Variant report

Variant	rs58776118
Chromosome Location	chr4:148917490-148917491
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10010996	1.00[EUR][1000 genomes]
rs10012122	1.00[EUR][1000 genomes]
rs10213616	1.00[EUR][1000 genomes]
rs10519932	1.00[EUR][1000 genomes]
rs1436492	1.00[EUR][1000 genomes]
rs17023950	1.00[EUR][1000 genomes]
rs17023959	1.00[EUR][1000 genomes]
rs17024108	1.00[EUR][1000 genomes]
rs17024163	1.00[EUR][1000 genomes]
rs17024397	1.00[EUR][1000 genomes]
rs28371967	1.00[EUR][1000 genomes]
rs28647457	1.00[EUR][1000 genomes]
rs41435251	1.00[EUR][1000 genomes]
rs55689306	1.00[EUR][1000 genomes]
rs56742479	1.00[EUR][1000 genomes]
rs57536956	0.83[AFR][1000 genomes]
rs59129054	1.00[EUR][1000 genomes]
rs59222333	1.00[EUR][1000 genomes]
rs59845678	1.00[EUR][1000 genomes]
rs6813344	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6814079	0.83[AFR][1000 genomes]
rs6814346	0.81[AFR][1000 genomes]
rs6815620	1.00[EUR][1000 genomes]
rs6848211	1.00[EUR][1000 genomes]
rs72957764	1.00[EUR][1000 genomes]
rs72957767	1.00[EUR][1000 genomes]
rs72957792	1.00[EUR][1000 genomes]
rs731989	1.00[EUR][1000 genomes]
rs73853711	1.00[EUR][1000 genomes]
rs7661589	1.00[EUR][1000 genomes]
rs7699281	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv498083	chr4:148519825-148917583	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv880244	chr4:148764252-148920089	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1017904	chr4:148814133-148975348	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148866400-148927400	Weak transcription	Thymus	Thymus
2	chr4:148885600-148939000	Weak transcription	Pancreas	Pancrea
3	chr4:148886000-148917600	Weak transcription	Esophagus	oesophagus
4	chr4:148889200-148936200	Weak transcription	Fetal Intestine Large	intestine
5	chr4:148891600-148920600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:148891600-148928000	Weak transcription	A549	lung
7	chr4:148896600-148928400	Weak transcription	Spleen	Spleen
8	chr4:148897200-148917600	Weak transcription	Lung	lung
9	chr4:148898200-148920600	Weak transcription	NHEK	skin
10	chr4:148898200-148925400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:148905800-148918000	Weak transcription	Stomach Mucosa	stomach
12	chr4:148906000-148925200	Weak transcription	Adipose Nuclei	Adipose
13	chr4:148906400-148928400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:148906600-148917600	Weak transcription	Gastric	stomach
15	chr4:148906600-148920600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr4:148906600-148920600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:148906600-148920800	Weak transcription	Fetal Intestine Small	intestine
18	chr4:148906800-148918000	Weak transcription	NHLF	lung
19	chr4:148907200-148928000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr4:148907400-148928400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:148907800-148920600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr4:148910200-148928400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr4:148911600-148936200	Weak transcription	H9 Cell Line	embryonic stem cell
24	chr4:148911800-148917600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr4:148911800-148925200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:148913000-148920000	Weak transcription	GM12878-XiMat	blood
27	chr4:148913200-148929200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr4:148913600-148917600	Weak transcription	Right Atrium	heart
29	chr4:148913600-148920600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:148913600-148933200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr4:148914400-148918000	Enhancers	Colon Smooth Muscle	Colon
32	chr4:148915200-148928200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:148915400-148917600	Weak transcription	HSMM	muscle
34	chr4:148915400-148920000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:148915600-148917600	Weak transcription	Left Ventricle	heart
36	chr4:148915600-148920200	Weak transcription	Aorta	Aorta
37	chr4:148915600-148920200	Weak transcription	Fetal Muscle Leg	muscle
38	chr4:148916000-148917600	Weak transcription	Right Ventricle	heart
39	chr4:148916200-148920600	Weak transcription	Fetal Stomach	stomach
40	chr4:148916400-148928200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr4:148916600-148917600	Weak transcription	Ovary	ovary
42	chr4:148916600-148922200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr4:148916600-148925400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr4:148916600-148925600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr4:148916600-148928800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr4:148916800-148917600	Weak transcription	Fetal Heart	heart
47	chr4:148916800-148927800	Weak transcription	HUVEC	blood vessel
48	chr4:148917200-148917800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:148917200-148918200	Enhancers	Psoas Muscle	Psoas
50	chr4:148917200-148918200	Enhancers	Stomach Smooth Muscle	stomach

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