| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04861 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:177912730-177913690 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:177913343-177913354 | GACAGCTGCGG | + | 6.32 | | Zfx | MA0146.2 | chr1:177913421-177913435 | CAGGCCGGGGCGGC | - | 6.47 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I177943 | chr1 | 177912808 | 177913774 |
|
Enhancer Sequence | CTCTACCTAA AGAAGATAAC TAAGGTAGGA AGATAAGATA CCTGTGCATA AAAGTCAAGA 60
AAACACAAGG CAGCGTGAGC TCAGTGTCAG TGGGGGGCCC TGGATTCGGC TGTGGGAGCC 120
ACACTGTGCC TGCCATGACG TCAACGCCGA AAGCAGTTGC TGTGTGCCAG GCGCTGTTCT 180
CGAGCATTAA GGAAACTAAC TCGATTTCAT GCCAGCTCCA TTACAAGGCA CCACTCTCAT 240
CCCATTTTAC AGCTGAGACC ACTGAAGGCT GCCATCTCAG TCATACTCGT AGGTGTGGCC 300
CAGGTAGTCT GCATGGAGGA AGGGATGGTG CTGGACGTCA GAGCTCACAG AGGATTTAGA 360
CGGAGGAGGA CACGATGTCA GCACTGGTCT TTACGAATGT AAGGTGACAA CAGCATCATG 420
TAGAAACGTT GAGAAGAGGG CGGAAACCAC AGTATGGACA CCACCCACAC AGCTGATGCT 480
CTGAGTGGGA CGAAGAAGGG TGAGGGCGGA GGTAGAGGAC AGAGGATTTC AAAAGAGGCC 540
GGAGAAGGAG TGCGGAGCAG AGGGAGGGTG AGCAGACACT GGGCTGGGCC TGCGCTCCCA 600
CTCCCTCCCA CAGGACAGCT GCGGAGGCTC AGAAGAAAGG GAGAGCTGTC TGGAGAGATG 660
GGGAGAAGGA GCTGACAGCA GGAGTGAGGC ACAGGCCGGG GCGGCAGGCA GGACGTTCAA 720
ACATCAGCAG TGAGGCAGGA GCCTCCAGCA GAGAGGCCTC TGCAAGGTTT TGCCTTCATA 780
TTATAAAATA CAGACCTTTA GGGGACATAA AAAGAAATCC TACACCCTCC CACGCTTAAG 840
CTAATGAGGA AAAGTTCAGT AGATAACTTA GCCCCAGGTA CTAAGTGCCA AAAAGCAAAG 900
CTGCAAATAC AGCTGCCTGC AGCTGCCTGA CAGTGACGGT GGTGGCCTCA TCTGGGCTCA 960
|
