| Tag | Content |
|---|
EnhancerAtlas ID | HS105-39265 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:15223380-15224370 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr19:15224314-15224325 | AGCCAATCAGA | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr19:15223933-15223948 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr19:15224069-15224084 | TGAACTCCTGACCTC | - | 6.22 | | SP1 | MA0079.4 | chr19:15223471-15223486 | GAAGCTACGCCCCCT | + | 6.02 | | SP4 | MA0685.1 | chr19:15223471-15223488 | GAAGCTACGCCCCCTCA | + | 6.25 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I015112 | chr19 | 15223341 | 15223490 | | GH19I015113 | chr19 | 15224201 | 15224350 |
|
Enhancer Sequence | AGGTGAGTTC ATGCCCAGGG CCTGCACCAC CAATCTGAGC CAGGCTGCTA CAGTGATGCC 60
ACCTTAAGGG ACCAATCAGT GTCTTAGGCT TGAAGCTACG CCCCCTCATG GAGTAAACTG 120
GTACCTGGTT GCCTCAGCAA CCAGTTCAGA TCCAACCAAT CTGTCTGTTT TGTCTTTTTT 180
TATTTTCATT TTTTTGTAAA GACAGGGTTT CTCTATATTG CCCAAGCTGG TCTCAAACGC 240
ATGATCTCAA GCCATCCTTC CGCCTCAGCC TCCCAAAGTA CTGGGATTAT AAACCAAATC 300
ACCTTGCCCC ACAGAGCTGA TTCATCTTTT TATTTTTATT TTTTATTTTT TTTGAGATGG 360
AGTCTTGCTC TCTAGCCCAG GCTGGGGTGT GGTGGCATGA TCTCAGCTCA CTGCAACCTC 420
TGCCTCCCAG GTTCAAGGGA TTCTCCCACC TCAGCCTCCC GAGTAGCTGG GATTATAGGC 480
ACGCACCACC AGTCCTGGCT AATTTTTATA TTTTAAGTAG AGCAGGGTTT CACTGTGTTG 540
GCCAGGCTGG TCTTGAACTC CTGACCTCAA GTGATCCACC CATTTCAGGC CTCTCAAAGT 600
GCTGGGATTA CAGGCATGCA CTACCAATCC TAGCTAATTT TTGTATTTTT AGTGGAGATG 660
GGGCTTCACG GTGTTGGCCA GGCTGGTCTT GAACTCCTGA CCTCAAGTGA TCCGCCTGCC 720
TCAGGCCTCC CAAAGTGCTG GGATTACAGG CATGATCCAG GCATGATCCA CAGACCTGCC 780
CCTACCCATC TTTGATGCAG TCAGAGGCCC TGCCTCTTGA CATGCCAATC AGAGGCCTAG 840
TTGCGTAAGC AACCAGTCCT AGCTCTGCCA GTGAAAACCT GAAAGGGTCG AAGGCCGCTT 900
TCCACAGGCC AATCAGGAGC CTAGTTCCCT AAGCAGCCAA TCAGAGGTCG GCTGTCGCCT 960
CTTTCTATGA CCTACCCTGT CTCCCTTCAG 990
|
