Variant report

Variant	rs3770087
Chromosome Location	chr2:86267068-86267069
allele	A/G
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	chr2:86266947-86267290	K562	blood:	n/a	n/a
2	POLR2A	chr2:86267029-86267684	K562	blood:	n/a	n/a
3	POLR2A	chr2:86267003-86267189	H1-hESC	embryonic stem cell:	n/a	n/a
4	POLR2A	chr2:86266757-86267133	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr2:86265726-86267954	K562	blood:	n/a	n/a
6	POLR2A	chr2:86266988-86267074	HepG2	liver:	n/a	n/a
7	POLR2A	chr2:86266326-86267980	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:86263075..86266284-chr2:86266783..86270779,4	MCF-7	breast:

Variant related genes	Relation type
POLR1A	TF binding region
ENSG00000068654	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10165327	0.82[ASN][1000 genomes]
rs10168635	0.82[ASN][1000 genomes]
rs10174095	0.87[ASN][1000 genomes]
rs10179090	0.82[ASN][1000 genomes]
rs1019591	1.00[CEU][hapmap];0.94[ASN][1000 genomes]
rs1036554	0.96[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10427394	0.82[ASN][1000 genomes]
rs11899576	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12612513	0.94[ASN][1000 genomes]
rs12614260	0.94[ASN][1000 genomes]
rs12620810	1.00[CEU][hapmap];0.82[ASN][1000 genomes]
rs12621992	1.00[CEU][hapmap]
rs12622009	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12622715	1.00[CEU][hapmap]
rs12624126	1.00[CEU][hapmap]
rs13384563	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13390702	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1561328	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17026701	1.00[CEU][hapmap]
rs17026729	1.00[CEU][hapmap]
rs17026854	0.96[ASN][1000 genomes]
rs17027011	0.82[ASN][1000 genomes]
rs17584578	1.00[CEU][hapmap];0.94[ASN][1000 genomes]
rs17618001	1.00[CEU][hapmap];0.94[ASN][1000 genomes]
rs2012798	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2118521	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2164879	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2241435	1.00[CEU][hapmap]
rs2241437	1.00[CEU][hapmap];0.89[ASN][1000 genomes]
rs2278085	0.96[ASN][1000 genomes]
rs2278086	1.00[CEU][hapmap]
rs2278087	0.94[ASN][1000 genomes]
rs2278088	1.00[CEU][hapmap];0.94[ASN][1000 genomes]
rs2288121	0.84[ASN][1000 genomes]
rs2289237	1.00[CEU][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303339	1.00[CEU][hapmap]
rs2303340	1.00[CEU][hapmap];0.92[ASN][1000 genomes]
rs311562	0.84[ASN][1000 genomes]
rs311566	0.84[ASN][1000 genomes]
rs311567	0.84[ASN][1000 genomes]
rs34522092	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3731819	1.00[CEU][hapmap];0.90[ASN][1000 genomes]
rs3770066	0.82[ASN][1000 genomes]
rs3770081	0.90[ASN][1000 genomes]
rs3770089	1.00[CEU][hapmap];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3770090	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3810827	1.00[CEU][hapmap];0.92[ASN][1000 genomes]
rs3815840	0.84[ASN][1000 genomes]
rs4832242	0.84[ASN][1000 genomes]
rs56104203	0.92[ASN][1000 genomes]
rs56326127	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56977454	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs57083584	0.94[ASN][1000 genomes]
rs57398459	0.94[ASN][1000 genomes]
rs58186343	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs58365138	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs58898686	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59835600	0.92[ASN][1000 genomes]
rs59891296	0.99[AFR][1000 genomes]
rs60649958	0.94[ASN][1000 genomes]
rs6750765	0.91[ASN][1000 genomes]
rs73943946	0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73947314	0.96[ASN][1000 genomes]
rs7562837	0.81[AMR][1000 genomes]
rs7608262	0.98[ASN][1000 genomes]
rs918857	0.94[AFR][1000 genomes]
rs918858	0.92[AFR][1000 genomes]
rs9789563	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9973880	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1001104	chr2:86182021-86271923	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv535807	chr2:86182021-86271923	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	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
4	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
5	nsv870120	chr2:86265437-86343058	Strong transcription Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86251200-86273200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
2	chr2:86251200-86281400	Strong transcription	H9 Cell Line	embryonic stem cell
3	chr2:86251200-86283000	Strong transcription	HepG2	liver
4	chr2:86251200-86283200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:86251200-86285000	Strong transcription	HUES6 Cell Line	embryonic stem cell
6	chr2:86251200-86285200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr2:86252000-86331200	Strong transcription	HUES64 Cell Line	embryonic stem cell
8	chr2:86252200-86282600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
9	chr2:86252200-86285200	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr2:86252400-86283200	Strong transcription	H1 Cell Line	embryonic stem cell
11	chr2:86252600-86267800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
12	chr2:86252600-86276800	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:86260600-86268800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
14	chr2:86260600-86269000	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr2:86260800-86268800	Weak transcription	Ovary	ovary
16	chr2:86261200-86272000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr2:86262400-86268400	Flanking Active TSS	Thymus	Thymus
18	chr2:86263800-86267200	Enhancers	Primary B cells from peripheral blood	blood
19	chr2:86263800-86268000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr2:86263800-86268800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr2:86263800-86269200	Enhancers	Primary T cells fromperipheralblood	blood
22	chr2:86264000-86268200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr2:86264000-86269000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr2:86264000-86281800	Strong transcription	Fetal Brain Female	brain
25	chr2:86264000-86332000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr2:86264200-86267200	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr2:86264200-86268400	Enhancers	Primary T cells from cord blood	blood
28	chr2:86264200-86269600	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr2:86264200-86275400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:86264400-86269000	Enhancers	Primary T helper cells PMA-I stimulated	--
31	chr2:86264400-86269800	Genic enhancers	Fetal Muscle Trunk	muscle
32	chr2:86264400-86279400	Strong transcription	Hela-S3	cervix
33	chr2:86264400-86285400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:86264400-86285400	Strong transcription	A549	lung
35	chr2:86264600-86267600	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr2:86264600-86267600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
37	chr2:86264600-86273800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr2:86264800-86269800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
39	chr2:86264800-86273000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr2:86264800-86275400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
41	chr2:86265000-86268200	Transcr. at gene 5' and 3'	Fetal Thymus	thymus
42	chr2:86265000-86269800	Genic enhancers	Fetal Muscle Leg	muscle
43	chr2:86265200-86268800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr2:86265200-86268800	Genic enhancers	Dnd41	blood
45	chr2:86265200-86281600	Strong transcription	HMEC	breast
46	chr2:86265200-86284000	Strong transcription	NHEK	skin
47	chr2:86265200-86330000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr2:86265400-86267200	Enhancers	Spleen	Spleen
49	chr2:86265400-86269000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr2:86265400-86269200	Enhancers	Primary T helper naive cells from peripheral blood	blood

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