Variant report

Variant	rs9469965
Chromosome Location	chr6:35194287-35194288
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:35192773..35195560-chr6:35195988..35198811,2	MCF-7	breast:
2	chr6:35192627..35195181-chr6:35418062..35420714,2	K562	blood:
3	chr6:35190929..35192629-chr6:35194228..35196176,2	K562	blood:

Variant related genes	Relation type
ENSG00000112039	Chromatin interaction
ENSG00000272374	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1034450	0.81[AMR][1000 genomes]
rs12332985	0.92[AMR][1000 genomes]
rs16874062	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16874262	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2187903	0.81[AMR][1000 genomes]
rs2228265	0.81[AMR][1000 genomes]
rs28627111	0.81[AMR][1000 genomes]
rs59895076	0.81[AMR][1000 genomes]
rs60569490	0.81[AMR][1000 genomes]
rs60812576	0.83[AFR][1000 genomes]
rs62403573	1.00[EUR][1000 genomes]
rs6901580	0.81[AMR][1000 genomes]
rs6906117	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs743965	0.81[AMR][1000 genomes]
rs9462061	0.83[AFR][1000 genomes]
rs9462062	0.81[AMR][1000 genomes]
rs9462064	0.81[AMR][1000 genomes]
rs9462066	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469959	0.82[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs9469960	0.81[AMR][1000 genomes]
rs9469962	0.82[AFR][1000 genomes]
rs9469966	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469967	0.81[AMR][1000 genomes]
rs9469969	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs9469973	0.82[AFR][1000 genomes]
rs9469977	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469984	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9469993	0.92[AMR][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	esv3428128	chr6:35150524-35225843	Bivalent Enhancer Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	esv2758047	chr6:35168116-35291002	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	esv2759419	chr6:35168116-35291002	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35182400-35209000	Weak transcription	A549	lung
2	chr6:35182600-35198600	Weak transcription	Gastric	stomach
3	chr6:35183200-35198800	Weak transcription	Ovary	ovary
4	chr6:35184800-35205600	Weak transcription	Fetal Brain Female	brain
5	chr6:35185400-35198800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:35185800-35198400	Weak transcription	Brain Cingulate Gyrus	brain
7	chr6:35186200-35202800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:35186400-35198000	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:35186400-35212000	Weak transcription	NHDF-Ad	bronchial
10	chr6:35186600-35198200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:35186600-35204600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr6:35186600-35205400	Weak transcription	Fetal Muscle Trunk	muscle
13	chr6:35186800-35212000	Weak transcription	Dnd41	blood
14	chr6:35187000-35196400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr6:35187000-35197600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr6:35187400-35198400	Weak transcription	Brain Hippocampus Middle	brain
17	chr6:35187600-35198400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:35188000-35195200	Weak transcription	Lung	lung
19	chr6:35188000-35198400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:35188000-35198600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr6:35188000-35199400	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr6:35188200-35200400	Genic enhancers	Osteobl	bone
23	chr6:35188200-35205800	Weak transcription	Fetal Kidney	kidney
24	chr6:35188200-35206400	Weak transcription	NH-A	brain
25	chr6:35188400-35197200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:35188400-35199600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr6:35188600-35195400	Weak transcription	Aorta	Aorta
28	chr6:35188800-35194600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:35188800-35195200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:35189000-35195200	Weak transcription	Fetal Intestine Small	intestine
31	chr6:35189200-35200000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:35189600-35205800	Weak transcription	Brain Germinal Matrix	brain
33	chr6:35189800-35197600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr6:35190000-35205600	Weak transcription	Fetal Muscle Leg	muscle
35	chr6:35190200-35212000	Weak transcription	Brain Angular Gyrus	brain
36	chr6:35190400-35196600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr6:35190600-35201800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:35191200-35194800	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:35191200-35212000	Weak transcription	Primary T cells from cord blood	blood
40	chr6:35191400-35198400	Weak transcription	Brain Substantia Nigra	brain
41	chr6:35191400-35226000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:35191600-35198000	Weak transcription	Adipose Nuclei	Adipose
43	chr6:35192200-35195200	Weak transcription	Right Ventricle	heart
44	chr6:35192200-35211400	Weak transcription	Skeletal Muscle Female	skeletal muscle
45	chr6:35192600-35198400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr6:35192800-35198000	Weak transcription	Colon Smooth Muscle	Colon
47	chr6:35193000-35194800	Weak transcription	Fetal Stomach	stomach
48	chr6:35193000-35195200	Weak transcription	Left Ventricle	heart
49	chr6:35193400-35195200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:35193400-35195800	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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