Variant report

Variant	rs726020
Chromosome Location	chr14:81425425-81425426
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81420793..81423189-chr14:81424553..81427836,4	MCF-7	breast:
2	chr14:81421283..81423197-chr14:81423259..81426025,2	K562	blood:

Variant related genes	Relation type
ENSG00000165409	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs10149689	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs11845052	0.80[ASN][1000 genomes]
rs11850464	0.84[ASN][1000 genomes]
rs12050077	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs12050078	1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs12050278	0.89[CHB][hapmap];0.83[JPT][hapmap]
rs12050350	1.00[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs17544968	0.80[ASN][1000 genomes]
rs17545038	0.80[ASN][1000 genomes]
rs179243	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs179245	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs179249	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs179251	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs179254	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs179257	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2024427	0.83[CHB][hapmap];0.81[JPT][hapmap]
rs2110696	0.94[CHB][hapmap];0.81[JPT][hapmap]
rs2114705	0.89[CHB][hapmap];0.83[JPT][hapmap]
rs2195103	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs2217177	0.88[CHB][hapmap];0.88[JPT][hapmap]
rs2217178	0.89[CHB][hapmap];0.83[JPT][hapmap]
rs2239610	0.89[CHB][hapmap];0.83[JPT][hapmap];0.82[ASN][1000 genomes]
rs2268451	0.88[CHB][hapmap];0.80[YRI][hapmap];0.80[ASN][1000 genomes]
rs2268452	0.89[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs2268458	0.87[JPT][hapmap]
rs2268460	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs2284718	0.86[ASN][1000 genomes]
rs2284719	0.86[ASN][1000 genomes]
rs2284720	0.94[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs2284722	0.88[CHB][hapmap];0.81[JPT][hapmap]
rs3783945	0.81[ASN][1000 genomes]
rs3783951	0.88[CHB][hapmap]
rs4903957	0.88[CHB][hapmap]
rs4903958	0.88[CHB][hapmap]
rs5002906	0.88[CHB][hapmap];0.80[JPT][hapmap]
rs55751898	0.81[ASN][1000 genomes]
rs55945219	0.80[ASN][1000 genomes]
rs59431750	0.83[ASN][1000 genomes]
rs59711583	0.80[ASN][1000 genomes]
rs7154269	0.89[CHB][hapmap]
rs724169	0.80[ASN][1000 genomes]
rs726018	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72693053	0.83[ASN][1000 genomes]
rs72693057	0.86[ASN][1000 genomes]
rs72693075	0.82[ASN][1000 genomes]
rs72693090	0.80[ASN][1000 genomes]
rs72693096	0.80[ASN][1000 genomes]
rs74064796	0.80[ASN][1000 genomes]
rs8009058	0.82[YRI][hapmap]
rs8022600	0.88[CHB][hapmap];0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	esv2761847	chr14:81392124-81453137	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	n/a
3	nsv456346	chr14:81399692-81448382	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	n/a
4	nsv565291	chr14:81399692-81448382	Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81421000-81426400	Active TSS	Thymus	Thymus
2	chr14:81422000-81425800	Weak transcription	Brain Angular Gyrus	brain
3	chr14:81422200-81425800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:81422200-81425800	Weak transcription	Brain Substantia Nigra	brain
5	chr14:81422200-81426600	Weak transcription	Spleen	Spleen
6	chr14:81422200-81427200	Weak transcription	Right Ventricle	heart
7	chr14:81422400-81425800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr14:81422400-81425800	Weak transcription	Brain Anterior Caudate	brain
9	chr14:81423200-81427600	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:81423600-81425800	Weak transcription	Adipose Nuclei	Adipose
11	chr14:81423800-81425600	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr14:81423800-81426600	Active TSS	Fetal Thymus	thymus
13	chr14:81424200-81425600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr14:81424400-81425800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr14:81424600-81425600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr14:81424800-81426600	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr14:81424800-81427200	Flanking Active TSS	Dnd41	blood
18	chr14:81425000-81425800	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr14:81425200-81425800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr14:81425200-81426800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr14:81425400-81425600	Enhancers	Primary T cells fromperipheralblood	blood
22	chr14:81425400-81425600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
23	chr14:81425400-81425600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
24	chr14:81425400-81425600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr14:81425400-81425800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr14:81425400-81425800	Enhancers	Brain Germinal Matrix	brain
27	chr14:81425400-81425800	Enhancers	Brain Hippocampus Middle	brain
28	chr14:81425400-81426000	Enhancers	Primary monocytes fromperipheralblood	blood
29	chr14:81425400-81426000	Enhancers	Primary B cells from cord blood	blood
30	chr14:81425400-81426200	Enhancers	Psoas Muscle	Psoas
31	chr14:81425400-81426400	Flanking Active TSS	GM12878-XiMat	blood
32	chr14:81425400-81426600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
33	chr14:81425400-81426600	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
34	chr14:81425400-81426800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr14:81425400-81426800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
36	chr14:81425400-81426800	Enhancers	Fetal Brain Male	brain
37	chr14:81425400-81426800	Enhancers	Rectal Mucosa Donor 31	rectum

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