| Tag | Content |
|---|
EnhancerAtlas ID | HS034-16741 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:88526830-88527710 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:88527275-88527285 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:88527275-88527285 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:88527275-88527285 | AATGGAAAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AATGTTTGAC ACACAATGAG CATTTAATAA ATGTTAGAAT GTTATTATTA ATTGTGAAAT 60
ATGAGTAACA GTACCATTTG TAGGACTGTT GTGGTATTAA ATTAGAAATA TTCATACACC 120
CTAACACACT TAGTATACTG CCTGGGGTAC GATAGGTCGC CCTTACTCTC TACCCTAAGC 180
TGCCTCCCTA GTGAATGCTT TTTTTCTTCT TTTTCTTTTT CCACTTCCCT GTCAGTTTTG 240
ATGAGGATAT AGGCTGGGCT GGTGACTCTG GGAGCAGGAA TGTGCATGTT GAGCTCAGTC 300
ACGGGTGACA GGATCAGAAG TCTTTGGTTT GCCTCTTGGG GAGAGGTGGA TTACGACTCC 360
CCAGGGGTCA GCCCAGGCTT TAGCCTGCAG TCACTTCCTG ACAGGGAGCT ACTCTCCCCC 420
AACTTGGTCT CAGGGCAAAA GGCAAAATGG AAAATGCAAG AATGGAAAGG AAACAGGAGC 480
CACAGGGAAG CTGCTGGGAG ATGGCTGGGC CACACGTTTT TGTCATAGGC CAGCCTTGGA 540
GAACTCCTGT GCTGGGTGAT CTTAATTATA ACCTTACATG ATCATGAGTA AGAATTGAAC 600
AGAGCTCTCC CTGTCTGAAC TCTTTGCTGT GCGCCCCTTC CTTATCCTAA GAGAAAAACA 660
AGAACAAGAG AACGGAAACT AACCAAGCCC TAAAGGACCT CTCTTCACAC ACATTTCTGT 720
CAAAATGGAC AGTAGACTGA AAAGTATGTT TCTCTACCAG GTGATTCCAG GACCTGATGG 780
TGAAGCCTCA GCATCAGAAA GGACCTTAAT CATAATACAG GACATGCTTT CAGATGGGAC 840
TTACACCCAC TGAGGTATTG CAGCCATTGA GGAGGGGGTG 880
|
