Variant report

Variant	rs802618
Chromosome Location	chr6:143006214-143006215
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:143005255..143006929-chr6:143007126..143009083,2	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12214216	1.00[ASN][1000 genomes]
rs62430690	1.00[ASN][1000 genomes]
rs62430703	1.00[ASN][1000 genomes]
rs6900521	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72984377	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72995085	1.00[ASN][1000 genomes]
rs7757965	1.00[ASN][1000 genomes]
rs9689935	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	nsv949088	chr6:142561402-143128849	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv830827	chr6:142840734-143015005	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv830828	chr6:142970134-143116517	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142998200-143008200	Weak transcription	Fetal Stomach	stomach
2	chr6:142999400-143007800	Enhancers	Fetal Brain Male	brain
3	chr6:143001800-143013600	Weak transcription	NH-A	brain
4	chr6:143002400-143006400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr6:143002400-143007000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr6:143002600-143013800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr6:143003600-143006800	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr6:143004000-143006400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr6:143004000-143006400	Enhancers	NHEK	skin
10	chr6:143004000-143006800	Enhancers	HMEC	breast
11	chr6:143004200-143006400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:143004400-143007400	Enhancers	Primary T cells from cord blood	blood
13	chr6:143005000-143008400	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr6:143005200-143014200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr6:143005800-143006600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:143005800-143007400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr6:143006000-143008000	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr6:143006000-143008000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
19	chr6:143006000-143008600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr6:143006000-143009000	Enhancers	Fetal Lung	lung
21	chr6:143006200-143007000	Weak transcription	Fetal Brain Female	brain
22	chr6:143006200-143008000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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