Variant report

Variant	rs73954970
Chromosome Location	chr2:111916531-111916532
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:111914389..111917112-chr2:111917290..111919823,3	MCF-7	breast:
2	chr2:111911560..111915041-chr2:111915359..111919056,5	K562	blood:
3	chr2:111914059..111916689-chr2:111925221..111929362,3	MCF-7	breast:
4	chr2:111915696..111917657-chr2:111917984..111921314,3	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs55675010	0.85[AFR][1000 genomes]
rs55798204	1.00[AFR][1000 genomes]
rs56038719	1.00[AFR][1000 genomes]
rs56205524	0.85[AFR][1000 genomes]
rs56354417	0.85[AFR][1000 genomes]
rs56405634	1.00[AFR][1000 genomes]
rs57293149	0.85[AFR][1000 genomes]
rs61584108	0.85[AFR][1000 genomes]
rs61634451	0.85[AFR][1000 genomes]
rs73954940	0.85[AFR][1000 genomes]
rs73954955	0.85[AFR][1000 genomes]
rs73954956	0.85[AFR][1000 genomes]
rs73954957	0.85[AFR][1000 genomes]
rs73954960	0.85[AFR][1000 genomes]
rs73954961	0.85[AFR][1000 genomes]
rs73954968	1.00[AFR][1000 genomes]
rs73954969	1.00[AFR][1000 genomes]
rs73954972	0.85[AFR][1000 genomes]
rs73954973	0.85[AFR][1000 genomes]
rs73954974	0.85[AFR][1000 genomes]
rs73954978	0.85[AFR][1000 genomes]
rs73954981	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv874838	chr2:111376870-112046226	Weak transcription Strong transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv834331	chr2:111812139-112004678	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	esv1803356	chr2:111899783-112662597	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS 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	44 gene(s)	inside rSNPs	diseases
4	nsv428402	chr2:111899783-112662597	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
5	esv1801950	chr2:111899783-112746937	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
6	esv2757825	chr2:111899783-112746937	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
7	esv2759083	chr2:111899783-112746937	Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111881800-111919800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr2:111884800-111925400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr2:111893600-111916800	Weak transcription	HSMM	muscle
4	chr2:111893600-111918600	Weak transcription	Colon Smooth Muscle	Colon
5	chr2:111894200-111917200	Weak transcription	NH-A	brain
6	chr2:111897800-111916600	Weak transcription	Psoas Muscle	Psoas
7	chr2:111898800-111920600	Weak transcription	Fetal Kidney	kidney
8	chr2:111904400-111920800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:111906400-111919600	Strong transcription	HUES48 Cell Line	embryonic stem cell
10	chr2:111906600-111927000	Weak transcription	Rectal Smooth Muscle	rectum
11	chr2:111906800-111918200	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr2:111907400-111917000	Strong transcription	Placenta	Placenta
13	chr2:111907400-111920000	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr2:111907400-111920200	Strong transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:111907600-111919200	Strong transcription	Fetal Intestine Small	intestine
16	chr2:111907600-111919200	Strong transcription	Fetal Stomach	stomach
17	chr2:111907600-111919800	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr2:111908000-111917200	Strong transcription	Duodenum Mucosa	Duodenum
19	chr2:111908000-111920000	Strong transcription	Fetal Intestine Large	intestine
20	chr2:111909200-111919200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr2:111909400-111916600	Strong transcription	Fetal Muscle Leg	muscle
22	chr2:111909600-111918600	Weak transcription	Fetal Brain Male	brain
23	chr2:111909600-111922600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr2:111910000-111925200	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr2:111910200-111916600	Weak transcription	Right Ventricle	heart
26	chr2:111910200-111916600	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr2:111910200-111917200	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr2:111910200-111917400	Weak transcription	NHLF	lung
29	chr2:111910200-111922800	Weak transcription	Aorta	Aorta
30	chr2:111910400-111916800	Weak transcription	Fetal Heart	heart
31	chr2:111910400-111919600	Weak transcription	Small Intestine	intestine
32	chr2:111910400-111922400	Weak transcription	Ovary	ovary
33	chr2:111910600-111918000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr2:111911400-111919000	Weak transcription	K562	blood
35	chr2:111911600-111918600	Weak transcription	Colonic Mucosa	Colon
36	chr2:111912000-111916800	Strong transcription	Fetal Muscle Trunk	muscle
37	chr2:111912400-111917200	Strong transcription	Hela-S3	cervix
38	chr2:111912400-111919800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr2:111912600-111916800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr2:111912600-111917000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr2:111912800-111919600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
42	chr2:111913400-111916600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:111913400-111916600	Weak transcription	Left Ventricle	heart
44	chr2:111913400-111916600	Weak transcription	Right Atrium	heart
45	chr2:111913400-111916800	Weak transcription	Gastric	stomach
46	chr2:111913600-111917200	Enhancers	Primary B cells from cord blood	blood
47	chr2:111913600-111917200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr2:111913600-111917200	Weak transcription	A549	lung
49	chr2:111913600-111919000	Weak transcription	Stomach Mucosa	stomach
50	chr2:111913800-111917000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links