| Tag | Content |
|---|
EnhancerAtlas ID | HS108-11699 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:20954850-20955770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT3 | MA0757.1 | chr14:20955576-20955590 | TTTATTGATTATTG | - | 6.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH14I020489 | chr14 | 20955641 | 20955790 | | GH14I020486 | chr14 | 20954970 | 20955510 |
|
Enhancer Sequence | TAAAAAATAG GAATTTAGAA AGGTTCCTAA GTTTTCAGCT TGACCTGCTG GGTGAATGGA 60
GTTGCCATCT ACCAAGACAC CGCTAACAGA GGAGCAGTTT TGGCATGGTA ATCAAAAGTT 120
TCTTTTAAGG CTGTCACGTT TGAAAAGCTA GACCTCCAGA TGGACATGTG GATTACACAG 180
TTGGGTATAT GAGTTTGGAG TCCAAGGGAA GAGGTTTAAG CTAGATAAAT ACATTTGGAA 240
GTCATTAGCA CATAGGTGGT GTTTAAACCA AATTATCTGG ACGATATCAC TTGGGGACAG 300
AAGTCAGGAG AAGGAGAAGG ATCTAGCAAA TGTGTTTGAG GAGACATTAA TGAGGTAGAA 360
GGAAAACCAA GAAGTAGGAT GCCTTGGAGG GCAAGTGAAG AAAGCGTTTT AACACAAGAG 420
ACTGATCGAG GTCACTGCTC ACCTTGACGA GCAGTCTCAG CGGGGTAACA AAGATGATAT 480
CTTTATTAGA GCGGACACCA GAAAGAATGA GAGGTGAGGA AATAGAGGCA GCAAGTGCAA 540
ACCATGAAAT TTTGCTATAA AGGGAAGTGG TAGCTGGGGG AAAGGATGTG GGTTCAGGAG 600
AAGGTTTTTT CCTTTTTTTT TAAATGATGG GAGGCATTTT GAACTGGAAA GAAGCCAACT 660
GGGACTTGGG TGTGATCTGA AGAAGAGAAG ATGGCCTGTA CCATAGTCTG AGAGTTAAAT 720
GGCACCTTTA TTGATTATTG ATATAATACC CTATGGCTTG CTTATAGTAC AGTTACACCT 780
GTGTTGTGTG ATAGGGAGCC TTGCCAGTGG AAGCAAATTG GTCTAAGATA GAAGCTTGGT 840
TTTGACTTGA TAGCTGCCCA TAAGAGGGCA GCAGAGCAGA GCTAGGAAAT TAAAAACAAC 900
AACAACAATA ATAACAACAA 920
|
