Variant report

Variant	rs12679619
Chromosome Location	chr8:6340475-6340476
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	chr8:6339705..6342364-chr8:6348069..6350911,2	K562	blood:

Extended variants
information (count: 139 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:125)

rs_ID	r²[population]
rs1054073	0.88[CHD][hapmap];0.94[JPT][hapmap]
rs11137028	0.82[CHB][hapmap]
rs11137029	0.90[CHB][hapmap];0.89[GIH][hapmap];0.88[JPT][hapmap];0.82[MEX][hapmap];0.88[ASN][1000 genomes]
rs11137033	0.94[JPT][hapmap]
rs1129703	0.88[CHD][hapmap];0.88[JPT][hapmap]
rs1129704	0.88[JPT][hapmap]
rs1129706	0.88[CHD][hapmap];0.94[JPT][hapmap]
rs12545613	0.85[ASN][1000 genomes]
rs12546890	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs12550299	0.90[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs12674488	0.90[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];0.92[YRI][hapmap];0.82[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12675930	0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs12676907	0.90[CHB][hapmap];0.94[JPT][hapmap];0.88[ASN][1000 genomes]
rs12676922	0.90[CHB][hapmap];0.88[JPT][hapmap];0.85[YRI][hapmap];0.88[ASN][1000 genomes]
rs12677501	1.00[GIH][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap];0.83[ASN][1000 genomes]
rs12680048	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12681009	0.95[ASN][1000 genomes]
rs12681195	0.86[ASN][1000 genomes]
rs13248420	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs13267816	0.82[CHB][hapmap];0.94[JPT][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs13281793	0.98[ASN][1000 genomes]
rs13281967	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs13282022	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs13282116	0.98[ASN][1000 genomes]
rs13282577	0.82[CHB][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1373307	0.88[JPT][hapmap]
rs1550690	0.82[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs17077031	0.85[ASN][1000 genomes]
rs17077056	0.90[CHB][hapmap];0.94[JPT][hapmap];0.91[ASN][1000 genomes]
rs17077067	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs17077083	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs17077094	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17077109	1.00[GIH][hapmap];0.94[JPT][hapmap];0.82[MEX][hapmap];0.83[ASN][1000 genomes]
rs17613024	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.82[MEX][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1867385	0.88[JPT][hapmap]
rs1867386	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs1868551	0.84[CHD][hapmap];0.94[JPT][hapmap]
rs2034143	0.88[JPT][hapmap]
rs2166010	0.82[CHB][hapmap]
rs2251956	0.88[JPT][hapmap]
rs2254903	0.82[CHD][hapmap];0.88[JPT][hapmap]
rs2277136	1.00[CHB][hapmap];0.96[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2305022	0.84[JPT][hapmap]
rs2440395	0.88[ASN][1000 genomes]
rs2440396	0.89[GIH][hapmap];0.88[JPT][hapmap]
rs2440397	0.88[JPT][hapmap]
rs2440406	0.84[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2440412	0.88[JPT][hapmap]
rs2440414	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs2440416	0.84[CHD][hapmap];1.00[JPT][hapmap]
rs2440422	0.83[JPT][hapmap]
rs2440423	0.88[JPT][hapmap]
rs2440424	0.82[CHD][hapmap];0.88[JPT][hapmap]
rs2440428	0.94[JPT][hapmap]
rs2440432	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2442485	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2442491	0.86[JPT][hapmap]
rs2442493	0.88[JPT][hapmap]
rs2442497	0.90[CHB][hapmap];0.88[CHD][hapmap];0.89[GIH][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs2442500	0.84[JPT][hapmap]
rs2442502	0.88[JPT][hapmap]
rs2442510	0.88[CHD][hapmap];0.94[JPT][hapmap]
rs2442511	0.88[CHD][hapmap];1.00[JPT][hapmap]
rs2442514	0.83[JPT][hapmap]
rs2442516	0.83[JPT][hapmap]
rs2442517	0.83[JPT][hapmap]
rs2442518	0.88[JPT][hapmap]
rs2442522	0.88[JPT][hapmap]
rs2442523	0.89[JPT][hapmap]
rs2442524	0.89[JPT][hapmap]
rs2515555	0.84[JPT][hapmap]
rs2515564	0.81[JPT][hapmap]
rs2515572	0.88[JPT][hapmap]
rs2515585	0.89[GIH][hapmap];0.88[JPT][hapmap]
rs2515592	0.90[ASN][1000 genomes]
rs2916723	0.89[ASN][1000 genomes]
rs2916740	0.94[JPT][hapmap]
rs2916741	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs2916742	0.94[JPT][hapmap]
rs2916743	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs2916746	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs2916750	0.88[CHD][hapmap];0.94[JPT][hapmap]
rs2920659	0.94[JPT][hapmap]
rs2920660	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs2920665	0.83[JPT][hapmap]
rs2920671	0.94[JPT][hapmap]
rs2920674	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2920676	0.82[CHB][hapmap]
rs2920677	0.94[JPT][hapmap]
rs2920681	0.82[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2920689	0.94[JPT][hapmap]
rs2922811	0.94[JPT][hapmap]
rs2922813	0.94[JPT][hapmap]
rs2922814	0.94[JPT][hapmap]
rs2922815	0.94[JPT][hapmap]
rs2922818	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs2922820	0.84[CHD][hapmap];0.94[JPT][hapmap]
rs2979648	0.94[JPT][hapmap]
rs2979652	0.94[JPT][hapmap]
rs3020270	0.88[CHD][hapmap];0.94[JPT][hapmap]
rs34009442	0.82[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs34635086	0.83[ASN][1000 genomes]
rs34748476	0.99[ASN][1000 genomes]
rs35150903	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56073811	0.87[ASN][1000 genomes]
rs58679306	0.81[ASN][1000 genomes]
rs59635757	0.96[ASN][1000 genomes]
rs60915478	0.91[ASN][1000 genomes]
rs6559161	0.83[JPT][hapmap]
rs6559162	0.83[JPT][hapmap]
rs6559164	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6989935	0.88[JPT][hapmap]
rs6995735	0.84[JPT][hapmap]
rs7002187	0.82[CHD][hapmap];0.88[JPT][hapmap]
rs7002509	0.94[JPT][hapmap]
rs7008227	0.84[JPT][hapmap]
rs73196802	0.94[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs73661775	0.95[ASN][1000 genomes]
rs7824209	0.85[CHD][hapmap];0.94[JPT][hapmap]
rs7833479	0.95[ASN][1000 genomes]
rs7833481	0.86[CHB][hapmap];0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs7833484	0.95[ASN][1000 genomes]
rs894895	0.94[JPT][hapmap]
rs930557	0.88[JPT][hapmap]
rs9644411	0.82[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890034	chr8:5926632-6427868	Enhancers Strong transcription Active TSS Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1021175	chr8:5965453-6880364	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1027682	chr8:6018123-6920312	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
4	esv3506199	chr8:6116693-6536592	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
5	esv3506200	chr8:6116693-6536592	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers 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	11 gene(s)	inside rSNPs	diseases
6	nsv482828	chr8:6182711-6355710	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv890055	chr8:6237397-6351252	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv933282	chr8:6261036-6440592	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1015981	chr8:6286575-6578450	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS 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	17 gene(s)	inside rSNPs	diseases
10	nsv1027313	chr8:6286575-6920312	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
11	nsv890056	chr8:6314486-6343727	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	nsv890057	chr8:6317165-6427868	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv1025860	chr8:6328628-6360743	Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
14	nsv890058	chr8:6329510-6367302	Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6287600-6344400	Weak transcription	Small Intestine	intestine
2	chr8:6304400-6360200	Weak transcription	Esophagus	oesophagus
3	chr8:6308000-6372600	Weak transcription	HMEC	breast
4	chr8:6316400-6345600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:6317800-6380200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr8:6321800-6342000	Weak transcription	Aorta	Aorta
7	chr8:6321800-6343800	Weak transcription	Hela-S3	cervix
8	chr8:6322000-6346800	Weak transcription	Colon Smooth Muscle	Colon
9	chr8:6323400-6342000	Weak transcription	NHEK	skin
10	chr8:6325800-6374400	Weak transcription	K562	blood
11	chr8:6331400-6345600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr8:6333000-6342000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr8:6335000-6344200	Weak transcription	NHLF	lung
14	chr8:6335000-6345200	Weak transcription	Ovary	ovary
15	chr8:6335400-6341200	Weak transcription	Fetal Lung	lung
16	chr8:6335600-6344400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr8:6336800-6377600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr8:6337000-6342200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr8:6337000-6342400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
20	chr8:6337800-6342200	Strong transcription	Lung	lung
21	chr8:6337800-6342400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr8:6337800-6347600	Strong transcription	Primary T cells from cord blood	blood
23	chr8:6338000-6340800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr8:6338000-6342400	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr8:6338000-6342400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr8:6338000-6342600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr8:6338000-6343600	Strong transcription	GM12878-XiMat	blood
28	chr8:6338200-6340600	Strong transcription	Liver	Liver
29	chr8:6338200-6340600	Strong transcription	Fetal Muscle Trunk	muscle
30	chr8:6338200-6340800	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr8:6338200-6341000	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr8:6338200-6341000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr8:6338200-6341000	Strong transcription	Brain Hippocampus Middle	brain
34	chr8:6338200-6341000	Strong transcription	Duodenum Mucosa	Duodenum
35	chr8:6338200-6341000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr8:6338200-6341200	Strong transcription	Primary B cells from cord blood	blood
37	chr8:6338200-6341800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:6338200-6342000	Strong transcription	Primary B cells from peripheral blood	blood
39	chr8:6338200-6342400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:6338200-6342400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr8:6338200-6342400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr8:6338200-6342400	Strong transcription	Adipose Nuclei	Adipose
43	chr8:6338200-6342400	Strong transcription	Rectal Mucosa Donor 29	rectum
44	chr8:6338200-6342400	Strong transcription	Rectal Smooth Muscle	rectum
45	chr8:6338200-6342400	Strong transcription	HSMM	muscle
46	chr8:6338200-6343400	Strong transcription	Fetal Intestine Large	intestine
47	chr8:6338200-6343400	Strong transcription	Thymus	Thymus
48	chr8:6338400-6340800	Strong transcription	Primary monocytes fromperipheralblood	blood
49	chr8:6338400-6341200	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr8:6338400-6341200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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