Variant report

Variant	rs2668216
Chromosome Location	chr3:112295615-112295616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:112280239..112282206-chr3:112293782..112295982,2	K562	blood:
2	chr3:112294905..112297769-chr3:112358184..112360725,3	MCF-7	breast:
3	chr3:112290282..112294480-chr3:112295112..112298665,4	K562	blood:

Variant related genes	Relation type
ENSG00000144848	Chromatin interaction
ENSG00000138459	Chromatin interaction
ENSG00000091986	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10934177	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1385527	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1386896	1.00[ASN][1000 genomes]
rs1388442	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1472106	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1472107	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1488260	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1488262	1.00[ASN][1000 genomes]
rs1491629	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1532198	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1552707	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1814053	1.00[ASN][1000 genomes]
rs1817694	1.00[ASN][1000 genomes]
rs1844864	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1877362	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1877364	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1906519	1.00[ASN][1000 genomes]
rs2029317	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2399431	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2464612	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2638025	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2638030	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2638033	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2638034	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2638036	1.00[ASN][1000 genomes]
rs2638041	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2638043	1.00[ASN][1000 genomes]
rs2638044	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2705506	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2705510	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2705514	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2705520	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2705524	1.00[ASN][1000 genomes]
rs2705551	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2705554	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2705563	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2933139	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2933140	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2969894	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3109033	0.86[ASN][1000 genomes]
rs62264580	0.83[ASN][1000 genomes]
rs6793232	1.00[ASN][1000 genomes]
rs7618978	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs901829	1.00[ASN][1000 genomes]
rs971832	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs986883	0.89[EUR][1000 genomes];1.00[ASN][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	nsv877342	chr3:112185025-112332629	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	esv3329419	chr3:112236688-112620544	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS 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	39 gene(s)	inside rSNPs	diseases
3	nsv591301	chr3:112252532-112332629	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS 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 target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112281800-112299400	Weak transcription	Left Ventricle	heart
2	chr3:112281800-112301600	Weak transcription	HepG2	liver
3	chr3:112281800-112312000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr3:112281800-112315400	Weak transcription	Pancreas	Pancrea
5	chr3:112281800-112324200	Weak transcription	Spleen	Spleen
6	chr3:112281800-112325400	Weak transcription	Gastric	stomach
7	chr3:112282000-112312200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr3:112282000-112330400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr3:112282000-112330600	Weak transcription	Esophagus	oesophagus
10	chr3:112282200-112303400	Weak transcription	Psoas Muscle	Psoas
11	chr3:112282400-112299400	Weak transcription	Fetal Stomach	stomach
12	chr3:112282400-112301600	Weak transcription	Hela-S3	cervix
13	chr3:112282400-112304400	Weak transcription	Fetal Heart	heart
14	chr3:112282400-112306600	Weak transcription	Right Ventricle	heart
15	chr3:112282400-112307200	Weak transcription	Small Intestine	intestine
16	chr3:112282400-112312400	Weak transcription	Rectal Smooth Muscle	rectum
17	chr3:112282400-112316800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr3:112282400-112322800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:112282400-112324200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr3:112282400-112340000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:112282600-112297200	Weak transcription	Thymus	Thymus
22	chr3:112282600-112298200	Weak transcription	NHEK	skin
23	chr3:112282600-112301200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr3:112282600-112301400	Weak transcription	A549	lung
25	chr3:112282600-112306800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:112282800-112298600	Weak transcription	Brain Angular Gyrus	brain
27	chr3:112282800-112301400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr3:112282800-112302200	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr3:112283000-112299200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr3:112283000-112301800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr3:112283000-112316400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr3:112283600-112295800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
33	chr3:112284000-112297600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr3:112284000-112298600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr3:112286600-112298000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr3:112287600-112304000	Weak transcription	HMEC	breast
37	chr3:112287800-112298000	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr3:112287800-112299400	Weak transcription	Aorta	Aorta
39	chr3:112287800-112299400	Weak transcription	GM12878-XiMat	blood
40	chr3:112290200-112299800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr3:112290400-112317400	Weak transcription	Placenta Amnion	Placenta Amnion
42	chr3:112290600-112297200	Weak transcription	HSMMtube	muscle
43	chr3:112290600-112297800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr3:112290600-112299400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr3:112290600-112299400	Weak transcription	Lung	lung
46	chr3:112290600-112299800	Weak transcription	Brain Germinal Matrix	brain
47	chr3:112290600-112300400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr3:112290600-112301600	Weak transcription	Brain Substantia Nigra	brain
49	chr3:112290600-112306400	Weak transcription	Colonic Mucosa	Colon
50	chr3:112290600-112315600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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