Variant report

Variant	rs12205788
Chromosome Location	chr6:149335629-149335630
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:149334123..149335650-chr6:149338219..149339983,2	K562	blood:
2	chr6:149334123..149336930-chr6:149338219..149339983,3	K562	blood:
3	chr6:149335195..149337795-chr6:149343011..149345785,3	MCF-7	breast:
4	chr6:149326735..149329434-chr6:149335396..149337104,2	K562	blood:
5	chr6:149335068..149337695-chr6:149751708..149753851,2	MCF-7	breast:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10457838	0.91[EUR][1000 genomes]
rs10782309	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10872630	0.88[JPT][hapmap];0.84[EUR][1000 genomes]
rs10872631	0.84[EUR][1000 genomes]
rs10872632	0.81[EUR][1000 genomes]
rs11155611	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11155615	0.86[EUR][1000 genomes]
rs11755470	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11759315	0.80[JPT][hapmap];0.89[EUR][1000 genomes]
rs11759624	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11967885	1.00[CEU][hapmap];0.94[JPT][hapmap];0.95[EUR][1000 genomes]
rs12201653	0.96[CEU][hapmap];0.94[CHB][hapmap];0.81[JPT][hapmap];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12203658	1.00[CEU][hapmap];0.93[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12211152	0.81[CHB][hapmap];0.88[EUR][1000 genomes]
rs17669693	0.80[CEU][hapmap];0.82[JPT][hapmap];0.89[EUR][1000 genomes]
rs17732007	0.84[EUR][1000 genomes]
rs1934218	0.95[CEU][hapmap];0.81[CHB][hapmap];0.87[JPT][hapmap];0.93[EUR][1000 genomes]
rs1934220	0.89[EUR][1000 genomes]
rs2500542	0.96[CEU][hapmap]
rs2500544	0.81[CEU][hapmap]
rs2879862	0.84[EUR][1000 genomes]
rs4897077	0.84[EUR][1000 genomes]
rs4897078	0.82[JPT][hapmap]
rs56358125	0.85[EUR][1000 genomes]
rs62426145	0.85[EUR][1000 genomes]
rs62426146	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62426150	0.95[EUR][1000 genomes]
rs62426156	0.84[EUR][1000 genomes]
rs6903827	0.81[EUR][1000 genomes]
rs6911677	0.96[CEU][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6932386	0.80[CEU][hapmap];0.82[JPT][hapmap];0.84[EUR][1000 genomes]
rs6938335	0.95[EUR][1000 genomes]
rs6939103	0.84[CEU][hapmap];0.82[JPT][hapmap];0.83[EUR][1000 genomes]
rs7756263	0.92[CEU][hapmap];0.83[CHB][hapmap];0.88[JPT][hapmap];0.95[EUR][1000 genomes]
rs7772696	0.82[JPT][hapmap]
rs9322164	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032690	chr6:149206106-149398712	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1032319	chr6:149271433-149550525	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv538470	chr6:149271433-149550525	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv830842	chr6:149272321-149427340	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149305400-149381400	Weak transcription	Gastric	stomach
2	chr6:149320200-149344800	Weak transcription	Left Ventricle	heart
3	chr6:149321600-149336000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr6:149321600-149340600	Weak transcription	Aorta	Aorta
5	chr6:149321800-149340200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:149321800-149349800	Weak transcription	Rectal Smooth Muscle	rectum
7	chr6:149323000-149342600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr6:149327200-149340200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr6:149327200-149340600	Weak transcription	Primary B cells from cord blood	blood
10	chr6:149327200-149353000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr6:149327600-149335800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr6:149327600-149342200	Weak transcription	Dnd41	blood
13	chr6:149329400-149340600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:149329800-149340200	Weak transcription	Ovary	ovary
15	chr6:149332600-149336200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr6:149332600-149337800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:149333000-149337600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr6:149333000-149337600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:149333400-149340800	Weak transcription	Colon Smooth Muscle	Colon
20	chr6:149333600-149340400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:149333800-149335800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr6:149333800-149336000	Weak transcription	HSMM	muscle
23	chr6:149333800-149341400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr6:149333800-149341800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:149333800-149342200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:149334000-149336800	Enhancers	Fetal Brain Male	brain
27	chr6:149334000-149353400	Weak transcription	Spleen	Spleen
28	chr6:149334200-149337200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr6:149334200-149337200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr6:149334400-149336400	Enhancers	Fetal Brain Female	brain
31	chr6:149334400-149352800	Weak transcription	HSMMtube	muscle
32	chr6:149334600-149336200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr6:149334600-149336200	Enhancers	Brain Angular Gyrus	brain
34	chr6:149334600-149336400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr6:149334600-149337000	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr6:149334600-149337600	Enhancers	H9 Cell Line	embryonic stem cell
37	chr6:149334800-149336200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr6:149334800-149336200	Enhancers	Brain Anterior Caudate	brain
39	chr6:149334800-149336800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr6:149334800-149337200	Enhancers	Fetal Heart	heart
41	chr6:149334800-149337400	Enhancers	Fetal Stomach	stomach
42	chr6:149335000-149336000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr6:149335000-149336200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:149335000-149336400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:149335000-149337000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:149335000-149337600	Enhancers	Fetal Muscle Trunk	muscle
47	chr6:149335200-149336000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr6:149335200-149336200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
49	chr6:149335200-149336200	Enhancers	Esophagus	oesophagus
50	chr6:149335200-149336200	Enhancers	Right Atrium	heart

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