| Tag | Content |
|---|
EnhancerAtlas ID | HS047-16767 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:10325280-10326460 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:10325902-10325917 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I010214 | chr19 | 10325384 | 10325869 |
|
Enhancer Sequence | GAGTGCAATG GTGCAGCCTT GACTCACCGC AACCTCTGCC TCCAGGGTTC AAGCGATTCT 60
CCTGCCTCAG CCTCCCAAGT AGCTGGGATT ACAGGCATGC GCCACCATGC CCGGCTAATT 120
CTGTATTTTT AGTAGAGACA GGGTTTCTCC ATGTTGATCA AGCTGGTCTC AAACTCCTGA 180
CCTCAGATGG TCCACCCGCC TCAGCTTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACT 240
GTTCCCCGGC CAAGGACTAC ATATTTTTAA ATTATTAGGG GTTCCTGGTA AGAAACACAC 300
ATTTCTAGGT TCATTCCAGA CCTGTTTAGT CAGAATCTCT GACCATAGAG CTTGAGAATT 360
TGCATTTAAG CAGGTTCTTC CAGGTCATTC CTTTGTTGGT CCCTATTAGG CAACAGCCTC 420
CCTAGGGGAA AAAGGAGGTG AAAGTCATCT TGTGTTTCCT GCTGGAAGGA CCACTTTAAT 480
TTGGGCTCCA AGATTTGAGA GCTATCAACA AATGGGATCT TCAGATCCAG ATATTGAGGA 540
GGATCAGATA TGATTGTGGG CCCGGCGCAG TGGCTCATGC CTGTAATCCC AGCACTTTGG 600
GAGGCCAAGG TGGGTGGATC ATGAGGTCAG GAGTTCAAGA CCAGCCTGGC TAACATGGTG 660
AAACCCTGTC TCTACTAAAA ATACAAAAAA ATTAGCCAGG CATGGTGGCG GGCACCTGTC 720
ATCCCAGCTA CTTGAGAGGC TGAGGCAAGG AGAATCTCTT GAACCTGGGA GGCGGAGGTT 780
GCAGTGAGCC GAGATCGCAC CATTGCACTA CAGCCTGGGC GACAGTGCAA GACTCCATCT 840
CAAAAAAATT AGCTGGGTAT GATGGTGCAC GCCTGTAATC CCAGCTACTT GGAAGGCTGA 900
GGCGGGAGAA GCGCTTGAAC CTGGGAGGCA GAGGTTGCAG TGAGCCAAGA CTGCGCCATT 960
GCACTCCAGC CTGGGTGACA AGAGAGAAAC TCTGTCTCAA AAAAAAAAAA ATTAGCTAGG 1020
CGTGGTGGTG CGTGCCTGTA ATCACCGCTA CTAGAGAAGC TGAGGCGGAA GAAACTCTCG 1080
AACCTGGGAG GTGGAGGTTG CAGTGAGCCG AGACTGTGCC ACTGCACTCC AGCCTGGGCG 1140
ATAGAGTGAG ACTCTATCTC CAAAAATAAA TAAATAAATA 1180
|
