| Tag | Content |
|---|
EnhancerAtlas ID | HS093-11611 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:30177100-30178120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr16:30177515-30177530 | TGAACTCCTGACCTC | - | 6.22 | | SPI1 | MA0080.4 | chr16:30177660-30177674 | GAAATGAGGAAGTG | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 30177400 | 30178000 | | chr16 | 30177560 | 30178034 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I030165 | chr16 | 30177294 | 30178330 |
|
Enhancer Sequence | AGAGGAAGAG ACACCCCACA GGGGATTGAC AGAGAAAGCC ATAGAGAAAG ATGAGAACAA 60
GGGGAGGGTG CGTCGTCGCA TATTCGAAAG GAACATGTTC AAGGAGGAGG CATAGTCAGT 120
AGCATTGGAT GGACACCAAA ACGTGTTTGC CTGATTTGAT GACCAGGAAG TTACTGGTGG 180
CCCTGCTGAG GGCAAATCTT TTTTTTTTTT TTTTTTAATG GAGTTTCGCT CTGTCACCCA 240
GGCTGGAGTG CAATGGCTCA ATCTCGGCTC ACTGCAACCT CTGTCTCCCG GGTTCAAGCG 300
ATTCTCCTGC CTCAGCCTCC CCAGTAGCTG GGATTACAGG TGTGCGCCAC CACACCCAGC 360
TAATTTTTGT GTTTTTAGTA GAGATGGGGT TTCACCATGT TGGCCAGGGT GGTCTTGAAC 420
TCCTGACCTC AGGTGATCTG CCTGCCTCAG CCTCCCAAAG TGTTGGGATA ACAGGCGTGA 480
GCCACCGGGC CTGGCTGGTG AGGGCAAATA TATGTGGAAT GGCGAGGGCA GAAGACAGAC 540
TCAAGTAGGT GGAAAAGTAG GAAATGAGGA AGTGGAGACA GTGAGTGTCC ACCACTCTCT 600
CAAGAAACTC ACATGTGAAC AATAGGAGTG AAATAGGGAA GTGGTTTGAG GTTGCCAAGT 660
TGAGAGAGGT TCCCCCTGCA CACAGGAACC TGGGTGTGTT TTATATCCTG AAAAGAGAGG 720
GTCTGCAGAG AGAGGCCTGC CAGTAGAGGA GAAAAGGGTG AAACGATGAG GTGAGATCAC 780
TGAAGAAATG GGAGGAATGT GTCCCAAGAG GGATCGGCCT TGGGCCCAAT GAGAACCATT 840
ACTTTAAAAA CATTTTTTTA GAGACAGGGT CTCCTTCTGT CATCCAGGCT GGAATGCAGT 900
GGCGCAATCA TAGTTCACTG AAGCCTCCAA CTCCTGGGCT CAAGGGATCC TCCTGCTTCA 960
GCCTCCCGAG TAGTTAGGAC TACAGGCACA TGCCATCACA CGTGGCTAAT ATTTTATTTT 1020
|
