Variant report

Variant	nsv548420
Chromosome Location	chr1:187513281-187599437
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	ATF2	chr1:187593954-187594448	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr1:187547417-187547428	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL11A	chr1:187594147-187594356	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:187591096-187591473	GM12878	blood:	n/a	n/a
5	CEBPB	chr1:187584503-187584826	IMR90	lung:	n/a	chr1:187584652-187584661 chr1:187584781-187584794 chr1:187584652-187584663
6	CEBPB	chr1:187597341-187597369	A549	lung:	n/a	n/a
7	CEBPB	chr1:187546801-187547159	IMR90	lung:	n/a	chr1:187546981-187546994 chr1:187546982-187546993 chr1:187546981-187546992 chr1:187546980-187546997 chr1:187546981-187546994 chr1:187546981-187546994
8	CEBPB	chr1:187553736-187554088	A549	lung:	n/a	chr1:187553867-187553878
9	CEBPB	chr1:187546810-187547135	H1-hESC	embryonic stem cell:	n/a	chr1:187546981-187546994 chr1:187546982-187546993 chr1:187546981-187546992 chr1:187546980-187546997 chr1:187546981-187546994 chr1:187546981-187546994
10	CEBPB	chr1:187514839-187515039	HepG2	liver:	n/a	chr1:187514935-187514946
11	CEBPB	chr1:187546803-187547133	HepG2	liver:	n/a	chr1:187546981-187546994 chr1:187546982-187546993 chr1:187546981-187546992 chr1:187546980-187546997 chr1:187546981-187546994 chr1:187546981-187546994
12	CEBPB	chr1:187594008-187594675	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr1:187594338-187594675	A549	lung:	n/a	n/a
14	CEBPB	chr1:187584503-187584806	HepG2	liver:	n/a	chr1:187584652-187584661 chr1:187584781-187584794 chr1:187584652-187584663
15	CEBPB	chr1:187546820-187547113	A549	lung:	n/a	chr1:187546981-187546994 chr1:187546982-187546993 chr1:187546981-187546992 chr1:187546980-187546997 chr1:187546981-187546994 chr1:187546981-187546994
16	CEBPB	chr1:187539491-187539703	HepG2	liver:	n/a	chr1:187539643-187539652 chr1:187539643-187539652 chr1:187539650-187539661 chr1:187539641-187539654 chr1:187539643-187539652
17	CEBPB	chr1:187553697-187554169	IMR90	lung:	n/a	chr1:187553867-187553878
18	CEBPB	chr1:187594332-187594668	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr1:187546803-187547151	Hela-S3	cervix:	n/a	chr1:187546981-187546994 chr1:187546982-187546993 chr1:187546981-187546992 chr1:187546980-187546997 chr1:187546981-187546994 chr1:187546981-187546994
20	CEBPB	chr1:187539467-187539785	IMR90	lung:	n/a	chr1:187539643-187539652 chr1:187539643-187539652 chr1:187539650-187539661 chr1:187539641-187539654 chr1:187539643-187539652
21	CEBPB	chr1:187539554-187539736	H1-hESC	embryonic stem cell:	n/a	chr1:187539643-187539652 chr1:187539643-187539652 chr1:187539650-187539661 chr1:187539641-187539654 chr1:187539643-187539652
22	CEBPB	chr1:187553739-187554038	HepG2	liver:	n/a	chr1:187553867-187553878
23	CEBPB	chr1:187556182-187556310	A549	lung:	n/a	n/a
24	CEBPB	chr1:187529831-187530020	HepG2	liver:	n/a	chr1:187529948-187529959
25	CEBPB	chr1:187594334-187594684	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:187538353-187538590	IMR90	lung:	n/a	n/a
27	CEBPB	chr1:187539465-187539743	A549	lung:	n/a	chr1:187539643-187539652 chr1:187539643-187539652 chr1:187539650-187539661 chr1:187539641-187539654 chr1:187539643-187539652
28	CEBPB	chr1:187556120-187556764	IMR90	lung:	n/a	n/a
29	CHD1	chr1:187594556-187594929	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr1:187520340-187520490	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:187520311-187520547	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:187520403-187520445	NHEK	skin:	n/a	n/a
33	CTCF	chr1:187572981-187573038	GM10248	blood:	n/a	n/a
34	CTCF	chr1:187520360-187520510	HepG2	liver:	n/a	n/a
35	CTCF	chr1:187520360-187520510	BE2_C	brain:	n/a	n/a
36	CTCF	chr1:187520360-187520510	NB4	blood:	n/a	n/a
37	CTCF	chr1:187520348-187520509	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:187520360-187520510	GM12874	blood:	n/a	n/a
39	CTCF	chr1:187595767-187595849	GM20000	blood:	n/a	n/a
40	CTCF	chr1:187520323-187520537	MCF-7	breast:	n/a	n/a
41	CTCF	chr1:187520325-187520507	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:187520300-187520450	HBMEC	blood vessel:	n/a	n/a
43	CTCF	chr1:187520300-187520450	HMEC	breast:	n/a	n/a
44	CTCF	chr1:187520280-187520430	HCT-116	colon:	n/a	n/a
45	CTCF	chr1:187520320-187520470	A549	lung:	n/a	n/a
46	CTCF	chr1:187520420-187520570	A549	lung:	n/a	n/a
47	CTCF	chr1:187520360-187520510	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr1:187520365-187520494	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:187520280-187520430	HRE	kidney:	n/a	n/a
50	CTCF	chr1:187520349-187520528	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:187593849-187593899	SK-N-SH	brain:	n/a
2	chr1:187593849-187593899	HRCEpiC	kidney:	n/a
3	chr1:187593849-187593899	NT2-D1	testis:	n/a
4	chr1:187593849-187593899	LNCaP	prostate:	n/a
5	chr1:187593849-187593899	HAEpiC	amniotic membrane:	n/a
6	chr1:187593849-187593899	HL-60	blood:	n/a
7	chr1:187593849-187593899	HUVEC	blood vessel:	n/a
8	chr1:187593849-187593899	T-47D	breast:	n/a
9	chr1:187593849-187593899	HNPCEpiC	eye:	n/a
10	chr1:187593849-187593899	ECC-1	luminal epithelium:	n/a
11	chr1:187593849-187593899	GM12878	blood:	n/a
12	chr1:187593849-187593899	HEEpiC	esophagus:	n/a
13	chr1:187593849-187593899	AG09309	skin:	n/a
14	chr1:187593849-187593899	NB4	blood:	n/a
15	chr1:187593849-187593899	RPTEC	kidney:	n/a
16	chr1:187593849-187593899	HCPEpiC	choroid plexus:	n/a
17	chr1:187593849-187593899	HRE	kidney:	n/a
18	chr1:187593849-187593899	Hela-S3	cervix:	n/a
19	chr1:187593849-187593899	GM19239	blood:	n/a
20	chr1:187593849-187593899	SAEC	small airway:	n/a
21	chr1:187593849-187593899	Jurkat	blood:	n/a
22	chr1:187593849-187593899	HepG2	liver:	n/a
23	chr1:187593849-187593899	MCF-7	breast:	n/a
24	chr1:187593849-187593899	PrEC	prostate:	n/a
25	chr1:187593849-187593899	HCF	heart:	n/a
26	chr1:187593849-187593899	HCM	heart:	n/a
27	chr1:187593849-187593899	Hepatocyte	liver:	n/a
28	chr1:187593849-187593899	GM12891	blood:	n/a
29	chr1:187593849-187593899	U87	brain:	n/a
30	chr1:187593849-187593899	HRPEpiC	eye:	n/a
31	chr1:187593849-187593899	AG04449	skin:	fetal
32	chr1:187593849-187593899	PFSK-1	brain:	n/a
33	chr1:187593849-187593899	K562	blood:	n/a
34	chr1:187593849-187593899	AoSMC	blood vessel:	n/a
35	chr1:187593849-187593899	SK-N-SH_RA	brain:	n/a
36	chr1:187593849-187593899	HPAEpiC	pulmonary alveolar:	n/a
37	chr1:187593849-187593899	Caco-2	colon:	n/a
38	chr1:187593849-187593899	SK-N-MC	brain:	n/a
39	chr1:187593849-187593899	MCF10A-Er-Src	breast:	n/a
40	chr1:187593849-187593899	NH-A	brain:	n/a
41	chr1:187593849-187593899	SKMC	muscle:	n/a
42	chr1:187593849-187593899	AG10803	skin:	n/a
43	chr1:187593849-187593899	HMEC	breast:	n/a
44	chr1:187593849-187593899	NHBE	bronchial:	n/a
45	chr1:187593849-187593899	BE2_C	brain:	n/a
46	chr1:187593849-187593899	PANC-1	pancreas:	n/a
47	chr1:187593849-187593899	A549	lung:	n/a
48	chr1:187593849-187593899	HEK293	kidney:	embryo
49	chr1:187593849-187593899	HIPEpiC	eye:	n/a
50	chr1:187593849-187593899	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr1:187587843..187589982-chr1:187592058..187594369,2	MCF-7	breast:
2	chr1:187557147..187558747-chr1:187665623..187667137,2	K562	blood:
3	chr1:187580745..187582461-chr1:187606188..187607711,2	K562	blood:
4	chr1:187552134..187555012-chr1:187591423..187593251,2	MCF-7	breast:
5	chr1:187587843..187589982-chr1:187592058..187594369,2	MCF-7	breast:
6	chr1:187539532..187540502-chr14:23585032..23585801,2	MCF-7	breast:
7	chr1:187552134..187555012-chr1:187591423..187593251,2	MCF-7	breast:

Variant related genes	Relation type
FDPSP1	TF binding region
FDPSP1	CpG island

Extended variants
information (count: 1367 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1367 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549612444	chr1:187517440-187517441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565036197	chr1:187517455-187517456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75274551	chr1:187517456-187517457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116709458	chr1:187517527-187517528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11799315	chr1:187517551-187517552	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs180975402	chr1:187517557-187517558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11808975	chr1:187517582-187517583	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs185005923	chr1:187517592-187517593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368276191	chr1:187517598-187517599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559039527	chr1:187517614-187517615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs149967759	chr1:187517622-187517623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189521207	chr1:187517668-187517669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77670296	chr1:187517689-187517690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11802548	chr1:187517700-187517701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs375354144	chr1:187517755-187517756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542175522	chr1:187517779-187517780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559076630	chr1:187517800-187517801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145099895	chr1:187517815-187517816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs116321882	chr1:187517897-187517898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs182345474	chr1:187517953-187517954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551729642	chr1:187518005-187518006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs150912286	chr1:187518011-187518012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34145814	chr1:187518012-187518013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs550813677	chr1:187518032-187518033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567529459	chr1:187518033-187518034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536543435	chr1:187518038-187518039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs145945756	chr1:187518042-187518043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187004568	chr1:187518052-187518053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs71955236	chr1:187518061-187518062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs201148230	chr1:187518064-187518065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566732751	chr1:187518066-187518067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs2050742	chr1:187518067-187518068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12022374	chr1:187518068-187518069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558749661	chr1:187518069-187518070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575715635	chr1:187518080-187518081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs144724248	chr1:187518083-187518084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191863325	chr1:187518091-187518092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35965457	chr1:187518097-187518098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs11809380	chr1:187518107-187518108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs574731500	chr1:187518126-187518127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551239600	chr1:187518174-187518175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571597834	chr1:187518184-187518185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs183313475	chr1:187518210-187518211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs143037412	chr1:187518218-187518219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572732856	chr1:187518250-187518251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146684653	chr1:187518293-187518294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140305682	chr1:187518321-187518322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145794940	chr1:187518339-187518340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550738053	chr1:187518362-187518363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114287147	chr1:187518375-187518376	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Schizophrenia	19197363	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17899364	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:187517400-187517800	Enhancers	Fetal Heart	heart
2	chr1:187517800-187518200	Weak transcription	Fetal Heart	heart
3	chr1:187518200-187519800	Enhancers	Fetal Heart	heart
4	chr1:187542600-187543000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:187543000-187546200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:187546200-187547000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr1:187546200-187547400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:187546600-187547400	Enhancers	Fetal Lung	lung
9	chr1:187559800-187560200	Enhancers	Fetal Lung	lung
10	chr1:187572800-187573000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr1:187573000-187573200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr1:187573000-187573200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr1:187573000-187573400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr1:187573000-187573600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
15	chr1:187573000-187575400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr1:187573000-187575400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr1:187573200-187573400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr1:187573200-187574400	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr1:187573200-187575400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr1:187573400-187574800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr1:187573400-187575000	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr1:187573600-187573800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr1:187573800-187574800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr1:187574400-187575400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr1:187574800-187575000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr1:187574800-187575200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr1:187574800-187575200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr1:187574800-187575400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr1:187574800-187575400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr1:187575000-187575200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr1:187579000-187595400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr1:187581000-187581400	Weak transcription	Pancreas	Pancrea
33	chr1:187581400-187581600	ZNF genes & repeats	Pancreas	Pancrea
34	chr1:187584200-187586400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
35	chr1:187584400-187585000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
36	chr1:187584800-187586400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr1:187585000-187587000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr1:187586400-187591200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr1:187587000-187587600	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
40	chr1:187587600-187591000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr1:187588400-187595000	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr1:187589200-187592800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
43	chr1:187591000-187592200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr1:187591200-187591400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr1:187591200-187591400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:187591200-187591600	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr1:187591200-187591600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr1:187591200-187593600	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr1:187591600-187592600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr1:187591600-187592800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links