Variant report

Variant	rs4150982
Chromosome Location	chr19:40933487-40933488
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr19:40932720-40933684	HepG2	liver:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40919789..40935162-chr19:40946854..40955873,58	MCF-7	breast:
2	chr19:40929000..40933496-chr19:40948111..40953156,29	MCF-7	breast:
3	chr19:40930494..40933522-chr19:41110007..41112597,3	K562	blood:
4	chr19:40929942..40935093-chr19:40947472..40955743,23	K562	blood:
5	chr19:40929630..40934621-chr19:40969030..40973237,9	K562	blood:
6	chr19:40925098..40933993-chr19:40944045..40956524,41	K562	blood:
7	chr19:40930456..40933734-chr19:41119113..41120830,3	K562	blood:

No data

Variant related genes	Relation type
SERTAD1	TF binding region
ENSG00000167565	Chromatin interaction
ENSG00000160460	Chromatin interaction
ENSG00000090006	Chromatin interaction
ENSG00000268366	Chromatin interaction
ENSG00000090013	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10423800	1.00[EUR][1000 genomes]
rs268682	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs366973	1.00[EUR][1000 genomes]
rs398162	1.00[EUR][1000 genomes]
rs400195	1.00[EUR][1000 genomes]
rs403842	1.00[EUR][1000 genomes]
rs4150980	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57554707	1.00[EUR][1000 genomes]
rs8112927	1.00[EUR][1000 genomes]
rs922216	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9630860	1.00[EUR][1000 genomes]
rs9630868	1.00[EUR][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	esv1826663	chr19:40529943-41023601	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv833831	chr19:40796740-40960865	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
3	nsv911706	chr19:40842529-40969203	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
4	nsv911707	chr19:40855255-40948202	Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
5	nsv911708	chr19:40855255-40982375	Weak transcription Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
6	esv1830682	chr19:40880127-41270055	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer 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 target site	139 gene(s)	inside rSNPs	diseases
7	nsv911709	chr19:40928944-41060616	Bivalent/Poised TSS Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40932400-40938400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr19:40932600-40934800	Weak transcription	Esophagus	oesophagus
3	chr19:40932600-40935000	Weak transcription	Placenta	Placenta
4	chr19:40932600-40937200	Weak transcription	Fetal Lung	lung
5	chr19:40932600-40937400	Weak transcription	Fetal Stomach	stomach
6	chr19:40932600-40937600	Weak transcription	Fetal Muscle Leg	muscle
7	chr19:40932600-40937800	Weak transcription	Fetal Heart	heart
8	chr19:40932600-40937800	Weak transcription	Fetal Kidney	kidney
9	chr19:40932600-40938000	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr19:40932600-40938000	Weak transcription	Adipose Nuclei	Adipose
11	chr19:40932600-40938000	Weak transcription	Fetal Intestine Small	intestine
12	chr19:40932600-40938200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr19:40932600-40938400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr19:40932600-40938400	Weak transcription	Liver	Liver
15	chr19:40932600-40938400	Weak transcription	Brain Hippocampus Middle	brain
16	chr19:40932600-40938400	Weak transcription	Duodenum Mucosa	Duodenum
17	chr19:40932600-40938400	Weak transcription	Stomach Smooth Muscle	stomach
18	chr19:40932600-40938400	Weak transcription	HSMM	muscle
19	chr19:40932600-40938600	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr19:40932600-40938600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:40932600-40938600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr19:40932600-40938600	Weak transcription	Right Atrium	heart
23	chr19:40932600-40939000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr19:40932600-40939200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr19:40932600-40939200	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr19:40932600-40939200	Weak transcription	Primary T cells from cord blood	blood
27	chr19:40932600-40939200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr19:40932600-40939200	Weak transcription	GM12878-XiMat	blood
29	chr19:40933000-40935200	Enhancers	HepG2	liver
30	chr19:40933000-40937600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr19:40933000-40938600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:40933200-40937600	Weak transcription	Fetal Muscle Trunk	muscle
33	chr19:40933200-40937800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr19:40933200-40938000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr19:40933200-40938400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr19:40933200-40938600	Weak transcription	Colonic Mucosa	Colon
37	chr19:40933200-40938600	Weak transcription	Pancreas	Pancrea
38	chr19:40933200-40939200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr19:40933400-40937400	Weak transcription	K562	blood
40	chr19:40933400-40937800	Weak transcription	A549	lung
41	chr19:40933400-40937800	Weak transcription	Hela-S3	cervix
42	chr19:40933400-40938400	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr19:40933400-40938400	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr19:40933400-40938600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr19:40933400-40938600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr19:40933400-40938600	Weak transcription	HMEC	breast

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