Variant report

Variant	rs4771662
Chromosome Location	chr13:110946729-110946730
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs2029767	0.90[AMR][1000 genomes]
rs55997809	0.90[AMR][1000 genomes]
rs58910650	0.90[AMR][1000 genomes]
rs73617472	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs903355	0.84[ASW][hapmap];1.00[CHD][hapmap];0.90[AMR][1000 genomes]
rs9301444	1.00[ASW][hapmap]
rs9559763	0.81[YRI][hapmap]
rs9559764	0.81[YRI][hapmap]
rs958521	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038914	chr13:110860219-111190104	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1046423	chr13:110936104-111286607	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:110920200-110951200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr13:110925400-110949000	Weak transcription	Fetal Kidney	kidney
3	chr13:110928600-110951000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr13:110936200-110951000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr13:110936200-110958800	Weak transcription	Gastric	stomach
6	chr13:110937000-110955400	Weak transcription	A549	lung
7	chr13:110937400-110951000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr13:110937400-110952000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr13:110937800-110947600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr13:110937800-110950600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr13:110938000-110951200	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr13:110938400-110947000	Strong transcription	Osteobl	bone
13	chr13:110939200-110949400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr13:110939600-110951000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:110939600-110951400	Weak transcription	Fetal Intestine Large	intestine
16	chr13:110939800-110950800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr13:110940000-110946800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr13:110940200-110948400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr13:110940200-110949200	Weak transcription	Psoas Muscle	Psoas
20	chr13:110940400-110948200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr13:110940400-110951200	Weak transcription	HSMMtube	muscle
22	chr13:110940400-110953600	Weak transcription	NHEK	skin
23	chr13:110941000-110951000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr13:110941600-110946800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr13:110941600-110947000	Enhancers	Fetal Heart	heart
26	chr13:110942200-110949000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr13:110942200-110950000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr13:110942400-110951200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr13:110942600-110948400	Weak transcription	HSMM	muscle
30	chr13:110942600-110949000	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr13:110942800-110946800	Enhancers	Left Ventricle	heart
32	chr13:110943000-110948200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr13:110943400-110951000	Weak transcription	Colonic Mucosa	Colon
34	chr13:110943600-110946800	Enhancers	Spleen	Spleen
35	chr13:110943600-110951000	Weak transcription	Esophagus	oesophagus
36	chr13:110943800-110947000	Genic enhancers	Fetal Muscle Leg	muscle
37	chr13:110943800-110951000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr13:110944400-110950000	Enhancers	Adipose Nuclei	Adipose
39	chr13:110945000-110946800	Enhancers	Right Atrium	heart
40	chr13:110945400-110946800	Enhancers	Ovary	ovary
41	chr13:110945400-110947600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr13:110945400-110947600	Enhancers	Fetal Lung	lung
43	chr13:110945600-110948600	Weak transcription	NH-A	brain
44	chr13:110945600-110949400	Enhancers	Colon Smooth Muscle	Colon
45	chr13:110945600-110955600	Weak transcription	Pancreas	Pancrea
46	chr13:110945800-110946800	Enhancers	Fetal Stomach	stomach
47	chr13:110945800-110950000	Weak transcription	Fetal Intestine Small	intestine
48	chr13:110946000-110947000	Enhancers	HUVEC	blood vessel
49	chr13:110946000-110947400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr13:110946000-110947600	Enhancers	NHDF-Ad	bronchial

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