| Tag | Content |
|---|
EnhancerAtlas ID | HS133-20037 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr20:61700830-61701770 |
Target genes | | Number: 32 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr20:61701380-61701401 | GGCCCTCTCCAAGGTGCTGAC | - | 8.87 | | RREB1 | MA0073.1 | chr20:61701608-61701628 | CCCCACCCCACCCTCCCTCC | + | 6.21 | | ZNF263 | MA0528.1 | chr20:61701606-61701627 | CTCCCCACCCCACCCTCCCTC | - | 6.42 | | ZNF263 | MA0528.1 | chr20:61701592-61701613 | TTCCCCTGCTCCTCCTCCCCA | - | 6.84 | | ZNF263 | MA0528.1 | chr20:61701589-61701610 | TTCTTCCCCTGCTCCTCCTCC | - | 7.68 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGCTGGGATT ACAGGCGTGA GCCACCGTGC CTGGCCGGGA GGGAGTTTTT AAAGAGGTCA 60
GACCTCTTCC TGATTTTGGG GTGCAGAGCC AGCACCATCC AAGGAGATGC TGCGGGGTTG 120
GGAGGGAGGA CCGGGTCCAT GCTCCCCAGT GGAGGTGCCG GCTCTGGGAG ACACAGGGCC 180
CCTCGCCCTG CATGCATGCA CATGCGGCTT CTCAGGGCAG CTGGACTTGC TCTGTTCATG 240
AGCTCTTGGC CTTCTGAAAC TGCTAGTTAG AGGCCAGTTA GAATGCTTGG CCTAGAGAGG 300
CCCCTGTTCC CCCATCGGAG CTGAGCTGCC ATCTCTCATC AGAGGCTCGT GTCAGAAAGC 360
CCTGGTGGAG GAAAGCCAAC ACTTGGGAAG CACAGGGAGG CAGGCTGGAC CCGGCGTCCT 420
TGCGGGCTGT TGGCAACACC GTCTGGAGAG GGACCGGGCC CTGTGCCCGC CAGTCCCCAG 480
GGCGGGGCGG CCTGAGCTGG CCTGGTCTGC TGTCCTTGGG ATCAGGCCAG GACTCAGCTC 540
TGTGCCTGGG GGCCCTCTCC AAGGTGCTGA CGACACCATG TTCCAGCCTT CACTCCTGCC 600
AGCCTGGGAG ACCTTCGAGC GGCTTTAACA AACCCCATCG CAACTGGGCT TGCCTTGAAC 660
ACAGCCCTGG ACAATGGCTC TGTCTGGGTG TCTTTGGGAA TACACGTCTT TTTACTAACT 720
TCAGTCAGAC CTTCAGCCTT CCTTGATCCA GCCTCTCTGT TCTTCCCCTG CTCCTCCTCC 780
CCACCCCACC CTCCCTCCCA CAGCAATTCC CCAAAGGAGC AGAGGCAGAG GGAGAGCCTT 840
CCTCTGCTTG TCCCTTGAGA AGAGGATGTG GAAACGTCAG AGATTCTCCT GAGAGTTGCA 900
GGCAGGCAGG GAGGACAGAC GTACTTGGGA CACTTCCTGC 940
|
