Variant report

Variant	rs61272099
Chromosome Location	chr6:11426310-11426311
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:11355983..11357680-chr6:11424097..11426477,2	MCF-7	breast:
2	chr6:11231660..11236076-chr6:11425416..11429561,7	MCF-7	breast:
3	chr6:11423621..11427169-chr6:11433589..11436531,3	MCF-7	breast:
4	chr6:11420850..11423411-chr6:11425046..11427068,2	K562	blood:
5	chr6:11424121..11426419-chr6:11426537..11429403,3	MCF-7	breast:
6	chr6:11424461..11426917-chr6:11430880..11433034,2	K562	blood:
7	chr6:11230046..11231611-chr6:11426271..11428690,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000111859	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11963692	1.00[ASN][1000 genomes]
rs6935901	0.96[ASN][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	nsv1021078	chr6:10819083-11558560	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers 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 target site	47 gene(s)	inside rSNPs	diseases
2	nsv538135	chr6:10819083-11558560	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv432848	chr6:11371614-11560114	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	esv3340894	chr6:11425466-11429864	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11417800-11426400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:11420200-11427400	Weak transcription	Aorta	Aorta
3	chr6:11423200-11431800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:11423400-11427800	Enhancers	A549	lung
5	chr6:11423400-11430200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:11423400-11430400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr6:11423400-11430600	Enhancers	NHDF-Ad	bronchial
8	chr6:11423400-11434200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr6:11423600-11427600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:11423600-11430400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr6:11423600-11432200	Enhancers	Muscle Satellite Cultured Cells	--
12	chr6:11423600-11435200	Enhancers	HepG2	liver
13	chr6:11423800-11427000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr6:11423800-11427400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:11423800-11435600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr6:11424000-11427000	Enhancers	Fetal Kidney	kidney
17	chr6:11424000-11427600	Weak transcription	Esophagus	oesophagus
18	chr6:11424000-11427600	Weak transcription	Left Ventricle	heart
19	chr6:11424000-11428600	Enhancers	Lung	lung
20	chr6:11424000-11429600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr6:11424000-11429600	Enhancers	Stomach Mucosa	stomach
22	chr6:11424000-11430400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr6:11424600-11430600	Enhancers	Placenta	Placenta
24	chr6:11424600-11430800	Enhancers	Osteobl	bone
25	chr6:11424800-11426800	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:11424800-11428000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr6:11424800-11430800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:11425000-11426800	Weak transcription	Fetal Stomach	stomach
29	chr6:11425000-11427400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr6:11425000-11427400	Weak transcription	Gastric	stomach
31	chr6:11425000-11427800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr6:11425000-11428200	Weak transcription	GM12878-XiMat	blood
33	chr6:11425000-11432200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr6:11425200-11429000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr6:11425200-11429800	Enhancers	HUVEC	blood vessel
36	chr6:11425400-11427400	Weak transcription	Right Atrium	heart
37	chr6:11425600-11426400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr6:11425600-11426600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr6:11425600-11426600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
40	chr6:11425600-11426600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:11425600-11426600	Enhancers	HSMM	muscle
42	chr6:11425600-11427200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:11425600-11427600	Enhancers	Fetal Lung	lung
44	chr6:11425600-11430600	Enhancers	NHLF	lung
45	chr6:11425600-11436200	Enhancers	Adipose Nuclei	Adipose
46	chr6:11425800-11426400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr6:11425800-11426400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr6:11425800-11426600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr6:11425800-11426600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr6:11425800-11427000	Enhancers	H9 Cell Line	embryonic stem cell

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