Variant report

Variant	nsv3865
Chromosome Location	chr3:70326908-70372109
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:251)
CpG islands
(count:184)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:251 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr3:70330643-70331286	A549	lung:	n/a	n/a
2	BACH1	chr3:70360134-70360158	K562	blood:	n/a	n/a
3	BCL3	chr3:70330686-70331249	A549	lung:	n/a	n/a
4	BCL3	chr3:70330602-70331311	A549	lung:	n/a	n/a
5	BHLHE40	chr3:70345132-70345162	GM12878	blood:	n/a	n/a
6	CBX3	chr3:70340237-70340430	K562	blood:	n/a	n/a
7	CEBPB	chr3:70348297-70348536	IMR90	lung:	n/a	n/a
8	CEBPB	chr3:70330783-70331335	A549	lung:	n/a	n/a
9	CEBPB	chr3:70347482-70347867	Hela-S3	cervix:	n/a	chr3:70347639-70347652
10	CEBPB	chr3:70348318-70348533	A549	lung:	n/a	n/a
11	CEBPB	chr3:70353517-70353712	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:70330602-70331397	A549	lung:	n/a	n/a
13	CEBPB	chr3:70330700-70331346	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:70330850-70331283	A549	lung:	n/a	n/a
15	CEBPB	chr3:70353466-70353709	A549	lung:	n/a	n/a
16	CEBPB	chr3:70355088-70355214	HepG2	liver:	n/a	n/a
17	CTCF	chr3:70358000-70358150	GM12868	blood:	n/a	n/a
18	CTCF	chr3:70358040-70358190	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr3:70358060-70358210	GM12874	blood:	n/a	n/a
20	CTCF	chr3:70358000-70358150	GM12878	blood:	n/a	n/a
21	CTCF	chr3:70357980-70358130	GM12865	blood:	n/a	n/a
22	CTCF	chr3:70358000-70358150	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr3:70358060-70358210	A549	lung:	n/a	n/a
24	CTCF	chr3:70357880-70358030	A549	lung:	n/a	n/a
25	CTCF	chr3:70358072-70358152	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:70358080-70358230	AG09319	gingival:	n/a	n/a
27	CTCF	chr3:70358060-70358210	HMF	breast:	n/a	n/a
28	CTCF	chr3:70358060-70358210	AG04450	lung:	n/a	n/a
29	CTCF	chr3:70358000-70358150	AG04450	lung:	n/a	n/a
30	CTCF	chr3:70358004-70358200	HepG2	liver:	n/a	n/a
31	CTCF	chr3:70357980-70358130	GM12866	blood:	n/a	n/a
32	CTCF	chr3:70358000-70358150	GM12873	blood:	n/a	n/a
33	CTCF	chr3:70358040-70358190	SK-N-SH_RA	brain:	n/a	n/a
34	CTCF	chr3:70358018-70358181	GM19240	blood:	n/a	n/a
35	CTCF	chr3:70358000-70358150	GM12864	blood:	n/a	n/a
36	CTCF	chr3:70358000-70358226	LNCaP	prostate:	n/a	n/a
37	CTCF	chr3:70358018-70358151	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr3:70358100-70358250	BJ	skin:	n/a	n/a
39	CTCF	chr3:70358040-70358190	HAc	cerebellar:	n/a	n/a
40	CTCF	chr3:70357980-70358130	AoAF	blood vessel:	n/a	n/a
41	CTCF	chr3:70358070-70358125	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr3:70358040-70358190	GM12864	blood:	n/a	n/a
43	CTCF	chr3:70357907-70358312	MCF-7	breast:	n/a	n/a
44	CTCF	chr3:70357980-70358130	NHEK	skin:	n/a	n/a
45	CTCF	chr3:70358040-70358190	AG04449	skin:	n/a	n/a
46	CTCF	chr3:70358080-70358230	NHLF	lung:	n/a	n/a
47	CTCF	chr3:70358160-70358310	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr3:70358040-70358190	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr3:70358020-70358170	HMEC	breast:	n/a	n/a
50	CTCF	chr3:70358040-70358190	HMEC	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:70360572-70360622	HIPEpiC	eye:	n/a
2	chr3:70360572-70360622	HIPEpiC	eye:	n/a
3	chr3:70339967-70340017	SK-N-SH_RA	brain:	n/a
4	chr3:70360572-70360622	SK-N-SH	brain:	n/a
5	chr3:70360572-70360622	IMR90	lung:	fetal
6	chr3:70339935-70339985	AG10803	skin:	n/a
7	chr3:70360572-70360622	PrEC	prostate:	n/a
8	chr3:70339967-70340017	HCM	heart:	n/a
9	chr3:70360572-70360622	H1-hESC	embryonic stem cell:	embryo
10	chr3:70339935-70339985	Hepatocyte	liver:	n/a
11	chr3:70339967-70340017	HL-60	blood:	n/a
12	chr3:70339967-70340017	ProgFib	skin:	n/a
13	chr3:70339935-70339985	HRE	kidney:	n/a
14	chr3:70339935-70339985	HPAEpiC	pulmonary alveolar:	n/a
15	chr3:70360572-70360622	A549	lung:	n/a
16	chr3:70360572-70360622	Hela-S3	cervix:	n/a
17	chr3:70339935-70339985	NH-A	brain:	n/a
18	chr3:70360572-70360622	HCF	heart:	n/a
19	chr3:70339967-70340017	A549	lung:	n/a
20	chr3:70360572-70360622	Jurkat	blood:	n/a
21	chr3:70339967-70340017	NH-A	brain:	n/a
22	chr3:70339967-70340017	GM19239	blood:	n/a
23	chr3:70339967-70340017	IMR90	lung:	fetal
24	chr3:70339967-70340017	ovcar-3	ovarian:	n/a
25	chr3:70360572-70360622	HL-60	blood:	n/a
26	chr3:70339935-70339985	HRCEpiC	kidney:	n/a
27	chr3:70339967-70340017	NB4	blood:	n/a
28	chr3:70360572-70360622	HUVEC	blood vessel:	n/a
29	chr3:70339967-70340017	HCPEpiC	choroid plexus:	n/a
30	chr3:70339967-70340017	CMK	blood:	n/a
31	chr3:70360572-70360622	Hepatocyte	liver:	n/a
32	chr3:70339935-70339985	HUVEC	blood vessel:	n/a
33	chr3:70339935-70339985	CMK	blood:	n/a
34	chr3:70339935-70339985	Caco-2	colon:	n/a
35	chr3:70339967-70340017	Hepatocyte	liver:	n/a
36	chr3:70339967-70340017	SK-N-MC	brain:	n/a
37	chr3:70339967-70340017	H1-hESC	embryonic stem cell:	embryo
38	chr3:70360572-70360622	BJ	skin:	n/a
39	chr3:70360572-70360622	GM19239	blood:	n/a
40	chr3:70360572-70360622	HMEC	breast:	n/a
41	chr3:70339967-70340017	HCT-116	colon:	n/a
42	chr3:70339935-70339985	SK-N-SH	brain:	n/a
43	chr3:70339967-70340017	NHBE	bronchial:	n/a
44	chr3:70360572-70360622	MCF10A-Er-Src	breast:	n/a
45	chr3:70339935-70339985	ECC-1	luminal epithelium:	n/a
46	chr3:70339935-70339985	HRPEpiC	eye:	n/a
47	chr3:70339967-70340017	AG04450	lung:	fetal
48	chr3:70339935-70339985	Jurkat	blood:	n/a
49	chr3:70339935-70339985	NHDF-neo	bronchial:	n/a
50	chr3:70339935-70339985	SK-N-SH_RA	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:70339740..70342430-chr3:70343681..70346313,2	K562	blood:
2	chr3:70339740..70342430-chr3:70343681..70346313,2	K562	blood:
3	chr3:70367804..70369875-chr3:70383298..70385013,2	K562	blood:
4	chr3:70322866..70326501-chr3:70330007..70332995,3	MCF-7	breast:
5	chr3:70348474..70350327-chr3:70352138..70355044,2	K562	blood:
6	chr3:70348474..70350327-chr3:70352138..70355044,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000242120	TF binding region
ENSG00000242120	CpG island

Extended variants
information (count: 1097 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549442651	chr3:70326918-70326919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147431084	chr3:70326960-70326961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6549327	chr3:70326994-70326995	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs77523646	chr3:70327012-70327013	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551618831	chr3:70327059-70327060	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs571612353	chr3:70327066-70327067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537222751	chr3:70327083-70327084	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115839398	chr3:70327105-70327106	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs75646981	chr3:70327133-70327134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114299455	chr3:70327134-70327135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553080606	chr3:70327148-70327149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9681827	chr3:70327161-70327162	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs187980989	chr3:70327190-70327191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375026295	chr3:70327218-70327219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2320474	chr3:70327250-70327251	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs193030715	chr3:70327334-70327335	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566196666	chr3:70327352-70327353	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561164341	chr3:70327371-70327372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535363680	chr3:70327387-70327388	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs9682662	chr3:70327391-70327392	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs185622806	chr3:70327400-70327401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559826857	chr3:70327410-70327411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531936409	chr3:70327458-70327459	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551780115	chr3:70327461-70327462	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571655546	chr3:70327502-70327503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs571576316	chr3:70327514-70327515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556327657	chr3:70327591-70327592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531272947	chr3:70327616-70327617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138207949	chr3:70327647-70327648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs537474282	chr3:70327665-70327666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576468957	chr3:70327666-70327667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs557161899	chr3:70327681-70327682	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545178080	chr3:70327700-70327701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1522345	chr3:70327747-70327748	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs1522346	chr3:70327750-70327751	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs190104382	chr3:70327811-70327812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs181874972	chr3:70327855-70327856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72628621	chr3:70327922-70327923	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs143382508	chr3:70327927-70327928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575587775	chr3:70327928-70327929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147145317	chr3:70327950-70327951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554459237	chr3:70327955-70327956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139476170	chr3:70327965-70327966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540058431	chr3:70328002-70328003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs111500396	chr3:70328005-70328006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116628952	chr3:70328028-70328029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149687948	chr3:70328039-70328040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144515796	chr3:70328040-70328041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562176363	chr3:70328096-70328097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540905919	chr3:70328113-70328114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	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
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	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
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Mental retardation	17847001	CNVD

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:70325800-70327000	Enhancers	Fetal Intestine Large	intestine
2	chr3:70325800-70327000	Enhancers	Fetal Lung	lung
3	chr3:70325800-70327400	Enhancers	Fetal Intestine Small	intestine
4	chr3:70326600-70327000	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr3:70326600-70327000	Enhancers	A549	lung
6	chr3:70326800-70328000	Enhancers	Pancreatic Islets	Pancreatic Islet
7	chr3:70327000-70328600	Weak transcription	A549	lung
8	chr3:70328000-70329000	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr3:70328200-70329400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr3:70328600-70329200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr3:70328600-70329200	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr3:70328600-70329600	Enhancers	H9 Cell Line	embryonic stem cell
13	chr3:70328600-70330400	Enhancers	A549	lung
14	chr3:70328800-70329200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:70329000-70329200	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr3:70329000-70329400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr3:70330200-70332600	Enhancers	Hela-S3	cervix
18	chr3:70330400-70331600	Enhancers	NH-A	brain
19	chr3:70330400-70331800	Flanking Active TSS	A549	lung
20	chr3:70331000-70331600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr3:70331800-70332600	Enhancers	A549	lung
22	chr3:70332400-70347800	Weak transcription	Aorta	Aorta
23	chr3:70339800-70340000	Active TSS	Placenta	Placenta
24	chr3:70339800-70340200	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr3:70339800-70340200	Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr3:70339800-70340200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:70339800-70340400	Active TSS	iPS-15b Cell Line	embryonic stem cell
28	chr3:70339800-70340400	Active TSS	K562	blood
29	chr3:70340000-70340200	Flanking Active TSS	Placenta	Placenta
30	chr3:70343000-70343200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr3:70343200-70344000	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr3:70344000-70344200	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr3:70344200-70346600	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr3:70346600-70347800	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr3:70347400-70348200	Enhancers	A549	lung
36	chr3:70347400-70348400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr3:70347800-70348200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr3:70347800-70348200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr3:70347800-70348200	Enhancers	Aorta	Aorta
40	chr3:70357800-70358200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:70357800-70358400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr3:70358000-70358800	Enhancers	Aorta	Aorta
43	chr3:70358200-70360800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr3:70360400-70360600	Enhancers	A549	lung
45	chr3:70360600-70361200	Weak transcription	A549	lung
46	chr3:70360600-70361600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr3:70360800-70361600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr3:70360800-70361800	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:70360800-70361800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr3:70361000-70361800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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