| Tag | Content |
|---|
EnhancerAtlas ID | HS062-01231 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr1:178470390-178471320 |
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 | TAGAAGAGGC TCAGCTAGAC TTCCTTCCAT TTCTTCAGAG AAAGGAAGGT TTTCTCCTCT 60
CCCTGTGGGA GGCGCTGTGA ACTGGAGACC AGGGCTGTGC TCTGAGGGCA GTACGGGGAC 120
AGCACCTGTG TCCTCCGAAG GCTCCATCAG CTGCGTGGGT TCAGATCATC CTCAAGGACC 180
GCAGGACCTC AAGCTCGGCT GCACTTTGTT CATTTTGTGG ACACTGGAGA GCCACAGGCC 240
ATGTCCCATT GGATGGAGGG GCAGCTCTTA GGAACACCTG CCCACCCTGA AAGGTAGGGT 300
GTCTGCGGTG AGGAGCTTGT TCCCTTTATT CCTGCTCCCT GCTCTGAACT GTTTATTCGG 360
CTTGTAACCT AAATCTGTTT CCACATCCTC TGTTATAAGT GTGGGTTGCC ATGCCTGGCA 420
AGGAGGGGCA GTCGGTATAT GTTGACTGAA TGAGTGGTTG GATAAAAATG ATTTCCTGCT 480
GATGATTGTG TGGGTTTGGA CATGACCTGT GAAGTCGCCT GTGCCTCGTG GGGCCATTTC 540
TGCCCAAGGG AAAAGTTCTG CTCTAAATCC CTATGCAGGC AGGGAAAGCA GGGGAGCAGC 600
TGGGGCAGGT CACTGGGGTA CTTCTGGAAC ACTTGGATCC CTTGGCGAGA GCCTCTGTTC 660
TTGGGCGCCC CCTAGGGGCA AACACTCAGT ACTGGGCAGC CAGACCGGCT TCCTTCAACC 720
TGAAGAGCCC TTTTTGCTGG TGGGGGAGAG GAAGGGTGAA CCCTTGCATT CTAAGCTACT 780
GCTGCTTGTA TCTTTCATTT ATTCCACCCC CTTCCCCCTG TTTAAGTGCT GCTTTAATAG 840
CTAGTCTTAA ATAGAAACAA TTCTACTTGA TTCCTTTACA ACTAAATATT GAGTTAATAC 900
TAGGTACCTA ATTTGACTAT TTTTCTTCCC 930
|
