Variant report

Variant	nsv427718
Chromosome Location	chr5:45713018-45896090
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	ATF1	chr5:45779869-45779893	K562	blood:	n/a	n/a
2	ATF2	chr5:45793733-45794112	GM12878	blood:	n/a	n/a
3	ATF2	chr5:45793625-45794610	GM12878	blood:	n/a	n/a
4	BATF	chr5:45794116-45794419	GM12878	blood:	n/a	n/a
5	BATF	chr5:45793742-45794099	GM12878	blood:	n/a	n/a
6	BATF	chr5:45793691-45794568	GM12878	blood:	n/a	n/a
7	BCL11A	chr5:45848140-45848326	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr5:45793646-45794647	GM12878	blood:	n/a	n/a
9	BCL11A	chr5:45793739-45794103	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:45794121-45794555	GM12878	blood:	n/a	n/a
11	BHLHE40	chr5:45799491-45799496	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:45793537-45794787	GM12878	blood:	n/a	n/a
13	CEBPB	chr5:45740115-45740413	HepG2	liver:	n/a	chr5:45740245-45740256
14	CEBPB	chr5:45893475-45893744	Hela-S3	cervix:	n/a	chr5:45893595-45893608 chr5:45893595-45893608 chr5:45893597-45893608 chr5:45893595-45893608 chr5:45893696-45893709 chr5:45893595-45893606
15	CEBPB	chr5:45787466-45787674	HepG2	liver:	n/a	chr5:45787597-45787608
16	CEBPB	chr5:45893506-45893786	IMR90	lung:	n/a	chr5:45893595-45893608 chr5:45893595-45893608 chr5:45893597-45893608 chr5:45893595-45893608 chr5:45893696-45893709 chr5:45893595-45893606
17	CEBPB	chr5:45740075-45740364	A549	lung:	n/a	chr5:45740245-45740256
18	CEBPB	chr5:45822073-45822347	HepG2	liver:	n/a	chr5:45822202-45822215 chr5:45822242-45822253 chr5:45822202-45822213
19	CEBPB	chr5:45893484-45893777	A549	lung:	n/a	chr5:45893595-45893608 chr5:45893595-45893608 chr5:45893597-45893608 chr5:45893595-45893608 chr5:45893696-45893709 chr5:45893595-45893606
20	CEBPB	chr5:45775648-45775852	HepG2	liver:	n/a	chr5:45775697-45775708 chr5:45775698-45775709 chr5:45775697-45775710 chr5:45775697-45775710 chr5:45775697-45775710
21	CEBPB	chr5:45781873-45782081	HepG2	liver:	n/a	chr5:45782013-45782024
22	CEBPB	chr5:45893568-45893768	K562	blood:	n/a	chr5:45893595-45893608 chr5:45893595-45893608 chr5:45893597-45893608 chr5:45893595-45893608 chr5:45893696-45893709 chr5:45893595-45893606
23	CEBPB	chr5:45787482-45787676	A549	lung:	n/a	chr5:45787597-45787608
24	CEBPB	chr5:45893462-45893790	HepG2	liver:	n/a	chr5:45893595-45893608 chr5:45893595-45893608 chr5:45893597-45893608 chr5:45893595-45893608 chr5:45893696-45893709 chr5:45893595-45893606
25	CEBPB	chr5:45774730-45775060	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr5:45787427-45787684	IMR90	lung:	n/a	chr5:45787597-45787608
27	CEBPB	chr5:45808983-45809181	A549	lung:	n/a	n/a
28	CHD2	chr5:45799665-45799856	GM12878	blood:	n/a	n/a
29	CHD2	chr5:45793709-45794421	GM12878	blood:	n/a	n/a
30	CHD2	chr5:45848073-45848341	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr5:45797180-45797330	AG04449	skin:	n/a	n/a
32	CTCF	chr5:45795823-45795826	MCF-7	breast:	n/a	n/a
33	CTCF	chr5:45796740-45796890	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr5:45774780-45774930	GM12867	blood:	n/a	n/a
35	CTCF	chr5:45862980-45863130	GM12864	blood:	n/a	n/a
36	CTCF	chr5:45795640-45795790	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:45797220-45797370	GM06990	blood:	n/a	n/a
38	CTCF	chr5:45797180-45797330	GM12870	blood:	n/a	n/a
39	CTCF	chr5:45796980-45797516	HCT-116	colon:	n/a	n/a
40	CTCF	chr5:45857862-45857963	GM13977	blood:	n/a	n/a
41	CTCF	chr5:45713800-45713950	HCT-116	colon:	n/a	n/a
42	CTCF	chr5:45774780-45774930	HMEC	breast:	n/a	n/a
43	CTCF	chr5:45797060-45797210	WI-38	lung:	n/a	n/a
44	CTCF	chr5:45857814-45858029	GM10248	blood:	n/a	n/a
45	CTCF	chr5:45797180-45797330	BE2_C	brain:	n/a	n/a
46	CTCF	chr5:45774848-45774857	GM10248	blood:	n/a	n/a
47	CTCF	chr5:45863020-45863170	BE2_C	brain:	n/a	n/a
48	CTCF	chr5:45797181-45797290	Pancreas_OC	pancreas:	n/a	n/a
49	CTCF	chr5:45797160-45797310	HMF	breast:	n/a	n/a
50	CTCF	chr5:45795620-45795770	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:45724903-45724953	SK-N-SH_RA	brain:	n/a
2	chr5:45724903-45724953	RPTEC	kidney:	n/a
3	chr5:45724903-45724953	GM12891	blood:	n/a
4	chr5:45724903-45724953	AG10803	skin:	n/a
5	chr5:45724903-45724953	HRPEpiC	eye:	n/a
6	chr5:45724903-45724953	HL-60	blood:	n/a
7	chr5:45724903-45724953	PANC-1	pancreas:	n/a
8	chr5:45724903-45724953	SK-N-SH	brain:	n/a
9	chr5:45724903-45724953	HCT-116	colon:	n/a
10	chr5:45724903-45724953	LNCaP	prostate:	n/a
11	chr5:45724903-45724953	HEK293	kidney:	embryo
12	chr5:45724903-45724953	MCF10A-Er-Src	breast:	n/a
13	chr5:45724903-45724953	AG04449	skin:	fetal
14	chr5:45724903-45724953	BE2_C	brain:	n/a
15	chr5:45724903-45724953	AG09309	skin:	n/a
16	chr5:45724903-45724953	SAEC	small airway:	n/a
17	chr5:45724903-45724953	ECC-1	luminal epithelium:	n/a
18	chr5:45724903-45724953	U87	brain:	n/a
19	chr5:45724903-45724953	BJ	skin:	n/a
20	chr5:45724903-45724953	SKMC	muscle:	n/a
21	chr5:45724903-45724953	HUVEC	blood vessel:	n/a
22	chr5:45724903-45724953	Jurkat	blood:	n/a
23	chr5:45724903-45724953	K562	blood:	n/a
24	chr5:45724903-45724953	HCF	heart:	n/a
25	chr5:45724903-45724953	H1-hESC	embryonic stem cell:	embryo
26	chr5:45724903-45724953	Caco-2	colon:	n/a
27	chr5:45724903-45724953	AoSMC	blood vessel:	n/a
28	chr5:45724903-45724953	PrEC	prostate:	n/a
29	chr5:45724903-45724953	HMEC	breast:	n/a
30	chr5:45724903-45724953	PFSK-1	brain:	n/a
31	chr5:45724903-45724953	SK-N-MC	brain:	n/a
32	chr5:45724903-45724953	NHBE	bronchial:	n/a
33	chr5:45724903-45724953	AG09319	gingival:	n/a
34	chr5:45724903-45724953	HIPEpiC	eye:	n/a
35	chr5:45724903-45724953	NHDF-neo	bronchial:	n/a
36	chr5:45724903-45724953	MCF-7	breast:	n/a
37	chr5:45724903-45724953	GM12892	blood:	n/a
38	chr5:45724903-45724953	NB4	blood:	n/a
39	chr5:45724903-45724953	Hepatocyte	liver:	n/a
40	chr5:45724903-45724953	HepG2	liver:	n/a
41	chr5:45724903-45724953	GM12878	blood:	n/a
42	chr5:45724903-45724953	ProgFib	skin:	n/a
43	chr5:45724903-45724953	NT2-D1	testis:	n/a
44	chr5:45724903-45724953	A549	lung:	n/a
45	chr5:45724903-45724953	IMR90	lung:	fetal
46	chr5:45724903-45724953	T-47D	breast:	n/a
47	chr5:45724903-45724953	HNPCEpiC	eye:	n/a
48	chr5:45724903-45724953	HEEpiC	esophagus:	n/a
49	chr5:45724903-45724953	CMK	blood:	n/a
50	chr5:45724903-45724953	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:45038244..45038751-chr5:45773997..45774955,2	MCF-7	breast:
2	chr5:45700474..45703420-chr5:45719507..45722171,2	MCF-7	breast:
3	chr5:44952363..44953098-chr5:45773975..45774930,2	MCF-7	breast:
4	chr17:56742322..56745282-chr5:45859385..45861280,2	MCF-7	breast:
5	chr11:62608627..62609151-chr5:45773998..45774657,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS30-14	chr5:45752904-45753159	NONHSAT101363
2	lnc-MRPS30-14	chr5:45753168-45753300	NONHSAT101363
3	lnc-MRPS30-14	chr5:45749057-45749335	NONHSAT101363

Variant related genes	Relation type
ENSG00000250122	TF binding region
ENSG00000250122	CpG island
ENSG00000199426	chromatin interactions

Extended variants
information (count: 1139 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1139 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549181465	chr5:45722839-45722840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs138768014	chr5:45722842-45722843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72763966	chr5:45722843-45722844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551887500	chr5:45722904-45722905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190266361	chr5:45722919-45722920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181087203	chr5:45722949-45722950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553545342	chr5:45722966-45722967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6892627	chr5:45722994-45722995	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs62367670	chr5:45722997-45722998	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs573052095	chr5:45724244-45724245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12520275	chr5:45724280-45724281	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs79693999	chr5:45724299-45724300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141887392	chr5:45724300-45724301	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372469465	chr5:45724330-45724331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552968744	chr5:45724345-45724346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550826200	chr5:45724351-45724352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs150653105	chr5:45724362-45724363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs551615387	chr5:45724427-45724428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9986198	chr5:45724549-45724550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs113128893	chr5:45724553-45724554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549295571	chr5:45724594-45724595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs570021300	chr5:45724605-45724606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537091675	chr5:45724606-45724607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs549218156	chr5:45724621-45724622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567629283	chr5:45724639-45724640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565983949	chr5:45724654-45724655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs374401308	chr5:45724748-45724749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138382890	chr5:45724749-45724750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534477939	chr5:45724750-45724751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs202229041	chr5:45724752-45724753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71000647	chr5:45724780-45724781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10070753	chr5:45724786-45724787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114477590	chr5:45724792-45724793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553551994	chr5:45724809-45724810	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10077615	chr5:45724828-45724829	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs537133824	chr5:45724855-45724856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs12655211	chr5:45724857-45724858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs376674550	chr5:45724903-45724904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535845346	chr5:45724915-45724916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369395644	chr5:45724964-45724965	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573499425	chr5:45725014-45725015	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs1852595	chr5:45725052-45725053	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545245814	chr5:45725055-45725056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149359175	chr5:45725099-45725100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147526754	chr5:45725130-45725131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544685088	chr5:45725131-45725132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1852596	chr5:45725139-45725140	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561415310	chr5:45725165-45725166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140210507	chr5:45725185-45725186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs539512142	chr5:45725187-45725188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45722800-45723000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:45724200-45724400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr5:45724400-45724600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr5:45724400-45724600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:45724400-45725000	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr5:45724600-45724800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr5:45724600-45729000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:45724800-45725200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr5:45724800-45725800	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr5:45725000-45725800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr5:45725200-45725800	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:45725200-45725800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr5:45725400-45725600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr5:45725400-45725800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr5:45728800-45729400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr5:45729000-45729600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:45740600-45741200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr5:45741000-45742000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr5:45741200-45742000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr5:45741400-45741800	Enhancers	H9 Cell Line	embryonic stem cell
21	chr5:45741600-45742400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr5:45748800-45749400	Active TSS	Hela-S3	cervix
23	chr5:45749000-45749400	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr5:45750800-45751400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr5:45777600-45777800	Enhancers	Pancreas	Pancrea
26	chr5:45794400-45794800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr5:45795400-45795800	Active TSS	Primary T killer memory cells from peripheral blood	blood
28	chr5:45795600-45796000	ZNF genes & repeats	GM12878-XiMat	blood
29	chr5:45800200-45802600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:45800400-45801600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:45844200-45844800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr5:45844800-45847600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr5:45847600-45848200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr5:45847600-45848400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr5:45847600-45848800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr5:45847600-45848800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr5:45847600-45848800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
38	chr5:45847600-45848800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
39	chr5:45847600-45848800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr5:45847600-45848800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:45847800-45848600	Enhancers	H1 Cell Line	embryonic stem cell
42	chr5:45847800-45848600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr5:45890800-45891200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
44	chr5:45891400-45891600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell

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