Variant report

Variant	rs74135713
Chromosome Location	chr10:43810859-43810860
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs57169447	1.00[AMR][1000 genomes]
rs58340819	1.00[AMR][1000 genomes]
rs58594005	1.00[AMR][1000 genomes]
rs58609636	1.00[AMR][1000 genomes]
rs74135709	1.00[AMR][1000 genomes]
rs74135712	1.00[AMR][1000 genomes]
rs74135718	1.00[AMR][1000 genomes]
rs74135728	1.00[AMR][1000 genomes]
rs74135737	1.00[AMR][1000 genomes]
rs7915588	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430159	chr10:43291894-43946294	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv916378	chr10:43622151-43868356	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv1043661	chr10:43626619-43890162	Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv540574	chr10:43626619-43890162	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1035873	chr10:43721143-43873664	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv466882	chr10:43721481-43849358	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv550697	chr10:43721481-43849358	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1044422	chr10:43731521-43860307	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv895087	chr10:43783339-43982390	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43805000-43818000	Weak transcription	Right Atrium	heart
2	chr10:43807000-43813800	Weak transcription	A549	lung
3	chr10:43810000-43813200	Enhancers	Fetal Intestine Small	intestine
4	chr10:43810200-43812600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:43810400-43811800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr10:43810400-43812600	Enhancers	Colonic Mucosa	Colon
7	chr10:43810600-43811000	Enhancers	HepG2	liver
8	chr10:43810600-43813200	Enhancers	Stomach Mucosa	stomach
9	chr10:43810800-43811000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
10	chr10:43810800-43811000	Enhancers	Sigmoid Colon	Sigmoid Colon
11	chr10:43810800-43811000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
12	chr10:43810800-43811200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr10:43810800-43811200	Flanking Active TSS	Fetal Intestine Large	intestine
14	chr10:43810800-43811200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
15	chr10:43810800-43811400	Active TSS	Rectal Smooth Muscle	rectum
16	chr10:43810800-43811600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
17	chr10:43810800-43811600	Active TSS	Duodenum Mucosa	Duodenum

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