Variant report

Variant	rs4894944
Chromosome Location	chr3:105449328-105449329
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 45 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11708360	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs13061514	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1372982	0.93[CEU][hapmap];0.86[EUR][1000 genomes]
rs1522287	0.88[CHB][hapmap];0.82[JPT][hapmap]
rs1546733	0.92[CEU][hapmap];0.88[CHB][hapmap];0.87[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1550711	1.00[CEU][hapmap];0.88[CHB][hapmap];0.87[JPT][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1561919	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1584028	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16851440	0.92[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1867191	1.00[CEU][hapmap];0.88[CHB][hapmap];0.86[JPT][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2010718	0.81[ASN][1000 genomes]
rs2034157	0.87[CHB][hapmap];0.80[JPT][hapmap];0.81[AMR][1000 genomes]
rs2120105	0.88[CHB][hapmap];0.80[JPT][hapmap];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2293148	0.92[CEU][hapmap];0.88[CHB][hapmap];0.87[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2301044	0.88[CHB][hapmap];0.87[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2301045	0.88[CHB][hapmap];0.82[JPT][hapmap];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2301046	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs35903551	0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3772539	0.96[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4476538	1.00[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4894940	0.88[CEU][hapmap];0.88[CHB][hapmap];0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6437612	0.86[EUR][1000 genomes]
rs6767808	0.93[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6777124	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6787175	0.93[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6800344	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs726443	0.88[CHB][hapmap];0.87[JPT][hapmap];0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7640740	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7644634	0.85[EUR][1000 genomes]
rs7645026	0.81[AMR][1000 genomes]
rs7646159	0.88[CHB][hapmap];0.82[JPT][hapmap];0.96[AFR][1000 genomes];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9832882	0.93[CEU][hapmap];0.88[CHB][hapmap];0.82[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9873655	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9876007	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[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	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs4894944	CBLB	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105375800-105464600	Weak transcription	Small Intestine	intestine
2	chr3:105378000-105455400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:105389200-105467200	Weak transcription	Stomach Mucosa	stomach
4	chr3:105407800-105457800	Weak transcription	HepG2	liver
5	chr3:105421200-105465400	Weak transcription	Colonic Mucosa	Colon
6	chr3:105432800-105463800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr3:105433600-105465600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr3:105434800-105463800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr3:105438800-105464000	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr3:105438800-105465400	Weak transcription	Fetal Heart	heart
11	chr3:105439000-105450600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr3:105439000-105457800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr3:105439000-105461600	Weak transcription	Dnd41	blood
14	chr3:105439000-105464000	Weak transcription	Duodenum Mucosa	Duodenum
15	chr3:105439000-105464200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr3:105439000-105465400	Weak transcription	Colon Smooth Muscle	Colon
17	chr3:105439000-105465800	Weak transcription	NHLF	lung
18	chr3:105439000-105466200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr3:105439000-105466600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr3:105439000-105471200	Weak transcription	Fetal Thymus	thymus
21	chr3:105439000-105471400	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr3:105439000-105471400	Weak transcription	HMEC	breast
23	chr3:105439000-105471600	Weak transcription	Fetal Brain Male	brain
24	chr3:105439000-105475800	Weak transcription	Esophagus	oesophagus
25	chr3:105439000-105477400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr3:105439000-105477400	Weak transcription	Lung	lung
27	chr3:105439000-105477400	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr3:105439200-105449800	Weak transcription	NHDF-Ad	bronchial
29	chr3:105439200-105450400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr3:105439200-105450600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr3:105439200-105452200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr3:105439200-105457800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr3:105439200-105457800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr3:105439200-105457800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr3:105439200-105457800	Weak transcription	Liver	Liver
36	chr3:105439200-105457800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr3:105439200-105457800	Weak transcription	Pancreas	Pancrea
38	chr3:105439200-105458200	Weak transcription	Fetal Muscle Trunk	muscle
39	chr3:105439200-105463400	Weak transcription	Fetal Stomach	stomach
40	chr3:105439200-105464600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr3:105439200-105464600	Weak transcription	HUVEC	blood vessel
42	chr3:105439200-105465200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr3:105439200-105465400	Weak transcription	Ovary	ovary
44	chr3:105439200-105465400	Weak transcription	Psoas Muscle	Psoas
45	chr3:105439200-105465600	Weak transcription	Rectal Smooth Muscle	rectum
46	chr3:105439200-105465600	Weak transcription	Right Ventricle	heart
47	chr3:105439200-105465600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr3:105439200-105477200	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr3:105439600-105465200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr3:105439800-105464000	Weak transcription	Stomach Smooth Muscle	stomach

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