Variant report

Variant	rs17101577
Chromosome Location	chr14:64514433-64514434
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10129174	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10136783	0.88[CEU][hapmap]
rs10137916	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10138308	0.85[EUR][1000 genomes]
rs10145173	0.88[CEU][hapmap]
rs11158527	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11158528	1.00[CEU][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11847087	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1556587	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101600	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101624	1.00[CEU][hapmap];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101626	1.00[CEU][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17101637	0.88[CEU][hapmap]
rs17101640	0.88[CEU][hapmap]
rs17101651	0.88[CEU][hapmap]
rs57608795	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs59807631	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718389	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718390	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718391	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718393	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718394	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718399	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72718402	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8017952	0.87[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:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64457000-64519200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr14:64466600-64593200	Weak transcription	Colon Smooth Muscle	Colon
3	chr14:64468800-64527200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr14:64469600-64518400	Weak transcription	HMEC	breast
5	chr14:64473000-64515000	Weak transcription	Hela-S3	cervix
6	chr14:64475200-64527200	Weak transcription	Fetal Heart	heart
7	chr14:64475600-64518400	Weak transcription	Gastric	stomach
8	chr14:64479200-64526200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr14:64481400-64574000	Weak transcription	Stomach Mucosa	stomach
10	chr14:64489000-64518400	Weak transcription	HUVEC	blood vessel
11	chr14:64489200-64526600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr14:64489400-64568600	Weak transcription	Small Intestine	intestine
13	chr14:64490000-64515800	Weak transcription	Right Ventricle	heart
14	chr14:64491200-64518400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr14:64491200-64565200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr14:64492000-64518600	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr14:64492200-64518400	Weak transcription	Fetal Brain Male	brain
18	chr14:64492200-64547400	Weak transcription	Colonic Mucosa	Colon
19	chr14:64492400-64518600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr14:64498200-64516600	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr14:64498600-64518400	Weak transcription	Primary B cells from cord blood	blood
22	chr14:64498800-64518400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr14:64498800-64518400	Weak transcription	Fetal Kidney	kidney
24	chr14:64499000-64515600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr14:64499000-64518600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr14:64499000-64518600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr14:64499000-64538800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr14:64499200-64516400	Weak transcription	Ovary	ovary
29	chr14:64499200-64516400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr14:64499200-64518200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr14:64499200-64518400	Weak transcription	Liver	Liver
32	chr14:64500400-64515200	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr14:64502000-64515200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr14:64502400-64518200	Weak transcription	GM12878-XiMat	blood
35	chr14:64503800-64515200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr14:64505400-64518400	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr14:64505800-64515200	Weak transcription	Fetal Intestine Large	intestine
38	chr14:64506200-64516200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr14:64506200-64518400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:64506200-64518400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr14:64506200-64518400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr14:64509800-64518400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr14:64510000-64517600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr14:64510600-64518400	Weak transcription	Fetal Lung	lung
45	chr14:64510600-64518600	Weak transcription	Primary B cells from peripheral blood	blood
46	chr14:64510600-64518600	Weak transcription	Brain Germinal Matrix	brain
47	chr14:64510600-64527200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr14:64510800-64518400	Weak transcription	Fetal Brain Female	brain
49	chr14:64510800-64526400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr14:64511000-64515200	Weak transcription	Left Ventricle	heart

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