Variant report

Variant	rs34783816
Chromosome Location	chr5:36099755-36099756
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT3A2-3	chr5:36098658-36102483	NONHSAT101022

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1113073	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12513526	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12522542	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12654974	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12655763	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12658867	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13156321	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13163292	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13177876	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13180445	0.93[AFR][1000 genomes]
rs13181789	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1353269	1.00[AFR][1000 genomes]
rs1393158	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1501817	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17343598	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1827369	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1827371	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2012367	1.00[AFR][1000 genomes]
rs267766	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34165875	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35746165	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs36064347	0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3898058	0.84[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs3913488	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4021314	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs40499	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4415106	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4869468	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4869614	0.81[AFR][1000 genomes]
rs766064	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7705825	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7705975	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7706216	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv32711	chr5:36047797-36146166	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv830262	chr5:36074311-36293872	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	63 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36090800-36107000	Weak transcription	HSMMtube	muscle
2	chr5:36092200-36106000	Weak transcription	Primary B cells from cord blood	blood
3	chr5:36092800-36116200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:36093600-36104000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr5:36093600-36107600	Weak transcription	Psoas Muscle	Psoas
6	chr5:36095600-36103000	Weak transcription	HSMM	muscle
7	chr5:36096600-36128600	Weak transcription	Fetal Brain Male	brain
8	chr5:36096800-36104000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr5:36097200-36104000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
10	chr5:36098200-36100000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr5:36098200-36104200	Weak transcription	Primary T cells from cord blood	blood
12	chr5:36098200-36106800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:36098400-36102000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr5:36098400-36103800	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr5:36098600-36102200	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr5:36098600-36103200	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr5:36098600-36104000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr5:36098600-36104000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr5:36098600-36104200	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr5:36098600-36106200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr5:36098600-36106800	Weak transcription	Left Ventricle	heart
22	chr5:36098600-36107400	Weak transcription	Right Ventricle	heart
23	chr5:36098600-36107800	Weak transcription	Cortex derived primary cultured neurospheres	brain
24	chr5:36098800-36104000	Weak transcription	Brain Angular Gyrus	brain
25	chr5:36098800-36113200	Weak transcription	Fetal Stomach	stomach
26	chr5:36099000-36102400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
27	chr5:36099000-36102600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr5:36099000-36104000	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr5:36099000-36104200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr5:36099000-36116800	Weak transcription	Fetal Intestine Small	intestine
31	chr5:36099200-36103800	Weak transcription	Liver	Liver
32	chr5:36099400-36102200	Weak transcription	Duodenum Smooth Muscle	Duodenum
33	chr5:36099600-36103000	Enhancers	iPS-15b Cell Line	embryonic stem cell

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