Variant report

Variant	nsv470783
Chromosome Location	chr3:98431225-98466222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:98450665-98451258	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:98452261-98452798	HepG2	liver:	n/a	n/a
3	ATF2	chr3:98452576-98453067	GM12878	blood:	n/a	n/a
4	ATF2	chr3:98463918-98464617	GM12878	blood:	n/a	n/a
5	ATF2	chr3:98449166-98449665	GM12878	blood:	n/a	n/a
6	ATF2	chr3:98464024-98464663	GM12878	blood:	n/a	n/a
7	ATF2	chr3:98449138-98449542	GM12878	blood:	n/a	n/a
8	ATF2	chr3:98451907-98452363	GM12878	blood:	n/a	n/a
9	BACH1	chr3:98431536-98431728	H1-hESC	embryonic stem cell:	n/a	chr3:98431553-98431567
10	BACH1	chr3:98464794-98464817	K562	blood:	n/a	n/a
11	BATF	chr3:98463086-98463485	GM12878	blood:	n/a	chr3:98463356-98463364 chr3:98463286-98463297
12	BATF	chr3:98464079-98464417	GM12878	blood:	n/a	n/a
13	BATF	chr3:98449120-98449561	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:98463954-98464325	GM12878	blood:	n/a	n/a
15	BCL3	chr3:98452563-98452971	GM12878	blood:	n/a	n/a
16	BCL3	chr3:98449125-98449705	GM12878	blood:	n/a	n/a
17	BCL3	chr3:98463921-98464568	GM12878	blood:	n/a	n/a
18	BCLAF1	chr3:98452265-98453111	GM12878	blood:	n/a	chr3:98452505-98452518
19	BCLAF1	chr3:98452587-98452996	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:98449165-98449730	GM12878	blood:	n/a	n/a
21	BCLAF1	chr3:98450976-98451691	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:98464059-98464616	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:98449132-98449698	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:98463982-98464596	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:98452700-98453327	HepG2	liver:	n/a	n/a
26	BHLHE40	chr3:98450588-98452100	HepG2	liver:	n/a	chr3:98450776-98450785 chr3:98450776-98450785 chr3:98450774-98450787 chr3:98450775-98450784 chr3:98450770-98450791
27	BHLHE40	chr3:98447479-98447534	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:98452642-98453330	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:98450607-98452299	GM12878	blood:	n/a	chr3:98450776-98450785 chr3:98450776-98450785 chr3:98450774-98450787 chr3:98450775-98450784 chr3:98450770-98450791
30	BRCA1	chr3:98451646-98451685	HepG2	liver:	n/a	n/a
31	BRCA1	chr3:98463032-98463181	GM12878	blood:	n/a	n/a
32	BRCA1	chr3:98450923-98451322	GM12878	blood:	n/a	n/a
33	CBX3	chr3:98460084-98460644	HCT-116	colon:	n/a	chr3:98460542-98460553
34	CEBPB	chr3:98452066-98452405	H1-hESC	embryonic stem cell:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
35	CEBPB	chr3:98452008-98452434	MCF-7	breast:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
36	CEBPB	chr3:98463902-98464559	GM12878	blood:	n/a	n/a
37	CEBPB	chr3:98452119-98452277	HepG2	liver:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
38	CEBPB	chr3:98452128-98452429	ECC-1	luminal epithelium:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
39	CEBPB	chr3:98452081-98452433	A549	lung:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
40	CEBPB	chr3:98460131-98460472	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:98451975-98452513	A549	lung:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
42	CEBPB	chr3:98452187-98452302	K562	blood:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
43	CEBPB	chr3:98452044-98452412	HepG2	liver:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
44	CEBPB	chr3:98451999-98452468	ECC-1	luminal epithelium:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
45	CEBPB	chr3:98452074-98452357	A549	lung:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
46	CEBPB	chr3:98460042-98460398	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr3:98452041-98452387	IMR90	lung:	n/a	chr3:98452226-98452239 chr3:98452227-98452238 chr3:98452228-98452237 chr3:98452226-98452237
48	CEBPB	chr3:98453276-98453504	HepG2	liver:	n/a	chr3:98453422-98453435 chr3:98453422-98453433
49	CHD1	chr3:98456600-98456646	GM12878	blood:	n/a	n/a
50	CHD1	chr3:98449349-98449629	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:98452940-98452990	HCPEpiC	choroid plexus:	n/a
2	chr3:98451398-98451448	HRCEpiC	kidney:	n/a
3	chr3:98452940-98452990	HCPEpiC	choroid plexus:	n/a
4	chr3:98451398-98451448	HRCEpiC	kidney:	n/a
5	chr3:98452812-98452862	SKMC	muscle:	n/a
6	chr3:98451002-98451052	GM12891	blood:	n/a
7	chr3:98451398-98451448	HRPEpiC	eye:	n/a
8	chr3:98451002-98451052	HCT-116	colon:	n/a
9	chr3:98453086-98453136	AG04450	lung:	fetal
10	chr3:98451002-98451052	Caco-2	colon:	n/a
11	chr3:98451287-98451337	HL-60	blood:	n/a
12	chr3:98452218-98452268	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:98451002-98451052	PANC-1	pancreas:	n/a
14	chr3:98451002-98451052	AG04449	skin:	fetal
15	chr3:98452812-98452862	NB4	blood:	n/a
16	chr3:98451287-98451337	GM06990	blood:	n/a
17	chr3:98453086-98453136	NT2-D1	testis:	n/a
18	chr3:98450242-98450292	Hepatocyte	liver:	n/a
19	chr3:98450242-98450292	HPAEpiC	pulmonary alveolar:	n/a
20	chr3:98452879-98452929	GM12878	blood:	n/a
21	chr3:98451119-98451169	AG04449	skin:	fetal
22	chr3:98451398-98451448	Caco-2	colon:	n/a
23	chr3:98451116-98451166	BE2_C	brain:	n/a
24	chr3:98452812-98452862	ECC-1	luminal epithelium:	n/a
25	chr3:98452940-98452990	NB4	blood:	n/a
26	chr3:98452218-98452268	HCM	heart:	n/a
27	chr3:98452218-98452268	NHDF-neo	bronchial:	n/a
28	chr3:98452812-98452862	A549	lung:	n/a
29	chr3:98451718-98451768	Jurkat	blood:	n/a
30	chr3:98452812-98452862	NHBE	bronchial:	n/a
31	chr3:98441923-98441973	HMEC	breast:	n/a
32	chr3:98452812-98452862	T-47D	breast:	n/a
33	chr3:98451718-98451768	ProgFib	skin:	n/a
34	chr3:98451119-98451169	CMK	blood:	n/a
35	chr3:98451287-98451337	SK-N-SH	brain:	n/a
36	chr3:98452940-98452990	HepG2	liver:	n/a
37	chr3:98451398-98451448	NHBE	bronchial:	n/a
38	chr3:98452812-98452862	GM19239	blood:	n/a
39	chr3:98452218-98452268	CMK	blood:	n/a
40	chr3:98450242-98450292	NHDF-neo	bronchial:	n/a
41	chr3:98451287-98451337	ovcar-3	ovarian:	n/a
42	chr3:98451002-98451052	IMR90	lung:	fetal
43	chr3:98452812-98452862	HNPCEpiC	eye:	n/a
44	chr3:98451287-98451337	HMEC	breast:	n/a
45	chr3:98451718-98451768	HUVEC	blood vessel:	n/a
46	chr3:98451398-98451448	Hepatocyte	liver:	n/a
47	chr3:98451119-98451169	NHDF-neo	bronchial:	n/a
48	chr3:98451116-98451166	AG10803	skin:	n/a
49	chr3:98451718-98451768	HAEpiC	amniotic membrane:	n/a
50	chr3:98452218-98452268	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:98457980..98458905-chr6:108437117..108437659,2	MCF-7	breast:
2	chr3:98438833..98441641-chr3:98449159..98451733,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCBLD2-1	chr3:98434149-98434365	ENSG00000239445.1
2	lnc-DCBLD2-1	chr3:98433176-98433342	ENSG00000239445.1
3	lnc-DCBLD2-1	chr3:98434494-98434622	NONHSAT090810
4	lnc-ST3GAL6-3	chr3:98451558-98451855	NONHSAT090816
5	lnc-DCBLD2-1	chr3:98437263-98437365	NR_046683
6	lnc-DCBLD2-1	chr3:98434494-98434645	NONHSAT147243
7	lnc-DCBLD2-1	chr3:98433174-98433342	ENSG00000239445.1
8	lnc-DCBLD2-1	chr3:98451270-98451492	ENSG00000239445.1
9	lnc-DCBLD2-1	chr3:98434494-98434621	ENSG00000239445.1
10	lnc-DCBLD2-1	chr3:98434220-98434365	NONHSAT090810
11	lnc-ST3GAL6-3	chr3:98452300-98452435	NONHSAT090817
12	lnc-ST3GAL6-3	chr3:98451213-98451376	NONHSAT090815
13	lnc-DCBLD2-1	chr3:98434256-98434365	NONHSAT147243
14	lnc-DCBLD2-1	chr3:98434220-98434365	ENSG00000239445.1
15	lnc-DCBLD2-1	chr3:98434220-98434365	NR_046683
16	lnc-ST3GAL6-3	chr3:98451080-98451376	NONHSAT090814
17	lnc-DCBLD2-1	chr3:98433177-98433342	NR_046683
18	lnc-DCBLD2-1	chr3:98451270-98451495	NR_046683
19	lnc-DCBLD2-1	chr3:98437268-98437365	ENSG00000239445.1
20	lnc-DCBLD2-1	chr3:98432741-98433342	NONHSAT090810
21	lnc-DCBLD2-1	chr3:98434494-98434621	ENSG00000239445.1
22	lnc-DCBLD2-1	chr3:98434220-98434365	ENSG00000239445.1
23	lnc-DCBLD2-1	chr3:98434494-98434621	ENSG00000239445.1
24	lnc-DCBLD2-1	chr3:98451270-98451352	ENSG00000239445.1
25	lnc-DCBLD2-1	chr3:98437263-98437365	ENSG00000239445.1
26	lnc-DCBLD2-1	chr3:98451270-98451495	ENSG00000239445.1
27	lnc-DCBLD2-1	chr3:98434494-98434621	NR_046683

Variant related genes	Relation type
ST3GAL6	TF binding region
ST3GAL6-AS1	TF binding region
ST3GAL6	CpG island
ST3GAL6-AS1	CpG island
ENSG00000064225	chromatin interactions
ENSG00000239445	chromatin interactions

Extended variants
information (count: 1277 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16840083	chr3:98431225-98431226	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549551038	chr3:98431226-98431227	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs367936766	chr3:98431242-98431243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190607870	chr3:98431268-98431269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144095837	chr3:98431291-98431292	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370932327	chr3:98431297-98431298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs150964974	chr3:98431318-98431319	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181071860	chr3:98431339-98431340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140768520	chr3:98431353-98431354	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557834636	chr3:98431388-98431389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs577589533	chr3:98431416-98431417	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs184380616	chr3:98431491-98431492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11385511	chr3:98431493-98431494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs397752586	chr3:98431506-98431507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs74983524	chr3:98431507-98431508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs73858607	chr3:98431511-98431512	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs369140946	chr3:98431522-98431523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531538889	chr3:98431527-98431528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189729826	chr3:98431530-98431531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181330495	chr3:98431725-98431726	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562218788	chr3:98431732-98431733	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549363043	chr3:98431749-98431750	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185516893	chr3:98431783-98431784	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs112792154	chr3:98431852-98431853	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541022108	chr3:98431857-98431858	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs138365532	chr3:98431873-98431874	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190673380	chr3:98431908-98431909	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs115043894	chr3:98431909-98431910	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569707246	chr3:98431915-98431916	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs528174438	chr3:98431917-98431918	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79267271	chr3:98431934-98431935	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181558469	chr3:98431942-98431943	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534738459	chr3:98431985-98431986	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs10935480	chr3:98431986-98431987	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs563367489	chr3:98432016-98432017	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146890040	chr3:98432040-98432041	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187407412	chr3:98432067-98432068	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576517427	chr3:98432094-98432095	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542398104	chr3:98432106-98432107	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555729083	chr3:98432120-98432121	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572183602	chr3:98432124-98432125	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs1136551	chr3:98432202-98432203	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs1136550	chr3:98432205-98432206	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs192189514	chr3:98432209-98432210	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543314910	chr3:98432255-98432256	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139336883	chr3:98432284-98432285	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs536820629	chr3:98432323-98432324	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs549141407	chr3:98432360-98432361	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs555236772	chr3:98432425-98432426	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs559620174	chr3:98432437-98432438	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	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
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:98425000-98431600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:98425600-98438600	Weak transcription	Aorta	Aorta
3	chr3:98427400-98432800	Enhancers	Placenta	Placenta
4	chr3:98428800-98432600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:98428800-98432800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr3:98429000-98432600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr3:98429000-98432600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr3:98429000-98432800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr3:98429400-98432800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr3:98431000-98449200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr3:98431600-98433400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:98432600-98433000	Enhancers	H9 Cell Line	embryonic stem cell
13	chr3:98432600-98433000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr3:98432600-98433000	Enhancers	Stomach Mucosa	stomach
15	chr3:98432600-98433600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:98432600-98433800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr3:98432800-98433000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr3:98432800-98433200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr3:98432800-98433800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr3:98432800-98437400	Weak transcription	Placenta	Placenta
21	chr3:98433000-98435000	Weak transcription	Stomach Mucosa	stomach
22	chr3:98433200-98433800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr3:98433400-98446000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:98436200-98436400	Enhancers	Stomach Mucosa	stomach
25	chr3:98437200-98438000	Enhancers	GM12878-XiMat	blood
26	chr3:98437400-98437800	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr3:98437400-98438400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr3:98437400-98438400	Enhancers	Placenta	Placenta
29	chr3:98438200-98438600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr3:98438400-98438600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr3:98438400-98441800	Weak transcription	Placenta	Placenta
32	chr3:98438600-98441400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr3:98438800-98441000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:98439400-98439600	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr3:98439600-98440800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr3:98440800-98441200	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr3:98440800-98442000	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr3:98440800-98442800	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr3:98441000-98441200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:98441000-98441600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr3:98441000-98442000	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr3:98441200-98441400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr3:98441200-98441600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:98441200-98441600	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr3:98441200-98441800	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr3:98441200-98441800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr3:98441200-98443000	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr3:98441400-98441600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr3:98441400-98441600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr3:98441600-98442000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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