| Tag | Content |
|---|
EnhancerAtlas ID | HS104-39219 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr22:46027150-46027990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr22:46027973-46027985 | ACAAAGTAAACA | - | 6.18 | | Foxd3 | MA0041.1 | chr22:46027725-46027737 | AAACAAACAATT | - | 6.22 | | RFX2 | MA0600.2 | chr22:46027195-46027211 | AGTTGCCCTGGCAACG | + | 6.04 | | RFX5 | MA0510.2 | chr22:46027195-46027211 | AGTTGCCCTGGCAACG | - | 6.31 | | RFX5 | MA0510.2 | chr22:46027195-46027211 | AGTTGCCCTGGCAACG | + | 6.53 |
|
| | 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 |
| GH22I045631 | chr22 | 46027069 | 46027259 |
|
Enhancer Sequence | TGGTCTCCCA GACAGCCAAG GAAGGAGGGA GCCCGCCCTG CTCTCAGTTG CCCTGGCAAC 60
GCAGCCAGCC TTGGTTCAGG GAATTAGAAT GAAAAAGCTG CATGCAAATG AGGTAAATTG 120
CAATTAGGGG GGAAGAGCAA ACACTTGGCC TGTTCTTGAG GCCGCACTAG GGAGGTGTCC 180
AGGAGGTATT TGTGCAGCAA AGAATGAGGC CGCAAAAAGA AGAACTCACA TTGCATAAAA 240
GCCTACACCA GGCCCAGGGT GCCCAGGGGT CCCTTGGGTC CTGGTGGATC CCCCGCTTAA 300
TGTTGGTGGT GGTCAGATGT CTGGTGAACG TCAGGAGTCC CACGGCTGCC CCTGACCAGT 360
ATAATGCCTG CTGCAGAGAC CAGAGGGAGC AGGATCAGCT GTCAGCACTA CCAGAATTAT 420
CTCCTTCTTA CAGATGAGAA AGCAGAGGCT TGGAAAGAGT GCACAACTCA CCCAAGCTCA 480
CACAGCTGGT GATAAATTCA AAAGTCAGAT TCCAGACCCC TCAACCATTC ACTCACTAAG 540
AACCCCAGGG GACTGGGCAT CTGCCCTCAT ACCAAAAACA AACAATTCTC TAAAGATGAA 600
CCCCCCATAT TCTGACAAGT ATTCTGCTAC CCACCTCGTT GCTCCAAACT GAAACCCACC 660
AATGCAGCCC TGCCCACCTG TATCGTTAAT GACTTTATAA AACATGAGGG AGGGCCAGGG 720
ACCATGACGC ACGCCTGTAA ACCCAGCACT TTGGGAGGCT AAGGCAGGAG GATCAATGGA 780
GAACAGCCTG GGCAACACAG CGAGACCCCA TCTCTATAAA TAAACAAAGT AAACATAAAA 840
|
