Variant report

Variant	rs6463470
Chromosome Location	chr7:48179227-48179228
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:48179050..48179761-chr7:48194036..48194625,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10081256	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10215134	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10224302	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10224538	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10227666	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10227773	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10227781	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10244950	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10253481	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10257019	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10282492	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10951948	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10951950	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11771288	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12540937	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6415281	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6463468	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6963458	0.81[AFR][1000 genomes]
rs7384280	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7457043	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7457060	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7802128	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9639996	0.81[EUR][1000 genomes]
rs9791970	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[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	nsv1026223	chr7:47560728-48243287	Genic enhancers Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv532120	chr7:47882757-48195869	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv470221	chr7:47917495-48354363	Strong transcription Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv464442	chr7:47917495-48354820	Genic enhancers Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv606893	chr7:47917495-48354820	Flanking Active TSS Strong transcription Genic enhancers Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv1027414	chr7:48117684-48438543	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1033738	chr7:48143988-48349357	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:48171000-48179800	Weak transcription	NH-A	brain
2	chr7:48174400-48186600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr7:48175200-48179800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr7:48178400-48179400	Enhancers	Liver	Liver
5	chr7:48178400-48179800	Flanking Active TSS	HepG2	liver
6	chr7:48178400-48181000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr7:48178600-48179400	Enhancers	A549	lung
8	chr7:48178600-48179600	Enhancers	Duodenum Mucosa	Duodenum
9	chr7:48178600-48180600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:48178600-48181400	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:48178800-48179800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:48178800-48180000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr7:48178800-48180000	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr7:48178800-48181200	Enhancers	Small Intestine	intestine
15	chr7:48179000-48179800	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr7:48179000-48180400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr7:48179200-48179600	Enhancers	Hela-S3	cervix
18	chr7:48179200-48179800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:48179200-48179800	Enhancers	Adipose Nuclei	Adipose
20	chr7:48179200-48180000	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr7:48179200-48180000	Enhancers	Skeletal Muscle Female	skeletal muscle
22	chr7:48179200-48180400	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr7:48179200-48180400	Enhancers	Primary hematopoietic stem cells	blood
24	chr7:48179200-48180600	Enhancers	Pancreas	Pancrea
25	chr7:48179200-48181000	Enhancers	Fetal Stomach	stomach
26	chr7:48179200-48181200	Enhancers	Colonic Mucosa	Colon
27	chr7:48179200-48181400	Enhancers	Sigmoid Colon	Sigmoid Colon
28	chr7:48179200-48184600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr7:48179200-48184600	Enhancers	Stomach Mucosa	stomach

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