| Tag | Content |
|---|
EnhancerAtlas ID | HS034-15971 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:15792840-15793700 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX2 | MA0706.1 | chr2:15793455-15793465 | AGTAATTAAC | + | 6.02 | | NFYA | MA0060.3 | chr2:15792905-15792916 | AACCAATCAGA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCTGCTTTTA TCGCCCCAAA ATCTCTTCGA GGTAGGCTAT ACCACCTCTG CTTTACCAAT 60
CAGGAAACCA ATCAGAGAAG TTACATAAAA TGTCCCAGAG TCTCACAGCT GGTCCATATC 120
ATGGGCCTGG GATTCGAACT TTGACACCTG TGACTCAGAG CTCATGTTCT TTCGGCTCCA 180
CTGCTCTGCC TCCTTGGAAA TAATACTGAT GAGCATCCTT CCTCCTCCCA ACTCGGGCCC 240
TCTGGCTGCC CAATACAGCC ATAAGTCAGG CTCTGTCCCA AGGTCCAGCC CAGTCAGGCC 300
ATGCTAGCCA TGGGCTGGTA ATGGGACCCC TGTGGGTGGG GGAGGGATGG ACGCACTAAT 360
GCACTCAGCC CTCAGGCTGG AGATCAAACG GCCCAGCAGA GAGAGATGTA AATCACCCCT 420
CAAAGAGCAG CAGTTCCAAG TGACCGGTGA ACTCAAAGAT TCCCACAGAC ACCCAATACC 480
CCCCTCCAAG CCTCCCTGCT GCCCTGTGGG TGGGGGCCTA GCACACCCTG GGAACCCAGG 540
TCCACCGAGG CCTCACAGGC CTCACCTCTT CACTTAGGAT TCTTCTGCGG CCAAACCCAG 600
GACTGGGGTC CCTGTAGTAA TTAACATGCT CACCTTTGTG AAATGGTGTA GAGCAAGCCG 660
ATCCCAGATT CAAAACCTCC AGCCACTTCC TGCCTGGGTG ATGTGAGGCA AGTCATTTAA 720
CCCTGAGTGG TTCTTCATTG ATAGCATAGG GATGAGAAAA ACAACCTCGC ACTGTTGTTG 780
GGAGACGAAA CAGGTAGCGT GTGAAACCGT GGTGTCTGGT TGACACTAGA AGGTGCTAGC 840
TCCCTTCCCC ACTGTAGCCC 860
|
