Variant report

Variant	rs12891263
Chromosome Location	chr14:21974645-21974646
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:21973399..21975434-chr14:22010976..22012541,2	K562	blood:
2	chr14:21959084..21961956-chr14:21974490..21976293,2	K562	blood:
3	chr14:21973675..21975896-chr14:22025670..22027377,2	K562	blood:
4	chr14:21922971..21924665-chr14:21973742..21975845,3	MCF-7	breast:
5	chr14:21972318..21975113-chr14:21978008..21980143,3	K562	blood:
6	chr14:21944053..21946667-chr14:21973536..21975748,2	MCF-7	breast:
7	chr14:21974369..21977190-chr14:22017356..22019662,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000100888	Chromatin interaction
ENSG00000129472	Chromatin interaction
ENSG00000165819	Chromatin interaction
ENSG00000092203	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1061026	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12878084	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12880071	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12884313	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12894578	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106830	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs33919729	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34765612	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35446048	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35463722	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35582631	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35856604	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3752411	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3762161	0.90[AMR][1000 genomes]
rs4982449	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67492181	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67802283	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73581403	0.85[AMR][1000 genomes]
rs73581411	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73581416	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs73581419	0.90[AMR][1000 genomes]
rs9322989	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530009	chr14:21377022-22044608	Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
2	nsv530769	chr14:21407536-22139126	Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
3	nsv1036762	chr14:21507093-22101805	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
4	nsv541976	chr14:21507093-22101805	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
5	esv3518898	chr14:21805983-22077584	Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	esv3518899	chr14:21805983-22077584	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv1054013	chr14:21868964-21992109	Enhancers Genic enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	nsv541991	chr14:21868964-21992109	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
9	nsv530011	chr14:21876973-21985341	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	esv2422459	chr14:21931624-22169502	Genic enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21946200-21977600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr14:21947000-21978000	Weak transcription	Fetal Heart	heart
3	chr14:21954800-21977400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr14:21955600-21977200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr14:21964000-21977800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr14:21967200-21975800	Strong transcription	HepG2	liver
7	chr14:21967200-21977400	Weak transcription	Small Intestine	intestine
8	chr14:21967600-21977400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr14:21967600-21977400	Strong transcription	HUES6 Cell Line	embryonic stem cell
10	chr14:21967800-21977200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr14:21967800-21977400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr14:21967800-21978600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr14:21971600-21975400	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr14:21971800-21978000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr14:21971800-21978000	Weak transcription	Brain Cingulate Gyrus	brain
16	chr14:21971800-21978200	Weak transcription	Pancreatic Islets	Pancreatic Islet
17	chr14:21971800-21978200	Weak transcription	Stomach Mucosa	stomach
18	chr14:21972000-21974800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr14:21972000-21974800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr14:21972000-21974800	Weak transcription	Fetal Muscle Leg	muscle
21	chr14:21972000-21975400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr14:21972000-21975400	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr14:21972000-21975400	Weak transcription	Duodenum Mucosa	Duodenum
24	chr14:21972000-21975400	Weak transcription	Fetal Intestine Large	intestine
25	chr14:21972000-21975400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr14:21972000-21975400	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr14:21972000-21975400	Weak transcription	HSMMtube	muscle
28	chr14:21972000-21975600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr14:21972000-21975600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr14:21972000-21975600	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr14:21972000-21975600	Weak transcription	Adipose Nuclei	Adipose
32	chr14:21972000-21975600	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr14:21972000-21975600	Weak transcription	Lung	lung
34	chr14:21972000-21975800	Weak transcription	Primary T cells from cord blood	blood
35	chr14:21972000-21975800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr14:21972000-21975800	Weak transcription	Fetal Lung	lung
37	chr14:21972000-21975800	Weak transcription	HMEC	breast
38	chr14:21972000-21975800	Weak transcription	NHEK	skin
39	chr14:21972000-21976000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr14:21972000-21976000	Weak transcription	Ovary	ovary
41	chr14:21972000-21976000	Weak transcription	NHLF	lung
42	chr14:21972000-21976200	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr14:21972000-21976200	Weak transcription	Stomach Smooth Muscle	stomach
44	chr14:21972000-21977200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr14:21972000-21977200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr14:21972000-21977200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr14:21972000-21977200	Weak transcription	Left Ventricle	heart
48	chr14:21972000-21977200	Weak transcription	Psoas Muscle	Psoas
49	chr14:21972000-21977200	Weak transcription	Thymus	Thymus
50	chr14:21972000-21977400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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