| Tag | Content |
|---|
EnhancerAtlas ID | HS050-40704 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:239799860-239800830 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr2:239799874-239799891 | GAGGCCACCTTGACCCT | - | 6 | | GCM1 | MA0646.1 | chr2:239800677-239800688 | CATGCGGGTGC | + | 6.02 | | ZEB1 | MA0103.3 | chr2:239800743-239800754 | CCCACCTGCCC | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_00303 | chr2:239798579-239802139 | Adipose_Nuclei |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I238888 | chr2 | 239797600 | 239801752 |
|
Enhancer Sequence | GCTCTTAGAT CAGCGAGGCC ACCTTGACCC TATCGGGAGC ATTCGGACTC CTGGTAAACC 60
TCTCTCAGTG GACAGCAGAG CTGTGCTTGT GAACGGCCTT CAGGCCCAGC GCCCTCACTG 120
TGCCCAGTGG GGATATCACT GGTCATGGCT GATGACTGGC CGAGCACCTG TGTGTCTCCT 180
CAAAAGGAAC CTGGGGCTTG GCCGGCATGG CCTATTCCTT GTTCTGGTCT GCATTTCGGC 240
CTGGACTTCT GTGTCTCTGT GTGCTGTCCT GAGGCCTGCG GGCTCCCAGG TGTCTGTGTT 300
CCAGTGTAGG GGGAGCTGGA GGGTGAGAGG ACGGTCTGGC AAACGTCCTT CCCCTGGCAG 360
ATCTAGGAGG CATGTGAACA GGGGGACGGT TTCCCCCAGG AGGAGGCCGA GGTCCTGAAA 420
GGCAGGTGGG GGCCTTGAGA CAAGAAAGCG AGAAGGTTCG AGGGTCATCC TTGGCTGGCT 480
GACAGCACCC TCACTCTGGG AGCTGGAAGC TGGGAAGGCA GAGGCGTGCA CATTTTCCAG 540
GCTTGAGTCC AAAAACCCCG CTATTCTCCG TGTCTCCGCT GCCTCACTGC CTTCCTCTGT 600
TTGCTCCTAG AGACCCAGGC GCTGGGTCTG CGGAGTCCGC GGGGATGTCT TTCTGTGTGA 660
ATGAGCAGCC ACTGCGTGTG GGAAGATTGG GCTATGTAGG ACAAGCTGTA TTTGTGCACC 720
TGCGCAAGGC GGGACCACTG AAATTTAGCC CTGGAGTTCG TTCACGGAGC CGCTGACCAC 780
TTATCCCTTC CTCTTCAGCA TGTGCTTGCC GCTGAGCCAT GCGGGTGCTG TGTTCTCTGT 840
TATGTGCCGG TGTGTGGACT GGAACCCGCC TGCAGCAGCC ACTCCCACCT GCCCTCGGGA 900
CCCTGACTGT ACATGGGCTG AGCCAGGCAA CCACCGGAAG GGTGAGTCCT TCCCCAGGAC 960
TCAGCGGGTG 970
|
