| Tag | Content |
|---|
EnhancerAtlas ID | HS182-06745 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr14:92726190-92727130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr14:92726358-92726379 | GACGAGAAAATGAAACCACAG | - | 6.16 | | RUNX1 | MA0002.2 | chr14:92726370-92726381 | AAACCACAGAA | - | 6.32 |
|
| | 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 |
| GH14I092258 | chr14 | 92725037 | 92727108 |
|
Enhancer Sequence | TGCTTCCTTG GCATGTTGTA AAGAATAAGT GAGTCCATGT AAAGGGCTTG GCACACTTAG 60
TGAGCTCTGT AATTACTGCT CTCCTACTGG GCACCCAGCA TCACGTTATA TGCGCTGCAA 120
TCCATCTAAT CTCTATGCCT CCTCTGTTAT TAGCAGACTT GTTTTACAGA CGAGAAAATG 180
AAACCACAGA AATGTCAAGT GACTTACATG AGTCCCTTGG CTGAGGCCAC ACTGAGTTTC 240
AAACCCACAT CTGGCTGCCT CCAGAAGCCC AAGCCCTTAG CTGCCTTGCC ATTCTGTCCC 300
CACCACATGG CGTTCTGCTT CTTGGTTCCT CTATGGCAAA CAAAGAAACC TAGGCCCAGG 360
GAGGTCAACC CATTGTTCAC AGTCACCCAG CTAGTAAATG AAACAGGAAT TAGGATGCAC 420
GAGTCCGTCC ATGACCCCAC ACTTCCTCTA CAGGGACAGA AGCTCTGTAG CATCCTGCAG 480
CAAGATTGTT CTCAGCCACC CTATCAGGCA GTTCCTCCTT GTGTCAAACC AAGATCTGTC 540
CTGCTTTAGT TTATGCTTAT TTTCTTTTGC TGCATTCTTG AAAGAGGCCT TTCTCTGGTC 600
TATTTGAATC TTTAGCTTGT GACCTACCTG CCTACTGCCC AGCTCTGACC TGTCTGTCCC 660
CACATGTCCA CTTCAGCACC TCTCCTTGAG ATGAGGCTAA GGCTTCATGA GCCACCTTCA 720
GGGACAAGTG GACCAAGGGT CTCTAGGGAG TGTCACTCCT CCCGCAGTCT CTGCTGAGCC 780
TCAGTGGGAT CTGGTTTTTT TCTCAGGCCT GGCAGTGAAG TGCCTCCTTC CTGATGTCTT 840
TTGTCCATAC TTCTCCGGAC CGCCACCTTC CCACCTTGCT GGAGATTCGT GTGCTCTTTC 900
TGATATGTGA TCTGGGGGTG GGCGAGAGTG TCCTCTAGAC 940
|
