Variant report

Variant	rs884216
Chromosome Location	chr2:36743696-36743697
allele	A/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	STAT3	chr2:36743662-36743893	MCF10A-Er-Src	breast:	n/a	chr2:36743858-36743865
2	POLR2A	chr2:36742645-36744973	HUVEC	blood vessel:	n/a	n/a
3	POLR2A	chr2:36743654-36743702	ProgFib	skin:	n/a	n/a
4	POLR2A	chr2:36741393-36744578	HUVEC	blood vessel:	n/a	n/a
5	POLR2A	chr2:36742644-36743716	HUVEC	blood vessel:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:36743424..36745842-chr2:36763620..36766499,2	K562	blood:
2	chr2:36742000..36743740-chr2:36761834..36763560,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000273090	TF binding region

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10490671	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2023408	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2888369	0.83[CHB][hapmap]
rs3770827	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3770834	0.88[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3770841	0.89[CHB][hapmap]
rs3821155	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs66484476	0.80[ASN][1000 genomes]
rs711247	1.00[CEU][hapmap];0.85[EUR][1000 genomes]
rs848519	0.94[CHB][hapmap];0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs848520	0.93[CEU][hapmap]
rs848521	0.93[CEU][hapmap]
rs848524	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs848526	0.87[CEU][hapmap]
rs848539	0.84[CHB][hapmap]
rs848543	0.84[CHB][hapmap]
rs848563	0.84[EUR][1000 genomes]
rs867701	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833803	chr2:36589065-36745779	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1010985	chr2:36707157-36942066	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv535642	chr2:36707157-36942066	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:36713800-36789600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr2:36717400-36744400	Weak transcription	Brain Angular Gyrus	brain
3	chr2:36720000-36760600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr2:36721800-36746000	Strong transcription	HUVEC	blood vessel
5	chr2:36722600-36752400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr2:36725200-36756800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:36726800-36751800	Strong transcription	Skeletal Muscle Female	skeletal muscle
8	chr2:36727400-36757200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr2:36728400-36749200	Weak transcription	Fetal Brain Male	brain
10	chr2:36729600-36790200	Weak transcription	Small Intestine	intestine
11	chr2:36733000-36752000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr2:36733200-36774200	Weak transcription	Fetal Thymus	thymus
13	chr2:36733400-36764400	Weak transcription	Pancreas	Pancrea
14	chr2:36733600-36748800	Weak transcription	Stomach Mucosa	stomach
15	chr2:36733600-36750200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr2:36734600-36756800	Strong transcription	HepG2	liver
17	chr2:36735400-36744200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr2:36735600-36754200	Strong transcription	Hela-S3	cervix
19	chr2:36735800-36751000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr2:36735800-36752600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:36736000-36745000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr2:36736000-36755800	Strong transcription	HUES64 Cell Line	embryonic stem cell
23	chr2:36736400-36751400	Strong transcription	Left Ventricle	heart
24	chr2:36736800-36751400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr2:36737200-36745200	Strong transcription	Fetal Stomach	stomach
26	chr2:36737800-36748600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr2:36737800-36750600	Strong transcription	A549	lung
28	chr2:36738000-36744600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr2:36738000-36745000	Genic enhancers	Placenta	Placenta
30	chr2:36738000-36747200	Weak transcription	Thymus	Thymus
31	chr2:36738200-36745000	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr2:36738200-36745200	Strong transcription	Skeletal Muscle Male	skeletal muscle
33	chr2:36738200-36754000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr2:36738400-36745200	Strong transcription	Aorta	Aorta
35	chr2:36738400-36751600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr2:36738400-36751600	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr2:36738600-36754200	Strong transcription	HUES6 Cell Line	embryonic stem cell
38	chr2:36738800-36745000	Strong transcription	Lung	lung
39	chr2:36738800-36748200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr2:36738800-36754000	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr2:36739000-36745000	Strong transcription	H9 Cell Line	embryonic stem cell
42	chr2:36739000-36745200	Strong transcription	Ovary	ovary
43	chr2:36739000-36751200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr2:36739000-36778200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr2:36739200-36745000	Strong transcription	Fetal Brain Female	brain
46	chr2:36739200-36745000	Strong transcription	Fetal Lung	lung
47	chr2:36739200-36745200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr2:36739200-36748000	Strong transcription	Colon Smooth Muscle	Colon
49	chr2:36739200-36749200	Strong transcription	Primary B cells from cord blood	blood
50	chr2:36739200-36751200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood

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