| Tag | Content |
|---|
EnhancerAtlas ID | HS003-12033 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr12:121443000-121443910 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr12:121443116-121443127 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr12:121443116-121443126 | AAAACAAAGG | - | 6.02 | | TFAP2A | MA0003.3 | chr12:121443499-121443510 | CGCCTCAGGCA | + | 6.62 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121005 | chr12 | 121443201 | 121443390 |
|
Enhancer Sequence | AAACGAAAGA AAGAAAAGAT AAAGAGAAAC AAAAAAAAAA TTTTAAGAAG ACACAAAATA 60
AAAAAATTTA AAAAAGAAAC AATAACAAAA AAACCCAACC AAGCAAACAA ACAAAAAAAA 120
CAAAGGAGCA GAGTCAGCAC CCCCAGATGC CAGCCCCTCC TCCCAGGTGC CAGGTGCTGA 180
AGCTGCCCCG CCTCTGCCCT CAGGAGCTCC TGGTCCAGAG GCAAAGACCC AGGAATCAGT 240
CGTCTAACTA CAAAGTGATT CTGCATCTGC CAAGGGTCAT GCTGATGCCT GATGGAGCCA 300
GTGGAGGGCG CGCTGGAGCA GGAGCCAGCA GCCACATCAG CTCAGCAAGC CCTCAGAGGC 360
TTCTGGAAGT CAGCACTTGA GCTCCTGACC TAAGGCAGCC TTCAAAGTGG CAAATGTGTT 420
GGTACAGGAC AGACGCAGAT GGGCGAGGCT GTGGAGGGCA GCAGTAAAGT GCTCCTGCTC 480
AGGGTGACAC AGACGAGGCC GCCTCAGGCA AATGACTTCG TTTCTCAGGG CCTCAGTCTC 540
CTTGTCTGTA CATGGGGTTC AATCATAATA CCTGCCTCAC CACAGGGGCT GAGCAGATGA 600
AAGAATGGTG AGGTGGCCCA TGCCTGTAAC CCCAGTACTT TGGTAGTCTG AGGCGGGAGG 660
ATAGCTTGAG GCCAGGAGTT TAAGACCAGC CTGGGCAACA TGACAGAACC CTGTCTCTAA 720
AAAAAAATAC AAAAATTAGC CAGGTGTGGT GGTGCACGCC TGTAGTCCCA GAACTTTGGA 780
AGGCTAAGGT GGGCAGATGG CTTGAGGCCA GGAGTTCAAG ACCAGCCTGG GCAACATAGC 840
GAGATCCTGT CTCTAAAAAA CATAAATAAT TAGCCAGGGG TGGTGGTGTG TGTCTGTGGT 900
CCCAGCTACT 910
|
