Variant report

Variant	rs55674397
Chromosome Location	chr6:34300987-34300988
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:34299992..34302647-chr6:34315891..34318733,2	MCF-7	breast:
2	chr6:34285140..34288176-chr6:34300410..34302551,3	MCF-7	breast:
3	chr6:34300486..34302209-chr6:34305816..34308305,2	MCF-7	breast:
4	chr6:34299261..34302272-chr6:34303453..34305944,3	K562	blood:
5	chr6:34298245..34300492-chr6:34300638..34303123,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10484267	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484268	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1057691	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1060308	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10648	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1127084	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1265	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12654	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13466	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16883137	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16883475	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16883896	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16888452	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17628798	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17628946	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17629180	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17629270	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696774	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696829	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1994923	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs206922	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs3798554	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3798557	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41269032	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41269034	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41269036	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs41269038	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713771	0.87[EUR][1000 genomes]
rs55684754	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55694290	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55763242	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55779010	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55798596	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55812200	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55833185	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55863933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55864834	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56033036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56039915	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56107559	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56188036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56274913	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56309550	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56323997	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56330729	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59832183	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62399870	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6911272	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7738665	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7741127	0.80[AMR][1000 genomes]
rs7760373	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7770443	0.84[EUR][1000 genomes]
rs875274	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9368811	0.80[EUR][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	esv1798756	chr6:34203406-34319041	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	esv1798835	chr6:34204183-34319041	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv1792088	chr6:34204285-34318837	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	esv1793127	chr6:34204285-34319041	Weak transcription Flanking Active TSS Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
5	esv1794528	chr6:34267024-34308816	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs55674397	NUDT3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34261800-34330800	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr6:34262200-34301200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr6:34274400-34306400	Weak transcription	Brain Germinal Matrix	brain
4	chr6:34274400-34309000	Weak transcription	NHDF-Ad	bronchial
5	chr6:34284000-34301600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:34284000-34308200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:34284800-34310800	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr6:34285000-34305600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr6:34285200-34330600	Weak transcription	Thymus	Thymus
10	chr6:34285400-34305200	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr6:34285400-34305400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr6:34285400-34307800	Weak transcription	Liver	Liver
13	chr6:34285800-34308800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:34285800-34326600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr6:34286000-34308200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr6:34286600-34302800	Weak transcription	Osteobl	bone
17	chr6:34287000-34301200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:34287000-34305000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:34287400-34301600	Weak transcription	Spleen	Spleen
20	chr6:34287400-34304000	Weak transcription	Colonic Mucosa	Colon
21	chr6:34287600-34305400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr6:34287600-34305400	Weak transcription	Right Atrium	heart
23	chr6:34287600-34306400	Weak transcription	Fetal Lung	lung
24	chr6:34287600-34309200	Weak transcription	Pancreas	Pancrea
25	chr6:34289000-34325200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:34289400-34308200	Weak transcription	Fetal Intestine Large	intestine
27	chr6:34291400-34301800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr6:34291800-34307000	Weak transcription	Hela-S3	cervix
29	chr6:34292400-34305800	Weak transcription	HMEC	breast
30	chr6:34292600-34308200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr6:34292800-34302000	Weak transcription	HSMMtube	muscle
32	chr6:34293000-34301200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr6:34293000-34304600	Weak transcription	Colon Smooth Muscle	Colon
34	chr6:34293000-34305000	Weak transcription	Brain Cingulate Gyrus	brain
35	chr6:34293000-34305200	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr6:34293000-34305400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:34293000-34306400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr6:34293000-34308200	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr6:34293200-34301800	Weak transcription	NHEK	skin
40	chr6:34293400-34304600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr6:34293400-34305800	Weak transcription	Placenta	Placenta
42	chr6:34293400-34307600	Weak transcription	Fetal Thymus	thymus
43	chr6:34294000-34308800	Weak transcription	NH-A	brain
44	chr6:34294800-34305600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:34295000-34302800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr6:34295800-34301800	Weak transcription	Fetal Intestine Small	intestine
47	chr6:34296200-34301400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr6:34296200-34301600	Weak transcription	NHLF	lung
49	chr6:34296200-34305600	Weak transcription	Duodenum Mucosa	Duodenum
50	chr6:34296200-34309400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--

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