| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01262 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:26002460-26003450 |
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 | ACCTGGGGCT CTTGTTAAAC TGCTGCTACA GATTCAGCAG GTGGGAGAGT GGAACTGAGG 60
TACTCTGTTT CTGACGTGCC CCCTGGGTGG CCCTACTCCT GGTCCCTGGA GCACTTTGAG 120
CAGCGAGAGT TTCTCTGCCT GTATGGCCCA CACTCTCGAC CCTGATGCCT TAGAAACAGC 180
TGCAGACAGG ATGCGATTCC TGAGACTGCT CAAACCTGAA ACCCCATGGG CAGGATGTGG 240
GTGAGCTGTC TGGACCTCAG GTGGGTGGGA GTTGTATCAT ATGCTCATTT CCCACATTGG 300
CCTTTCAATA GCTTGAGTAA ACCCGAAACT GAGAGGGTTG GAGGCAGCAT CTCCCCTTCT 360
ACTCCCCCGC TTCACCTCCC CGGGCAACCA AACCCCACCC GTGCCCAGCT TCTGAGCGAT 420
AGACCTGGGC TGTGTATTTG CAGGAGCCTC ACTGGGGTCA CCAACCAGGT CATGTTGTGT 480
TGCCCCAATA AATGGAACTG GATCAGAAAA TCCAACGTGG ATAGTTTTTA GGTGCCAAGC 540
TGTCAGCTCT TCCCTTGGAC TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT CAACCCAATG 600
TTCTAAGCTC TCTGTCTACA TAGTCATTAG ATCCCAGGAT CGTTAGAGAC CAAATCCCTT 660
CCCACTTGGC CCCTGCAAAT GGGGCCAGGT GTCACTGCTG GGAGACGCCA GTAAGGCTGC 720
ACGTCATGGT GTGAGCACTT GTCTTTAATG ACTGGGAAAA TCCATTTCCT TCCTTGGCAG 780
CTTTGAATGT AGCAACTGTG GTTCTGGGTC ACTGCCAGAG CCAGCCTTGT GTGTATGTGT 840
GTGATTTTTT AAAGTGGGGG AGAATGTCTC AATATTCAAT GCTCACCCCC TTCCTTCCAA 900
GTTGTACCCC CAGAGAACTG TCCAACACAA ACTTTGGAGT TTTCCACTCT GGGAGTGGTC 960
TGCTGGCACC CACGTGTCCT CCCCTCCTCT 990
|
