Variant report

Variant	rs11946732
Chromosome Location	chr4:148835530-148835531
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11930900	0.83[AFR][1000 genomes]
rs11934409	1.00[CHB][hapmap];0.95[JPT][hapmap];0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11937178	1.00[CHB][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes]
rs11939997	0.92[AMR][1000 genomes]
rs11941546	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs11942547	0.95[CHB][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes]
rs13434578	1.00[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes]
rs13435747	0.92[AMR][1000 genomes]
rs17024143	0.92[AMR][1000 genomes]
rs187006	0.86[CHB][hapmap]
rs2118033	0.86[CHB][hapmap]
rs2118035	0.82[AMR][1000 genomes]
rs2164530	0.95[CHB][hapmap];0.84[JPT][hapmap];0.81[YRI][hapmap];0.87[AMR][1000 genomes]
rs2164531	0.95[CHB][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes]
rs2358180	0.85[AMR][1000 genomes]
rs2358181	0.86[CHB][hapmap]
rs2635256	0.86[CHB][hapmap]
rs2635266	0.86[CHB][hapmap]
rs2635267	0.95[CHB][hapmap];0.84[JPT][hapmap];0.80[AMR][1000 genomes]
rs2635268	0.86[CHB][hapmap]
rs4027115	0.85[YRI][hapmap];0.81[AFR][1000 genomes]
rs4337713	0.89[AMR][1000 genomes]
rs55752555	0.82[AMR][1000 genomes]
rs67913037	0.87[AMR][1000 genomes]
rs72617450	0.82[AMR][1000 genomes]
rs72959726	0.83[AFR][1000 genomes]
rs7655265	1.00[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs7666206	0.87[AMR][1000 genomes]
rs7669783	0.95[CHB][hapmap];0.81[JPT][hapmap];0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7672161	0.95[CHB][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes]
rs975371	1.00[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes]
rs975372	0.92[AMR][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	nsv498083	chr4:148519825-148917583	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer 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	20 gene(s)	inside rSNPs	diseases
2	nsv880243	chr4:148735644-148879583	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv880244	chr4:148764252-148920089	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1029845	chr4:148766290-148916437	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1030001	chr4:148773479-148916437	Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1017904	chr4:148814133-148975348	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1024596	chr4:148830472-148886915	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148786000-148861400	Weak transcription	Pancreas	Pancrea
2	chr4:148796800-148863200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr4:148796800-148866000	Weak transcription	Thymus	Thymus
4	chr4:148797000-148835800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr4:148797400-148879600	Weak transcription	Gastric	stomach
6	chr4:148804600-148854400	Weak transcription	Psoas Muscle	Psoas
7	chr4:148820600-148861200	Weak transcription	Esophagus	oesophagus
8	chr4:148820800-148848800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr4:148823400-148836600	Weak transcription	Placenta	Placenta
10	chr4:148824400-148842800	Weak transcription	Lung	lung
11	chr4:148824400-148854600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr4:148824600-148854400	Weak transcription	Right Ventricle	heart
13	chr4:148825000-148836200	Weak transcription	HMEC	breast
14	chr4:148825200-148839600	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr4:148825200-148847400	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr4:148825200-148848400	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr4:148825400-148843400	Weak transcription	Fetal Heart	heart
18	chr4:148825400-148844200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr4:148825400-148846200	Weak transcription	Fetal Kidney	kidney
20	chr4:148825400-148861200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr4:148825400-148865800	Weak transcription	Fetal Lung	lung
22	chr4:148826600-148888200	Weak transcription	Fetal Thymus	thymus
23	chr4:148827400-148861200	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr4:148828400-148836400	Strong transcription	Aorta	Aorta
25	chr4:148829000-148836400	Weak transcription	Ovary	ovary
26	chr4:148829400-148836200	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr4:148829400-148864200	Weak transcription	Primary T cells from cord blood	blood
28	chr4:148830200-148841200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr4:148830600-148840200	Weak transcription	Spleen	Spleen
30	chr4:148830800-148845600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr4:148831400-148842800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:148831600-148849000	Weak transcription	NH-A	brain
33	chr4:148832000-148838400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:148832000-148839000	Strong transcription	Fetal Muscle Leg	muscle
35	chr4:148832200-148848800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr4:148832200-148854400	Weak transcription	NHEK	skin
37	chr4:148832600-148837000	Weak transcription	HUVEC	blood vessel
38	chr4:148832600-148845600	Weak transcription	Colon Smooth Muscle	Colon
39	chr4:148833400-148835600	Strong transcription	Fetal Intestine Small	intestine
40	chr4:148833400-148835600	Strong transcription	Fetal Stomach	stomach
41	chr4:148833400-148836600	Strong transcription	Stomach Smooth Muscle	stomach
42	chr4:148833400-148837800	Strong transcription	Left Ventricle	heart
43	chr4:148833400-148838600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr4:148833600-148848400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:148833600-148877400	Weak transcription	Small Intestine	intestine
46	chr4:148833800-148836400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr4:148833800-148836800	Strong transcription	Muscle Satellite Cultured Cells	--
48	chr4:148833800-148836800	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr4:148833800-148836800	Strong transcription	HSMMtube	muscle
50	chr4:148834000-148835600	Strong transcription	Osteobl	bone

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links