| Tag | Content |
|---|
EnhancerAtlas ID | HS092-00513 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:17613670-17614560 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr1:17614474-17614487 | CACGTGACCTCTG | - | 6.04 |
|
| | 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 |
| GH01I017286 | chr1 | 17613436 | 17614463 |
|
Enhancer Sequence | TAAAATGGGC AAAATAACTG CCGCTTCATA GAGCTTGCAT GGGGATGAAG TAGGGTAACT 60
CACAAGATAT ACTTAGTGTC AATAGCACAG TGCATGGTGC ATAGTAAGTG CTCAGTAAAT 120
GATGACTGCT GTTACATAAC ATCCCCCAGC CCTTCCTCAA GCATCTGCTG TGTAGAACAC 180
TCCTAATCTC CGCGCTTTAA TAGATGACAA AGACCCTTTG AGACCCAGAG GTGAAATGAG 240
GGAGGTAGGG ACAGGACAGC TGTCTTGGCT ACTCTCAGAT CATACCCTGC TTGTCTCAGC 300
TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT GCCTGGACAA GAAGCTGACA AGAAAGCCTG 360
TCTTTTTTGT GGGGATTTGC AGCTCTGGGT GGCCCTGACT CATGCTTTAT TCAGAATTTG 420
GAATAAGTAG CTGCAGGGCT TCCGCAGGCA TTGCCCAACT CTGTGGCCTC CTGCGGCTTC 480
CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA GGATGGCTGG AAAGGAATTC TGGATGGCTG 540
GACAGAGTCC ATGGGACCTA TCACTTCCTA CAAAGTCACT GTCATCCCAA GTCCCCTCCA 600
GCATAATGAC GGCAAGTGCA AGCATTGTGC CAGCAGGTAC TGAATGCTTC CTGAGCACCA 660
TCTGATATAG CCCTCACAGC ATGCCAGCAG GCAGCTATTA CTATTGTTCT CACTTTATAG 720
ACAGGGAAAC TGAGGCACAG CCACATGAAA GCGCTTGCCC TGGTCACAGA GCTATTAAGT 780
GGGGGAAACA AATTTGAGCC TAGACACGTG ACCTCTGTAC CCAGTCACAC CAGTGGTTCT 840
CAACCCATCT ACACATTAGA ATCACCTGGA AGGCTCTCAT GAAAACCTAG 890
|
