Variant report

Variant	esv1839152
Chromosome Location	chr4:48979634-48993377
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:78)
CpG islands
(count:794)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:78 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:48984018-48984328	HepG2	liver:	n/a	chr4:48984158-48984169
2	CEBPB	chr4:48984066-48984268	K562	blood:	n/a	chr4:48984158-48984169
3	CEBPB	chr4:48984034-48984293	A549	lung:	n/a	chr4:48984158-48984169
4	CHD2	chr4:48988138-48988159	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTBP2	chr4:48987811-48989013	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:48987938-48988255	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr4:48988120-48988195	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr4:48988326-48988564	H1-hESC	embryonic stem cell:	n/a	chr4:48988371-48988381
9	CTCF	chr4:48988420-48988570	HRE	kidney:	n/a	n/a
10	CTCF	chr4:48988000-48988150	HEEpiC	esophagus:	n/a	n/a
11	CTCF	chr4:48988020-48988170	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr4:48988120-48988270	SAEC	small airway:	n/a	n/a
13	CTCF	chr4:48988081-48988275	NHEK	skin:	n/a	n/a
14	CTCF	chr4:48987880-48988030	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr4:48988454-48988501	LNCaP	prostate:	n/a	n/a
16	CTCF	chr4:48988860-48989010	NHEK	skin:	n/a	chr4:48988927-48988940
17	CTCF	chr4:48980648-48980736	K562	blood:	n/a	n/a
18	CTCF	chr4:48988196-48988213	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr4:48988080-48988230	SAEC	small airway:	n/a	n/a
20	CTCF	chr4:48987885-48988628	H1-hESC	embryonic stem cell:	n/a	chr4:48988371-48988381
21	CTCF	chr4:48988060-48988210	HMEC	breast:	n/a	n/a
22	CTCF	chr4:48988040-48988190	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr4:48988108-48988204	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:48988020-48988170	NHEK	skin:	n/a	n/a
25	CTCF	chr4:48988103-48988251	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr4:48980606-48980762	K562	blood:	n/a	n/a
27	CTCF	chr4:48987896-48988248	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr4:48988399-48988561	NHEK	skin:	n/a	n/a
29	CTCF	chr4:48988440-48988590	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr4:48988000-48988150	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr4:48988150-48988177	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:48987040-48987190	GM12801	blood:	n/a	n/a
33	CTCF	chr4:48988340-48988561	H1-hESC	embryonic stem cell:	n/a	chr4:48988371-48988381
34	CTCF	chr4:48988200-48988350	A549	lung:	n/a	n/a
35	CTCF	chr4:48988400-48988550	WERI-Rb-1	eye:	n/a	n/a
36	E2F4	chr4:48992359-48992446	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F6	chr4:48987909-48988595	H1-hESC	embryonic stem cell:	n/a	chr4:48988361-48988373 chr4:48988359-48988369 chr4:48988318-48988330 chr4:48988132-48988143
38	EP300	chr4:48982207-48982502	SK-N-SH_RA	brain:	n/a	n/a
39	FOS	chr4:48979376-48979650	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr4:48982257-48982614	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr4:48982260-48982614	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr4:48982349-48982569	HUVEC	blood vessel:	n/a	n/a
43	FOS	chr4:48982234-48982620	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr4:48983021-48983065	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr4:48983024-48983035	MCF10A-Er-Src	breast:	n/a	n/a
46	FOSL2	chr4:48982236-48982545	SK-N-SH	brain:	n/a	n/a
47	GABPA	chr4:48987867-48988282	H1-hESC	embryonic stem cell:	n/a	n/a
48	GABPA	chr4:48987971-48988493	H1-hESC	embryonic stem cell:	n/a	n/a
49	GATA3	chr4:48988481-48988718	T-47D	breast:	n/a	chr4:48988659-48988669
50	GATA3	chr4:48982114-48982538	SK-N-SH	brain:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:48991973-48992023	ECC-1	luminal epithelium:	n/a
2	chr4:48991973-48992023	ECC-1	luminal epithelium:	n/a
3	chr4:48987024-48987074	T-47D	breast:	n/a
4	chr4:48991973-48992023	AG09309	skin:	n/a
5	chr4:48987791-48987841	AG09309	skin:	n/a
6	chr4:48988090-48988140	NH-A	brain:	n/a
7	chr4:48988321-48988371	NT2-D1	testis:	n/a
8	chr4:48990530-48990580	HEEpiC	esophagus:	n/a
9	chr4:48988124-48988174	ECC-1	luminal epithelium:	n/a
10	chr4:48988801-48988851	ProgFib	skin:	n/a
11	chr4:48988124-48988174	NB4	blood:	n/a
12	chr4:48988038-48988088	T-47D	breast:	n/a
13	chr4:48988066-48988116	Jurkat	blood:	n/a
14	chr4:48991973-48992023	HIPEpiC	eye:	n/a
15	chr4:48988124-48988174	PANC-1	pancreas:	n/a
16	chr4:48988124-48988174	HCT-116	colon:	n/a
17	chr4:48988038-48988088	NB4	blood:	n/a
18	chr4:48988038-48988088	ProgFib	skin:	n/a
19	chr4:48990530-48990580	Hepatocyte	liver:	n/a
20	chr4:48990530-48990580	ProgFib	skin:	n/a
21	chr4:48984176-48984226	HRPEpiC	eye:	n/a
22	chr4:48988090-48988140	GM12891	blood:	n/a
23	chr4:48987024-48987074	ProgFib	skin:	n/a
24	chr4:48988124-48988174	AG10803	skin:	n/a
25	chr4:48988321-48988371	HCPEpiC	choroid plexus:	n/a
26	chr4:48987024-48987074	AG04450	lung:	fetal
27	chr4:48990530-48990580	HL-60	blood:	n/a
28	chr4:48990530-48990580	NHBE	bronchial:	n/a
29	chr4:48991973-48992023	HRCEpiC	kidney:	n/a
30	chr4:48987791-48987841	RPTEC	kidney:	n/a
31	chr4:48988321-48988371	ovcar-3	ovarian:	n/a
32	chr4:48988253-48988303	GM06990	blood:	n/a
33	chr4:48988090-48988140	MCF10A-Er-Src	breast:	n/a
34	chr4:48984176-48984226	BJ	skin:	n/a
35	chr4:48990530-48990580	HNPCEpiC	eye:	n/a
36	chr4:48984176-48984226	BE2_C	brain:	n/a
37	chr4:48988090-48988140	HEK293	kidney:	embryo
38	chr4:48987024-48987074	HepG2	liver:	n/a
39	chr4:48988038-48988088	AG04450	lung:	fetal
40	chr4:48988801-48988851	LNCaP	prostate:	n/a
41	chr4:48984176-48984226	LNCaP	prostate:	n/a
42	chr4:48988124-48988174	NHBE	bronchial:	n/a
43	chr4:48988066-48988116	HCF	heart:	n/a
44	chr4:48988321-48988371	HRE	kidney:	n/a
45	chr4:48988066-48988116	HPAEpiC	pulmonary alveolar:	n/a
46	chr4:48987024-48987074	GM06990	blood:	n/a
47	chr4:48991973-48992023	CMK	blood:	n/a
48	chr4:48988124-48988174	HIPEpiC	eye:	n/a
49	chr4:48990530-48990580	GM19239	blood:	n/a
50	chr4:48988253-48988303	SK-N-SH	brain:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:48977539..48979962-chr4:48981392..48983640,2	MCF-7	breast:
2	chr4:48973617..48975284-chr4:48977428..48979706,2	K562	blood:
3	chr4:48987005..48989182-chr4:48992277..48994580,2	K562	blood:
4	chr4:48977539..48979962-chr4:48981392..48983640,2	MCF-7	breast:

No data

Variant related genes	Relation type
CWH43	TF binding region
CWH43	CpG island
ENSG00000109182	chromatin interactions

Extended variants
information (count: 533 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187968000	chr4:48979697-48979698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34969634	chr4:48979702-48979703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs397692021	chr4:48979713-48979714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115515390	chr4:48979742-48979743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570074865	chr4:48979793-48979794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536933446	chr4:48979808-48979809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555605505	chr4:48979836-48979837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573866211	chr4:48979871-48979872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534772789	chr4:48979913-48979914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553205995	chr4:48979950-48979951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140607156	chr4:48979953-48979954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545163622	chr4:48980085-48980086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144414353	chr4:48980144-48980145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575224281	chr4:48980147-48980148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542280368	chr4:48980152-48980153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs59683836	chr4:48980189-48980190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200301538	chr4:48980203-48980204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs373058766	chr4:48980212-48980213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562372948	chr4:48980317-48980318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529571998	chr4:48980328-48980329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs547539700	chr4:48980331-48980332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559568463	chr4:48980353-48980354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs180877200	chr4:48980414-48980415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147813682	chr4:48980421-48980422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs551496435	chr4:48980436-48980437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs112404700	chr4:48980524-48980525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142449893	chr4:48980569-48980570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549116324	chr4:48980582-48980583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149790595	chr4:48980586-48980587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534962683	chr4:48980634-48980635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186403356	chr4:48980655-48980656	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577945257	chr4:48980697-48980698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538715509	chr4:48980764-48980765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545554644	chr4:48980797-48980798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563633540	chr4:48980817-48980818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191089844	chr4:48980829-48980830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs575259357	chr4:48980859-48980860	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542570052	chr4:48980879-48980880	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530994653	chr4:48980891-48980892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554273263	chr4:48980906-48980907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542700737	chr4:48980921-48980922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183403004	chr4:48981029-48981030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541367808	chr4:48981097-48981098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559508496	chr4:48981166-48981167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs62309602	chr4:48981172-48981173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114408445	chr4:48981177-48981178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369118873	chr4:48981199-48981200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576552808	chr4:48981207-48981208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145749761	chr4:48981268-48981269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115919007	chr4:48981280-48981281	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Breast cancer	16272173	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:48973400-48981600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:48979000-48981600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr4:48980600-48981800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:48981200-48981600	Enhancers	GM12878-XiMat	blood
5	chr4:48981600-48983200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr4:48981600-48983400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr4:48981800-48983000	Enhancers	HMEC	breast
8	chr4:48981800-48983200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:48981800-48983200	Enhancers	NHEK	skin
10	chr4:48982000-48982400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr4:48982000-48982800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:48982200-48982400	Enhancers	Brain Anterior Caudate	brain
13	chr4:48983200-48987400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr4:48987400-48987600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:48987400-48987800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr4:48987600-48987800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:48987600-48987800	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:48987600-48987800	Bivalent Enhancer	Primary hematopoietic stem cells	blood
19	chr4:48987600-48987800	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
20	chr4:48987600-48987800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
21	chr4:48987600-48987800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:48987600-48987800	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr4:48987600-48988000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr4:48987600-48988000	Bivalent Enhancer	Stomach Mucosa	stomach
25	chr4:48987600-48988600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
26	chr4:48987600-48988600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:48987600-48988800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
28	chr4:48987600-48988800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
29	chr4:48987600-48988800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
30	chr4:48987600-48988800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
31	chr4:48987600-48988800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
32	chr4:48987600-48988800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
33	chr4:48987600-48989200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:48987600-48989200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:48987800-48988000	Flanking Bivalent TSS/Enh	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr4:48987800-48988000	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:48987800-48988000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr4:48987800-48988000	Enhancers	Liver	Liver
39	chr4:48987800-48988000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
40	chr4:48987800-48988000	Bivalent/Poised TSS	Colonic Mucosa	Colon
41	chr4:48987800-48988000	Enhancers	Gastric	stomach
42	chr4:48987800-48988000	Flanking Bivalent TSS/Enh	Psoas Muscle	Psoas
43	chr4:48987800-48988000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
44	chr4:48987800-48988000	Bivalent/Poised TSS	Right Atrium	heart
45	chr4:48987800-48988000	Flanking Bivalent TSS/Enh	Right Ventricle	heart
46	chr4:48987800-48988000	Bivalent Enhancer	Osteobl	bone
47	chr4:48987800-48988200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr4:48987800-48988200	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:48987800-48988200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
50	chr4:48987800-48988200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links