine_Large | SE_31786 | chr12:56472465-56478174 | Gastric | SE_48005 | chr12:56477266-56477747 | Pancreas | SE_50964 | chr12:56472347-56478225 | Sigmoid_Colon |
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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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Enhancer Sequence | GTGAGCCCAC CCTCCTTCCT CAACCTGCTC CTCTTTATTC TCCCCTAGAA CCCTCCTTCC 60 TTCTTCAGGG CTACCTTCTG CTGGAGTTCA CCCTTCCTAA GACTCAGGAG TTCCTAAGAT 120 TCAAAACCGT GTATTTATGG GGACAGTGGC TGTCATCTGG GACCTATGGT CTCACTGTTG 180 TAGCCAGGGA TATATAGGGG GCAGGGTCAG GGGCAGGTGG TGTTCTGTGG ATAGTGCAAG 240 GTCAGCAGGG ACTAGTGCAG AGAGAAACCT GAGGACCAAG AGGTTACCTG GGGAGATGAG 300 GAAGGGGCCC TACTGGTATG AGGCACTTTG AGGAGAAAGC TGCCTGTCTT CACTCCCAGA 360 AGTGACACAG CAGTGTGACA CAGTCTACTC CCTACTCCCA AATAGGAATT AGCAAGAGTT 420 AAGGCCAGGT GCAGTGGCTC ATGCCTGTAA TCCCAGCACT TTGGGAGGCC AAGGAAGGCA 480 GATCACTTGA GGTCAGGAGT TCAAGACCAG CCTGGGCAAT GTGGTGAAAC GCTGTCTCTA 540 CAAAAATACA AAAATTAGCT GGGTATGGTG 570
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