| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10513 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:69251140-69253640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr11:69252217-69252228 | GACAGCTGCTG | + | 6.14 | | PLAG1 | MA0163.1 | chr11:69252705-69252719 | GGGGCCAACGGGGG | + | 7.38 | | SPI1 | MA0080.4 | chr11:69251435-69251449 | TAAAAGAGGAAGTT | + | 6.83 | | SPIC | MA0687.1 | chr11:69251435-69251449 | TAAAAGAGGAAGTT | + | 6.34 | | Tcf12 | MA0521.1 | chr11:69252217-69252228 | GACAGCTGCTG | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_57195 | chr11:69251639-69252438 | VACO_400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I069434 | chr11 | 69248988 | 69253103 |
|
Enhancer Sequence | TAACAGCAAA TGGGATAAAG ACGCCGCCCT CACAGGGCTT ACCGTGGAAG AGATGGGAAA 60
TCCAGACCCA CAGCTAAGGG CAGGGCCAGA GGGTGCTGAG TGCTGGACGA AGTGAGACGA 120
GGGAAGCGGG TGTGGACTGA ATTGCAACCC CCCTCCAACA AGATGTTTGT GTTGAAGTCT 180
TAACCCCCAG GACCCCGGAA CATTTCCTGA TTTGGAGATA GGGCCTTTAC AGTGGTCACC 240
AAGTTCTGAG GAGGCCATTA GGGTGGGCCC TAATCCAATA TGACCGCAGT CCTACTAAAA 300
GAGGAAGTTC AGGCACAGAG GCCGCATGGG AGGGAAGCTG ATGTGGAGAG GCATGGGCCA 360
CCTGCAAGCC AAGGAGAGAA ACCTGGGCCA GTTCCTTCCC CGCAGCCTCA GAAGGAGCCT 420
GCCCTGCTGA CACCTTGATC TTGGACTTTC ATTTCTATCA GTTAAGCTGC CTGGTCTGCG 480
GATCTTTTGG CCTAGCGTAT GGGGCTTGTA CTCCACACGT CTCCCAGGGC TCTGCAGGCC 540
AGCACCGGGG ACCCCACCCA TGTTATGCTC CACTTTCCAG GGAGGGAAAC TGAGGCTCAC 600
AGAGGTGAAG TCACCCTGAC AAGCCCCACA GACCATGGCC CAGGCTTGCT AGACTCTAGG 660
GACAGAGCCC TTCTTCCCCT CAATGAGGCC ACTGACCTCT CCAGGTGAAC GTTGTTGGTG 720
CAGCAGGGCA TGAACCAGCT CACGTGCCTG GCCCACTGGC CAGACCACAG CATGGCTCTA 780
GCTGCCCTGT CCCTGGCTGC ATTGCTCACA GCCGACAGGG GCAGACAGGT GTAGACACAG 840
CCGCCCAGCC CTGCAGCCCG GCATCCCAGG AATGTGGTCA GCCACCCACA CCACTGCCCC 900
CACCCCAGCC AGGCGTGCTG TGTCAGCCCT GGGCCCTCCT GCCCTTCCCT CCAAGCCCCG 960
CAGGTCGCCC AACTCCCAGG GCGGCTGCAT TCACTGTTCA TCCCCCAGGG GAAGAAAGGC 1020
CGGGACCAGG GGCTGGCCCT GGGCCTGCAC CAACCAGGGA TCCTGCTCTA AGGACCTGAC 1080
AGCTGCTGCT TTGCCCTTAG AGGAAAGGAG ACCTTTAGAG AGACAGGAGG AAAGAGAGAG 1140
CAAGAGAGAG TGAGAGAGAG AGAGAGAGAG AGAGACAGGG AGAGAGGGAG AGAGAGAGAG 1200
AGACAGAGAG AAAGGGAGAG AGAGAGACAG AGAGGCAGAG ACGGAGAACA CTCCAACCCA 1260
AATATCCTGT CCCAGTTTTG AGCACAGCTT GGAGGTGTCC CCCTGCTAGG GGAGGGGTTC 1320
CAGACTCCAA TGTGTCTCTT TAGTGAAGAA TGCCCTGAAA GCCTTCTAGA GAATTGTGGG 1380
TGCTTCTCCC ACCCACCCCA TCTTGTTGGG AGCCTTGCTG ATTGAATACC TGGCTCCCCT 1440
GAATATGTCT CGGGACACTG CAAGTCAGAG GGCGGGCACA AGTGCCGGCA CCAGGCTTCA 1500
CCGCCACAGT GACCCTCAGG GTGGGTCTGG GGGGCAGAAA GGTCACGCCC TTCCTTTGAA 1560
GACAAGGGGC CAACGGGGGT GGGGAGGGGT CTTCCCTCTG AACACCTCCT CCTCCCCTCT 1620
CTTGCTGCAC TGGGGCCCCA GCGGCTGCCT TTCCTCATAC AAACCAGGTT GTACAGCCTG 1680
ATCCACTAGG GAGAGCCTGG CGTGGGGGCA GGCGAGTCCT GACTGCAGGG GAGACGTGCA 1740
AGTGAGGAAG GGTGGTCCTG AGGAAGGGTG GTCCGCAGGG AGACTTCAGC CTCCAGAGAC 1800
AGGTGGCCGC AGCTCCCCTA AGTCGCATCC CATCCCCTAG TCCAAAGCGC AGTGTCTGGT 1860
CACAGTGAGG CCCCAGAAAG GCTGGGCCTG TGTGGACACA CTTCTCGCTT ATTGCTTCCA 1920
CTAACCCCAC AAAGAAGACA GCTCCATTTC ACAGATGAGG AACCTGAGTC GTGAGAGGTT 1980
AAAAGACTAG GGTGAGGGCA CGGGATTGCA GTGGGCAAAG CCAGGCTCCT TGCACGGTGC 2040
GCCCTGGCAC TCACTCAGAG GAGGCTCTGA ATACAAAACC AGGATTGCAC TGAGATAGCC 2100
CTGCTGTTTC CGCGCGGACG TGGAATGAAG TCAGCCCTGG CGATGCCAGA GAGAGACAGG 2160
CGGAGAGACG ATCAGAGCCT CCCGGCTCCT AGTGGCTCAG GTGTGGCCCG GTGTGAAAAC 2220
CTCAACCGTC CCAGAATTGA GGTGTTGAAG GCTCCTCTTG TTCCCTGATC AGCCAGACAT 2280
TGGCTCCGGG ACCAAGGCGG GGCCCACGTA GGGTCTGGTT GGTGGGGTGG GCCTGCCCAT 2340
GGCCCTGACA GCCCCCGTTG TCCTAGGCAG GGAGTGGGGG ACAGGTATTC AGGGCCTGGA 2400
GAGGTATTCC CAGGACAGGC GGGCTGTGGG GTGTGTGGGC GCTCCCGGGA GGTCCTGGCA 2460
GCCGCTGAGT GCAGACCAGG CCTGCAGACA AAGGAGAGAG 2500
|
