| Tag | Content |
|---|
EnhancerAtlas ID | HS179-00296 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:17613470-17614550 |
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 | GGAAATTTCC CTTCACCCTA TTGTGGTTCC CCTAACACAG TGGGCAACCT TGACCAGGCC 60
TGAGGATAAG GGAAGATACC CAACCGACTC ACCTACTCCC AGCTGGCTGC CTGAAACCCC 120
TCGGAGTTGG ACCATCAGAT GCTGAACTCG TACTCTCTAG CTGAGCACAT AACTTGGGTG 180
AGCCTCAGTT TCCCCCTCCA TAAAATGGGC AAAATAACTG CCGCTTCATA GAGCTTGCAT 240
GGGGATGAAG TAGGGTAACT CACAAGATAT ACTTAGTGTC AATAGCACAG TGCATGGTGC 300
ATAGTAAGTG CTCAGTAAAT GATGACTGCT GTTACATAAC ATCCCCCAGC CCTTCCTCAA 360
GCATCTGCTG TGTAGAACAC TCCTAATCTC CGCGCTTTAA TAGATGACAA AGACCCTTTG 420
AGACCCAGAG GTGAAATGAG GGAGGTAGGG ACAGGACAGC TGTCTTGGCT ACTCTCAGAT 480
CATACCCTGC TTGTCTCAGC TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT GCCTGGACAA 540
GAAGCTGACA AGAAAGCCTG TCTTTTTTGT GGGGATTTGC AGCTCTGGGT GGCCCTGACT 600
CATGCTTTAT TCAGAATTTG GAATAAGTAG CTGCAGGGCT TCCGCAGGCA TTGCCCAACT 660
CTGTGGCCTC CTGCGGCTTC CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA GGATGGCTGG 720
AAAGGAATTC TGGATGGCTG GACAGAGTCC ATGGGACCTA TCACTTCCTA CAAAGTCACT 780
GTCATCCCAA GTCCCCTCCA GCATAATGAC GGCAAGTGCA AGCATTGTGC CAGCAGGTAC 840
TGAATGCTTC CTGAGCACCA TCTGATATAG CCCTCACAGC ATGCCAGCAG GCAGCTATTA 900
CTATTGTTCT CACTTTATAG ACAGGGAAAC TGAGGCACAG CCACATGAAA GCGCTTGCCC 960
TGGTCACAGA GCTATTAAGT GGGGGAAACA AATTTGAGCC TAGACACGTG ACCTCTGTAC 1020
CCAGTCACAC CAGTGGTTCT CAACCCATCT ACACATTAGA ATCACCTGGA AGGCTCTCAT 1080
|
