| Tag | Content |
|---|
EnhancerAtlas ID | HS088-00861 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr1:21816930-21817860 |
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 | TTGATTTAAG AGTAAATTAA TTTCCATTTA CTTTTTATTT TTATTTTTTT AGAGACAGGG 60
TCTTGTTCTG TCACCCAGGC TGGAGTGCAG TGGTGCGATC ATATTGATAG CAGCAGGAGG 120
CAGACAAATG CCTAGGTAGA TAGGGGCGGG TCCCCGGTGA AACCACAGCT TCAAGCCAAA 180
AACAGCTGGA CTGCTGGTTC CAGAGGAGTG AGAACTTCTG TTCCTGTTTG CCTACCCTTT 240
ACTGACTGGC TCTTTCTGAA TAATGCTCTT TAACCAATCA AATGTTGCCT TTTTCAATAC 300
TACTTACAGC CTGCCCCTCC CTAATGCTAT GCCTGTAAAA ATCCCAGACT CAGCCACACT 360
GAGGGAGATG ACCTGACTTT GGGTGAGACA CCACCTACCC ATCCCCTTTC CTCCAAGAGC 420
TGTTTTGTAG CTCAATAACA TTCTCAGCCC TCATCACCCT TCAATCGTCG GCATGACTTC 480
ATTTTTCTTG GACGAGGGAC AAGAGCTAGG GACCTACCGA ATGTGAGTAC CCAGAAGGCT 540
GTAGCACTGT GGCCCTCTGC CCTCTGCTGG TGGAGGGCAG CCGCTCCATC TGACAGAAGC 600
AGTGGTGAGG CTGAGCCAGT CCTGGAGCCC TGGGCCAGAG CAGGGCAAGG AGCTGAGTGA 660
GCTGCTAACA CACTGCTGTC CATCAGGCTG CAGATGGTGG AACTGAGAGC TAATTAGCAT 720
ACTGTAACAC CCCCTCTGGG GCTTTGGCAT TGAAAACACC CCTGCCTGGG CACCACTGTG 780
TTCCCTTCTG GGCAACACGC CTGGTCCAGC CACCAGCCTT GCACGGAGCC TGCTCCTGTG 840
TTGGGGCTCA GCGCTCAGAA CAGCCAGCCA GACCCCACAA TCACTTACTC ACACACCCCC 900
TCCCTCCTGG GACTGAGTGC ACAGTCACAG 930
|
