Variant report

Variant	rs55727224
Chromosome Location	chr14:66416226-66416227
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:66414502..66416771-chr14:66536392..66538001,2	MCF-7	breast:
2	chr14:66410164..66412047-chr14:66415656..66417761,2	MCF-7	breast:
3	chr14:66404813..66406809-chr14:66413591..66416552,2	MCF-7	breast:
4	chr14:65876878..65880763-chr14:66413907..66416423,3	MCF-7	breast:
5	chr14:66407663..66410306-chr14:66414738..66417001,2	K562	blood:
6	chr14:66407663..66410728-chr14:66412233..66417001,4	K562	blood:

Variant related genes	Relation type
ENSG00000033170	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs72718412	1.00[AFR][1000 genomes]
rs72718417	0.91[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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
12	nsv1313	chr14:66410061-66437297	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66405000-66416400	Weak transcription	Primary hematopoietic stem cells	blood
2	chr14:66405400-66416600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:66411600-66416400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr14:66412800-66417200	Weak transcription	Spleen	Spleen
5	chr14:66413200-66424200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr14:66415000-66417600	Enhancers	Primary T cells fromperipheralblood	blood
7	chr14:66415200-66417000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr14:66415400-66416400	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr14:66415400-66416600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr14:66415800-66417600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:66416000-66417200	Enhancers	Fetal Heart	heart
12	chr14:66416000-66417400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr14:66416200-66416800	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr14:66416200-66416800	Enhancers	GM12878-XiMat	blood
15	chr14:66416200-66417200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:66416200-66417400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
17	chr14:66416200-66417600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr14:66416200-66417600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr14:66416200-66417800	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr14:66416200-66418000	Enhancers	Primary T cells from cord blood	blood
21	chr14:66416200-66418000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr14:66416200-66418200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
23	chr14:66416200-66418400	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr14:66416200-66418800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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