Variant report

Variant	rs11111762
Chromosome Location	chr12:104170124-104170125
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:104168330..104170721-chr12:104177797..104180026,2	MCF-7	breast:
2	chr12:104167428..104170420-chr12:104235158..104237169,3	K562	blood:
3	chr12:104168307..104171120-chr12:104193442..104196343,2	K562	blood:
4	chr12:104166229..104169114-chr12:104169303..104172896,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111696	Chromatin interaction
ENSG00000257327	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10861092	0.82[AFR][1000 genomes]
rs10861094	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861095	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10861096	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861097	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861104	0.88[ASN][1000 genomes]
rs11111750	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11111752	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11111754	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11111755	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11111757	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11111758	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11111759	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11111763	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11111765	0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11111767	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11111771	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11111776	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11111778	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11111779	0.81[AMR][1000 genomes]
rs11111791	0.80[ASN][1000 genomes]
rs12228207	0.80[ASN][1000 genomes]
rs1565773	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs15918	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1866292	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1976256	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2292682	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3751204	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3812805	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4964298	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4964823	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4964827	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4964830	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4981032	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4981036	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs751448	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs869993	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9132	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs934847	0.81[AMR][1000 genomes]
rs954920	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv899480	chr12:104092996-104211440	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv899481	chr12:104092996-104213731	Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv899482	chr12:104092996-104218956	Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv34031	chr12:104114277-104298546	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
5	nsv899483	chr12:104117462-104218956	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv899486	chr12:104118587-104170474	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv899487	chr12:104118587-104218956	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv899489	chr12:104144835-104218956	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv899490	chr12:104149022-104218956	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	nsv899491	chr12:104151560-104175575	Genic enhancers Strong transcription Enhancers Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv899492	chr12:104151560-104183658	Transcr. at gene 5' and 3' Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs11111762	RP11-341G23.4	cis	Artery Aorta	GTEx
rs11111762	RP11-341G23.4	cis	Thyroid	GTEx
rs11111762	RP11-341G23.4	cis	Adipose Subcutaneous	GTEx
rs11111762	RP11-341G23.4	cis	Artery Tibial	GTEx
rs11111762	RP11-341G23.4	cis	Esophagus Muscularis	GTEx

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104151600-104170400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr12:104152600-104171200	Weak transcription	Esophagus	oesophagus
3	chr12:104153200-104185200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr12:104154400-104186400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr12:104154800-104170600	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr12:104155000-104170600	Weak transcription	Primary T cells from cord blood	blood
7	chr12:104155000-104170800	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr12:104155000-104171000	Weak transcription	Osteobl	bone
9	chr12:104155000-104178000	Weak transcription	Colonic Mucosa	Colon
10	chr12:104155200-104173400	Weak transcription	NHDF-Ad	bronchial
11	chr12:104156000-104170800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr12:104156200-104170600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:104157400-104172400	Weak transcription	GM12878-XiMat	blood
14	chr12:104157400-104191200	Weak transcription	HUVEC	blood vessel
15	chr12:104157600-104170200	Weak transcription	K562	blood
16	chr12:104157800-104170600	Weak transcription	Primary monocytes fromperipheralblood	blood
17	chr12:104158200-104170400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr12:104158600-104170600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr12:104158600-104170600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr12:104159200-104170400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr12:104159400-104170400	Weak transcription	Fetal Brain Female	brain
22	chr12:104160400-104170800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr12:104160400-104185800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr12:104160600-104170400	Weak transcription	Primary B cells from cord blood	blood
25	chr12:104160600-104170400	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr12:104160800-104170400	Weak transcription	Placenta	Placenta
27	chr12:104162400-104170800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr12:104163000-104178400	Strong transcription	NHEK	skin
29	chr12:104163200-104175200	Weak transcription	Psoas Muscle	Psoas
30	chr12:104163400-104170400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr12:104163600-104174000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr12:104163600-104185000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr12:104163600-104204200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr12:104163800-104170600	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr12:104163800-104170600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr12:104163800-104170600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr12:104163800-104170600	Weak transcription	NHLF	lung
38	chr12:104163800-104170800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr12:104163800-104171000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr12:104164400-104171600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:104165000-104170600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr12:104165200-104170600	Weak transcription	Primary T cells fromperipheralblood	blood
43	chr12:104165600-104170200	Weak transcription	Fetal Stomach	stomach
44	chr12:104165600-104170600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr12:104165600-104170600	Weak transcription	Aorta	Aorta
46	chr12:104165800-104173800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr12:104165800-104193400	Weak transcription	Fetal Lung	lung
48	chr12:104166400-104188400	Weak transcription	Fetal Thymus	thymus
49	chr12:104166800-104170800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr12:104166800-104170800	Weak transcription	Lung	lung

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