Variant report

Variant	rs9426218
Chromosome Location	chr1:246904532-246904533
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:246851356..246854003-chr1:246902517..246904591,2	K562	blood:
2	chr1:246897168..246899913-chr1:246904406..246907114,2	K562	blood:

Variant related genes	Relation type
ENSG00000235021	Chromatin interaction

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10127783	0.93[CHB][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10159002	0.85[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10754532	0.93[CHB][hapmap];0.84[JPT][hapmap];0.83[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs10754533	0.82[CHB][hapmap]
rs10802442	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10924820	0.84[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap];0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10924823	0.84[CEU][hapmap];0.93[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10924824	0.84[CEU][hapmap];0.93[CHB][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12027222	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12085330	0.92[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12090470	0.87[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12122102	0.93[CHB][hapmap];1.00[YRI][hapmap]
rs12132038	0.93[CHB][hapmap]
rs12142760	0.85[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs12144408	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs3007316	0.93[CHB][hapmap];0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3007317	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3007318	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3007319	1.00[YRI][hapmap]
rs3007322	1.00[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3007323	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3007324	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3007411	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34649985	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs34989088	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3795463	0.81[CEU][hapmap];0.93[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3795464	1.00[CEU][hapmap];0.93[CHB][hapmap];0.87[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4130316	0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4130317	0.92[CEU][hapmap];0.81[CHB][hapmap];0.84[JPT][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4244627	0.84[CEU][hapmap];0.93[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4244630	0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4926454	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4926455	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4926457	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4926459	0.84[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.91[ASN][1000 genomes]
rs6426323	0.81[CHB][hapmap]
rs6426326	0.86[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6664883	0.85[CEU][hapmap];0.94[CHB][hapmap];0.89[JPT][hapmap];0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6685364	0.92[CEU][hapmap];0.93[CHB][hapmap];0.89[JPT][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72764626	0.92[ASN][1000 genomes]
rs7364715	0.96[ASN][1000 genomes]
rs7365076	0.86[ASN][1000 genomes]
rs7366377	0.81[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7416239	0.88[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7532928	0.81[CHB][hapmap]
rs9426267	0.81[EUR][1000 genomes]
rs9426269	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9426271	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[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	nsv949571	chr1:246688635-247240863	Active TSS Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv873421	chr1:246818634-247044692	Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	esv2762192	chr1:246823857-247069232	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS 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 target site	21 gene(s)	inside rSNPs	diseases
4	nsv1006271	chr1:246832606-247276182	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
5	nsv535416	chr1:246832606-247276182	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
6	nsv430413	chr1:246845971-246975015	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
7	nsv873422	chr1:246854862-247002638	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv1011346	chr1:246868799-247133898	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
9	nsv870294	chr1:246877043-246927940	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS 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	3 gene(s)	inside rSNPs	diseases
10	nsv1006262	chr1:246892826-246964775	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
11	nsv523531	chr1:246893948-246967899	Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
12	nsv999756	chr1:246894542-246969660	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:246888400-246946400	Weak transcription	Small Intestine	intestine
2	chr1:246888600-246945600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
3	chr1:246888800-246904800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr1:246889000-246929000	Weak transcription	Stomach Mucosa	stomach
5	chr1:246889600-246907000	Strong transcription	Fetal Muscle Trunk	muscle
6	chr1:246890200-246905000	Strong transcription	Duodenum Mucosa	Duodenum
7	chr1:246890200-246906600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:246890200-246913200	Strong transcription	Fetal Muscle Leg	muscle
9	chr1:246890400-246907400	Strong transcription	Stomach Smooth Muscle	stomach
10	chr1:246890400-246909000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr1:246890600-246905000	Strong transcription	Brain Anterior Caudate	brain
12	chr1:246890600-246907600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:246890600-246914000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:246891800-246911600	Strong transcription	Liver	Liver
15	chr1:246892400-246912000	Strong transcription	Dnd41	blood
16	chr1:246892600-246904600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr1:246892600-246908800	Strong transcription	Fetal Stomach	stomach
18	chr1:246892600-246909200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr1:246892600-246924400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr1:246893400-246906800	Strong transcription	Brain Cingulate Gyrus	brain
21	chr1:246893600-246905000	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr1:246893800-246912800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr1:246894400-246909600	Strong transcription	Placenta	Placenta
24	chr1:246894600-246923800	Weak transcription	Pancreas	Pancrea
25	chr1:246895000-246904600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:246895000-246906600	Strong transcription	Fetal Intestine Large	intestine
27	chr1:246895000-246907400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:246895000-246909000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:246895000-246909200	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr1:246895000-246912000	Weak transcription	Spleen	Spleen
31	chr1:246895000-246942200	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr1:246895400-246938600	Weak transcription	Fetal Heart	heart
33	chr1:246896400-246917000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr1:246897400-246909000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:246897400-246909200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:246897600-246909200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr1:246897600-246912400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:246897800-246907400	Strong transcription	Adipose Nuclei	Adipose
39	chr1:246899200-246905400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr1:246899400-246906600	Strong transcription	Ovary	ovary
41	chr1:246899600-246905000	Strong transcription	Brain Germinal Matrix	brain
42	chr1:246900000-246917600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:246900400-246905200	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr1:246900400-246910400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr1:246900600-246907200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr1:246900600-246908200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
47	chr1:246900800-246908400	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr1:246900800-246912200	Weak transcription	Esophagus	oesophagus
49	chr1:246901000-246908000	Weak transcription	Right Ventricle	heart
50	chr1:246901200-246905400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links