Variant report

Variant	rs9347743
Chromosome Location	chr6:163776018-163776019
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:163757896..163760585-chr6:163774528..163776997,2	MCF-7	breast:
2	chr6:163772638..163774453-chr6:163775997..163777514,2	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs13194411	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1737311	0.90[ASN][1000 genomes]
rs1737323	1.00[JPT][hapmap]
rs1744933	1.00[CHB][hapmap]
rs1763999	0.90[ASN][1000 genomes]
rs2143070	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2784874	1.00[JPT][hapmap]
rs4709712	0.90[ASN][1000 genomes]
rs6901488	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6905064	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6920269	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6922650	0.90[ASN][1000 genomes]
rs735751	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9346957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9347742	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9355427	1.00[JPT][hapmap]
rs9365560	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9365561	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1022610	chr6:163591786-163814041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv534621	chr6:163731741-163950870	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163767600-163776200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:163767600-163776600	Enhancers	Brain Cingulate Gyrus	brain
3	chr6:163768200-163776400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:163768200-163776400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:163772200-163778000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:163772200-163778600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr6:163772400-163778800	Enhancers	Placenta	Placenta
8	chr6:163773400-163776800	Enhancers	Brain Angular Gyrus	brain
9	chr6:163773400-163777600	Enhancers	Fetal Muscle Leg	muscle
10	chr6:163773600-163778000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr6:163773800-163776200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:163774400-163776600	Enhancers	Brain Substantia Nigra	brain
13	chr6:163775000-163777600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:163775000-163777600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr6:163775000-163778000	Enhancers	Hela-S3	cervix
16	chr6:163775000-163778400	Enhancers	Fetal Heart	heart
17	chr6:163775200-163776200	Enhancers	NH-A	brain
18	chr6:163775200-163776200	Enhancers	NHDF-Ad	bronchial
19	chr6:163775200-163776400	Enhancers	Right Ventricle	heart
20	chr6:163775200-163777200	Enhancers	Fetal Lung	lung
21	chr6:163775200-163777400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:163775200-163777400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:163775200-163777400	Enhancers	Spleen	Spleen
24	chr6:163775200-163777400	Enhancers	HSMMtube	muscle
25	chr6:163775200-163777800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr6:163775200-163778000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:163775200-163778000	Enhancers	NHEK	skin
28	chr6:163775200-163778200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr6:163775200-163778400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:163775200-163778400	Enhancers	Lung	lung
31	chr6:163775400-163777200	Enhancers	Fetal Stomach	stomach
32	chr6:163775400-163777400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:163775400-163777400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr6:163775400-163777400	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr6:163775600-163776200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr6:163775600-163776200	Enhancers	Colon Smooth Muscle	Colon
37	chr6:163775600-163777000	Enhancers	Placenta Amnion	Placenta Amnion
38	chr6:163775800-163776200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr6:163775800-163776200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr6:163775800-163776400	Enhancers	Fetal Kidney	kidney
41	chr6:163775800-163776400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr6:163775800-163776600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr6:163775800-163776800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr6:163775800-163776800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr6:163775800-163776800	Enhancers	Esophagus	oesophagus
46	chr6:163775800-163776800	Active TSS	Rectal Smooth Muscle	rectum
47	chr6:163775800-163777000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr6:163775800-163777200	Enhancers	Primary hematopoietic stem cells	blood
49	chr6:163775800-163777200	Flanking Active TSS	Osteobl	bone
50	chr6:163775800-163777400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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