Variant report

Variant	rs4903612
Chromosome Location	chr14:78043929-78043930
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10136221	1.00[AMR][1000 genomes]
rs10142919	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs12889681	1.00[AMR][1000 genomes]
rs1474504	1.00[AMR][1000 genomes]
rs176902	0.82[AFR][1000 genomes]
rs1973866	1.00[AMR][1000 genomes]
rs2091915	1.00[MEX][hapmap];0.85[MKK][hapmap];1.00[AMR][1000 genomes]
rs2142186	1.00[AMR][1000 genomes]
rs2178876	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs2364603	1.00[LWK][hapmap];0.93[MKK][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes]
rs4145508	1.00[MEX][hapmap]
rs4899657	1.00[AMR][1000 genomes]
rs4903601	1.00[AMR][1000 genomes]
rs4903609	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6574381	1.00[AMR][1000 genomes]
rs7143656	0.92[LWK][hapmap]
rs7156665	1.00[AMR][1000 genomes]
rs7157643	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs7400794	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8003293	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs8004422	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8010591	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8022297	1.00[AMR][1000 genomes]
rs926115	1.00[AMR][1000 genomes]
rs963897	1.00[AMR][1000 genomes]
rs9972134	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832835	chr14:77906706-78095207	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1053810	chr14:77987871-78148320	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv1051554	chr14:78004196-78122980	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv1794863	chr14:78024926-78048715	Strong transcription Weak transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	esv3433816	chr14:78043490-78043981	Weak transcription Strong transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:77970200-78047200	Weak transcription	Fetal Heart	heart
2	chr14:77987800-78060000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr14:78009800-78050800	Weak transcription	Psoas Muscle	Psoas
4	chr14:78011200-78045800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:78013200-78066200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr14:78016400-78061000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:78018600-78044200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr14:78018800-78047000	Weak transcription	Placenta	Placenta
9	chr14:78021600-78047000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr14:78021800-78061000	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr14:78021800-78068400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr14:78021800-78071600	Weak transcription	Colon Smooth Muscle	Colon
13	chr14:78022000-78060800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr14:78022400-78047200	Weak transcription	Brain Germinal Matrix	brain
15	chr14:78022400-78049000	Weak transcription	Right Ventricle	heart
16	chr14:78022400-78055000	Weak transcription	Colonic Mucosa	Colon
17	chr14:78024000-78046400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:78024200-78046800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr14:78024200-78047200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr14:78026200-78045600	Weak transcription	Fetal Lung	lung
21	chr14:78028600-78047200	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr14:78029800-78047600	Weak transcription	K562	blood
23	chr14:78030200-78056800	Weak transcription	HMEC	breast
24	chr14:78033600-78044600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr14:78034800-78046000	Strong transcription	Monocytes-CD14+_RO01746	blood
26	chr14:78036000-78046800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
27	chr14:78036200-78044000	Strong transcription	Primary hematopoietic stem cells	blood
28	chr14:78037600-78049000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr14:78038200-78044400	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr14:78038200-78045400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr14:78038400-78045800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
32	chr14:78038400-78045800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr14:78038600-78045600	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr14:78039400-78044000	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr14:78039400-78044400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr14:78039800-78044600	Strong transcription	Primary T helper cells PMA-I stimulated	--
37	chr14:78040000-78044600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr14:78040000-78045200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr14:78040200-78044800	Strong transcription	NHEK	skin
40	chr14:78040200-78045600	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr14:78040400-78044000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr14:78040400-78051800	Weak transcription	HepG2	liver
43	chr14:78040600-78049000	Weak transcription	Ovary	ovary
44	chr14:78040800-78047000	Weak transcription	Stomach Mucosa	stomach
45	chr14:78041000-78047000	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr14:78041200-78044600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr14:78041200-78044600	Strong transcription	Thymus	Thymus
48	chr14:78041200-78045200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr14:78041400-78044200	Strong transcription	Lung	lung
50	chr14:78041600-78044000	Strong transcription	iPS-18 Cell Line	embryonic stem cell

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