Variant report

Variant	rs2091547
Chromosome Location	chr4:99440635-99440636
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10004753	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs10005781	0.89[CEU][hapmap];0.85[EUR][1000 genomes]
rs13116201	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs13137132	0.94[CHB][hapmap]
rs13435698	0.83[EUR][1000 genomes]
rs17027628	0.82[JPT][hapmap];0.88[LWK][hapmap];0.91[YRI][hapmap];0.80[AFR][1000 genomes]
rs17191936	0.96[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17192060	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.96[TSI][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2156504	0.81[CHB][hapmap]
rs2866018	0.81[JPT][hapmap];0.91[YRI][hapmap]
rs4282188	0.80[AFR][1000 genomes]
rs4399995	0.82[JPT][hapmap];0.88[LWK][hapmap];0.91[YRI][hapmap];0.80[AFR][1000 genomes]
rs4535338	0.82[JPT][hapmap];0.88[LWK][hapmap];0.91[YRI][hapmap];0.80[AFR][1000 genomes]
rs6812597	0.88[ASN][1000 genomes]
rs7668981	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7695093	0.96[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529623	chr4:98501338-99460166	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv2754250	chr4:99094922-99527122	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers 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	20 gene(s)	inside rSNPs	diseases
3	nsv879651	chr4:99105055-99441349	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv1004181	chr4:99208152-99529576	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99431200-99443600	Weak transcription	Fetal Brain Male	brain
2	chr4:99433000-99443200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr4:99434000-99441600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:99434400-99443800	Weak transcription	Aorta	Aorta
5	chr4:99435600-99440800	Enhancers	Brain Hippocampus Middle	brain
6	chr4:99435600-99441800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr4:99436200-99441800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr4:99436200-99441800	Enhancers	NHDF-Ad	bronchial
9	chr4:99436400-99440800	Enhancers	Fetal Stomach	stomach
10	chr4:99436600-99441400	Enhancers	NHLF	lung
11	chr4:99436600-99443600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr4:99436600-99446400	Weak transcription	Left Ventricle	heart
13	chr4:99437000-99441400	Enhancers	Brain Cingulate Gyrus	brain
14	chr4:99437200-99440800	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr4:99437200-99443400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr4:99438000-99441800	Enhancers	Osteobl	bone
17	chr4:99438000-99442600	Weak transcription	Dnd41	blood
18	chr4:99438400-99441200	Enhancers	Brain Anterior Caudate	brain
19	chr4:99438400-99443200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr4:99438600-99441400	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr4:99438600-99441600	Enhancers	Brain Angular Gyrus	brain
22	chr4:99438800-99441000	Weak transcription	Right Ventricle	heart
23	chr4:99438800-99443400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr4:99438800-99452000	Enhancers	Fetal Heart	heart
25	chr4:99439000-99441600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr4:99439000-99442600	Weak transcription	HMEC	breast
27	chr4:99439000-99442800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:99439000-99443200	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr4:99439200-99441200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:99439200-99441400	Enhancers	Primary B cells from peripheral blood	blood
31	chr4:99439200-99441600	Enhancers	Fetal Lung	lung
32	chr4:99439200-99441800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr4:99439200-99442400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:99439200-99442600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:99439200-99442600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr4:99439200-99443200	Enhancers	NH-A	brain
37	chr4:99439400-99440800	Enhancers	Primary B cells from cord blood	blood
38	chr4:99439400-99441600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:99439400-99441600	Enhancers	Fetal Muscle Leg	muscle
40	chr4:99439400-99443200	Weak transcription	Colon Smooth Muscle	Colon
41	chr4:99439600-99441000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr4:99439600-99441200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr4:99439600-99441400	Enhancers	Primary T helper cells PMA-I stimulated	--
44	chr4:99439600-99445800	Enhancers	Ovary	ovary
45	chr4:99439800-99440800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:99439800-99440800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:99439800-99440800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr4:99439800-99441200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr4:99439800-99441400	Enhancers	Fetal Thymus	thymus
50	chr4:99439800-99441800	Enhancers	Spleen	Spleen

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