Variant report

Variant	nsv598681
Chromosome Location	chr5:75863987-75902533
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	chr5:75879112-75879647	K562	blood:	n/a	n/a
2	ARID3A	chr5:75879372-75879648	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:75894704-75894734	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:75878262-75878267	K562	blood:	n/a	n/a
5	ATF2	chr5:75877922-75878580	GM12878	blood:	n/a	n/a
6	ATF2	chr5:75885636-75886289	GM12878	blood:	n/a	n/a
7	ATF2	chr5:75877962-75878487	GM12878	blood:	n/a	n/a
8	ATF2	chr5:75885854-75886295	GM12878	blood:	n/a	n/a
9	BATF	chr5:75885837-75886185	GM12878	blood:	n/a	chr5:75886008-75886019 chr5:75886009-75886019
10	BATF	chr5:75885818-75886149	GM12878	blood:	n/a	chr5:75886008-75886019 chr5:75886009-75886019
11	BATF	chr5:75878063-75878435	GM12878	blood:	n/a	n/a
12	BATF	chr5:75878120-75878359	GM12878	blood:	n/a	n/a
13	BCL11A	chr5:75878053-75878407	GM12878	blood:	n/a	n/a
14	BCL11A	chr5:75878060-75878454	GM12878	blood:	n/a	n/a
15	BCL3	chr5:75878087-75878399	GM12878	blood:	n/a	n/a
16	BCLAF1	chr5:75885718-75886254	GM12878	blood:	n/a	chr5:75886011-75886020
17	BCLAF1	chr5:75877985-75878556	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:75877874-75878590	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:75885807-75886280	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:75879352-75879536	GM12878	blood:	n/a	n/a
21	BHLHE40	chr5:75897312-75897624	K562	blood:	n/a	n/a
22	BHLHE40	chr5:75878083-75878443	K562	blood:	n/a	n/a
23	BRCA1	chr5:75886137-75886143	HepG2	liver:	n/a	n/a
24	CCNT2	chr5:75879032-75879277	K562	blood:	n/a	n/a
25	CEBPB	chr5:75875019-75875341	A549	lung:	n/a	n/a
26	CEBPB	chr5:75875047-75875337	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:75874997-75875377	IMR90	lung:	n/a	n/a
28	CEBPB	chr5:75875118-75875326	HepG2	liver:	n/a	n/a
29	CEBPB	chr5:75875056-75875399	ECC-1	luminal epithelium:	n/a	n/a
30	CHD1	chr5:75878098-75878698	GM12878	blood:	n/a	n/a
31	CHD2	chr5:75877945-75878436	GM12878	blood:	n/a	n/a
32	CHD2	chr5:75885853-75886221	GM12878	blood:	n/a	n/a
33	CREB1	chr5:75885789-75886317	GM12878	blood:	n/a	n/a
34	CREB1	chr5:75885846-75886292	GM12878	blood:	n/a	n/a
35	CTCF	chr5:75867540-75867830	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr5:75879378-75879561	GM12878	blood:	n/a	chr5:75879454-75879475 chr5:75879459-75879477 chr5:75879461-75879474 chr5:75879460-75879476
37	CTCF	chr5:75897400-75897550	HRE	kidney:	n/a	chr5:75897475-75897493 chr5:75897476-75897492 chr5:75897478-75897487 chr5:75897480-75897490 chr5:75897477-75897498
38	CTCF	chr5:75897000-75897150	HCM	heart:	n/a	n/a
39	CTCF	chr5:75897327-75897629	Medullo	brain:	n/a	chr5:75897475-75897493 chr5:75897476-75897492 chr5:75897478-75897487 chr5:75897480-75897490 chr5:75897477-75897498
40	CTCF	chr5:75897359-75897598	Pancreas_OC	pancreas:	n/a	chr5:75897475-75897493 chr5:75897476-75897492 chr5:75897478-75897487 chr5:75897480-75897490 chr5:75897477-75897498
41	CTCF	chr5:75897259-75897646	A549	lung:	n/a	chr5:75897475-75897493 chr5:75897476-75897492 chr5:75897478-75897487 chr5:75897480-75897490 chr5:75897477-75897498
42	CTCF	chr5:75897400-75897550	AG04450	lung:	n/a	chr5:75897475-75897493 chr5:75897476-75897492 chr5:75897478-75897487 chr5:75897480-75897490 chr5:75897477-75897498
43	CTCF	chr5:75898120-75898270	NHEK	skin:	n/a	n/a
44	CTCF	chr5:75867522-75867688	LNCaP	prostate:	n/a	n/a
45	CTCF	chr5:75897420-75897570	HFF	foreskin:	n/a	chr5:75897475-75897493 chr5:75897476-75897492 chr5:75897478-75897487 chr5:75897480-75897490 chr5:75897477-75897498
46	CTCF	chr5:75879360-75879510	AG04450	lung:	n/a	chr5:75879454-75879475 chr5:75879459-75879477 chr5:75879461-75879474 chr5:75879460-75879476
47	CTCF	chr5:75897040-75897190	RPTEC	kidney:	n/a	n/a
48	CTCF	chr5:75897420-75897570	NB4	blood:	n/a	chr5:75897475-75897493 chr5:75897476-75897492 chr5:75897478-75897487 chr5:75897480-75897490 chr5:75897477-75897498
49	CTCF	chr5:75898260-75898410	BJ	skin:	n/a	n/a
50	CTCF	chr5:75898272-75898440	A549	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75878300-75878350	HRPEpiC	eye:	n/a
2	chr5:75878300-75878350	H1-hESC	embryonic stem cell:	embryo
3	chr5:75878300-75878350	GM12878	blood:	n/a
4	chr5:75878300-75878350	Caco-2	colon:	n/a
5	chr5:75878300-75878350	BJ	skin:	n/a
6	chr5:75878300-75878350	HIPEpiC	eye:	n/a
7	chr5:75878300-75878350	PrEC	prostate:	n/a
8	chr5:75878300-75878350	U87	brain:	n/a
9	chr5:75878300-75878350	HRE	kidney:	n/a
10	chr5:75878300-75878350	ProgFib	skin:	n/a
11	chr5:75878300-75878350	AG10803	skin:	n/a
12	chr5:75878300-75878350	ECC-1	luminal epithelium:	n/a
13	chr5:75878300-75878350	HEK293	kidney:	embryo
14	chr5:75878300-75878350	AG09319	gingival:	n/a
15	chr5:75878300-75878350	IMR90	lung:	fetal
16	chr5:75878300-75878350	AG09309	skin:	n/a
17	chr5:75878300-75878350	SAEC	small airway:	n/a
18	chr5:75878300-75878350	LNCaP	prostate:	n/a
19	chr5:75878300-75878350	HCM	heart:	n/a
20	chr5:75878300-75878350	GM12892	blood:	n/a
21	chr5:75878300-75878350	CMK	blood:	n/a
22	chr5:75878300-75878350	Hela-S3	cervix:	n/a
23	chr5:75878300-75878350	HRCEpiC	kidney:	n/a
24	chr5:75878300-75878350	GM06990	blood:	n/a
25	chr5:75878300-75878350	T-47D	breast:	n/a
26	chr5:75878300-75878350	AG04450	lung:	fetal
27	chr5:75878300-75878350	HEEpiC	esophagus:	n/a
28	chr5:75878300-75878350	NB4	blood:	n/a
29	chr5:75878300-75878350	NHDF-neo	bronchial:	n/a
30	chr5:75878300-75878350	NHBE	bronchial:	n/a
31	chr5:75878300-75878350	Hepatocyte	liver:	n/a
32	chr5:75878300-75878350	A549	lung:	n/a
33	chr5:75878300-75878350	SK-N-MC	brain:	n/a
34	chr5:75878300-75878350	GM12891	blood:	n/a
35	chr5:75878300-75878350	SK-N-SH	brain:	n/a
36	chr5:75878300-75878350	RPTEC	kidney:	n/a
37	chr5:75878300-75878350	SK-N-SH_RA	brain:	n/a
38	chr5:75878300-75878350	HCT-116	colon:	n/a
39	chr5:75878300-75878350	HCPEpiC	choroid plexus:	n/a
40	chr5:75878300-75878350	AG04449	skin:	fetal
41	chr5:75878300-75878350	HepG2	liver:	n/a
42	chr5:75878300-75878350	BE2_C	brain:	n/a
43	chr5:75878300-75878350	MCF10A-Er-Src	breast:	n/a
44	chr5:75878300-75878350	HMEC	breast:	n/a
45	chr5:75878300-75878350	NH-A	brain:	n/a
46	chr5:75878300-75878350	MCF-7	breast:	n/a
47	chr5:75878300-75878350	SKMC	muscle:	n/a
48	chr5:75878300-75878350	HCF	heart:	n/a
49	chr5:75878300-75878350	GM19239	blood:	n/a
50	chr5:75878300-75878350	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:75897979..75898810-chr5:75937080..75938018,3	K562	blood:
2	chr5:75699826..75701586-chr5:75896000..75897576,2	K562	blood:
3	chr5:75896999..75898252-chr5:76070091..76071474,10	K562	blood:
4	chr5:75861596..75864384-chr5:75866146..75868439,3	K562	blood:
5	chr5:75897714..75898323-chr5:75934762..75935296,2	MCF-7	breast:
6	chr5:75897329..75897974-chr5:132288926..132289426,2	MCF-7	breast:
7	chr5:75861596..75864384-chr5:75866146..75868439,3	K562	blood:
8	chr5:75896964..75897974-chr5:75936696..75938042,13	K562	blood:
9	chr5:75873843..75876744-chr5:75876856..75878367,2	K562	blood:
10	chr5:75896963..75898061-chr5:76070096..76071180,9	MCF-7	breast:
11	chr5:75897247..75898569-chr5:75937033..75938017,10	MCF-7	breast:
12	chr5:75878372..75880301-chr5:75883948..75885454,2	K562	blood:
13	chr5:75898209..75899288-chr5:76070136..76071088,4	MCF-7	breast:
14	chr5:75901625..75904371-chr5:75985828..75988323,2	MCF-7	breast:
15	chr5:75878372..75880301-chr5:75883948..75885454,2	K562	blood:
16	chr5:75699529..75700200-chr5:75878922..75879530,2	K562	blood:
17	chr5:75873843..75876744-chr5:75876856..75878367,2	K562	blood:
18	chr5:75826263..75829016-chr5:75865983..75867633,2	K562	blood:
19	chr5:75858031..75860083-chr5:75863526..75866442,2	K562	blood:
20	chr5:75899104..75902387-chr5:75903056..75906871,6	K562	blood:
21	chr5:75899087..75901579-chr5:75954997..75956885,2	K562	blood:
22	chr5:75896478..75897915-chr5:75936605..75938172,9	MCF-7	breast:
23	chr5:75633485..75634409-chr5:75878986..75879511,2	K562	blood:
24	chr5:75897975..75898494-chr5:75937296..75938025,2	MCF-7	breast:
25	chr5:75897438..75897959-chr5:76070126..76070803,2	MCF-7	breast:
26	chr5:75897144..75897771-chr5:103707251..103707772,2	MCF-7	breast:
27	chr5:75199631..75200148-chr5:75897260..75897978,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-F2RL2-1	chr5:75902433-75903909	ENSG00000249713.1

Variant related genes	Relation type
IQGAP2	TF binding region
IQGAP2	CpG island
ENSG00000145703	chromatin interactions
ENSG00000249713	chromatin interactions

Extended variants
information (count: 1450 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1450 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12523647	chr5:75863987-75863988	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573203371	chr5:75864033-75864034	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs375604860	chr5:75864057-75864058	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185096026	chr5:75864067-75864068	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189954137	chr5:75864070-75864071	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs575376182	chr5:75864095-75864096	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12513400	chr5:75864144-75864145	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs562058885	chr5:75864183-75864184	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs56356240	chr5:75864218-75864219	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs55650900	chr5:75864219-75864220	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529125942	chr5:75864292-75864293	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145063272	chr5:75864312-75864313	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs541731632	chr5:75864334-75864335	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs115901567	chr5:75864342-75864343	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528067189	chr5:75864343-75864344	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551136918	chr5:75864379-75864380	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs543290657	chr5:75864402-75864403	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537152685	chr5:75864419-75864420	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183434976	chr5:75864432-75864433	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs567879674	chr5:75864515-75864516	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373095131	chr5:75864529-75864530	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533704236	chr5:75864533-75864534	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs201035278	chr5:75864566-75864567	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs550062876	chr5:75864643-75864644	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553611224	chr5:75864658-75864659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570240354	chr5:75864707-75864708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72777513	chr5:75864720-75864721	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs188374301	chr5:75864738-75864739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11742152	chr5:75864807-75864808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547930247	chr5:75864830-75864831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148642221	chr5:75865004-75865005	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371149005	chr5:75865025-75865026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575288755	chr5:75865036-75865037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544323688	chr5:75865086-75865087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561631286	chr5:75865117-75865118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142903156	chr5:75865125-75865126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs193185439	chr5:75865169-75865170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35438972	chr5:75865258-75865259	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs398084212	chr5:75865267-75865268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199782131	chr5:75865268-75865269	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs56370891	chr5:75865271-75865272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573486110	chr5:75865284-75865285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542484640	chr5:75865309-75865310	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs72777514	chr5:75865463-75865464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113048615	chr5:75865479-75865480	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183485590	chr5:75865499-75865500	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs114876818	chr5:75865504-75865505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187772942	chr5:75865597-75865598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192521873	chr5:75865613-75865614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183629422	chr5:75865696-75865697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	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
Hepatocellular carcinoma	16750200	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	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
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:601 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75835600-75871200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:75843800-75884400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:75845400-75876600	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr5:75846800-75902600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr5:75851800-75892000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr5:75852000-75864400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr5:75852800-75877800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr5:75852800-75877800	Weak transcription	Small Intestine	intestine
9	chr5:75853200-75896400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr5:75856400-75873000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr5:75857400-75866200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr5:75857600-75864000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr5:75858000-75864000	Strong transcription	Primary B cells from cord blood	blood
14	chr5:75858800-75866000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr5:75858800-75876600	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr5:75859000-75866000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr5:75859000-75866200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr5:75859000-75873200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
19	chr5:75859000-75878600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:75859800-75864800	Strong transcription	Primary hematopoietic stem cells	blood
21	chr5:75860800-75872000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr5:75861200-75864600	Enhancers	Stomach Mucosa	stomach
23	chr5:75861200-75872200	Weak transcription	Fetal Lung	lung
24	chr5:75861200-75889600	Weak transcription	Fetal Stomach	stomach
25	chr5:75861400-75878600	Weak transcription	Pancreas	Pancrea
26	chr5:75861600-75866000	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr5:75861600-75866200	Weak transcription	Duodenum Mucosa	Duodenum
28	chr5:75862000-75866400	Weak transcription	Primary T helper cells fromperipheralblood	blood
29	chr5:75862200-75885400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr5:75862400-75865600	Weak transcription	Placenta	Placenta
31	chr5:75862400-75867600	Weak transcription	Fetal Brain Male	brain
32	chr5:75862600-75866200	Weak transcription	Liver	Liver
33	chr5:75862600-75873600	Weak transcription	HepG2	liver
34	chr5:75862600-75877800	Weak transcription	K562	blood
35	chr5:75862800-75880200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr5:75863000-75864200	Weak transcription	Fetal Intestine Small	intestine
37	chr5:75863000-75866200	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr5:75863000-75866200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr5:75863200-75864400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr5:75863200-75866000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr5:75863400-75866400	Weak transcription	Primary T cells from cord blood	blood
42	chr5:75863400-75872800	Weak transcription	Gastric	stomach
43	chr5:75863600-75864600	Enhancers	Primary neutrophils fromperipheralblood	blood
44	chr5:75863600-75866000	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr5:75863800-75866000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr5:75863800-75866200	Weak transcription	Primary T cells fromperipheralblood	blood
47	chr5:75864000-75866000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr5:75864000-75867000	Weak transcription	Primary B cells from cord blood	blood
49	chr5:75864200-75864600	Enhancers	Fetal Intestine Small	intestine
50	chr5:75864400-75864600	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--

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