Variant report

Variant	rs7191138
Chromosome Location	chr16:69925981-69925982
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:69756730..69759339-chr16:69925366..69928011,2	K562	blood:
2	chr16:69899911..69901440-chr16:69925824..69928776,2	K562	blood:

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10400955	1.00[EUR][1000 genomes]
rs11510266	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11860910	1.00[EUR][1000 genomes]
rs13333561	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13335267	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13335499	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13338793	0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28522432	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28538568	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28611042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28753861	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28788800	1.00[EUR][1000 genomes]
rs45568735	1.00[EUR][1000 genomes]
rs45608334	1.00[EUR][1000 genomes]
rs56182388	1.00[EUR][1000 genomes]
rs57154889	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58892726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60137705	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs60683406	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60949042	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61731358	1.00[EUR][1000 genomes]
rs7184392	0.96[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs7185321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7185659	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7186422	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7188693	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7189022	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7189521	0.81[YRI][hapmap];1.00[EUR][1000 genomes]
rs7190665	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7193149	0.81[YRI][hapmap];1.00[EUR][1000 genomes]
rs7197774	1.00[EUR][1000 genomes]
rs7199881	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7200168	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7200242	1.00[EUR][1000 genomes]
rs74029722	1.00[EUR][1000 genomes]
rs74029725	1.00[EUR][1000 genomes]
rs74029732	1.00[EUR][1000 genomes]
rs74029733	0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74029738	1.00[EUR][1000 genomes]
rs74029748	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8052959	1.00[EUR][1000 genomes]
rs9921205	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9925155	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9929073	0.82[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9934685	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9934743	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9934983	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9935008	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9939065	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9940805	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv906823	chr16:69711533-69959223	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
2	nsv1062171	chr16:69854267-70188585	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	nsv542941	chr16:69854267-70188585	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	nsv1059249	chr16:69854467-70188446	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
5	nsv542942	chr16:69854467-70188446	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	esv2758428	chr16:69855122-70313222	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
7	esv2758652	chr16:69855122-70313222	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:106 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69893000-69934800	Weak transcription	Hela-S3	cervix
2	chr16:69900800-69933400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr16:69904200-69951200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr16:69907600-69942600	Weak transcription	Small Intestine	intestine
5	chr16:69908200-69943000	Weak transcription	Right Ventricle	heart
6	chr16:69910600-69937400	Strong transcription	Primary monocytes fromperipheralblood	blood
7	chr16:69911400-69970200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr16:69913600-69950400	Weak transcription	A549	lung
9	chr16:69916400-69931600	Strong transcription	Primary B cells from cord blood	blood
10	chr16:69916400-69931600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr16:69917200-69930600	Strong transcription	Primary T helper cells fromperipheralblood	blood
12	chr16:69919800-69932400	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr16:69920600-69928000	Strong transcription	Primary T cells from cord blood	blood
14	chr16:69921400-69938800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr16:69921600-69932800	Strong transcription	Primary neutrophils fromperipheralblood	blood
16	chr16:69921800-69926000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr16:69921800-69926000	Strong transcription	Thymus	Thymus
18	chr16:69921800-69926400	Strong transcription	Duodenum Mucosa	Duodenum
19	chr16:69921800-69926600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr16:69922000-69926000	Enhancers	Brain Substantia Nigra	brain
21	chr16:69923200-69938600	Weak transcription	Ovary	ovary
22	chr16:69923400-69926000	Enhancers	Brain Hippocampus Middle	brain
23	chr16:69923600-69926000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr16:69923600-69926000	Enhancers	Brain Anterior Caudate	brain
25	chr16:69923600-69928600	Weak transcription	Liver	Liver
26	chr16:69923600-69942600	Weak transcription	Pancreas	Pancrea
27	chr16:69923600-69944800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr16:69923800-69926000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr16:69923800-69926000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr16:69923800-69927800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr16:69923800-69929000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr16:69923800-69929800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr16:69923800-69931400	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr16:69923800-69936000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr16:69923800-69936400	Weak transcription	Lung	lung
36	chr16:69923800-69938600	Weak transcription	Aorta	Aorta
37	chr16:69923800-69938600	Weak transcription	K562	blood
38	chr16:69923800-69939800	Weak transcription	HSMM	muscle
39	chr16:69923800-69940400	Weak transcription	HSMMtube	muscle
40	chr16:69923800-69942400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr16:69923800-69949200	Weak transcription	Dnd41	blood
42	chr16:69923800-69951800	Weak transcription	GM12878-XiMat	blood
43	chr16:69924000-69926000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr16:69924000-69942600	Weak transcription	NHEK	skin
45	chr16:69924200-69926200	Enhancers	Fetal Heart	heart
46	chr16:69924200-69936000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr16:69924400-69927600	Weak transcription	Fetal Intestine Large	intestine
48	chr16:69924400-69936000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr16:69924400-69965000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr16:69924600-69926800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links