| Tag | Content |
|---|
EnhancerAtlas ID | HS184-01877 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:178470660-178471320 |
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 | GGAACACCTG CCCACCCTGA AAGGTAGGGT GTCTGCGGTG AGGAGCTTGT TCCCTTTATT 60
CCTGCTCCCT GCTCTGAACT GTTTATTCGG CTTGTAACCT AAATCTGTTT CCACATCCTC 120
TGTTATAAGT GTGGGTTGCC ATGCCTGGCA AGGAGGGGCA GTCGGTATAT GTTGACTGAA 180
TGAGTGGTTG GATAAAAATG ATTTCCTGCT GATGATTGTG TGGGTTTGGA CATGACCTGT 240
GAAGTCGCCT GTGCCTCGTG GGGCCATTTC TGCCCAAGGG AAAAGTTCTG CTCTAAATCC 300
CTATGCAGGC AGGGAAAGCA GGGGAGCAGC TGGGGCAGGT CACTGGGGTA CTTCTGGAAC 360
ACTTGGATCC CTTGGCGAGA GCCTCTGTTC TTGGGCGCCC CCTAGGGGCA AACACTCAGT 420
ACTGGGCAGC CAGACCGGCT TCCTTCAACC TGAAGAGCCC TTTTTGCTGG TGGGGGAGAG 480
GAAGGGTGAA CCCTTGCATT CTAAGCTACT GCTGCTTGTA TCTTTCATTT ATTCCACCCC 540
CTTCCCCCTG TTTAAGTGCT GCTTTAATAG CTAGTCTTAA ATAGAAACAA TTCTACTTGA 600
TTCCTTTACA ACTAAATATT GAGTTAATAC TAGGTACCTA ATTTGACTAT TTTTCTTCCC 660
|
