Variant report

Variant	rs10099928
Chromosome Location	chr8:10665290-10665291
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	chr8:10533955..10536464-chr8:10664070..10665725,2	K562	blood:
2	chr8:10663898..10666534-chr8:10670905..10672921,2	K562	blood:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10091961	0.84[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs10092781	0.87[JPT][hapmap]
rs10094907	0.89[CEU][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10097531	0.85[CEU][hapmap];0.94[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10099021	1.00[CEU][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10099137	1.00[CEU][hapmap];0.95[JPT][hapmap];0.82[YRI][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10107180	0.95[CEU][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10107303	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10109034	0.84[CEU][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs10109550	0.85[CEU][hapmap];0.92[YRI][hapmap];0.85[EUR][1000 genomes]
rs10113332	1.00[CEU][hapmap];0.80[JPT][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10113343	0.89[JPT][hapmap]
rs11250069	0.80[EUR][1000 genomes]
rs11250079	0.88[CHB][hapmap];0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs12056936	0.84[EUR][1000 genomes]
rs12544044	0.81[EUR][1000 genomes]
rs12550169	0.95[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12550720	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12679010	0.83[JPT][hapmap]
rs12679155	0.83[JPT][hapmap]
rs12680846	0.82[JPT][hapmap]
rs12681175	0.80[AFR][1000 genomes];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12681375	0.83[JPT][hapmap]
rs1469557	1.00[YRI][hapmap]
rs1544981	0.80[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1549794	0.95[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17152520	0.95[CEU][hapmap];0.86[CHB][hapmap];0.94[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2005311	0.89[JPT][hapmap]
rs2033369	0.89[JPT][hapmap]
rs2052963	0.95[CEU][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2116096	0.84[EUR][1000 genomes]
rs2271356	0.89[CEU][hapmap];0.89[YRI][hapmap]
rs2409651	0.89[CEU][hapmap];0.80[JPT][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28429578	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28592638	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs60011038	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs6601524	0.89[CEU][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs6601525	0.89[JPT][hapmap]
rs6985218	1.00[CEU][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6985890	0.85[EUR][1000 genomes]
rs6989072	0.81[EUR][1000 genomes]
rs6989846	0.84[CEU][hapmap];0.85[YRI][hapmap];0.85[EUR][1000 genomes]
rs6992039	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6994595	0.81[EUR][1000 genomes]
rs6995541	0.81[CHB][hapmap];0.95[JPT][hapmap];0.84[ASN][1000 genomes]
rs7005531	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs7010709	1.00[YRI][hapmap]
rs7010926	0.80[EUR][1000 genomes]
rs7014168	0.95[CEU][hapmap]
rs714371	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7820819	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7823088	0.83[EUR][1000 genomes]
rs7823521	0.94[CEU][hapmap];0.91[YRI][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7824384	0.85[CEU][hapmap];0.93[YRI][hapmap];0.86[EUR][1000 genomes]
rs7826180	0.89[CEU][hapmap];0.83[JPT][hapmap];0.80[EUR][1000 genomes]
rs7826189	0.83[JPT][hapmap]
rs7826458	1.00[CEU][hapmap];0.94[JPT][hapmap];0.86[YRI][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7838341	0.89[CEU][hapmap];0.94[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs891554	0.95[CEU][hapmap];0.95[JPT][hapmap];0.83[EUR][1000 genomes]
rs891555	0.81[EUR][1000 genomes]
rs9644730	1.00[CEU][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9657541	1.00[YRI][hapmap]

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	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv1017836	chr8:10591801-10803617	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1034988	chr8:10591801-10804243	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
6	nsv519768	chr8:10600254-10691993	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
7	nsv831232	chr8:10606053-10774948	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
8	nsv519376	chr8:10611708-10691993	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
9	nsv429860	chr8:10615990-10685890	Strong transcription Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1019754	chr8:10617908-10700140	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
11	nsv539471	chr8:10617908-10700140	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
12	nsv1031726	chr8:10627742-10749369	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10620000-10669800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr8:10623600-10667000	Weak transcription	Thymus	Thymus
3	chr8:10640200-10669800	Weak transcription	Aorta	Aorta
4	chr8:10645000-10670000	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr8:10647000-10674400	Weak transcription	Right Ventricle	heart
6	chr8:10647000-10681200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr8:10647200-10673600	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr8:10647800-10669800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr8:10648200-10669800	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr8:10648200-10683400	Weak transcription	Brain Angular Gyrus	brain
11	chr8:10650000-10676200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:10650600-10669000	Weak transcription	Fetal Stomach	stomach
13	chr8:10650600-10671200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr8:10650800-10669400	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr8:10657200-10670000	Weak transcription	Lung	lung
16	chr8:10657400-10681400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr8:10657400-10685800	Weak transcription	Psoas Muscle	Psoas
18	chr8:10657600-10670000	Weak transcription	Gastric	stomach
19	chr8:10657600-10674200	Weak transcription	Pancreas	Pancrea
20	chr8:10657600-10674600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:10657600-10674600	Weak transcription	Esophagus	oesophagus
22	chr8:10657600-10674600	Weak transcription	Left Ventricle	heart
23	chr8:10657600-10681800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr8:10657800-10673000	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr8:10657800-10673200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr8:10657800-10674400	Weak transcription	Stomach Smooth Muscle	stomach
27	chr8:10657800-10674600	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr8:10657800-10680600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr8:10657800-10680600	Weak transcription	HSMMtube	muscle
30	chr8:10658000-10669400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr8:10658000-10669400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr8:10658400-10673000	Weak transcription	Liver	Liver
33	chr8:10658400-10676000	Weak transcription	HepG2	liver
34	chr8:10658600-10673400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr8:10658600-10676000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr8:10659400-10673400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr8:10659400-10676000	Weak transcription	NHLF	lung
38	chr8:10659600-10682400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr8:10659800-10669800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr8:10660000-10679200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:10660200-10669600	Weak transcription	K562	blood
42	chr8:10660200-10673400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr8:10660400-10665400	Weak transcription	A549	lung
44	chr8:10660400-10667800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr8:10660400-10670600	Weak transcription	Osteobl	bone
46	chr8:10660400-10677000	Weak transcription	NHDF-Ad	bronchial
47	chr8:10661800-10665400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr8:10662000-10667200	Weak transcription	NHEK	skin
49	chr8:10662000-10667400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr8:10662000-10673400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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