| Tag | Content |
|---|
EnhancerAtlas ID | HS047-03281 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:230843880-230845010 |
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 | chr1:230843972-230843993 | TATTCTTCCTCCTCTTCCTCC | - | 6.98 |
|
| | 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 |
| GH01I230707 | chr1 | 230843691 | 230845900 |
|
Enhancer Sequence | AAGTTAGGAA GTGGGGCAGG GTCAGGGCAG CATGCGGTGG AGGCCGGCGA GGATCCTGGG 60
CTTCCTTTGA GTCCCGATGT GGTTGGCTTT TTTATTCTTC CTCCTCTTCC TCCTGGCCTG 120
GCTCTGCGGT CTGGGTCAGG TGGATGTGCT CTCTTTCGAA GGGAGACCCA TTTCAGATGC 180
CACTGGCTTT CTTGCCTTTG CCTTCTGCAG GACCCTCCTT CTCAGTGAGC GCTCCTCCCA 240
GCACTTCTCC TAGGGACAGC AGGCTAAGTC CATGTGTCCC TGCTCTGCCC TGCACAGTGT 300
GCTGCCACCC TCAACCGGGC AACCCTCGGG CTGGCCTCTG CCCCTGTGAC CAGTCAGTGC 360
CAGGGCTGAG CAATCCCCCC ATCTATCACC TCTCCCTGAA CCCGAAGGGA AAGACCTCAA 420
GGAGGTTGTT GTGGTAAGAA AAATCACTAT GCGCCACTGA ACCTCTTTCT CCACAGTCTT 480
GTCTTTCACC TCCCGCCTGG CTCTCTGTCC CTCACGAGGT TAACATCTTG ACAGAGCCTC 540
CTCAGTGTCT CTTAGACACA CCCCTCAGCC CCACCCCACC CATGGATTTG CCGAGCTGCT 600
CCCTGAGCAC GTGTTCCCGT GACTGTGTGC CTGGACTCTT GCGTAACCTT CAAACAATCC 660
TCCCTGCCTC CAGTCTGCAC ACGGCAGGCT TCCGGGATGA CCTCTGAACA GAACGCGTCC 720
CCATTCCCAC ACCTACCAAG CATGGCGTTC AAAGTGTCTC CAGCTCTGCC CTCCCCAGGC 780
CCATTTTCTG GTTCAACACT CATGCCAAGC CAACCGCCCC ATCCTCGTTC CTTGCCCCAA 840
ACTCTGCAGG CTGGGCTCAT CATGCTTGCT CCTAGCTTCA CCAGCCCTGT TGCCCTCACT 900
GCCAGGCAAG GCCTGCTCTC CGCTCCCCAG TGACCTCTGT CCTCTGAGAG CCCCGAGGCT 960
TCCCTGAGTT ACCTTGTGGA GCACGTTTCC CTGCAGCTCC AAATCCTAGG CATTTGCCCA 1020
TTGACCTTTA AAAGCCTGGA GGCAGGGCCT ATACAGCCCT CCTCTGGCCT CCTCTGAGAT 1080
GCCAGGCTTA AAGTCTTACA AGTAGCAAAT CCTCAACAAG TATTTGTTAA 1130
|
