| Tag | Content |
|---|
EnhancerAtlas ID | HS108-14482 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr16:3746420-3747500 |
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 | GCAAACATCG GTGCACACTT AAACAGAGGA GGAGCAGCAG CTCTTCATCA CAGCAGAATT 60
CCAATGAATA AACACAAGGA ATGGCAGAAA ACAGAAAGCA CACCATCAGG AAACACCACA 120
GCAATAACTG GCTGGTGTAA GTTACTACTA TTTTGAGACA GGGTCTCACT CTGTTGCCCA 180
GGCTGGATCA CAATGGCACA ATCACAGCTC ACTGCAGCCT CGACCTTCCC GGGCTCAGGT 240
GATCCTCCCA CCTCAGCCTC CTGAGTAGCT GGGACTATAG GCCGTGTATT ACCACTCCTA 300
GCTAATTTTT TTTTTCTTTT TTTTTTTGAC TGGGTCTCAC TCTGTCGCCC AGGCTGAAGT 360
GCAGTAGAGT GATCTTGGCT CACAGCAGCC TCAACCCTCC GGATTCAAGT GATCCTCCCA 420
CCTCAACCTT CCGAGTAGCT GAGACTACAG GCTCATGCCA CCATACCCGG CTAATTTTTG 480
TGTTTTCTGT AGAGACAGGG ATTCACCATG TTGCCCAGGC TGGTCTCAAA CTCCTGAGCT 540
CAAGTGATCC CCCGGCCTCT GCCTCCCAAG CGCTGGGATT AGAGCCGTAA GACACCACGC 600
CCAGCCTAAG GTTATGTATT TGAAGCAGTG GTAGATACTG CCAAGTCACA CTCCACAGAG 660
ATCCTATCAG TTTACGTTCC CACAGCAATG TACTAAAGTG CATATCATCC TACATTCCTG 720
CCAAGTCAGT GTTGAGATGA AACTCTTGGA TCTTTGCCTA TTGGTCAGAT AAAATTTTCA 780
CTGCAGTTTT CACTTACATT TCTCTTATTA TAAGCAAAAC TGAGCACTGT CCCGTATTTT 840
TAAATATTTC CTATTTCCTT TTTTGTTAAG GGACTGTTGG TATCCTCTGA TAATTTTTCT 900
ACTACATTTT AAATCTTCTT CTTATTGATT TGTAAGAGCT TTTTATATAT TAAGGAAATT 960
AGTCGCCAGG AGCGGTGGCT CACACCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGCGGGA 1020
GGATCACGAG GTCAGGAGAT TGAGACCATC CTGGCTAACA CGGTGAAACC CCGTCTCTAC 1080
|
