Variant report

Variant	rs571939107
Chromosome Location	chr14:105443986-105443987
allele	A/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:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:105397847..105399946-chr14:105442912..105445708,2	MCF-7	breast:
2	chr14:105261681..105264088-chr14:105440432..105444268,3	MCF-7	breast:
3	chr14:105442748..105444564-chr14:105532745..105535377,2	MCF-7	breast:
4	chr14:105441981..105444790-chr14:105863308..105866164,2	MCF-7	breast:
5	chr14:105443757..105444660-chr14:105510431..105511022,2	MCF-7	breast:
6	chr14:105440890..105445623-chr14:105485614..105489562,6	MCF-7	breast:
7	chr14:105443928..105445902-chr14:105765680..105767557,2	MCF-7	breast:
8	chr14:105329992..105332567-chr14:105443160..105445644,3	MCF-7	breast:
9	chr14:105442175..105444429-chr14:105444520..105447131,2	K562	blood:
10	chr14:105440794..105444073-chr14:105510721..105514386,4	K562	blood:
11	chr14:105265965..105267568-chr14:105442748..105445496,2	MCF-7	breast:
12	chr14:105389558..105391968-chr14:105443207..105445217,2	MCF-7	breast:
13	chr14:105442698..105444680-chr14:105485412..105488707,3	K562	blood:
14	chr14:105441584..105444154-chr14:105510721..105515062,5	K562	blood:
15	chr14:105443512..105446839-chr14:105449245..105453481,5	K562	blood:
16	chr14:105441389..105444198-chr14:105485839..105488707,2	K562	blood:
17	chr14:105441966..105444390-chr14:105493852..105497490,3	MCF-7	breast:
18	chr14:105433937..105458439-chr14:105476653..105492775,70	MCF-7	breast:
19	chr14:105442218..105444582-chr14:105521648..105524128,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000170779	Chromatin interaction
ENSG00000166428	Chromatin interaction
ENSG00000140104	Chromatin interaction
ENSG00000226174	Chromatin interaction
ENSG00000185567	Chromatin interaction
ENSG00000183484	Chromatin interaction
ENSG00000185024	Chromatin interaction
ENSG00000179627	Chromatin interaction
ENSG00000179364	Chromatin interaction
ENSG00000099814	Chromatin interaction
ENSG00000142208	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053591	chr14:105024558-105475931	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
2	nsv542224	chr14:105024558-105475931	Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	nsv902419	chr14:105381763-105494262	Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
8	nsv1049253	chr14:105384959-105471855	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
9	nsv542228	chr14:105390569-105459912	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
10	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
11	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
12	nsv1036224	chr14:105404755-105470333	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
13	nsv902420	chr14:105410183-105494262	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
14	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
15	nsv1438	chr14:105412728-105457581	Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	esv3355872	chr14:105443532-105446080	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
24	esv3389914	chr14:105443857-105446155	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases
25	esv3403786	chr14:105443932-105446780	Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105433000-105445400	Flanking Active TSS	Stomach Smooth Muscle	stomach
2	chr14:105434600-105444000	Weak transcription	Aorta	Aorta
3	chr14:105437400-105444000	Enhancers	Pancreas	Pancrea
4	chr14:105438000-105446800	Enhancers	Lung	lung
5	chr14:105439600-105445400	Enhancers	Spleen	Spleen
6	chr14:105440200-105444000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr14:105440400-105444000	Enhancers	Right Ventricle	heart
8	chr14:105440600-105444000	Bivalent Enhancer	Stomach Mucosa	stomach
9	chr14:105441600-105444000	Enhancers	Gastric	stomach
10	chr14:105441800-105444400	Bivalent Enhancer	Placenta	Placenta
11	chr14:105441800-105446800	Enhancers	Fetal Heart	heart
12	chr14:105442000-105444000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:105442000-105444000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
14	chr14:105442000-105444000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr14:105442200-105444000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr14:105442200-105444000	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
17	chr14:105442200-105444000	Enhancers	Liver	Liver
18	chr14:105442200-105444000	Enhancers	NH-A	brain
19	chr14:105442600-105444000	Flanking Active TSS	Hela-S3	cervix
20	chr14:105442800-105444000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
21	chr14:105442800-105444000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
22	chr14:105442800-105444000	Flanking Active TSS	NHEK	skin
23	chr14:105442800-105444400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr14:105443000-105444000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr14:105443000-105444000	Enhancers	Adipose Nuclei	Adipose
26	chr14:105443000-105444000	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
27	chr14:105443000-105444000	Weak transcription	HUVEC	blood vessel
28	chr14:105443000-105444000	Weak transcription	K562	blood
29	chr14:105443000-105444200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:105443000-105444400	Flanking Active TSS	HMEC	breast
31	chr14:105443000-105445600	Enhancers	Fetal Brain Male	brain
32	chr14:105443200-105444000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr14:105443200-105444200	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr14:105443200-105444200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr14:105443400-105444000	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr14:105443400-105444000	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
37	chr14:105443400-105444000	Enhancers	Brain Substantia Nigra	brain
38	chr14:105443400-105444200	Flanking Active TSS	Colon Smooth Muscle	Colon
39	chr14:105443400-105444200	Enhancers	Fetal Lung	lung
40	chr14:105443400-105444600	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
41	chr14:105443400-105444600	Flanking Active TSS	Esophagus	oesophagus
42	chr14:105443400-105444600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
43	chr14:105443600-105444000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr14:105443600-105444000	Bivalent Enhancer	Primary hematopoietic stem cells	blood
45	chr14:105443600-105444000	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
46	chr14:105443600-105444000	Flanking Bivalent TSS/Enh	Brain Hippocampus Middle	brain
47	chr14:105443600-105444000	Enhancers	Psoas Muscle	Psoas
48	chr14:105443600-105444000	Active TSS	HSMMtube	muscle
49	chr14:105443600-105444200	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
50	chr14:105443600-105444400	Bivalent Enhancer	Primary B cells from cord blood	blood

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