Variant report

Variant	rs13353034
Chromosome Location	chr1:171220811-171220812
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	chr1:171219827..171222241-chr1:171222983..171225833,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYOC-2	chr1:171220662-171220933	ENSG00000231424.1
2	lnc-MYOC-2	chr1:171220662-171220933	ENSG00000231424.2

Variant related genes	Relation type
ENSG00000206692	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12064117	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12066662	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12067810	0.86[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12071595	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12072321	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12082112	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12087971	1.00[GIH][hapmap]
rs12091865	1.00[GIH][hapmap]
rs16864165	1.00[GIH][hapmap]
rs16864191	1.00[GIH][hapmap];0.84[LWK][hapmap];0.81[TSI][hapmap];0.82[YRI][hapmap];0.83[EUR][1000 genomes]
rs16864245	0.85[YRI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17350523	0.85[YRI][hapmap]
rs2020860	1.00[GIH][hapmap]
rs2020865	1.00[GIH][hapmap];0.81[TSI][hapmap];0.83[EUR][1000 genomes]
rs2075991	0.83[YRI][hapmap]
rs2205726	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56060753	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56159716	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs56233063	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs57182460	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58324390	0.83[EUR][1000 genomes]
rs58956470	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs59910498	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61225278	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs61233777	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6668231	0.80[EUR][1000 genomes]
rs6673781	0.80[EUR][1000 genomes]
rs6684218	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6689616	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs73032526	0.80[EUR][1000 genomes]
rs74122287	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7527107	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001228	chr1:170885787-171452579	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
2	esv14617	chr1:171016086-171726961	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats 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 miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1005902	chr1:171036690-171254916	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
4	nsv535203	chr1:171036690-171254916	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	esv10193	chr1:171128845-171414611	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv831882	chr1:171166224-171326083	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171217600-171221000	Active TSS	Fetal Intestine Small	intestine
2	chr1:171217600-171221200	Active TSS	Fetal Intestine Large	intestine
3	chr1:171219600-171221200	Active TSS	Fetal Lung	lung
4	chr1:171220000-171221200	Active TSS	Breast Myoepithelial Primary Cells	Breast
5	chr1:171220200-171221000	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr1:171220200-171221000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr1:171220200-171221000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:171220200-171221000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
9	chr1:171220200-171221000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
10	chr1:171220200-171221000	Bivalent/Poised TSS	Fetal Brain Male	brain
11	chr1:171220200-171221000	Active TSS	Fetal Heart	heart
12	chr1:171220200-171221200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr1:171220200-171221200	Flanking Active TSS	Primary B cells from cord blood	blood
14	chr1:171220200-171221200	Active TSS	Brain Cingulate Gyrus	brain
15	chr1:171220200-171221200	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr1:171220200-171221200	Active TSS	K562	blood
17	chr1:171220200-171221200	Flanking Active TSS	NHEK	skin
18	chr1:171220200-171221200	Active TSS	NHLF	lung
19	chr1:171220200-171221200	Active TSS	Osteobl	bone
20	chr1:171220200-171221400	Active TSS	Right Ventricle	heart
21	chr1:171220200-171221800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
22	chr1:171220400-171221000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr1:171220400-171221000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:171220400-171221000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr1:171220400-171221000	Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr1:171220400-171221000	Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr1:171220400-171221000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr1:171220400-171221000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr1:171220400-171221000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	Primary monocytes fromperipheralblood	blood
33	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
34	chr1:171220400-171221000	Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr1:171220400-171221000	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
37	chr1:171220400-171221000	Active TSS	Aorta	Aorta
38	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	Placenta	Placenta
39	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
40	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
41	chr1:171220400-171221000	Active TSS	Gastric	stomach
42	chr1:171220400-171221000	Flanking Active TSS	Lung	lung
43	chr1:171220400-171221000	Flanking Active TSS	Pancreas	Pancrea
44	chr1:171220400-171221000	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
45	chr1:171220400-171221000	Bivalent/Poised TSS	HepG2	liver
46	chr1:171220400-171221000	Active TSS	NHDF-Ad	bronchial
47	chr1:171220400-171221200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:171220400-171221200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells short term culture	blood
49	chr1:171220400-171221200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr1:171220400-171221200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin

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