Variant report

Variant	rs73410446
Chromosome Location	chr6:2030999-2031000
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:1608425..1611671-chr6:2030333..2034108,4	MCF-7	breast:
2	chr6:2030064..2032046-chr6:2035936..2037834,2	K562	blood:

Variant related genes	Relation type
ENSG00000054598	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10484947	1.00[ASN][1000 genomes]
rs10484948	1.00[ASN][1000 genomes]
rs11242727	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11966735	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17134626	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17134684	1.00[ASN][1000 genomes]
rs2076854	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28736862	1.00[ASN][1000 genomes]
rs35781270	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56905405	1.00[ASN][1000 genomes]
rs57366578	1.00[ASN][1000 genomes]
rs58499654	1.00[ASN][1000 genomes]
rs59275343	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59609802	1.00[ASN][1000 genomes]
rs59936111	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59952501	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61109748	1.00[ASN][1000 genomes]
rs625781	1.00[ASN][1000 genomes]
rs6930064	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72494599	0.81[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410414	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410419	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410422	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410424	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410429	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410440	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73410461	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73412535	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73412542	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73412553	0.86[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73412554	1.00[EUR][1000 genomes]
rs73414521	1.00[ASN][1000 genomes]
rs73414524	1.00[ASN][1000 genomes]
rs73414527	1.00[ASN][1000 genomes]
rs73414530	1.00[ASN][1000 genomes]
rs73414544	1.00[ASN][1000 genomes]
rs73416657	1.00[ASN][1000 genomes]
rs73416659	1.00[ASN][1000 genomes]
rs73427457	1.00[ASN][1000 genomes]
rs73716941	1.00[ASN][1000 genomes]
rs73716945	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	nsv530548	chr6:1441421-2351608	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv931941	chr6:1768439-2246781	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv531295	chr6:1773436-2724986	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
4	nsv1032727	chr6:1900622-2064690	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv538095	chr6:1900622-2064690	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv883386	chr6:1910108-2122454	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv981098	chr6:2008599-2102267	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv527735	chr6:2028237-2097654	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:2006200-2034800	Weak transcription	HepG2	liver
2	chr6:2019800-2040000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:2022200-2031600	Weak transcription	Esophagus	oesophagus
4	chr6:2022400-2035000	Weak transcription	Gastric	stomach
5	chr6:2022400-2042800	Weak transcription	Right Atrium	heart
6	chr6:2022400-2055600	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr6:2022400-2080600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr6:2026600-2031600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:2026800-2031000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr6:2027000-2035000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:2028800-2032000	Enhancers	Fetal Thymus	thymus
12	chr6:2028800-2032600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:2029200-2031800	Weak transcription	Dnd41	blood
14	chr6:2029200-2032000	Enhancers	HUVEC	blood vessel
15	chr6:2029200-2032600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr6:2029200-2037000	Weak transcription	Primary T cells from cord blood	blood
17	chr6:2029600-2032000	Enhancers	Thymus	Thymus
18	chr6:2029800-2040400	Weak transcription	Stomach Mucosa	stomach
19	chr6:2030000-2053600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr6:2030200-2032000	Enhancers	H9 Cell Line	embryonic stem cell
21	chr6:2030200-2032000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr6:2030400-2032000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:2030400-2032000	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr6:2030400-2032000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:2030400-2035000	Weak transcription	Pancreas	Pancrea
26	chr6:2030600-2031600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr6:2030600-2031800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:2030600-2031800	Enhancers	Rectal Mucosa Donor 31	rectum
29	chr6:2030600-2031800	Enhancers	Osteobl	bone
30	chr6:2030600-2034800	Weak transcription	Fetal Kidney	kidney
31	chr6:2030800-2031200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr6:2030800-2031400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:2030800-2038400	Weak transcription	Primary hematopoietic stem cells	blood

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