| Tag | Content |
|---|
EnhancerAtlas ID | HS105-38367 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr19:2182350-2183530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr19:2183413-2183427 | CCCGCCTCGGCCTC | + | 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 |
| GH19I002181 | chr19 | 2181002 | 2183356 |
|
Enhancer Sequence | GCAACATAAT GAGACCCCAA GTCTACAAAA AAGTAAAAAA TTAGCTGGGC ATGGTGGTGC 60
ACACCTGTGG TCCCAGCTAC TTGCGGGGCT GAGGTGGGAG GATCACTTGA GACCAGTGGC 120
GCTGTGATTG TGCCACCGCC CTCCAGCCAG GCAACAGAGT GAGACCCTGT CTCAAGAAAC 180
AAAACCCAAA CAAGAAAGAG TGCTCCAGGG CTGTGGCTTC CCGGGGCTGT GACTGTGCAG 240
GTTCTGCCAG TGCTGCCCAG ACGTGGTCTC TCTGGGTTAG GATCTCGGTG CAGCAGGGGT 300
GGAAGCCCCT CTCTGACCAG GCGCTTGCTA GTGTGTCTGG AGGTGCTCAG CAGCAGGGGA 360
GCTGCACCTG CTCCCCATGG GAAGGGGCCT GCACAGACTT CTGGGGTCAG AGGAGACCCC 420
AGGCCCCCGG ATCTCAGGCA GTGGCGGTGA GAGTGCCTCT CTGGCTGCAT GCTCGCCTTC 480
TGCAGGGCTC GGAGCTGACT GTCTTGTTTG AACCTTGTGT GTTTTCTGGG GAGCGCATCT 540
GGAGTCTGGA GCTTAAGCGT TGTAGGGAGC AGGGTCCAGG CACAGGGGCG TGCACCAACA 600
CCTGGGCATC CGCGACGTAG GCAGAGACCT CGAAACTCGA ACCCCCACCA CCTGGAGAGG 660
CTGCTTTCTC CCGTGCATCC CCAGCATGTG GCCAGGGTTC TCACGGTGTG GCTGCACAGA 720
CCTTTTCTGT CTCACTTCCT CTAGAAACAC CGACGACGTT CTTACACAGC AAACACCATT 780
CAGTCCCCAT ACGGCCAGTG TCCCAAGCAC GTCCTCCCAC AGTGGTGTTG TTTTTTTGAG 840
TCAGCGTCTG GCTCTGCTGC TCAGGCTGGG GTGCAGTGGT GCCATCTCAG CTCACTGCAA 900
CTTCCACCTC CCAGGTTCAA GCAATTCTCC TGCCTCAGCC TCCCGAGTAG CAGGGATTAC 960
AGGTGCCTGC AACCACGCCC AGCTAATTTT TGTATTTTTA GTAGAGGCGA GGTTTTGCCA 1020
CCTTGGCCAG GCTGGTCTCA AACTCCTGGC CTCAAGTGAT CCACCCGCCT CGGCCTCCCG 1080
AAGTGTGGGG AGGGCTGTTG TTTAAAGATG ATTGGGCTGT CCTAGGCTCT CCTCGTTTGG 1140
ATGTCCGTTG AGAATCAGCC TTTCCATTTC TCCAGAAAAG 1180
|
