| Tag | Content |
|---|
EnhancerAtlas ID | HS157-04572 |
Organism | Homo sapiens |
Tissue/cell | PANC-1 |
Coordinate | chr14:105243110-105244360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr14:105244100-105244118 | CACAAGGGGGCCTGGCCA | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CGGGCAGGCA GAGCCTCTGT CTGCGTGCAT CCCCCTGCCC CTCCCAGGGC CCTCACCACA 60
GCCCCCGCTG CACCAGCCAG CTCCCCTTGC ATACCACCCA CCAGGTCCTG GGAAGCCCCA 120
TCTCTTCCTC TCTCCAAGCC TCAGTTTCTC GCCTCACAGA GTGGGGCTAG GACCCCTGTT 180
CCAGCTCAGA CACTCTACTC CAGGCTGAGG CAGCCACACA GGGCATCTGG CCCGGCGTCA 240
GGTCAAACCC CCACCATCGT CCACTCCTAC AGTCCTTCCT TCAGTCTCTG AGCCCCGCCG 300
TGCGCCAGGC CTCAGAGGAT GAGGGGTATG GAGATCCCAC AGAGGGGCTG GCATGAGGGG 360
GGCACCCCAG AAACCTGCTT GTCCCACCTA GTGTAGAAAT GTCCTGCTTT TTTCCCAACC 420
TCACCCTGAG TACCTGGGAA ATACAGCCAC CTGGAGCACA CCCACACCTG GGGCACACCC 480
ACACCTGGGG CACAGGCACA CCTGGGGCAC AGCCACACCT GGGGCACAGG CACACCTGGG 540
GCACAGCCAC ACCTGGGGCA CACATACATC TGGGGCACAC ACACACTGGA GGCAAAGCCA 600
CACCTGGGGC ACACGCACAC CTGAGGCACA CACCTGGGGC ACACGCACAC CTGGGACACA 660
GCCACACTGG AATACACAGA CATCTAGAAC ACATCTAGAC ACCTAGCCAC ATCTGGGGCA 720
CACGAACACC TGGGGCACAC GCACACCTGG GGCACAGCCA CACCTGGGGC ACAAGCACAC 780
CTGGGGAACA CATACCTGGG GCACAGCCAC ACCTACAGCA CGTACACCCT GAGGGCTGTG 840
GGAACGTGCG GGGCCCTGAG AGGTGTGAGT GAGTGGAGTG TGTAGCCGCT GGGGCTCCGT 900
GGCAGGCTCT GGCCCAGCCT GTGCAAAGCA GGAGGAGGCT GAGGGGCCAG TGGGGGGCCT 960
CTGACATTCC AGCATCGAGG CCCTGGCAAC CACAAGGGGG CCTGGCCAGG CAGCAAGGAA 1020
GCTGTCTTCC AGGCCTGGGG GCCAGGAGGG GGCTCGGGAC CAGCCTGGTG GGGAGGGTGG 1080
CCTGTGTCAA CACAGGCCAG AGAAGTGGAA ACCGGTGTGA AGCCCCGGCA CACCCACCTC 1140
CCACTCGCTC CTGGATGGTC CGATCTGCCC CAGTATGCAA TCCCCAGGGC CAGAGTCTCG 1200
AGCCCACTGC CCCGGAACCG TTCCCCGGAG AAAAGCCCCG GACAGAGGCC 1250
|
