Variant report

Variant	rs10167916
Chromosome Location	chr2:186943933-186943934
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:186943617..186946004-chr2:186946269..186949362,3	K562	blood:

Variant related genes	Relation type
ENSG00000237877	Chromatin interaction

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10169303	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10169495	0.83[EUR][1000 genomes]
rs10170460	1.00[ASN][1000 genomes]
rs10172385	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10177674	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10188935	1.00[ASN][1000 genomes]
rs10190643	1.00[ASN][1000 genomes]
rs10194279	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10195894	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10196464	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10199503	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10199590	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10202753	1.00[ASN][1000 genomes]
rs10202978	1.00[ASN][1000 genomes]
rs10206032	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10206285	1.00[ASN][1000 genomes]
rs10208050	1.00[ASN][1000 genomes]
rs10208364	1.00[ASN][1000 genomes]
rs10208438	1.00[ASN][1000 genomes]
rs10208476	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13403627	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13413555	1.00[ASN][1000 genomes]
rs13414293	1.00[ASN][1000 genomes]
rs13417380	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13421890	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13423512	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13424471	1.00[ASN][1000 genomes]
rs13430022	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34468721	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36103051	1.00[ASN][1000 genomes]
rs60597870	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62197162	1.00[ASN][1000 genomes]
rs62197163	1.00[ASN][1000 genomes]
rs62197188	1.00[ASN][1000 genomes]
rs62197196	1.00[ASN][1000 genomes]
rs62197200	1.00[ASN][1000 genomes]
rs62197201	1.00[ASN][1000 genomes]
rs62197202	1.00[ASN][1000 genomes]
rs62197203	1.00[ASN][1000 genomes]
rs62197214	1.00[ASN][1000 genomes]
rs62197216	1.00[ASN][1000 genomes]
rs62197217	1.00[ASN][1000 genomes]
rs62197218	1.00[ASN][1000 genomes]
rs62197222	1.00[ASN][1000 genomes]
rs62197223	1.00[ASN][1000 genomes]
rs62197226	1.00[ASN][1000 genomes]
rs62198978	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62198988	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199016	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199017	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199018	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199020	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199022	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199023	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199039	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199040	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199047	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62199048	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73981042	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73981045	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv875545	chr2:186566024-187280164	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv817325	chr2:186625679-187200841	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv868949	chr2:186657142-187327560	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv1002243	chr2:186692815-187150225	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv536077	chr2:186692815-187150225	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv932296	chr2:186737443-187265790	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv875547	chr2:186798249-187014815	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv875548	chr2:186798249-187164657	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv875550	chr2:186807268-186965143	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv875551	chr2:186844579-186965143	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv1007635	chr2:186847770-186947882	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1001737	chr2:186847770-186953324	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv1007803	chr2:186847770-186959288	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
14	nsv431846	chr2:186848494-186945624	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	nsv431835	chr2:186848494-186960817	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
16	nsv1005089	chr2:186848664-186953324	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
17	nsv584026	chr2:186851224-186944663	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
18	nsv584027	chr2:186851224-186954427	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
19	nsv584028	chr2:186851224-186965143	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
20	nsv584029	chr2:186851224-186971595	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
21	nsv584030	chr2:186915437-187001076	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
22	nsv1014798	chr2:186933314-186965502	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186928600-186948600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr2:186935600-186946200	Weak transcription	HepG2	liver
3	chr2:186940800-186946800	Weak transcription	Adipose Nuclei	Adipose
4	chr2:186940800-186946800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr2:186942000-186944400	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr2:186942400-186944200	Weak transcription	Liver	Liver
7	chr2:186942800-186946200	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr2:186943000-186944000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr2:186943200-186945400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr2:186943400-186944800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr2:186943800-186946000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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