Variant report

Variant	rs7832933
Chromosome Location	chr8:121490344-121490345
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	chr8:121489947..121491586-chr8:121494046..121495561,2	K562	blood:
2	chr8:121490309..121492059-chr8:121495586..121498161,2	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10098436	0.94[ASN][1000 genomes]
rs10109431	0.96[ASN][1000 genomes]
rs10955971	0.87[ASN][1000 genomes]
rs1129080	0.89[ASN][1000 genomes]
rs1129353	0.89[ASN][1000 genomes]
rs11780830	0.98[ASN][1000 genomes]
rs11781786	0.96[ASN][1000 genomes]
rs12545308	0.89[ASN][1000 genomes]
rs12546007	0.93[ASN][1000 genomes]
rs12674727	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12675235	0.94[ASN][1000 genomes]
rs12676755	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12678531	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12678788	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12680641	0.80[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs13252173	0.96[ASN][1000 genomes]
rs13263962	0.94[ASN][1000 genomes]
rs16893976	0.89[ASN][1000 genomes]
rs2429	0.89[ASN][1000 genomes]
rs4242313	0.90[ASN][1000 genomes]
rs4448321	0.91[ASN][1000 genomes]
rs4452825	0.94[ASN][1000 genomes]
rs4463470	0.89[ASN][1000 genomes]
rs4565499	0.98[ASN][1000 genomes]
rs4573322	0.91[ASN][1000 genomes]
rs4590476	0.89[ASN][1000 genomes]
rs4871067	0.98[ASN][1000 genomes]
rs61203971	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61424477	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6415474	0.98[ASN][1000 genomes]
rs6469920	0.87[ASN][1000 genomes]
rs6469921	0.87[ASN][1000 genomes]
rs6984090	0.96[ASN][1000 genomes]
rs6985660	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7002445	0.96[ASN][1000 genomes]
rs7015443	0.89[ASN][1000 genomes]
rs73315165	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73315171	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73315174	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73315182	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7812590	0.96[ASN][1000 genomes]
rs7814949	0.94[ASN][1000 genomes]
rs7818026	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7819405	0.89[ASN][1000 genomes]
rs7826906	0.98[ASN][1000 genomes]
rs7834496	0.87[ASN][1000 genomes]
rs7835198	0.89[ASN][1000 genomes]
rs7835363	0.89[ASN][1000 genomes]
rs9297619	0.98[ASN][1000 genomes]
rs9650081	0.91[ASN][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	nsv891420	chr8:121194900-121561369	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv891421	chr8:121292407-121653902	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
3	nsv1033386	chr8:121369943-121501239	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv470235	chr8:121437222-121526747	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv519152	chr8:121458457-121571266	Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:121458000-121510400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr8:121458200-121505200	Weak transcription	Placenta	Placenta
3	chr8:121458400-121501000	Weak transcription	Ovary	ovary
4	chr8:121458600-121504200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr8:121458600-121516400	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr8:121458800-121491000	Weak transcription	HMEC	breast
7	chr8:121458800-121504000	Weak transcription	Fetal Heart	heart
8	chr8:121458800-121510200	Weak transcription	Brain Germinal Matrix	brain
9	chr8:121458800-121510400	Weak transcription	NHLF	lung
10	chr8:121458800-121539000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr8:121459000-121528600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr8:121461000-121491000	Weak transcription	Primary hematopoietic stem cells	blood
13	chr8:121468600-121501800	Weak transcription	HUVEC	blood vessel
14	chr8:121469200-121515200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr8:121470000-121502400	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr8:121470400-121491000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr8:121470600-121490400	Weak transcription	Liver	Liver
18	chr8:121474600-121553600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
19	chr8:121477800-121503800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr8:121480000-121501000	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr8:121481200-121491000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:121481800-121501600	Weak transcription	Fetal Stomach	stomach
23	chr8:121482600-121503800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr8:121483400-121501600	Weak transcription	Primary B cells from cord blood	blood
25	chr8:121484400-121541800	Weak transcription	Left Ventricle	heart
26	chr8:121486000-121490800	Weak transcription	A549	lung
27	chr8:121486000-121500400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
28	chr8:121486400-121499800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr8:121486800-121501000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr8:121487400-121500400	Weak transcription	Dnd41	blood
31	chr8:121487400-121500800	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr8:121487600-121512200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:121488400-121539200	Weak transcription	HSMM	muscle
34	chr8:121489200-121500000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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