Variant report

Variant	rs73700626
Chromosome Location	chr8:110533428-110533429
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2)
CpG islands
(count:0)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MEF2A	chr8:110533142-110533508	K562	blood:	n/a	n/a
2	SPI1	chr8:110533372-110534218	GM12878	blood:	n/a	n/a

No data

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:110532017..110535509-chr8:110550359..110553902,4	K562	blood:
2	chr8:110531754..110534652-chr8:110551713..110553240,2	MCF-7	breast:
3	chr8:110528262..110531056-chr8:110532730..110534557,2	MCF-7	breast:
4	chr8:110525756..110528832-chr8:110532009..110534427,3	K562	blood:
5	chr8:110532422..110535509-chr8:110550359..110553902,3	K562	blood:
6	chr8:110530935..110534382-chr8:110534655..110537155,3	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs55680107	1.00[AFR][1000 genomes]
rs56266884	1.00[AFR][1000 genomes]
rs59905170	1.00[AFR][1000 genomes]
rs73700632	1.00[AFR][1000 genomes]
rs73700648	1.00[AFR][1000 genomes]
rs73700949	1.00[AFR][1000 genomes]
rs73704029	1.00[AFR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891281	chr8:110450092-110558622	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	15 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	chr8:110531000-110535000	Enhancers	Primary B cells from peripheral blood	blood
2	chr8:110531600-110534200	Enhancers	GM12878-XiMat	blood
3	chr8:110532400-110533800	Enhancers	K562	blood
4	chr8:110533200-110534400	Enhancers	Primary B cells from cord blood	blood

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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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