| Tag | Content |
|---|
EnhancerAtlas ID | HS074-01127 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:183163780-183164960 |
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 | chr1:183164111-183164122 | CAGCAGCTGTC | - | 6.14 | | Nr5a2 | MA0505.1 | chr1:183164925-183164940 | AAGTTCAAGGCCAGT | + | 7.44 | | Tcf12 | MA0521.1 | chr1:183164111-183164122 | CAGCAGCTGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_35834 | chr1:183163338-183165417 | HMEC | | SE_64350 | chr1:183163237-183165340 | NHEK |
|
| | 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 |
| GH01I183194 | chr1 | 183163373 | 183169370 |
|
Enhancer Sequence | TCATAGAAGG TTTCTTTCCT TTTGGTCCTC TTTGCTTCAG GTATTTACCT CTGGCATCCC 60
TGGAATCTCT GATTCCCTTT ATTTCAACTG CTTCTTAGAG GGGCATAGGA TACCTTTTTC 120
TAGGCCATGC AAGAAATGTC CAGAGAACAC TATGCTCTTT GAATAACAGT TAAATGTCCT 180
TTCTATGCTG GAATGCTTTT CTTTGTAGGT AACTTCACAG AAATGTATAA CCCTTTATTT 240
CTGTGGTCAG AAGAGTGTGG AGTTCCATGG AGGTGGTTGC TGTCATATAG AATCTTACCA 300
CAATCACTTC CTGAGTCTAT GCTGCAGCTG ACAGCAGCTG TCTTGCGGTA GAGCCTTTGA 360
CAGTGCCAGC TATAACTCTA ATGTCCTCAG TTTGCCTTCC CTTTCACCTG TGAGCTTACT 420
CAGACTGAAC CCTCAGTTTT ACCTTTACCC TCCACTCCTT TGCTAGTCAG ACAAAACTTG 480
GTGTCCCCAG TTTCCCTGTT CACTGGGACT TTCTTCCCCC TCCTCATTGT CTGCCTGGGC 540
ACTGGTGTCC CAGTGGAGTG TCAGGGGAAG ACATCTCCAG GTGTGAACTC CTGATGGAGT 600
CCTCACCAGG CTGAGTCATC TACAGTTCAC ACGGGTACAT TCCCAAGTCT AGGCTGTGAT 660
ATAATGTACT ATGAACTCTC GGTGAAACAG GTGTCTCCTC TGAAGCCATA ATCATTCAAA 720
AGGAAATGGC AGTGATCTGA GTTTCACTGA CTCTTGATGA CTTTGGAGTA TTCAGAGTTG 780
AAAAAACTGA CCCATACTTT ATGATTCAAA ATTGCCTGTG AGATTAGAGA ACTGAGCTCT 840
GTCATTCCTC TCATCCTAGC ACTTCCTGCC TCAGCCTTAC TCACATTGCT TGGACATTTA 900
AATGTCAACT GGTGCCGTGC CCTTTATTTA AATGAAACAA ATGGATCAGG CAGGATATGG 960
TATCAGTTTT CTGGCTGTGG TGGCTTAAAA TGTGGCTATG AAAAATTTGC AAAAGAAGCC 1020
TAAATTCAGC TAAAAGCCTT AGTGAGAGAA GTACCATTTC AGTTTTCTTA TTCTAATTAG 1080
GGAACATATT GTGACATTCT TTAAGAAGAT AAAACTAGAA GCAGATATTC ACACATTAAA 1140
CAATGAAGTT CAAGGCCAGT TTAAATGATG AAGGATTCAG 1180
|
