Variant report

Variant	rs7202233
Chromosome Location	chr16:69894432-69894433
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:69756797..69758977-chr16:69893050..69895419,2	K562	blood:
2	chr16:69787646..69790099-chr16:69892380..69895088,2	MCF-7	breast:
3	chr16:69756797..69760411-chr16:69892588..69895419,3	K562	blood:

Variant related genes	Relation type
ENSG00000141101	Chromatin interaction
ENSG00000181019	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10852460	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10852461	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11075742	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11075744	0.84[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.88[ASN][1000 genomes]
rs1116544	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11642008	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11645565	0.86[AMR][1000 genomes]
rs11648348	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12927168	0.81[EUR][1000 genomes]
rs1466863	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1500337	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1566453	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs1566454	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1566456	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2133799	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2362642	0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs3790075	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3790076	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3790080	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs3790082	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3790083	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4146819	0.86[CHB][hapmap]
rs4985447	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4985448	0.90[ASN][1000 genomes]
rs4985449	0.90[ASN][1000 genomes]
rs4985450	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55887947	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6499263	0.86[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6499265	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6499268	0.86[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6499270	0.86[CHB][hapmap]
rs7190013	0.90[ASN][1000 genomes]
rs7196842	0.86[CHB][hapmap]
rs7196917	0.80[CEU][hapmap];0.87[AMR][1000 genomes]
rs7200258	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8047194	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8047682	0.86[ASN][1000 genomes]
rs8048550	0.86[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs8049373	0.86[ASN][1000 genomes]
rs8050414	0.82[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs8050516	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8051168	0.94[ASN][1000 genomes]
rs8060478	0.86[ASN][1000 genomes]
rs8063226	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9927967	0.95[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9936589	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9936723	0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][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

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs7202233	LOC283970	cis	multi-tissue	Pritchard
rs7202233	LOC440348	Cis_chr	lymphoblastoid	RTeQTL

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:69834000-69910600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr16:69837000-69905600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr16:69874000-69905800	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr16:69876000-69895000	Weak transcription	Fetal Brain Female	brain
5	chr16:69876000-69904400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr16:69876000-69905800	Weak transcription	Dnd41	blood
7	chr16:69876200-69905800	Weak transcription	Brain Germinal Matrix	brain
8	chr16:69879800-69895000	Weak transcription	Primary hematopoietic stem cells	blood
9	chr16:69882800-69894800	Weak transcription	Colonic Mucosa	Colon
10	chr16:69883000-69899400	Weak transcription	NHLF	lung
11	chr16:69883400-69894800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr16:69883400-69899600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr16:69883400-69903800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr16:69883600-69904400	Weak transcription	HMEC	breast
15	chr16:69883800-69895200	Weak transcription	HSMMtube	muscle
16	chr16:69885200-69895600	Strong transcription	Primary T helper cells fromperipheralblood	blood
17	chr16:69887600-69901400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr16:69888000-69901400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr16:69888000-69905600	Weak transcription	Gastric	stomach
20	chr16:69888200-69895000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr16:69888200-69895000	Weak transcription	Fetal Stomach	stomach
22	chr16:69888800-69894800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr16:69889200-69899800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr16:69889600-69905600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr16:69889800-69895000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr16:69889800-69895200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr16:69889800-69895400	Weak transcription	NHDF-Ad	bronchial
28	chr16:69890000-69895200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr16:69890400-69923400	Weak transcription	HUVEC	blood vessel
30	chr16:69891000-69898600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr16:69891200-69896800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr16:69891200-69898400	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr16:69891600-69898600	Enhancers	Pancreas	Pancrea
34	chr16:69892000-69895200	Strong transcription	Primary B cells from peripheral blood	blood
35	chr16:69892200-69895400	Strong transcription	Primary neutrophils fromperipheralblood	blood
36	chr16:69892200-69895400	Strong transcription	Primary B cells from cord blood	blood
37	chr16:69892200-69896200	Strong transcription	Primary T cells from cord blood	blood
38	chr16:69892200-69896400	Enhancers	Duodenum Mucosa	Duodenum
39	chr16:69892200-69897000	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr16:69892400-69894600	Strong transcription	Thymus	Thymus
41	chr16:69892400-69895200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr16:69892400-69895200	Enhancers	Fetal Heart	heart
43	chr16:69892400-69896600	Enhancers	Adipose Nuclei	Adipose
44	chr16:69892600-69895000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr16:69892600-69905400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr16:69892800-69895000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr16:69892800-69895200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr16:69893000-69894800	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr16:69893000-69906800	Weak transcription	GM12878-XiMat	blood
50	chr16:69893000-69907000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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