Variant report

Variant	nsv882375
Chromosome Location	chr5:91144658-91383848
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	chr5:91225091-91225393	HepG2	liver:	n/a	n/a
2	ATF1	chr5:91148131-91148258	K562	blood:	n/a	n/a
3	BATF	chr5:91227634-91227833	GM12878	blood:	n/a	chr5:91227743-91227754
4	BCL11A	chr5:91171038-91171201	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr5:91375827-91375830	GM12878	blood:	n/a	n/a
6	CBX3	chr5:91144174-91144682	HCT-116	colon:	n/a	n/a
7	CBX3	chr5:91313395-91314027	HCT-116	colon:	n/a	n/a
8	CBX3	chr5:91315122-91315650	HCT-116	colon:	n/a	n/a
9	CBX3	chr5:91144125-91144870	HCT-116	colon:	n/a	n/a
10	CEBPB	chr5:91315118-91315514	Hela-S3	cervix:	n/a	chr5:91315210-91315221 chr5:91315210-91315223
11	CEBPB	chr5:91280927-91281141	HepG2	liver:	n/a	chr5:91281056-91281067
12	CEBPB	chr5:91202357-91202629	A549	lung:	n/a	n/a
13	CEBPB	chr5:91297576-91297842	A549	lung:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
14	CEBPB	chr5:91313622-91314038	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:91366092-91366382	HepG2	liver:	n/a	chr5:91366257-91366268 chr5:91366316-91366327
16	CEBPB	chr5:91144100-91144745	HCT-116	colon:	n/a	n/a
17	CEBPB	chr5:91261230-91261315	HepG2	liver:	n/a	n/a
18	CEBPB	chr5:91298859-91299124	IMR90	lung:	n/a	chr5:91299044-91299056
19	CEBPB	chr5:91144946-91145322	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr5:91194000-91194193	H1-hESC	embryonic stem cell:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087
21	CEBPB	chr5:91297546-91297863	IMR90	lung:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
22	CEBPB	chr5:91152417-91152693	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:91244707-91244803	HepG2	liver:	n/a	chr5:91244717-91244728 chr5:91244716-91244729 chr5:91244716-91244727 chr5:91244716-91244727
24	CEBPB	chr5:91209578-91209801	HepG2	liver:	n/a	chr5:91209684-91209695
25	CEBPB	chr5:91181195-91181277	A549	lung:	n/a	n/a
26	CEBPB	chr5:91297518-91297861	Hela-S3	cervix:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
27	CEBPB	chr5:91193969-91194233	A549	lung:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087
28	CEBPB	chr5:91261232-91261348	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr5:91250007-91250340	MCF-7	breast:	n/a	chr5:91250037-91250050
30	CEBPB	chr5:91298908-91299168	HepG2	liver:	n/a	chr5:91299044-91299056
31	CEBPB	chr5:91327553-91327814	A549	lung:	n/a	n/a
32	CEBPB	chr5:91296321-91296513	HepG2	liver:	n/a	chr5:91296386-91296397
33	CEBPB	chr5:91199500-91199796	H1-hESC	embryonic stem cell:	n/a	chr5:91199715-91199726
34	CEBPB	chr5:91297589-91297834	HepG2	liver:	n/a	chr5:91297703-91297714 chr5:91297702-91297713
35	CEBPB	chr5:91281741-91282081	HepG2	liver:	n/a	chr5:91281924-91281935 chr5:91281925-91281936
36	CEBPB	chr5:91143989-91144785	HCT-116	colon:	n/a	n/a
37	CEBPB	chr5:91145762-91146149	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:91375748-91376042	A549	lung:	n/a	chr5:91375852-91375863 chr5:91375852-91375865 chr5:91375853-91375864
39	CEBPB	chr5:91193946-91194198	IMR90	lung:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087
40	CEBPB	chr5:91224209-91224484	A549	lung:	n/a	chr5:91224253-91224264
41	CEBPB	chr5:91144241-91144690	A549	lung:	n/a	n/a
42	CEBPB	chr5:91250031-91250152	H1-hESC	embryonic stem cell:	n/a	chr5:91250037-91250050
43	CEBPB	chr5:91221103-91221469	HepG2	liver:	n/a	n/a
44	CEBPB	chr5:91249914-91250302	Hela-S3	cervix:	n/a	chr5:91250037-91250050
45	CEBPB	chr5:91152497-91152724	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:91375704-91376012	HepG2	liver:	n/a	chr5:91375852-91375863 chr5:91375852-91375865 chr5:91375853-91375864
47	CEBPB	chr5:91252099-91252272	HepG2	liver:	n/a	chr5:91252162-91252175 chr5:91252162-91252173 chr5:91252164-91252175
48	CEBPB	chr5:91274856-91275061	A549	lung:	n/a	chr5:91274933-91274946
49	CEBPB	chr5:91144102-91144750	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:91193926-91194211	HepG2	liver:	n/a	chr5:91194074-91194087 chr5:91194074-91194085 chr5:91194075-91194086 chr5:91194074-91194087

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:91303031-91303081	HMEC	breast:	n/a
2	chr5:91213435-91213485	H1-hESC	embryonic stem cell:	embryo
3	chr5:91213190-91213240	AG04450	lung:	fetal
4	chr5:91303031-91303081	NHBE	bronchial:	n/a
5	chr5:91213435-91213485	NB4	blood:	n/a
6	chr5:91298666-91298716	GM06990	blood:	n/a
7	chr5:91213435-91213485	A549	lung:	n/a
8	chr5:91303031-91303081	Hela-S3	cervix:	n/a
9	chr5:91298666-91298716	IMR90	lung:	fetal
10	chr5:91213435-91213485	MCF-7	breast:	n/a
11	chr5:91213190-91213240	U87	brain:	n/a
12	chr5:91303031-91303081	NH-A	brain:	n/a
13	chr5:91298666-91298716	Hepatocyte	liver:	n/a
14	chr5:91298666-91298716	AG04450	lung:	fetal
15	chr5:91303031-91303081	HepG2	liver:	n/a
16	chr5:91298666-91298716	AoSMC	blood vessel:	n/a
17	chr5:91303031-91303081	HIPEpiC	eye:	n/a
18	chr5:91213190-91213240	MCF10A-Er-Src	breast:	n/a
19	chr5:91213190-91213240	K562	blood:	n/a
20	chr5:91303031-91303081	HL-60	blood:	n/a
21	chr5:91303031-91303081	HCF	heart:	n/a
22	chr5:91213435-91213485	AoSMC	blood vessel:	n/a
23	chr5:91303031-91303081	BJ	skin:	n/a
24	chr5:91213435-91213485	HMEC	breast:	n/a
25	chr5:91213435-91213485	Hela-S3	cervix:	n/a
26	chr5:91298666-91298716	ECC-1	luminal epithelium:	n/a
27	chr5:91213190-91213240	NHDF-neo	bronchial:	n/a
28	chr5:91213435-91213485	ovcar-3	ovarian:	n/a
29	chr5:91298666-91298716	HRCEpiC	kidney:	n/a
30	chr5:91298666-91298716	HCPEpiC	choroid plexus:	n/a
31	chr5:91298666-91298716	HRPEpiC	eye:	n/a
32	chr5:91303031-91303081	K562	blood:	n/a
33	chr5:91303031-91303081	Hepatocyte	liver:	n/a
34	chr5:91303031-91303081	PFSK-1	brain:	n/a
35	chr5:91213435-91213485	SK-N-MC	brain:	n/a
36	chr5:91213435-91213485	SKMC	muscle:	n/a
37	chr5:91303031-91303081	BE2_C	brain:	n/a
38	chr5:91303031-91303081	GM06990	blood:	n/a
39	chr5:91303031-91303081	SK-N-MC	brain:	n/a
40	chr5:91298666-91298716	HL-60	blood:	n/a
41	chr5:91298666-91298716	Caco-2	colon:	n/a
42	chr5:91298666-91298716	BE2_C	brain:	n/a
43	chr5:91213190-91213240	RPTEC	kidney:	n/a
44	chr5:91213435-91213485	HPAEpiC	pulmonary alveolar:	n/a
45	chr5:91213190-91213240	T-47D	breast:	n/a
46	chr5:91303031-91303081	AG09309	skin:	n/a
47	chr5:91213435-91213485	HCPEpiC	choroid plexus:	n/a
48	chr5:91303031-91303081	RPTEC	kidney:	n/a
49	chr5:91303031-91303081	A549	lung:	n/a
50	chr5:91213435-91213485	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:91164822..91166961-chr5:91195203..91197338,2	K562	blood:
2	chr5:91164822..91166961-chr5:91195203..91197338,2	K562	blood:
3	chr5:91264205..91265908-chr5:91266164..91267839,2	MCF-7	breast:
4	chr5:91165736..91168298-chr5:91169196..91172814,3	K562	blood:
5	chr5:91164818..91166462-chr5:91169540..91172351,2	MCF-7	breast:
6	chr11:118661976..118663890-chr5:91336617..91338563,2	MCF-7	breast:
7	chr5:91224612..91225895-chr5:91517942..91518899,6	MCF-7	breast:
8	chr5:91264205..91265908-chr5:91266164..91267839,2	MCF-7	breast:
9	chr5:91164818..91166462-chr5:91169540..91172351,2	MCF-7	breast:
10	chr5:91315876..91316579-chr6:144774937..144775884,2	MCF-7	breast:
11	chr5:90141991..90142609-chr5:91326921..91327421,2	MCF-7	breast:
12	chr5:91233124..91235467-chr5:91239612..91241761,2	MCF-7	breast:
13	chr5:91194593..91196093-chr6:26282424..26284564,2	MCF-7	breast:
14	chr20:13765598..13766099-chr5:91346247..91346777,2	MCF-7	breast:
15	chr5:91148456..91150162-chr5:91156168..91158769,2	K562	blood:
16	chr5:91233124..91235467-chr5:91239612..91241761,2	MCF-7	breast:
17	chr5:91164129..91166638-chr5:91167068..91169772,2	MCF-7	breast:
18	chr5:91309512..91311831-chr5:91321119..91323779,2	K562	blood:
19	chr5:91309512..91311831-chr5:91321119..91323779,2	K562	blood:
20	chr5:91164129..91166638-chr5:91167068..91169772,2	MCF-7	breast:
21	chr5:91148456..91150162-chr5:91156168..91158769,2	K562	blood:
22	chr5:91165736..91168298-chr5:91169196..91172814,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR98-5	chr5:91378414-91378637	XLOC_004470

Variant related genes	Relation type
ENSG00000250049	TF binding region
PCBP2P3	TF binding region
ENSG00000250049	CpG island
PCBP2P3	CpG island
ENSG00000164199	chromatin interactions
ENSG00000101247	chromatin interactions

Extended variants
information (count: 4185 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4185 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6887393	chr5:91144658-91144659	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs183604323	chr5:91144775-91144776	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs75165148	chr5:91144890-91144891	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs10062507	chr5:91144915-91144916	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs567578703	chr5:91144932-91144933	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs536053485	chr5:91144966-91144967	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs556363822	chr5:91144970-91144971	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs576167193	chr5:91144983-91144984	Flanking Active TSS Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs538709409	chr5:91145036-91145037	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs558701800	chr5:91145120-91145121	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs572055465	chr5:91145158-91145159	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs541057332	chr5:91145187-91145188	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs561421922	chr5:91145191-91145192	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs185964035	chr5:91145202-91145203	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs543771828	chr5:91145211-91145212	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs374987699	chr5:91145214-91145215	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs10077502	chr5:91145230-91145231	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs567478508	chr5:91145232-91145233	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs190728979	chr5:91145287-91145288	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs545856597	chr5:91145346-91145347	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536020829	chr5:91145350-91145351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs114481863	chr5:91145355-91145356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs528444093	chr5:91145392-91145393	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548609128	chr5:91145530-91145531	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567437941	chr5:91145547-91145548	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11953383	chr5:91145549-91145550	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs549809606	chr5:91145593-91145594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569833367	chr5:91145609-91145610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117895040	chr5:91145617-91145618	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549101752	chr5:91145630-91145631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182515357	chr5:91145644-91145645	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116130474	chr5:91145665-91145666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs543682877	chr5:91145677-91145678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187221932	chr5:91145869-91145870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565827956	chr5:91145915-91145916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs546807040	chr5:91145920-91145921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574355320	chr5:91145939-91145940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148320918	chr5:91145940-91145941	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12521016	chr5:91145965-91145966	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372462354	chr5:91145975-91145976	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577004953	chr5:91146008-91146009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs80037808	chr5:91146082-91146083	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6898058	chr5:91146088-91146089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10079624	chr5:91146100-91146101	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs116101451	chr5:91146126-91146127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562066990	chr5:91146177-91146178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146370809	chr5:91146185-91146186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10072732	chr5:91146203-91146204	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs114204067	chr5:91146215-91146216	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376661197	chr5:91146249-91146250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91142800-91146400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr5:91143200-91146600	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr5:91143800-91146200	Enhancers	Hela-S3	cervix
4	chr5:91143800-91147400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr5:91144000-91146000	Enhancers	A549	lung
6	chr5:91144200-91145000	Enhancers	HMEC	breast
7	chr5:91144200-91145600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr5:91144200-91146200	Enhancers	NH-A	brain
9	chr5:91144200-91146400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:91144400-91145000	Enhancers	H9 Cell Line	embryonic stem cell
11	chr5:91144400-91146200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:91144400-91146400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr5:91144400-91146400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr5:91144400-91146400	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr5:91144400-91146400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr5:91144400-91146600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr5:91144600-91145000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr5:91144800-91145200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr5:91145000-91146000	Weak transcription	HMEC	breast
20	chr5:91145000-91147800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr5:91146000-91146200	Enhancers	HMEC	breast
22	chr5:91146400-91146600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr5:91146600-91152600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr5:91146800-91147600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr5:91147800-91152600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr5:91152400-91153200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr5:91152600-91153200	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr5:91152600-91153200	Enhancers	H9 Cell Line	embryonic stem cell
29	chr5:91152600-91153200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr5:91160200-91161000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr5:91160400-91162400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr5:91160400-91162600	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr5:91160400-91163200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:91160600-91161000	Enhancers	Fetal Brain Male	brain
35	chr5:91160600-91161200	Enhancers	Brain Germinal Matrix	brain
36	chr5:91160600-91161800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr5:91160600-91162000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr5:91160600-91162000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr5:91160600-91162400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:91160600-91162400	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr5:91160600-91162600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr5:91160600-91162600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr5:91161000-91161800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:91161000-91161800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:91161000-91161800	Enhancers	Fetal Lung	lung
46	chr5:91161000-91162400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr5:91161600-91162000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:91161800-91162600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:91161800-91169600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr5:91162400-91165200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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