Variant report

Variant	rs9468033
Chromosome Location	chr6:27266490-27266491
allele	A/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

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:27264794..27266821-chr6:27355400..27358259,2	K562	blood:
2	chr6:27265877..27267509-chr6:27513280..27515497,2	K562	blood:
3	chr6:27266213..27267894-chr6:27269235..27271066,2	K562	blood:
4	chr6:27113560..27116380-chr6:27265078..27267189,2	K562	blood:
5	chr6:27172666..27175265-chr6:27265465..27267285,2	K562	blood:
6	chr6:27264602..27266621-chr6:27277586..27279716,2	MCF-7	breast:
7	chr6:27112367..27116319-chr6:27264620..27267784,3	K562	blood:
8	chr6:27155262..27157566-chr6:27266020..27269001,2	K562	blood:
9	chr6:27197041..27202373-chr6:27261458..27267425,7	K562	blood:
10	chr6:27260999..27263500-chr6:27265988..27267831,3	K562	blood:
11	chr6:27263999..27267440-chr6:27299677..27302604,5	K562	blood:
12	chr6:27264150..27266831-chr6:27300629..27302449,2	K562	blood:
13	chr6:27097573..27099800-chr6:27264464..27267307,2	K562	blood:

No data

No data

No data

Variant related genes	Relation type
ENSG00000184825	Chromatin interaction
ENSG00000158553	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000124613	Chromatin interaction
ENSG00000265565	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13218537	1.00[ASN][1000 genomes]
rs28360634	1.00[ASN][1000 genomes]
rs34332556	1.00[ASN][1000 genomes]
rs34953377	1.00[ASN][1000 genomes]
rs35120058	1.00[ASN][1000 genomes]
rs35984974	1.00[ASN][1000 genomes]
rs56401801	1.00[ASN][1000 genomes]
rs66841633	1.00[ASN][1000 genomes]
rs71537559	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	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases
2	nsv1017328	chr6:27177147-27369588	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
3	nsv883505	chr6:27210614-27300580	Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 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	chr6:27261000-27266800	Active TSS	A549	lung
2	chr6:27266400-27266600	Active TSS	K562	blood
3	chr6:27266400-27268800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:27266400-27268800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:27266400-27269400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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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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