Variant report

Variant	rs6926829
Chromosome Location	chr6:139970521-139970522
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17069144	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6941139	0.84[AFR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7776303	0.85[EUR][1000 genomes];1.00[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	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv516840	chr6:139960833-140053704	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:139957200-139976000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:139966200-139974200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:139966400-139974000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr6:139966800-139974200	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:139969200-139971000	Flanking Active TSS	K562	blood
6	chr6:139969200-139971800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:139969400-139970800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr6:139969400-139972000	Weak transcription	Adipose Nuclei	Adipose
9	chr6:139969600-139971000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:139970000-139974000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr6:139970000-139976000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:139970200-139970600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr6:139970200-139974600	Weak transcription	HUES64 Cell Line	embryonic stem cell

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

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