Variant report

Variant	rs2682506
Chromosome Location	chr12:10564963-10564964
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr12:10564886-10566124	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr12:10560564-10566250	Hela-S3	cervix:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:10563346..10565218-chr12:11316267..11318781,2	K562	blood:
2	chr12:10514090..10517702-chr12:10563594..10568036,4	K562	blood:

Variant related genes	Relation type
KLRC4	TF binding region
KLRC4-KLRK1	TF binding region
ENSG00000245648	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10743890	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10845102	1.00[AMR][1000 genomes]
rs11610719	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11830753	1.00[AMR][1000 genomes]
rs12099689	1.00[AMR][1000 genomes]
rs12322217	1.00[AMR][1000 genomes]
rs1915326	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2253722	1.00[AMR][1000 genomes]
rs2253849	1.00[AMR][1000 genomes]
rs2447701	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2447702	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2460730	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2460731	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2460732	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2460733	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2460734	1.00[AFR][1000 genomes]
rs2460735	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682494	0.95[AFR][1000 genomes]
rs2682495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682496	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682498	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682499	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682500	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682501	1.00[AFR][1000 genomes]
rs2682502	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682503	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682505	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682507	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2682510	1.00[AMR][1000 genomes]
rs2734434	1.00[AMR][1000 genomes]
rs2741881	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2741885	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2741886	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2741887	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2741888	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2741889	0.83[AFR][1000 genomes]
rs28425178	1.00[AMR][1000 genomes]
rs2981589	1.00[AMR][1000 genomes]
rs2981590	1.00[AMR][1000 genomes]
rs4275705	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4394921	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4579992	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4612903	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57872510	1.00[AMR][1000 genomes]
rs58350988	1.00[AMR][1000 genomes]
rs9668214	1.00[AMR][1000 genomes]
rs9804977	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898757	chr12:10229281-10614641	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv832328	chr12:10398071-10620443	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv898759	chr12:10454556-10583365	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	nsv1036390	chr12:10496724-10596720	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv898763	chr12:10514528-10603670	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv8914	chr12:10532300-10662676	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv557456	chr12:10532326-10698255	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
8	nsv898764	chr12:10537269-10698255	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
9	nsv898765	chr12:10537269-10701992	Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	nsv898766	chr12:10537269-10722585	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	nsv557457	chr12:10545925-10698255	Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	nsv557458	chr12:10546140-10698255	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
13	nsv1051292	chr12:10547900-10596720	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	esv1809664	chr12:10551852-10598784	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
15	nsv606	chr12:10552632-10612899	Weak transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
16	nsv898767	chr12:10553930-10622047	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
17	nsv973196	chr12:10559010-10573933	Flanking Active TSS Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
18	nsv983434	chr12:10559010-10600415	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
19	nsv557459	chr12:10560591-10729821	Genic enhancers Enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
20	nsv521062	chr12:10560957-10604945	Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
21	esv3503718	chr12:10562526-10589131	Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
22	esv3503730	chr12:10562526-10589131	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
23	esv4003	chr12:10562591-10589105	Weak transcription Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
24	esv1813897	chr12:10563876-10602124	Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10562200-10566600	Weak transcription	Hela-S3	cervix
2	chr12:10562200-10572800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr12:10564400-10565400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr12:10564400-10570200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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