| Tag | Content |
|---|
EnhancerAtlas ID | HS061-00461 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr1:26002030-26003130 |
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 | TAAATGTGTA TGCAAGTGTC TTTTTCATAT AATGACTTAT TTTGCGGGGG GGGGGGGAGG 60
TGGTTACCCA GTGTGGGATT GCTGGATCAA ATGATAGTTC TACTTTTAGT TCTTTAAGGA 120
ATCTCCATAC TGTTTTCCAT AGTGGTTGTA CTAACTTATA TTCCCACCAG CAGTGTAAAA 180
GTGTTCACTT TTCACCACAT CCATGCCATG GCTGCTTTTT ATTGAGCACA TATTATATAC 240
GAGCCATTGT GCTCAACACT TTACATCTGT TATTTACTCT TAGGGTTATT CTAAGGATTA 300
AGTATTTCTG TCCTTTTACA GATGAGGAAA CTGAGACTTA CAGGGGTTAA GTCACTCACT 360
CAAGGCCACA CAGCCAGTAA GGTGGCAGAG CCCTAGAGCA GCCTCTCAAG CTTCAATGTG 420
CGTTTGAATC ACCTGGGGCT CTTGTTAAAC TGCTGCTACA GATTCAGCAG GTGGGAGAGT 480
GGAACTGAGG TACTCTGTTT CTGACGTGCC CCCTGGGTGG CCCTACTCCT GGTCCCTGGA 540
GCACTTTGAG CAGCGAGAGT TTCTCTGCCT GTATGGCCCA CACTCTCGAC CCTGATGCCT 600
TAGAAACAGC TGCAGACAGG ATGCGATTCC TGAGACTGCT CAAACCTGAA ACCCCATGGG 660
CAGGATGTGG GTGAGCTGTC TGGACCTCAG GTGGGTGGGA GTTGTATCAT ATGCTCATTT 720
CCCACATTGG CCTTTCAATA GCTTGAGTAA ACCCGAAACT GAGAGGGTTG GAGGCAGCAT 780
CTCCCCTTCT ACTCCCCCGC TTCACCTCCC CGGGCAACCA AACCCCACCC GTGCCCAGCT 840
TCTGAGCGAT AGACCTGGGC TGTGTATTTG CAGGAGCCTC ACTGGGGTCA CCAACCAGGT 900
CATGTTGTGT TGCCCCAATA AATGGAACTG GATCAGAAAA TCCAACGTGG ATAGTTTTTA 960
GGTGCCAAGC TGTCAGCTCT TCCCTTGGAC TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT 1020
CAACCCAATG TTCTAAGCTC TCTGTCTACA TAGTCATTAG ATCCCAGGAT CGTTAGAGAC 1080
CAAATCCCTT CCCACTTGGC 1100
|
