Variant report

Variant	rs491336
Chromosome Location	chr6:150402342-150402343
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:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:150400674..150403275-chr6:150407304..150409849,2	K562	blood:
2	chr6:150401711..150402469-chr6:150716292..150716821,2	K562	blood:
3	chr6:150401548..150402447-chr6:150655810..150657501,10	K562	blood:
4	chr6:150401151..150402465-chr6:150656027..150656922,6	MCF-7	breast:
5	chr6:150401196..150403539-chr6:150662242..150665059,2	K562	blood:
6	chr6:150401003..150402693-chr6:150655609..150656984,12	MCF-7	breast:
7	chr6:150400447..150403376-chr6:150651283..150654200,2	K562	blood:
8	chr6:150401082..150403253-chr6:150656281..150658165,2	MCF-7	breast:
9	chr6:150401453..150402381-chr6:150464218..150464794,3	MCF-7	breast:
10	chr6:150388542..150390431-chr6:150401978..150404443,2	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11754434	0.94[ASN][1000 genomes]
rs11754488	0.94[ASN][1000 genomes]
rs11755079	0.84[ASN][1000 genomes]
rs11756904	0.93[ASN][1000 genomes]
rs11756945	0.94[ASN][1000 genomes]
rs11759611	0.92[ASN][1000 genomes]
rs1194970	0.84[ASN][1000 genomes]
rs13201209	0.95[ASN][1000 genomes]
rs13216978	0.93[ASN][1000 genomes]
rs1748295	0.95[ASN][1000 genomes]
rs35742354	0.96[ASN][1000 genomes]
rs489664	0.94[ASN][1000 genomes]
rs682942	0.88[ASN][1000 genomes]
rs683002	0.82[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7738164	0.89[ASN][1000 genomes]
rs7753353	0.89[ASN][1000 genomes]
rs7765587	0.89[ASN][1000 genomes]
rs789819	0.94[ASN][1000 genomes]
rs789820	0.86[ASN][1000 genomes]
rs789821	0.86[ASN][1000 genomes]
rs789822	0.85[ASN][1000 genomes]
rs789823	0.85[ASN][1000 genomes]
rs789824	0.94[ASN][1000 genomes]
rs789825	0.94[ASN][1000 genomes]
rs789826	0.94[ASN][1000 genomes]
rs789827	0.94[ASN][1000 genomes]
rs789828	0.93[ASN][1000 genomes]
rs789829	0.94[ASN][1000 genomes]
rs806072	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	nsv517022	chr6:150145001-150426272	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv1026236	chr6:150360882-150408946	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv886770	chr6:150395424-150499889	Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Weak transcription Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150391200-150410000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:150400800-150408400	Weak transcription	NHEK	skin
3	chr6:150401000-150408200	Weak transcription	HMEC	breast
4	chr6:150401000-150408400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:150401000-150408400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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