| Tag | Content |
|---|
EnhancerAtlas ID | HS133-20956 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr22:20111020-20112520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr22:20111724-20111744 | GGTTGTGGGTTGTTGTGTGT | - | 6.2 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH22I020123 | chr22 | 20110603 | 20111350 |
| Enhancer Sequence | GTGTGAGAGA GATTGGGGGT GTTCGGGCAG TGTAAGAGCA GATGTGTGAG GTGCCCAGGC 60
ACCAGCCTCC CCAGTTATGG TGTGTTCTAC CCTCACCAGG ATCTTCCTGG GGAGGAAACG 120
GGAGGGGAAC GGGGCTGAGA AGGTGGCCAG GTCCTGGGCG CCTCTGAAGC TACATAAGTA 180
GAGGCCCTTG GGCAGGTTCA GCCAAGAGCT CCAGCCACCC TGTGAGGGGT CCAGCCTGGC 240
CTGCAAAGAA GTGGCAGTAG GTTGTCCTGA GTATGGCTGG CTGCCAGCTG TCTTTAGATT 300
GAACCTGCAC TGCCCAGCTT GTTGGCATGT TTGGAAGTAC ACTTGTCCTG GGGTGTCCCT 360
TGGTAAGCTT CCTAGTGTCG TTTGCTGAGT GTCATGCGTG TCCGGCGGGG CAGGGTCCCT 420
CATCCCAGGT GCAGGATGAC TGCTGGCAGG AGCCTGAGTG GCTCAGCCCT TGAGGGCGAT 480
GCAGAGGGGT GGGTGGTGGT CTGCCTATGC CATGGGCACC TCACTGCACG GCCTGGCCTG 540
CCAGACTTCC TTGGGAACTG GCTCCTGGGT TCCCCTCCCT CCCTGCTCAG CATGTCTAGT 600
CCTGGGGAAG CTTGCACTCT GGCTGGTCCT CCTCCTCGAG CCGTTTGAAT CATTTCCTTG 660
GGGGTCTTCC CTGATGCCCT GTGCTGCTCC CAGAGCCTGG GTCAGGTTGT GGGTTGTTGT 720
GTGTGCATCA TAAGTTGGTT CTGGGCTCCT GGGCATCTGG GCAGAGCCAT CTGTGTAGCC 780
AGCAGTGTCT TGTGCCCATC ATGGGCCCTT GGTAGACAGG GAAAGTGGCA GTGGGTAGAG 840
GCTGGCTTCT GGGTAAGGTG TCGAAGAGGC TGTGGGCTGG GTCGGGGCGG GGTGTGAAGG 900
GGGCATGCAG GGGGCTTGGC ATCCGCTGTG GCAGGCTGCA GTAGACGAGA CCCCCCCCCA 960
GCTCCCAGTT CAGATAGTGA CGTGTAGGGG TATCCTGGGG GTGCATGTGG CCTGGACTGG 1020
GCATGGGCAC CTGGGATGGT CTGGGTTCTC AGGGAGCTGT TCTGAAGAGT GGTCACCTGC 1080
AGGGCCATCT CCCCTTGGGG CTGCCTGTGC CTGGGGAGTT GGGGTGGAGG CGTCCATTGC 1140
AGGCCGTGGC TCTGTCTCCT GTGCCCTCCA GGCTTCAGTC ATGGGGATGC AGGTGGGCAC 1200
TCCTGCATCA ATCATGGGGA TGCATGGCCA CGGCCCCCAG TGGGCTCCCT TCTGGCAACT 1260
GCCCCACTTT CTAGCCTTCT GCTGCCCCCC ACTTTCAGAT AGGCTGGCTC TATGTGTTGG 1320
GTTCCCTTAG GAAAGACTGG GCCCCCTGGG CCTTGTGCCC TGATATCTGA CCCTGGGCTT 1380
CTGACTTCAC GGCCAGGGTC AGAATCAAGG GGATCAGGGT TGGGCTTGAG TGCAGCCCTG 1440
GGATACAGCT GGGGCCTGCT TTGCCAGCTC TGCTTCTCTG CATTTCTGGA GGTGGGGGTC 1500
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