| Tag | Content |
|---|
EnhancerAtlas ID | HS139-32269 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr2:241790270-241791600 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr2:241790893-241790908 | TGACCTCTGACCCCA | - | 7.91 | | Nr2f6 | MA0677.1 | chr2:241790893-241790907 | TGACCTCTGACCCC | - | 7.03 | | Rxra | MA0512.2 | chr2:241790893-241790907 | TGACCTCTGACCCC | - | 6.98 | | SRF | MA0083.3 | chr2:241791493-241791509 | TCTCCAAATATGGTCA | + | 6.02 | | Zfx | MA0146.2 | chr2:241790605-241790619 | CAGGCCCAGGCGGG | - | 6.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 241790525 | 241791266 | | chr2 | 241791304 | 241791424 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I240851 | chr2 | 241790721 | 241790890 |
|
Enhancer Sequence | GCCGTCCCCC ATTGCTGCCG TCCCCCACTG CATCCACCCC ATGTGCAGGC TGCTCCCACC 60
CCAGAAGCCT CGAAGGCCAG GGACCCGTGG GGTCCCTCCG TGACTCGGTA CCCTTCCCCT 120
CGCTGTCCCC TGAGTTTCCT TCAAATCAGG AAGCCTCCAC CAGCCCTGGC CCGCTGGCTG 180
GGTCCCTCCC CGAGAGCCAG GTCACCTGTC ACTGTCTCTC ACCATCCTCA GCCCCATGGA 240
CTGTGCTGCA GGTGGCCACT GTCACGTCAC CCAGGCCAAG CACACCCGTC AGGATTCCCA 300
AGGCAGGTCG GTGTCCAGCC GCTTCCCTGA GGCTGCAGGC CCAGGCGGGC TGCGGAGTCT 360
GTGCCTACAT ACCGCGGGCC GAGCTTGCTC CAGGCAGGGA CGGCGCGGGA GGCACAGGTC 420
CTCTTTGGGC CTTTCTGCAG GTCCTCCTGC CCCACATGGA CATGCCAGCT GTCACTTGCA 480
CCATCAGGAA GAACAAGAAT CCTGTGTGCC CTGTGGTGGG GCCACAGTCG GCCGCTAGGT 540
GTCACTGTTT CCTCAGAGAC CAGCACATTG TCCCTATGCT TTCTCTCTGC AGTCCCTGGC 600
TGGCAGCTCC TTGGGCAGGG TGGTGACCTC TGACCCCAGA CCCGTCCCCC CTGAGCTGGT 660
CCTGGCTCCA CCGGGAGCTC CGTCCCCTGG GCTTCCTGCT GATATGTAAG TCAAGCCTGA 720
GCTGCCGCGT TGGGGCCACT GATCTGGGCA GAGCCTCGTG GGGTCTCCCA GGGGCTCAGA 780
CGTTGGCCAG GACCCCACAG GGAGGATGCT CAGGTCAAAA AGATGCCCGC ACTCCGGGCG 840
CTGCCCAGAG CTCTTAACTC TCATGCTGAG AACAGCTTTG TGTGCTGAGT GTTTCGCACA 900
CCCGCAGGCC CCGCACGTTC TGCCTGCTGT TCCCTGTAAT CCTGACCTCG CCTGGGAGTG 960
GCAGGGCCAC CCACTTCGGG AGCGGTGGAG ATTGGACTAT TTAGAGCACA CACGCTGGGG 1020
AACCAGGGGA AGAGTTGTGA AGGGGTTAAG CAAAAGAAGC CTTTCTCCTG GGCTTGTAGA 1080
TGGCCGTCTT CTCCCTGTGT TTCCACATGG CTGCCCCCCA TGTCTGTGTC CTAATCCCCT 1140
CTACTTATTA AGACACAGTG GGGTTGGATT AGGGTCCATC CTAACAGCCT TATTTAACCT 1200
TAATTAGCTC TTTAAAGACC TTATCTCCAA ATATGGTCAC ATCCTGAGGG ACTGGAGGCA 1260
AGGACTTCAA CACATACATT TTGGATGGCA CAATTTAGTT CAAAACACCT CCCAGCCCCA 1320
GCTGGCACTG 1330
|
