Variant report

Variant	rs11677350
Chromosome Location	chr2:48771605-48771606
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:48767423..48771041-chr2:48771579..48775293,4	K562	blood:
2	chr2:48676760..48679121-chr2:48771521..48774088,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11674217	0.87[CEU][hapmap]
rs11674683	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11675947	1.00[AFR][1000 genomes]
rs11678934	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[AFR][1000 genomes]
rs11682008	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs11682838	1.00[AFR][1000 genomes]
rs11683259	0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11688465	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11689285	0.87[CEU][hapmap]
rs11690526	0.87[CEU][hapmap]
rs11691302	1.00[AFR][1000 genomes]
rs11691407	1.00[AFR][1000 genomes]
rs11692537	0.87[CEU][hapmap]
rs11694094	1.00[AFR][1000 genomes]
rs11694955	1.00[AFR][1000 genomes]
rs17325698	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs17397449	1.00[ASW][hapmap]
rs17397707	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2937	0.87[CEU][hapmap]
rs4364065	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005954	chr2:48692696-48905723	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv535682	chr2:48692696-48905723	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv833981	chr2:48705444-48878179	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1007491	chr2:48752185-48796441	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv535683	chr2:48752185-48796441	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv581776	chr2:48763382-48913019	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv1000419	chr2:48766957-48795327	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1010494	chr2:48767055-49027310	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
9	nsv1002793	chr2:48771220-49466550	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11677350	EMR1	trans	lymphoblastoid	seeQTL

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48758800-48772400	Weak transcription	Fetal Muscle Trunk	muscle
2	chr2:48759000-48772600	Weak transcription	Fetal Muscle Leg	muscle
3	chr2:48759000-48775200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:48759000-48787000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:48759000-48787400	Weak transcription	Psoas Muscle	Psoas
6	chr2:48759000-48827600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr2:48759200-48793200	Weak transcription	Fetal Lung	lung
8	chr2:48759400-48775200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:48760000-48772000	Weak transcription	Lung	lung
10	chr2:48760000-48772400	Weak transcription	Right Atrium	heart
11	chr2:48760400-48772800	Weak transcription	Left Ventricle	heart
12	chr2:48762600-48775000	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr2:48766800-48779600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr2:48767200-48772600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:48767200-48807800	Weak transcription	Aorta	Aorta
16	chr2:48767400-48775200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr2:48767600-48772400	Weak transcription	K562	blood
18	chr2:48767800-48772600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr2:48767800-48776400	Weak transcription	Fetal Stomach	stomach
20	chr2:48768000-48772000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr2:48768000-48772400	Weak transcription	Placenta	Placenta
22	chr2:48768000-48787600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:48768000-48793800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:48768200-48772400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr2:48768600-48777000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr2:48769000-48776000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:48769400-48774400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:48769400-48778800	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr2:48769400-48780200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr2:48769800-48772400	Weak transcription	Fetal Heart	heart
31	chr2:48769800-48778200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr2:48770800-48771800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr2:48770800-48771800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr2:48770800-48772400	Enhancers	Stomach Smooth Muscle	stomach
35	chr2:48770800-48776800	Enhancers	Colon Smooth Muscle	Colon
36	chr2:48771000-48772000	Enhancers	Duodenum Smooth Muscle	Duodenum
37	chr2:48771000-48772000	Enhancers	Osteobl	bone
38	chr2:48771000-48781200	Weak transcription	HSMMtube	muscle
39	chr2:48771200-48777600	Weak transcription	Adipose Nuclei	Adipose
40	chr2:48771400-48771800	Weak transcription	Ovary	ovary
41	chr2:48771400-48772800	Weak transcription	Rectal Smooth Muscle	rectum
42	chr2:48771600-48772400	Weak transcription	NHDF-Ad	bronchial
43	chr2:48771600-48776000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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