| Tag | Content |
|---|
EnhancerAtlas ID | HS191-14110 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr16:1343930-1344840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX5 | MA0510.2 | chr16:1343993-1344009 | GGTTGCCATGGCATCT | + | 6.11 | | SRF | MA0083.3 | chr16:1343969-1343985 | AGACCATATATGGTGA | + | 7.15 | | SRF | MA0083.3 | chr16:1343969-1343985 | AGACCATATATGGTGA | - | 7.31 |
|
| | 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 |
| GH16I001294 | chr16 | 1344323 | 1344595 |
|
Enhancer Sequence | TGCTAAACAA GGGGTGGATT ATTCATACCT CCCCTTTTTA GACCATATAT GGTGACTTCC 60
TGAGGTTGCC ATGGCATCTG TAAACTGTCA CGGCTGGTGG GAGTGTGGCA GTGAGGACGG 120
CCAGAGGTCA CTCTTGTCAC CATCTTGGTT TTGGTGGGAT TTGGACGGCT CCTTTGCTGC 180
AACCTGTTTT ATCAGCAAGG TCTTTATGAC CTGTATCTTG TGCTGACCTC CTGTCTCACC 240
CTGTGACTCA GAATGCCACA GCGGTCTGGG AATGCAGCCC CACAGGTCTC AGCTTCATTT 300
TACGCAGCCC CATTCAAGAT GGAGTTGCTC TGGTTCACAC GCCTCTGACA ACTTGAGCCC 360
AGGAGGTTGA GGCTGCCATG AGGCTACACT CTATCTCAAA AAAAAAAAAA AAATTCCAGG 420
AACATGAAGA TAATGAGTGA TGGTTACATT GTGCATCTTG TGGTAACATT TTAGGTAATT 480
TATCAGCTAG TCTGAAACTA CAGGGAAAGA AAGGCAAATT CCCTGAAACA GCTTCCCTCC 540
TCGCACAGGC GCAGGGGCTT CACACGCCTC CTGCTCAGGT CTCTCTGGGC CTGATCCAGG 600
TCACAGACCT CACGTTTCCC AGGCTCTCTG AGCCACATCC ATGGGGTGGG CCTGGTGCAC 660
CTTCCAAACC TCACCCTGAG TATCTCTTCA TCTGCCCGCT CATTTTTATC CTCTAAGACA 720
TCTGCAAAAC AAAAATAAAA TTATAAGCCC CCAACTGATG AAACAGACCC CTCCTCTCCT 780
CCAAGGGGAT TCGAAAGTGG CTCAAAACAC TAGTTCAGGC CACGCTGGGA AGGGGGATTG 840
GACATGCCTC ATTACACCCT CCTCCCTTTG GGATTCAGGC CCCACTGACC AGCCTTAACA 900
TTAAAACAGA 910
|
