| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17649 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:127832600-127833710 |
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 | AAAATTGTTC TCTCAATATC AATATATGGC TCTGACCTAA TTGCTCCGAA TACACCACTG 60
GATCTTTGAG ATACCTGCTT TCTCTTTTTA CAAATACAGG AAAACACCAA TCTACAACCC 120
ATCAGAAATA ATGAAGGAAT GAATGAATGG ATTGTTCATT TTATGTTATG TAGCCCACAA 180
AGAGTGAAGA AGGATACCTC AAGTAGGATT TTGAAGCTAT GAGTTGGTCT TAACAAGTTA 240
CACTTAAACA CGCCCTGTGG TAAACTACAA ATTGATTTTT GACAAGATAA TTACAGCTGG 300
CAAATGCTAA ACAGAACCAG ACTTCACAGG TGTACGGTCA AATGTCAAGT ATGGCAAGCA 360
AATGCTTTAA AGTTGGTACA GAACTGGGCA ATGCCATGGC CTCTAAATGC CATTTTCATC 420
TTTCCTCAAC TCTGAAACAG GAGCACGAGT AAGGCCAGCT CCCCAGGTAT ATGGGCTAAG 480
ACTGAAAACA AGCTTGTTAC TGAAGAACAA AGTGAAACTG AGACGGTGTC TTAAAATTAA 540
CAGTCAAGGT TCCTCTCAGA TTTTCTTTTC TATGCCCTTT TGGTGATAGT TTTGAGGTAG 600
TAAAATCTGG TAGAGAATCA GTGTATAGCA CAGTATAAAA TGCACTAGCC AGGAACAGAA 660
AGATTAGTGC TGGTTCTGCC ACTAATTTTC AGTGTGACCT TGGGCACTCA GCAAATCTCA 720
GGTGCCCGAT TTCCTCATCT GTCAAATGAA AGTACTAAAG TGCCATGCTA GATCACAAGT 780
GGCAAACTCG TTGCTCACAG CCTGGTTCTG TTTGGCCTGC AGTCTCATGG TGACCTTCAG 840
CAAGGCCGAG CACCTGGGGC TCAAGGCAGA CACGCCACAG TGCACCCAGC CACTTCCCTC 900
ATCCCCGTTG CCTGCCTCAT TAGGCATCTG CACTTGTGAG CTCAAGGCTG ACACCTTGAA 960
AACTGGTATT CTTCTAAGAG CAAAGGAAAA AAATCTCTGG AACATGAAAG GGCACAATGA 1020
GAGGAGCAGC ACTCTAACAG CAGACTCCCC GTGGGGCCAC AGGCTGGACA GGACCACCCC 1080
TTCCCAGTTA CTCCTTTCTC TTCCTTGTAT 1110
|
