| Tag | Content |
|---|
EnhancerAtlas ID | HS139-33493 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr20:49471710-49473190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr20:49472924-49472935 | TCAAGGTCAAA | + | 6.14 | | FOXH1 | MA0479.1 | chr20:49472742-49472753 | TGTGGATTGGG | - | 6.14 |
|
| | 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 |
| GH20I050855 | chr20 | 49472328 | 49473295 |
|
Enhancer Sequence | ACCCTCACCC CCAGCCCTGC TTGGTGGAGA TTTCGGCCTC TGGCTCTGCA TCCCCAACAA 60
TTCTGTTTCC TGCTGTCTCT CTTCCCATCT CCATCTCTGT TGGTATTCTG GTCTGTCTCT 120
ATCTTTGTGT CACTGCCTGG ATCCATGTCT CTTGCGTTCA TCTTGCTTGT CTCTGCGTCT 180
CTCCATGTGT CTCTGCATCC CTATCTGTGC CACTCCATCT CCTCGTCTCT CCTGCCTGTG 240
TCTCTGTCCC ATGTCTCTCT GTGTGTCACC TACACAATCA CAAACCTTCA CTGTGCCCCC 300
TGTCCCCCAG GCCACAATCC TCGCATCCCC CTTCGTGCCC CACCTCCACC TGCATCTCTG 360
GCTCCTCCAA GAGACCTTCC TGGGACCCCT TCCTCCTCAG ACTGGAAGGG GAAGGGGAAG 420
GGTGTGGGCC GGCAGGGCTA GGACAGGTCT GAGTCTGTCT GCCGTCCACC AGCCTGGCCG 480
GCCCAGGCTG GGCCGTGGGC ACCCATTGCC CTTCTCTGAG CCCTGATGTC CACATCAGGG 540
CATAAGTGCG CCCACAGGAG GGCCCCCCAG GGACGCTTTT GACTGTGTCA CTAGAGAGCA 600
ACACTTGGTA CGTGGGAACT GTTAGTAACA ACAGCCATGA ACCTGAGGAT GAATAAATGG 660
AGGACCTGGG TCCCCGCCTG GGCTTAGGGT CTCTCTGGAG AATAAAACTC ACAGGCAGAA 720
ACTATCAGCG GATAATAACA AGGTGGGCTG CATGCATCTC ACTTCCATGC CTCACAGAGA 780
AAAAGAGGAA CGAGCTCAAG GGAAGCTGCA GAGGACAGGC TGGGAAAGGC CTGCGGGAGG 840
GAAGAGCCTG GCCCATGTGT GGCATTCGCA GCACAGCCCA CGACAGGCTG CTGGGTCGCA 900
GGCATTCCTG AGTGAGGTTG GGCCCGGCAG GGGATGGCAG GTGTGATCGG TGTCAGAACG 960
CAGGTTCTGG AATCAAGCAG TGTGCAGAGG TGAGTCGTTT GTCAGTGCAG ACTCCTGCCT 1020
GCTGCCTGCA GCTGTGGATT GGGTCTGGAA AAGGTGCAAT CCCTTTGATG CCCACGGAGC 1080
CTGGGAAGTA CTTGGCTCTG TTCCTGGTCA ACTTTCTGCT GGGAAAATAA ACCGTGTCTC 1140
ATTAGGCAGT GAGTTCATCC CGATGCCTGT TCTGGCTGAT AACATCACAC CTTGTCATGC 1200
TGCCAGGCCC AAAGTCAAGG TCAAAGTTCC TGTTACTTAG GGAATCCTAA TAATTAACCT 1260
GGGAACCTCA GCCGGAGAGG GAGATGCTGG TTTTTAAATG GAGTGAGAAG CTGGAGCAGG 1320
GAGGTGGCTG TTTCGGGGCT GGGCATCTCC AAGCACCAAT TTCAAGGTGC CACCCTGATC 1380
AGGATTGGTG ATCACAGTCT TCCAGCCTCC TTGTCCCTTT TGTGTCTGGT AGCTCTTTGC 1440
TGGCCTAGAC CTGGCTCCAG AGGCCTTGGG CAGTGCCCCT 1480
|
