Variant report

Variant	rs9469611
Chromosome Location	chr6:33802248-33802249
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs9461919	1.00[AFR][1000 genomes]
rs9461920	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv885773	chr6:33778964-33813043	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv885774	chr6:33778964-33840121	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv885775	chr6:33788055-33828178	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1032074	chr6:33795671-33835988	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1022403	chr6:33795671-33847345	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33797200-33805600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:33799800-33803800	Weak transcription	K562	blood
3	chr6:33801200-33802400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:33801400-33803000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr6:33801400-33803200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:33801400-33803200	Enhancers	Esophagus	oesophagus
7	chr6:33801400-33809400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr6:33801600-33802600	Enhancers	HMEC	breast
9	chr6:33801600-33803200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:33801600-33803200	Enhancers	NHEK	skin
11	chr6:33801600-33806000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr6:33801800-33802400	Enhancers	A549	lung
13	chr6:33801800-33802600	Enhancers	Gastric	stomach
14	chr6:33801800-33802800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:33801800-33803200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:33801800-33803200	Enhancers	Placenta	Placenta

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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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