| Tag | Content |
|---|
EnhancerAtlas ID | HS073-00263 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:26002170-26003310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:26002631-26002644 | AGAAACAGCTGCA | - | 6.29 | | Myog | MA0500.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.62 | | Znf423 | MA0116.1 | chr1:26002536-26002551 | TGCCCCCTGGGTGGC | - | 6.13 |
|
| | 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 |
| GH01I025675 | chr1 | 26002283 | 26003398 |
|
Enhancer Sequence | AGTGGTTGTA CTAACTTATA TTCCCACCAG CAGTGTAAAA GTGTTCACTT TTCACCACAT 60
CCATGCCATG GCTGCTTTTT ATTGAGCACA TATTATATAC GAGCCATTGT GCTCAACACT 120
TTACATCTGT TATTTACTCT TAGGGTTATT CTAAGGATTA AGTATTTCTG TCCTTTTACA 180
GATGAGGAAA CTGAGACTTA CAGGGGTTAA GTCACTCACT CAAGGCCACA CAGCCAGTAA 240
GGTGGCAGAG CCCTAGAGCA GCCTCTCAAG CTTCAATGTG CGTTTGAATC ACCTGGGGCT 300
CTTGTTAAAC TGCTGCTACA GATTCAGCAG GTGGGAGAGT GGAACTGAGG TACTCTGTTT 360
CTGACGTGCC CCCTGGGTGG CCCTACTCCT GGTCCCTGGA GCACTTTGAG CAGCGAGAGT 420
TTCTCTGCCT GTATGGCCCA CACTCTCGAC CCTGATGCCT TAGAAACAGC TGCAGACAGG 480
ATGCGATTCC TGAGACTGCT CAAACCTGAA ACCCCATGGG CAGGATGTGG GTGAGCTGTC 540
TGGACCTCAG GTGGGTGGGA GTTGTATCAT ATGCTCATTT CCCACATTGG CCTTTCAATA 600
GCTTGAGTAA ACCCGAAACT GAGAGGGTTG GAGGCAGCAT CTCCCCTTCT ACTCCCCCGC 660
TTCACCTCCC CGGGCAACCA AACCCCACCC GTGCCCAGCT TCTGAGCGAT AGACCTGGGC 720
TGTGTATTTG CAGGAGCCTC ACTGGGGTCA CCAACCAGGT CATGTTGTGT TGCCCCAATA 780
AATGGAACTG GATCAGAAAA TCCAACGTGG ATAGTTTTTA GGTGCCAAGC TGTCAGCTCT 840
TCCCTTGGAC TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT CAACCCAATG TTCTAAGCTC 900
TCTGTCTACA TAGTCATTAG ATCCCAGGAT CGTTAGAGAC CAAATCCCTT CCCACTTGGC 960
CCCTGCAAAT GGGGCCAGGT GTCACTGCTG GGAGACGCCA GTAAGGCTGC ACGTCATGGT 1020
GTGAGCACTT GTCTTTAATG ACTGGGAAAA TCCATTTCCT TCCTTGGCAG CTTTGAATGT 1080
AGCAACTGTG GTTCTGGGTC ACTGCCAGAG CCAGCCTTGT GTGTATGTGT GTGATTTTTT 1140
|
