Variant report

Variant	rs7149529
Chromosome Location	chr14:66425874-66425875
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:66396499..66397053-chr14:66425648..66426403,2	MCF-7	breast:
2	chr14:65881389..65882114-chr14:66425535..66426219,3	MCF-7	breast:
3	chr14:66281810..66282561-chr14:66425521..66426262,2	MCF-7	breast:
4	chr14:66291136..66291696-chr14:66425702..66426318,2	MCF-7	breast:
5	chr14:65628473..65630943-chr14:66425441..66427693,2	MCF-7	breast:
6	chr14:65630510..65631490-chr14:66425640..66426199,2	K562	blood:

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs11625540	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17827524	1.00[ASN][1000 genomes]
rs55871008	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61989042	1.00[ASN][1000 genomes]
rs61989044	1.00[ASN][1000 genomes]
rs61990006	1.00[ASN][1000 genomes]
rs61990009	1.00[ASN][1000 genomes]
rs61990010	1.00[ASN][1000 genomes]
rs61990011	1.00[ASN][1000 genomes]
rs61990013	1.00[ASN][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	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66423200-66426000	Enhancers	H9 Cell Line	embryonic stem cell
2	chr14:66424200-66426000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr14:66424200-66426000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr14:66424200-66426400	Enhancers	H1 Cell Line	embryonic stem cell
5	chr14:66424200-66426600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr14:66424400-66426000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:66424600-66426000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:66424800-66426800	Enhancers	Rectal Mucosa Donor 31	rectum
9	chr14:66425000-66426600	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr14:66425000-66426600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr14:66425200-66427800	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr14:66425200-66439000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr14:66425400-66426000	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr14:66425400-66426600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr14:66425400-66426800	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr14:66425400-66426800	Enhancers	Dnd41	blood
17	chr14:66425400-66427400	Enhancers	Primary T cells from cord blood	blood
18	chr14:66425400-66427800	Enhancers	Primary T cells fromperipheralblood	blood
19	chr14:66425400-66428000	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr14:66425600-66426200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
21	chr14:66425600-66426400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr14:66425600-66426400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr14:66425600-66426400	Enhancers	Brain Cingulate Gyrus	brain
24	chr14:66425600-66426800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
25	chr14:66425600-66427000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
26	chr14:66425600-66427000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:66425600-66427000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr14:66425800-66426000	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr14:66425800-66426200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr14:66425800-66426400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr14:66425800-66427600	Enhancers	Primary T killer memory cells from peripheral blood	blood

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