| Tag | Content |
|---|
EnhancerAtlas ID | HS076-04623 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:178470300-178471270 |
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 | chr1:178471052-178471071 | GGGCGCCCCCTAGGGGCAA | - | 6.19 |
|
| | 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 |
| GH01I178501 | chr1 | 178470961 | 178471150 |
|
Enhancer Sequence | CCTAGGGCTC TGGGAAAAAA ACACAAATTA CTACCTAACA AGCTTATCCT GCCTCGTGTC 60
TATAAAGCAC TCAACCTCAT CCCAGACCCA TAGAAGAGGC TCAGCTAGAC TTCCTTCCAT 120
TTCTTCAGAG AAAGGAAGGT TTTCTCCTCT CCCTGTGGGA GGCGCTGTGA ACTGGAGACC 180
AGGGCTGTGC TCTGAGGGCA GTACGGGGAC AGCACCTGTG TCCTCCGAAG GCTCCATCAG 240
CTGCGTGGGT TCAGATCATC CTCAAGGACC GCAGGACCTC AAGCTCGGCT GCACTTTGTT 300
CATTTTGTGG ACACTGGAGA GCCACAGGCC ATGTCCCATT GGATGGAGGG GCAGCTCTTA 360
GGAACACCTG CCCACCCTGA AAGGTAGGGT GTCTGCGGTG AGGAGCTTGT TCCCTTTATT 420
CCTGCTCCCT GCTCTGAACT GTTTATTCGG CTTGTAACCT AAATCTGTTT CCACATCCTC 480
TGTTATAAGT GTGGGTTGCC ATGCCTGGCA AGGAGGGGCA GTCGGTATAT GTTGACTGAA 540
TGAGTGGTTG GATAAAAATG ATTTCCTGCT GATGATTGTG TGGGTTTGGA CATGACCTGT 600
GAAGTCGCCT GTGCCTCGTG GGGCCATTTC TGCCCAAGGG AAAAGTTCTG CTCTAAATCC 660
CTATGCAGGC AGGGAAAGCA GGGGAGCAGC TGGGGCAGGT CACTGGGGTA CTTCTGGAAC 720
ACTTGGATCC CTTGGCGAGA GCCTCTGTTC TTGGGCGCCC CCTAGGGGCA AACACTCAGT 780
ACTGGGCAGC CAGACCGGCT TCCTTCAACC TGAAGAGCCC TTTTTGCTGG TGGGGGAGAG 840
GAAGGGTGAA CCCTTGCATT CTAAGCTACT GCTGCTTGTA TCTTTCATTT ATTCCACCCC 900
CTTCCCCCTG TTTAAGTGCT GCTTTAATAG CTAGTCTTAA ATAGAAACAA TTCTACTTGA 960
TTCCTTTACA 970
|
