| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00510 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:21817080-21818020 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:21817484-21817503 | CTCTGCCCTCTGCTGGTGG | - | 6.39 | | NOTO | MA0710.1 | chr1:21817638-21817648 | GCTAATTAGC | + | 6.02 | | NOTO | MA0710.1 | chr1:21817638-21817648 | GCTAATTAGC | - | 6.02 | | Pou2f3 | MA0627.1 | chr1:21817638-21817654 | GCTAATTAGCATACTG | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 21817107 | 21817342 | | chr1 | 21817263 | 21817646 |
|
Enhancer Sequence | TCCCCGGTGA AACCACAGCT TCAAGCCAAA AACAGCTGGA CTGCTGGTTC CAGAGGAGTG 60
AGAACTTCTG TTCCTGTTTG CCTACCCTTT ACTGACTGGC TCTTTCTGAA TAATGCTCTT 120
TAACCAATCA AATGTTGCCT TTTTCAATAC TACTTACAGC CTGCCCCTCC CTAATGCTAT 180
GCCTGTAAAA ATCCCAGACT CAGCCACACT GAGGGAGATG ACCTGACTTT GGGTGAGACA 240
CCACCTACCC ATCCCCTTTC CTCCAAGAGC TGTTTTGTAG CTCAATAACA TTCTCAGCCC 300
TCATCACCCT TCAATCGTCG GCATGACTTC ATTTTTCTTG GACGAGGGAC AAGAGCTAGG 360
GACCTACCGA ATGTGAGTAC CCAGAAGGCT GTAGCACTGT GGCCCTCTGC CCTCTGCTGG 420
TGGAGGGCAG CCGCTCCATC TGACAGAAGC AGTGGTGAGG CTGAGCCAGT CCTGGAGCCC 480
TGGGCCAGAG CAGGGCAAGG AGCTGAGTGA GCTGCTAACA CACTGCTGTC CATCAGGCTG 540
CAGATGGTGG AACTGAGAGC TAATTAGCAT ACTGTAACAC CCCCTCTGGG GCTTTGGCAT 600
TGAAAACACC CCTGCCTGGG CACCACTGTG TTCCCTTCTG GGCAACACGC CTGGTCCAGC 660
CACCAGCCTT GCACGGAGCC TGCTCCTGTG TTGGGGCTCA GCGCTCAGAA CAGCCAGCCA 720
GACCCCACAA TCACTTACTC ACACACCCCC TCCCTCCTGG GACTGAGTGC ACAGTCACAG 780
GGGCCACAGG ATCCACACTG GAAGCTTGCC TTCAAGCACA GCCCAGCGGG CCAAGTTGAC 840
GGGGCATCTC CTGCTGTGAG CCTGACAAAG GGAGCAAAAA AAATCCTGCG CCAATAGCTC 900
ACTGCAGTCT CGACCTCCCG GGCTCCAGTG ATCCCCCTCC 940
|
