Variant report

Variant	rs10132667
Chromosome Location	chr14:105553351-105553352
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105439903..105442825-chr14:105553149..105554969,2	MCF-7	breast:
2	chr14:105444537..105448423-chr14:105550882..105555382,4	MCF-7	breast:
3	chr14:105399436..105400309-chr14:105552835..105553556,2	MCF-7	breast:
4	chr14:105552235..105554666-chr14:105628025..105629965,2	MCF-7	breast:
5	chr14:105441809..105443191-chr14:105552782..105553787,10	MCF-7	breast:
6	chr14:105541634..105546414-chr14:105550039..105556215,6	MCF-7	breast:
7	chr14:105362768..105363662-chr14:105553187..105553782,2	MCF-7	breast:
8	chr14:105550862..105553369-chr14:105650448..105653112,3	MCF-7	breast:
9	chr14:105553187..105555561-chr14:105589136..105591325,2	MCF-7	breast:
10	chr14:105441876..105443118-chr14:105552847..105553563,3	MCF-7	breast:
11	chr14:105539179..105546592-chr14:105547833..105554421,6	K562	blood:
12	chr14:105551472..105556224-chr14:105557135..105561197,4	K562	blood:
13	chr14:105511795..105512498-chr14:105553098..105553751,3	MCF-7	breast:
14	chr14:105552947..105555057-chr14:105555509..105557119,2	K562	blood:
15	chr14:105441542..105446524-chr14:105551776..105555830,4	K562	blood:
16	chr14:105444336..105445214-chr14:105553267..105554067,2	K562	blood:
17	chr14:105487065..105489354-chr14:105552819..105555083,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000185567	Chromatin interaction
ENSG00000170779	Chromatin interaction
ENSG00000257556	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10130160	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10149404	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28407946	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28535454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28634831	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58358810	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59176538	0.87[AMR][1000 genomes]
rs59819555	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60165074	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61043267	0.87[AMR][1000 genomes]
rs61556877	0.87[AMR][1000 genomes]
rs74092711	1.00[EUR][1000 genomes]
rs74092712	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1828345	chr14:105100787-105803170	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
2	nsv542225	chr14:105133688-105803170	Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	nsv542227	chr14:105157572-105803170	Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	147 gene(s)	inside rSNPs	diseases
4	nsv917106	chr14:105339195-105803170	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	94 gene(s)	inside rSNPs	diseases
5	nsv456457	chr14:105404384-105555396	Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
6	nsv566141	chr14:105404384-105555396	Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
7	nsv902421	chr14:105410183-105574843	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
8	nsv902422	chr14:105420215-105803170	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
9	nsv1052190	chr14:105423761-105722653	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
10	nsv902423	chr14:105430890-105803170	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
11	nsv1042303	chr14:105435649-105633544	Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
12	nsv456458	chr14:105435649-105690092	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
13	nsv566150	chr14:105435649-105690092	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
14	nsv902424	chr14:105436222-105803170	Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	86 gene(s)	inside rSNPs	diseases
15	nsv566151	chr14:105459140-105555396	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
16	nsv456459	chr14:105459140-105617891	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
17	nsv566152	chr14:105459140-105617891	Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
18	nsv902425	chr14:105463936-105690092	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
19	nsv9175	chr14:105496509-105688941	Enhancers Strong transcription Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
20	nsv902427	chr14:105508577-105585347	Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
21	esv2758369	chr14:105513346-105803170	Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
22	esv2760014	chr14:105513346-105803170	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
23	nsv902428	chr14:105531945-105555396	Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105542400-105553400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:105551600-105559000	Enhancers	Placenta	Placenta
3	chr14:105552200-105553400	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr14:105552400-105553400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
5	chr14:105552800-105553400	Enhancers	Primary B cells from cord blood	blood
6	chr14:105552800-105553800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr14:105552800-105553800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr14:105552800-105553800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr14:105552800-105554000	Active TSS	Breast Myoepithelial Primary Cells	Breast
10	chr14:105552800-105554000	Flanking Active TSS	HMEC	breast
11	chr14:105552800-105554000	Active TSS	NH-A	brain
12	chr14:105552800-105554000	Active TSS	NHLF	lung
13	chr14:105552800-105554200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr14:105552800-105554200	Bivalent Enhancer	Fetal Brain Male	brain
15	chr14:105553000-105553400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
16	chr14:105553000-105553400	Enhancers	Primary hematopoietic stem cells	blood
17	chr14:105553000-105553400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
18	chr14:105553000-105553400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr14:105553000-105553400	Bivalent Enhancer	Liver	Liver
20	chr14:105553000-105553400	Enhancers	Brain Angular Gyrus	brain
21	chr14:105553000-105553400	Active TSS	Brain Cingulate Gyrus	brain
22	chr14:105553000-105553400	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
23	chr14:105553000-105553400	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr14:105553000-105553400	Active TSS	Duodenum Smooth Muscle	Duodenum
25	chr14:105553000-105553400	Enhancers	Gastric	stomach
26	chr14:105553000-105553400	Enhancers	Lung	lung
27	chr14:105553000-105553400	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
28	chr14:105553000-105553400	Bivalent Enhancer	Stomach Mucosa	stomach
29	chr14:105553000-105553400	Bivalent/Poised TSS	Thymus	Thymus
30	chr14:105553000-105553400	Active TSS	Hela-S3	cervix
31	chr14:105553000-105553600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:105553000-105553600	Bivalent Enhancer	Brain Substantia Nigra	brain
33	chr14:105553000-105553600	Enhancers	Dnd41	blood
34	chr14:105553000-105553800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chr14:105553000-105553800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
36	chr14:105553000-105553800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:105553000-105553800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
38	chr14:105553000-105553800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
39	chr14:105553000-105553800	Active TSS	Sigmoid Colon	Sigmoid Colon
40	chr14:105553000-105553800	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
41	chr14:105553000-105553800	Active TSS	HSMM	muscle
42	chr14:105553000-105553800	Active TSS	HSMMtube	muscle
43	chr14:105553000-105554000	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
44	chr14:105553000-105554000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
45	chr14:105553000-105554000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr14:105553000-105554000	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr14:105553000-105554200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:105553000-105554200	Active TSS	H9 Cell Line	embryonic stem cell
49	chr14:105553000-105554200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr14:105553000-105554200	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon

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