Variant report

Variant	rs28481772
Chromosome Location	chr14:66408492-66408493
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:66407238..66409314-chr14:66412717..66414386,2	MCF-7	breast:
2	chr14:66403172..66405104-chr14:66407998..66409669,3	MCF-7	breast:
3	chr14:66407663..66410306-chr14:66414738..66417001,2	K562	blood:
4	chr14:66407663..66410728-chr14:66412233..66417001,4	K562	blood:

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10144902	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2022847	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2022848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28489937	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28492007	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28532911	1.00[AMR][1000 genomes]
rs28579424	1.00[AMR][1000 genomes]
rs28636801	1.00[AMR][1000 genomes]
rs28679781	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 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	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
4	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
5	nsv564953	chr14:66287921-67046960	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
6	nsv1050485	chr14:66308283-67109270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
7	nsv530775	chr14:66316836-67079049	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv530793	chr14:66317036-67078908	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
9	nsv1046455	chr14:66345369-66848234	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
10	nsv1043864	chr14:66372458-66845503	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	nsv917338	chr14:66376591-66841403	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66404600-66415000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr14:66404600-66415200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr14:66404800-66410000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr14:66405000-66416400	Weak transcription	Primary hematopoietic stem cells	blood
5	chr14:66405400-66410200	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr14:66405400-66416600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:66405600-66409800	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr14:66405600-66410000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr14:66405600-66410000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr14:66406400-66409800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr14:66406800-66408600	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr14:66407000-66409000	Enhancers	Brain Germinal Matrix	brain
13	chr14:66407200-66409800	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr14:66407800-66408600	Enhancers	H1 Cell Line	embryonic stem cell
15	chr14:66407800-66408800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr14:66408000-66408600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr14:66408000-66408600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr14:66408200-66408600	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr14:66408200-66408600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr14:66408200-66408600	Enhancers	Fetal Brain Male	brain
21	chr14:66408200-66409800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr14:66408200-66410600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr14:66408400-66409800	Weak transcription	Primary T cells from cord blood	blood
24	chr14:66408400-66409800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
25	chr14:66408400-66415000	Weak transcription	HUES6 Cell Line	embryonic stem cell

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