| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01229 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:25333000-25334410 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:25333767-25333779 | AAACAAACATTT | - | 6.27 | | HES2 | MA0616.2 | chr1:25334087-25334097 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:25334087-25334097 | GGCACGTGCC | - | 6.02 | | IRF1 | MA0050.2 | chr1:25333939-25333960 | CCTTTCTTTCTTTTTCTTTTT | + | 6.68 | | ZNF263 | MA0528.1 | chr1:25333229-25333250 | GGGGGATGGGAGAGAAGGAGA | + | 6.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59636 | chr1:25332603-25364666 | Ly4 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I025007 | chr1 | 25333492 | 25334553 |
|
Enhancer Sequence | CCCAGCACTG GGTTCACTTG CCTAGAGATG AAGGATTAGT CAGAGCTCTG AGGTGTCCTT 60
GTATCCCCCC TCTACCCCAC TGGAAGGATT GACATGTAAG TTCATAAATG CTGGGAGCCA 120
ACGGGTTGCA GAGATGACAG TGGCAGGGTT TCAGTCATGG CTTTCCTTCC AGGCTTACTG 180
TCTTCATTCT TGGCTTCCAC GGCCAGGCAG TGGCCAGATC ATGCTAGGAG GGGGATGGGA 240
GAGAAGGAGA GAGGGTGAGA AGGGAGGTTT AGCTGGCCCT GGGAAGCCGT GAAAGAGCCG 300
ATGTGAATGA AAGTCAGACT TTCAGAGGAG AAGCTGGGGC TCCGGGAGGA GCACTAGCCA 360
GGGAGTCAGA GACCCAGGGT CCAGCGTGAG GAGCTCCCTG CCTTCTGTGT GCTTCGACAT 420
TCATTTCATT GATGCAGTGA ATACCGGCTA AGGAACTACA TGCCTGGCCC TGTGCCAGGA 480
AAGGGAGAGG GAAAAATCAA GCCGACTTGG TCAGTTACAG AAGCTCACTG TTCAGCGGGC 540
GAGAGAACAC GTGGGGATCT TGTTGAGATA TAAAGTTTGA TCACGACTGC AAGGGAAAAT 600
AGAGAGGGAG GGCTGCGGGG CTTTAGGGTG GGGGTGCTGG GAGAGGAAGC CCATCAGGTG 660
AGATGTGGGA AGGGCATTTC AGGCACAGAC ACTGCAGGAG CAAAGGTGGG GAAGAAGGGG 720
TGGGCATATG GCCCTGCTCA GCTGGAACCC CGTCCTAGGG AAGGAGGAAA CAAACATTTG 780
GAACGTGTGC ATGGTACCAG ATCAGAGTGG GTCTTGAATG ACCAGCTAAA GATTTTGGAC 840
TTCATTCTGC AGGTGGCAGG AGCCACTGAA GGTTTTTGAG TGCAGACATG CCAATAAATG 900
TGTGAAGCAG GAAGAGGCAC ATTTTGAAAG TTTAATGCCC CTTTCTTTCT TTTTCTTTTT 960
TTTGAGACAG GGTCTCACTC TATCTCCCAG GCTGGAGTGC AGTGACACAA TCACAGCTCG 1020
CTGCAGCCTT GACCTCCTGG GCTGAGGCAA GCTTTGCGTT TCAGCTTCCT GAGTAGCTAG 1080
GACTACAGGC ACGTGCCACC ACACCCAGTT TGCTTTTTAG AGATGGTTTT TCGCCATGTT 1140
GCCCCGGCTG GTCTTGAACT CCTGGGCTCA AGGGATCCAC TTGCCTCTGC CTTCCGAAGT 1200
GCTAGGATTC CAGGGGAGAG CCACTGCACC TGGCCACTCC TCTATTTCTT TCTTTCTTTC 1260
TTTCTTTTTT TTTCTTTTGA GACGGAGTCT TGCTCTGTTG CCAGGCTGGA GTGTAGTGGC 1320
GCAATCTTGC ACTGCAACCT CCGCCTCCCA GGTTCAAGCG ATTTTCCTGC CTCAGCCCCG 1380
CAAGCAGATG GCACTACAGG CACCCGCCCC 1410
|
