Variant report

Variant	rs55938117
Chromosome Location	chr14:35094710-35094711
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:35089260..35092373-chr14:35092594..35095994,3	MCF-7	breast:
2	chr14:35093463..35096571-chr14:35096710..35101951,6	K562	blood:
3	chr14:35091495..35095564-chr14:35101048..35103200,4	MCF-7	breast:
4	chr14:35087584..35096037-chr14:35096409..35100819,12	MCF-7	breast:

Variant related genes	Relation type
ENSG00000129515	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10131004	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10134534	0.85[EUR][1000 genomes]
rs10136826	0.92[ASN][1000 genomes]
rs10151832	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10220690	0.95[ASN][1000 genomes]
rs10872887	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11156850	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11620787	0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12432069	0.86[EUR][1000 genomes]
rs12432539	0.90[ASN][1000 genomes]
rs12717240	0.85[ASN][1000 genomes]
rs12880885	0.85[ASN][1000 genomes]
rs12885600	0.85[EUR][1000 genomes]
rs12891984	0.92[ASN][1000 genomes]
rs28537636	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34612921	0.97[ASN][1000 genomes]
rs4258505	0.82[ASN][1000 genomes]
rs4304943	0.86[EUR][1000 genomes]
rs4403967	0.85[ASN][1000 genomes]
rs4453379	0.86[EUR][1000 genomes]
rs4562976	0.85[EUR][1000 genomes]
rs4567613	0.82[EUR][1000 genomes]
rs4598814	0.85[ASN][1000 genomes]
rs4612970	0.95[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs4981244	0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60370017	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7144882	0.92[ASN][1000 genomes]
rs7146283	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7148910	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7149128	0.85[EUR][1000 genomes]
rs7149200	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7151774	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7155411	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7158783	0.92[ASN][1000 genomes]
rs72675226	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72675236	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72675245	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72675282	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7493420	0.92[ASN][1000 genomes]
rs7493480	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8008918	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8013554	0.84[EUR][1000 genomes]
rs8018552	0.85[ASN][1000 genomes]
rs8018701	0.85[ASN][1000 genomes]
rs8018918	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040980	chr14:34345018-35255592	Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
2	nsv1048408	chr14:34958352-35255592	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
3	esv3392700	chr14:34989406-35365530	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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 miRNA target site	85 gene(s)	inside rSNPs	diseases
4	nsv1040303	chr14:35040853-35101044	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv542027	chr14:35040853-35101044	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv1038360	chr14:35040853-35152886	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
7	esv3408652	chr14:35069966-35110821	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv523334	chr14:35075022-35131862	Flanking Active TSS Strong transcription Active TSS Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1041857	chr14:35084889-35417180	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35054600-35098400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:35060800-35097800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr14:35063000-35098400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:35068400-35098000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr14:35070400-35098600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:35073600-35097800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:35076600-35098000	Weak transcription	HSMMtube	muscle
8	chr14:35077000-35097600	Weak transcription	Esophagus	oesophagus
9	chr14:35077000-35098600	Weak transcription	Pancreas	Pancrea
10	chr14:35077600-35097800	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr14:35077600-35098000	Weak transcription	Aorta	Aorta
12	chr14:35077600-35098200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:35077600-35098600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr14:35078000-35098000	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr14:35078000-35098000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr14:35078000-35098200	Weak transcription	Ovary	ovary
17	chr14:35078200-35098600	Weak transcription	Gastric	stomach
18	chr14:35079400-35097800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr14:35081200-35095200	Strong transcription	Fetal Muscle Leg	muscle
20	chr14:35081200-35097000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr14:35085400-35097800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr14:35085600-35098000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr14:35086000-35095800	Strong transcription	HepG2	liver
24	chr14:35086200-35097600	Weak transcription	Lung	lung
25	chr14:35087800-35095400	Strong transcription	Fetal Muscle Trunk	muscle
26	chr14:35088800-35095400	Strong transcription	Primary B cells from peripheral blood	blood
27	chr14:35089400-35095200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr14:35089400-35097200	Weak transcription	Right Ventricle	heart
29	chr14:35089600-35095200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr14:35089600-35097600	Weak transcription	Stomach Mucosa	stomach
31	chr14:35089600-35098000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr14:35089800-35097600	Weak transcription	Colonic Mucosa	Colon
33	chr14:35090400-35097600	Weak transcription	Spleen	Spleen
34	chr14:35090600-35096200	Strong transcription	Placenta	Placenta
35	chr14:35091000-35095800	Weak transcription	Fetal Heart	heart
36	chr14:35091000-35096000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr14:35091000-35097000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr14:35091000-35097800	Weak transcription	Fetal Lung	lung
39	chr14:35091000-35098000	Weak transcription	Rectal Smooth Muscle	rectum
40	chr14:35091200-35095000	Strong transcription	Primary T helper cells fromperipheralblood	blood
41	chr14:35091200-35095200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
42	chr14:35091800-35095400	Strong transcription	Primary monocytes fromperipheralblood	blood
43	chr14:35091800-35095600	Strong transcription	Primary neutrophils fromperipheralblood	blood
44	chr14:35091800-35096200	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr14:35092000-35098000	Weak transcription	Fetal Thymus	thymus
46	chr14:35092400-35098000	Weak transcription	Fetal Kidney	kidney
47	chr14:35092600-35097000	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr14:35092600-35097200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr14:35092600-35097800	Weak transcription	Stomach Smooth Muscle	stomach
50	chr14:35092800-35095600	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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