Variant report

Variant	rs8021889
Chromosome Location	chr14:66214811-66214812
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:65879004..65881155-chr14:66213120..66215142,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000033170	Chromatin interaction

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10083363	1.00[CEU][hapmap];0.89[YRI][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10143206	0.84[YRI][hapmap]
rs10148699	1.00[CEU][hapmap];0.90[YRI][hapmap];0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10873191	0.84[YRI][hapmap]
rs10873192	1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11158603	0.84[YRI][hapmap]
rs1121885	0.84[YRI][hapmap]
rs11622767	0.83[EUR][1000 genomes]
rs11848209	1.00[CEU][hapmap];0.83[YRI][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12433597	0.84[YRI][hapmap]
rs1956008	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1956009	0.85[EUR][1000 genomes]
rs2180299	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2268956	0.84[YRI][hapmap]
rs2411349	1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2411354	1.00[CEU][hapmap];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2411813	1.00[ASN][1000 genomes]
rs2411815	0.84[YRI][hapmap]
rs2898814	0.84[YRI][hapmap]
rs2898816	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3825639	0.84[YRI][hapmap]
rs4902404	0.84[YRI][hapmap]
rs4902408	1.00[CEU][hapmap];0.94[LWK][hapmap];0.98[MKK][hapmap];0.84[YRI][hapmap];0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902413	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6573616	0.84[YRI][hapmap]
rs7144345	0.84[YRI][hapmap]
rs7144971	0.84[YRI][hapmap]
rs7146993	0.84[YRI][hapmap]
rs7147002	0.85[YRI][hapmap]
rs7147231	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7150233	1.00[CEU][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7153497	1.00[ASN][1000 genomes]
rs7158153	0.80[YRI][hapmap]
rs7160390	1.00[CEU][hapmap];0.84[YRI][hapmap];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72714491	1.00[ASN][1000 genomes]
rs72714498	1.00[ASN][1000 genomes]
rs8017258	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs8019762	0.83[YRI][hapmap]
rs9323461	0.85[YRI][hapmap]
rs9671406	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][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	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
2	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	nsv1039168	chr14:65811750-66308343	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
4	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
5	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66190400-66217000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr14:66191800-66217800	Weak transcription	Small Intestine	intestine
3	chr14:66193000-66218800	Weak transcription	Colonic Mucosa	Colon
4	chr14:66200600-66215600	Weak transcription	Brain Substantia Nigra	brain
5	chr14:66201200-66216400	Weak transcription	Fetal Thymus	thymus
6	chr14:66201800-66219200	Weak transcription	Brain Anterior Caudate	brain
7	chr14:66202200-66215000	Weak transcription	Psoas Muscle	Psoas
8	chr14:66207400-66215400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:66209400-66215000	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr14:66209400-66217400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr14:66209400-66217600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr14:66209400-66219200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr14:66209600-66215200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr14:66209600-66216600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr14:66209600-66217800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr14:66209600-66217800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr14:66209600-66219000	Weak transcription	Thymus	Thymus
18	chr14:66209600-66219200	Weak transcription	Stomach Mucosa	stomach
19	chr14:66210600-66217400	Weak transcription	GM12878-XiMat	blood
20	chr14:66210600-66217800	Weak transcription	Duodenum Mucosa	Duodenum
21	chr14:66210800-66217400	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr14:66211000-66218000	Weak transcription	Fetal Intestine Large	intestine
23	chr14:66211800-66217600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr14:66212400-66217800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:66212600-66217800	Weak transcription	HepG2	liver
26	chr14:66213400-66218000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr14:66213600-66217600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr14:66213600-66217800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr14:66213800-66215600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr14:66214400-66215200	Weak transcription	Primary T cells from cord blood	blood

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