Variant report

Variant	rs16970463
Chromosome Location	chr16:70759585-70759586
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	chr16:70725942..70727688-chr16:70759419..70762080,2	K562	blood:
2	chr16:70758547..70760441-chr16:70762170..70763955,2	K562	blood:

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11864186	1.00[CEU][hapmap]
rs16970439	1.00[AMR][1000 genomes]
rs4985422	1.00[EUR][1000 genomes]
rs60002562	1.00[AMR][1000 genomes]
rs7189559	1.00[EUR][1000 genomes]
rs7189695	1.00[EUR][1000 genomes]
rs731697	1.00[EUR][1000 genomes]
rs744844	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv517391	chr16:70666410-70840490	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	nsv457517	chr16:70666722-70840490	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv572945	chr16:70666722-70840490	Weak transcription Genic enhancers Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv906877	chr16:70677785-70766378	Enhancers Genic enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats 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	18 gene(s)	inside rSNPs	diseases
5	nsv906878	chr16:70677785-70782922	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS 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	19 gene(s)	inside rSNPs	diseases
6	nsv906879	chr16:70677785-70790831	Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv906880	chr16:70677785-70796515	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv1059226	chr16:70708698-70779144	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	14 gene(s)	inside rSNPs	diseases
9	nsv906889	chr16:70724001-70790831	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
10	nsv906890	chr16:70740707-70790831	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
11	nsv1061191	chr16:70754975-71201367	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70727000-70770800	Weak transcription	GM12878-XiMat	blood
2	chr16:70749800-70759600	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr16:70750200-70759600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr16:70750400-70759600	Weak transcription	NHEK	skin
5	chr16:70750400-70764800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr16:70750400-70767000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr16:70750600-70766600	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr16:70750800-70771800	Weak transcription	A549	lung
9	chr16:70752600-70770800	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr16:70753200-70766400	Strong transcription	Primary T cells from cord blood	blood
11	chr16:70753400-70767200	Strong transcription	Primary B cells from peripheral blood	blood
12	chr16:70753800-70761600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr16:70753800-70764800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr16:70754000-70759600	Weak transcription	Fetal Kidney	kidney
15	chr16:70754200-70761800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr16:70754200-70768800	Weak transcription	Osteobl	bone
17	chr16:70754400-70764800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr16:70754400-70776600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr16:70754400-70780000	Weak transcription	Hela-S3	cervix
20	chr16:70754600-70759600	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr16:70754600-70760400	Strong transcription	Spleen	Spleen
22	chr16:70754600-70761600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr16:70754600-70761600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr16:70754600-70761800	Weak transcription	Aorta	Aorta
25	chr16:70754600-70764800	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr16:70754800-70764800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr16:70755000-70759800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr16:70755200-70769600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr16:70755600-70774200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr16:70755800-70761800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr16:70755800-70772000	Weak transcription	Small Intestine	intestine
32	chr16:70756000-70760600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr16:70756000-70762200	Weak transcription	Dnd41	blood
34	chr16:70756200-70759600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr16:70756200-70760600	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr16:70756600-70768600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr16:70756800-70760200	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr16:70756800-70760400	Weak transcription	Primary B cells from cord blood	blood
39	chr16:70757000-70760400	Enhancers	Fetal Lung	lung
40	chr16:70757200-70761600	Enhancers	Fetal Muscle Leg	muscle
41	chr16:70757400-70759600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr16:70757400-70761200	Enhancers	Fetal Heart	heart
43	chr16:70757600-70760600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr16:70757600-70761000	Enhancers	Lung	lung
45	chr16:70757600-70762200	Enhancers	Right Ventricle	heart
46	chr16:70757800-70759800	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chr16:70757800-70760200	Weak transcription	Duodenum Mucosa	Duodenum
48	chr16:70757800-70760200	Enhancers	Pancreas	Pancrea
49	chr16:70757800-70766000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
50	chr16:70758000-70759600	Enhancers	Brain Cingulate Gyrus	brain

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