Tag | Content |
---|
EnhancerAtlas ID | HS047-12856 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:31171110-31172070 |
Target genes | Number: 10 | 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 | chr16:31171731-31171746 | TGAACTATTGAGCTC | - | 6.03 |
|
| 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 |
GH16I031159 | chr16 | 31171101 | 31171250 |
|
Enhancer Sequence | TGGGAACATG TTGTGTGTTG ACTCCACGCT TGACTGATAT GATCAAGACA TCCCCTTGGT 60 GCTCCCTCTC GTGGCAAGAA GAGTAACTGC TCCTTCAATT TCACTCCCAG ACTCTGCCCC 120 CACCTCCCCA CCCACCTCTT GGTCTCCAGG GACCATGCTG GTACCCTGAG CCTGTCGGAG 180 CCAGAGATTG CCCCAGGACT CAGCGCTTTA GCCTCAAATG AGTTGCCCTA CTTCAAAGGG 240 ACCTCACTTT GTGAGATGCA CTGTATAGAA TTTTTTTTTT TTTTTGAGAT GGAGTCTCGC 300 TGTGTCGCCC AGGCTGGAGT GCAATGGCAT GATCTCAGCT CACCGCAACC TCTGCCTCCC 360 GGGTTCAAGT GATTCTTGCC CCAGCCTCCC GAGTAGCTGG GATTACAGGC ATGTGCCACC 420 ACGCCCAGCT AATTTTGTAT TTTTTAGCAG AGACAGGGGT TCTCCATGTT GGCCAGGTTG 480 GTCTCGAACT CCCAACCTCA GGTGATCCGC CCACCTTGGC CTCCCAAAGC GCTGGGATTA 540 CAGGTGTGAG CCACCGTGCC TGGCCCTAAT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA 600 CTATGTTGGC CAGGCTGGTC TTGAACTATT GAGCTCAGGT TATCCACCTG CCTCAGCCTC 660 CCAAAGTGCT GGGATGACAG GCATGAGCCA CCGTGCCTGG CCATTGTATG CAATTTGGAG 720 GGTGGTTCCT GAGACACAGA GAGAACAATC CGAGTTGGAG TCTGAGGAGG TGGCAGCTCA 780 TTGCTGGGAG AGAGACGTCC TCCTGCTTCT GAGGGGAGCA GTTTTGGGGT GCTCCTGCAT 840 AAACTGTATG GGGTCCGGGA GAGCTCTTGG GGGCAAGAGA GGAGGTCAGG ATGGGATGGG 900 GGTGAGGGCG AGGTTTTTGA GTCATGGCTG GAGGCAACAA GGCTTATGGC CCTGACTTGG 960
|