Variant report

Variant	nsv882390
Chromosome Location	chr5:95486940-95591580
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:971)
CpG islands
(count:549)
Chromatin interactive
region (count:14)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:971 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:95550628-95550982	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:95523195-95523769	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:95535336-95536476	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:95581064-95581603	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:95531796-95532242	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:95562820-95563009	HepG2	liver:	n/a	n/a
7	ATF1	chr5:95515236-95515349	K562	blood:	n/a	n/a
8	ATF2	chr5:95556378-95556814	GM12878	blood:	n/a	n/a
9	ATF2	chr5:95556405-95556814	GM12878	blood:	n/a	n/a
10	ATF2	chr5:95513034-95513668	GM12878	blood:	n/a	n/a
11	ATF2	chr5:95512965-95513671	GM12878	blood:	n/a	n/a
12	BACH1	chr5:95546561-95546757	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr5:95556266-95556804	GM12878	blood:	n/a	chr5:95556552-95556563
14	BATF	chr5:95513032-95513607	GM12878	blood:	n/a	chr5:95513318-95513329
15	BATF	chr5:95556408-95556754	GM12878	blood:	n/a	chr5:95556552-95556563
16	BATF	chr5:95564194-95564485	GM12878	blood:	n/a	chr5:95564355-95564366
17	BATF	chr5:95513119-95513616	GM12878	blood:	n/a	chr5:95513318-95513329
18	BCL11A	chr5:95564243-95564493	GM12878	blood:	n/a	chr5:95564355-95564364
19	BCL11A	chr5:95513024-95513657	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:95556405-95556726	GM12878	blood:	n/a	n/a
21	BCL3	chr5:95487725-95488076	GM12878	blood:	n/a	chr5:95487770-95487779
22	BCL3	chr5:95590615-95591173	A549	lung:	n/a	chr5:95590792-95590801 chr5:95590791-95590800
23	BCL3	chr5:95513115-95513601	GM12878	blood:	n/a	n/a
24	BCL3	chr5:95581015-95581512	A549	lung:	n/a	n/a
25	BCL3	chr5:95590537-95591423	A549	lung:	n/a	chr5:95590792-95590801 chr5:95590791-95590800
26	BCLAF1	chr5:95513077-95513561	GM12878	blood:	n/a	n/a
27	BCLAF1	chr5:95513016-95513698	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:95523524-95523764	HepG2	liver:	n/a	n/a
29	BHLHE40	chr5:95535587-95535874	HepG2	liver:	n/a	n/a
30	BHLHE40	chr5:95513053-95513596	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:95515259-95515455	K562	blood:	n/a	n/a
32	BRCA1	chr5:95590520-95591511	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr5:95589078-95589088	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr5:95515032-95515640	HCT-116	colon:	n/a	n/a
35	CEBPB	chr5:95581049-95581396	A549	lung:	n/a	chr5:95581050-95581062 chr5:95581204-95581215
36	CEBPB	chr5:95586207-95586325	K562	blood:	n/a	chr5:95586274-95586285
37	CEBPB	chr5:95550670-95550801	A549	lung:	n/a	n/a
38	CEBPB	chr5:95581025-95581468	HepG2	liver:	n/a	chr5:95581050-95581062 chr5:95581204-95581215
39	CEBPB	chr5:95571768-95572062	IMR90	lung:	n/a	chr5:95572006-95572017
40	CEBPB	chr5:95581081-95581444	MCF-7	breast:	n/a	chr5:95581204-95581215
41	CEBPB	chr5:95523544-95523768	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:95590564-95591420	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:95523193-95523565	HepG2	liver:	n/a	chr5:95523338-95523349
44	CEBPB	chr5:95537035-95537186	HepG2	liver:	n/a	n/a
45	CEBPB	chr5:95590629-95590893	A549	lung:	n/a	n/a
46	CEBPB	chr5:95580975-95581490	A549	lung:	n/a	chr5:95581050-95581062 chr5:95581204-95581215
47	CEBPB	chr5:95556497-95556768	HepG2	liver:	n/a	chr5:95556626-95556637
48	CEBPB	chr5:95586219-95586336	HepG2	liver:	n/a	chr5:95586274-95586285
49	CEBPB	chr5:95590555-95591120	A549	lung:	n/a	n/a
50	CEBPB	chr5:95504716-95504797	Hela-S3	cervix:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:95590917-95590967	AG09319	gingival:	n/a
2	chr5:95514729-95514779	AoSMC	blood vessel:	n/a
3	chr5:95580517-95580567	SKMC	muscle:	n/a
4	chr5:95580517-95580567	HUVEC	blood vessel:	n/a
5	chr5:95553592-95553642	HCT-116	colon:	n/a
6	chr5:95562504-95562554	RPTEC	kidney:	n/a
7	chr5:95590917-95590967	AG04450	lung:	fetal
8	chr5:95583220-95583270	AG09309	skin:	n/a
9	chr5:95553592-95553642	HRCEpiC	kidney:	n/a
10	chr5:95509647-95509697	HNPCEpiC	eye:	n/a
11	chr5:95580517-95580567	U87	brain:	n/a
12	chr5:95553592-95553642	CMK	blood:	n/a
13	chr5:95514729-95514779	HepG2	liver:	n/a
14	chr5:95555970-95556020	NHBE	bronchial:	n/a
15	chr5:95590917-95590967	HCT-116	colon:	n/a
16	chr5:95590917-95590967	HMEC	breast:	n/a
17	chr5:95571107-95571157	GM19239	blood:	n/a
18	chr5:95562504-95562554	Caco-2	colon:	n/a
19	chr5:95571107-95571157	Hepatocyte	liver:	n/a
20	chr5:95580517-95580567	MCF10A-Er-Src	breast:	n/a
21	chr5:95562504-95562554	PANC-1	pancreas:	n/a
22	chr5:95571107-95571157	SK-N-MC	brain:	n/a
23	chr5:95553592-95553642	LNCaP	prostate:	n/a
24	chr5:95580517-95580567	NHDF-neo	bronchial:	n/a
25	chr5:95571107-95571157	PANC-1	pancreas:	n/a
26	chr5:95509647-95509697	GM12892	blood:	n/a
27	chr5:95583220-95583270	ProgFib	skin:	n/a
28	chr5:95514729-95514779	SAEC	small airway:	n/a
29	chr5:95580517-95580567	AG04450	lung:	fetal
30	chr5:95590917-95590967	HUVEC	blood vessel:	n/a
31	chr5:95580517-95580567	ovcar-3	ovarian:	n/a
32	chr5:95580517-95580567	AG09309	skin:	n/a
33	chr5:95590917-95590967	SK-N-MC	brain:	n/a
34	chr5:95562504-95562554	NH-A	brain:	n/a
35	chr5:95580517-95580567	T-47D	breast:	n/a
36	chr5:95562504-95562554	HCT-116	colon:	n/a
37	chr5:95583220-95583270	HIPEpiC	eye:	n/a
38	chr5:95553592-95553642	GM06990	blood:	n/a
39	chr5:95555970-95556020	ECC-1	luminal epithelium:	n/a
40	chr5:95514729-95514779	NH-A	brain:	n/a
41	chr5:95514729-95514779	Caco-2	colon:	n/a
42	chr5:95555970-95556020	SK-N-SH	brain:	n/a
43	chr5:95509647-95509697	AoSMC	blood vessel:	n/a
44	chr5:95590917-95590967	HepG2	liver:	n/a
45	chr5:95562504-95562554	CMK	blood:	n/a
46	chr5:95590917-95590967	ECC-1	luminal epithelium:	n/a
47	chr5:95509647-95509697	ECC-1	luminal epithelium:	n/a
48	chr5:95514729-95514779	HEK293	kidney:	embryo
49	chr5:95571107-95571157	ECC-1	luminal epithelium:	n/a
50	chr5:95571107-95571157	K562	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:95588143..95588958-chr9:139052512..139053354,2	Hela-S3	cervix:
2	chr5:95525860..95527522-chr5:95528640..95530648,2	K562	blood:
3	chr5:95562010..95564635-chr5:95566152..95567653,2	K562	blood:
4	chr5:95514396..95516278-chr5:95516334..95518457,2	MCF-7	breast:
5	chr5:95295813..95297730-chr5:95509691..95513158,3	MCF-7	breast:
6	chr5:95482304..95484710-chr5:95487757..95489395,2	K562	blood:
7	chr5:95478380..95480797-chr5:95483671..95486972,3	K562	blood:
8	chr5:95525860..95527522-chr5:95528640..95530648,2	K562	blood:
9	chr5:95514396..95516278-chr5:95516334..95518457,2	MCF-7	breast:
10	chr5:95473116..95474627-chr5:95485772..95487685,2	MCF-7	breast:
11	chr5:95559323..95562073-chr5:95563803..95565354,2	K562	blood:
12	chr5:95559323..95562073-chr5:95563803..95565354,2	K562	blood:
13	chr5:95562010..95564635-chr5:95566152..95567653,2	K562	blood:
14	chr5:95296142..95297757-chr5:95548308..95551059,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCSK1-1	chr5:95550572-95550869	NONHSAT102885
2	lnc-PCSK1-1	chr5:95549050-95549493	XLOC_004933
3	lnc-PCSK1-1	chr5:95550572-95550779	XLOC_004933
4	lnc-CAST-3	chr5:95583480-95583721	XLOC_004479
5	lnc-C5orf27-3	chr5:95550679-95551223	ENSG00000250551
6	lnc-CAST-10	chr5:95546905-95548572	NONHSAT102887
7	lnc-PCSK1-1	chr5:95545140-95549493	NONHSAT102885

No data

Variant related genes	Relation type
ENSG00000249746	TF binding region
RNU6-524P	TF binding region
ENSG00000250158	TF binding region
ENSG00000249746	CpG island
RNU6-524P	CpG island
ENSG00000250158	CpG island
ENSG00000251314	chromatin interactions
ENSG00000118985	chromatin interactions

Extended variants
information (count: 3679 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:3679 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4869266	chr5:95486940-95486941	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs573761217	chr5:95486942-95486943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555125598	chr5:95486974-95486975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542671511	chr5:95487046-95487047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574957792	chr5:95487047-95487048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562461810	chr5:95487054-95487055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs35450775	chr5:95487062-95487063	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs544445082	chr5:95487232-95487233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531274656	chr5:95487241-95487242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370761534	chr5:95487272-95487273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551002296	chr5:95487308-95487309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4869126	chr5:95487326-95487327	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533384546	chr5:95487336-95487337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs546759498	chr5:95487390-95487391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566659308	chr5:95487424-95487425	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185388796	chr5:95487463-95487464	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs549013679	chr5:95487464-95487465	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs569148844	chr5:95487470-95487471	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs13159130	chr5:95487536-95487537	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs557789139	chr5:95487615-95487616	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577832720	chr5:95487636-95487637	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138217784	chr5:95487637-95487638	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs576779617	chr5:95487671-95487672	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs143603987	chr5:95487688-95487689	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542732864	chr5:95487698-95487699	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs545790784	chr5:95487706-95487707	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190680808	chr5:95487719-95487720	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575954155	chr5:95487735-95487736	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs569486118	chr5:95487753-95487754	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs544962990	chr5:95487762-95487763	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs564643997	chr5:95487779-95487780	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs66853776	chr5:95487872-95487873	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs546819180	chr5:95487896-95487897	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180744364	chr5:95487938-95487939	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146021875	chr5:95488063-95488064	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10069928	chr5:95488078-95488079	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569306486	chr5:95488082-95488083	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs186176556	chr5:95488196-95488197	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551735783	chr5:95488419-95488420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200249644	chr5:95488480-95488481	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs201538077	chr5:95488483-95488484	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200350894	chr5:95488484-95488485	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76182565	chr5:95488485-95488486	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571476905	chr5:95488509-95488510	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188397369	chr5:95488534-95488535	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs181206564	chr5:95488555-95488556	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114117381	chr5:95488580-95488581	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567476155	chr5:95488588-95488589	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536408217	chr5:95488597-95488598	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73773918	chr5:95488624-95488625	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Williams Syndrome	20824207	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Renal cell carcinoma	21215367	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:1159 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:95478200-95493200	Weak transcription	Gastric	stomach
2	chr5:95479400-95489000	Weak transcription	Pancreas	Pancrea
3	chr5:95480200-95491000	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr5:95481600-95488000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr5:95482200-95491800	Weak transcription	Fetal Intestine Large	intestine
6	chr5:95482600-95487400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr5:95482600-95494800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:95482800-95487200	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr5:95482800-95494800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr5:95483400-95487400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr5:95483600-95488400	Enhancers	NHEK	skin
12	chr5:95483800-95488200	Enhancers	HMEC	breast
13	chr5:95484800-95488600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:95485600-95487600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:95486400-95493400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr5:95486400-95494600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr5:95486400-95495000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr5:95486600-95487600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr5:95486600-95491000	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr5:95486600-95493200	Weak transcription	A549	lung
21	chr5:95486800-95488200	Enhancers	Stomach Smooth Muscle	stomach
22	chr5:95486800-95490600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr5:95486800-95490600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr5:95486800-95491000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr5:95486800-95491400	Weak transcription	Esophagus	oesophagus
26	chr5:95486800-95506400	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr5:95487200-95488200	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr5:95487400-95488000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:95487400-95488200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr5:95487400-95488200	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr5:95487400-95488400	Enhancers	Stomach Mucosa	stomach
32	chr5:95487600-95487800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr5:95487600-95488000	Enhancers	Brain Substantia Nigra	brain
34	chr5:95487600-95488000	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr5:95487600-95488400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:95487800-95489000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr5:95488000-95490600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr5:95488200-95489800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr5:95488200-95490600	Weak transcription	HMEC	breast
40	chr5:95488400-95490400	Weak transcription	NHEK	skin
41	chr5:95488600-95489000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr5:95489000-95489200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr5:95489000-95489200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr5:95489000-95489200	Enhancers	Pancreas	Pancrea
45	chr5:95489200-95493200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:95489800-95490400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr5:95490400-95491200	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr5:95490400-95491800	Enhancers	NHEK	skin
49	chr5:95490400-95495000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:95490600-95491800	Enhancers	HMEC	breast

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