| Tag | Content |
|---|
EnhancerAtlas ID | HS003-31379 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr22:43624030-43625070 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr22:43624969-43624984 | GCCCCCCAGGGTTGA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGGCCCAGG GAAGGGGTGC CCAAGTTTTC GAGAGTCTTT CCAGAAGAAT CTGTAGCCCG 60
CCTCCAGAAG CCCAAGCACC AGCTATGTCC TGATCACATT CTTGCCTGAC CCTGTCTGAT 120
CTTCAAGTGG CCTGGCATCG TGAGTGTGGC TACCCCCAGG TCACAGAAAA GGAAGAGAGA 180
GGGGGACCGT CCTTGGCTTC CTAATCTTCA CCCACCATGC CCATATAACA CCAAGTCCCA 240
GCAGCCTGGC TCTGACTCCT AAATACATCT AGAATCTTCC TCTTTGTTCC GTCGCTGCCC 300
ACCCTGCCCC GGCTCCAGCA GTGCATGCTC CCATGCCTGG AGCTGTCTTC CCAGTGGTAC 360
CCTGGATTCC ACTCTCCTTT CCATGTGGTC ACTGGGGCAT CTAGTTCCAT GAACTTGACC 420
ATATCACACC CCTGCTTAAA CCCTCCACAG GCTTCTCATC TGACTGGGAA TAAACCCTCA 480
ACTCCCCTGC GGGCTCACGC AGCCTGCATG GTGGGATGGC GCCCCCTATC CGCATCTTCC 540
TCTGAGCTCC CTCCTGTGGG CTCCAGTCCT GTGGCTGCCT CTCGGTCCTT CTGTCCACTG 600
CTTTCTCATG CGGATCCCTC TGGAGTGCCT CCCTACCCCC AGCCAAACAC TCCCCCTTGA 660
GGATCCCGAA TTGCCCCTCT ACTCTGCCCC TCTCTGCTGT GAGCCTCCCT GGAACGAGCT 720
GTCTGGAATT TCCATGTATT GGTGCCCCCG CTCCTGGCCC GAGTTCTCTA GTAAATGGGG 780
TTTCCAGCCC CGTGCCCATC TGGCCAAGGC CTGGCACTGG CAGAGACCTG CTACCCACCT 840
CTAACCGTTC CCTGCTACCC CTTGTCTCCC CAGCCCTGCC TCACTTGTCC TTGGCTGAGC 900
CCCTCTGCCC AGGAGTCCCC ATCCTTGCTG AGGCCTCAGG CCCCCCAGGG TTGAGGGCAG 960
GGTTGGGATG CGGGGTGCAG TGTAGGTGGC CGTGCGGCCA GGCGCGTGCC TCGGGGGGGA 1020
GGTGGCCCTG GCGGGCAGGC 1040
|
