Variant report

Variant	nsv547860
Chromosome Location	chr1:152497685-152553365
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	chr1:152497800-152498135	HepG2	liver:	n/a	n/a
2	ATF2	chr1:152549641-152550036	GM12878	blood:	n/a	n/a
3	ATF2	chr1:152537532-152538062	GM12878	blood:	n/a	n/a
4	BATF	chr1:152549573-152550008	GM12878	blood:	n/a	n/a
5	BATF	chr1:152537583-152537985	GM12878	blood:	n/a	n/a
6	BATF	chr1:152549615-152549949	GM12878	blood:	n/a	n/a
7	BATF	chr1:152537564-152537953	GM12878	blood:	n/a	n/a
8	BHLHE40	chr1:152516435-152516557	K562	blood:	n/a	n/a
9	CEBPB	chr1:152535552-152535869	IMR90	lung:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
10	CEBPB	chr1:152535595-152535869	Hela-S3	cervix:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
11	CEBPB	chr1:152497663-152498081	HepG2	liver:	n/a	chr1:152497788-152497801
12	CEBPB	chr1:152546403-152546497	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr1:152497742-152497999	HepG2	liver:	n/a	chr1:152497788-152497801
14	CEBPB	chr1:152497662-152498094	A549	lung:	n/a	chr1:152497788-152497801
15	CEBPB	chr1:152497790-152497957	K562	blood:	n/a	n/a
16	CEBPB	chr1:152497570-152498264	A549	lung:	n/a	chr1:152497788-152497801
17	CEBPB	chr1:152497676-152498092	A549	lung:	n/a	chr1:152497788-152497801
18	CEBPB	chr1:152535544-152535899	A549	lung:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
19	CEBPB	chr1:152535518-152535885	HepG2	liver:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
20	CEBPB	chr1:152497637-152498096	HepG2	liver:	n/a	chr1:152497788-152497801
21	CTCF	chr1:152516380-152516530	GM12872	blood:	n/a	n/a
22	CTCF	chr1:152505900-152506050	HBMEC	blood vessel:	n/a	chr1:152505986-152506007
23	CTCF	chr1:152505960-152506110	GM12874	blood:	n/a	chr1:152505986-152506007
24	CTCF	chr1:152516424-152516590	GM13977	blood:	n/a	n/a
25	CTCF	chr1:152516660-152516810	GM12871	blood:	n/a	n/a
26	CTCF	chr1:152505940-152506090	NB4	blood:	n/a	chr1:152505986-152506007
27	CTCF	chr1:152506180-152506330	GM12868	blood:	n/a	n/a
28	CTCF	chr1:152516371-152516610	GM19240	blood:	n/a	n/a
29	CTCF	chr1:152544300-152544450	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr1:152514180-152514330	GM12872	blood:	n/a	n/a
31	CTCF	chr1:152516400-152516550	HEK293	kidney:	n/a	n/a
32	CTCF	chr1:152516393-152516533	A549	lung:	n/a	n/a
33	CTCF	chr1:152516380-152516530	NHLF	lung:	n/a	n/a
34	CTCF	chr1:152505906-152506061	H1-hESC	embryonic stem cell:	n/a	chr1:152505986-152506007
35	CTCF	chr1:152516769-152516828	GM12892	blood:	n/a	chr1:152516812-152516820 chr1:152516800-152516821 chr1:152516805-152516823
36	CTCF	chr1:152505875-152506129	GM19240	blood:	n/a	chr1:152505986-152506007
37	CTCF	chr1:152505880-152506141	LNCaP	prostate:	n/a	chr1:152505986-152506007
38	CTCF	chr1:152516336-152516667	K562	blood:	n/a	n/a
39	CTCF	chr1:152516400-152516550	GM12874	blood:	n/a	n/a
40	CTCF	chr1:152516420-152516570	GM12872	blood:	n/a	n/a
41	CTCF	chr1:152516400-152516550	HL-60	blood:	n/a	n/a
42	CTCF	chr1:152516460-152516610	BJ	skin:	n/a	n/a
43	CTCF	chr1:152516480-152516630	HMF	breast:	n/a	n/a
44	CTCF	chr1:152505900-152506050	NHEK	skin:	n/a	chr1:152505986-152506007
45	CTCF	chr1:152516409-152516579	GM10266	blood:	n/a	n/a
46	CTCF	chr1:152505872-152506145	GM12878	blood:	n/a	chr1:152505986-152506007
47	CTCF	chr1:152526172-152526231	A549	lung:	n/a	n/a
48	CTCF	chr1:152516380-152516530	SAEC	small airway:	n/a	n/a
49	CTCF	chr1:152516440-152516590	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr1:152528954-152529048	Kidney_OC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152552175-152552225	SK-N-SH_RA	brain:	n/a
2	chr1:152538380-152538430	PrEC	prostate:	n/a
3	chr1:152552175-152552225	LNCaP	prostate:	n/a
4	chr1:152506922-152506972	A549	lung:	n/a
5	chr1:152538426-152538476	AG10803	skin:	n/a
6	chr1:152538857-152538907	AG04449	skin:	fetal
7	chr1:152538857-152538907	AG04450	lung:	fetal
8	chr1:152538857-152538907	HRCEpiC	kidney:	n/a
9	chr1:152538888-152538938	GM12891	blood:	n/a
10	chr1:152506842-152506892	HRPEpiC	eye:	n/a
11	chr1:152552175-152552225	ovcar-3	ovarian:	n/a
12	chr1:152506922-152506972	AG09309	skin:	n/a
13	chr1:152553096-152553146	AG10803	skin:	n/a
14	chr1:152506886-152506936	SAEC	small airway:	n/a
15	chr1:152506886-152506936	ProgFib	skin:	n/a
16	chr1:152538380-152538430	Hepatocyte	liver:	n/a
17	chr1:152552494-152552544	SKMC	muscle:	n/a
18	chr1:152553244-152553294	AG04449	skin:	fetal
19	chr1:152553244-152553294	NB4	blood:	n/a
20	chr1:152538888-152538938	PFSK-1	brain:	n/a
21	chr1:152538857-152538907	GM12892	blood:	n/a
22	chr1:152538888-152538938	LNCaP	prostate:	n/a
23	chr1:152538888-152538938	HL-60	blood:	n/a
24	chr1:152553096-152553146	HMEC	breast:	n/a
25	chr1:152506842-152506892	GM12892	blood:	n/a
26	chr1:152506842-152506892	HCPEpiC	choroid plexus:	n/a
27	chr1:152538857-152538907	HPAEpiC	pulmonary alveolar:	n/a
28	chr1:152552175-152552225	AG10803	skin:	n/a
29	chr1:152538380-152538430	NT2-D1	testis:	n/a
30	chr1:152506886-152506936	NB4	blood:	n/a
31	chr1:152552175-152552225	PFSK-1	brain:	n/a
32	chr1:152506886-152506936	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:152506922-152506972	SAEC	small airway:	n/a
34	chr1:152552175-152552225	HUVEC	blood vessel:	n/a
35	chr1:152553244-152553294	HCM	heart:	n/a
36	chr1:152506922-152506972	SKMC	muscle:	n/a
37	chr1:152538857-152538907	ovcar-3	ovarian:	n/a
38	chr1:152538426-152538476	ECC-1	luminal epithelium:	n/a
39	chr1:152552175-152552225	SK-N-SH	brain:	n/a
40	chr1:152553244-152553294	HCPEpiC	choroid plexus:	n/a
41	chr1:152506922-152506972	Caco-2	colon:	n/a
42	chr1:152552494-152552544	NHBE	bronchial:	n/a
43	chr1:152506922-152506972	NHBE	bronchial:	n/a
44	chr1:152506922-152506972	HIPEpiC	eye:	n/a
45	chr1:152538888-152538938	AG09309	skin:	n/a
46	chr1:152506886-152506936	GM12891	blood:	n/a
47	chr1:152552494-152552544	HEEpiC	esophagus:	n/a
48	chr1:152553244-152553294	HRPEpiC	eye:	n/a
49	chr1:152553096-152553146	HUVEC	blood vessel:	n/a
50	chr1:152506886-152506936	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:152469001..152470435-chr1:152505453..152506443,13	MCF-7	breast:
2	chr1:152508160..152510844-chr1:152518388..152520386,2	K562	blood:
3	chr1:152469495..152470816-chr1:152505489..152506516,11	MCF-7	breast:
4	chr1:152433729..152434269-chr1:152505524..152506462,2	MCF-7	breast:
5	chr1:152458591..152459582-chr1:152505807..152506392,3	MCF-7	breast:
6	chr1:152433975..152434768-chr1:152504695..152505339,2	MCF-7	breast:
7	chr1:152467226..152468092-chr1:152505547..152506816,7	MCF-7	breast:
8	chr1:152508160..152510844-chr1:152518388..152520386,2	K562	blood:
9	chr1:152469492..152471247-chr1:152505473..152506875,7	K562	blood:
10	chr1:152467377..152468575-chr1:152505519..152506463,7	MCF-7	breast:
11	chr1:152512266..152512767-chr16:8754919..8755481,3	MCF-7	breast:
12	chr1:152507658..152510511-chr1:152512542..152515138,2	MCF-7	breast:
13	chr1:152494849..152497210-chr1:152499471..152502246,2	MCF-7	breast:
14	chr1:152507658..152510511-chr1:152512542..152515138,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRCT1-2	chr1:152502924-152503231	expReg_chr1_17005_+

Variant related genes	Relation type
LCE3D	TF binding region
LCE3E	TF binding region
LCE3D	CpG island
LCE3E	CpG island

Extended variants
information (count: 1384 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:1384 , 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	rs12116609	chr1:152497685-152497686	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs367803389	chr1:152497687-152497688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575814838	chr1:152497727-152497728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs372710672	chr1:152497758-152497759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs526099	chr1:152497811-152497812	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs146966813	chr1:152497813-152497814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546390306	chr1:152497832-152497833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540276407	chr1:152497833-152497834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73004888	chr1:152497844-152497845	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs525960	chr1:152497866-152497867	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs79563434	chr1:152497925-152497926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34940634	chr1:152497953-152497954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs370492078	chr1:152497994-152497995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs182208859	chr1:152498006-152498007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531550832	chr1:152498014-152498015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74128255	chr1:152498018-152498019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs185796925	chr1:152498025-152498026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571570744	chr1:152498041-152498042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377086208	chr1:152498042-152498043	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547459768	chr1:152498058-152498059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538490162	chr1:152498066-152498067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73004889	chr1:152498077-152498078	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs112860734	chr1:152498122-152498123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs556237303	chr1:152498141-152498142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550110373	chr1:152498156-152498157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576013368	chr1:152498183-152498184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538435449	chr1:152498243-152498244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs558065157	chr1:152498375-152498376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189925797	chr1:152498470-152498471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181678517	chr1:152498514-152498515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568635000	chr1:152498524-152498525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs373835879	chr1:152498539-152498540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540509731	chr1:152498558-152498559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369494369	chr1:152498567-152498568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs541640778	chr1:152498657-152498658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560143643	chr1:152498699-152498700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs573720538	chr1:152498815-152498816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185461557	chr1:152498817-152498818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs563011427	chr1:152498859-152498860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7531805	chr1:152498878-152498879	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs551602311	chr1:152498896-152498897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs142035935	chr1:152498909-152498910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527609787	chr1:152498932-152498933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554289576	chr1:152498950-152498951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74482377	chr1:152498965-152498966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7531924	chr1:152498992-152498993	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs190122005	chr1:152499008-152499009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs58674564	chr1:152499038-152499039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs397943711	chr1:152499043-152499044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572498505	chr1:152499067-152499068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	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
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	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
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152496600-152503400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:152497400-152497800	Enhancers	Liver	Liver
3	chr1:152497600-152498000	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr1:152497600-152498400	Enhancers	Duodenum Mucosa	Duodenum
5	chr1:152497600-152499400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:152497800-152498200	Enhancers	A549	lung
7	chr1:152498200-152499000	Weak transcription	A549	lung
8	chr1:152499000-152499200	Enhancers	A549	lung
9	chr1:152503400-152503800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:152503800-152510000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:152508400-152513400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:152510000-152510600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr1:152510000-152510600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:152512000-152512800	Enhancers	A549	lung
15	chr1:152516600-152517000	Enhancers	Esophagus	oesophagus
16	chr1:152519200-152519600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr1:152531600-152532200	Active TSS	Spleen	Spleen
18	chr1:152534800-152535000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:152535000-152538400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr1:152537400-152537800	Enhancers	GM12878-XiMat	blood
21	chr1:152537800-152538200	Flanking Active TSS	GM12878-XiMat	blood
22	chr1:152538200-152538400	Enhancers	GM12878-XiMat	blood
23	chr1:152538400-152539600	Enhancers	HMEC	breast
24	chr1:152538400-152539800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr1:152538800-152539400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:152538800-152539800	Enhancers	NHEK	skin
27	chr1:152539000-152539600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr1:152539400-152541800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:152541800-152542400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:152542000-152544400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
31	chr1:152542400-152543000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr1:152543000-152552600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:152546400-152547000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:152547000-152552400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr1:152549400-152549800	Enhancers	GM12878-XiMat	blood
36	chr1:152549400-152550800	Enhancers	Muscle Satellite Cultured Cells	--
37	chr1:152549400-152551400	Enhancers	HSMMtube	muscle
38	chr1:152549400-152551600	Enhancers	HSMM	muscle
39	chr1:152549800-152551400	Weak transcription	GM12878-XiMat	blood
40	chr1:152550800-152555200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr1:152551400-152552600	Enhancers	GM12878-XiMat	blood
42	chr1:152551600-152552800	Weak transcription	HSMM	muscle
43	chr1:152552400-152553200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr1:152552400-152553400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr1:152552600-152553200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:152552600-152553200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:152552600-152553400	Enhancers	HMEC	breast
48	chr1:152552800-152553200	Enhancers	HSMM	muscle
49	chr1:152552800-152553400	Enhancers	NHEK	skin

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