| Tag | Content |
|---|
EnhancerAtlas ID | HS047-13678 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:89969130-89970520 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
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 | chr16:89969997-89970012 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr16:89969997-89970015 | GAGGTCAAGAGTTCAAGA | + | 6.45 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 89969323 | 89969738 | | chr16 | 89969221 | 89969292 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I089903 | chr16 | 89970330 | 89971828 |
|
Enhancer Sequence | TCCGAGGGGC TGTGAGGGGT GAGGGTGAAA TCCCTCCTTA AGACGGGCCT CCTCCGAGGG 60
GCGGTGAGGG GTGAGGGTTA TTTGCGTGCA GCTAGTATAC ACACATTACG TGACCACTCA 120
TCGCCTATTA GGATGTCCTG GAAGCAGCAT CCCTTTCTCG GTTCTGTGGG TTTCCAGGGC 180
TCTGTCTGGG CCCCGAGGAG GCCCACGGCG TGGGGTTGGG CAGCTTCTAG CACAGGCAGA 240
AACGTGCCCC CCAGAGGGGC CTGGCCAGGC CTCAGTCTGC TCGCTGACCC CAAAAGTTTC 300
GTCCCCTGTG TCTAAGAAGC ACCTTTGTCC TCCTCTGGGG CTGCATGCAG CTGGCCATAT 360
GCTCCACCAG TGCAGCCGTG TCTGGAAACG CGGCTGGGAG GCCCTGTCCT TTGTGGCAGA 420
GCTGTGCTGC TGTGTCACAG GCTGTAGCGT CAGCACCTCC CTTGAAGGCA GGTGGGCTGC 480
CAAGAAGCCG CTGCCACTTA CCCCAGAACA CTGGAGATCA CTGCAGGCTC TGCCCTCGGG 540
GCCCGTTCCC CTACATGGCG GCCTCTGCCC TCAACCTGCA GTGCTGGCTC TTCCACTGGG 600
CACAGGTGGC CTCCGCTCCC ACCAGCCTGC CATGGGGTCC AGTCTTTGTG ATTAAAACAT 660
CCAACCGGCC GGGCACGGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCA 720
GGAGGATCGC TTGAGCATAG GAGTTCGAGA CCAGCCTGGT CAACACGGTG AAACCCTTTC 780
TCTACCAAAA ATATAAAAAT TAGCCGGGTG TGGTGGCGGA CGCCTGTAAT CCCAGCACTT 840
TCGGAGGCTG AGGCAGGTGG ATCACCTGAG GTCAAGAGTT CAAGACCAGC CTGGCCAGCA 900
TGGTGAAACC CTGTCTCTAC TAAACATACA AAAATTAACC GGGGCGTGGT AGTGTGCGCC 960
TGTGATCCCA GCTACTCGGG AGGCTGAGGC AGGAGAATCG CTTGAGCCTG GGAGGTGGAG 1020
GTTGCAGTGA GCCGAGATTT CGCCAACGCA CTCCAGCCTG AGCAACAGAG TGAGACCCTG 1080
TCTCAGAAAA ACAAAAAAAA ACCCAACCCC ATGTGTGTGG AGGGTGGTGG GTGAGTCTTC 1140
CCTTGGATGC AAATGGGGGC CCTGGCAGCC TCCTTGGGGC TGGTGTGAAG GAGACCCCCA 1200
GCCTCAGACC CTGGGCACGC CAGCAGCAGC AACTCAGAAT ACCACCCGGA AGCAAGCCGC 1260
TGGCCCTGCA GACTCTCCAC CTTAGAACAG CTGTGTCTGT GACAAGGACC TCGCTGTGTC 1320
CCTTACTGCC TTGGGGGCTA GGAGTGGCTG GGGTGTGTGC TGAGGGCCCC CACAGAGCCT 1380
CCGCTTCCCC 1390
|
