Variant report

Variant	rs12855185
Chromosome Location	chr13:49176517-49176518
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs1009719	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11148110	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12050047	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12859099	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12864882	0.85[EUR][1000 genomes]
rs12876717	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12877288	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12877954	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1359688	0.83[EUR][1000 genomes]
rs1536396	0.85[AFR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1536397	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1808060	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1887154	0.86[EUR][1000 genomes]
rs198590	0.80[EUR][1000 genomes]
rs2104532	0.81[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2407095	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs3092904	0.80[EUR][1000 genomes]
rs4497565	0.86[EUR][1000 genomes]
rs4635233	0.85[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs7325719	0.86[EUR][1000 genomes]
rs7332322	0.86[EUR][1000 genomes]
rs8002098	0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9316381	0.80[EUR][1000 genomes]
rs9316388	0.83[EUR][1000 genomes]
rs9316393	0.83[EUR][1000 genomes]
rs9316407	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs943280	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9526481	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9526483	0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9535038	0.81[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs9535042	0.92[AFR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9535043	0.88[EUR][1000 genomes]
rs9535045	0.85[AFR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9535046	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9535049	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9535055	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9535056	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9535058	0.84[EUR][1000 genomes]
rs9568047	0.84[EUR][1000 genomes]
rs9568049	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9568050	0.85[AFR][1000 genomes];0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9568051	0.91[EUR][1000 genomes]
rs9568057	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9568060	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9568063	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9595937	0.84[EUR][1000 genomes]
rs9634680	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1041275	chr13:49045566-49242357	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv541769	chr13:49045566-49242357	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv832604	chr13:49061081-49281807	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1049117	chr13:49089476-49928945	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv832605	chr13:49171305-49344970	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs12855185	ITM2B	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49169800-49177800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:49170000-49176600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr13:49170400-49176600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr13:49173800-49176600	Enhancers	Ovary	ovary
5	chr13:49174000-49176800	Enhancers	Fetal Stomach	stomach
6	chr13:49174200-49176800	Enhancers	NH-A	brain
7	chr13:49174200-49177400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr13:49174400-49177000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr13:49174600-49177000	Enhancers	Placenta Amnion	Placenta Amnion
10	chr13:49174600-49178000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr13:49174800-49176800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr13:49174800-49177000	Enhancers	Primary hematopoietic stem cells	blood
13	chr13:49174800-49177200	Enhancers	Placenta	Placenta
14	chr13:49174800-49177400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr13:49175200-49176800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr13:49175200-49176800	Enhancers	Pancreas	Pancrea
17	chr13:49175400-49176600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr13:49175400-49176600	Weak transcription	HSMMtube	muscle
19	chr13:49175400-49177000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr13:49175400-49177000	Enhancers	Hela-S3	cervix
21	chr13:49175600-49176800	Weak transcription	Fetal Muscle Leg	muscle
22	chr13:49175800-49176600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr13:49175800-49176800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr13:49175800-49177600	Enhancers	Dnd41	blood
25	chr13:49176000-49176600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr13:49176200-49176600	Enhancers	Fetal Muscle Trunk	muscle
27	chr13:49176400-49176600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr13:49176400-49176600	Enhancers	Right Ventricle	heart
29	chr13:49176400-49176600	Bivalent Enhancer	HepG2	liver
30	chr13:49176400-49176800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr13:49176400-49176800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr13:49176400-49177200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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