Variant report

Variant	rs13032876
Chromosome Location	chr2:86426132-86426133
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:86425990-86427055	PFSK-1	brain:	n/a	n/a
2	POLR2A	chr2:86426027-86427133	PANC-1	pancreas:	n/a	n/a
3	ZNF384	chr2:86425985-86426845	K562	blood:	n/a	n/a
4	GTF3C2	chr2:86426068-86426806	Hela-S3	cervix:	n/a	n/a
5	MYBL2	chr2:86426103-86427195	HepG2	liver:	n/a	n/a
6	ELF1	chr2:86425955-86426923	GM12878	blood:	n/a	chr2:86426517-86426528
7	NR2F2	chr2:86426089-86427257	K562	blood:	n/a	n/a
8	POLR2A	chr2:86425265-86427120	HepG2	liver:	n/a	n/a
9	TCF12	chr2:86426039-86427298	A549	lung:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:86424285..86426477-chr5:133860624..133863238,2	MCF-7	breast:
2	chr2:86420213..86424453-chr2:86424933..86430971,16	MCF-7	breast:
3	chr2:86331612..86333310-chr2:86425160..86426981,2	MCF-7	breast:

Variant related genes	Relation type
IMMT	TF binding region
MRPL35	TF binding region
ENSG00000132300	Chromatin interaction
ENSG00000043143	Chromatin interaction
ENSG00000068654	Chromatin interaction
ENSG00000132305	Chromatin interaction
ENSG00000273080	Chromatin interaction
ENSG00000265420	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10170676	0.95[ASN][1000 genomes]
rs10184462	0.93[ASN][1000 genomes]
rs10208602	0.92[ASN][1000 genomes]
rs10901	0.93[ASN][1000 genomes]
rs12714173	0.92[ASN][1000 genomes]
rs12714174	0.93[ASN][1000 genomes]
rs12714175	0.89[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs12714177	0.93[ASN][1000 genomes]
rs12994382	0.95[ASN][1000 genomes]
rs13001470	0.95[ASN][1000 genomes]
rs13027248	0.95[ASN][1000 genomes]
rs13035593	0.93[ASN][1000 genomes]
rs1540391	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs35615768	0.95[ASN][1000 genomes]
rs6547665	0.93[ASN][1000 genomes]
rs6740287	0.94[ASN][1000 genomes]
rs7560376	0.95[ASN][1000 genomes]
rs7563742	0.95[ASN][1000 genomes]
rs7590445	0.95[ASN][1000 genomes]
rs9789526	0.93[ASN][1000 genomes]
rs9808316	0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2751903	chr2:86253542-86505453	Active TSS Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv531380	chr2:86253552-86469217	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv1007474	chr2:86281967-86505453	Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv997563	chr2:86281967-86506132	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
5	nsv1008924	chr2:86282722-86499402	Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
6	nsv999956	chr2:86285944-86505453	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
7	nsv1012768	chr2:86285944-86506132	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv1003207	chr2:86286314-86496732	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1000441	chr2:86286314-86508168	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
10	nsv535808	chr2:86286314-86508168	Genic enhancers Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
11	nsv1004442	chr2:86286480-86506132	Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
12	nsv916616	chr2:86289130-86509326	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv458563	chr2:86292341-86507688	Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
14	nsv582370	chr2:86292341-86507688	Flanking Active TSS Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
15	nsv1009140	chr2:86294939-86506132	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
16	nsv582371	chr2:86296566-86507688	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv531381	chr2:86301091-86478346	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
18	nsv1001157	chr2:86301440-86508168	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
19	esv3412938	chr2:86370969-86867936	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
20	nsv458574	chr2:86385728-86507688	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
21	nsv582372	chr2:86385728-86507688	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs13032876	IMMT	cis	Whole Blood	GTEx
rs13032876	IMMT	cis	Artery Aorta	GTEx
rs13032876	MRPL35	Cis_1M	lymphoblastoid	RTeQTL
rs13032876	IMMT	Cis_1M	lymphoblastoid	RTeQTL
rs13032876	IMMT	cis	Esophagus Muscularis	GTEx

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86423200-86426200	Weak transcription	Ovary	ovary
2	chr2:86423400-86426200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:86423400-86426200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr2:86423400-86426200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:86423400-86426200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:86423400-86426200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:86423400-86426200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr2:86423400-86426200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:86423400-86426200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr2:86423400-86426200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr2:86423400-86426200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr2:86423400-86426200	Weak transcription	Aorta	Aorta
13	chr2:86423400-86426200	Weak transcription	Liver	Liver
14	chr2:86423400-86426200	Weak transcription	Brain Angular Gyrus	brain
15	chr2:86423400-86426200	Weak transcription	Brain Anterior Caudate	brain
16	chr2:86423400-86426200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr2:86423400-86426200	Weak transcription	Esophagus	oesophagus
18	chr2:86423400-86426200	Weak transcription	Fetal Kidney	kidney
19	chr2:86423400-86426200	Weak transcription	Pancreatic Islets	Pancreatic Islet
20	chr2:86423400-86426200	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr2:86423400-86426200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr2:86423400-86426200	Weak transcription	Small Intestine	intestine
23	chr2:86423400-86426200	Weak transcription	HUVEC	blood vessel
24	chr2:86423400-86426200	Weak transcription	NHLF	lung
25	chr2:86423400-86426400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr2:86423400-86426400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr2:86423400-86426400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr2:86423400-86426400	Weak transcription	Gastric	stomach
29	chr2:86423400-86426400	Weak transcription	Spleen	Spleen
30	chr2:86423400-86426400	Weak transcription	NHDF-Ad	bronchial
31	chr2:86423600-86426200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr2:86423600-86426200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr2:86423600-86426200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr2:86423600-86426200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr2:86423600-86426200	Weak transcription	Primary hematopoietic stem cells	blood
36	chr2:86423600-86426200	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr2:86423600-86426200	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr2:86423800-86426200	Weak transcription	HMEC	breast
39	chr2:86424000-86426200	Weak transcription	Osteobl	bone
40	chr2:86424200-86426200	Weak transcription	NHEK	skin
41	chr2:86424200-86426600	Weak transcription	Fetal Heart	heart
42	chr2:86424400-86426200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr2:86424400-86426200	Weak transcription	HSMMtube	muscle
44	chr2:86424600-86426200	Weak transcription	K562	blood
45	chr2:86425400-86426200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr2:86425600-86427200	Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr2:86425600-86427200	Active TSS	Skeletal Muscle Male	skeletal muscle
48	chr2:86425800-86426200	Enhancers	Primary B cells from cord blood	blood
49	chr2:86425800-86426200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr2:86425800-86426200	Enhancers	Primary T helper naive cells from peripheral blood	blood

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