Variant report

Variant	nsv428414
Chromosome Location	chr3:20376250-20540628
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:609)
CpG islands
(count:244)
Chromatin interactive
region (count:29)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:609 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20382933-20383181	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:20381827-20382195	K562	blood:	n/a	n/a
3	ARID3A	chr3:20378141-20378394	K562	blood:	n/a	n/a
4	ARID3A	chr3:20394102-20394581	K562	blood:	n/a	n/a
5	ATF1	chr3:20521702-20521870	K562	blood:	n/a	n/a
6	ATF2	chr3:20385829-20386232	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr3:20394287-20394634	K562	blood:	n/a	n/a
8	BACH1	chr3:20394395-20394609	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr3:20536253-20536368	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:20535546-20535645	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:20492139-20492474	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:20394371-20394578	K562	blood:	n/a	n/a
13	BACH1	chr3:20381913-20382270	K562	blood:	n/a	n/a
14	BACH1	chr3:20492146-20492486	K562	blood:	n/a	n/a
15	BATF	chr3:20416798-20417091	GM12878	blood:	n/a	n/a
16	BHLHE40	chr3:20394266-20394730	K562	blood:	n/a	n/a
17	BHLHE40	chr3:20381816-20382255	K562	blood:	n/a	n/a
18	BRCA1	chr3:20381852-20382113	Hela-S3	cervix:	n/a	n/a
19	CBX3	chr3:20394150-20394723	K562	blood:	n/a	chr3:20394644-20394655
20	CCNT2	chr3:20394423-20394638	K562	blood:	n/a	n/a
21	CCNT2	chr3:20500973-20501023	K562	blood:	n/a	n/a
22	CEBPB	chr3:20381826-20382307	K562	blood:	n/a	n/a
23	CEBPB	chr3:20421949-20421971	HepG2	liver:	n/a	n/a
24	CEBPB	chr3:20447358-20447747	HepG2	liver:	n/a	chr3:20447481-20447492
25	CEBPB	chr3:20394053-20394628	K562	blood:	n/a	chr3:20394224-20394235
26	CEBPB	chr3:20394124-20394372	IMR90	lung:	n/a	chr3:20394224-20394235
27	CEBPB	chr3:20394114-20394325	K562	blood:	n/a	chr3:20394224-20394235
28	CEBPB	chr3:20394100-20394376	HepG2	liver:	n/a	chr3:20394224-20394235
29	CEBPB	chr3:20416950-20417260	K562	blood:	n/a	n/a
30	CEBPB	chr3:20439757-20440083	IMR90	lung:	n/a	n/a
31	CEBPB	chr3:20439770-20440049	A549	lung:	n/a	n/a
32	CEBPB	chr3:20439732-20440080	HepG2	liver:	n/a	n/a
33	CEBPB	chr3:20405252-20405383	K562	blood:	n/a	n/a
34	CEBPB	chr3:20421835-20421992	K562	blood:	n/a	n/a
35	CEBPB	chr3:20439795-20440063	K562	blood:	n/a	n/a
36	CEBPB	chr3:20394121-20394364	A549	lung:	n/a	chr3:20394224-20394235
37	CEBPB	chr3:20439832-20440032	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr3:20442866-20443121	HepG2	liver:	n/a	chr3:20442974-20442985
39	CEBPB	chr3:20393995-20394652	K562	blood:	n/a	chr3:20394224-20394235
40	CEBPB	chr3:20381803-20382270	K562	blood:	n/a	n/a
41	CEBPB	chr3:20417034-20417209	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr3:20381826-20382192	Hela-S3	cervix:	n/a	n/a
43	CEBPD	chr3:20394123-20394654	K562	blood:	n/a	n/a
44	CEBPD	chr3:20394035-20394664	K562	blood:	n/a	n/a
45	CTCF	chr3:20381900-20382050	GM12868	blood:	n/a	chr3:20381990-20382011 chr3:20381988-20382006 chr3:20381991-20382004
46	CTCF	chr3:20381960-20382110	SAEC	small airway:	n/a	chr3:20381990-20382011 chr3:20381988-20382006 chr3:20381991-20382004
47	CTCF	chr3:20381940-20382090	GM12869	blood:	n/a	chr3:20381990-20382011 chr3:20381988-20382006 chr3:20381991-20382004
48	CTCF	chr3:20381839-20382139	GM12878	blood:	n/a	chr3:20381990-20382011 chr3:20381988-20382006 chr3:20381991-20382004
49	CTCF	chr3:20381940-20382090	HEK293	kidney:	n/a	chr3:20381990-20382011 chr3:20381988-20382006 chr3:20381991-20382004
50	CTCF	chr3:20381980-20382130	HA-sp	spinal cord:	n/a	chr3:20381990-20382011 chr3:20381988-20382006 chr3:20381991-20382004

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20418856-20418906	SK-N-MC	brain:	n/a
2	chr3:20522301-20522351	HAEpiC	amniotic membrane:	n/a
3	chr3:20418856-20418906	A549	lung:	n/a
4	chr3:20448283-20448333	SK-N-SH	brain:	n/a
5	chr3:20522301-20522351	HCM	heart:	n/a
6	chr3:20522301-20522351	GM12892	blood:	n/a
7	chr3:20412342-20412392	PrEC	prostate:	n/a
8	chr3:20522301-20522351	GM12891	blood:	n/a
9	chr3:20412342-20412392	NT2-D1	testis:	n/a
10	chr3:20522301-20522351	SK-N-SH_RA	brain:	n/a
11	chr3:20522301-20522351	HPAEpiC	pulmonary alveolar:	n/a
12	chr3:20412342-20412392	Hela-S3	cervix:	n/a
13	chr3:20418856-20418906	K562	blood:	n/a
14	chr3:20412342-20412392	GM19239	blood:	n/a
15	chr3:20522301-20522351	GM19239	blood:	n/a
16	chr3:20522301-20522351	AG04449	skin:	fetal
17	chr3:20448283-20448333	SAEC	small airway:	n/a
18	chr3:20412342-20412392	MCF10A-Er-Src	breast:	n/a
19	chr3:20448283-20448333	NT2-D1	testis:	n/a
20	chr3:20522301-20522351	SKMC	muscle:	n/a
21	chr3:20418856-20418906	GM06990	blood:	n/a
22	chr3:20522301-20522351	NH-A	brain:	n/a
23	chr3:20522301-20522351	A549	lung:	n/a
24	chr3:20522301-20522351	RPTEC	kidney:	n/a
25	chr3:20412342-20412392	HCPEpiC	choroid plexus:	n/a
26	chr3:20448283-20448333	CMK	blood:	n/a
27	chr3:20448283-20448333	MCF-7	breast:	n/a
28	chr3:20522301-20522351	Hela-S3	cervix:	n/a
29	chr3:20412342-20412392	HCF	heart:	n/a
30	chr3:20412342-20412392	K562	blood:	n/a
31	chr3:20448283-20448333	HEEpiC	esophagus:	n/a
32	chr3:20412342-20412392	HMEC	breast:	n/a
33	chr3:20412342-20412392	RPTEC	kidney:	n/a
34	chr3:20522301-20522351	BE2_C	brain:	n/a
35	chr3:20412342-20412392	AG09309	skin:	n/a
36	chr3:20448283-20448333	HAEpiC	amniotic membrane:	n/a
37	chr3:20412342-20412392	BJ	skin:	n/a
38	chr3:20418856-20418906	HCT-116	colon:	n/a
39	chr3:20418856-20418906	HCPEpiC	choroid plexus:	n/a
40	chr3:20418856-20418906	Hela-S3	cervix:	n/a
41	chr3:20418856-20418906	PFSK-1	brain:	n/a
42	chr3:20448283-20448333	ProgFib	skin:	n/a
43	chr3:20418856-20418906	SKMC	muscle:	n/a
44	chr3:20412342-20412392	GM12891	blood:	n/a
45	chr3:20448283-20448333	RPTEC	kidney:	n/a
46	chr3:20418856-20418906	U87	brain:	n/a
47	chr3:20522301-20522351	HEK293	kidney:	embryo
48	chr3:20522301-20522351	HepG2	liver:	n/a
49	chr3:20522301-20522351	SK-N-MC	brain:	n/a
50	chr3:20522301-20522351	Hepatocyte	liver:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
2	chr3:20364762..20367629-chr3:20378813..20381206,2	K562	blood:
3	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
4	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
5	chr3:20381763..20382471-chr3:21525223..21526354,4	MCF-7	breast:
6	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
7	chr3:20460438..20462411-chr3:20516734..20518648,2	MCF-7	breast:
8	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
9	chr3:20378280..20380658-chr3:21571258..21574044,2	K562	blood:
10	chr3:20381603..20382455-chr3:22159036..22159808,2	K562	blood:
11	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
12	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
13	chr3:20436330..20438604-chr3:20439437..20442062,2	MCF-7	breast:
14	chr3:20384572..20387306-chr3:20389164..20391622,2	K562	blood:
15	chr3:20381671..20382483-chr3:21592493..21593315,3	MCF-7	breast:
16	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
17	chr3:20451777..20453884-chr3:20476566..20478123,2	K562	blood:
18	chr3:20375934..20377835-chr3:20379796..20382067,2	MCF-7	breast:
19	chr3:20381543..20382061-chr3:21935726..21936559,2	MCF-7	breast:
20	chr3:20381610..20382290-chr3:22159023..22159894,2	MCF-7	breast:
21	chr3:20413525..20416049-chr3:20420124..20421856,2	K562	blood:
22	chr3:20447764..20450202-chr3:20450641..20452829,2	MCF-7	breast:
23	chr3:20381373..20383643-chr3:20384207..20386125,2	K562	blood:
24	chr20:55749599..55750399-chr3:20381742..20382481,2	MCF-7	breast:
25	chr3:20381636..20382451-chr3:20971371..20972187,4	MCF-7	breast:
26	chr3:20370553..20372483-chr3:20373507..20376475,2	K562	blood:
27	chr3:20514130..20516158-chr3:20517415..20519398,2	K562	blood:
28	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
29	chr3:20514130..20516158-chr3:20517415..20519398,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-2	chr3:20387156-20387558	NONHSAT088622
2	lnc-KAT2B-2	chr3:20389488-20389501	NONHSAT088622
3	lnc-KAT2B-2	chr3:20392207-20392420	XLOC_002595
4	lnc-KAT2B-2	chr3:20387157-20387558	XLOC_002595
5	lnc-KAT2B-2	chr3:20389489-20389501	XLOC_002595
6	lnc-KAT2B-2	chr3:20387152-20387274	XLOC_002595
7	lnc-KAT2B-3	chr3:20429741-20432054	ENSG00000261734.1
8	lnc-KAT2B-2	chr3:20383960-20385528	XLOC_002595
9	lnc-KAT2B-2	chr3:20387517-20387558	XLOC_002595
10	lnc-KAT2B-2	chr3:20389489-20389581	XLOC_002595

No data

Variant related genes	Relation type
ENSG00000231304	TF binding region
ENSG00000261734	TF binding region
ENSG00000231304	CpG island
ENSG00000261734	CpG island

Extended variants
information (count: 4629 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:4629 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190548181	chr3:20376254-20376255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538938561	chr3:20376302-20376303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149768300	chr3:20376315-20376316	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs77453049	chr3:20376341-20376342	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572281594	chr3:20376345-20376346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34585492	chr3:20376430-20376431	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs114562008	chr3:20376446-20376447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554331348	chr3:20376471-20376472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377419672	chr3:20376472-20376473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565021223	chr3:20376563-20376564	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182938473	chr3:20376575-20376576	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9821725	chr3:20376684-20376685	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs565299463	chr3:20376698-20376699	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187032040	chr3:20376709-20376710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541396660	chr3:20376725-20376726	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs191826499	chr3:20376740-20376741	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530410062	chr3:20376785-20376786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145668608	chr3:20376791-20376792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs570217144	chr3:20376802-20376803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531456016	chr3:20376860-20376861	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184068535	chr3:20376897-20376898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141432288	chr3:20376919-20376920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs547296725	chr3:20376999-20377000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145270680	chr3:20377043-20377044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs6791417	chr3:20377100-20377101	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs373596952	chr3:20377116-20377117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565874172	chr3:20377136-20377137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs536099641	chr3:20377142-20377143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554343570	chr3:20377172-20377173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575801046	chr3:20377219-20377220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565362720	chr3:20377230-20377231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs117323354	chr3:20377245-20377246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558815105	chr3:20377267-20377268	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77368449	chr3:20377288-20377289	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541109507	chr3:20377305-20377306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559661234	chr3:20377309-20377310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs368097737	chr3:20377331-20377332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575215169	chr3:20377364-20377365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542513833	chr3:20377395-20377396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs563888430	chr3:20377402-20377403	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs533008138	chr3:20377432-20377433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373915097	chr3:20377530-20377531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187590033	chr3:20377586-20377587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536356976	chr3:20377590-20377591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs11293807	chr3:20377609-20377610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs60538383	chr3:20377638-20377639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs57107964	chr3:20377644-20377645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1356791	chr3:20377724-20377725	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs191452680	chr3:20377762-20377763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs182483176	chr3:20377808-20377809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20354000-20381800	Weak transcription	Aorta	Aorta
2	chr3:20373400-20376600	Weak transcription	K562	blood
3	chr3:20375000-20377000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:20376400-20376600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr3:20376600-20378400	Enhancers	K562	blood
6	chr3:20376600-20380200	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr3:20377000-20377400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:20377400-20378800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:20377600-20378200	Enhancers	Stomach Mucosa	stomach
10	chr3:20378000-20378200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr3:20378200-20380400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr3:20378400-20378800	Weak transcription	K562	blood
13	chr3:20378800-20379000	Enhancers	K562	blood
14	chr3:20378800-20381000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:20379000-20379200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:20379000-20382000	Weak transcription	K562	blood
17	chr3:20379200-20380400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr3:20380200-20382400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr3:20380200-20382600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr3:20380400-20380800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr3:20380400-20380800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr3:20380400-20382000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr3:20380400-20382200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr3:20380400-20382400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:20380600-20381800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
26	chr3:20380600-20382000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr3:20381000-20382000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:20381800-20382000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr3:20381800-20382400	Enhancers	Aorta	Aorta
30	chr3:20382000-20382200	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr3:20382000-20382200	Enhancers	Brain Substantia Nigra	brain
32	chr3:20382000-20382200	Enhancers	Fetal Intestine Large	intestine
33	chr3:20382000-20382200	Enhancers	Fetal Kidney	kidney
34	chr3:20382000-20382200	Enhancers	Pancreas	Pancrea
35	chr3:20382000-20382200	Enhancers	Rectal Smooth Muscle	rectum
36	chr3:20382000-20382200	Enhancers	K562	blood
37	chr3:20382000-20382400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr3:20382000-20382400	Active TSS	Brain Anterior Caudate	brain
39	chr3:20382000-20382400	Active TSS	Pancreatic Islets	Pancreatic Islet
40	chr3:20382000-20382400	Active TSS	Fetal Lung	lung
41	chr3:20382000-20382400	Active TSS	Stomach Smooth Muscle	stomach
42	chr3:20382000-20383800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:20382000-20385400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr3:20382200-20385200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr3:20382200-20390000	Weak transcription	Pancreas	Pancrea
46	chr3:20382400-20384000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
47	chr3:20382400-20385200	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr3:20382400-20394600	Weak transcription	Aorta	Aorta
49	chr3:20382600-20384400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr3:20383800-20384200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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