Variant report

Variant	rs55675010
Chromosome Location	chr2:111927144-111927145
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:111914059..111916689-chr2:111925221..111929362,3	MCF-7	breast:
2	chr2:111923929..111929033-chr2:111931509..111935010,6	K562	blood:
3	chr2:111926311..111928837-chr2:111932498..111934410,2	MCF-7	breast:
4	chr2:111920278..111923982-chr2:111925821..111929846,4	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs55751209	0.81[AFR][1000 genomes]
rs55798204	0.85[AFR][1000 genomes]
rs56038719	0.85[AFR][1000 genomes]
rs56205524	1.00[AFR][1000 genomes]
rs56405634	0.85[AFR][1000 genomes]
rs57293149	1.00[AFR][1000 genomes]
rs57730861	0.92[AFR][1000 genomes]
rs61634451	1.00[AFR][1000 genomes]
rs73954968	0.85[AFR][1000 genomes]
rs73954969	0.85[AFR][1000 genomes]
rs73954970	0.85[AFR][1000 genomes]
rs73954972	1.00[AFR][1000 genomes]
rs73954973	1.00[AFR][1000 genomes]
rs73954974	1.00[AFR][1000 genomes]
rs73954978	1.00[AFR][1000 genomes]
rs73954981	1.00[AFR][1000 genomes]
rs73954987	0.92[AFR][1000 genomes]
rs73954996	0.92[AFR][1000 genomes]
rs73954997	0.92[AFR][1000 genomes]
rs73956803	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:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111920600-111928000	Weak transcription	Brain Angular Gyrus	brain
2	chr2:111920800-111943000	Weak transcription	Right Ventricle	heart
3	chr2:111921200-111939400	Weak transcription	Right Atrium	heart
4	chr2:111921400-111928800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:111921400-111932200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:111922200-111928600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr2:111923000-111927800	Weak transcription	Colonic Mucosa	Colon
8	chr2:111923000-111929000	Weak transcription	Spleen	Spleen
9	chr2:111923400-111928000	Weak transcription	Primary B cells from cord blood	blood
10	chr2:111923800-111929600	Weak transcription	Aorta	Aorta
11	chr2:111924000-111929000	Weak transcription	Pancreas	Pancrea
12	chr2:111924000-111931600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr2:111924200-111927400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
14	chr2:111924400-111928200	Weak transcription	Stomach Smooth Muscle	stomach
15	chr2:111924400-111931600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:111924800-111927200	Enhancers	HSMMtube	muscle
17	chr2:111924800-111927200	Enhancers	K562	blood
18	chr2:111925000-111928400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr2:111925000-111932200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr2:111925000-111934000	Weak transcription	Fetal Intestine Large	intestine
21	chr2:111925200-111927200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr2:111925200-111927200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:111925200-111927200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr2:111925200-111927200	Enhancers	Gastric	stomach
25	chr2:111925200-111927200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr2:111925200-111928800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr2:111925400-111927400	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr2:111925400-111927800	Weak transcription	Ovary	ovary
29	chr2:111925400-111929000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:111925600-111927400	Weak transcription	Fetal Stomach	stomach
31	chr2:111925600-111927800	Weak transcription	Primary monocytes fromperipheralblood	blood
32	chr2:111925600-111929000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:111925600-111929000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr2:111925600-111929000	Weak transcription	Placenta Amnion	Placenta Amnion
35	chr2:111925600-111929000	Weak transcription	HepG2	liver
36	chr2:111925600-111931600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:111925800-111931600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr2:111926200-111928600	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:111926200-111931400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr2:111926200-111933400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr2:111926200-111934400	Weak transcription	Adipose Nuclei	Adipose
42	chr2:111926400-111927200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr2:111926400-111927200	Enhancers	Fetal Muscle Trunk	muscle
44	chr2:111926400-111927400	Enhancers	A549	lung
45	chr2:111926400-111930200	Weak transcription	Thymus	Thymus
46	chr2:111926600-111927200	Enhancers	Osteobl	bone
47	chr2:111926600-111927800	Weak transcription	Fetal Intestine Small	intestine
48	chr2:111926600-111928800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:111926600-111929000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr2:111926600-111929000	Weak transcription	Esophagus	oesophagus

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