| Tag | Content |
|---|
EnhancerAtlas ID | HS147-15963 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr16:3746370-3747550 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr16:3747425-3747439 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH16I003694 | chr16 | 3744630 | 3747751 |
|
Enhancer Sequence | AAAATAACGA ACGACAATAA TGGATTGTAA GCTGTGACCC GGCAAATCAA GCAAACATCG 60
GTGCACACTT AAACAGAGGA GGAGCAGCAG CTCTTCATCA CAGCAGAATT CCAATGAATA 120
AACACAAGGA ATGGCAGAAA ACAGAAAGCA CACCATCAGG AAACACCACA GCAATAACTG 180
GCTGGTGTAA GTTACTACTA TTTTGAGACA GGGTCTCACT CTGTTGCCCA GGCTGGATCA 240
CAATGGCACA ATCACAGCTC ACTGCAGCCT CGACCTTCCC GGGCTCAGGT GATCCTCCCA 300
CCTCAGCCTC CTGAGTAGCT GGGACTATAG GCCGTGTATT ACCACTCCTA GCTAATTTTT 360
TTTTTCTTTT TTTTTTTGAC TGGGTCTCAC TCTGTCGCCC AGGCTGAAGT GCAGTAGAGT 420
GATCTTGGCT CACAGCAGCC TCAACCCTCC GGATTCAAGT GATCCTCCCA CCTCAACCTT 480
CCGAGTAGCT GAGACTACAG GCTCATGCCA CCATACCCGG CTAATTTTTG TGTTTTCTGT 540
AGAGACAGGG ATTCACCATG TTGCCCAGGC TGGTCTCAAA CTCCTGAGCT CAAGTGATCC 600
CCCGGCCTCT GCCTCCCAAG CGCTGGGATT AGAGCCGTAA GACACCACGC CCAGCCTAAG 660
GTTATGTATT TGAAGCAGTG GTAGATACTG CCAAGTCACA CTCCACAGAG ATCCTATCAG 720
TTTACGTTCC CACAGCAATG TACTAAAGTG CATATCATCC TACATTCCTG CCAAGTCAGT 780
GTTGAGATGA AACTCTTGGA TCTTTGCCTA TTGGTCAGAT AAAATTTTCA CTGCAGTTTT 840
CACTTACATT TCTCTTATTA TAAGCAAAAC TGAGCACTGT CCCGTATTTT TAAATATTTC 900
CTATTTCCTT TTTTGTTAAG GGACTGTTGG TATCCTCTGA TAATTTTTCT ACTACATTTT 960
AAATCTTCTT CTTATTGATT TGTAAGAGCT TTTTATATAT TAAGGAAATT AGTCGCCAGG 1020
AGCGGTGGCT CACACCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGA GGATCACGAG 1080
GTCAGGAGAT TGAGACCATC CTGGCTAACA CGGTGAAACC CCGTCTCTAC TAAAAATACA 1140
AAAAATTAGC CAGGCGTAGT GGTGGGCGCC TGTAGTCCCA 1180
|
