Variant report

Variant	rs7185691
Chromosome Location	chr16:31910324-31910325
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:31908381..31911064-chr16:31928039..31930191,2	K562	blood:

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs11150651	0.88[AFR][1000 genomes]
rs12599066	0.85[AFR][1000 genomes]
rs3843960	0.87[AFR][1000 genomes]
rs3843961	0.89[AFR][1000 genomes]
rs3861268	0.87[AFR][1000 genomes]
rs3913868	0.87[AFR][1000 genomes]
rs4026652	0.87[AFR][1000 genomes]
rs4026653	0.87[AFR][1000 genomes]
rs4026654	0.87[AFR][1000 genomes]
rs4402587	0.89[AFR][1000 genomes]
rs4889517	0.87[AFR][1000 genomes]
rs4889518	0.87[AFR][1000 genomes]
rs7200162	0.80[AFR][1000 genomes]
rs9928704	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
2	nsv918074	chr16:31669781-31935033	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS 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	43 gene(s)	inside rSNPs	diseases
3	nsv1063037	chr16:31669981-31934894	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv542903	chr16:31669981-31934894	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1066522	chr16:31831196-31959992	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers 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	26 gene(s)	inside rSNPs	diseases
6	nsv1057300	chr16:31862900-31959992	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv833196	chr16:31897381-32068953	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	esv1850460	chr16:31905688-32097085	Strong transcription ZNF genes & repeats Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31889400-31911600	ZNF genes & repeats	Primary B cells from cord blood	blood
2	chr16:31892000-31910400	ZNF genes & repeats	GM12878-XiMat	blood
3	chr16:31893000-31913200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr16:31893200-31911800	ZNF genes & repeats	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr16:31893400-31911400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr16:31893400-31911800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr16:31893400-31912000	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
8	chr16:31893600-31917800	Weak transcription	Colon Smooth Muscle	Colon
9	chr16:31896600-31910400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
10	chr16:31897600-31912000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
11	chr16:31900000-31911000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr16:31900000-31911400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr16:31903600-31911600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr16:31903600-31916800	Weak transcription	Stomach Mucosa	stomach
15	chr16:31904800-31910400	Strong transcription	HSMM	muscle
16	chr16:31905000-31912000	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr16:31906000-31911800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
18	chr16:31906200-31910400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr16:31906400-31910800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr16:31906600-31910600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr16:31906600-31910800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr16:31906600-31917200	Weak transcription	Pancreas	Pancrea
23	chr16:31907000-31910400	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
24	chr16:31907000-31911000	Weak transcription	Fetal Kidney	kidney
25	chr16:31907400-31917200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr16:31907600-31912000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr16:31907600-31917200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr16:31907600-31921400	Weak transcription	Hela-S3	cervix
29	chr16:31907800-31911000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
30	chr16:31907800-31911600	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr16:31907800-31911800	Weak transcription	Fetal Intestine Small	intestine
32	chr16:31907800-31917000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr16:31907800-31917000	Weak transcription	Fetal Stomach	stomach
34	chr16:31907800-31917200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr16:31907800-31917200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr16:31907800-31917200	Weak transcription	Aorta	Aorta
37	chr16:31907800-31917200	Weak transcription	Esophagus	oesophagus
38	chr16:31907800-31917400	Weak transcription	Gastric	stomach
39	chr16:31907800-31924400	Weak transcription	HSMMtube	muscle
40	chr16:31908000-31911600	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr16:31908000-31913200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr16:31908000-31917000	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr16:31908000-31917000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr16:31908000-31917000	Weak transcription	Thymus	Thymus
45	chr16:31908000-31917200	Weak transcription	Left Ventricle	heart
46	chr16:31908000-31917200	Weak transcription	Rectal Smooth Muscle	rectum
47	chr16:31908000-31917200	Weak transcription	Right Ventricle	heart
48	chr16:31908000-31917400	Weak transcription	Ovary	ovary
49	chr16:31908000-31924600	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr16:31908200-31910400	Weak transcription	Osteobl	bone

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