Variant report

Variant	rs1844696
Chromosome Location	chr5:52936538-52936539
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10063311	0.82[EUR][1000 genomes]
rs10471875	0.82[ASN][1000 genomes]
rs1465445	1.00[CEU][hapmap];0.93[JPT][hapmap]
rs1532163	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1552649	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1559266	0.92[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs173905	0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1844698	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs185603	0.81[CHB][hapmap];1.00[YRI][hapmap]
rs187659	0.82[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs198941	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2130744	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs256083	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs256085	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs256087	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs256090	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs256095	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256097	0.81[CHB][hapmap];0.87[ASN][1000 genomes]
rs256100	0.86[ASN][1000 genomes]
rs256107	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs256108	0.92[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs256110	0.92[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs256112	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs256113	0.96[ASN][1000 genomes]
rs256116	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs256117	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2607501	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2607502	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2607509	0.83[CHB][hapmap];0.87[ASN][1000 genomes]
rs2607511	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2636991	0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2636999	0.80[ASN][1000 genomes]
rs2637004	0.83[CHB][hapmap];0.82[ASN][1000 genomes]
rs2637027	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2637030	0.81[CHB][hapmap];0.87[ASN][1000 genomes]
rs269415	0.84[AFR][1000 genomes]
rs271213	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs271214	0.82[ASN][1000 genomes]
rs271216	0.80[ASN][1000 genomes]
rs271217	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs31302	0.81[CHB][hapmap];0.87[ASN][1000 genomes]
rs31303	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs31304	1.00[YRI][hapmap]
rs31305	0.81[CHB][hapmap];1.00[YRI][hapmap]
rs370594	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs372006	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs372135	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs375956	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs376566	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs381374	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs399141	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs403207	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4147740	0.83[CEU][hapmap]
rs423014	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs423872	0.81[CHB][hapmap];0.87[ASN][1000 genomes]
rs424955	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs429384	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs430427	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs431602	0.81[CHB][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs435187	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs439552	0.92[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs439641	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs449160	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs530216	0.83[ASN][1000 genomes]
rs549131	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6881928	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs693995	0.82[ASN][1000 genomes]
rs7728496	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7731940	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs786333	0.87[ASN][1000 genomes]
rs786335	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs813301	0.86[CHB][hapmap];0.87[ASN][1000 genomes]
rs889291	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs889292	0.92[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap]
rs923609	0.83[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]

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	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv1032632	chr5:52667145-53655624	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv880868	chr5:52799618-53002783	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv880689	chr5:52847995-53002783	ZNF genes & repeats Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv881348	chr5:52885100-52942083	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv881237	chr5:52885100-52944428	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv880426	chr5:52885100-52953048	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv881604	chr5:52885100-53035301	Weak transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv880762	chr5:52894276-52944428	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv4828	chr5:52895470-52940279	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv1032504	chr5:52908394-53398435	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
12	nsv537763	chr5:52908394-53398435	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52900800-52936600	Weak transcription	NHEK	skin
2	chr5:52903000-52943800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr5:52903200-52939200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr5:52904200-52936800	Weak transcription	NHDF-Ad	bronchial
5	chr5:52904400-52966600	Weak transcription	Osteobl	bone
6	chr5:52904600-52937000	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr5:52909600-52937600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:52910600-52941000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr5:52919200-52944000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr5:52920800-52940800	Weak transcription	HepG2	liver
11	chr5:52920800-52978800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr5:52921000-52941800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr5:52921200-52937000	Weak transcription	Brain Substantia Nigra	brain
14	chr5:52921600-52963400	Weak transcription	A549	lung
15	chr5:52922000-52936600	Weak transcription	Fetal Lung	lung
16	chr5:52922000-52939400	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr5:52922000-52942000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:52925600-52961200	Weak transcription	Esophagus	oesophagus
19	chr5:52925800-52952000	Weak transcription	Colonic Mucosa	Colon
20	chr5:52926000-52941800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr5:52926000-52943800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr5:52926600-52948800	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr5:52926800-52963600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr5:52927400-52937800	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr5:52927400-52945000	Weak transcription	Fetal Brain Female	brain
26	chr5:52927400-52961000	Weak transcription	Placenta	Placenta
27	chr5:52927600-52937800	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr5:52927600-52942400	Weak transcription	Fetal Thymus	thymus
29	chr5:52927800-52937000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:52927800-52937000	Weak transcription	Fetal Stomach	stomach
31	chr5:52927800-52937800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr5:52927800-52937800	Weak transcription	Ovary	ovary
33	chr5:52927800-52938000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr5:52927800-52948600	Weak transcription	Pancreas	Pancrea
35	chr5:52927800-52961200	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr5:52927800-52961200	Weak transcription	Stomach Smooth Muscle	stomach
37	chr5:52927800-52961200	Weak transcription	Thymus	Thymus
38	chr5:52928000-52937200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr5:52928000-52937800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr5:52928000-52937800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr5:52928000-52945000	Weak transcription	Fetal Intestine Small	intestine
42	chr5:52928000-52946000	Weak transcription	Gastric	stomach
43	chr5:52928000-52962200	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr5:52928200-52944000	Weak transcription	GM12878-XiMat	blood
45	chr5:52928400-52942000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr5:52928600-52944400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr5:52929000-52937000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr5:52929000-52981800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr5:52929200-52941800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr5:52929200-52942000	Weak transcription	Dnd41	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links