Variant report

Variant	rs55925976
Chromosome Location	chr14:64328108-64328109
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:64319325..64321479-chr14:64326717..64328387,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000054654	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1000904	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10873171	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12435958	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12436656	0.83[ASN][1000 genomes]
rs12587452	0.80[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs12893838	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2151763	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2357001	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34486661	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35234298	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs36050513	0.93[ASN][1000 genomes]
rs4902249	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4902251	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4902252	0.81[EUR][1000 genomes]
rs61985747	0.94[ASN][1000 genomes]
rs6573532	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6573533	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6573535	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6573536	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7144370	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7145302	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7145810	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7149609	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7150540	0.80[EUR][1000 genomes]
rs7153723	0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7158960	0.89[ASN][1000 genomes]
rs7161586	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8004989	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8009846	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8010094	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8013611	0.80[ASN][1000 genomes]
rs945031	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs951250	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][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	nsv1038825	chr14:64109441-64491720	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1037140	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv542119	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64321200-64333800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:64321200-64334600	Weak transcription	Pancreas	Pancrea
3	chr14:64321200-64340600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr14:64321400-64330600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr14:64321400-64331200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr14:64321400-64350200	Weak transcription	Fetal Stomach	stomach
7	chr14:64322400-64334400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr14:64322600-64331200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr14:64322600-64331200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr14:64322800-64329000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
11	chr14:64322800-64330000	Weak transcription	Fetal Kidney	kidney
12	chr14:64322800-64330000	Weak transcription	HepG2	liver
13	chr14:64322800-64330600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
14	chr14:64322800-64330800	Enhancers	Primary T cells fromperipheralblood	blood
15	chr14:64322800-64340400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:64322800-64340600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:64323000-64329000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr14:64323000-64330000	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr14:64323000-64330200	Weak transcription	Primary T cells from cord blood	blood
20	chr14:64323000-64330400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr14:64323000-64332800	Weak transcription	Fetal Intestine Small	intestine
22	chr14:64323000-64333000	Weak transcription	Ovary	ovary
23	chr14:64323200-64331200	Weak transcription	Right Atrium	heart
24	chr14:64323200-64334400	Weak transcription	Aorta	Aorta
25	chr14:64323200-64340200	Weak transcription	Left Ventricle	heart
26	chr14:64323200-64340400	Weak transcription	Spleen	Spleen
27	chr14:64324000-64330200	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr14:64324200-64329800	Weak transcription	Brain Germinal Matrix	brain
29	chr14:64324200-64330800	Weak transcription	Hela-S3	cervix
30	chr14:64324400-64329200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr14:64324400-64330800	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr14:64324400-64331200	Enhancers	Primary T killer memory cells from peripheral blood	blood
33	chr14:64324600-64328800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr14:64324600-64331000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr14:64324600-64331200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
36	chr14:64324600-64341400	Weak transcription	HSMM	muscle
37	chr14:64324800-64328800	Weak transcription	NHEK	skin
38	chr14:64324800-64329000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:64324800-64329800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr14:64324800-64330000	Weak transcription	HMEC	breast
41	chr14:64325800-64331000	Enhancers	Placenta	Placenta
42	chr14:64326600-64330800	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr14:64326800-64331600	Enhancers	Stomach Mucosa	stomach
44	chr14:64327000-64330600	Enhancers	Dnd41	blood
45	chr14:64327000-64331400	Weak transcription	Thymus	Thymus
46	chr14:64327200-64328400	Weak transcription	GM12878-XiMat	blood
47	chr14:64327200-64331200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr14:64327200-64332000	Weak transcription	Fetal Brain Female	brain
49	chr14:64327200-64340600	Weak transcription	Right Ventricle	heart
50	chr14:64327400-64330800	Weak transcription	HUES64 Cell Line	embryonic stem cell

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