Variant report

Variant	rs17398399
Chromosome Location	chr2:153005484-153005485
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10194916	0.85[CEU][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10930984	0.85[EUR][1000 genomes]
rs10930988	0.85[EUR][1000 genomes]
rs11683326	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11684002	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11684622	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11695538	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17326195	0.89[CEU][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17398246	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17398253	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2004544	1.00[CHB][hapmap]
rs2345644	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2345646	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2345811	1.00[CHB][hapmap]
rs2345894	0.85[CEU][hapmap]
rs2345897	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2345900	0.85[EUR][1000 genomes]
rs4233656	0.85[EUR][1000 genomes]
rs4233657	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4284784	0.85[EUR][1000 genomes]
rs4664090	0.89[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4664092	0.85[EUR][1000 genomes]
rs4664558	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs56853020	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58761402	0.82[EUR][1000 genomes]
rs60098187	0.85[EUR][1000 genomes]
rs60847003	0.85[EUR][1000 genomes]
rs6433898	0.81[EUR][1000 genomes]
rs6433929	0.85[EUR][1000 genomes]
rs66529470	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs66530032	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs66673544	0.82[EUR][1000 genomes]
rs66733611	0.85[EUR][1000 genomes]
rs66782719	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs67135983	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67157738	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6745311	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs67874818	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs68008008	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68036808	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72857737	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72859833	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72859836	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs72864740	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72864741	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72864754	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72864765	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73002815	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7597103	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005746	chr2:152361972-153059840	Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv535984	chr2:152361972-153059840	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv875287	chr2:152714680-153110573	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv875288	chr2:152716628-153183646	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
5	nsv875289	chr2:152720030-153183646	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	esv1847028	chr2:152863856-153045036	Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
7	nsv1004308	chr2:152980087-153154534	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	nsv535985	chr2:152980087-153154534	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
9	nsv459740	chr2:152986041-153045036	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
10	nsv583316	chr2:152986041-153045036	Bivalent/Poised TSS ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
11	esv3693434	chr2:152998467-153208713	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription 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	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:152971200-153008400	Weak transcription	Esophagus	oesophagus
2	chr2:152974200-153017000	Weak transcription	Colonic Mucosa	Colon
3	chr2:152974800-153008200	Weak transcription	Fetal Brain Female	brain
4	chr2:152976000-153014800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:152976200-153010200	Weak transcription	Fetal Brain Male	brain
6	chr2:152976200-153013400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr2:152976400-153013400	Weak transcription	Brain Angular Gyrus	brain
8	chr2:152977400-153006200	Weak transcription	HMEC	breast
9	chr2:152978200-153021400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr2:152981800-153024800	Weak transcription	Brain Substantia Nigra	brain
11	chr2:152982400-153013400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr2:152983800-153013400	Weak transcription	Psoas Muscle	Psoas
13	chr2:152988400-153007400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:152991600-153010600	Weak transcription	Gastric	stomach
15	chr2:152991800-153008600	Weak transcription	NHLF	lung
16	chr2:152991800-153018400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:152992000-153008200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr2:152992000-153011600	Weak transcription	Stomach Mucosa	stomach
19	chr2:152992200-153005800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr2:152995200-153006800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr2:152995200-153006800	Strong transcription	Liver	Liver
22	chr2:152996200-153013400	Weak transcription	Right Ventricle	heart
23	chr2:152998400-153007400	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr2:152998400-153013200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:152998400-153013400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr2:152999800-153007400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr2:153000000-153007400	Strong transcription	Placenta	Placenta
28	chr2:153000200-153031000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr2:153001800-153013600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr2:153001800-153013600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:153002200-153006400	Strong transcription	GM12878-XiMat	blood
32	chr2:153002200-153008400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:153002200-153013400	Weak transcription	Aorta	Aorta
34	chr2:153002200-153023600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr2:153002400-153010600	Weak transcription	Pancreas	Pancrea
36	chr2:153002400-153022000	Weak transcription	Lung	lung
37	chr2:153002600-153010800	Weak transcription	Primary T cells from cord blood	blood
38	chr2:153002800-153006800	Weak transcription	Fetal Stomach	stomach
39	chr2:153002800-153030400	Weak transcription	Thymus	Thymus
40	chr2:153003000-153006600	Weak transcription	Small Intestine	intestine
41	chr2:153003200-153007400	Weak transcription	Fetal Muscle Leg	muscle
42	chr2:153003200-153011800	Weak transcription	Spleen	Spleen
43	chr2:153003200-153013400	Weak transcription	Left Ventricle	heart
44	chr2:153003200-153013600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr2:153003200-153028400	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr2:153003600-153006000	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr2:153003600-153013400	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr2:153003600-153013400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr2:153003600-153013800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr2:153003600-153014000	Weak transcription	Ovary	ovary

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