Variant report

Variant	esv3365586
Chromosome Location	chr3:51995312-51998710
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:21)
CpG islands
(count:489)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr3:51998273-51998472	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD2	chr3:51998014-51998456	H1-hESC	embryonic stem cell:	n/a	chr3:51998261-51998271
3	MAX	chr3:51997840-51998085	K562	blood:	n/a	chr3:51998001-51998010 chr3:51998000-51998011 chr3:51998000-51998010 chr3:51998001-51998010 chr3:51998001-51998010
4	MXI1	chr3:51998225-51998385	H1-hESC	embryonic stem cell:	n/a	n/a
5	POLR2A	chr3:51996060-51996068	Hela-S3	cervix:	n/a	n/a
6	POLR2A	chr3:51997184-51997606	HepG2	liver:	n/a	n/a
7	POLR2A	chr3:51997964-51998074	H1-hESC	embryonic stem cell:	n/a	n/a
8	POLR2A	chr3:51996599-51996603	K562	blood:	n/a	n/a
9	POLR2A	chr3:51996551-51996596	K562	blood:	n/a	n/a
10	POLR2A	chr3:51997165-51999885	K562	blood:	n/a	n/a
11	POLR2A	chr3:51998638-51998696	HepG2	liver:	n/a	n/a
12	POLR2A	chr3:51996413-51996900	K562	blood:	n/a	n/a
13	POLR2A	chr3:51995770-51996201	K562	blood:	n/a	n/a
14	POLR2A	chr3:51995922-51996015	K562	blood:	n/a	n/a
15	SIN3A	chr3:51998103-51998494	H1-hESC	embryonic stem cell:	n/a	chr3:51998455-51998466
16	SIN3AK20	chr3:51998118-51998444	H1-hESC	embryonic stem cell:	n/a	n/a
17	UBTF	chr3:51995827-51995916	K562	blood:	n/a	n/a
18	USF2	chr3:51996090-51996126	HepG2	liver:	n/a	n/a
19	ZNF143	chr3:51998221-51998370	H1-hESC	embryonic stem cell:	n/a	chr3:51998257-51998275
20	ZNF263	chr3:51995604-51996175	HEK293-T-REx	kidney:	n/a	chr3:51995826-51995835 chr3:51995689-51995698 chr3:51995799-51995820
21	ZNF263	chr3:51996412-51996916	HEK293-T-REx	kidney:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:51995784-51995834	HNPCEpiC	eye:	n/a
2	chr3:51995784-51995834	HNPCEpiC	eye:	n/a
3	chr3:51998051-51998101	GM12891	blood:	n/a
4	chr3:51995784-51995834	BE2_C	brain:	n/a
5	chr3:51996834-51996884	ovcar-3	ovarian:	n/a
6	chr3:51997033-51997083	HRPEpiC	eye:	n/a
7	chr3:51998051-51998101	HL-60	blood:	n/a
8	chr3:51995445-51995495	HCPEpiC	choroid plexus:	n/a
9	chr3:51996834-51996884	A549	lung:	n/a
10	chr3:51995445-51995495	HEEpiC	esophagus:	n/a
11	chr3:51997492-51997542	SAEC	small airway:	n/a
12	chr3:51997385-51997435	Hepatocyte	liver:	n/a
13	chr3:51996834-51996884	HRCEpiC	kidney:	n/a
14	chr3:51996797-51996847	HNPCEpiC	eye:	n/a
15	chr3:51995445-51995495	PFSK-1	brain:	n/a
16	chr3:51997033-51997083	ovcar-3	ovarian:	n/a
17	chr3:51996797-51996847	ovcar-3	ovarian:	n/a
18	chr3:51996797-51996847	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:51997492-51997542	SK-N-MC	brain:	n/a
20	chr3:51995784-51995834	H1-hESC	embryonic stem cell:	embryo
21	chr3:51998051-51998101	NB4	blood:	n/a
22	chr3:51997385-51997435	AG04450	lung:	fetal
23	chr3:51997492-51997542	AG09309	skin:	n/a
24	chr3:51997033-51997083	HPAEpiC	pulmonary alveolar:	n/a
25	chr3:51998051-51998101	HepG2	liver:	n/a
26	chr3:51995784-51995834	SKMC	muscle:	n/a
27	chr3:51995445-51995495	GM19239	blood:	n/a
28	chr3:51996834-51996884	HepG2	liver:	n/a
29	chr3:51996797-51996847	HCF	heart:	n/a
30	chr3:51997492-51997542	ECC-1	luminal epithelium:	n/a
31	chr3:51996834-51996884	MCF10A-Er-Src	breast:	n/a
32	chr3:51997033-51997083	SK-N-SH_RA	brain:	n/a
33	chr3:51997033-51997083	ProgFib	skin:	n/a
34	chr3:51997385-51997435	NT2-D1	testis:	n/a
35	chr3:51996797-51996847	NT2-D1	testis:	n/a
36	chr3:51998051-51998101	BE2_C	brain:	n/a
37	chr3:51997492-51997542	NH-A	brain:	n/a
38	chr3:51996834-51996884	HCT-116	colon:	n/a
39	chr3:51997492-51997542	HepG2	liver:	n/a
40	chr3:51995445-51995495	SK-N-SH_RA	brain:	n/a
41	chr3:51997033-51997083	AoSMC	blood vessel:	n/a
42	chr3:51998051-51998101	MCF10A-Er-Src	breast:	n/a
43	chr3:51997033-51997083	GM12878	blood:	n/a
44	chr3:51996834-51996884	BE2_C	brain:	n/a
45	chr3:51997033-51997083	Jurkat	blood:	n/a
46	chr3:51997033-51997083	AG09309	skin:	n/a
47	chr3:51998051-51998101	Jurkat	blood:	n/a
48	chr3:51995445-51995495	AoSMC	blood vessel:	n/a
49	chr3:51997492-51997542	CMK	blood:	n/a
50	chr3:51996797-51996847	AG04449	skin:	fetal

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:51997651..51999473-chr3:52171714..52174151,2	K562	blood:
2	chr3:51992685..51994681-chr3:51997289..51999303,2	MCF-7	breast:
3	chr3:51977352..51979030-chr3:51995876..51997693,2	MCF-7	breast:
4	chr3:51972287..51978873-chr3:51998179..52003667,9	MCF-7	breast:
5	chr3:51988009..51992311-chr3:51992660..51997455,6	K562	blood:
6	chr3:51997248..52000056-chr3:52000079..52001783,2	MCF-7	breast:
7	chr3:51970192..51973030-chr3:51997697..51999602,2	K562	blood:
8	chr3:51980428..51982546-chr3:51998419..52000085,2	K562	blood:
9	chr3:51976676..51979243-chr3:51995471..51997610,2	K562	blood:
10	chr3:51976909..51979243-chr3:51994383..51996203,2	MCF-7	breast:
11	chr3:51976078..51979243-chr3:51993727..51997610,4	K562	blood:

No data

Variant related genes	Relation type
PCBP4	TF binding region
PCBP4	CpG island
ENSG00000180929	chromatin interactions
ENSG00000041880	chromatin interactions
ENSG00000114767	chromatin interactions
ENSG00000090097	chromatin interactions

Extended variants
information (count: 131 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:131 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571476874	chr3:51995347-51995348	Strong transcription Genic enhancers Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs78433790	chr3:51995401-51995402	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs114593478	chr3:51995419-51995420	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs565863591	chr3:51995430-51995431	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561514911	chr3:51995443-51995444	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs554202385	chr3:51995446-51995447	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs191496851	chr3:51995468-51995469	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs569240540	chr3:51995486-51995487	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs550828191	chr3:51995489-51995490	Weak transcription Genic enhancers Strong transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs558505126	chr3:51995580-51995581	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538270374	chr3:51995606-51995607	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs529637219	chr3:51995622-51995623	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs560571216	chr3:51995663-51995664	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs183194504	chr3:51995675-51995676	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs187852368	chr3:51995770-51995771	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs369498457	chr3:51995771-51995772	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs561334479	chr3:51995818-51995819	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs531816451	chr3:51995842-51995843	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs559553842	chr3:51995861-51995862	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs2740338	chr3:51995868-51995869	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs549940135	chr3:51995875-51995876	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs565269421	chr3:51995876-51995877	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs532347811	chr3:51995885-51995886	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs564128952	chr3:51995916-51995917	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs2657314	chr3:51995920-51995921	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs547622001	chr3:51995923-51995924	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs192548818	chr3:51995938-51995939	Weak transcription Genic enhancers Strong transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs368053232	chr3:51996005-51996006	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs547901961	chr3:51996040-51996041	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs371915340	chr3:51996070-51996071	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs374802840	chr3:51996137-51996138	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs569440683	chr3:51996172-51996173	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs537135949	chr3:51996176-51996177	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs538054764	chr3:51996223-51996224	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs558310174	chr3:51996271-51996272	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs183607529	chr3:51996273-51996274	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs538969481	chr3:51996325-51996326	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs143476227	chr3:51996368-51996369	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs554644806	chr3:51996379-51996380	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs148008368	chr3:51996386-51996387	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs533363271	chr3:51996435-51996436	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs543218320	chr3:51996489-51996490	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs551531010	chr3:51996539-51996540	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs370096184	chr3:51996549-51996550	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs141519176	chr3:51996555-51996556	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs576648148	chr3:51996589-51996590	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs150888630	chr3:51996596-51996597	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs13072003	chr3:51996604-51996605	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs568035392	chr3:51996612-51996613	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs565137492	chr3:51996632-51996633	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:51988400-52000600	Weak transcription	Hela-S3	cervix
2	chr3:51989400-51997000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:51990600-52000200	Weak transcription	NHDF-Ad	bronchial
4	chr3:51990600-52000400	Weak transcription	Small Intestine	intestine
5	chr3:51990600-52000400	Weak transcription	HUVEC	blood vessel
6	chr3:51990600-52000800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr3:51990800-51996000	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr3:51990800-51997200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr3:51990800-51999600	Weak transcription	NH-A	brain
10	chr3:51990800-52000400	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr3:51991000-51995600	Weak transcription	Right Atrium	heart
12	chr3:51991000-51995800	Strong transcription	Fetal Stomach	stomach
13	chr3:51991000-51995800	Weak transcription	Psoas Muscle	Psoas
14	chr3:51991000-51996000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:51991000-51996400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr3:51991000-51996600	Weak transcription	Fetal Brain Male	brain
17	chr3:51991000-51997000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr3:51991000-51997000	Strong transcription	Muscle Satellite Cultured Cells	--
19	chr3:51991000-51997400	Strong transcription	NHLF	lung
20	chr3:51991000-51999600	Weak transcription	Colonic Mucosa	Colon
21	chr3:51991000-51999600	Weak transcription	HMEC	breast
22	chr3:51991000-51999800	Weak transcription	NHEK	skin
23	chr3:51991000-52000200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr3:51991000-52000400	Weak transcription	Stomach Mucosa	stomach
25	chr3:51991000-52000600	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr3:51991200-51995800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:51991200-51997400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr3:51991200-51997800	Genic enhancers	Brain Cingulate Gyrus	brain
29	chr3:51991200-52000000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr3:51991200-52000400	Weak transcription	Primary T helper cells fromperipheralblood	blood
31	chr3:51991200-52000400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr3:51991400-51995400	Strong transcription	Fetal Brain Female	brain
33	chr3:51991400-51996800	Weak transcription	Fetal Heart	heart
34	chr3:51991400-51997000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
35	chr3:51991400-51997600	Genic enhancers	Brain Hippocampus Middle	brain
36	chr3:51991400-52000200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr3:51991600-51995400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr3:51991600-51995400	Strong transcription	Gastric	stomach
39	chr3:51991600-51995600	Strong transcription	Brain Germinal Matrix	brain
40	chr3:51991600-51997200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr3:51991800-51996800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr3:51991800-51998200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr3:51992000-51996000	Strong transcription	Aorta	Aorta
44	chr3:51992200-51996000	Strong transcription	Stomach Smooth Muscle	stomach
45	chr3:51992400-51995400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr3:51992400-51995800	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr3:51992800-51995800	Strong transcription	HSMM	muscle
48	chr3:51992800-52000400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr3:51993000-51996000	Genic enhancers	Brain Substantia Nigra	brain
50	chr3:51993000-51996800	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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