Variant report

Variant	rs2295865
Chromosome Location	chr14:21820029-21820030
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:21814371..21817924-chr14:21819365..21822480,4	K562	blood:
2	chr14:21727359..21730774-chr14:21816654..21820383,4	K562	blood:
3	chr14:21814821..21817594-chr14:21819098..21821242,4	K562	blood:
4	chr14:21700378..21702346-chr14:21819126..21821504,2	MCF-7	breast:
5	chr14:21788171..21789709-chr14:21819035..21821503,2	K562	blood:

Variant related genes	Relation type
ENSG00000092200	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1008268	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1008269	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10132333	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10134108	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs10135022	0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10137743	1.00[CHB][hapmap]
rs10138699	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10139379	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10142205	0.81[ASN][1000 genomes]
rs10143061	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10146717	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs10150329	0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10151764	1.00[CHB][hapmap];0.83[AMR][1000 genomes]
rs10438064	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs10438065	0.86[ASN][1000 genomes]
rs10438066	0.86[ASN][1000 genomes]
rs1045842	0.84[AMR][1000 genomes]
rs10782384	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11623599	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs11623642	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs11623737	0.82[AMR][1000 genomes]
rs11624716	1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12885503	1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1543494	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1952554	1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1983768	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1998330	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1998331	0.85[EUR][1000 genomes]
rs1998332	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs1999139	0.84[AMR][1000 genomes]
rs2007434	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2065096	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2146062	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2149749	0.85[AMR][1000 genomes]
rs2181125	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2295866	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3762156	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3762157	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3762158	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3762159	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4144189	1.00[CHB][hapmap]
rs4982445	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4982446	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs58685090	0.83[ASN][1000 genomes]
rs61695584	0.86[ASN][1000 genomes]
rs6571770	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6571797	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs6571826	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7145002	0.82[CEU][hapmap]
rs7147024	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7148741	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs7152833	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7155123	1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7160488	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8004294	1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8004388	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8007893	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs8008670	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8009789	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8011945	0.82[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs8017451	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8017630	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8018369	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8020149	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8022395	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8022755	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs927412	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9322978	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:21 , 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	nsv916319	chr14:21507092-21896590	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
4	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
5	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
6	nsv530770	chr14:21526410-21852363	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
7	nsv1043570	chr14:21575068-21899964	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
8	nsv541977	chr14:21575068-21899964	Active TSS Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
9	nsv1048032	chr14:21602341-21847247	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
10	nsv541978	chr14:21602341-21847247	Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
11	nsv948957	chr14:21616875-21928338	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
12	nsv1044822	chr14:21659344-21860081	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
13	esv1825348	chr14:21691941-21829404	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
14	nsv1051407	chr14:21692670-21907366	Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
15	nsv541984	chr14:21692670-21907366	Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
16	nsv530010	chr14:21692670-21923767	Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
17	nsv428617	chr14:21721165-21871164	Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
18	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
19	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
20	nsv933465	chr14:21819353-21821015	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
21	nsv976317	chr14:21819802-21820890	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region miRNA target site	2 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	chr14:21803600-21820200	Weak transcription	K562	blood
2	chr14:21811800-21820200	Weak transcription	Gastric	stomach
3	chr14:21815600-21820200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:21816400-21820800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr14:21817000-21820200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr14:21817000-21820200	Weak transcription	Pancreas	Pancrea
7	chr14:21817600-21820600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr14:21817600-21822400	Weak transcription	Stomach Mucosa	stomach
9	chr14:21817800-21820200	Weak transcription	Colonic Mucosa	Colon
10	chr14:21817800-21825400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:21818000-21820200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr14:21818000-21843000	Strong transcription	A549	lung
13	chr14:21818000-21848800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr14:21818000-21849200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr14:21818200-21841200	Strong transcription	Fetal Brain Female	brain
16	chr14:21818400-21820200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:21818600-21820200	Strong transcription	Primary neutrophils fromperipheralblood	blood
18	chr14:21818600-21820200	Weak transcription	Brain Angular Gyrus	brain
19	chr14:21818600-21838800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:21818600-21841000	Strong transcription	HMEC	breast
21	chr14:21818600-21841200	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr14:21818800-21820200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr14:21818800-21820200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:21818800-21820200	Strong transcription	GM12878-XiMat	blood
25	chr14:21818800-21820800	Strong transcription	Liver	Liver
26	chr14:21818800-21823200	Strong transcription	Brain Substantia Nigra	brain
27	chr14:21818800-21836600	Strong transcription	Spleen	Spleen
28	chr14:21818800-21838400	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr14:21818800-21838600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr14:21818800-21839600	Strong transcription	Thymus	Thymus
31	chr14:21818800-21840600	Strong transcription	Rectal Mucosa Donor 29	rectum
32	chr14:21818800-21840800	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr14:21818800-21841000	Strong transcription	Brain Anterior Caudate	brain
34	chr14:21818800-21841200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr14:21818800-21841200	Strong transcription	Duodenum Mucosa	Duodenum
36	chr14:21818800-21841200	Strong transcription	Left Ventricle	heart
37	chr14:21818800-21841400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr14:21818800-21841400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr14:21818800-21841400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr14:21818800-21841400	Strong transcription	NHEK	skin
41	chr14:21818800-21841600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr14:21818800-21841600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr14:21818800-21841600	Strong transcription	Fetal Thymus	thymus
44	chr14:21818800-21841600	Strong transcription	Skeletal Muscle Female	skeletal muscle
45	chr14:21818800-21841600	Strong transcription	HSMM	muscle
46	chr14:21818800-21841800	Strong transcription	H1 Cell Line	embryonic stem cell
47	chr14:21818800-21841800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr14:21818800-21841800	Strong transcription	Fetal Muscle Leg	muscle
49	chr14:21818800-21842800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr14:21818800-21843200	Strong transcription	HUES48 Cell Line	embryonic stem cell

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