Variant report

Variant	rs16907873
Chromosome Location	chr9:94606115-94606116
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr9:94596679..94601637-chr9:94602257..94606458,6	K562	blood:
2	chr9:94603914..94606181-chr9:94621038..94623335,2	MCF-7	breast:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11999739	0.93[YRI][hapmap];0.83[AFR][1000 genomes]
rs12002460	0.86[YRI][hapmap]
rs12002478	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.94[GIH][hapmap];0.92[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12002827	1.00[CEU][hapmap];0.84[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12002851	0.84[CHB][hapmap];0.86[CHD][hapmap];0.94[GIH][hapmap];0.92[JPT][hapmap];0.85[MEX][hapmap];0.94[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12003273	0.96[YRI][hapmap];0.81[AFR][1000 genomes]
rs12004009	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16907830	0.81[YRI][hapmap]
rs16907877	0.93[YRI][hapmap];0.86[AFR][1000 genomes]
rs16907893	0.93[YRI][hapmap]
rs1881386	0.86[YRI][hapmap]
rs7031514	0.86[YRI][hapmap]
rs7032520	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7045708	0.86[YRI][hapmap]
rs73651567	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73651569	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73651570	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73651574	0.88[AFR][1000 genomes]
rs73651579	0.88[AFR][1000 genomes]
rs73651581	0.81[AFR][1000 genomes]
rs7847748	1.00[CEU][hapmap];0.84[CHB][hapmap];0.92[JPT][hapmap];0.86[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7849644	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7866996	1.00[CEU][hapmap];0.85[YRI][hapmap]
rs7874163	1.00[CEU][hapmap];0.84[CHB][hapmap];0.86[CHD][hapmap];0.94[GIH][hapmap];0.92[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9969713	0.82[YRI][hapmap]

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	nsv1045332	chr9:94352661-94656016	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv531631	chr9:94373847-94633213	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats 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
4	nsv1036176	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv540171	chr9:94500213-94639367	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv949008	chr9:94500776-95182133	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
7	nsv6614	chr9:94571349-94610085	ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94594600-94610800	Enhancers	Fetal Thymus	thymus
2	chr9:94601800-94607400	Weak transcription	Gastric	stomach
3	chr9:94601800-94618400	Weak transcription	K562	blood
4	chr9:94602800-94611200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr9:94602800-94611600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:94603800-94607800	Enhancers	Ovary	ovary
7	chr9:94604000-94606200	Enhancers	Duodenum Smooth Muscle	Duodenum
8	chr9:94604400-94606800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr9:94604800-94606800	Enhancers	Primary hematopoietic stem cells	blood
10	chr9:94604800-94607000	Enhancers	Thymus	Thymus
11	chr9:94604800-94607600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr9:94604800-94607800	Enhancers	Fetal Lung	lung
13	chr9:94604800-94610200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:94605000-94606200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:94605000-94606800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr9:94605000-94607000	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr9:94605000-94607000	Enhancers	Brain Germinal Matrix	brain
18	chr9:94605000-94608400	Enhancers	Fetal Stomach	stomach
19	chr9:94605200-94606600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:94605200-94606800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:94605200-94607600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr9:94605200-94607600	Enhancers	Fetal Muscle Leg	muscle
23	chr9:94605400-94606200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr9:94605400-94606600	Enhancers	Primary B cells from cord blood	blood
25	chr9:94605400-94606800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr9:94605400-94606800	Enhancers	Fetal Kidney	kidney
27	chr9:94605400-94607000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr9:94605400-94607400	Enhancers	NHLF	lung
29	chr9:94605400-94607600	Enhancers	H1 Cell Line	embryonic stem cell
30	chr9:94605600-94606200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:94605600-94606200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr9:94605600-94606200	Flanking Active TSS	Colon Smooth Muscle	Colon
33	chr9:94605600-94606200	Enhancers	NHDF-Ad	bronchial
34	chr9:94605600-94606600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr9:94605600-94606600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr9:94605600-94606800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr9:94605600-94606800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr9:94605600-94606800	Enhancers	Colonic Mucosa	Colon
39	chr9:94605600-94606800	Enhancers	Lung	lung
40	chr9:94605600-94607000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr9:94605600-94607000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr9:94605600-94607000	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr9:94605600-94607000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr9:94605600-94607000	Enhancers	Brain Cingulate Gyrus	brain
45	chr9:94605600-94607000	Genic enhancers	Fetal Intestine Small	intestine
46	chr9:94605600-94607000	Enhancers	Placenta	Placenta
47	chr9:94605600-94607000	Enhancers	Placenta Amnion	Placenta Amnion
48	chr9:94605600-94607000	Flanking Active TSS	Stomach Smooth Muscle	stomach
49	chr9:94605600-94607200	Enhancers	Fetal Intestine Large	intestine
50	chr9:94605600-94609600	Weak transcription	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links