Variant report

Variant	rs41269032
Chromosome Location	chr6:34251905-34251906
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Distal block	Cell Line	Cell type
1	chr6:34251031..34253241-chr6:34259138..34261085,2	MCF-7	breast:
2	chr6:34216498..34218663-chr6:34250285..34252688,2	K562	blood:
3	chr6:34249917..34252313-chr6:34359035..34361576,2	MCF-7	breast:
4	chr6:34243359..34245671-chr6:34250933..34253670,2	MCF-7	breast:
5	chr6:34203148..34206017-chr6:34251263..34253790,3	K562	blood:
6	chr6:34250015..34252529-chr6:34278374..34280844,2	K562	blood:
7	chr6:34251466..34254255-chr6:34254972..34256784,2	MCF-7	breast:
8	chr6:34251313..34254635-chr6:34272399..34275413,3	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGA1-2	chr6:34247482-34252266	ENSG00000225339
2	lnc-HMGA1-2	chr6:34251650-34254539	NONHSAT112120
3	lnc-HMGA1-2	chr6:34251650-34252045	ENSG00000225339.2
4	lnc-HMGA1-2	chr6:34246917-34254539	NONHSAT112121
5	lnc-HMGA1-2	chr6:34247456-34254545	ENSG00000225339.2
6	lnc-HMGA1-2	chr6:34251650-34252231	ENSG00000225339.2

No data

Variant related genes	Relation type
ENSG00000272325	Chromatin interaction
ENSG00000137309	Chromatin interaction
ENSG00000186577	Chromatin interaction

Extended variants
information (count: 62 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10484267	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10484268	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1057691	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1060308	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10648	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1127084	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1265	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12654	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13466	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16883137	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16883475	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16883896	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs16888452	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17628798	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17628946	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17629180	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17629270	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696583	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696774	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17696829	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1994923	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs206922	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs3798554	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3798557	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs41269034	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41269036	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs41269038	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713771	0.88[EUR][1000 genomes]
rs4713782	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs55674397	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55684754	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55694290	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55763242	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55779010	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55798596	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55812200	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55833185	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55863933	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs55864834	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56033036	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56039915	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56107559	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56188036	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56274913	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56309550	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56323997	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs56330729	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs59832183	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs62399870	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6457775	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6911272	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7738665	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7760373	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7770443	0.83[EUR][1000 genomes]
rs875274	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9368811	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv462903	chr6:34110257-34263743	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv602863	chr6:34110257-34263743	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs41269032	NUDT3	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34218200-34255000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:34238400-34259400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:34240200-34255200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:34240400-34255000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr6:34240400-34259800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr6:34240400-34259800	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr6:34240600-34269200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr6:34240800-34261000	Weak transcription	Fetal Kidney	kidney
9	chr6:34241400-34260000	Weak transcription	Esophagus	oesophagus
10	chr6:34241600-34252800	Weak transcription	Stomach Mucosa	stomach
11	chr6:34242000-34252800	Weak transcription	Colon Smooth Muscle	Colon
12	chr6:34243600-34252600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr6:34243600-34257200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:34244200-34260000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:34244400-34256600	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr6:34244400-34273400	Weak transcription	Rectal Smooth Muscle	rectum
17	chr6:34245000-34259800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr6:34245000-34260000	Weak transcription	NH-A	brain
19	chr6:34245000-34262600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:34245000-34263400	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr6:34245200-34252200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr6:34245200-34255000	Weak transcription	Ovary	ovary
23	chr6:34245200-34259600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr6:34245200-34260800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr6:34245400-34253000	Strong transcription	Fetal Stomach	stomach
26	chr6:34245400-34260800	Weak transcription	Aorta	Aorta
27	chr6:34245600-34255200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr6:34245600-34257400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:34245600-34261600	Weak transcription	Gastric	stomach
30	chr6:34245800-34254800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr6:34245800-34255000	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr6:34245800-34260000	Weak transcription	HSMMtube	muscle
33	chr6:34246000-34253800	Strong transcription	Fetal Muscle Trunk	muscle
34	chr6:34246000-34264400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr6:34246200-34252000	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr6:34246600-34252600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:34246600-34256800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
38	chr6:34246600-34264000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:34246600-34264000	Strong transcription	Dnd41	blood
40	chr6:34247200-34259600	Weak transcription	Fetal Heart	heart
41	chr6:34247400-34256400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr6:34247400-34259800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr6:34247800-34252000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr6:34247800-34260600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr6:34248000-34252600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:34248000-34252600	Weak transcription	Brain Germinal Matrix	brain
47	chr6:34248200-34256400	Weak transcription	Hela-S3	cervix
48	chr6:34248400-34252400	Weak transcription	Fetal Brain Female	brain
49	chr6:34248400-34255000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr6:34248600-34255000	Weak transcription	Stomach Smooth Muscle	stomach

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