Variant report

Variant	esv3414088
Chromosome Location	chr5:90744553-90861592
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	chr5:90795795-90796098	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:90764927-90765546	K562	blood:	n/a	n/a
3	ATF1	chr5:90765488-90766019	K562	blood:	n/a	n/a
4	BACH1	chr5:90786343-90786533	K562	blood:	n/a	n/a
5	BATF	chr5:90751095-90751405	GM12878	blood:	n/a	chr5:90751256-90751267
6	BHLHE40	chr5:90765406-90765732	K562	blood:	n/a	n/a
7	CBX3	chr5:90837471-90837905	HCT-116	colon:	n/a	n/a
8	CEBPB	chr5:90750057-90750384	HepG2	liver:	n/a	chr5:90750215-90750226
9	CEBPB	chr5:90750102-90750383	A549	lung:	n/a	chr5:90750215-90750226
10	CEBPB	chr5:90750063-90750364	IMR90	lung:	n/a	chr5:90750215-90750226
11	CEBPB	chr5:90782535-90782728	A549	lung:	n/a	n/a
12	CEBPB	chr5:90785648-90785848	HepG2	liver:	n/a	chr5:90785778-90785789
13	CEBPB	chr5:90791584-90791784	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:90782399-90782801	A549	lung:	n/a	n/a
15	CEBPB	chr5:90780537-90780906	A549	lung:	n/a	chr5:90780752-90780763
16	CEBPB	chr5:90792630-90792654	A549	lung:	n/a	n/a
17	CEBPB	chr5:90780617-90780857	A549	lung:	n/a	chr5:90780752-90780763
18	CTCF	chr5:90795860-90796010	HPAF	blood vessel:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
19	CTCF	chr5:90795860-90796010	SAEC	small airway:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
20	CTCF	chr5:90795898-90796014	MCF-7	breast:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
21	CTCF	chr5:90795760-90796070	K562	blood:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
22	CTCF	chr5:90795920-90796070	HAc	cerebellar:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
23	CTCF	chr5:90795780-90795930	HCT-116	colon:	n/a	n/a
24	CTCF	chr5:90795780-90795930	NHLF	lung:	n/a	n/a
25	CTCF	chr5:90795900-90796050	HUVEC	blood vessel:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
26	CTCF	chr5:90795860-90796010	MCF-7	breast:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
27	CTCF	chr5:90795768-90796144	A549	lung:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
28	CTCF	chr5:90795860-90796010	GM12869	blood:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
29	CTCF	chr5:90825264-90825304	GM20000	blood:	n/a	n/a
30	CTCF	chr5:90795872-90796041	GM13976	blood:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
31	CTCF	chr5:90795880-90796030	GM12875	blood:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
32	CTCF	chr5:90791560-90791710	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr5:90795720-90795870	GM12878	blood:	n/a	n/a
34	CTCF	chr5:90795836-90796074	A549	lung:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
35	CTCF	chr5:90795870-90796030	MCF-7	breast:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
36	CTCF	chr5:90795800-90795950	RPTEC	kidney:	n/a	n/a
37	CTCF	chr5:90795756-90796112	K562	blood:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
38	CTCF	chr5:90795760-90795910	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr5:90795780-90795930	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr5:90795900-90796050	Hela-S3	cervix:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
41	CTCF	chr5:90795900-90796050	HCPEpiC	choroid plexus:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
42	CTCF	chr5:90795820-90795970	HCM	heart:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
43	CTCF	chr5:90795860-90796010	HAc	cerebellar:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
44	CTCF	chr5:90795920-90796070	AG09309	skin:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
45	CTCF	chr5:90795820-90795970	GM12873	blood:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
46	CTCF	chr5:90795752-90796135	K562	blood:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
47	CTCF	chr5:90795880-90796030	HRE	kidney:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
48	CTCF	chr5:90795853-90796017	LNCaP	prostate:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
49	CTCF	chr5:90795860-90796010	AG09319	gingival:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956
50	CTCF	chr5:90795860-90796010	RPTEC	kidney:	n/a	chr5:90795941-90795962 chr5:90795939-90795957 chr5:90795940-90795956

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:90790737-90790787	GM12891	blood:	n/a
2	chr5:90790737-90790787	Hela-S3	cervix:	n/a
3	chr5:90790737-90790787	A549	lung:	n/a
4	chr5:90790737-90790787	HCF	heart:	n/a
5	chr5:90790737-90790787	HRE	kidney:	n/a
6	chr5:90790737-90790787	GM12892	blood:	n/a
7	chr5:90753493-90753543	K562	blood:	n/a
8	chr5:90753493-90753543	AoSMC	blood vessel:	n/a
9	chr5:90753493-90753543	AG04449	skin:	fetal
10	chr5:90790737-90790787	SAEC	small airway:	n/a
11	chr5:90753493-90753543	HCM	heart:	n/a
12	chr5:90753493-90753543	GM19239	blood:	n/a
13	chr5:90753493-90753543	GM12878	blood:	n/a
14	chr5:90753493-90753543	HRCEpiC	kidney:	n/a
15	chr5:90753493-90753543	PANC-1	pancreas:	n/a
16	chr5:90753493-90753543	A549	lung:	n/a
17	chr5:90790737-90790787	PFSK-1	brain:	n/a
18	chr5:90790737-90790787	NB4	blood:	n/a
19	chr5:90790737-90790787	GM06990	blood:	n/a
20	chr5:90753493-90753543	BE2_C	brain:	n/a
21	chr5:90790737-90790787	BJ	skin:	n/a
22	chr5:90753493-90753543	HRE	kidney:	n/a
23	chr5:90753493-90753543	Caco-2	colon:	n/a
24	chr5:90790737-90790787	SKMC	muscle:	n/a
25	chr5:90753493-90753543	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:90753493-90753543	HepG2	liver:	n/a
27	chr5:90790737-90790787	ovcar-3	ovarian:	n/a
28	chr5:90790737-90790787	HL-60	blood:	n/a
29	chr5:90753493-90753543	NHBE	bronchial:	n/a
30	chr5:90790737-90790787	MCF-7	breast:	n/a
31	chr5:90753493-90753543	NH-A	brain:	n/a
32	chr5:90753493-90753543	HCPEpiC	choroid plexus:	n/a
33	chr5:90753493-90753543	LNCaP	prostate:	n/a
34	chr5:90790737-90790787	RPTEC	kidney:	n/a
35	chr5:90753493-90753543	ovcar-3	ovarian:	n/a
36	chr5:90753493-90753543	RPTEC	kidney:	n/a
37	chr5:90753493-90753543	GM12892	blood:	n/a
38	chr5:90790737-90790787	AoSMC	blood vessel:	n/a
39	chr5:90790737-90790787	MCF10A-Er-Src	breast:	n/a
40	chr5:90790737-90790787	PANC-1	pancreas:	n/a
41	chr5:90753493-90753543	U87	brain:	n/a
42	chr5:90753493-90753543	SK-N-SH	brain:	n/a
43	chr5:90790737-90790787	SK-N-SH_RA	brain:	n/a
44	chr5:90753493-90753543	HCF	heart:	n/a
45	chr5:90753493-90753543	BJ	skin:	n/a
46	chr5:90753493-90753543	T-47D	breast:	n/a
47	chr5:90753493-90753543	MCF-7	breast:	n/a
48	chr5:90753493-90753543	AG04450	lung:	fetal
49	chr5:90753493-90753543	AG09309	skin:	n/a
50	chr5:90790737-90790787	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:90783798..90785591-chr5:90786884..90789599,2	K562	blood:
2	chr5:90745132..90747371-chr5:90754761..90757366,2	MCF-7	breast:
3	chr5:90745132..90747371-chr5:90754761..90757366,2	MCF-7	breast:
4	chr5:90745652..90748041-chr5:90748498..90750732,2	K562	blood:
5	chr5:90790806..90792338-chr5:90794426..90796044,2	MCF-7	breast:
6	chr5:90805327..90807145-chr5:90810854..90813797,2	MCF-7	breast:
7	chr5:90745652..90748041-chr5:90748498..90750732,2	K562	blood:
8	chr5:90779830..90782085-chr5:90782633..90785121,2	MCF-7	breast:
9	chr5:90742935..90745412-chr5:90752752..90755455,2	K562	blood:
10	chr5:90771920..90773679-chr5:90776565..90778220,2	K562	blood:
11	chr5:90783798..90785591-chr5:90786884..90789599,2	K562	blood:
12	chr5:90779830..90782085-chr5:90782633..90785121,2	MCF-7	breast:
13	chr5:90805327..90807145-chr5:90810854..90813797,2	MCF-7	breast:
14	chr5:90674940..90676801-chr5:90743157..90745200,2	K562	blood:
15	chr5:90790806..90792338-chr5:90794426..90796044,2	MCF-7	breast:
16	chr5:90742935..90745412-chr5:90752752..90755455,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR98-11	chr5:90750428-90752287	ucscGeneNc_uc003kka_2
2	lnc-GPR98-11	chr5:90750282-90750344	ucscGeneNc_uc003kka_2

Variant related genes	Relation type
RAB5CP2	TF binding region
RAB5CP2	CpG island
ENSG00000113369	chromatin interactions
ENSG00000251356	chromatin interactions

Extended variants
information (count: 2586 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2586 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549079401	chr5:90744595-90744596	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568981945	chr5:90744598-90744599	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536877355	chr5:90744621-90744622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs557100729	chr5:90744767-90744768	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs570692940	chr5:90744778-90744779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs538883929	chr5:90744789-90744790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189063712	chr5:90744800-90744801	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs985433	chr5:90744871-90744872	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572893384	chr5:90744901-90744902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs181704802	chr5:90744903-90744904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs368897438	chr5:90744911-90744912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555532390	chr5:90744924-90744925	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs575285027	chr5:90744925-90744926	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs145373474	chr5:90744941-90744942	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs186421095	chr5:90745015-90745016	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533318633	chr5:90745030-90745031	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548168207	chr5:90745038-90745039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs116324937	chr5:90745050-90745051	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs529269964	chr5:90745102-90745103	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548944166	chr5:90745103-90745104	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7720132	chr5:90745105-90745106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs191067826	chr5:90745179-90745180	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs146463747	chr5:90745181-90745182	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs200218223	chr5:90745247-90745248	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570626636	chr5:90745248-90745249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs397688231	chr5:90745255-90745256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs57551844	chr5:90745277-90745278	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571044733	chr5:90745336-90745337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs17638833	chr5:90745387-90745388	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs566675426	chr5:90745438-90745439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535480781	chr5:90745459-90745460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555392297	chr5:90745498-90745499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs373571888	chr5:90745531-90745532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs575293804	chr5:90745612-90745613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs544300081	chr5:90745636-90745637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs111596688	chr5:90745664-90745665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs578134894	chr5:90745679-90745680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540398797	chr5:90745715-90745716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560441192	chr5:90745726-90745727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs113689682	chr5:90745743-90745744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs367655339	chr5:90745770-90745771	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529527008	chr5:90745779-90745780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs140878724	chr5:90745866-90745867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143156120	chr5:90745889-90745890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs386690037	chr5:90745892-90745893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs78154992	chr5:90745943-90745944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1035476	chr5:90745976-90745977	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565208760	chr5:90745985-90745986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs113029567	chr5:90746003-90746004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546803402	chr5:90746041-90746042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	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
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
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
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
Ovarian cancer	21720365	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
Myelofibrosis	22110671	CNVD
Mental retardation	19592390	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
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:90740200-90752000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr5:90741400-90744600	Weak transcription	Stomach Mucosa	stomach
3	chr5:90744600-90745000	Enhancers	Duodenum Mucosa	Duodenum
4	chr5:90744600-90745000	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr5:90744600-90745400	Enhancers	Liver	Liver
6	chr5:90744600-90746000	Enhancers	Stomach Mucosa	stomach
7	chr5:90751000-90751400	ZNF genes & repeats	Aorta	Aorta
8	chr5:90751400-90764800	Weak transcription	Aorta	Aorta
9	chr5:90752000-90752200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:90752000-90754400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr5:90752200-90752600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr5:90752200-90754400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr5:90752200-90754600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr5:90752400-90752800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:90752400-90754200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:90752600-90752800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr5:90752600-90753600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr5:90752600-90753800	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr5:90752600-90754200	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr5:90752800-90753000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr5:90752800-90753200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr5:90752800-90753400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr5:90752800-90753800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr5:90753000-90753200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr5:90753000-90753800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:90753200-90753400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr5:90753200-90753400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr5:90753200-90753600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr5:90753400-90753800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr5:90753400-90753800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr5:90753600-90753800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
32	chr5:90753800-90754200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr5:90757600-90757800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:90762200-90762400	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr5:90764400-90764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr5:90764400-90764600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:90764400-90764600	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr5:90764400-90764800	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr5:90764400-90765200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr5:90764400-90765400	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr5:90764600-90765000	Enhancers	HSMMtube	muscle
42	chr5:90764600-90765000	Enhancers	NHDF-Ad	bronchial
43	chr5:90764600-90765400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr5:90764600-90765600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr5:90764600-90765800	Active TSS	Adipose Nuclei	Adipose
46	chr5:90764600-90766000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr5:90764600-90766000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr5:90764600-90766000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr5:90764600-90766200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr5:90764800-90765200	Enhancers	Primary T helper cells PMA-I stimulated	--

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