| Tag | Content |
|---|
EnhancerAtlas ID | HS050-10586 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr10:131425110-131426300 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr10:131425653-131425671 | TCTTCCCTGCTTCCCTCC | - | 6.04 | | MEF2A | MA0052.3 | chr10:131425911-131425923 | TCTAAAAATAAA | + | 6.07 | | ZNF263 | MA0528.1 | chr10:131425653-131425674 | TCTTCCCTGCTTCCCTCCTCT | - | 6.08 | | ZNF263 | MA0528.1 | chr10:131425645-131425666 | CCTCCCTCTCTTCCCTGCTTC | - | 6.78 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I129627 | chr10 | 131425113 | 131426444 |
|
Enhancer Sequence | TTTTATAAAC TGACTATGGA GCTGGTGTAA GGAGATGCAG GGAAGGCTTC TCATCTGAGT 60
CGGTAGCAGA GTACATAGTG CAAGAAGCGT GGGCAGGCTC CCAGCGCACC CAGAGATCAA 120
GGAGAGTGAT GGGTGCTGCC CGCCTCTGAG GGGACGGAGG CAGCTGCCAC CCGCCGTGTC 180
CCTCACGCTG GCTTTCAGAA GGCTTCACGC AAGTGGGCTC ACAGGCAAGA AGAAAAGCTG 240
TGGGCCGTGT GTCTCCCTTG GCTATGGCTC AGTTTTAATG TAATTAGAAG CTCAACTTGA 300
AAGTGAGATA TCAAAGGAAG CCTTCAGTTG CTGAAGATGG GTGTGCTGGG GGATGAGGGC 360
GTGGGTTGAA AAGTATCCAG TTACTGTTTT TCTCACGTGG ATCAGTCTAA CATATGTGAC 420
TCTGGTAATT GAAGATGGTG ACAGGCTAAA CTAAGCTGGG ATTCCCCAGG GAGAGACTAG 480
GATTTCTGGA ACCAGTCTAA CAAAAACAGA AACTTGAAGG AGAAAACAGA ATATGCCTCC 540
CTCTCTTCCC TGCTTCCCTC CTCTACTCAA AAAAAAGAAA GAAAGAAAAA AGCAGCTTTT 600
GCAATGAAGA ATTCAGTTTT TCGCCCCCGA GTGTATGATG GTAGTGACTT TGGTGTTCCT 660
GGTGCAGACC TGTATTTTTT TGTGATGTCT TCATCTGGCC CCTCGCCCTC CACTCTTCAT 720
GATGAATATG AGACCTGTGC ACTGAGGGTC CTCACCAACA CTTCCTTCCT CACAGCCGTA 780
TGATTTCATC CGGAAGCGGC CTCTAAAAAT AAACACCCTC ATGTTAGCCT TTTTCCACCA 840
TGCTTCATAT TTGGCTCTTG TATAAATATC TGCCACGTTT CCACTGGGAA TTATTGCTGT 900
TATATATTTT ATAGACACTC GACTGTCATC TAAGTGGCTT ATTTTATTCC CATAGCTAGA 960
AGAAAAATAC AAAAATAATT TTGTAATGTG AGTGTGATTG TGGGCCAGGA GTTATGTTCT 1020
GAGAAGGAGC TGAGAGTAAA TTATATTCCT GCTTTATTGT GTTGATATTG TCTTCCCTGT 1080
TGTGTCCTGA GTTAGCCTTT GTTGTTCCAA GTTATTAACC AGAGGTGGCT TGATAATGAC 1140
GCCACTTTGG AAGCGTCTGG CTGGTGTTTA AAACTCTAGC TGGTGATAAA 1190
|
