Variant report

Variant	rs74098137
Chromosome Location	chr12:67295966-67295967
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:11)

rs_ID	r²[population]
rs55916974	0.91[AFR][1000 genomes]
rs58864847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60934939	1.00[AMR][1000 genomes]
rs74098138	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098139	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098140	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098141	1.00[AMR][1000 genomes]
rs74098144	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098145	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74098147	1.00[AFR][1000 genomes]
rs74098148	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1053250	chr12:67067995-67381411	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1050547	chr12:67122154-67314886	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv541521	chr12:67122154-67314886	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1037144	chr12:67203280-67325187	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv1044939	chr12:67207260-67377982	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1036984	chr12:67273098-67427543	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	esv17595	chr12:67295958-67301314	Enhancers Weak transcription	Chromatin interactive region lncRNA	2 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	chr12:67292200-67296400	Enhancers	Primary T cells from cord blood	blood
2	chr12:67292600-67296000	Enhancers	Primary T helper naive cells from peripheral blood	blood
3	chr12:67292800-67296200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr12:67293000-67298800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr12:67293200-67296000	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr12:67293200-67296200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr12:67293200-67296200	Weak transcription	HMEC	breast
8	chr12:67293200-67298000	Weak transcription	Colon Smooth Muscle	Colon
9	chr12:67293200-67298000	Weak transcription	Psoas Muscle	Psoas
10	chr12:67293400-67296000	Enhancers	Primary B cells from peripheral blood	blood
11	chr12:67293400-67296200	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr12:67293400-67304000	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr12:67293600-67296000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr12:67294200-67296000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr12:67295400-67296000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr12:67295800-67296000	Enhancers	NHEK	skin
17	chr12:67295800-67296400	Enhancers	Small Intestine	intestine

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

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