Variant report

Variant	rs9821956
Chromosome Location	chr3:105462289-105462290
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs12493560	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs12695122	0.83[EUR][1000 genomes]
rs13064310	0.82[EUR][1000 genomes]
rs13317635	0.81[CEU][hapmap]
rs1545304	0.86[CEU][hapmap];0.82[EUR][1000 genomes]
rs17202348	0.83[EUR][1000 genomes]
rs1838046	0.92[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1867190	0.90[CEU][hapmap]
rs2301029	0.91[CEU][hapmap]
rs2301030	0.83[EUR][1000 genomes]
rs2301037	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs2301040	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs2301041	0.82[EUR][1000 genomes]
rs2301043	0.90[CEU][hapmap];0.82[EUR][1000 genomes]
rs2305034	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2305035	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs2305036	0.90[CEU][hapmap];0.82[EUR][1000 genomes]
rs2399054	0.91[CEU][hapmap];0.83[EUR][1000 genomes]
rs3772536	0.81[CEU][hapmap]
rs3772537	0.81[CEU][hapmap]
rs4627779	0.83[EUR][1000 genomes]
rs726444	0.91[CEU][hapmap]
rs7615317	0.93[CEU][hapmap]
rs7624530	0.81[CEU][hapmap]
rs7652702	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs9288815	0.91[CEU][hapmap];0.82[EUR][1000 genomes]
rs9840891	0.82[CEU][hapmap]
rs9859953	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9872897	0.91[CEU][hapmap]
rs9877805	0.81[CEU][hapmap]
rs9878058	0.80[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877306	chr3:105372196-105495841	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv877307	chr3:105373836-105465189	Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv591242	chr3:105373836-105470134	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv877308	chr3:105373836-105495841	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv877309	chr3:105373836-105542435	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv2755185	chr3:105378310-105597310	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv877310	chr3:105409321-105495841	ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv591243	chr3:105438320-105470134	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
9	nsv591244	chr3:105438320-105495841	ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv591245	chr3:105438806-105469882	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv591246	chr3:105439522-105504129	ZNF genes & repeats Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv877311	chr3:105449986-105493286	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9821956	CBLB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105375800-105464600	Weak transcription	Small Intestine	intestine
2	chr3:105389200-105467200	Weak transcription	Stomach Mucosa	stomach
3	chr3:105421200-105465400	Weak transcription	Colonic Mucosa	Colon
4	chr3:105432800-105463800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr3:105433600-105465600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr3:105434800-105463800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:105438800-105464000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr3:105438800-105465400	Weak transcription	Fetal Heart	heart
9	chr3:105439000-105464000	Weak transcription	Duodenum Mucosa	Duodenum
10	chr3:105439000-105464200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr3:105439000-105465400	Weak transcription	Colon Smooth Muscle	Colon
12	chr3:105439000-105465800	Weak transcription	NHLF	lung
13	chr3:105439000-105466200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr3:105439000-105466600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:105439000-105471200	Weak transcription	Fetal Thymus	thymus
16	chr3:105439000-105471400	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr3:105439000-105471400	Weak transcription	HMEC	breast
18	chr3:105439000-105471600	Weak transcription	Fetal Brain Male	brain
19	chr3:105439000-105475800	Weak transcription	Esophagus	oesophagus
20	chr3:105439000-105477400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr3:105439000-105477400	Weak transcription	Lung	lung
22	chr3:105439000-105477400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr3:105439200-105463400	Weak transcription	Fetal Stomach	stomach
24	chr3:105439200-105464600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr3:105439200-105464600	Weak transcription	HUVEC	blood vessel
26	chr3:105439200-105465200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr3:105439200-105465400	Weak transcription	Ovary	ovary
28	chr3:105439200-105465400	Weak transcription	Psoas Muscle	Psoas
29	chr3:105439200-105465600	Weak transcription	Rectal Smooth Muscle	rectum
30	chr3:105439200-105465600	Weak transcription	Right Ventricle	heart
31	chr3:105439200-105465600	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr3:105439200-105477200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr3:105439600-105465200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr3:105439800-105464000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr3:105445800-105465600	Weak transcription	Gastric	stomach
36	chr3:105446600-105477600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:105447800-105462800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr3:105447800-105463400	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr3:105448600-105465400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:105449000-105465000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:105449000-105465400	Weak transcription	Aorta	Aorta
42	chr3:105450000-105462800	Weak transcription	NHDF-Ad	bronchial
43	chr3:105450200-105464800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:105450200-105465000	Weak transcription	Adipose Nuclei	Adipose
45	chr3:105450400-105463800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr3:105450400-105465400	Strong transcription	Osteobl	bone
47	chr3:105451000-105464600	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr3:105451200-105465200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:105452400-105465400	Weak transcription	Left Ventricle	heart
50	chr3:105452400-105477400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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