Variant report

Variant	rs34195234
Chromosome Location	chr19:39446799-39446800
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:39445673-39446942	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:39445648..39448441-chr19:39522316..39524736,2	MCF-7	breast:
2	chr19:39442111..39444861-chr19:39446173..39448020,2	K562	blood:
3	chr19:39436055..39437829-chr19:39444775..39447617,2	MCF-7	breast:

Variant related genes	Relation type
FBXO17	TF binding region
ENSG00000269190	Chromatin interaction
ENSG00000161243	Chromatin interaction

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11669210	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11669212	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11880780	0.89[EUR][1000 genomes]
rs12974911	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12979835	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28479912	0.82[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057899	chr19:39088319-39475493	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv2762038	chr19:39444417-39455548	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39422600-39453000	Weak transcription	HSMMtube	muscle
2	chr19:39435800-39453000	Weak transcription	K562	blood
3	chr19:39438200-39447000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:39438400-39453000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr19:39439200-39452600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr19:39441000-39453000	Weak transcription	Aorta	Aorta
7	chr19:39441000-39459200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr19:39441200-39447600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr19:39441200-39448200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr19:39441200-39449200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr19:39441200-39449200	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr19:39441200-39450400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr19:39441200-39452800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr19:39441200-39453000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr19:39441200-39453000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr19:39441200-39453000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr19:39441200-39453000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr19:39441200-39453000	Weak transcription	Brain Hippocampus Middle	brain
19	chr19:39441200-39453000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr19:39441200-39453000	Weak transcription	Lung	lung
21	chr19:39441200-39453000	Weak transcription	Pancreas	Pancrea
22	chr19:39441200-39453000	Weak transcription	Osteobl	bone
23	chr19:39441200-39455800	Weak transcription	Psoas Muscle	Psoas
24	chr19:39441200-39459400	Weak transcription	Fetal Lung	lung
25	chr19:39441200-39465200	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr19:39441200-39465200	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr19:39441200-39465200	Weak transcription	NHLF	lung
28	chr19:39441200-39465400	Weak transcription	Right Atrium	heart
29	chr19:39441400-39447600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr19:39441400-39447600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr19:39441400-39452600	Weak transcription	Adipose Nuclei	Adipose
32	chr19:39441400-39452600	Weak transcription	Colon Smooth Muscle	Colon
33	chr19:39441400-39453000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr19:39441400-39453000	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr19:39441400-39453000	Weak transcription	Fetal Brain Male	brain
36	chr19:39441400-39453000	Weak transcription	Fetal Brain Female	brain
37	chr19:39441400-39453000	Weak transcription	Ovary	ovary
38	chr19:39441400-39453000	Weak transcription	Stomach Smooth Muscle	stomach
39	chr19:39441400-39453200	Weak transcription	Fetal Heart	heart
40	chr19:39441400-39462000	Weak transcription	Small Intestine	intestine
41	chr19:39441400-39465000	Weak transcription	HUVEC	blood vessel
42	chr19:39441600-39450200	Strong transcription	Fetal Stomach	stomach
43	chr19:39443400-39453000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr19:39443600-39452800	Weak transcription	Fetal Kidney	kidney
45	chr19:39443600-39453000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr19:39443600-39453000	Weak transcription	HSMM	muscle
47	chr19:39444600-39448200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr19:39444600-39452200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr19:39444800-39447600	Weak transcription	Fetal Muscle Trunk	muscle
50	chr19:39444800-39450200	Weak transcription	HepG2	liver

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