Variant report

Variant	rs73427430
Chromosome Location	chr8:131442993-131442994
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:131441459..131443636-chr8:131445223..131447112,2	K562	blood:
2	chr8:131442973..131445344-chr8:131451202..131452908,2	MCF-7	breast:
3	chr8:131442808..131445703-chr8:131454691..131456819,2	MCF-7	breast:
4	chr8:131442195..131445335-chr8:131452635..131456457,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000153317	Chromatin interaction

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

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

rs_ID	r²[population]
rs57129132	0.83[AFR][1000 genomes]
rs59496740	0.83[AFR][1000 genomes]
rs73409308	1.00[AFR][1000 genomes]
rs73409312	1.00[AFR][1000 genomes]
rs73409315	0.83[AFR][1000 genomes]
rs73409341	1.00[AFR][1000 genomes]
rs73409344	1.00[AFR][1000 genomes]
rs73409350	1.00[AFR][1000 genomes]
rs73409355	0.83[AFR][1000 genomes]
rs73417906	1.00[AFR][1000 genomes]
rs73417935	1.00[AFR][1000 genomes]
rs73417940	0.83[AFR][1000 genomes]
rs73417948	1.00[AFR][1000 genomes]
rs73417951	1.00[AFR][1000 genomes]
rs73425601	1.00[AFR][1000 genomes]
rs73427358	0.83[AFR][1000 genomes]
rs73427361	0.83[AFR][1000 genomes]
rs73427414	1.00[AFR][1000 genomes]
rs73427426	1.00[AFR][1000 genomes]
rs73427428	1.00[AFR][1000 genomes]
rs73427429	1.00[AFR][1000 genomes]
rs73427432	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869334	chr8:131025093-131651487	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv915580	chr8:131025093-131667578	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv533085	chr8:131042781-131755007	Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv3321933	chr8:131438670-131443068	Enhancers ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	esv3324025	chr8:131439370-131443168	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:131429000-131446800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr8:131429000-131454800	Weak transcription	Aorta	Aorta
3	chr8:131429200-131444800	Weak transcription	HSMMtube	muscle
4	chr8:131429400-131447200	Weak transcription	Gastric	stomach
5	chr8:131429400-131449400	Weak transcription	Brain Hippocampus Middle	brain
6	chr8:131429600-131453800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr8:131432000-131445000	Weak transcription	Psoas Muscle	Psoas
8	chr8:131432200-131449400	Weak transcription	Ovary	ovary
9	chr8:131434000-131443000	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr8:131434200-131443000	Weak transcription	Brain Substantia Nigra	brain
11	chr8:131434600-131447000	Weak transcription	HSMM	muscle
12	chr8:131434600-131447200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:131434800-131453000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr8:131435000-131446600	Weak transcription	NH-A	brain
15	chr8:131435200-131443400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr8:131435800-131443200	Weak transcription	Stomach Smooth Muscle	stomach
17	chr8:131437000-131449800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr8:131437000-131449800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr8:131437800-131443400	Weak transcription	Primary B cells from peripheral blood	blood
20	chr8:131438200-131443600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr8:131438200-131451400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:131438800-131451400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:131439200-131443000	Weak transcription	Placenta	Placenta
24	chr8:131439200-131443200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr8:131439200-131449800	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr8:131439200-131450200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr8:131439400-131447400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:131439400-131450000	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr8:131439600-131447000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr8:131440800-131443200	Strong transcription	A549	lung
31	chr8:131440800-131443600	Strong transcription	Cortex derived primary cultured neurospheres	brain
32	chr8:131440800-131444000	Enhancers	Right Ventricle	heart
33	chr8:131440800-131445800	Weak transcription	HepG2	liver
34	chr8:131441000-131443000	Weak transcription	Fetal Kidney	kidney
35	chr8:131441000-131444000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr8:131441000-131444000	Enhancers	NHDF-Ad	bronchial
37	chr8:131441000-131446800	Weak transcription	Pancreas	Pancrea
38	chr8:131441000-131449600	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr8:131441000-131449800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr8:131441000-131450600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr8:131441200-131443600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr8:131441200-131453400	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr8:131441400-131443000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr8:131441400-131443400	Strong transcription	Fetal Brain Female	brain
45	chr8:131441600-131443000	Strong transcription	Fetal Muscle Trunk	muscle
46	chr8:131441600-131443400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr8:131441600-131443600	Strong transcription	Hela-S3	cervix
48	chr8:131441600-131444200	Strong transcription	HMEC	breast
49	chr8:131441800-131443200	Genic enhancers	NHEK	skin
50	chr8:131441800-131443800	Enhancers	Adipose Nuclei	Adipose

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links