| Tag | Content |
|---|
EnhancerAtlas ID | HS076-00998 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:21816600-21818120 |
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 | TTGGGAGGCT AAGGTGGGCA GATCACTTGA GTTCAGGAGC TCGAGACCAG CCTGGTCAAA 60
ATGGTGAAAC CCCGTATCAA CTAAAAATAC AAAAAAAATT AGCTGGGCTT GGTGACACAC 120
GCCTGTAATC CCAGCTACTT GGGAGGCTGA GGCACAAGAA TCACTTGAAT CTCAGAGGTG 180
GAGGTTGCAC TGAGCTAAGA TCAGGACACT GCACTCTAGC CTGGGTGACA GAGTAAGACT 240
CTGTCTCAAA AAAAAAAAGA AAAAGAAAAC CTACTGCATG ACAGGGACAA TGCTGGTCTT 300
TACACCTATT CTGAAGATTT AATTACTAGA TTGATTTAAG AGTAAATTAA TTTCCATTTA 360
CTTTTTATTT TTATTTTTTT AGAGACAGGG TCTTGTTCTG TCACCCAGGC TGGAGTGCAG 420
TGGTGCGATC ATATTGATAG CAGCAGGAGG CAGACAAATG CCTAGGTAGA TAGGGGCGGG 480
TCCCCGGTGA AACCACAGCT TCAAGCCAAA AACAGCTGGA CTGCTGGTTC CAGAGGAGTG 540
AGAACTTCTG TTCCTGTTTG CCTACCCTTT ACTGACTGGC TCTTTCTGAA TAATGCTCTT 600
TAACCAATCA AATGTTGCCT TTTTCAATAC TACTTACAGC CTGCCCCTCC CTAATGCTAT 660
GCCTGTAAAA ATCCCAGACT CAGCCACACT GAGGGAGATG ACCTGACTTT GGGTGAGACA 720
CCACCTACCC ATCCCCTTTC CTCCAAGAGC TGTTTTGTAG CTCAATAACA TTCTCAGCCC 780
TCATCACCCT TCAATCGTCG GCATGACTTC ATTTTTCTTG GACGAGGGAC AAGAGCTAGG 840
GACCTACCGA ATGTGAGTAC CCAGAAGGCT GTAGCACTGT GGCCCTCTGC CCTCTGCTGG 900
TGGAGGGCAG CCGCTCCATC TGACAGAAGC AGTGGTGAGG CTGAGCCAGT CCTGGAGCCC 960
TGGGCCAGAG CAGGGCAAGG AGCTGAGTGA GCTGCTAACA CACTGCTGTC CATCAGGCTG 1020
CAGATGGTGG AACTGAGAGC TAATTAGCAT ACTGTAACAC CCCCTCTGGG GCTTTGGCAT 1080
TGAAAACACC CCTGCCTGGG CACCACTGTG TTCCCTTCTG GGCAACACGC CTGGTCCAGC 1140
CACCAGCCTT GCACGGAGCC TGCTCCTGTG TTGGGGCTCA GCGCTCAGAA CAGCCAGCCA 1200
GACCCCACAA TCACTTACTC ACACACCCCC TCCCTCCTGG GACTGAGTGC ACAGTCACAG 1260
GGGCCACAGG ATCCACACTG GAAGCTTGCC TTCAAGCACA GCCCAGCGGG CCAAGTTGAC 1320
GGGGCATCTC CTGCTGTGAG CCTGACAAAG GGAGCAAAAA AAATCCTGCG CCAATAGCTC 1380
ACTGCAGTCT CGACCTCCCG GGCTCCAGTG ATCCCCCTCC CACATCAGCC TCCTGAGTAA 1440
CTGGGACTGC AAGTGCGCAC CACCATGCCC AGCTAAGTTT TTTGACTTTT TGTAGAGATG 1500
GGAGTCTCAC TATGTTGCCT 1520
|
