Variant report

Variant	rs17101626
Chromosome Location	chr14:64548419-64548420
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	chr14:64547416..64549627-chr14:64558968..64561021,2	MCF-7	breast:
2	chr14:64538983..64542739-chr14:64547728..64551234,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000054654	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10129174	0.93[YRI][hapmap];0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10136783	0.88[CEU][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes]
rs10137916	1.00[CEU][hapmap];0.94[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10137972	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs10138292	0.88[AFR][1000 genomes]
rs10138308	0.90[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10141709	0.92[AFR][1000 genomes]
rs10145173	0.88[CEU][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes]
rs11158527	1.00[CEU][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11158528	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11847087	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1556587	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101577	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101600	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101624	1.00[CEU][hapmap];0.88[YRI][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101637	0.88[CEU][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes]
rs17101640	0.88[CEU][hapmap];0.83[AFR][1000 genomes]
rs17101651	0.88[CEU][hapmap]
rs57608795	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59807631	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718389	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718390	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718391	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718393	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718394	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718399	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718402	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72720306	0.93[AFR][1000 genomes]
rs72720309	0.93[AFR][1000 genomes]
rs72720312	0.96[AFR][1000 genomes]
rs72720319	0.86[AFR][1000 genomes]
rs8017952	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv902019	chr14:64395569-64882380	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv456326	chr14:64420413-64754361	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv564905	chr14:64420413-64754361	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64466600-64593200	Weak transcription	Colon Smooth Muscle	Colon
2	chr14:64481400-64574000	Weak transcription	Stomach Mucosa	stomach
3	chr14:64489400-64568600	Weak transcription	Small Intestine	intestine
4	chr14:64491200-64565200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr14:64519400-64592000	Weak transcription	Fetal Brain Male	brain
6	chr14:64525400-64566600	Strong transcription	Primary T helper cells fromperipheralblood	blood
7	chr14:64526000-64552200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr14:64526800-64577000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr14:64527600-64551800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:64527800-64549000	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr14:64527800-64552000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr14:64527800-64556600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:64528000-64557000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr14:64528000-64567400	Weak transcription	Fetal Heart	heart
15	chr14:64529000-64553200	Strong transcription	Dnd41	blood
16	chr14:64529400-64566800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr14:64536800-64552200	Strong transcription	Placenta	Placenta
18	chr14:64539600-64549400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr14:64539600-64552400	Weak transcription	Brain Anterior Caudate	brain
20	chr14:64541400-64549200	Weak transcription	Psoas Muscle	Psoas
21	chr14:64541600-64549200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:64542200-64557800	Weak transcription	HMEC	breast
23	chr14:64542600-64549000	Weak transcription	HSMM	muscle
24	chr14:64542600-64550600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr14:64542600-64552000	Strong transcription	HUES64 Cell Line	embryonic stem cell
26	chr14:64542800-64549200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr14:64542800-64556200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr14:64542800-64574000	Weak transcription	HUVEC	blood vessel
29	chr14:64542800-64575400	Weak transcription	Hela-S3	cervix
30	chr14:64543000-64576400	Weak transcription	NHDF-Ad	bronchial
31	chr14:64544000-64616200	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr14:64544200-64552400	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr14:64544400-64550400	Strong transcription	Primary T helper cells PMA-I stimulated	--
34	chr14:64544600-64551800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr14:64545000-64550600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr14:64545000-64551600	Strong transcription	Primary B cells from cord blood	blood
37	chr14:64545200-64549200	Strong transcription	Left Ventricle	heart
38	chr14:64545200-64549800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr14:64545200-64550400	Strong transcription	Primary T helper naive cells from peripheral blood	blood
40	chr14:64545200-64550400	Strong transcription	Duodenum Mucosa	Duodenum
41	chr14:64545200-64550400	Strong transcription	Fetal Muscle Leg	muscle
42	chr14:64545200-64550400	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr14:64545200-64550400	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr14:64545200-64552000	Strong transcription	Primary T cells from cord blood	blood
45	chr14:64545200-64552000	Strong transcription	Fetal Intestine Large	intestine
46	chr14:64545400-64549800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr14:64545400-64550400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr14:64545400-64550400	Strong transcription	Sigmoid Colon	Sigmoid Colon
49	chr14:64545400-64552000	Strong transcription	Fetal Stomach	stomach
50	chr14:64545600-64550200	Strong transcription	Adipose Nuclei	Adipose

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