Variant report

Variant	rs11111755
Chromosome Location	chr12:104159667-104159668
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10861094	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10861095	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10861096	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10861097	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10861098	0.83[AFR][1000 genomes]
rs10861099	0.83[AFR][1000 genomes]
rs10861105	0.83[ASN][1000 genomes]
rs11111750	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11111752	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11111754	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11111757	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11111758	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11111759	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11111762	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11111763	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11111765	0.85[AMR][1000 genomes]
rs11111767	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11111771	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11111776	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11111779	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11111788	0.83[ASN][1000 genomes]
rs11111789	0.83[ASN][1000 genomes]
rs1565773	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs15918	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1866292	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1866295	0.88[ASN][1000 genomes]
rs1976256	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2292682	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3751204	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3812805	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4964298	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4964812	0.84[ASN][1000 genomes]
rs4964823	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4964827	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4964830	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4981032	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4981036	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs751448	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs869993	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9132	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs934847	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs954920	0.86[AMR][1000 genomes];0.94[EUR][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
rs11111755	RP11-341G23.4	cis	Artery Aorta	GTEx
rs11111755	RP11-341G23.4	cis	Esophagus Muscularis	GTEx
rs11111755	RP11-341G23.4	cis	Thyroid	GTEx
rs11111755	RP11-341G23.4	cis	Artery Tibial	GTEx
rs11111755	RP11-341G23.4	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104145800-104166800	Weak transcription	Right Atrium	heart
2	chr12:104146200-104169400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr12:104147000-104165400	Strong transcription	Stomach Smooth Muscle	stomach
4	chr12:104150000-104166800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr12:104151600-104170400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr12:104152000-104159800	Weak transcription	Lung	lung
7	chr12:104152400-104160000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr12:104152400-104162600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:104152400-104162800	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:104152600-104160600	Strong transcription	Spleen	Spleen
11	chr12:104152600-104161600	Strong transcription	HMEC	breast
12	chr12:104152600-104162600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr12:104152600-104162600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:104152600-104162800	Weak transcription	Psoas Muscle	Psoas
15	chr12:104152600-104171200	Weak transcription	Esophagus	oesophagus
16	chr12:104152800-104162800	Weak transcription	Brain Angular Gyrus	brain
17	chr12:104152800-104165400	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr12:104153200-104162800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:104153200-104185200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr12:104153800-104161600	Strong transcription	Liver	Liver
21	chr12:104154200-104161800	Strong transcription	Colon Smooth Muscle	Colon
22	chr12:104154400-104186400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr12:104154600-104160400	Strong transcription	NHEK	skin
24	chr12:104154600-104160600	Strong transcription	Aorta	Aorta
25	chr12:104154600-104160600	Strong transcription	Fetal Stomach	stomach
26	chr12:104154800-104161400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr12:104154800-104161600	Strong transcription	NH-A	brain
28	chr12:104154800-104170600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr12:104155000-104161200	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr12:104155000-104169000	Weak transcription	Primary B cells from peripheral blood	blood
31	chr12:104155000-104170600	Weak transcription	Primary T cells from cord blood	blood
32	chr12:104155000-104170800	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr12:104155000-104171000	Weak transcription	Osteobl	bone
34	chr12:104155000-104178000	Weak transcription	Colonic Mucosa	Colon
35	chr12:104155200-104162800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr12:104155200-104163200	Weak transcription	NHLF	lung
37	chr12:104155200-104173400	Weak transcription	NHDF-Ad	bronchial
38	chr12:104155400-104160800	Strong transcription	Duodenum Smooth Muscle	Duodenum
39	chr12:104155600-104159800	Weak transcription	Monocytes-CD14+_RO01746	blood
40	chr12:104155600-104161200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:104155600-104162800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr12:104155800-104160000	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr12:104155800-104169000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr12:104156000-104170800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr12:104156200-104160000	Weak transcription	Adipose Nuclei	Adipose
46	chr12:104156200-104161000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:104156200-104170600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:104156600-104166600	Weak transcription	Brain Anterior Caudate	brain
49	chr12:104157400-104166400	Weak transcription	HSMMtube	muscle
50	chr12:104157400-104169000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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