Variant report

Variant	rs192543167
Chromosome Location	chr6:44282390-44282391
allele	A/G
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:44279584..44282464-chr6:44309477..44312125,3	K562	blood:
2	chr6:44213575..44218708-chr6:44278177..44283526,11	K562	blood:
3	chr6:44281673..44282583-chr6:102995671..102996294,2	MCF-7	breast:
4	chr6:44272619..44273140-chr6:44281766..44282700,2	K562	blood:
5	chr6:44279978..44282464-chr6:44309513..44313447,3	K562	blood:
6	chr6:44213056..44218708-chr6:44277561..44284910,14	K562	blood:
7	chr6:44281326..44282860-chr6:44296235..44298156,2	K562	blood:
8	chr6:44223815..44226053-chr6:44279566..44282424,2	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv931987	chr6:43624625-44350167	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	201 gene(s)	inside rSNPs	diseases
2	nsv522456	chr6:44281716-44288847	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
3	nsv516456	chr6:44282316-44298309	Enhancers Bivalent Enhancer 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	chr6:44281200-44283200	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr6:44281200-44283200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr6:44281400-44283200	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr6:44281400-44283400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:44281600-44283600	Weak transcription	iPS-15b 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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