Variant report

Variant	rs9636429
Chromosome Location	chr2:37215607-37215608
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10084334	0.84[ASN][1000 genomes]
rs10167385	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10176270	0.83[ASN][1000 genomes]
rs10190027	0.81[EUR][1000 genomes]
rs10865119	0.81[ASN][1000 genomes]
rs11124556	0.91[ASN][1000 genomes]
rs1123648	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11682782	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11684340	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11694342	0.86[AMR][1000 genomes]
rs11895180	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17020136	0.80[EUR][1000 genomes]
rs17038861	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2110992	0.91[ASN][1000 genomes]
rs2110998	0.83[ASN][1000 genomes]
rs2247357	0.88[ASN][1000 genomes]
rs2247935	0.83[ASN][1000 genomes]
rs2372788	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2541004	0.81[ASN][1000 genomes]
rs2541007	0.91[ASN][1000 genomes]
rs3770770	0.80[AMR][1000 genomes]
rs3796041	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4255943	0.83[ASN][1000 genomes]
rs4606899	0.84[ASN][1000 genomes]
rs4670181	0.83[ASN][1000 genomes]
rs4670642	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4670643	0.91[ASN][1000 genomes]
rs4670645	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4670647	0.81[ASN][1000 genomes]
rs59952755	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs60572996	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs61380056	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61689754	0.80[AMR][1000 genomes]
rs62133071	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62133077	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62133080	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62133081	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62133082	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62133104	0.82[EUR][1000 genomes]
rs62133105	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62133108	0.81[EUR][1000 genomes]
rs6709006	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6712162	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6723869	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6728062	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6733188	0.84[ASN][1000 genomes]
rs6739171	0.89[ASN][1000 genomes]
rs6753260	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs9636428	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1004483	chr2:36875235-37356812	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS 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	23 gene(s)	inside rSNPs	diseases
2	nsv535644	chr2:36875235-37356812	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv428395	chr2:36990348-37300352	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv456363	chr2:37109281-37235324	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
5	nsv581470	chr2:37109281-37235324	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
6	nsv873879	chr2:37200033-37299145	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv581471	chr2:37213186-37257386	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:37194400-37229000	Weak transcription	Gastric	stomach
2	chr2:37194800-37226400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr2:37194800-37232400	Weak transcription	NHLF	lung
4	chr2:37195000-37224200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr2:37195200-37217400	Weak transcription	NHDF-Ad	bronchial
6	chr2:37195200-37225400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr2:37195200-37252800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr2:37195400-37217600	Weak transcription	Brain Cingulate Gyrus	brain
9	chr2:37195400-37227400	Weak transcription	A549	lung
10	chr2:37195400-37227600	Weak transcription	HUVEC	blood vessel
11	chr2:37195400-37248600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr2:37195600-37231400	Weak transcription	Brain Angular Gyrus	brain
13	chr2:37195800-37229000	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr2:37196200-37226400	Weak transcription	Dnd41	blood
15	chr2:37201000-37225200	Weak transcription	K562	blood
16	chr2:37202000-37228800	Weak transcription	Spleen	Spleen
17	chr2:37202800-37228800	Weak transcription	Aorta	Aorta
18	chr2:37203600-37231600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr2:37204200-37227600	Weak transcription	HepG2	liver
20	chr2:37204400-37228800	Weak transcription	Esophagus	oesophagus
21	chr2:37205200-37220800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr2:37205200-37229400	Weak transcription	Brain Substantia Nigra	brain
23	chr2:37205600-37225200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:37206200-37218400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr2:37206400-37218200	Strong transcription	Primary T cells fromperipheralblood	blood
26	chr2:37206800-37227400	Weak transcription	NHEK	skin
27	chr2:37207000-37225200	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr2:37207800-37224400	Weak transcription	Fetal Lung	lung
29	chr2:37207800-37225400	Weak transcription	Primary B cells from cord blood	blood
30	chr2:37208600-37226400	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr2:37208800-37227600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr2:37209000-37217400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:37209000-37225400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr2:37209000-37225400	Weak transcription	GM12878-XiMat	blood
35	chr2:37209000-37228600	Weak transcription	Psoas Muscle	Psoas
36	chr2:37209000-37290200	Weak transcription	Small Intestine	intestine
37	chr2:37210200-37217600	Weak transcription	Rectal Mucosa Donor 31	rectum
38	chr2:37210200-37227600	Weak transcription	Fetal Heart	heart
39	chr2:37210600-37224000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr2:37211200-37221800	Strong transcription	Primary monocytes fromperipheralblood	blood
41	chr2:37211400-37238200	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr2:37211800-37218200	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr2:37211800-37221200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr2:37212400-37229000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr2:37212600-37216000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr2:37212600-37225400	Weak transcription	HSMM	muscle
47	chr2:37212800-37218000	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr2:37212800-37218400	Strong transcription	Adipose Nuclei	Adipose
49	chr2:37212800-37232000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:37213000-37218400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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