Variant report

Variant	rs11211139
Chromosome Location	chr1:46015751-46015752
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:46015672-46015815	GM12878	blood:	n/a	n/a
2	POLR2A	chr1:46015687-46017328	HepG2	liver:	n/a	n/a
3	POLR2A	chr1:46015701-46017433	GM12891	blood:	n/a	n/a

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:46014904..46019071-chr1:46034504..46037164,4	K562	blood:
2	chr1:46012797..46020877-chr1:46047985..46055272,23	K562	blood:
3	chr1:45985569..45992282-chr1:46014173..46025125,38	MCF-7	breast:
4	chr1:45195042..45198446-chr1:46014587..46018125,4	K562	blood:
5	chr1:46014878..46016600-chr1:46048610..46051417,2	MCF-7	breast:
6	chr1:46015193..46018509-chr1:46048657..46051369,3	MCF-7	breast:
7	chr1:45982342..45989534-chr1:46006947..46020678,57	K562	blood:
8	chr1:45974939..45977846-chr1:46015282..46017928,2	MCF-7	breast:
9	chr1:45184676..45187669-chr1:46014660..46016558,3	K562	blood:
10	chr1:45985342..45989391-chr1:46011113..46019467,18	MCF-7	breast:
11	chr1:45976870..45989534-chr1:46007918..46019226,54	K562	blood:
12	chr1:46012228..46018632-chr1:46046407..46053601,17	K562	blood:
13	chr1:45271619..45273419-chr1:46014827..46017277,2	K562	blood:
14	chr1:46014904..46020261-chr1:46034308..46041374,10	K562	blood:
15	chr1:45196137..45198081-chr1:46014587..46016947,2	K562	blood:
16	chr1:45964150..45967582-chr1:46014583..46018871,5	K562	blood:

No data

Variant related genes	Relation type
AKR1A1	TF binding region
ENSG00000199377	Chromatin interaction
ENSG00000117448	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000132780	Chromatin interaction
ENSG00000188396	Chromatin interaction
ENSG00000117450	Chromatin interaction
ENSG00000236624	Chromatin interaction
ENSG00000132763	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11211128	0.81[AMR][1000 genomes]
rs11211137	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12049503	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12077621	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2883968	0.80[EUR][1000 genomes]
rs34673142	0.83[EUR][1000 genomes]
rs34768551	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3790585	0.84[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs4633317	0.83[EUR][1000 genomes]
rs5015340	0.83[EUR][1000 genomes]
rs61788356	0.80[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs666720	0.84[ASN][1000 genomes]
rs713358	0.83[EUR][1000 genomes]
rs868351	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9727262	0.84[AMR][1000 genomes];0.83[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	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
2	nsv530016	chr1:45868543-46069020	Flanking Active TSS Genic enhancers Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
3	nsv829726	chr1:45897581-46103186	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
4	nsv529631	chr1:45905936-46335246	Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	207 gene(s)	inside rSNPs	diseases
5	nsv932680	chr1:45935520-46686477	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases
6	nsv868828	chr1:45953923-46686477	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	232 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs11211139	PRDX1	cis	Thyroid	GTEx
rs11211139	TESK2	cis	Whole Blood	GTEx
rs11211139	MMACHC	cis	multi-tissue	Pritchard
rs11211139	C2orf49	trans	lymphoblastoid	RTeQTL
rs11211139	MUTYH	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46000800-46016000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:46009600-46016000	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr1:46010000-46015800	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr1:46010000-46016000	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr1:46010000-46016000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:46010000-46016000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr1:46010000-46016000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr1:46010000-46016000	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr1:46010000-46016000	Weak transcription	Pancreas	Pancrea
10	chr1:46010000-46016000	Weak transcription	Thymus	Thymus
11	chr1:46010000-46016000	Weak transcription	NHLF	lung
12	chr1:46010000-46016000	Weak transcription	Osteobl	bone
13	chr1:46010200-46016000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr1:46010200-46016000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:46010200-46016000	Weak transcription	Fetal Kidney	kidney
16	chr1:46010200-46016200	Weak transcription	Small Intestine	intestine
17	chr1:46010400-46016000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr1:46010400-46016000	Weak transcription	Lung	lung
19	chr1:46010800-46016000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr1:46010800-46016000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr1:46010800-46016000	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr1:46011000-46016000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr1:46011000-46016000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr1:46011000-46016200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr1:46011200-46016000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr1:46011200-46016000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr1:46011200-46016000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:46011400-46015800	Weak transcription	Primary T cells fromperipheralblood	blood
29	chr1:46011400-46015800	Weak transcription	Adipose Nuclei	Adipose
30	chr1:46011400-46016000	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr1:46011400-46016000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:46011400-46016000	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr1:46011400-46016000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr1:46011600-46015800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:46011600-46015800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr1:46011600-46015800	Weak transcription	Placenta	Placenta
37	chr1:46011600-46016000	Weak transcription	Primary T helper cells fromperipheralblood	blood
38	chr1:46011600-46016000	Weak transcription	HUVEC	blood vessel
39	chr1:46011800-46015800	Weak transcription	Stomach Mucosa	stomach
40	chr1:46012000-46015800	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr1:46012000-46015800	Weak transcription	HepG2	liver
42	chr1:46012000-46016000	Weak transcription	Fetal Intestine Large	intestine
43	chr1:46012200-46015800	Weak transcription	Primary B cells from peripheral blood	blood
44	chr1:46012200-46015800	Weak transcription	Fetal Intestine Small	intestine
45	chr1:46012200-46015800	Weak transcription	Fetal Thymus	thymus
46	chr1:46012200-46016000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr1:46012200-46016000	Weak transcription	Liver	Liver
48	chr1:46012200-46016000	Weak transcription	GM12878-XiMat	blood
49	chr1:46013600-46015800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr1:46014000-46016200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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