| Tag | Content |
|---|
EnhancerAtlas ID | HS059-27934 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:234564440-234565510 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:234564537-234564558 | TCTCACTTTCACTTTTACACC | + | 6.5 | | PRDM1 | MA0508.2 | chr2:234564539-234564549 | TCACTTTCAC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTGAGCCCCA GCCATTCTCT TAACAATTCT TTTAGTTAAG TATCAGTTCC CCCATCCCCT 60
CACTCCAGCA TTTTTTGCCT CTTGCTATGA TCAGTTTTCT CACTTTCACT TTTACACCTC 120
TGATCACTGA AAAATTACAG AATTATAAGT TTGGAAAAGG AGTCTATATT TCTTGGAAAA 180
GGTTACAACC TTCAAGGTGG CCATCTAGCT GGCTGGGAAG CATGACCTCT GGCAAATACC 240
AGAGACAGGC CCTTGAAAGG AGAAGGGATG GGGTAGGAGC TTTATGCTGA ACAAACAGGG 300
TAAACATACA TATTCACCAG GTTACAGAAG GAGCTATGAA TATTTATGAA GGCCATCCTG 360
ACTCATGCGT ATTGAACACA CATGCATGTT ACATATGACC CGTGTTCACC CTGGGGTGGA 420
GACATCATAT TTAAATGGAT TACAATTAGG CCCTATACAT CAAAAGGTCT CTTCAGGGCA 480
CAAAGGCACT CAAATTCACA GTCTCCGTAA ACTGGCCAGA ACCAGTCTGT GATCACCAGT 540
CACTGGTCTT CTTACCAGGA GAAAGTTACT GAAATCAGCC TCTTGTCCAA TGAAAGCAGT 600
ATTTGTGGCT TATGGAACAA GGAATGGACG TCAGTTAGTC AGTGTCCGGT GGAGGTGCAC 660
TTGTTTAACA TTGTTTTTCT CTAGACCTGT GCTTATTTAG CTGCTAGAGA AAAAGAAAAA 720
CTCTGTGGCA GTTGGAACAT AGTTTATTCT TTAAGTGTAG GCGCCCATGA CTCAACTCTT 780
GCCTGGCGTG GTTTGAGGTC TTGTGTGTAG TTTTGTATCT GATTGCCACA AAAAGTCCAC 840
TGAGTCCATC TCATCTCTAT TTTAACACTA AAGTGGGTCA GTTGTGTTTA AACCACAAAA 900
GGGAGGGAGT GTGACGAGGC GTGTCCAGCC TTCTGTCCCG TCGTGGCTGT GACTCAGTTT 960
TGAAGGTTTC TTTGGGGTCC CGCTGGCCAG GAGGGTTCGA TTCACTTGTT GTGGGAGACG 1020
GGCGGCACTT AGTATTTTCT TTTCAGTTTA CACGTTCCTG GGCATCCCTA 1070
|
