Variant report

Variant	rs1204184
Chromosome Location	chr6:13853685-13853686
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:13852875..13854622-chr6:13856529..13860893,3	K562	blood:
2	chr6:13852220..13855025-chr6:13864513..13866779,2	MCF-7	breast:
3	chr6:13837585..13839319-chr6:13852270..13854306,2	K562	blood:
4	chr6:13852047..13854247-chr6:13855833..13857845,2	K562	blood:
5	chr6:13852875..13856749-chr6:13858134..13861261,5	K562	blood:

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1078046	0.95[ASN][1000 genomes]
rs10949002	0.95[ASN][1000 genomes]
rs1107758	0.95[ASN][1000 genomes]
rs1107759	0.94[ASN][1000 genomes]
rs1204191	0.94[ASN][1000 genomes]
rs1204195	0.94[ASN][1000 genomes]
rs1204197	0.94[ASN][1000 genomes]
rs1204202	0.94[ASN][1000 genomes]
rs1204205	0.92[ASN][1000 genomes]
rs1204207	0.91[ASN][1000 genomes]
rs1204208	0.91[ASN][1000 genomes]
rs1204209	0.92[ASN][1000 genomes]
rs1204210	0.88[ASN][1000 genomes]
rs1204214	0.93[ASN][1000 genomes]
rs1204217	0.91[ASN][1000 genomes]
rs1204219	0.85[ASN][1000 genomes]
rs1204224	0.85[ASN][1000 genomes]
rs1204229	0.83[ASN][1000 genomes]
rs1204232	0.83[ASN][1000 genomes]
rs1204234	0.83[ASN][1000 genomes]
rs1204235	0.83[ASN][1000 genomes]
rs1204237	0.82[ASN][1000 genomes]
rs1204240	0.81[ASN][1000 genomes]
rs1204241	0.80[ASN][1000 genomes]
rs12192978	0.81[ASN][1000 genomes]
rs12200710	0.84[EUR][1000 genomes]
rs12205612	0.96[ASN][1000 genomes]
rs12214124	0.94[ASN][1000 genomes]
rs12662217	0.94[ASN][1000 genomes]
rs12662221	0.86[ASN][1000 genomes]
rs12662533	0.95[ASN][1000 genomes]
rs12662534	0.94[ASN][1000 genomes]
rs12662535	0.94[ASN][1000 genomes]
rs1309311	0.94[ASN][1000 genomes]
rs13216137	0.95[ASN][1000 genomes]
rs13216246	0.96[ASN][1000 genomes]
rs1535811	0.95[ASN][1000 genomes]
rs1535812	0.95[ASN][1000 genomes]
rs1570623	0.83[ASN][1000 genomes]
rs1807919	0.92[ASN][1000 genomes]
rs1924461	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2014484	0.92[ASN][1000 genomes]
rs28594083	0.95[ASN][1000 genomes]
rs28619173	0.95[ASN][1000 genomes]
rs28716055	0.94[ASN][1000 genomes]
rs2876328	0.95[ASN][1000 genomes]
rs34901968	0.91[ASN][1000 genomes]
rs34957554	0.93[ASN][1000 genomes]
rs35198802	0.91[ASN][1000 genomes]
rs35904457	0.95[ASN][1000 genomes]
rs55742155	0.85[ASN][1000 genomes]
rs56759353	0.80[ASN][1000 genomes]
rs6899735	0.86[EUR][1000 genomes]
rs6903075	0.86[EUR][1000 genomes]
rs6904311	0.87[EUR][1000 genomes]
rs6906019	0.95[ASN][1000 genomes]
rs6919520	0.95[ASN][1000 genomes]
rs6919523	0.95[ASN][1000 genomes]
rs6924753	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6927092	0.95[ASN][1000 genomes]
rs72833105	0.94[ASN][1000 genomes]
rs72833108	0.91[ASN][1000 genomes]
rs72833112	0.93[ASN][1000 genomes]
rs72833113	0.93[ASN][1000 genomes]
rs72833115	0.92[ASN][1000 genomes]
rs72833116	0.92[ASN][1000 genomes]
rs72833124	0.83[ASN][1000 genomes]
rs7753981	0.91[ASN][1000 genomes]
rs7755582	0.95[ASN][1000 genomes]
rs7758088	0.91[ASN][1000 genomes]
rs7770830	0.83[ASN][1000 genomes]
rs7771874	0.83[ASN][1000 genomes]
rs7772023	0.83[ASN][1000 genomes]
rs7772769	0.95[ASN][1000 genomes]
rs9357909	0.82[EUR][1000 genomes]
rs9357919	0.95[ASN][1000 genomes]
rs9357920	0.95[ASN][1000 genomes]
rs9357925	0.85[ASN][1000 genomes]
rs9367682	0.84[EUR][1000 genomes]
rs9367691	0.86[ASN][1000 genomes]
rs9367692	0.84[ASN][1000 genomes]
rs9367696	0.83[ASN][1000 genomes]
rs9367697	0.83[ASN][1000 genomes]
rs9370526	0.83[EUR][1000 genomes]
rs9370532	0.94[ASN][1000 genomes]
rs9370537	0.92[ASN][1000 genomes]
rs9370546	0.81[ASN][1000 genomes]
rs9382632	0.94[ASN][1000 genomes]
rs9382633	0.95[ASN][1000 genomes]
rs9382634	0.91[ASN][1000 genomes]
rs9382641	0.95[ASN][1000 genomes]
rs9382651	0.85[ASN][1000 genomes]
rs9382660	0.83[ASN][1000 genomes]
rs9382661	0.83[ASN][1000 genomes]
rs9396212	0.95[ASN][1000 genomes]
rs9396227	0.84[ASN][1000 genomes]
rs9464395	0.85[ASN][1000 genomes]
rs9464398	0.81[ASN][1000 genomes]
rs9475703	0.93[ASN][1000 genomes]
rs9475705	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3475107	chr6:13834840-13863839	Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	esv3475109	chr6:13835023-13863759	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13847800-13864000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:13849400-13860000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:13852000-13854000	Weak transcription	Fetal Intestine Small	intestine
4	chr6:13853400-13854400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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