| Tag | Content |
|---|
EnhancerAtlas ID | HS099-06019 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr12:133053360-133054770 |
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 | chr12:133053920-133053931 | CTGCAGCTGTC | - | 6.62 | | NFKB1 | MA0105.4 | chr12:133054534-133054547 | TGGGGATTCCCCT | + | 6.67 | | NFKB1 | MA0105.4 | chr12:133054534-133054547 | TGGGGATTCCCCT | - | 6.87 | | Tcf12 | MA0521.1 | chr12:133053920-133053931 | CTGCAGCTGTC | - | 6.14 | | ZNF263 | MA0528.1 | chr12:133054006-133054027 | CCCATCCCCCACCCCTCCCCC | - | 6.21 | | ZNF263 | MA0528.1 | chr12:133054108-133054129 | TCTCTCTCCCCTGCCTCCTCA | - | 6.7 |
|
| | 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 |
| GH12I132473 | chr12 | 133050369 | 133054231 |
|
Enhancer Sequence | CCCGCACCCT GCGCCCTGGC AGGAGCCCCC AGAGGCCAGG ACGGCTGGAG TCCCCCCAGC 60
TTCCATCACT GTCCAGTTCT CCCCAGCCTG CCCTCTCCTT CCTCAGACAC ATTCACCCCA 120
TGACACCTGG CCTGTTGGAA ACAACCCAGC CCTGAGCTGC CCTCAGTGCT TCCGGCCCCT 180
CATGGGATGC AGCTTCCCCA CCAGCCCCCA GGCTGGGCTG CACCCCTCCT ACCACCGGCC 240
CCTAGGCTGA GCTACACCCC TCCCAACGCT GACCCGGCCG CACCTTCCTC CTCCCTCCAG 300
GTGGCTCCCG GCTCCACTGG CCTCCCCAGC TCTGGGCCTC TCTGCAGGGC CCCCTCACCC 360
CGAGTGCCTC CTCCAGGGGA AGCCCTGGAA CGCACAGATC AGATCGGCTC CTACCCCTGA 420
GCTTCCCTCC CCAGCCCTGC TGCAGCTGCT GCGGTTTGCT TGGGTGGGGC CTGTGCCCCG 480
GGTCAGCGTC CACCCCCTGC ACGCCGCAGA GGTTCTCCAA GTCCCTGCAG AACCAAGGGC 540
CAATTTGCAG CCTGACCACA CTGCAGCTGT CACACAGCCT GGTGGAGCAG TGACGTTTGG 600
GCTGATTGTG GTGGCTCCTC CCAGGTTGGG AGCCTCAAAG TGCCCTCCCA TCCCCCACCC 660
CTCCCCCACC ACAGCTGAGG CACTAGGAGG TCCTCCCCAA TCATGATCAC CAAGATGCAT 720
CCCCAACTGT CCTCTCACCC CACCTGCATC TCTCTCCCCT GCCTCCTCAG TGGGCTAGCC 780
TGGGCTCCTC CCAGGATCAG TGGGCTAGCC TGGGTGTGTC CTCTTGGGAT CAGTGGGCTA 840
GCCTGGGTGT GTCCTCTTGG GATCAGTGGG CTAGCCTGGG TGTGTCCTTT TGGGGCCAGT 900
GGACTAGCCT GGGCGCATCC TCCTGGGATC AGTGTCTGGA GTTGGGCTCG TGATAGGTTC 960
ACAATCACTT CCATCCCTTC TGTGAAGCAC CACAGCTGGC CAGACCCTGA GGTAGGGGTG 1020
AGAGAGGCCG AGGTGGGGGT GAGAGAGGCC GCCACCCCCA GCACTCTCCT GCCCCACAGC 1080
CTGAGGATCT GCCTGGGCCG TGCACCTCGG GGGCCCTGGG CTCCATCCAC TACATGTGGT 1140
GCTCAGCCGG GGGCTGATTC TTGAGCTCTG GCCCTGGGGA TTCCCCTTCT GGATACACCT 1200
TTTCCTCTTT CCTGACTGCA CAACCCCACA CAAGTCAGGG CATTCTGAAT TGTGACAGAA 1260
AAGGCAACAA AAGTGGTTGA AGCCAAGGGA GAAATTAGTG ACTCACATAA CCAGGACGTC 1320
CTGGAGTGGG TGGCTTCAGG TCTAGCTGGA TCCAGGGGCT CAAAGGACGT CATGGGGGCC 1380
TTGCTTCTGT CTCCCTCTCA CCTTCACTCT 1410
|
