Variant report

Variant	nsv1028181
Chromosome Location	chr5:111628901-111683317
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	BHLHE40	chr5:111665513-111665737	GM12878	blood:	n/a	n/a
2	BHLHE40	chr5:111672660-111672866	HepG2	liver:	n/a	chr5:111672779-111672800 chr5:111672784-111672793 chr5:111672783-111672796 chr5:111672785-111672794
3	BRCA1	chr5:111674313-111675097	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr5:111648598-111648854	HepG2	liver:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
5	CEBPB	chr5:111674572-111675011	H1-hESC	embryonic stem cell:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
6	CEBPB	chr5:111674386-111675014	A549	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
7	CEBPB	chr5:111644377-111644795	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr5:111648529-111648917	A549	lung:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
9	CEBPB	chr5:111674684-111675000	IMR90	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
10	CEBPB	chr5:111674525-111675177	MCF-7	breast:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
11	CEBPB	chr5:111660740-111660940	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr5:111674335-111675109	ECC-1	luminal epithelium:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
13	CEBPB	chr5:111674735-111675013	A549	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
14	CEBPB	chr5:111647976-111648996	Hela-S3	cervix:	n/a	chr5:111648694-111648711 chr5:111648118-111648131 chr5:111648696-111648707 chr5:111648437-111648448
15	CEBPB	chr5:111674743-111674884	HepG2	liver:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
16	CEBPB	chr5:111648479-111648970	ECC-1	luminal epithelium:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
17	CEBPB	chr5:111664552-111664647	HepG2	liver:	n/a	chr5:111664599-111664610
18	CEBPB	chr5:111674734-111674998	K562	blood:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
19	CEBPB	chr5:111674221-111675111	ECC-1	luminal epithelium:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
20	CEBPB	chr5:111674347-111675076	MCF-7	breast:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
21	CEBPB	chr5:111674383-111675019	HepG2	liver:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
22	CEBPB	chr5:111648486-111648956	ECC-1	luminal epithelium:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
23	CEBPB	chr5:111674424-111675026	K562	blood:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
24	CEBPB	chr5:111672672-111672946	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr5:111648622-111648781	K562	blood:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
26	CEBPB	chr5:111674223-111675149	Hela-S3	cervix:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
27	CEBPB	chr5:111649599-111649624	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr5:111648572-111648903	A549	lung:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
29	CEBPB	chr5:111660737-111660943	IMR90	lung:	n/a	n/a
30	CEBPB	chr5:111649518-111649702	K562	blood:	n/a	n/a
31	CEBPB	chr5:111674312-111675089	A549	lung:	n/a	chr5:111674833-111674842 chr5:111674831-111674842 chr5:111674833-111674842 chr5:111674833-111674842 chr5:111674833-111674842
32	CEBPB	chr5:111648588-111648889	IMR90	lung:	n/a	chr5:111648694-111648711 chr5:111648696-111648707
33	CHD2	chr5:111674287-111675069	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr5:111652427-111652570	MCF-7	breast:	n/a	n/a
35	CTCF	chr5:111637345-111637407	K562	blood:	n/a	n/a
36	CTCF	chr5:111650327-111650373	GM20000	blood:	n/a	n/a
37	CTCF	chr5:111673200-111673350	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr5:111652480-111652630	HMEC	breast:	n/a	n/a
39	CTCF	chr5:111637340-111637490	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr5:111638475-111638571	K562	blood:	n/a	n/a
41	CTCF	chr5:111630540-111630690	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr5:111652320-111652470	RPTEC	kidney:	n/a	n/a
43	CTCF	chr5:111637339-111637419	LNCaP	prostate:	n/a	n/a
44	CTCF	chr5:111652500-111652650	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:111652580-111652730	RPTEC	kidney:	n/a	n/a
46	CTCF	chr5:111630640-111630790	HCM	heart:	n/a	n/a
47	CTCF	chr5:111652400-111652550	MCF-7	breast:	n/a	n/a
48	CTCF	chr5:111652520-111652670	RPTEC	kidney:	n/a	n/a
49	CTCF	chr5:111652400-111652550	SAEC	small airway:	n/a	n/a
50	CTCF	chr5:111652468-111652543	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:111665548-111665598	HCT-116	colon:	n/a
2	chr5:111665548-111665598	AG04450	lung:	fetal
3	chr5:111665548-111665598	GM19239	blood:	n/a
4	chr5:111665548-111665598	AG09309	skin:	n/a
5	chr5:111665548-111665598	LNCaP	prostate:	n/a
6	chr5:111665548-111665598	RPTEC	kidney:	n/a
7	chr5:111665548-111665598	HCF	heart:	n/a
8	chr5:111665548-111665598	CMK	blood:	n/a
9	chr5:111665548-111665598	U87	brain:	n/a
10	chr5:111665548-111665598	SK-N-SH_RA	brain:	n/a
11	chr5:111665548-111665598	PANC-1	pancreas:	n/a
12	chr5:111665548-111665598	BE2_C	brain:	n/a
13	chr5:111665548-111665598	NH-A	brain:	n/a
14	chr5:111665548-111665598	NB4	blood:	n/a
15	chr5:111665548-111665598	HCM	heart:	n/a
16	chr5:111665548-111665598	HAEpiC	amniotic membrane:	n/a
17	chr5:111665548-111665598	HUVEC	blood vessel:	n/a
18	chr5:111665548-111665598	SKMC	muscle:	n/a
19	chr5:111665548-111665598	NHDF-neo	bronchial:	n/a
20	chr5:111665548-111665598	BJ	skin:	n/a
21	chr5:111665548-111665598	HL-60	blood:	n/a
22	chr5:111665548-111665598	HepG2	liver:	n/a
23	chr5:111665548-111665598	AG09319	gingival:	n/a
24	chr5:111665548-111665598	SK-N-MC	brain:	n/a
25	chr5:111665548-111665598	PrEC	prostate:	n/a
26	chr5:111665548-111665598	ECC-1	luminal epithelium:	n/a
27	chr5:111665548-111665598	HRCEpiC	kidney:	n/a
28	chr5:111665548-111665598	GM06990	blood:	n/a
29	chr5:111665548-111665598	IMR90	lung:	fetal
30	chr5:111665548-111665598	MCF-7	breast:	n/a
31	chr5:111665548-111665598	ProgFib	skin:	n/a
32	chr5:111665548-111665598	MCF10A-Er-Src	breast:	n/a
33	chr5:111665548-111665598	A549	lung:	n/a
34	chr5:111665548-111665598	GM12878	blood:	n/a
35	chr5:111665548-111665598	HEEpiC	esophagus:	n/a
36	chr5:111665548-111665598	Jurkat	blood:	n/a
37	chr5:111665548-111665598	HCPEpiC	choroid plexus:	n/a
38	chr5:111665548-111665598	HRE	kidney:	n/a
39	chr5:111665548-111665598	GM12891	blood:	n/a
40	chr5:111665548-111665598	Hela-S3	cervix:	n/a
41	chr5:111665548-111665598	HIPEpiC	eye:	n/a
42	chr5:111665548-111665598	HEK293	kidney:	embryo
43	chr5:111665548-111665598	HNPCEpiC	eye:	n/a
44	chr5:111665548-111665598	K562	blood:	n/a
45	chr5:111665548-111665598	PFSK-1	brain:	n/a
46	chr5:111665548-111665598	H1-hESC	embryonic stem cell:	embryo
47	chr5:111665548-111665598	NT2-D1	testis:	n/a
48	chr5:111665548-111665598	HRPEpiC	eye:	n/a
49	chr5:111665548-111665598	ovcar-3	ovarian:	n/a
50	chr5:111665548-111665598	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:111676724..111678269-chr5:111678976..111680650,2	MCF-7	breast:
2	chr5:111642905..111645831-chr5:111648722..111651593,3	K562	blood:
3	chr5:111681506..111684177-chr5:111711327..111713137,2	K562	blood:
4	chr5:111629073..111631228-chr5:111635645..111639350,3	K562	blood:
5	chr5:111676724..111678269-chr5:111678976..111680650,2	MCF-7	breast:
6	chr5:111496502..111498084-chr5:111652901..111655234,2	MCF-7	breast:
7	chr5:111672466..111674712-chr5:111689508..111691131,2	K562	blood:
8	chr5:111678130..111679875-chr5:111682477..111684112,2	K562	blood:
9	chr5:111629073..111631228-chr5:111635645..111639350,3	K562	blood:
10	chr5:111654503..111657162-chr5:111657627..111659825,2	K562	blood:
11	chr5:111638084..111640308-chr5:111646622..111650517,3	K562	blood:
12	chr5:111664622..111667062-chr5:111669246..111671249,2	K562	blood:
13	chr5:111664622..111667062-chr5:111669246..111671249,2	K562	blood:
14	chr5:111654503..111657162-chr5:111657627..111659825,2	K562	blood:
15	chr5:111638084..111640308-chr5:111646622..111650517,3	K562	blood:
16	chr5:111678130..111679875-chr5:111682477..111684112,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf13-5	chr5:111643083-111643099	NONHSAT103225

Variant related genes	Relation type
EPB41L4A	TF binding region
EPB41L4A	CpG island
ENSG00000238363	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000129595	chromatin interactions

Extended variants
information (count: 2291 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2291 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7706772	chr5:111628901-111628902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532383708	chr5:111628904-111628905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs71626659	chr5:111628911-111628912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34631751	chr5:111628918-111628919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs397811019	chr5:111628922-111628923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34996181	chr5:111628929-111628930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547365981	chr5:111628940-111628941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565990291	chr5:111628973-111628974	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534137462	chr5:111629041-111629042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs555822192	chr5:111629043-111629044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs149290819	chr5:111629057-111629058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374968122	chr5:111629064-111629065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs386691158	chr5:111629065-111629066	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs55898131	chr5:111629066-111629067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs61228559	chr5:111629068-111629069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371834728	chr5:111629073-111629074	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370477969	chr5:111629091-111629092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs17134324	chr5:111629108-111629109	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs578105484	chr5:111629111-111629112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs545626386	chr5:111629117-111629118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116530874	chr5:111629144-111629145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs140615368	chr5:111629174-111629175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs57428532	chr5:111629196-111629197	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs116193256	chr5:111629222-111629223	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs531372306	chr5:111629226-111629227	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs375849529	chr5:111629232-111629233	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs145733667	chr5:111629260-111629261	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs72781662	chr5:111629275-111629276	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs72781664	chr5:111629281-111629282	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs115534963	chr5:111629319-111629320	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs543708943	chr5:111629320-111629321	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs138315166	chr5:111629357-111629358	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548534647	chr5:111629387-111629388	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs113648319	chr5:111629392-111629393	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs538287063	chr5:111629393-111629394	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556376529	chr5:111629398-111629399	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs571725586	chr5:111629404-111629405	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs576897376	chr5:111629412-111629413	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538811674	chr5:111629415-111629416	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs557152907	chr5:111629427-111629428	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs62364140	chr5:111629484-111629485	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs559468659	chr5:111629493-111629494	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs542899014	chr5:111629506-111629507	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs554870913	chr5:111629541-111629542	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs373161472	chr5:111629587-111629588	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs141961032	chr5:111629601-111629602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs150662365	chr5:111629604-111629605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs576892235	chr5:111629683-111629684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs138106601	chr5:111629684-111629685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374331241	chr5:111629694-111629695	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Colorectal cancer	21297112	CNVD
Prostate cancer	22341455	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:111627000-111629400	Weak transcription	Right Atrium	heart
2	chr5:111627400-111630000	Weak transcription	Gastric	stomach
3	chr5:111628000-111629200	Weak transcription	Left Ventricle	heart
4	chr5:111628000-111629200	Weak transcription	Right Ventricle	heart
5	chr5:111628800-111631600	Enhancers	Fetal Heart	heart
6	chr5:111629200-111629600	Flanking Active TSS	Left Ventricle	heart
7	chr5:111629200-111629600	Flanking Active TSS	Right Ventricle	heart
8	chr5:111629200-111630200	Enhancers	Brain Hippocampus Middle	brain
9	chr5:111629400-111630000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr5:111629400-111630200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:111629400-111630600	Enhancers	Right Atrium	heart
12	chr5:111629600-111630400	Enhancers	Cortex derived primary cultured neurospheres	brain
13	chr5:111629600-111631000	Enhancers	Left Ventricle	heart
14	chr5:111629600-111631000	Enhancers	Right Ventricle	heart
15	chr5:111630000-111630200	Enhancers	Gastric	stomach
16	chr5:111630000-111630400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr5:111630000-111630400	Enhancers	Brain Anterior Caudate	brain
18	chr5:111630000-111630600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr5:111630000-111631000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr5:111630400-111639600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr5:111631000-111632200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:111631000-111639400	Weak transcription	Left Ventricle	heart
23	chr5:111631000-111639600	Weak transcription	Right Ventricle	heart
24	chr5:111631600-111634000	Weak transcription	Fetal Heart	heart
25	chr5:111634000-111634400	ZNF genes & repeats	Fetal Heart	heart
26	chr5:111634800-111637000	Weak transcription	Aorta	Aorta
27	chr5:111635200-111638600	Weak transcription	Fetal Heart	heart
28	chr5:111635600-111651800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr5:111636400-111639800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr5:111636400-111640400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr5:111636800-111637000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:111636800-111637200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:111637000-111637200	Weak transcription	Lung	lung
34	chr5:111637000-111637200	ZNF genes & repeats	Pancreas	Pancrea
35	chr5:111637000-111637400	ZNF genes & repeats	Aorta	Aorta
36	chr5:111637000-111639000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:111637000-111642200	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr5:111637200-111637400	Enhancers	Lung	lung
39	chr5:111637200-111639600	Weak transcription	Pancreas	Pancrea
40	chr5:111637400-111684600	Weak transcription	Aorta	Aorta
41	chr5:111638600-111643800	Enhancers	Fetal Heart	heart
42	chr5:111639000-111639600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr5:111639400-111639800	Enhancers	Left Ventricle	heart
44	chr5:111639400-111639800	Enhancers	Placenta Amnion	Placenta Amnion
45	chr5:111639400-111640000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr5:111639400-111640000	Enhancers	Right Atrium	heart
47	chr5:111639400-111640200	Enhancers	Psoas Muscle	Psoas
48	chr5:111639600-111639800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr5:111639600-111639800	ZNF genes & repeats	Pancreas	Pancrea
50	chr5:111639600-111640000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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