Variant report

Variant	rs2762323
Chromosome Location	chr6:14946025-14946026
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs12173704	0.88[ASN][1000 genomes]
rs12176066	0.88[ASN][1000 genomes]
rs1555642	0.94[ASN][1000 genomes]
rs2045222	0.97[ASN][1000 genomes]
rs2045223	0.88[ASN][1000 genomes]
rs28520668	0.94[ASN][1000 genomes]
rs371601	0.90[ASN][1000 genomes]
rs409391	0.90[ASN][1000 genomes]
rs4285324	0.88[ASN][1000 genomes]
rs4299834	0.87[ASN][1000 genomes]
rs447977	0.85[ASN][1000 genomes]
rs4515392	0.88[ASN][1000 genomes]
rs4574648	0.87[ASN][1000 genomes]
rs4715937	0.88[ASN][1000 genomes]
rs4715938	0.88[ASN][1000 genomes]
rs6917587	0.88[ASN][1000 genomes]
rs6918362	0.88[ASN][1000 genomes]
rs6922975	0.85[ASN][1000 genomes]
rs6930788	0.88[ASN][1000 genomes]
rs6931541	0.88[ASN][1000 genomes]
rs6942359	0.88[ASN][1000 genomes]
rs7755150	0.97[ASN][1000 genomes]
rs9349961	0.84[ASN][1000 genomes]
rs9349962	0.88[ASN][1000 genomes]
rs9370783	0.88[ASN][1000 genomes]
rs9396537	0.88[ASN][1000 genomes]
rs9396538	0.88[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	nsv1031668	chr6:14774036-15044308	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv538138	chr6:14774036-15044308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv883453	chr6:14926320-15001506	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14933600-14954000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:14933600-14964800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:14933800-14969600	Weak transcription	Right Atrium	heart
4	chr6:14944400-14946400	Enhancers	Fetal Thymus	thymus
5	chr6:14944600-14947200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr6:14945000-14949200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:14945400-14948800	Weak transcription	K562	blood
8	chr6:14945800-14946200	Enhancers	Fetal Stomach	stomach
9	chr6:14946000-14946200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr6:14946000-14946400	Enhancers	NHDF-Ad	bronchial

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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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