| Tag | Content |
|---|
EnhancerAtlas ID | HS047-14589 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr17:41797580-41798810 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr17:41797967-41797988 | GGAGGTGGGGTGGGAAGGGGA | + | 6.81 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GATGGCAGGT AGCCATTTGT GAGTGGAGGA AGATCTGTTG TAGGTGAGTA TTGAAAGCTT 60
TGCTGCAAGG TAGCTTCGTA TGGTGTCTGG CCACCATCTT CAGCAATGTC AATTTTGTTA 120
TCAAAGGCAT CCTCCTGACG GATGCTGGCG GAGTCAGTGA GTTGAGGTGG TTGTTGAACT 180
GTGTTTCCCG TGATCCCTTG CATGAAAGAG AAAGAGAAAT CCATTGTTCT GCTCCAGCAT 240
TCTTAACTTT CCCTTTCTCT CATCGGGCCT TCAGTTTGTC CCGTTCTAAC CGCCCGGCCG 300
TCTCAATGCG ATCACAGGAG GGACACGGAG ATCGAGGAGG GCCACAGCCG GACCAGGCCA 360
GGCGTGCTGC GGCAGGAGGA AGGCTCCGGA GGTGGGGTGG GAAGGGGAGG CCGAGAGACG 420
GGTGTCGCCG CGCCCCCGCT GCCGCCAGAG AGGAGCCTAC GGCTGGCAGC CTGGCCTGGG 480
CAGCAGGGTC CTCGGCGCTC GGCTGGGAAA TCGCACGTCT CTCCGCGGTG ACCTGTGCAC 540
AGCCCCTGGG CCTCCGCCTC CGTGCTGGCA GCCTCCGCCT CAGCGCACAA AGCCCCGTCA 600
CCCCGACTCT CGGGGCGCCG CCGCCGCCAA ATCCTCAGCC CCTCCCTCAT TGGCCGCGGC 660
GTCTGCCGGG AAGTGCAGTC CCGGGTTTGG GGCGATGGAG CCCAGGAGGA AGCGGCGAGT 720
CAGCGCGGCG GAAAGGGCGG AGGGGACGGA GGGGGCGGAG GGGACGAACC ACGAACGCCC 780
GCGGCCGCGA GGGTCTGGAC GACAAAGGAG AGACTAGGCG AGAGGGCTTG TTGCTTTTTT 840
TTTTTTTTTT TTTTTTTTTT TTTTTTTTGA GACGGAGTCT CGCTCTGTCA CCCAGGCTGG 900
AGTGCAATGG CGCGATCTCG GCTCGCTGCA ACCTCCGCCT CCCGGGTTCA AGCGATTCTC 960
CTGCTTCAGC CTCCGAGGAG CTGGGATTAC GGGGGCGCGC CTCCACGCCC AGCTAATTCT 1020
TTGTACTTTT AGTAGAGATG GGGTTTCACC ATGTTGGCCA GGCTGGTATC GAACTCCTGA 1080
CCTCGCGATC CACCCGCCTT GGTGTTGCAC TTTTATAACT CTTTTTACCT TCTCACCAAA 1140
CTAGCATTTA GGAAAAAAAA AAAATCAACA AAAACAAAAC AAAAAAACCA AAAACCTCTA 1200
TCAGTCATTT ACACGTTAGT TGGAAATAAT 1230
|
