| Tag | Content |
|---|
EnhancerAtlas ID | HS145-11041 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr18:45599170-45600170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr18:45599768-45599779 | CTGAGTCACCC | - | 6.02 | | JUNB | MA0490.1 | chr18:45599768-45599779 | CTGAGTCACCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26544 | chr18:45598310-45605257 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I048072 | chr18 | 45598970 | 45600373 |
|
Enhancer Sequence | ACTGCTGGGG AGAAGGCAGC CGCTCTCCGC TTCATCCTTG GGCTGGGACC CCAGATGTTT 60
GACCCTGGCC AGCCCCTTGC TGGCCTTCCC GACAGAGCCA CTTCCCTTTT GGGAGTGCAG 120
CCTGGAGTTC CCTTCCCCCT CCAGGCCACA GCCCCACTCT CCCTTAGGAT GACCTGAAAG 180
GGAAGTTTAT AAGAGGAAAA GGAATGAACG GGATCCTATT TAACAGCACA TGCTGGGCGG 240
AGGAACTTCC TGACAGGAAC CAATGTGGAA ACCAGGCCCA GTTTGGCCAT GGAAAACTGG 300
TTTGGCTCAG AACTGGCCAG AGTGGAGAGG AGACCTTGGG CAGCTGCACG TCGCAATTAA 360
ACTGGACTTG TCCGACTTCG CTTTCTTTCT TGTCCCCTCT AAGCAAGCAG ACACTATAAT 420
AATCTGCACA CCACAGGGGG TGTGCAGATT ATTTTTTTAA GTCTAGGGGA AAGAAACCCC 480
ACCCTCATTT AGGTCACAGA GACATAAAGG GCTACTGGCT AGGCTCAGCA AATCAGGAAC 540
AGATGTAGGC AGCGGAGCAG GGCCAGGCGA GCAGAGCCGC TGCCACCAGG CGCCCAGCCT 600
GAGTCACCCT GGCGGGGAGG GCGGGAGGTG GTGGGCAGGG GTGGCCGTCT TTATTTGTGG 660
GCTTGGGTGT GGGGTGCAGG AAACAATGCA AACAGAAGAG TCCCCGGGGC TGGGACAGGC 720
GCAGGGGTGC GGGCAGGTAC GGACAGGCTC CCAGTGGCTG CTCTTCTGGG CCAAAGGATT 780
AAAACAGGCC CTGAGTTTGA ACAGGGAGAA GGCTCTGCTC CTCCCTCAGC CTCTTTCTCT 840
CCTTCCCCTG CCCTCCCTCT CCCCCCACCC AAGAAGACCT TATTTCCAGG GCTGAGTCTG 900
GCTGTGGCTG GCCGGCTGGC CTCCGCCCTG GCTCCCCAAC CCCTCTCTTT AAGGGCCAGG 960
CTGTCCTGTG GCTGGCAGCT GGCAGGAGAG GCCTGGGGTG 1000
|
