| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14487 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:109982670-109983820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr12:109983668-109983681 | AGCAGCTGCCCCC | + | 6.03 |
|
| | 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 |
| GH12I109544 | chr12 | 109982612 | 109983475 |
|
Enhancer Sequence | TTGGTCAGTG GATCCCAGTC AACAAAATGT TTTTCCATCT GTTACCCACT TCCTCCTGCC 60
TGTGAAGGGG CAGTGCTCTC TCCTTCTTAT AGGTGAGGCT CTGAGAGGTG GAGTGAGTGA 120
CTTGCCCAGG GACTCAAAGC CAGGATATGA GGAACTGGGA TGTAAGCCCA AGCCTTTGAC 180
CAGGAAGGTG ACCTCACTCA CTCACTTGCC TTCCCTGATC GTCAGAGGCC TGGACAGAAG 240
CCTTCTGTCT CCCAGAGGGG CTAGTCCCAC TGACTCTCCT GACCTGCTCC CATCCCACTA 300
GGGACACTGT CCAGGGGAGG GAGCACACCC CATGTGGGGC TTGGTGTGAA GTCTGCTGGG 360
TGGCTTTGTC ACATTGCAGA TGGTGCCAGA TGAGCCGGGC CCCGCCCAGG AAGCCAGACT 420
GCCAGGGAGT TCAGACTCAG CCAACAAACA GACCCACAGG GCCTCCTGTG CCCCAGGCTG 480
GGTGCTGAGT TACAGCCGTG CACACGGTGG ACGTGATCCC TGCCCTACAG AGCTCACTCT 540
CTGGTGGGAA AGAGTCAGAA CTAATTCAAG GAGGAGGTGT ATGGCCACAT CCTGTGATCA 600
GCGTCCCTGG CATCTAGTGC TGTGCTATTC TGATGCCCAC TCAAGTGGGG AAAGCTGAGG 660
TCAGGAGCTG GTCATTCCCA TGCCCAAGGC CCCAGAGTCA GTTAAGTGGC AGAGCCAGGA 720
TTCAAACCCT GGTCTGCCAC ACTCCAGAGC CCTCACTCGG TTTGAGCAGG CAGAAGAGGG 780
GTGGGAGAAC ATTCTAGGCA AAGGGCTCAG CTTGAGCCAA GCCCCAGGGG CTGCTCTGTC 840
CCTTATCTGG AGCCCGCTGC CTCCACTGCT TGTCCCACTT ACCCTTGCCG GGGATGCTGC 900
AAACTGACAG ACACACCCAT TTTGCCAGTG AGTTCCCACA GCATTTTAAA GGACTTCTTC 960
AGGACCCTAG AGCCCTGGTC TCCCCAAGGC TGCAGAGCAG CAGCTGCCCC CCAGGCACAG 1020
AGCTGAAAGG CAGAGCTGGA TTTCAGGGTG TGCTGAGTAA AGGGCCGATC TACCCTGCAC 1080
TTTGGAAGCT CACCGGGTAG AGGGAGGCCA GAGGAATTTC AGGGACTCCA CGACTTCCTT 1140
AGCTTATCAT 1150
|
