| Tag | Content |
|---|
EnhancerAtlas ID | HS158-60245 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chrX:129065050-129066480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chrX:129066379-129066389 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chrX:129065683-129065693 | GGGGCGGGGC | - | 6.02 | | NFYB | MA0502.1 | chrX:129065502-129065517 | CTGATTGGTCCACTC | - | 6.77 | | SP2 | MA0516.2 | chrX:129066169-129066186 | CTAAGTCCCTCCCACAC | + | 6.48 | | ZNF263 | MA0528.1 | chrX:129065413-129065434 | TTTTTTTTCTTTTCTTCCTCC | - | 6.07 |
|
| | 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 |
| GH0XI129930 | chrX | 129064554 | 129067376 |
|
Enhancer Sequence | CGATCCACTC GCTGGTTGAC ACTTAAGTCA GTAGCCAGTG GTAGGGGATG CGGGAGCCCT 60
GCCCACTCCT GCCTCCGTTT AAGAGACCAC AACATTCTCT TGCACTCTTT TGAGCACAAA 120
GCTGCTACCT CCGTCCCACC CACCCCCCAA ATTGAGGCGC CCAATCAAGT GTCCCCGGTA 180
AATGGCCAAT CCCCGTCTAC TTTCCCCGGA CCCTCTTCAG CTCCGTTTGC TCCCCACTAC 240
CCAGGAGTGA TGCAAGCCAC CCCATCCTTC AAAGGAGAAG GCAGGTGCCA GAGCGTGCTA 300
TAAACGACGC CCATTCCCAG CCTTCCAAGC CCCCAAACAG ATTCGATTGT TGTTTCGTGG 360
GGCTTTTTTT TCTTTTCTTC CTCCGAACCT CCGAAGTGTT CTCCCTTCCC ATTGGCCGAA 420
GCTGCCCCTT GACGCCACCC TGGCCTTGCT CGCTGATTGG TCCACTCTGG ATGTGCCCAA 480
GCCTTTTTCC CAGGGTGTGG CGCCCCCCCG CCCCCAACAG GGTTCTGACC CCTGGCTCCT 540
CCCTTCCCCC CAAGCCCCCC TCTCTGTTCC GAATGGTTCC GCCCTGGCTC GGCTCCCCCA 600
CGGCCCAGGC CGCTGCCCTT AGGGCCCCCG GACGGGGCGG GGCACGCTGG GGACGGGCAG 660
AGGGCGGTGG TGGCGCCTTC CTGCCGAGTC CGAGGCCGCC CCCGCCACCC TTCTCTAATC 720
CTTGTAGGTC CCACTTTCCC CTGGGCAGTT CTCCTCCTGC ATCGGTAGCC CCGTCCCGTC 780
TGTGCAGCCC CCACCGTGGT CTTTGGGTCA TCTCGAAGAG CTGCGTTAAA TCCCTGCCCT 840
CAGCGCTGCA CACACGCCCA TCCGCCTCCA CCCTCGGGTC CCCGCACCAC CCCCTTTTCC 900
CGTGTCGGCT CCCCCTTCCC CTCCCGAGAC CGCGGAAGCT CCGACCCCCT TCCCTCGCTG 960
ACTGTCCATC CCCAGGACCC CCGTCCCTGT GTGTGGCCAG TCCCAGCGGC CTCTCCTTCG 1020
CGGCCTCCCT TCGCCTTCGT GGCCAGCGTG GTGGAGCACT CCCGCCCCCC TTTTCTCCGT 1080
ACCCCCGCGC TCCCTTATGT TGTCCCTTCT TGTCCCTCTC TAAGTCCCTC CCACACTATG 1140
CCCCCCCGCG GTACACACAC ACCCCTCCCC GCGAGGCGTC CCCCGGCGCC CCTCCCCTAC 1200
CCCCGCTCGT CTATGCCCCT CCCACCCACC CCGTCCTTTT GTCTCCTCTT TGGTCTCTAA 1260
GTCCCCCGCC CCTCCCTCGC TCCCGCCCTC ACTCCCCCGA GCACGCTCTT ATCTTCCCCA 1320
GGTCCCAGCG CCCCGCCCCG CGGCCGCGCC CCGCGGCCCC CTCCCTTCCG CGGCCCCGTC 1380
TCCGCCCTCC GCGCTCCGCC CTCCCCCCCG CGGCTCCTGC CCGCCAGCCC 1430
|
