Variant report

Variant	rs12893055
Chromosome Location	chr14:104318628-104318629
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:64)

rs_ID	r²[population]
rs10083367	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1040813	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10873539	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11160760	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11160761	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11160762	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11160765	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1155751	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11623546	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1187416	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12434686	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12878678	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12879501	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12880167	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12880233	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12880368	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12880413	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12880821	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12885018	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12886840	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12889993	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12891175	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12892186	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12894254	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12897150	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1475007	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2223937	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2368560	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28533661	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28612442	0.86[AMR][1000 genomes]
rs28698555	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2887282	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34066659	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34813623	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs35505672	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4606645	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4900594	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4900595	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4900598	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4900600	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4906371	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4906372	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4906373	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs55824307	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6575999	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7141473	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs71419615	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7147171	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7159810	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7401843	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7401901	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8003653	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8005225	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8005594	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8011109	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8011137	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8013637	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8015603	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8016014	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs8018062	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8020234	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs8021682	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8022783	0.82[EUR][1000 genomes]
rs9743799	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332028	chr14:103581471-104328811	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
2	nsv1045162	chr14:104140525-104594841	Flanking Active TSS Strong transcription Bivalent Enhancer Enhancers Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv542204	chr14:104140525-104594841	Active TSS Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
4	esv2758368	chr14:104147525-104412813	Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	esv2760013	chr14:104147525-104412813	Enhancers Genic enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv902313	chr14:104162263-104378087	Bivalent Enhancer Genic enhancers Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	nsv902318	chr14:104255083-104464809	Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
8	nsv902319	chr14:104255083-104620077	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	64 gene(s)	inside rSNPs	diseases
9	esv1838047	chr14:104283104-104359121	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	nsv902321	chr14:104283104-104378087	Strong transcription Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
11	esv1818596	chr14:104312697-104359121	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
12	esv1836134	chr14:104312697-104359121	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
13	esv1837236	chr14:104313426-104332759	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
14	nsv566028	chr14:104314023-104332759	Weak transcription Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104314800-104320200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:104315000-104320400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:104315000-104320400	Weak transcription	Primary hematopoietic stem cells	blood
4	chr14:104315200-104320400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr14:104315200-104320400	Weak transcription	Lung	lung
6	chr14:104315200-104327600	Weak transcription	Ovary	ovary
7	chr14:104315400-104320000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr14:104315400-104320200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr14:104315400-104320400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr14:104315400-104321200	Weak transcription	Stomach Smooth Muscle	stomach
11	chr14:104315600-104319800	Weak transcription	Placenta	Placenta
12	chr14:104315600-104320200	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr14:104315600-104320400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr14:104315600-104320400	Weak transcription	Fetal Lung	lung
15	chr14:104315800-104321000	Weak transcription	Gastric	stomach
16	chr14:104315800-104321000	Weak transcription	Pancreas	Pancrea
17	chr14:104315800-104321000	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr14:104316000-104320200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:104316000-104320400	Weak transcription	Esophagus	oesophagus
20	chr14:104316000-104320400	Weak transcription	Spleen	Spleen
21	chr14:104316000-104321400	Weak transcription	Colonic Mucosa	Colon
22	chr14:104316000-104321600	Weak transcription	Left Ventricle	heart
23	chr14:104316000-104321600	Weak transcription	Right Ventricle	heart
24	chr14:104316200-104321200	Weak transcription	Fetal Intestine Small	intestine
25	chr14:104316200-104321400	Weak transcription	Fetal Heart	heart
26	chr14:104316400-104321200	Weak transcription	Fetal Intestine Large	intestine
27	chr14:104316400-104321400	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr14:104316600-104321000	Weak transcription	Duodenum Mucosa	Duodenum
29	chr14:104317000-104320000	Weak transcription	HepG2	liver

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