Variant report

Variant	rs4074864
Chromosome Location	chr6:11390177-11390178
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:11388708..11391347-chr6:11433045..11435258,2	MCF-7	breast:
2	chr6:11252403..11254057-chr6:11387199..11390299,3	MCF-7	breast:
3	chr6:11356402..11359256-chr6:11386897..11390575,4	MCF-7	breast:
4	chr6:11363308..11365287-chr6:11389526..11391473,2	MCF-7	breast:
5	chr6:11343010..11348187-chr6:11388549..11393263,7	MCF-7	breast:
6	chr6:11229965..11235177-chr6:11385041..11393111,14	MCF-7	breast:
7	chr6:11230510..11233804-chr6:11387057..11390361,4	MCF-7	breast:
8	chr6:11389440..11392431-chr6:11393739..11396017,2	K562	blood:
9	chr6:11387321..11394874-chr6:11409302..11416244,8	MCF-7	breast:
10	chr6:11342539..11346028-chr6:11385686..11392115,8	MCF-7	breast:
11	chr6:11172296..11174854-chr6:11388458..11391129,2	MCF-7	breast:
12	chr6:11388874..11392122-chr6:11413409..11415866,5	MCF-7	breast:
13	chr6:11288344..11289961-chr6:11388125..11390631,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000247925	Chromatin interaction
ENSG00000111859	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1012503	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10947217	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11751505	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs11756278	1.00[CEU][hapmap];0.93[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12661807	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs17507230	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4318876	0.93[ASN][1000 genomes]
rs4713459	0.91[AMR][1000 genomes]
rs4713474	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4713475	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4713478	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55918622	0.93[ASN][1000 genomes]
rs56144403	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56155385	0.93[ASN][1000 genomes]
rs56317766	0.93[ASN][1000 genomes]
rs56711429	0.91[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs59349836	0.93[ASN][1000 genomes]
rs61650802	0.93[ASN][1000 genomes]
rs6901538	1.00[CEU][hapmap];0.80[CHB][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72832925	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs72832932	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72832935	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72832944	0.93[ASN][1000 genomes]
rs73366900	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7740502	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[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	nsv1021078	chr6:10819083-11558560	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS 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 target site	47 gene(s)	inside rSNPs	diseases
2	nsv538135	chr6:10819083-11558560	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS 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 target site	47 gene(s)	inside rSNPs	diseases
3	nsv432848	chr6:11371614-11560114	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11382600-11392400	Weak transcription	Right Atrium	heart
2	chr6:11383200-11390200	Weak transcription	Spleen	Spleen
3	chr6:11383400-11392600	Weak transcription	Duodenum Mucosa	Duodenum
4	chr6:11383600-11393000	Weak transcription	Small Intestine	intestine
5	chr6:11383800-11392600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr6:11385600-11390400	Enhancers	Primary B cells from peripheral blood	blood
7	chr6:11385800-11393400	Weak transcription	Aorta	Aorta
8	chr6:11386000-11393600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:11386600-11392200	Enhancers	HepG2	liver
10	chr6:11387200-11392800	Weak transcription	Stomach Mucosa	stomach
11	chr6:11387400-11390200	Weak transcription	Fetal Lung	lung
12	chr6:11387400-11392400	Weak transcription	Fetal Intestine Small	intestine
13	chr6:11388400-11392200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr6:11388800-11390800	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr6:11389200-11391000	Enhancers	Primary hematopoietic stem cells	blood
16	chr6:11389200-11394800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:11389400-11390400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:11389400-11392400	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr6:11389400-11392400	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr6:11389400-11394800	Enhancers	HUVEC	blood vessel
21	chr6:11389600-11390800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr6:11389600-11390800	Enhancers	Placenta	Placenta
23	chr6:11389600-11391600	Enhancers	Placenta Amnion	Placenta Amnion
24	chr6:11389600-11392600	Weak transcription	Primary neutrophils fromperipheralblood	blood
25	chr6:11389800-11390800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:11389800-11390800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:11389800-11391000	Enhancers	HMEC	breast
28	chr6:11389800-11392400	Weak transcription	Lung	lung
29	chr6:11389800-11393000	Weak transcription	Adipose Nuclei	Adipose
30	chr6:11390000-11390800	Enhancers	NHEK	skin
31	chr6:11390000-11391000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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