Variant report

Variant	rs3838955
Chromosome Location	chr1:45244051-45244052
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:62)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:62 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr1:45243922-45247518	U87	brain:	n/a	n/a
2	POLR2A	chr1:45243842-45247542	A549	lung:	n/a	n/a
3	POLR2A	chr1:45240631-45247540	HepG2	liver:	n/a	n/a
4	POLR2A	chr1:45240526-45248028	GM12892	blood:	n/a	n/a
5	POLR2A	chr1:45243731-45244254	HepG2	liver:	n/a	n/a
6	HEY1	chr1:45243695-45244848	K562	blood:	n/a	n/a
7	POLR2A	chr1:45240483-45248016	GM12892	blood:	n/a	n/a
8	POLR2A	chr1:45240295-45248263	H1-hESC	embryonic stem cell:	n/a	n/a
9	POLR2A	chr1:45242580-45247462	H1-hESC	embryonic stem cell:	n/a	n/a
10	POLR2A	chr1:45240547-45249219	HepG2	liver:	n/a	n/a
11	POLR2A	chr1:45239529-45250168	SK-N-MC	brain:	n/a	n/a
12	POLR2A	chr1:45242522-45244255	SK-N-SH	brain:	n/a	n/a
13	POLR2A	chr1:45243722-45244316	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr1:45242766-45248217	GM12891	blood:	n/a	n/a
15	SPI1	chr1:45243792-45244290	HL-60	blood:	n/a	n/a
16	POLR2A	chr1:45243808-45245472	GM12878	blood:	n/a	n/a
17	HEY1	chr1:45243859-45244323	HepG2	liver:	n/a	n/a
18	POLR2A	chr1:45242928-45247383	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr1:45243703-45244313	GM12891	blood:	n/a	n/a
20	SPI1	chr1:45243811-45244272	HL-60	blood:	n/a	n/a
21	POLR2A	chr1:45243740-45244061	GM12878	blood:	n/a	n/a
22	POLR2A	chr1:45240546-45248272	GM12892	blood:	n/a	n/a
23	POLR2A	chr1:45243686-45245094	K562	blood:	n/a	n/a
24	POLR2A	chr1:45243851-45245038	K562	blood:	n/a	n/a
25	POLR2A	chr1:45243725-45244347	GM12878	blood:	n/a	n/a
26	POLR2A	chr1:45243904-45244217	HUVEC	blood vessel:	n/a	n/a
27	HEY1	chr1:45243835-45245001	HepG2	liver:	n/a	n/a
28	POLR2A	chr1:45242629-45247224	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr1:45243708-45245616	K562	blood:	n/a	n/a
30	POLR2A	chr1:45242979-45245039	K562	blood:	n/a	n/a
31	JUND	chr1:45244050-45244077	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr1:45242783-45244071	HUVEC	blood vessel:	n/a	n/a
33	POLR2A	chr1:45240508-45247317	GM12878	blood:	n/a	n/a
34	POLR2A	chr1:45240713-45247745	PFSK-1	brain:	n/a	n/a
35	POLR2A	chr1:45243001-45245051	HepG2	liver:	n/a	n/a
36	POLR2A	chr1:45243853-45247621	U87	brain:	n/a	n/a
37	POLR2A	chr1:45243822-45244109	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr1:45240271-45247480	K562	blood:	n/a	n/a
39	POLR2A	chr1:45243714-45245109	HL-60	blood:	n/a	n/a
40	POLR2A	chr1:45239953-45247379	K562	blood:	n/a	n/a
41	POLR2A	chr1:45243812-45244286	HCT-116	colon:	n/a	n/a
42	POLR2A	chr1:45243824-45245068	K562	blood:	n/a	n/a
43	POLR2A	chr1:45240502-45248124	GM12878	blood:	n/a	n/a
44	SPI1	chr1:45243932-45244136	K562	blood:	n/a	n/a
45	POLR2A	chr1:45243011-45245009	K562	blood:	n/a	n/a
46	POLR2A	chr1:45240324-45245069	PANC-1	pancreas:	n/a	n/a
47	POLR2A	chr1:45243896-45244589	HUVEC	blood vessel:	n/a	n/a
48	POLR2A	chr1:45240539-45248722	PFSK-1	brain:	n/a	n/a
49	POLR2A	chr1:45242917-45245129	HL-60	blood:	n/a	n/a
50	POLR2A	chr1:45240524-45248015	GM12891	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:45194515..45198714-chr1:45239955..45244261,13	MCF-7	breast:
2	chr1:45238319..45262026-chr1:45262351..45301953,358	K562	blood:
3	chr1:45239592..45244618-chr1:45476667..45480609,10	K562	blood:
4	chr1:45239135..45244789-chr1:45475459..45482236,15	K562	blood:
5	chr1:45239101..45240995-chr1:45242933..45244701,2	MCF-7	breast:
6	chr1:45239959..45246724-chr1:45282430..45287057,13	MCF-7	breast:
7	chr1:45239942..45244585-chr1:45273690..45277023,5	MCF-7	breast:

No data

Variant related genes	Relation type
SNORD38B	TF binding region
ENSG00000225721	TF binding region
ENSG00000222009	Chromatin interaction
ENSG00000173846	Chromatin interaction
ENSG00000200169	Chromatin interaction
ENSG00000188396	Chromatin interaction
ENSG00000126107	Chromatin interaction
ENSG00000142937	Chromatin interaction
ENSG00000117425	Chromatin interaction
ENSG00000126088	Chromatin interaction
ENSG00000202444	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533037	chr1:44361728-45333408	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	469 gene(s)	inside rSNPs	diseases
2	nsv998476	chr1:45001278-45311757	Flanking Active TSS Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
3	nsv534941	chr1:45001278-45311757	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	426 gene(s)	inside rSNPs	diseases
4	nsv1014894	chr1:45139123-45397943	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	414 gene(s)	inside rSNPs	diseases
5	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
6	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
7	nsv998871	chr1:45196587-45251179	Genic enhancers Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	171 gene(s)	inside rSNPs	diseases
8	nsv461406	chr1:45218542-45293518	Strong transcription Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
9	nsv546145	chr1:45218542-45293518	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
10	nsv870815	chr1:45233638-45318752	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	127 gene(s)	inside rSNPs	diseases
11	nsv947252	chr1:45242176-45258816	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	30 gene(s)	inside rSNPs	diseases
12	nsv945912	chr1:45243841-45248516	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45241600-45244200	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
2	chr1:45241600-45244200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr1:45241600-45244200	Transcr. at gene 5' and 3'	NHEK	skin
4	chr1:45241600-45244600	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
5	chr1:45241600-45244600	Transcr. at gene 5' and 3'	Muscle Satellite Cultured Cells	--
6	chr1:45241600-45244600	Transcr. at gene 5' and 3'	Dnd41	blood
7	chr1:45241600-45244800	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:45241800-45244200	Transcr. at gene 5' and 3'	NHLF	lung
9	chr1:45241800-45244800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr1:45241800-45244800	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:45241800-45244800	Transcr. at gene 5' and 3'	A549	lung
12	chr1:45241800-45244800	Transcr. at gene 5' and 3'	K562	blood
13	chr1:45241800-45245000	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
14	chr1:45242000-45244200	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr1:45242000-45244400	Transcr. at gene 5' and 3'	Primary hematopoietic stem cells short term culture	blood
16	chr1:45242000-45244600	Transcr. at gene 5' and 3'	HepG2	liver
17	chr1:45242000-45245000	Transcr. at gene 5' and 3'	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:45242000-45245000	Transcr. at gene 5' and 3'	Hela-S3	cervix
19	chr1:45242200-45244400	Transcr. at gene 5' and 3'	Breast Myoepithelial Primary Cells	Breast
20	chr1:45242200-45244600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:45242200-45244600	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr1:45242200-45244800	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
23	chr1:45242400-45244600	Transcr. at gene 5' and 3'	NH-A	brain
24	chr1:45242400-45244800	Genic enhancers	Stomach Mucosa	stomach
25	chr1:45242400-45246400	Strong transcription	Aorta	Aorta
26	chr1:45242600-45244200	Genic enhancers	Primary T cells fromperipheralblood	blood
27	chr1:45242600-45244200	Genic enhancers	Primary T helper cells fromperipheralblood	blood
28	chr1:45242600-45244200	Enhancers	Fetal Brain Male	brain
29	chr1:45242600-45244200	Genic enhancers	Pancreas	Pancrea
30	chr1:45242600-45244200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
31	chr1:45242600-45244200	Genic enhancers	Thymus	Thymus
32	chr1:45242600-45244200	Genic enhancers	Monocytes-CD14+_RO01746	blood
33	chr1:45242600-45244600	Genic enhancers	Primary B cells from peripheral blood	blood
34	chr1:45242600-45244600	Genic enhancers	Placenta	Placenta
35	chr1:45242600-45247600	Strong transcription	Brain Hippocampus Middle	brain
36	chr1:45242800-45244200	Genic enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr1:45242800-45244200	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr1:45242800-45244200	Genic enhancers	Adipose Nuclei	Adipose
39	chr1:45242800-45244600	Genic enhancers	Fetal Muscle Trunk	muscle
40	chr1:45242800-45244600	Strong transcription	Small Intestine	intestine
41	chr1:45242800-45244800	Genic enhancers	NHDF-Ad	bronchial
42	chr1:45242800-45247400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr1:45242800-45247800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:45243000-45244200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
45	chr1:45243000-45244600	Genic enhancers	Fetal Muscle Leg	muscle
46	chr1:45243000-45244600	Genic enhancers	Fetal Stomach	stomach
47	chr1:45243000-45244800	Genic enhancers	Brain Cingulate Gyrus	brain
48	chr1:45243000-45244800	Strong transcription	Fetal Kidney	kidney
49	chr1:45243000-45244800	Genic enhancers	Fetal Thymus	thymus
50	chr1:45243000-45245400	Strong transcription	Rectal Smooth Muscle	rectum

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