| Tag | Content |
|---|
EnhancerAtlas ID | HS046-05684 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr11:2176960-2178340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:2177858-2177877 | TGATGCCATCTGCTGGTCG | - | 6.42 | | Nkx2-5(var.2) | MA0503.1 | chr11:2177240-2177251 | CTTGAGTGGCT | - | 6.62 | | STAT1 | MA0137.3 | chr11:2178008-2178019 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr11:2178008-2178019 | TTTCCCAGAAA | - | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65606 | chr11:2175710-2183172 | Pancreatic_islets |
|
| | 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 |
| GH11I002156 | chr11 | 2177781 | 2177930 |
|
Enhancer Sequence | TGTTCCTGCG GCCGAGGCCA GAAACAATAG TGGGAGGAAG GGCGGAGGGT GCGGAGGCGG 60
CACCCCAGTG TGTCATCTCC GCGTTCCCAG ACCCTGTCTA CCCCTGCCCT CAAACATTCT 120
TTCCAGAGTG GACCTCCCTC TCCTCACGGC GCTGGCGGAG GGGAGCGTGG GAACGCACTA 180
ACCCTCAGCC GCCTGGACCC CAGCTCCAGG CCTTCGGTGC CCCCAGGTCC CAGCCCCTGA 240
AGCCCCCTCC TCACATAGAA ACCAGGACTC GACCTTCTGG CTTGAGTGGC TGAGGGAGGG 300
ACCCTCCTGG CCACCGCTGG CCTCCAGCCT CAGTAGCCCC CAGGGGCCCT GGGGACCCTC 360
AGCAAAGGCC ACAGCCTGGT CCACCACCGG CCACAGTGGG CTCAGCCACG ACGAGGGTGG 420
GACGGAGTCC CCCTGGTCTT CTCACCCTAG CTCTCTGTGA TTCTAGGGGC TCGCAGGTGG 480
GGCTCAGAGT CCAGCCAGAG GCTTTCTTGG AATATTAGAG ACCCAGAACA TTTGTCCCGG 540
CCCTCTGAGA AACCCAGGCT GGTGAGAGGC TGGCCTGAGG CTTGACTTAG GGGCCGAGAC 600
TGGACCTGAG CAGGCCGGGG GCCTCTGCAA TGCCCCCACC ATCATCATCA GACAGCTCCT 660
CTCATTCCTA AGCCCCATGC CCTTCAGAGT GCCCAGCAGG GCCCCCCACA GCCCCCATAG 720
TCCCTGGGAG TGCCTGGCAG GGCCCCCCAC AGCCCCCAAG AGTGTCTGGC AGGGCCCCCA 780
CAGGCCCCAC AGCCCCCGGG AGTGCCCGGC AGGGGCAGGA TGCAGCTGCT CAGACCCTGG 840
GTGGTGGCCA GAACCTGGAC CCGTGGCTGG TGGCCGGAGT GCATCAAAAG TGAGGCTCTG 900
ATGCCATCTG CTGGTCGCAC CCGTGAATGG CGGCTCCTGG CCACATTGCT GGGTGTGGAA 960
AGGTGCCCAT CCTGGAAACA GCTACCTCAC AGCCTGGCTG GAGAGAGACA CTGGCCAACG 1020
TTCGGCCCAA GTTCTGCCCA GGGCTACCTT TCCCAGAAAC TCAGGCTTAA ACACTGCCTG 1080
TCCTGGCCTC AGTCTCTTCC CTGGGCTGGA CCCCTGCTGG GCACCAGGAC CCGAAGGGCA 1140
GGGGGCTACC CTCAGCACCG CTGAGTCCAC ACTCATCCCC CCGGGGTCTG CTCAGGCCTG 1200
GAGAGTCCTG GAGACGGAGG ACAGTAAATA TTTGCTGCCG ACAGGGGAAG GCAAACACTG 1260
CCCCAACGGC CAGGCAAAGG CGCCAGTTAT CCATGCCAGG AGCAGACGCA ATCTAGGGGG 1320
CCAGCCTGGA GGCAGCCACA CCGCAGTGTG TCCTGGGTGG GTGGGAGCAC GTGCCATGTG 1380
|
