Variant report

Variant	nsv880970
Chromosome Location	chr4:175434394-175444006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:250)
CpG islands
(count:427)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:250 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:175443570-175443858	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr4:175442908-175444261	K562	blood:	n/a	chr4:175443677-175443693
3	BHLHE40	chr4:175443469-175443773	A549	lung:	n/a	chr4:175443677-175443693
4	BHLHE40	chr4:175443462-175443846	HepG2	liver:	n/a	chr4:175443677-175443693
5	BHLHE40	chr4:175443428-175443853	GM12878	blood:	n/a	chr4:175443677-175443693
6	BRCA1	chr4:175443783-175444375	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr4:175443625-175444649	K562	blood:	n/a	n/a
8	CCNT2	chr4:175443310-175443912	K562	blood:	n/a	n/a
9	CEBPB	chr4:175437597-175437797	A549	lung:	n/a	chr4:175437702-175437713
10	CEBPB	chr4:175434240-175434498	IMR90	lung:	n/a	chr4:175434386-175434395 chr4:175434272-175434284 chr4:175434385-175434396
11	CEBPB	chr4:175434253-175434461	K562	blood:	n/a	chr4:175434386-175434395 chr4:175434272-175434284 chr4:175434385-175434396
12	CEBPB	chr4:175440069-175440443	A549	lung:	n/a	chr4:175440290-175440303
13	CEBPB	chr4:175443317-175443491	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr4:175437639-175437877	HepG2	liver:	n/a	chr4:175437702-175437713
15	CEBPB	chr4:175434271-175434535	HepG2	liver:	n/a	chr4:175434386-175434395 chr4:175434272-175434284 chr4:175434385-175434396
16	CHD2	chr4:175443638-175444009	HepG2	liver:	n/a	n/a
17	CHD2	chr4:175443570-175443770	Hela-S3	cervix:	n/a	n/a
18	CHD2	chr4:175443516-175443966	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr4:175443654-175443813	GM12878	blood:	n/a	n/a
20	CHD2	chr4:175443624-175443960	K562	blood:	n/a	n/a
21	CREB1	chr4:175443611-175444633	K562	blood:	n/a	n/a
22	CREB1	chr4:175443329-175443895	A549	lung:	n/a	n/a
23	CTBP2	chr4:175442870-175443914	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr4:175443120-175443270	HRPEpiC	eye:	n/a	n/a
25	CTCF	chr4:175443140-175443290	HCT-116	colon:	n/a	n/a
26	CTCF	chr4:175443100-175443397	K562	blood:	n/a	n/a
27	CTCF	chr4:175443140-175443290	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr4:175443180-175443330	GM06990	blood:	n/a	n/a
29	CTCF	chr4:175443267-175443277	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr4:175443180-175443330	HRE	kidney:	n/a	n/a
31	CTCF	chr4:175443165-175443293	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:175443162-175443305	K562	blood:	n/a	n/a
33	CTCF	chr4:175443160-175443310	Caco-2	colon:	n/a	n/a
34	CTCF	chr4:175443543-175443611	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:175443057-175443300	K562	blood:	n/a	n/a
36	CTCF	chr4:175443160-175443310	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr4:175443920-175444070	GM12867	blood:	n/a	n/a
38	CTCF	chr4:175443105-175443346	NHEK	skin:	n/a	n/a
39	CTCF	chr4:175443120-175443270	HRE	kidney:	n/a	n/a
40	CTCF	chr4:175443160-175443310	HMEC	breast:	n/a	n/a
41	CTCF	chr4:175443120-175443270	SAEC	small airway:	n/a	n/a
42	CTCF	chr4:175443560-175443710	GM12866	blood:	n/a	n/a
43	CTCF	chr4:175443080-175443230	NHEK	skin:	n/a	n/a
44	CTCF	chr4:175443784-175444133	K562	blood:	n/a	n/a
45	CTCF	chr4:175443120-175443270	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr4:175443380-175443530	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr4:175443140-175443290	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:175443440-175443590	Caco-2	colon:	n/a	n/a
49	CTCF	chr4:175443440-175443590	HRE	kidney:	n/a	n/a
50	CTCF	chr4:175443126-175443156	Lung_OC	lung:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:175443752-175443802	HRPEpiC	eye:	n/a
2	chr4:175443569-175443619	HUVEC	blood vessel:	n/a
3	chr4:175443797-175443847	SK-N-SH_RA	brain:	n/a
4	chr4:175443243-175443293	ovcar-3	ovarian:	n/a
5	chr4:175443407-175443457	HEEpiC	esophagus:	n/a
6	chr4:175443797-175443847	GM06990	blood:	n/a
7	chr4:175440325-175440375	GM19239	blood:	n/a
8	chr4:175440325-175440375	GM06990	blood:	n/a
9	chr4:175443867-175443917	AG04449	skin:	fetal
10	chr4:175443569-175443619	MCF-7	breast:	n/a
11	chr4:175443407-175443457	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:175443867-175443917	BJ	skin:	n/a
13	chr4:175443569-175443619	HIPEpiC	eye:	n/a
14	chr4:175440325-175440375	RPTEC	kidney:	n/a
15	chr4:175443569-175443619	A549	lung:	n/a
16	chr4:175443569-175443619	HAEpiC	amniotic membrane:	n/a
17	chr4:175440325-175440375	SKMC	muscle:	n/a
18	chr4:175443752-175443802	SK-N-SH_RA	brain:	n/a
19	chr4:175443797-175443847	CMK	blood:	n/a
20	chr4:175443797-175443847	IMR90	lung:	fetal
21	chr4:175443867-175443917	AG09309	skin:	n/a
22	chr4:175443797-175443847	HEEpiC	esophagus:	n/a
23	chr4:175443407-175443457	MCF-7	breast:	n/a
24	chr4:175443407-175443457	HCT-116	colon:	n/a
25	chr4:175443407-175443457	HIPEpiC	eye:	n/a
26	chr4:175443797-175443847	HCM	heart:	n/a
27	chr4:175443407-175443457	Jurkat	blood:	n/a
28	chr4:175443407-175443457	T-47D	breast:	n/a
29	chr4:175440325-175440375	Caco-2	colon:	n/a
30	chr4:175440325-175440375	GM12878	blood:	n/a
31	chr4:175443867-175443917	NHBE	bronchial:	n/a
32	chr4:175443243-175443293	Caco-2	colon:	n/a
33	chr4:175440325-175440375	CMK	blood:	n/a
34	chr4:175443569-175443619	AG09309	skin:	n/a
35	chr4:175443867-175443917	PANC-1	pancreas:	n/a
36	chr4:175443407-175443457	GM19239	blood:	n/a
37	chr4:175443867-175443917	NB4	blood:	n/a
38	chr4:175443797-175443847	NT2-D1	testis:	n/a
39	chr4:175443243-175443293	GM19239	blood:	n/a
40	chr4:175443752-175443802	Hepatocyte	liver:	n/a
41	chr4:175443797-175443847	RPTEC	kidney:	n/a
42	chr4:175443797-175443847	HRE	kidney:	n/a
43	chr4:175443569-175443619	AG04449	skin:	fetal
44	chr4:175440325-175440375	AG04450	lung:	fetal
45	chr4:175443797-175443847	PFSK-1	brain:	n/a
46	chr4:175443569-175443619	Caco-2	colon:	n/a
47	chr4:175440325-175440375	AG10803	skin:	n/a
48	chr4:175440325-175440375	NT2-D1	testis:	n/a
49	chr4:175443867-175443917	AG04450	lung:	fetal
50	chr4:175443752-175443802	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:175438441..175442290-chr4:175442561..175447463,6	K562	blood:
2	chr4:175441347..175443047-chr4:175456721..175458748,2	K562	blood:
3	chr4:175429876..175431764-chr4:175434191..175436356,2	K562	blood:
4	chr1:99961025..99961526-chr4:175442445..175442945,2	MCF-7	breast:

No data

Variant related genes	Relation type
HPGD	TF binding region
HPGD	CpG island
ENSG00000251584	chromatin interactions
ENSG00000164120	chromatin interactions

Extended variants
information (count: 375 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3797013	chr4:175434394-175434395	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182681459	chr4:175434406-175434407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs35011498	chr4:175434425-175434426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531418845	chr4:175434437-175434438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188255972	chr4:175434438-175434439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs564926950	chr4:175434448-175434449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192437169	chr4:175434464-175434465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs3797012	chr4:175434520-175434521	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567514208	chr4:175434565-175434566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150753455	chr4:175434569-175434570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs369816777	chr4:175434611-175434612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs578010334	chr4:175434612-175434613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548952556	chr4:175434613-175434614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs386402341	chr4:175434618-175434619	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76124797	chr4:175434623-175434624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79843646	chr4:175434624-175434625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79290819	chr4:175434626-175434627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562440812	chr4:175434674-175434675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184532131	chr4:175434716-175434717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187507855	chr4:175434718-175434719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192527284	chr4:175434720-175434721	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184742640	chr4:175434778-175434779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2254350	chr4:175434801-175434802	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs189221709	chr4:175434818-175434819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181583018	chr4:175434828-175434829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs368789454	chr4:175434847-175434848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2612660	chr4:175434849-175434850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs543377188	chr4:175434854-175434855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs59695808	chr4:175434953-175434954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs6846029	chr4:175434954-175434955	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs375644968	chr4:175434968-175434969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs576152431	chr4:175434972-175434973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199688408	chr4:175434995-175434996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs2612661	chr4:175435003-175435004	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs564951423	chr4:175435016-175435017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368727347	chr4:175435079-175435080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527408181	chr4:175435269-175435270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547538062	chr4:175435275-175435276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560785394	chr4:175435347-175435348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs3797011	chr4:175435356-175435357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529931940	chr4:175435393-175435394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549714198	chr4:175435450-175435451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs139139269	chr4:175435554-175435555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567883740	chr4:175435582-175435583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114815697	chr4:175435610-175435611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551500824	chr4:175435646-175435647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547126337	chr4:175435656-175435657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs2254225	chr4:175435658-175435659	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs79318084	chr4:175435740-175435741	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs73008775	chr4:175435760-175435761	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175396000-175442800	Weak transcription	Esophagus	oesophagus
2	chr4:175410000-175440800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:175410800-175440000	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr4:175418000-175438600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr4:175418600-175437800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr4:175418800-175435600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr4:175419200-175438600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr4:175420600-175441000	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr4:175421000-175439200	Weak transcription	Colon Smooth Muscle	Colon
10	chr4:175427400-175438400	Weak transcription	Primary hematopoietic stem cells	blood
11	chr4:175427400-175440600	Weak transcription	Duodenum Mucosa	Duodenum
12	chr4:175427400-175443000	Weak transcription	Lung	lung
13	chr4:175427600-175441800	Weak transcription	Fetal Thymus	thymus
14	chr4:175427800-175435800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:175428000-175439400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:175429200-175436200	Weak transcription	Stomach Mucosa	stomach
17	chr4:175429400-175435000	Weak transcription	Primary T cells from cord blood	blood
18	chr4:175429400-175441200	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr4:175429400-175442600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr4:175431000-175442400	Weak transcription	Fetal Intestine Large	intestine
21	chr4:175432800-175441600	Weak transcription	Placenta	Placenta
22	chr4:175433200-175442600	Weak transcription	Fetal Intestine Small	intestine
23	chr4:175433600-175434600	Enhancers	A549	lung
24	chr4:175434000-175435800	Enhancers	Liver	Liver
25	chr4:175434600-175437200	Weak transcription	A549	lung
26	chr4:175435000-175436400	Enhancers	Primary T cells from cord blood	blood
27	chr4:175435600-175435800	Enhancers	Rectal Smooth Muscle	rectum
28	chr4:175435800-175436000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:175435800-175436400	Weak transcription	Liver	Liver
30	chr4:175435800-175442000	Weak transcription	Rectal Smooth Muscle	rectum
31	chr4:175436200-175436800	Enhancers	Stomach Mucosa	stomach
32	chr4:175436400-175437600	Genic enhancers	Liver	Liver
33	chr4:175436400-175439200	Weak transcription	Primary T cells from cord blood	blood
34	chr4:175436800-175441400	Weak transcription	Stomach Mucosa	stomach
35	chr4:175437200-175438200	Strong transcription	A549	lung
36	chr4:175437600-175439600	Enhancers	Liver	Liver
37	chr4:175437800-175438200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr4:175438200-175439200	Weak transcription	A549	lung
39	chr4:175438200-175439400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr4:175438400-175440000	Enhancers	Primary hematopoietic stem cells	blood
41	chr4:175438400-175440200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr4:175438600-175439400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr4:175438600-175439600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr4:175438600-175439600	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr4:175438600-175439800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr4:175438600-175440400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:175439200-175439600	Enhancers	Colon Smooth Muscle	Colon
48	chr4:175439200-175440000	Flanking Active TSS	A549	lung
49	chr4:175439200-175441000	Enhancers	Primary T cells from cord blood	blood
50	chr4:175439400-175439600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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