Variant report

Variant	rs11070748
Chromosome Location	chr15:50380347-50380348
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11070745	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11070747	0.88[ASN][1000 genomes]
rs11857230	0.98[ASN][1000 genomes]
rs12148444	0.88[ASN][1000 genomes]
rs12441604	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12442280	0.97[ASN][1000 genomes]
rs12902530	0.84[ASN][1000 genomes]
rs2414016	0.98[ASN][1000 genomes]
rs28369108	0.84[ASN][1000 genomes]
rs41362650	0.84[ASN][1000 genomes]
rs4775849	0.88[ASN][1000 genomes]
rs4775851	0.98[ASN][1000 genomes]
rs4775852	0.98[ASN][1000 genomes]
rs6493402	0.94[ASN][1000 genomes]
rs7177318	0.88[ASN][1000 genomes]
rs7178944	0.98[ASN][1000 genomes]
rs7179392	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8040030	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8040357	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044277	chr15:49921547-50702386	Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
2	nsv542380	chr15:49921547-50702386	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
3	nsv1035983	chr15:50223334-50595170	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv542382	chr15:50223334-50595170	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv569395	chr15:50345393-50437494	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv3406350	chr15:50377385-50380658	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3321974	chr15:50378285-50380833	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50367200-50380600	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr15:50367400-50381600	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr15:50368000-50380800	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr15:50376800-50386200	Weak transcription	Primary hematopoietic stem cells	blood
5	chr15:50377400-50380400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr15:50378000-50380400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr15:50378000-50380400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr15:50379800-50381200	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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