Variant report

Variant	rs1706766
Chromosome Location	chr15:45567437-45567438
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10519020	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1618422	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16941188	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16941213	0.95[YRI][hapmap];0.95[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs16941238	0.80[YRI][hapmap]
rs16941242	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1706769	1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1706771	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1706773	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1719233	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2458226	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57259026	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58415206	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61449949	0.91[AMR][1000 genomes]
rs6493142	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6493146	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6493148	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74009617	0.81[AMR][1000 genomes]
rs8033317	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv869616	chr15:45401411-45736209	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv569315	chr15:45446156-45772448	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45550200-45570600	Weak transcription	Stomach Mucosa	stomach
2	chr15:45552600-45570600	Weak transcription	Pancreas	Pancrea
3	chr15:45553800-45569000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:45558000-45570400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr15:45560600-45570400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr15:45560600-45570600	Weak transcription	Fetal Stomach	stomach
7	chr15:45561200-45567600	Strong transcription	Duodenum Mucosa	Duodenum
8	chr15:45563000-45570400	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr15:45564800-45570400	Weak transcription	Fetal Brain Female	brain
10	chr15:45566000-45570400	Weak transcription	Brain Anterior Caudate	brain
11	chr15:45567000-45567800	Enhancers	Fetal Intestine Large	intestine
12	chr15:45567000-45567800	Enhancers	HepG2	liver
13	chr15:45567200-45570400	Weak transcription	A549	lung
14	chr15:45567400-45569000	Weak transcription	Fetal Intestine Small	intestine

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

what's new

Quick links