| Tag | Content |
|---|
EnhancerAtlas ID | HS133-20984 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:20882380-20883470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr22:20883447-20883458 | TTCTGTGGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_13928 | chr22:20882879-20883477 | CD34_Primary_RO01536 | | SE_14430 | chr22:20882563-20883761 | CD4_Memory_Primary_7pool | | SE_45715 | chr22:20882152-20883563 | Osteoblasts | | SE_53780 | chr22:20883004-20883484 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH22I020522 | chr22 | 20876463 | 20883405 | | GH22I020529 | chr22 | 20883464 | 20889824 |
|
Enhancer Sequence | TCTGTTACCG CTAAATTACT CTTTTCTTGT GGGGTCTTTA TTGGCCATGT TATGGCGTCT 60
GGCTGCCCTT GGCTGGTTGC TCACTCTGAG AGGGACCCTC CAAAGCCTAG GAGTCTCTTC 120
CAGCACGTGG AGCTTGTCGA CTGGGAACTT CATTGAAGGC TCATCTGGCT GCAGATTCTG 180
AGTCCTTCCT CCAGAACAAT GGTCCCCAAC CTTTTTAGCA CCAGGGACCG GTTTCACAGA 240
AGACAATTTT TCTACAGACC GGCAGATGAG GATGGTTTCA GGATGAAATT GTTCCACCTC 300
AGATCATCAG GCATTAGATT CTCATAAGGA GCATGCGACC TGGATCCCTC ACATGCACAG 360
TTTACAGTGG GGTTCGTGCT CCTATGAGAA TCTGATGCCA CCACTTATCT GACAGGAGGC 420
AGAGCTCAGG CAGTAATGCT TGCACACCCT CTGCTCACCT ACTGCTGTGA GGCCTGGTTC 480
CTAACAGCCC ACAGACCTGT ACTGGTCTGT GGCCCAGGGC TTGGGGACCC TGCCCTAGAG 540
CATGGTCTTC CAGACACTGG GCTGTGGGTG AAGACCTGGC TGCCAGCATG CTGCTCACTG 600
CGATGGAGGA GGCTGATGGG CCAGTGGGTC TCGGCAGTTA GCGTGCATCG ATCTAGTCAC 660
TTAGACCAGA GCACAGATGA CCACACAACC CACCTCTCTC AGTGTCCTAC CTGTGCCTTT 720
TCAACTGGGT GGGTTGGCCC CCTAGTCCAG TGACTATCCG TTTCATGCTT TTCCAGAGAG 780
TAAACCTCCT GTGGTCACCT GGTGCTGGAG TAGCTACCCA CAGTGTAAAG TTGGGGAGTG 840
AGGGATGCAG GGATATCTTT CACCCTCTGT CCCAGAGCAC TTGGTGCAGC CTGGCCTCAA 900
CCTGGCAAAG ACCTAGGGCT GTCACTGGGT GGGCGCACCC CCTCCTCACT GTTACTTAGG 960
ACTCTGGTTT CTTGGTCCTC TTGCTGTGTA CGTTACCACT GGGCCATCAG CTTTCCAGCT 1020
TCTAAAAGGC TGTTGAGGCC ACCATTTCCA TTCTTCCTGG TTTTTTTTTC TGTGGTTTTA 1080
GTCAGGTTTT 1090
|
