Variant report

Variant	rs9933022
Chromosome Location	chr16:70538585-70538586
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:70534426..70538037-chr16:70538279..70541133,3	K562	blood:
2	chr16:70536505..70539456-chr16:70548133..70550767,2	MCF-7	breast:
3	chr16:70538068..70540802-chr16:70542880..70545267,2	MCF-7	breast:
4	chr16:70536864..70540404-chr16:70556076..70558403,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000103051	Chromatin interaction
ENSG00000189091	Chromatin interaction

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs13331220	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13334577	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs13339216	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13339561	1.00[AMR][1000 genomes]
rs13339593	1.00[AMR][1000 genomes]
rs13339643	1.00[AMR][1000 genomes]
rs16970226	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16970240	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16970243	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16970253	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16970259	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16970260	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17878662	1.00[AMR][1000 genomes]
rs17879275	1.00[AMR][1000 genomes]
rs17881316	1.00[AMR][1000 genomes]
rs17885165	1.00[AMR][1000 genomes]
rs17886111	1.00[AMR][1000 genomes]
rs28419202	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28438025	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28475204	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28619389	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28777081	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55667445	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55885171	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55926204	0.97[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs56189591	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57451547	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58142695	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58144908	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59158714	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59460917	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60757048	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61641432	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6499318	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7184876	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7185011	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs7186436	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7188297	1.00[AMR][1000 genomes]
rs7188474	1.00[AMR][1000 genomes]
rs7188808	1.00[AMR][1000 genomes]
rs7191191	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7193228	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7196773	1.00[AMR][1000 genomes]
rs7199312	1.00[AMR][1000 genomes]
rs7200586	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7200978	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73573163	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73573175	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73578815	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73578819	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8047593	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8049929	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8050767	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes]
rs8051473	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8051618	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8057327	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8057732	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8058754	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8059200	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8061243	1.00[AMR][1000 genomes]
rs8061431	1.00[AMR][1000 genomes]
rs8062414	1.00[AMR][1000 genomes]
rs8062794	1.00[AMR][1000 genomes]
rs9302615	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9921410	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9926355	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9926435	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9928617	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9928808	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9929182	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9929354	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9929882	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9932065	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9932939	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9936085	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9937769	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9939252	0.89[AFR][1000 genomes]
rs9940353	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833272	chr16:70369769-70569723	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
2	esv2830027	chr16:70473934-70558039	Genic enhancers Enhancers Strong transcription Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	esv3330254	chr16:70536801-70538799	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:70489400-70556400	Weak transcription	Stomach Mucosa	stomach
2	chr16:70512800-70556400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr16:70517600-70538800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr16:70518000-70545800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr16:70523200-70542400	Weak transcription	Hela-S3	cervix
6	chr16:70524400-70542400	Weak transcription	Fetal Brain Male	brain
7	chr16:70526000-70539000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
8	chr16:70528000-70553800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr16:70528800-70556400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr16:70530000-70541200	Weak transcription	Fetal Heart	heart
11	chr16:70530600-70542400	Weak transcription	HMEC	breast
12	chr16:70530600-70545800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr16:70530800-70542200	Weak transcription	K562	blood
14	chr16:70531000-70541200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr16:70531000-70542400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr16:70531000-70542800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr16:70531200-70542200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr16:70531400-70543600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr16:70531600-70542000	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr16:70531600-70542800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr16:70531800-70540800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr16:70531800-70542400	Weak transcription	H9 Cell Line	embryonic stem cell
23	chr16:70531800-70542400	Weak transcription	Rectal Smooth Muscle	rectum
24	chr16:70532000-70540000	Weak transcription	Pancreas	Pancrea
25	chr16:70532000-70540600	Weak transcription	Psoas Muscle	Psoas
26	chr16:70532000-70540800	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr16:70532000-70540800	Weak transcription	Esophagus	oesophagus
28	chr16:70532000-70541000	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr16:70532000-70541000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr16:70532000-70541000	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr16:70532000-70541000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr16:70532000-70541200	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chr16:70532000-70542200	Weak transcription	HSMMtube	muscle
34	chr16:70532000-70542200	Weak transcription	HUVEC	blood vessel
35	chr16:70532000-70542200	Weak transcription	NHDF-Ad	bronchial
36	chr16:70532000-70542400	Weak transcription	Primary B cells from cord blood	blood
37	chr16:70532000-70542400	Weak transcription	Aorta	Aorta
38	chr16:70532000-70542400	Weak transcription	Fetal Lung	lung
39	chr16:70532000-70542800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr16:70532000-70543000	Weak transcription	Colonic Mucosa	Colon
41	chr16:70532000-70543000	Weak transcription	Small Intestine	intestine
42	chr16:70532000-70545600	Weak transcription	A549	lung
43	chr16:70532200-70540800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr16:70532600-70542200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr16:70533000-70538600	Strong transcription	Primary T cells fromperipheralblood	blood
46	chr16:70533000-70540600	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr16:70533000-70540600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr16:70533000-70540800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr16:70533000-70541000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr16:70533000-70542000	Weak transcription	Fetal Kidney	kidney

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