Variant report

Variant	rs35837037
Chromosome Location	chr2:46861300-46861301
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:46854125..46858531-chr2:46860398..46864023,5	K562	blood:
2	chr2:46845600..46848148-chr2:46860947..46862599,2	K562	blood:
3	chr2:46845764..46848148-chr2:46860387..46862849,3	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12105006	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13024534	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13406427	0.84[ASN][1000 genomes]
rs13417558	0.84[ASN][1000 genomes]
rs1378764	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs17767994	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17768018	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17768132	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17768138	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17768226	0.86[ASN][1000 genomes]
rs17819022	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1824050	0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2122715	0.95[ASN][1000 genomes]
rs34449783	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34748737	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34752561	0.90[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34996358	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35350086	0.86[AMR][1000 genomes]
rs35449212	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs35682608	0.87[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs35909669	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35949012	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4952837	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55742873	0.86[ASN][1000 genomes]
rs62136873	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62136894	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62136895	0.82[ASN][1000 genomes]
rs62136898	0.84[ASN][1000 genomes]
rs6746598	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7565274	0.95[ASN][1000 genomes]
rs7605089	0.84[ASN][1000 genomes]
rs896212	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757795	chr2:46532812-46874151	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2759046	chr2:46532812-46874151	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1014425	chr2:46670179-47033417	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv535678	chr2:46670179-47033417	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv873996	chr2:46670941-47065227	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS 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 target site	35 gene(s)	inside rSNPs	diseases
6	nsv1009735	chr2:46724523-46913152	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv533112	chr2:46800828-46959977	Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
8	nsv817517	chr2:46819371-47715140	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	152 gene(s)	inside rSNPs	diseases
9	nsv873997	chr2:46821640-46984627	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs35837037	ATP6V1E2	cis	Muscle Skeletal	GTEx
rs35837037	ATP6V1E2	cis	Heart Left Ventricle	GTEx
rs35837037	CRIPT	cis	Artery Tibial	GTEx
rs35837037	CRIPT	cis	multi-tissue	Pritchard
rs35837037	CRIPT	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46844800-46865600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:46844800-46868400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:46844800-46868400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr2:46844800-46868800	Weak transcription	Esophagus	oesophagus
5	chr2:46844800-46872200	Weak transcription	Pancreas	Pancrea
6	chr2:46845400-46864800	Weak transcription	Psoas Muscle	Psoas
7	chr2:46845400-46867000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr2:46845400-46871000	Weak transcription	Stomach Mucosa	stomach
9	chr2:46845400-46873000	Weak transcription	Right Ventricle	heart
10	chr2:46845600-46868200	Weak transcription	Aorta	Aorta
11	chr2:46845600-46868800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:46846000-46868600	Weak transcription	Fetal Intestine Small	intestine
13	chr2:46848600-46861800	Weak transcription	GM12878-XiMat	blood
14	chr2:46848600-46864800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:46848600-46867400	Weak transcription	Lung	lung
16	chr2:46848600-46871200	Weak transcription	HSMMtube	muscle
17	chr2:46848600-46872600	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr2:46848600-46872800	Weak transcription	Left Ventricle	heart
19	chr2:46848600-46872800	Weak transcription	Ovary	ovary
20	chr2:46848800-46868000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr2:46848800-46871000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr2:46848800-46872600	Weak transcription	Brain Cingulate Gyrus	brain
23	chr2:46848800-46873000	Weak transcription	Brain Angular Gyrus	brain
24	chr2:46849000-46861800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr2:46849000-46868600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr2:46849000-46868600	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr2:46849000-46877200	Weak transcription	Brain Substantia Nigra	brain
28	chr2:46849200-46861600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr2:46849200-46869400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr2:46849200-46869800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
31	chr2:46849200-46870800	Weak transcription	Hela-S3	cervix
32	chr2:46849200-46872600	Weak transcription	Colon Smooth Muscle	Colon
33	chr2:46849400-46872800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
34	chr2:46849800-46868200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr2:46850200-46868400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr2:46851000-46861600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
37	chr2:46851000-46861800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr2:46851600-46867600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
39	chr2:46852000-46861800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr2:46852000-46868200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:46852000-46872800	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr2:46852400-46869400	Weak transcription	Dnd41	blood
43	chr2:46853400-46865600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr2:46853400-46869600	Weak transcription	Brain Germinal Matrix	brain
45	chr2:46853400-46872600	Weak transcription	Brain Anterior Caudate	brain
46	chr2:46853400-46872800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr2:46853600-46862000	Weak transcription	HepG2	liver
48	chr2:46853600-46868600	Weak transcription	Fetal Intestine Large	intestine
49	chr2:46853600-46869400	Weak transcription	NH-A	brain
50	chr2:46853800-46861800	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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