Variant report

Variant	rs9825521
Chromosome Location	chr3:194882937-194882938
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:194882117..194884403-chr3:194909326..194911216,2	K562	blood:
2	chr3:194836997..194839918-chr3:194880679..194883112,2	K562	blood:
3	chr3:194872665..194876358-chr3:194881191..194883259,3	K562	blood:
4	chr3:194881175..194883958-chr3:194892435..194894199,2	K562	blood:

Variant related genes	Relation type
ENSG00000173950	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10433328	0.87[ASN][1000 genomes]
rs10433329	0.91[ASN][1000 genomes]
rs10433330	0.91[ASN][1000 genomes]
rs10933700	0.91[AMR][1000 genomes];0.80[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10933701	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12491661	0.89[ASN][1000 genomes]
rs12491663	0.82[ASN][1000 genomes]
rs2004553	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2088040	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2088041	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2410844	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2410846	0.81[ASN][1000 genomes]
rs28613110	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4677662	0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs4677811	0.91[ASN][1000 genomes]
rs4677814	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs59556963	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs59834989	0.84[AMR][1000 genomes]
rs60528401	0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6437460	0.89[ASN][1000 genomes]
rs6799346	0.91[ASN][1000 genomes]
rs73206648	0.86[ASN][1000 genomes]
rs73206650	0.86[ASN][1000 genomes]
rs73206651	0.91[ASN][1000 genomes]
rs7628775	0.83[ASN][1000 genomes]
rs7637593	0.83[ASN][1000 genomes]
rs7653355	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs903309	0.86[ASN][1000 genomes]
rs903311	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9809570	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9824084	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9835446	0.80[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1007697	chr3:194554814-195009930	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv536873	chr3:194554814-195009930	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
3	nsv997779	chr3:194687093-194885936	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv536874	chr3:194687093-194885936	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1009796	chr3:194737333-195124248	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
6	nsv1012592	chr3:194814446-194931562	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
7	nsv536875	chr3:194814446-194931562	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
8	nsv1001492	chr3:194814990-194935397	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
9	nsv461126	chr3:194817484-194961888	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
10	nsv592981	chr3:194817484-194961888	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
11	nsv878137	chr3:194822098-194900432	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
12	nsv461127	chr3:194833940-194934634	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
13	nsv592982	chr3:194833940-194934634	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
14	nsv1014826	chr3:194834615-195631793	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
15	nsv536876	chr3:194834615-195631793	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	73 gene(s)	inside rSNPs	diseases
16	nsv533904	chr3:194868329-195438728	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	65 gene(s)	inside rSNPs	diseases
17	nsv1009120	chr3:194874494-194974672	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
18	nsv1010168	chr3:194874494-195135790	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
19	nsv536877	chr3:194874494-195135790	Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
20	nsv997956	chr3:194879534-195087539	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
21	nsv536878	chr3:194879534-195087539	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:194862400-194897800	Weak transcription	Dnd41	blood
2	chr3:194868800-194885400	Enhancers	Fetal Muscle Leg	muscle
3	chr3:194871400-194887400	Enhancers	Primary hematopoietic stem cells	blood
4	chr3:194872000-194883000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr3:194872000-194883000	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr3:194873000-194884400	Enhancers	Primary B cells from peripheral blood	blood
7	chr3:194873000-194884600	Enhancers	Fetal Thymus	thymus
8	chr3:194874000-194889800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr3:194876600-194893000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr3:194876800-194893800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr3:194877200-194884200	Weak transcription	Gastric	stomach
12	chr3:194877200-194891200	Weak transcription	Psoas Muscle	Psoas
13	chr3:194877400-194883000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr3:194877400-194888600	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr3:194877400-194888800	Weak transcription	Brain Germinal Matrix	brain
16	chr3:194877800-194883000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr3:194878200-194885200	Enhancers	Fetal Stomach	stomach
18	chr3:194878600-194883000	Weak transcription	Brain Hippocampus Middle	brain
19	chr3:194879000-194883000	Weak transcription	Thymus	Thymus
20	chr3:194879600-194883400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:194880000-194883000	Enhancers	Placenta	Placenta
22	chr3:194880000-194883200	Enhancers	Left Ventricle	heart
23	chr3:194880000-194883400	Enhancers	Lung	lung
24	chr3:194880000-194883600	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr3:194880000-194887400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr3:194880200-194883400	Enhancers	Fetal Muscle Trunk	muscle
27	chr3:194880200-194883400	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr3:194880200-194885000	Enhancers	K562	blood
29	chr3:194880200-194886400	Enhancers	Spleen	Spleen
30	chr3:194880800-194883600	Enhancers	Primary B cells from cord blood	blood
31	chr3:194880800-194887200	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr3:194881000-194884600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
33	chr3:194881000-194888800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr3:194881200-194885000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr3:194881200-194887400	Enhancers	HUVEC	blood vessel
36	chr3:194881200-194888800	Weak transcription	NHEK	skin
37	chr3:194881400-194883400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:194881400-194884400	Enhancers	Stomach Smooth Muscle	stomach
39	chr3:194881400-194906000	Weak transcription	Hela-S3	cervix
40	chr3:194881600-194883000	Weak transcription	Colon Smooth Muscle	Colon
41	chr3:194881600-194885000	Enhancers	HepG2	liver
42	chr3:194881600-194885600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr3:194881600-194889200	Weak transcription	Esophagus	oesophagus
44	chr3:194881600-194892800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr3:194881600-194893000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr3:194881600-194903000	Weak transcription	HSMM	muscle
47	chr3:194881800-194883000	Weak transcription	Small Intestine	intestine
48	chr3:194881800-194883200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:194881800-194891000	Weak transcription	Right Ventricle	heart
50	chr3:194881800-194892800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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