Variant report

Variant	rs12422355
Chromosome Location	chr12:48456945-48456946
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10492081	0.81[CHB][hapmap];0.86[YRI][hapmap]
rs10492082	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1049392	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[EUR][1000 genomes]
rs10747529	0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10875733	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10875739	0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs10875752	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.82[EUR][1000 genomes]
rs10875754	1.00[JPT][hapmap]
rs10875761	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs10875766	1.00[JPT][hapmap]
rs11168350	0.94[JPT][hapmap]
rs11168353	1.00[JPT][hapmap]
rs11168354	1.00[JPT][hapmap]
rs11168358	1.00[JPT][hapmap]
rs11168361	0.81[ASN][1000 genomes]
rs11168363	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11168364	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11168373	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11168378	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11168404	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11168412	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11168417	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11168419	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11168424	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[EUR][1000 genomes]
rs11168434	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs11168435	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes]
rs11168438	1.00[JPT][hapmap]
rs11168445	0.81[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11168448	0.90[CEU][hapmap];0.88[CHB][hapmap];1.00[JPT][hapmap]
rs11168453	0.90[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11168454	0.90[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs11834818	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12228924	0.91[CEU][hapmap];0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12423250	0.94[JPT][hapmap]
rs12425679	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12426981	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17122567	1.00[JPT][hapmap]
rs1859443	0.94[JPT][hapmap]
rs1978161	0.82[JPT][hapmap];0.90[ASN][1000 genomes]
rs2107640	0.82[ASN][1000 genomes]
rs2240306	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2286020	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2408954	1.00[JPT][hapmap]
rs3742075	1.00[CHB][hapmap];0.94[JPT][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3825403	0.90[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4258439	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs4760678	0.84[ASN][1000 genomes]
rs57430775	0.80[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs58540891	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs58556309	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59667534	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6580658	0.82[JPT][hapmap]
rs7138917	0.91[ASN][1000 genomes]
rs7299704	0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs7302354	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7303677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73104071	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7484942	0.83[CEU][hapmap];1.00[JPT][hapmap]
rs765260	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7962390	0.90[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs7962569	0.94[JPT][hapmap]
rs8181670	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap]
rs886589	0.81[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs954326	0.94[JPT][hapmap]
rs9651981	0.94[JPT][hapmap]
rs9804751	0.94[JPT][hapmap]

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	nsv832401	chr12:48347453-48477999	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv2758307	chr12:48429702-48825499	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
3	esv2759898	chr12:48429702-48825499	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 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	chr12:48432000-48463400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr12:48432200-48498400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr12:48435200-48476200	Weak transcription	Stomach Mucosa	stomach
4	chr12:48435400-48457200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr12:48437200-48489000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:48439200-48468000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr12:48440000-48457200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr12:48441200-48457000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr12:48441400-48482600	Weak transcription	Small Intestine	intestine
10	chr12:48441600-48468000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr12:48443000-48478800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr12:48444200-48474600	Weak transcription	Gastric	stomach
13	chr12:48444800-48468000	Weak transcription	Spleen	Spleen
14	chr12:48449400-48464400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr12:48452000-48460200	Strong transcription	Hela-S3	cervix
16	chr12:48452000-48468600	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr12:48452000-48468800	Strong transcription	HUES64 Cell Line	embryonic stem cell
18	chr12:48452000-48468800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr12:48452000-48469400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:48452200-48459600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr12:48452200-48459600	Strong transcription	Cortex derived primary cultured neurospheres	brain
22	chr12:48452200-48459600	Strong transcription	NHDF-Ad	bronchial
23	chr12:48452200-48460000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr12:48452200-48460600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr12:48452200-48461200	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr12:48452200-48461600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr12:48452200-48468600	Strong transcription	NH-A	brain
28	chr12:48452200-48468800	Strong transcription	HUES6 Cell Line	embryonic stem cell
29	chr12:48452200-48469000	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr12:48452200-48469600	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr12:48452200-48470000	Strong transcription	Placenta	Placenta
32	chr12:48452400-48459400	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr12:48452400-48459600	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr12:48452400-48459600	Strong transcription	Rectal Mucosa Donor 31	rectum
35	chr12:48452400-48459600	Strong transcription	Osteobl	bone
36	chr12:48452400-48459800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr12:48452400-48460000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:48452400-48460600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr12:48452400-48460600	Strong transcription	Left Ventricle	heart
40	chr12:48452400-48461400	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr12:48452400-48461600	Strong transcription	Fetal Intestine Large	intestine
42	chr12:48452400-48463200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr12:48452400-48468800	Strong transcription	Adipose Nuclei	Adipose
44	chr12:48452400-48468800	Strong transcription	Duodenum Mucosa	Duodenum
45	chr12:48452400-48468800	Strong transcription	Fetal Thymus	thymus
46	chr12:48452400-48469600	Strong transcription	Primary T helper cells PMA-I stimulated	--
47	chr12:48452600-48468400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr12:48452800-48458000	Strong transcription	NHEK	skin
49	chr12:48452800-48460000	Strong transcription	HepG2	liver
50	chr12:48452800-48461600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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