Variant report

Variant	rs11174449
Chromosome Location	chr12:62768088-62768089
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:62653050..62656025-chr12:62764970..62768543,3	K562	blood:
2	chr12:62767512..62770487-chr12:62776323..62779154,2	K562	blood:

Variant related genes	Relation type
ENSG00000135655	Chromatin interaction
ENSG00000198673	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10160868	0.84[ASN][1000 genomes]
rs10160955	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs10431509	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10431510	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10431565	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10506440	0.89[CHB][hapmap]
rs10747958	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10784292	0.88[CHB][hapmap]
rs10877819	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10877820	0.89[CHB][hapmap]
rs10877824	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs10877826	0.86[CHB][hapmap]
rs10877829	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10877831	0.89[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs10877834	0.89[CHB][hapmap];0.85[ASN][1000 genomes]
rs11174401	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11174404	0.81[CHB][hapmap];0.87[CHD][hapmap];0.84[GIH][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs11174408	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs11174411	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11174412	1.00[CHB][hapmap];0.91[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11174416	0.84[ASN][1000 genomes]
rs11174417	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11174420	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11174423	0.86[ASN][1000 genomes]
rs11174424	0.89[CHB][hapmap];0.87[ASN][1000 genomes]
rs11174428	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs11174433	0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs11174435	0.88[ASN][1000 genomes]
rs11174436	0.89[CHB][hapmap]
rs11174438	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs11174446	0.89[CHB][hapmap]
rs11174458	0.89[CHB][hapmap];0.85[ASN][1000 genomes]
rs11174464	0.85[ASN][1000 genomes]
rs11504121	0.87[ASN][1000 genomes]
rs11561463	0.87[ASN][1000 genomes]
rs11830242	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11836268	0.89[CHB][hapmap]
rs12228015	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs12231778	0.89[ASN][1000 genomes]
rs12297474	0.89[CHB][hapmap]
rs12297480	0.81[ASN][1000 genomes]
rs12299072	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12306066	0.99[ASN][1000 genomes]
rs12307900	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12308455	0.89[CHB][hapmap];0.84[ASN][1000 genomes]
rs12310318	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs12310616	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs12310651	0.89[CHB][hapmap]
rs12311279	0.86[CHB][hapmap]
rs12314644	0.84[ASN][1000 genomes]
rs12318287	0.88[CHB][hapmap]
rs1376341	0.87[LWK][hapmap];0.96[MKK][hapmap];0.82[YRI][hapmap]
rs1376342	0.99[ASN][1000 genomes]
rs1496859	0.99[ASN][1000 genomes]
rs1901239	1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs2122660	0.85[ASN][1000 genomes]
rs2131434	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2132651	0.99[ASN][1000 genomes]
rs2167287	0.89[CHB][hapmap];0.85[ASN][1000 genomes]
rs2242032	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35634758	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3803106	0.89[CHB][hapmap]
rs66507062	0.85[ASN][1000 genomes]
rs7132814	0.88[ASN][1000 genomes]
rs7133294	0.99[ASN][1000 genomes]
rs7137068	0.87[ASN][1000 genomes]
rs7300928	0.89[CHB][hapmap]
rs7302033	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7302617	0.87[ASN][1000 genomes]
rs7309209	0.89[CHB][hapmap];0.83[ASN][1000 genomes]
rs73136889	0.84[ASN][1000 genomes]
rs73321563	0.83[ASN][1000 genomes]
rs7953967	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs7956332	0.83[ASN][1000 genomes]
rs7963950	0.89[CHB][hapmap];0.85[ASN][1000 genomes]
rs7965326	1.00[CHB][hapmap];0.87[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap]
rs7971588	0.85[ASN][1000 genomes]
rs7976058	1.00[CHB][hapmap];0.91[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9634284	0.89[CHB][hapmap];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035150	chr12:62615347-62785005	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv1049465	chr12:62657011-62785005	Weak transcription ZNF genes & repeats Enhancers Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv1053403	chr12:62657011-62809413	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv530690	chr12:62678463-62999462	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv899153	chr12:62716330-62817736	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	7 gene(s)	inside rSNPs	diseases
6	esv1803510	chr12:62729782-62802643	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv469417	chr12:62751242-62802643	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
8	nsv559155	chr12:62751242-62802643	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv899154	chr12:62764909-62811328	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
10	nsv899155	chr12:62764909-62817736	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:62701600-62769200	Weak transcription	NHEK	skin
2	chr12:62717000-62769200	Weak transcription	Fetal Kidney	kidney
3	chr12:62717000-62777000	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr12:62717000-62783200	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr12:62717000-62784600	Weak transcription	Colon Smooth Muscle	Colon
6	chr12:62717200-62778400	Weak transcription	Hela-S3	cervix
7	chr12:62729800-62776800	Weak transcription	HSMM	muscle
8	chr12:62737600-62784600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr12:62737600-62786600	Weak transcription	NHLF	lung
10	chr12:62737800-62780200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr12:62738200-62777000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr12:62738200-62787400	Weak transcription	Spleen	Spleen
13	chr12:62738200-62790600	Weak transcription	Esophagus	oesophagus
14	chr12:62738600-62783400	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr12:62738800-62769000	Weak transcription	Placenta	Placenta
16	chr12:62738800-62784000	Weak transcription	Rectal Smooth Muscle	rectum
17	chr12:62738800-62789600	Weak transcription	Ovary	ovary
18	chr12:62738800-62792800	Weak transcription	Lung	lung
19	chr12:62739000-62775400	Weak transcription	Adipose Nuclei	Adipose
20	chr12:62739600-62782000	Weak transcription	Thymus	Thymus
21	chr12:62739800-62782600	Weak transcription	Fetal Intestine Small	intestine
22	chr12:62741800-62783600	Weak transcription	NHDF-Ad	bronchial
23	chr12:62742000-62786800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr12:62742600-62775200	Weak transcription	NH-A	brain
25	chr12:62745600-62769000	Weak transcription	Rectal Mucosa Donor 31	rectum
26	chr12:62747600-62769200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr12:62747800-62777200	Weak transcription	A549	lung
28	chr12:62749600-62772600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr12:62751200-62782800	Weak transcription	Skeletal Muscle Female	skeletal muscle
30	chr12:62753400-62770200	Weak transcription	Liver	Liver
31	chr12:62753600-62779800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr12:62755200-62778800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr12:62757200-62782000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr12:62757600-62778400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr12:62758200-62787400	Weak transcription	Fetal Muscle Leg	muscle
36	chr12:62758600-62769200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr12:62758800-62774200	Weak transcription	Dnd41	blood
38	chr12:62758800-62775200	Weak transcription	Duodenum Mucosa	Duodenum
39	chr12:62759000-62775400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:62760000-62782200	Weak transcription	Fetal Lung	lung
41	chr12:62762400-62796600	Weak transcription	Fetal Brain Male	brain
42	chr12:62762800-62769000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr12:62763000-62805400	Strong transcription	Monocytes-CD14+_RO01746	blood
44	chr12:62763200-62777000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr12:62763400-62782600	Weak transcription	Fetal Brain Female	brain
46	chr12:62763800-62787600	Weak transcription	Brain Anterior Caudate	brain
47	chr12:62764200-62769400	Strong transcription	GM12878-XiMat	blood
48	chr12:62764200-62782600	Weak transcription	Left Ventricle	heart
49	chr12:62764200-62792000	Weak transcription	HepG2	liver
50	chr12:62764400-62774800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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