| Tag | Content |
|---|
EnhancerAtlas ID | HS116-22595 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr22:41703950-41704990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr22:41704155-41704166 | TCTGATTGGTT | - | 6.62 |
|
| | 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 |
| GH22I041307 | chr22 | 41703170 | 41705141 |
|
Enhancer Sequence | ACCACCAACA TTTGTGTCCT GCTGTGTCCA CAGTCTCTCA TTAATTGTCA TGACAGTCTT 60
TTGAGGTAAG GTAAGAGGTG TCCCTGTTTT TCAGAAGAAA AAGACTGAGG CATCATCACC 120
CACCCACTGC TCTTCCTACC CAGTCCACAA TGTGACTTGG GAGGGGAACA GGGTATTGGA 180
TTCCCTGAGA CCGAGAACCA TGTCTTCTGA TTGGTTTGTG TTACTGAAGT GCTGGAGTCA 240
GCTGATGATC ATTCCTTGAG CACTTCCTGT GAGGGCTGCA GGGAAGGTGG GGGCTCTGGC 300
CCTCCTGGGG TTTTTAGAGG TCGCCCTGGT TCAGCTATGC TCTTGTTCCC TGGAGCATCT 360
CTGTGTCATC CCTCTCCCTC CACAGGCTGA GGAACGCAGG GCAGGGAGCC CAAAGTCCTG 420
AGTTTCATTC CCAACTCCTG TTCATGCTGG CTGTATGATG GAGGCATTAT TATTTTGTCA 480
TTCTTGGCTT CTGTCTCCTT TTCTGTGAAA CGGCCGTACT GATCCTGTCG AATCTGCATC 540
AGGGGTTGTA GTTATGATCA TTTAATAGCC TTCAGAATAT TCCTGAATCT TCTTCACTGT 600
CTGCCTTGAT CCAGGCCTGA ACCACTGCAG TAGCCTCCTA ACCAATCTCC CAGTATCCTC 660
TCTTGTCATA CGTCCTCCCT GCAGTAGCCA AAAGGATCTT CTTGCGAAAT AAATAAGCTC 720
CTGTCACTCT TCTGCTGAAA ACTCTCCTGC AGTTTCCTGA CACACGCAAA ACACAGCCCT 780
GGCTCCCGGC ATGGCCTGTG AGTGGTTCTG AGACCAGCCT CGCCTGCCCC TTGCACTTTG 840
CCTCCCACGT GGCTTGCCCT TGCTTGGGTG TTGCAGCCAC GGTGGCCTTC TGAGTTTTCC 900
TGGAACATTA TCAGCTTGTT CCCACCTCAG GGCCATTGCC TGTGCCCTGT CCCCTGCTAG 960
GTAGGTGCCC TCTTACCCCA CCTCCTATCT TCCATGGCTG GCTACCTATC TCTCTTAAAT 1020
GTCAGCTTCC TCCTAAGGGC 1040
|
