Variant report

Variant	rs11183201
Chromosome Location	chr12:46170982-46170983
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:46157277..46159128-chr12:46169493..46171397,2	K562	blood:
2	chr12:46120828..46123681-chr12:46169798..46173669,4	K562	blood:
3	chr12:46145686..46147552-chr12:46169816..46172547,2	K562	blood:
4	chr12:46156363..46159128-chr12:46168846..46171397,2	K562	blood:

Variant related genes	Relation type
ENSG00000189079	Chromatin interaction
ENSG00000273015	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1012642	0.96[CEU][hapmap];0.83[JPT][hapmap]
rs10748432	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10880855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10880859	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10880860	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10880864	0.81[EUR][1000 genomes]
rs10880871	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes]
rs10880875	0.96[CEU][hapmap];0.82[AFR][1000 genomes]
rs10880879	0.96[CEU][hapmap];0.86[CHB][hapmap];0.86[JPT][hapmap]
rs11183184	1.00[YRI][hapmap]
rs11183243	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap]
rs12314770	0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.88[YRI][hapmap]
rs12319077	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12320533	0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1366024	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes]
rs1468993	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1863127	0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2059404	0.95[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2193749	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2216470	0.82[JPT][hapmap]
rs2408435	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs247917	0.83[EUR][1000 genomes]
rs247918	0.91[CEU][hapmap];0.89[CHB][hapmap];0.80[JPT][hapmap];0.83[EUR][1000 genomes]
rs247919	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs247920	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs247929	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap]
rs247930	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35115	0.96[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35117	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35121	1.00[CEU][hapmap];0.91[CHB][hapmap];0.86[JPT][hapmap];1.00[YRI][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35122	0.96[CEU][hapmap];0.81[CHB][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs35125	1.00[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6582574	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs67133230	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7132422	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7138997	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs724909	0.96[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap]
rs7306229	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap]
rs7315731	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap]
rs7955891	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7976870	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7979218	0.85[YRI][hapmap]
rs997307	0.96[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899052	chr12:46068394-46175469	Active TSS Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	51 gene(s)	inside rSNPs	diseases
2	esv2758306	chr12:46149338-46349891	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	esv2759897	chr12:46149338-46349891	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
4	nsv973961	chr12:46153815-46175394	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv832396	chr12:46155424-46310583	Enhancers Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	esv3502075	chr12:46160578-46175160	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	esv3372521	chr12:46160588-46175158	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	esv3502086	chr12:46160592-46175156	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:52 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:46132000-46205200	Weak transcription	HSMM	muscle
2	chr12:46137400-46174400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr12:46149600-46215400	Weak transcription	Fetal Kidney	kidney
4	chr12:46157400-46199600	Weak transcription	HepG2	liver
5	chr12:46162600-46175200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:46163000-46175400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr12:46164400-46187800	Weak transcription	Fetal Thymus	thymus
8	chr12:46164400-46193600	Weak transcription	Fetal Stomach	stomach
9	chr12:46164600-46187800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr12:46164600-46187800	Weak transcription	GM12878-XiMat	blood
11	chr12:46164600-46193400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr12:46164600-46205200	Weak transcription	Dnd41	blood
13	chr12:46164600-46230000	Weak transcription	Thymus	Thymus
14	chr12:46164800-46193200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr12:46165200-46187800	Weak transcription	Primary T cells fromperipheralblood	blood
16	chr12:46165400-46173200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr12:46165400-46176800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr12:46166200-46181200	Weak transcription	Hela-S3	cervix
19	chr12:46166800-46199800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:46167000-46175000	Weak transcription	Primary B cells from cord blood	blood
21	chr12:46167600-46205200	Weak transcription	Duodenum Mucosa	Duodenum
22	chr12:46168600-46174800	Weak transcription	Stomach Mucosa	stomach
23	chr12:46168600-46193400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:46168800-46181000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr12:46168800-46193600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr12:46169000-46177000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr12:46169000-46178400	Weak transcription	Gastric	stomach
28	chr12:46169000-46181800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
29	chr12:46169000-46182600	Weak transcription	NHDF-Ad	bronchial
30	chr12:46169000-46187800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr12:46169000-46197600	Weak transcription	Sigmoid Colon	Sigmoid Colon
32	chr12:46169000-46202400	Weak transcription	Aorta	Aorta
33	chr12:46169000-46202400	Weak transcription	Left Ventricle	heart
34	chr12:46169000-46202400	Weak transcription	Psoas Muscle	Psoas
35	chr12:46169000-46205200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr12:46169000-46208000	Weak transcription	Brain Angular Gyrus	brain
37	chr12:46169000-46215400	Weak transcription	Fetal Lung	lung
38	chr12:46169200-46182800	Weak transcription	Primary T helper cells PMA-I stimulated	--
39	chr12:46169200-46190000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr12:46170000-46173000	Weak transcription	A549	lung
41	chr12:46170000-46175000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr12:46170000-46177200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr12:46170000-46184200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr12:46170200-46172800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
45	chr12:46170200-46174600	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr12:46170200-46175200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr12:46170200-46175200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr12:46170200-46176000	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr12:46170200-46182400	Weak transcription	Primary T helper cells fromperipheralblood	blood
50	chr12:46170200-46183000	Weak transcription	Brain Substantia Nigra	brain

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