Variant report

Variant	rs10274669
Chromosome Location	chr7:17969206-17969207
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:17966773..17969755-chr7:17976526..17979737,3	K562	blood:
2	chr7:17967526..17969640-chr7:17977395..17979886,2	MCF-7	breast:
3	chr7:17967449..17969491-chr7:17974113..17976806,2	K562	blood:
4	chr7:17967449..17970656-chr7:17972677..17975613,3	K562	blood:

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10226396	0.94[YRI][hapmap];0.93[AFR][1000 genomes]
rs10228026	1.00[AMR][1000 genomes]
rs10228344	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs10229223	1.00[AMR][1000 genomes]
rs10229298	1.00[AMR][1000 genomes]
rs10230274	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10230644	1.00[AMR][1000 genomes]
rs10231226	1.00[AMR][1000 genomes]
rs10231951	1.00[AMR][1000 genomes]
rs10232014	1.00[AMR][1000 genomes]
rs10232030	1.00[AMR][1000 genomes]
rs10234457	1.00[AMR][1000 genomes]
rs10237285	1.00[AMR][1000 genomes]
rs10238514	0.93[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10242619	1.00[AMR][1000 genomes]
rs10242951	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs10244018	1.00[AMR][1000 genomes]
rs10244826	0.95[AFR][1000 genomes]
rs10252592	1.00[AMR][1000 genomes]
rs10264987	0.91[AFR][1000 genomes]
rs10268362	1.00[AMR][1000 genomes]
rs10269984	0.82[AFR][1000 genomes]
rs10270181	1.00[AMR][1000 genomes]
rs10270757	1.00[AMR][1000 genomes]
rs10274155	1.00[AMR][1000 genomes]
rs10274868	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10278523	1.00[AMR][1000 genomes]
rs10280913	1.00[AMR][1000 genomes]
rs10282571	1.00[AMR][1000 genomes]
rs11975603	1.00[AMR][1000 genomes]
rs11976744	0.94[YRI][hapmap]
rs11978117	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17138308	0.93[YRI][hapmap];1.00[AMR][1000 genomes]
rs17138311	1.00[AMR][1000 genomes]
rs17138418	0.86[YRI][hapmap]
rs17138437	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17138450	1.00[AMR][1000 genomes]
rs28468564	0.91[AFR][1000 genomes]
rs28476778	1.00[AMR][1000 genomes]
rs28566938	1.00[AMR][1000 genomes]
rs28637602	0.91[AFR][1000 genomes]
rs28663676	1.00[AMR][1000 genomes]
rs28862893	1.00[AMR][1000 genomes]
rs59568611	1.00[AMR][1000 genomes]
rs60138005	1.00[AMR][1000 genomes]
rs73308167	1.00[AMR][1000 genomes]
rs73308173	1.00[AMR][1000 genomes]
rs73308184	1.00[AMR][1000 genomes]
rs73310107	1.00[AMR][1000 genomes]
rs73310176	1.00[AMR][1000 genomes]
rs73310185	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73310190	1.00[AMR][1000 genomes]
rs73312112	1.00[AMR][1000 genomes]
rs73312146	0.93[AFR][1000 genomes]
rs73680509	0.87[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533938	chr7:17254118-18040301	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv830913	chr7:17848480-18034218	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1026629	chr7:17862477-18362404	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1025023	chr7:17865796-18357630	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1030201	chr7:17898410-18491985	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
8	nsv887808	chr7:17920613-18150005	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1018517	chr7:17926468-18127372	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv606357	chr7:17938491-18375245	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17911400-17977400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:17955000-17977400	Weak transcription	Fetal Intestine Small	intestine
3	chr7:17955400-17973000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr7:17959000-17971400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr7:17959600-17972800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr7:17960800-17970200	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr7:17961000-17971200	Weak transcription	Primary T cells from cord blood	blood
8	chr7:17961800-17977400	Weak transcription	Brain Angular Gyrus	brain
9	chr7:17961800-17978800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:17962000-17970200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr7:17962000-17970200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:17962000-17973400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr7:17962000-17975800	Weak transcription	Hela-S3	cervix
14	chr7:17962200-17973200	Weak transcription	Primary B cells from cord blood	blood
15	chr7:17962200-17977400	Weak transcription	Brain Cingulate Gyrus	brain
16	chr7:17962400-17978600	Weak transcription	Aorta	Aorta
17	chr7:17963400-17970200	Weak transcription	Ovary	ovary
18	chr7:17963400-17972400	Weak transcription	Right Ventricle	heart
19	chr7:17963400-17977000	Weak transcription	Fetal Lung	lung
20	chr7:17963400-17977400	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr7:17963800-17977800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr7:17964200-17970400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr7:17964200-17970800	Weak transcription	Colon Smooth Muscle	Colon
24	chr7:17964200-17971000	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr7:17964400-17969600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr7:17964800-17970400	Weak transcription	Gastric	stomach
27	chr7:17965000-17970200	Weak transcription	Psoas Muscle	Psoas
28	chr7:17965200-17970600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr7:17965400-17970200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr7:17965400-17977200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr7:17965600-17970400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr7:17966600-17969400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr7:17966600-17970200	Weak transcription	Left Ventricle	heart
34	chr7:17966600-17970200	Weak transcription	Pancreas	Pancrea
35	chr7:17966600-17970200	Weak transcription	Right Atrium	heart
36	chr7:17966600-17974800	Weak transcription	Duodenum Mucosa	Duodenum
37	chr7:17967000-17972400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr7:17967200-17972800	Weak transcription	Spleen	Spleen
39	chr7:17967200-17978800	Weak transcription	Lung	lung
40	chr7:17968000-17971600	Weak transcription	Small Intestine	intestine
41	chr7:17968200-17972200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr7:17968200-17973800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr7:17968400-17970600	Weak transcription	Fetal Heart	heart
44	chr7:17968800-17975200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr7:17969000-17970600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
46	chr7:17969000-17971200	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr7:17969200-17969400	Enhancers	Adipose Nuclei	Adipose
48	chr7:17969200-17969600	Enhancers	GM12878-XiMat	blood
49	chr7:17969200-17970200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr7:17969200-17970400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood

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