Variant report

Variant	nsv970439
Chromosome Location	chr7:4901682-4908069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:17)
CpG islands
(count:489)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:17 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:4905568-4906177	HepG2	liver:	n/a	chr7:4906010-4906021
2	CEBPB	chr7:4905888-4906177	K562	blood:	n/a	chr7:4906010-4906021
3	CEBPB	chr7:4905848-4906147	A549	lung:	n/a	chr7:4906010-4906021
4	CEBPB	chr7:4905893-4906174	IMR90	lung:	n/a	chr7:4906010-4906021
5	MAFK	chr7:4905571-4905764	HepG2	liver:	n/a	n/a
6	MAFK	chr7:4905583-4905754	HepG2	liver:	n/a	n/a
7	MAX	chr7:4906746-4906959	K562	blood:	n/a	n/a
8	MAX	chr7:4904827-4904910	NB4	blood:	n/a	chr7:4904850-4904860
9	POLR2A	chr7:4901715-4901719	MCF-7	breast:	n/a	n/a
10	POLR2A	chr7:4901613-4901690	MCF-7	breast:	n/a	n/a
11	REST	chr7:4906734-4906951	H1-hESC	embryonic stem cell:	n/a	chr7:4906856-4906865
12	REST	chr7:4906695-4907015	PFSK-1	brain:	n/a	chr7:4906856-4906865
13	REST	chr7:4906728-4906923	Hela-S3	cervix:	n/a	chr7:4906856-4906865
14	REST	chr7:4906748-4906931	K562	blood:	n/a	chr7:4906856-4906865
15	REST	chr7:4906740-4906982	H1-hESC	embryonic stem cell:	n/a	chr7:4906856-4906865
16	SPI1	chr7:4906342-4906525	K562	blood:	n/a	n/a
17	YY1	chr7:4901532-4901721	GM12878	blood:	n/a	chr7:4901615-4901632 chr7:4901609-4901631 chr7:4901620-4901628

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:4902015-4902065	PANC-1	pancreas:	n/a
2	chr7:4902015-4902065	PANC-1	pancreas:	n/a
3	chr7:4901798-4901848	SKMC	muscle:	n/a
4	chr7:4901750-4901800	Hela-S3	cervix:	n/a
5	chr7:4902603-4902653	PFSK-1	brain:	n/a
6	chr7:4902257-4902307	HEK293	kidney:	embryo
7	chr7:4902015-4902065	HL-60	blood:	n/a
8	chr7:4901750-4901800	NB4	blood:	n/a
9	chr7:4902015-4902065	K562	blood:	n/a
10	chr7:4901785-4901835	HPAEpiC	pulmonary alveolar:	n/a
11	chr7:4901785-4901835	NB4	blood:	n/a
12	chr7:4905117-4905167	HL-60	blood:	n/a
13	chr7:4901750-4901800	HCM	heart:	n/a
14	chr7:4902257-4902307	Hepatocyte	liver:	n/a
15	chr7:4902050-4902100	HEEpiC	esophagus:	n/a
16	chr7:4902050-4902100	CMK	blood:	n/a
17	chr7:4902050-4902100	Hepatocyte	liver:	n/a
18	chr7:4901785-4901835	AG04449	skin:	fetal
19	chr7:4901750-4901800	HUVEC	blood vessel:	n/a
20	chr7:4902050-4902100	HPAEpiC	pulmonary alveolar:	n/a
21	chr7:4902015-4902065	GM19239	blood:	n/a
22	chr7:4902050-4902100	BE2_C	brain:	n/a
23	chr7:4905117-4905167	PrEC	prostate:	n/a
24	chr7:4901785-4901835	HepG2	liver:	n/a
25	chr7:4905117-4905167	NHDF-neo	bronchial:	n/a
26	chr7:4901798-4901848	Hepatocyte	liver:	n/a
27	chr7:4905117-4905167	HMEC	breast:	n/a
28	chr7:4901785-4901835	HRCEpiC	kidney:	n/a
29	chr7:4902603-4902653	AG10803	skin:	n/a
30	chr7:4902603-4902653	HNPCEpiC	eye:	n/a
31	chr7:4901750-4901800	HPAEpiC	pulmonary alveolar:	n/a
32	chr7:4902257-4902307	MCF10A-Er-Src	breast:	n/a
33	chr7:4901785-4901835	HMEC	breast:	n/a
34	chr7:4901798-4901848	NHDF-neo	bronchial:	n/a
35	chr7:4902257-4902307	ovcar-3	ovarian:	n/a
36	chr7:4901785-4901835	PrEC	prostate:	n/a
37	chr7:4901785-4901835	AG09319	gingival:	n/a
38	chr7:4901750-4901800	AoSMC	blood vessel:	n/a
39	chr7:4902603-4902653	Caco-2	colon:	n/a
40	chr7:4902050-4902100	HIPEpiC	eye:	n/a
41	chr7:4901750-4901800	HEK293	kidney:	embryo
42	chr7:4902050-4902100	Hela-S3	cervix:	n/a
43	chr7:4902050-4902100	HCM	heart:	n/a
44	chr7:4901785-4901835	Jurkat	blood:	n/a
45	chr7:4902015-4902065	Hela-S3	cervix:	n/a
46	chr7:4902603-4902653	HPAEpiC	pulmonary alveolar:	n/a
47	chr7:4902603-4902653	HUVEC	blood vessel:	n/a
48	chr7:4901798-4901848	HNPCEpiC	eye:	n/a
49	chr7:4901750-4901800	GM19239	blood:	n/a
50	chr7:4901750-4901800	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:4906600..4908101-chr7:4911855..4914504,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAPOLB-2	chr7:4905063-4905435	NONHSAT118884
2	lnc-PAPOLB-1	chr7:4903425-4904999	ucscGeneNc_uc003snm_1

No data

Variant related genes	Relation type
PAPOLB	TF binding region
ENSG00000213935	TF binding region
PAPOLB	CpG island
ENSG00000213935	CpG island

Extended variants
information (count: 305 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559204555	chr7:4901691-4901692	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs112041262	chr7:4901696-4901697	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542058591	chr7:4901710-4901711	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs184441349	chr7:4901712-4901713	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs527592182	chr7:4901743-4901744	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs200752176	chr7:4901753-4901754	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs10275572	chr7:4901758-4901759	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs541138205	chr7:4901795-4901796	Bivalent/Poised TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs188853115	chr7:4901811-4901812	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs531676542	chr7:4901844-4901845	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs111751291	chr7:4901861-4901862	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs549890816	chr7:4901868-4901869	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568237485	chr7:4901889-4901890	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535620035	chr7:4901901-4901902	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs78637523	chr7:4901958-4901959	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs181239946	chr7:4901980-4901981	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533373646	chr7:4901986-4901987	Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs112702775	chr7:4902026-4902027	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs577358086	chr7:4902039-4902040	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs553481501	chr7:4902069-4902070	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs75709664	chr7:4902162-4902163	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568958129	chr7:4902212-4902213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539185006	chr7:4902243-4902244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs186120620	chr7:4902250-4902251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190596964	chr7:4902257-4902258	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs544245910	chr7:4902258-4902259	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs556257133	chr7:4902269-4902270	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs552785172	chr7:4902295-4902296	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs578093998	chr7:4902323-4902324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146881957	chr7:4902355-4902356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368496200	chr7:4902359-4902360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574593699	chr7:4902382-4902383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541997131	chr7:4902383-4902384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560135073	chr7:4902385-4902386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545408582	chr7:4902428-4902429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs527572697	chr7:4902501-4902502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs564017018	chr7:4902528-4902529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs11404610	chr7:4902529-4902530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs34119383	chr7:4902539-4902540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200459081	chr7:4902541-4902542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564483695	chr7:4902545-4902546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9801478	chr7:4902546-4902547	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs28405602	chr7:4902551-4902552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182449999	chr7:4902559-4902560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs28543671	chr7:4902564-4902565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561298282	chr7:4902565-4902566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186409850	chr7:4902574-4902575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs529351408	chr7:4902604-4902605	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs369629501	chr7:4902624-4902625	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs547968899	chr7:4902629-4902630	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD

Chromatin state (count:140 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:4900400-4902200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:4900800-4902000	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
3	chr7:4900800-4902200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
4	chr7:4901000-4901800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
5	chr7:4901000-4901800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr7:4901000-4902000	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:4901000-4902000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
8	chr7:4901000-4902000	Bivalent/Poised TSS	Primary B cells from cord blood	blood
9	chr7:4901000-4902000	Active TSS	Brain Anterior Caudate	brain
10	chr7:4901000-4902000	Active TSS	Fetal Kidney	kidney
11	chr7:4901000-4902200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
12	chr7:4901000-4902200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
13	chr7:4901000-4902200	Bivalent/Poised TSS	Primary T cells from cord blood	blood
14	chr7:4901000-4902200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr7:4901200-4901800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:4901200-4901800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:4901200-4901800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr7:4901200-4901800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr7:4901200-4901800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
20	chr7:4901200-4901800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
21	chr7:4901200-4901800	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:4901200-4901800	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
23	chr7:4901200-4901800	Active TSS	Adipose Nuclei	Adipose
24	chr7:4901200-4901800	Active TSS	Brain Inferior Temporal Lobe	brain
25	chr7:4901200-4901800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
26	chr7:4901200-4901800	Bivalent/Poised TSS	Fetal Intestine Large	intestine
27	chr7:4901200-4901800	Bivalent/Poised TSS	Fetal Intestine Small	intestine
28	chr7:4901200-4901800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
29	chr7:4901200-4901800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
30	chr7:4901200-4901800	Bivalent/Poised TSS	Fetal Thymus	thymus
31	chr7:4901200-4901800	Active TSS	Right Atrium	heart
32	chr7:4901200-4901800	Active TSS	Stomach Smooth Muscle	stomach
33	chr7:4901200-4901800	Bivalent/Poised TSS	HUVEC	blood vessel
34	chr7:4901200-4902000	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:4901200-4902000	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
36	chr7:4901200-4902000	Active TSS	Brain Angular Gyrus	brain
37	chr7:4901200-4902000	Bivalent/Poised TSS	Brain Germinal Matrix	brain
38	chr7:4901200-4902000	ZNF genes & repeats	Colon Smooth Muscle	Colon
39	chr7:4901200-4902000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
40	chr7:4901200-4902000	Bivalent/Poised TSS	Psoas Muscle	Psoas
41	chr7:4901200-4902000	Active TSS	Rectal Mucosa Donor 29	rectum
42	chr7:4901200-4902000	Active TSS	Right Ventricle	heart
43	chr7:4901200-4902000	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
44	chr7:4901200-4902000	ZNF genes & repeats	Spleen	Spleen
45	chr7:4901200-4902000	ZNF genes & repeats	HSMMtube	muscle
46	chr7:4901200-4902200	ZNF genes & repeats	Lung	lung
47	chr7:4901200-4902200	Active TSS	Rectal Smooth Muscle	rectum
48	chr7:4901400-4901800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr7:4901400-4901800	Flanking Bivalent TSS/Enh	Primary B cells from peripheral blood	blood
50	chr7:4901400-4901800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood

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