Variant report

Variant	rs74060252
Chromosome Location	chr14:70116380-70116381
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:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:70113887..70117052-chr14:70117331..70121263,5	K562	blood:
2	chr14:70108653..70111894-chr14:70113537..70117255,5	K562	blood:
3	chr14:70082796..70084596-chr14:70115953..70118660,2	MCF-7	breast:
4	chr14:70107632..70111411-chr14:70113640..70118051,5	MCF-7	breast:
5	chr14:70114480..70116769-chr14:70178429..70180282,2	MCF-7	breast:
6	chr14:70114857..70122560-chr14:70122603..70126754,12	MCF-7	breast:
7	chr14:70078253..70081194-chr14:70115455..70117698,3	MCF-7	breast:
8	chr14:70103316..70105220-chr14:70115351..70116992,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000100647	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11844465	1.00[EUR][1000 genomes]
rs11845465	1.00[EUR][1000 genomes]
rs11845528	1.00[EUR][1000 genomes]
rs11845658	1.00[EUR][1000 genomes]
rs11849924	1.00[EUR][1000 genomes]
rs12100899	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1803419	1.00[EUR][1000 genomes]
rs1957367	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55959724	1.00[EUR][1000 genomes]
rs56051240	1.00[EUR][1000 genomes]
rs56808476	1.00[EUR][1000 genomes]
rs56859443	1.00[EUR][1000 genomes]
rs57781039	1.00[EUR][1000 genomes]
rs58053579	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58140746	1.00[EUR][1000 genomes]
rs58503693	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58583730	1.00[EUR][1000 genomes]
rs60085780	1.00[EUR][1000 genomes]
rs60835679	1.00[EUR][1000 genomes]
rs61498582	1.00[EUR][1000 genomes]
rs61734222	1.00[EUR][1000 genomes]
rs61745930	1.00[EUR][1000 genomes]
rs7144597	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060205	1.00[EUR][1000 genomes]
rs74060220	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060234	1.00[EUR][1000 genomes]
rs74060251	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060256	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060258	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060261	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060263	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74060267	1.00[EUR][1000 genomes]
rs74060270	1.00[EUR][1000 genomes]
rs74060281	1.00[EUR][1000 genomes]
rs74060283	1.00[EUR][1000 genomes]
rs74060286	1.00[EUR][1000 genomes]
rs74060294	1.00[EUR][1000 genomes]
rs74060297	1.00[EUR][1000 genomes]
rs74060575	1.00[EUR][1000 genomes]
rs74061847	1.00[EUR][1000 genomes]
rs74061848	1.00[EUR][1000 genomes]
rs74061850	1.00[EUR][1000 genomes]
rs74061851	1.00[EUR][1000 genomes]
rs74061853	1.00[EUR][1000 genomes]
rs74061856	1.00[EUR][1000 genomes]
rs74061857	1.00[EUR][1000 genomes]
rs74061864	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049280	chr14:70036804-70172630	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv542124	chr14:70036804-70172630	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
4	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70104800-70125600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr14:70108400-70121200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr14:70109000-70121400	Enhancers	Stomach Mucosa	stomach
4	chr14:70109400-70121200	Enhancers	Small Intestine	intestine
5	chr14:70109600-70121200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
6	chr14:70109800-70125400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr14:70110000-70122800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr14:70110200-70121400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr14:70110400-70121400	Enhancers	Primary B cells from peripheral blood	blood
10	chr14:70110400-70124600	Weak transcription	Fetal Brain Female	brain
11	chr14:70112400-70117000	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr14:70112600-70123600	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr14:70113600-70120600	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr14:70113600-70121200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr14:70113800-70116400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr14:70113800-70116400	Enhancers	NHLF	lung
17	chr14:70113800-70116600	Enhancers	Osteobl	bone
18	chr14:70113800-70118000	Enhancers	Brain Angular Gyrus	brain
19	chr14:70113800-70118800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr14:70113800-70119400	Enhancers	Fetal Intestine Small	intestine
21	chr14:70113800-70119800	Enhancers	K562	blood
22	chr14:70113800-70121200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr14:70113800-70121200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr14:70114000-70116400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr14:70114000-70118400	Enhancers	Brain Substantia Nigra	brain
26	chr14:70114000-70118400	Enhancers	Fetal Muscle Leg	muscle
27	chr14:70114000-70118400	Enhancers	Fetal Stomach	stomach
28	chr14:70114000-70118800	Enhancers	Fetal Lung	lung
29	chr14:70114000-70119000	Enhancers	Primary T cells from cord blood	blood
30	chr14:70114000-70119200	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr14:70114000-70120000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr14:70114000-70120200	Enhancers	Skeletal Muscle Male	skeletal muscle
33	chr14:70114000-70120200	Enhancers	HUVEC	blood vessel
34	chr14:70114000-70121000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr14:70114000-70121000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr14:70114000-70121000	Enhancers	Adipose Nuclei	Adipose
37	chr14:70114000-70121200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr14:70114000-70121200	Enhancers	Right Ventricle	heart
39	chr14:70114000-70121200	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr14:70114000-70121200	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr14:70114000-70121400	Enhancers	Colonic Mucosa	Colon
42	chr14:70114000-70121800	Enhancers	Psoas Muscle	Psoas
43	chr14:70114000-70125000	Enhancers	Fetal Intestine Large	intestine
44	chr14:70114000-70126400	Enhancers	Left Ventricle	heart
45	chr14:70114200-70117000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr14:70114200-70118400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr14:70114200-70120400	Enhancers	Fetal Heart	heart
48	chr14:70114200-70121000	Enhancers	Primary T cells fromperipheralblood	blood
49	chr14:70114400-70117000	Flanking Active TSS	GM12878-XiMat	blood
50	chr14:70114400-70121200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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