| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01727 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:36573880-36575130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA13 | MA0650.2 | chr1:36574193-36574204 | CCCCATAAAAC | + | 6.02 | | Mafb | MA0117.2 | chr1:36574217-36574229 | AGTCAGCATTTT | - | 7.22 | | REL | MA0101.1 | chr1:36574167-36574177 | GGGGATTTCC | + | 6.02 | | ZNF263 | MA0528.1 | chr1:36574915-36574936 | GACTCCTCTCTCCCCTCCTCC | - | 6.52 | | ZNF263 | MA0528.1 | chr1:36574918-36574939 | TCCTCTCTCCCCTCCTCCTTC | - | 8.9 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_45971 | chr1:36574036-36575529 | Osteoblasts |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I036108 | chr1 | 36573751 | 36575310 |
|
Enhancer Sequence | TGTGTGTTCC TTGCTCTCCC CATGGGGAAC AGTGGCCAAG CAGGGCCGTC AAGGGTCAGG 60
GGCTGGGCCC TGAGGCTCAA GCCTGGCTCT GCCCACGACT GGCTGTGTGA CCCTGGGTAA 120
GCCATCACCC TCTCTGGTGA CCCCTTGGGA AATGAAGGTA GAAAGACGGC AGGGCTGGCA 180
GGGGCACGGA GCCCGAGGTG GGACGCACAC AGGAGACGCT GATTCAGAGG ACGGCGCAGT 240
GGCGGCCTCG GGTAGATGCA GTGTTTGGAC AGCTGCAAGT CCTTAACGGG GATTTCCCCC 300
CTTTTCAGCA AATCCCCATA AAACAGCATT CTGTCCAAGT CAGCATTTTG TGGCAGCCCG 360
GGCCTCCTCC CAGGGAGGCC AAGGAGACCG GCTGGGAGTG GGGAGTGCTC TGGGATCTTT 420
CAGACCAGTG GTGGCAGAGT GGCGGTGGTG TGCAGCAAAT GGGCCCCAGC AGAAATAATT 480
GGCAAGAAGC AGACCCCTTC ACTGCTCCCA GAAATGCCTG AAGAGGGGAA AGGACATTAG 540
CTAGCAGGGA CCCTTCCCAG CAGTCCTGGT CTCCGAAAGA GTCCTTTCCT AGAGGCGACC 600
AGCAGAGGAG GGCTATGTGG TAGCATGGAA TTGAAAGACC TGCCCACTCT CCCATCCCAT 660
TTCACAGGTG AGCGATCAGA GGTCTCAATA AAAAAGGGGG GCCTGAGAGT TGGTGCCTCA 720
GGACCCCAGG CACCCGCTAG GTTCCCAACG GACCGGCAGA CCCCCACAGG GTGGGTGGAT 780
GAAACGCAGC CCTGCGCAGG CCCCTACTGC TCCAAGCCCC CCACCCACCC CAGACAGAGC 840
AACTGCAGCT GAGGGAGCGG TGGGGGCACT CAGGCAGCCC CAGGGCCTGG CCAAACCACA 900
GGTATGTTAT GAGACGCTTC CTGTTGTGGA GACATTGCTG TGGGATCCGG CTGCCCTGCT 960
TGCTCACCCG CCCCGCGCTG CTCTCTCCTT GCTCCCCAGC CTTGCTCTCT GCGCTCTTGC 1020
TGGGTCTCTA CTCCTGACTC CTCTCTCCCC TCCTCCTTCT GGCTCTGTCT CTGTCATCAC 1080
AACAGGTGAA CAGCACTTCT GGCTCAGGCC CTCCCTATCA GGGACCCATC CCTGAGACCT 1140
CTAAGGCCCT CCTAGTTCCA GGCAGCCCCT GGACTCCTGT TTCAGCACAG CTACTTACCA 1200
GCTGGGTGAT CTTGGATGGG TCACTTAAAC ACTCTGAACC TCAGTGTCCT 1250
|
