| Tag | Content |
|---|
EnhancerAtlas ID | HS060-25067 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:127832790-127833790 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr3:127833102-127833123 | AAGAACAAAGTGAAACTGAGA | - | 6.18 |
|
| | 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 |
| GH03I128111 | chr3 | 127830362 | 127833950 |
|
Enhancer Sequence | AGGATACCTC AAGTAGGATT TTGAAGCTAT GAGTTGGTCT TAACAAGTTA CACTTAAACA 60
CGCCCTGTGG TAAACTACAA ATTGATTTTT GACAAGATAA TTACAGCTGG CAAATGCTAA 120
ACAGAACCAG ACTTCACAGG TGTACGGTCA AATGTCAAGT ATGGCAAGCA AATGCTTTAA 180
AGTTGGTACA GAACTGGGCA ATGCCATGGC CTCTAAATGC CATTTTCATC TTTCCTCAAC 240
TCTGAAACAG GAGCACGAGT AAGGCCAGCT CCCCAGGTAT ATGGGCTAAG ACTGAAAACA 300
AGCTTGTTAC TGAAGAACAA AGTGAAACTG AGACGGTGTC TTAAAATTAA CAGTCAAGGT 360
TCCTCTCAGA TTTTCTTTTC TATGCCCTTT TGGTGATAGT TTTGAGGTAG TAAAATCTGG 420
TAGAGAATCA GTGTATAGCA CAGTATAAAA TGCACTAGCC AGGAACAGAA AGATTAGTGC 480
TGGTTCTGCC ACTAATTTTC AGTGTGACCT TGGGCACTCA GCAAATCTCA GGTGCCCGAT 540
TTCCTCATCT GTCAAATGAA AGTACTAAAG TGCCATGCTA GATCACAAGT GGCAAACTCG 600
TTGCTCACAG CCTGGTTCTG TTTGGCCTGC AGTCTCATGG TGACCTTCAG CAAGGCCGAG 660
CACCTGGGGC TCAAGGCAGA CACGCCACAG TGCACCCAGC CACTTCCCTC ATCCCCGTTG 720
CCTGCCTCAT TAGGCATCTG CACTTGTGAG CTCAAGGCTG ACACCTTGAA AACTGGTATT 780
CTTCTAAGAG CAAAGGAAAA AAATCTCTGG AACATGAAAG GGCACAATGA GAGGAGCAGC 840
ACTCTAACAG CAGACTCCCC GTGGGGCCAC AGGCTGGACA GGACCACCCC TTCCCAGTTA 900
CTCCTTTCTC TTCCTTGTAT CTCTGCCAGC CCCAATTCCC TACCCTCAGT TTTGAACTTC 960
AAAGACAGTG ACCACATCCA ATTCAATGGC ACTCTCCCTC 1000
|
