Variant report

Variant	rs66794022
Chromosome Location	chr6:114080743-114080744
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:114080493..114083851-chr6:114178361..114180752,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155130	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs13193860	0.81[AMR][1000 genomes]
rs13200525	0.84[AMR][1000 genomes]
rs13201785	0.81[AMR][1000 genomes]
rs13204232	0.84[AMR][1000 genomes]
rs13207760	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13208937	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13209808	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs13220044	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17789266	0.84[AMR][1000 genomes]
rs2695454	0.81[AMR][1000 genomes]
rs34206951	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs34736881	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34753135	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34832025	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34950886	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs35384158	0.91[ASN][1000 genomes]
rs35409527	0.81[AMR][1000 genomes]
rs35470926	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs35542449	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35902942	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs36000791	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62417365	0.82[ASN][1000 genomes]
rs71541084	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72960759	0.84[AMR][1000 genomes];0.82[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	nsv1021774	chr6:114063971-114407280	Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv538422	chr6:114063971-114407280	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv464023	chr6:114071720-114114057	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
4	nsv604532	chr6:114071720-114114057	Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114077000-114085000	Weak transcription	Psoas Muscle	Psoas
2	chr6:114077600-114080800	Enhancers	GM12878-XiMat	blood
3	chr6:114077600-114083800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:114077600-114084600	Weak transcription	HSMM	muscle
5	chr6:114079200-114081400	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr6:114079400-114080800	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr6:114079600-114080800	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr6:114079600-114080800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:114079800-114080800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:114080000-114080800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr6:114080200-114080800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:114080400-114080800	Enhancers	Primary B cells from cord blood	blood
13	chr6:114080400-114080800	Enhancers	Primary hematopoietic stem cells	blood
14	chr6:114080400-114084200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:114080400-114085000	Weak transcription	A549	lung
16	chr6:114080600-114083400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr6:114080600-114083600	Weak transcription	HUVEC	blood vessel
18	chr6:114080600-114083800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:114080600-114083800	Weak transcription	Fetal Lung	lung
20	chr6:114080600-114083800	Weak transcription	Osteobl	bone
21	chr6:114080600-114084000	Weak transcription	Placenta	Placenta

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