Variant report

Variant	rs240403
Chromosome Location	chr6:75983882-75983883
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:75953197..75955267-chr6:75981448..75984407,2	K562	blood:
2	chr6:75983517..75986641-chr6:75988092..75990242,3	MCF-7	breast:
3	chr6:75982180..75984876-chr6:75993848..75995841,3	K562	blood:

Variant related genes	Relation type
ENSG00000225793	Chromatin interaction
ENSG00000112697	Chromatin interaction
ENSG00000112695	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs117512	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1203213	0.89[EUR][1000 genomes]
rs147523	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs15616	0.87[EUR][1000 genomes]
rs240361	1.00[JPT][hapmap]
rs240367	1.00[CEU][hapmap];0.86[EUR][1000 genomes]
rs240368	0.91[EUR][1000 genomes]
rs240369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes]
rs240381	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240382	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs240383	0.85[EUR][1000 genomes]
rs240385	0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240386	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240388	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs240389	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240390	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs240392	0.87[EUR][1000 genomes]
rs240393	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240396	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240398	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240400	0.87[EUR][1000 genomes]
rs240401	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240402	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240404	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs240405	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs240409	0.94[EUR][1000 genomes]
rs240410	0.84[EUR][1000 genomes]
rs240419	0.82[AMR][1000 genomes]
rs240423	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs240428	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs240429	1.00[CEU][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240430	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs240431	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs240432	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs381141	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs397039	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs414624	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs418485	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs429746	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs448854	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs507912	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes]
rs542717	0.91[EUR][1000 genomes]
rs638590	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs643707	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs654428	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs683943	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016804	chr6:75775846-76188585	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538310	chr6:75775846-76188585	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1024079	chr6:75848556-76238519	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv1027915	chr6:75893542-76510113	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv538311	chr6:75893542-76510113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
6	nsv603763	chr6:75923605-76009426	Genic enhancers Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
7	nsv603764	chr6:75963751-76025603	Weak transcription Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
8	nsv830698	chr6:75968810-76115592	Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 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	chr6:75954400-75986000	Weak transcription	Brain Germinal Matrix	brain
2	chr6:75954800-75988200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:75967800-75988200	Weak transcription	Fetal Brain Male	brain
4	chr6:75969600-75992200	Weak transcription	Colonic Mucosa	Colon
5	chr6:75970000-75992400	Weak transcription	Brain Substantia Nigra	brain
6	chr6:75973000-75985200	Weak transcription	HepG2	liver
7	chr6:75973200-75985000	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr6:75973400-75985600	Weak transcription	Lung	lung
9	chr6:75973400-75988200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr6:75974000-75986200	Weak transcription	K562	blood
11	chr6:75974000-75988000	Weak transcription	Stomach Smooth Muscle	stomach
12	chr6:75974200-75993000	Weak transcription	Placenta	Placenta
13	chr6:75974800-75989800	Weak transcription	Fetal Brain Female	brain
14	chr6:75975000-75988200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr6:75975000-75992400	Weak transcription	Fetal Stomach	stomach
16	chr6:75978200-75989400	Weak transcription	Rectal Smooth Muscle	rectum
17	chr6:75978200-75992400	Weak transcription	Fetal Kidney	kidney
18	chr6:75978400-75990000	Weak transcription	Fetal Intestine Small	intestine
19	chr6:75978600-75984800	Weak transcription	Hela-S3	cervix
20	chr6:75978600-75985600	Weak transcription	Left Ventricle	heart
21	chr6:75978600-75985600	Weak transcription	Right Ventricle	heart
22	chr6:75978600-75993600	Weak transcription	Esophagus	oesophagus
23	chr6:75979000-75984200	Weak transcription	Psoas Muscle	Psoas
24	chr6:75979000-75986400	Weak transcription	Gastric	stomach
25	chr6:75979800-75984400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:75979800-75984400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr6:75979800-75986200	ZNF genes & repeats	GM12878-XiMat	blood
28	chr6:75980000-75984400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr6:75981000-75984000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
30	chr6:75981400-75984000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr6:75981800-75984000	Genic enhancers	Dnd41	blood
32	chr6:75982200-75984400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
33	chr6:75982400-75984200	Enhancers	Colon Smooth Muscle	Colon
34	chr6:75982400-75986400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:75982600-75984000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr6:75982600-75984000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr6:75982600-75984800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:75982600-75988000	Weak transcription	Brain Angular Gyrus	brain
39	chr6:75982600-75988200	Weak transcription	Adipose Nuclei	Adipose
40	chr6:75982600-75991800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr6:75982600-75992400	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr6:75982600-75993600	Weak transcription	Spleen	Spleen
43	chr6:75982800-75984200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr6:75982800-75984200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr6:75982800-75984200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr6:75982800-75984600	Enhancers	NHLF	lung
47	chr6:75982800-75984800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr6:75982800-75984800	Weak transcription	Osteobl	bone
49	chr6:75982800-75985000	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr6:75982800-75985400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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