Variant report

Variant	nsv547920
Chromosome Location	chr1:153033406-153099345
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:414)
CpG islands
(count:671)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:414 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:153091851-153092463	K562	blood:	n/a	n/a
2	ARID3A	chr1:153045341-153045614	K562	blood:	n/a	n/a
3	ATF1	chr1:153045393-153045647	K562	blood:	n/a	n/a
4	ATF1	chr1:153092052-153092244	K562	blood:	n/a	n/a
5	ATF2	chr1:153095044-153096080	GM12878	blood:	n/a	n/a
6	ATF2	chr1:153095050-153096075	GM12878	blood:	n/a	n/a
7	BACH1	chr1:153095491-153095760	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr1:153095622-153095941	GM12878	blood:	n/a	n/a
9	BCL3	chr1:153095057-153096084	GM12878	blood:	n/a	n/a
10	BCL3	chr1:153095414-153095909	GM12878	blood:	n/a	n/a
11	BHLHE40	chr1:153095520-153095786	GM12878	blood:	n/a	n/a
12	BRCA1	chr1:153095487-153095747	H1-hESC	embryonic stem cell:	n/a	n/a
13	BRCA1	chr1:153072106-153072249	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr1:153098078-153098323	K562	blood:	n/a	n/a
15	CBX3	chr1:153072732-153073222	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:153095270-153096030	HCT-116	colon:	n/a	n/a
17	CBX3	chr1:153098003-153098342	K562	blood:	n/a	n/a
18	CBX3	chr1:153096241-153096560	K562	blood:	n/a	n/a
19	CBX3	chr1:153091834-153092294	K562	blood:	n/a	n/a
20	CCNT2	chr1:153045352-153045547	K562	blood:	n/a	n/a
21	CCNT2	chr1:153091982-153092181	K562	blood:	n/a	n/a
22	CEBPB	chr1:153072214-153073260	HCT-116	colon:	n/a	n/a
23	CEBPB	chr1:153072593-153073269	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:153072025-153072481	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr1:153091862-153092458	K562	blood:	n/a	n/a
26	CEBPB	chr1:153072685-153073167	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr1:153037628-153037762	K562	blood:	n/a	n/a
28	CEBPB	chr1:153070459-153070753	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr1:153072809-153073124	MCF-7	breast:	n/a	n/a
30	CEBPB	chr1:153045498-153045761	K562	blood:	n/a	n/a
31	CEBPB	chr1:153095343-153095899	Hela-S3	cervix:	n/a	n/a
32	CEBPD	chr1:153045266-153045639	K562	blood:	n/a	n/a
33	CHD1	chr1:153095590-153095751	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr1:153095404-153095710	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr1:153095434-153095592	GM12878	blood:	n/a	n/a
36	CHD2	chr1:153095274-153095886	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr1:153072795-153073086	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:153063890-153064040	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr1:153042620-153042770	HCT-116	colon:	n/a	n/a
40	CTCF	chr1:153063860-153064010	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr1:153043068-153043074	Fibrobl	skin:	n/a	n/a
42	CTCF	chr1:153075100-153075250	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr1:153042820-153042970	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr1:153063864-153064071	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:153063911-153064021	GM12878	blood:	n/a	n/a
46	CTCF	chr1:153042840-153042990	GM12873	blood:	n/a	n/a
47	CTCF	chr1:153042820-153042970	MCF-7	breast:	n/a	n/a
48	CTCF	chr1:153072114-153072181	LNCaP	prostate:	n/a	n/a
49	CTCF	chr1:153063909-153064013	NHEK	skin:	n/a	n/a
50	CTCF	chr1:153095643-153095687	MCF-7	breast:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153085969-153086019	HRE	kidney:	n/a
2	chr1:153065613-153065663	NB4	blood:	n/a
3	chr1:153068231-153068281	HL-60	blood:	n/a
4	chr1:153045274-153045324	HL-60	blood:	n/a
5	chr1:153044457-153044507	NHDF-neo	bronchial:	n/a
6	chr1:153044071-153044121	LNCaP	prostate:	n/a
7	chr1:153085649-153085699	HCM	heart:	n/a
8	chr1:153044457-153044507	HCM	heart:	n/a
9	chr1:153068236-153068286	SAEC	small airway:	n/a
10	chr1:153044071-153044121	NHBE	bronchial:	n/a
11	chr1:153065613-153065663	MCF10A-Er-Src	breast:	n/a
12	chr1:153085969-153086019	HL-60	blood:	n/a
13	chr1:153065613-153065663	H1-hESC	embryonic stem cell:	embryo
14	chr1:153043360-153043410	U87	brain:	n/a
15	chr1:153043360-153043410	PANC-1	pancreas:	n/a
16	chr1:153044457-153044507	ECC-1	luminal epithelium:	n/a
17	chr1:153085998-153086048	AG10803	skin:	n/a
18	chr1:153065613-153065663	K562	blood:	n/a
19	chr1:153085649-153085699	AoSMC	blood vessel:	n/a
20	chr1:153068231-153068281	A549	lung:	n/a
21	chr1:153085969-153086019	ovcar-3	ovarian:	n/a
22	chr1:153068231-153068281	NT2-D1	testis:	n/a
23	chr1:153085649-153085699	AG04450	lung:	fetal
24	chr1:153068231-153068281	AG09309	skin:	n/a
25	chr1:153068231-153068281	MCF10A-Er-Src	breast:	n/a
26	chr1:153044457-153044507	K562	blood:	n/a
27	chr1:153044457-153044507	PANC-1	pancreas:	n/a
28	chr1:153068231-153068281	HIPEpiC	eye:	n/a
29	chr1:153044457-153044507	BE2_C	brain:	n/a
30	chr1:153044457-153044507	HCT-116	colon:	n/a
31	chr1:153085649-153085699	LNCaP	prostate:	n/a
32	chr1:153068236-153068286	MCF10A-Er-Src	breast:	n/a
33	chr1:153045274-153045324	AG04449	skin:	fetal
34	chr1:153045274-153045324	H1-hESC	embryonic stem cell:	embryo
35	chr1:153043360-153043410	K562	blood:	n/a
36	chr1:153043360-153043410	AG10803	skin:	n/a
37	chr1:153085998-153086048	HEK293	kidney:	embryo
38	chr1:153065613-153065663	HL-60	blood:	n/a
39	chr1:153085649-153085699	HRCEpiC	kidney:	n/a
40	chr1:153068236-153068286	HEEpiC	esophagus:	n/a
41	chr1:153085969-153086019	GM12892	blood:	n/a
42	chr1:153065613-153065663	AG09309	skin:	n/a
43	chr1:153068236-153068286	GM19239	blood:	n/a
44	chr1:153085152-153085202	ProgFib	skin:	n/a
45	chr1:153085649-153085699	HNPCEpiC	eye:	n/a
46	chr1:153068231-153068281	ECC-1	luminal epithelium:	n/a
47	chr1:153068231-153068281	HRE	kidney:	n/a
48	chr1:153085969-153086019	ProgFib	skin:	n/a
49	chr1:153045274-153045324	Hepatocyte	liver:	n/a
50	chr1:153085998-153086048	SK-N-SH_RA	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:153040069..153041954-chr1:153044290..153046075,2	K562	blood:
2	chr1:153089902..153091539-chr1:153091672..153093377,2	MCF-7	breast:
3	chr1:153086209..153088647-chr1:153089320..153091909,2	K562	blood:
4	chr1:153034986..153036506-chr6:26033157..26034818,2	K562	blood:
5	chr1:153066495..153069197-chr1:153073553..153075701,2	K562	blood:
6	chr1:153089902..153091539-chr1:153091672..153093377,2	MCF-7	breast:
7	chr1:153086209..153088647-chr1:153089320..153091909,2	K562	blood:
8	chr1:153040069..153041954-chr1:153044290..153046075,2	K562	blood:
9	chr1:153093442..153095730-chr14:51247802..51249662,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPRR2E	TF binding region
SPRR2B	TF binding region
SPRR2A	TF binding region
SPRR2F	TF binding region
SPRR2E	CpG island
SPRR2B	CpG island
SPRR2A	CpG island
SPRR2F	CpG island
ENSG00000137259	chromatin interactions
ENSG00000203785	chromatin interactions

Extended variants
information (count: 2622 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:2622 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs582345	chr1:153033406-153033407	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs529229237	chr1:153033467-153033468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs417814	chr1:153033509-153033510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144663736	chr1:153033532-153033533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536122956	chr1:153033536-153033537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115432803	chr1:153033573-153033574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75285101	chr1:153033578-153033579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551550613	chr1:153033583-153033584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12748753	chr1:153033603-153033604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114790900	chr1:153033678-153033679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192099047	chr1:153033716-153033717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547017068	chr1:153033726-153033727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6675009	chr1:153033783-153033784	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs535760616	chr1:153033785-153033786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs117895495	chr1:153033831-153033832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569434822	chr1:153033889-153033890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76312314	chr1:153033899-153033900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs138414206	chr1:153033909-153033910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149245394	chr1:153033952-153033953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114081858	chr1:153033965-153033966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs144419885	chr1:153033985-153033986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552778490	chr1:153034014-153034015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368100498	chr1:153034057-153034058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574044799	chr1:153034096-153034097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184711775	chr1:153034150-153034151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs562687210	chr1:153034166-153034167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200962301	chr1:153034208-153034209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531626534	chr1:153034215-153034216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs12753609	chr1:153034230-153034231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs565068740	chr1:153034245-153034246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs527416363	chr1:153034273-153034274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370099942	chr1:153034295-153034296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545009128	chr1:153034301-153034302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377729093	chr1:153034366-153034367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563231813	chr1:153034398-153034399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115961649	chr1:153034418-153034419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs114677176	chr1:153034449-153034450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75349513	chr1:153034452-153034453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558964482	chr1:153034460-153034461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538237905	chr1:153034466-153034467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549361128	chr1:153034476-153034477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569488630	chr1:153034480-153034481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs6587724	chr1:153034501-153034502	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs535108133	chr1:153034535-153034536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558093528	chr1:153034560-153034561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571780872	chr1:153034612-153034613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs608509	chr1:153034650-153034651	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs554262498	chr1:153034715-153034716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562321931	chr1:153034743-153034744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs557873888	chr1:153034773-153034774	Weak transcription	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
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
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153032200-153053400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:153032400-153033600	Enhancers	K562	blood
3	chr1:153044000-153044600	Enhancers	Esophagus	oesophagus
4	chr1:153044000-153045400	Enhancers	K562	blood
5	chr1:153045400-153046400	Flanking Active TSS	K562	blood
6	chr1:153046400-153046800	Enhancers	K562	blood
7	chr1:153046800-153047400	Weak transcription	K562	blood
8	chr1:153047400-153047600	Enhancers	K562	blood
9	chr1:153050200-153050800	Enhancers	NHEK	skin
10	chr1:153050800-153053800	Weak transcription	NHEK	skin
11	chr1:153053400-153053600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:153053800-153055000	Enhancers	NHEK	skin
13	chr1:153054000-153054800	Enhancers	HMEC	breast
14	chr1:153055200-153068400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr1:153059800-153060600	Enhancers	K562	blood
16	chr1:153060600-153068200	Weak transcription	K562	blood
17	chr1:153067000-153067400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:153067000-153067400	Enhancers	NHEK	skin
19	chr1:153067200-153067400	Enhancers	Hela-S3	cervix
20	chr1:153067400-153067600	Enhancers	Esophagus	oesophagus
21	chr1:153067400-153068400	Weak transcription	Hela-S3	cervix
22	chr1:153067400-153070200	Weak transcription	NHEK	skin
23	chr1:153067400-153072000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr1:153068200-153069600	Enhancers	K562	blood
25	chr1:153068400-153069200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr1:153068400-153069200	Enhancers	Hela-S3	cervix
27	chr1:153069200-153070200	Weak transcription	Hela-S3	cervix
28	chr1:153070200-153072200	Enhancers	NHEK	skin
29	chr1:153070200-153073600	Enhancers	Hela-S3	cervix
30	chr1:153070400-153070600	Enhancers	HMEC	breast
31	chr1:153070800-153072000	Weak transcription	HMEC	breast
32	chr1:153072000-153072600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:153072000-153072600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:153072000-153072800	Enhancers	HMEC	breast
35	chr1:153072200-153072600	Flanking Active TSS	NHEK	skin
36	chr1:153072600-153073400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr1:153072600-153073800	Enhancers	NHEK	skin
38	chr1:153072600-153077600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr1:153072800-153073400	Weak transcription	HMEC	breast
40	chr1:153073400-153073600	Enhancers	HMEC	breast
41	chr1:153073400-153073800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr1:153075400-153075600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr1:153075600-153075800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr1:153075800-153076000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr1:153077600-153079200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:153079200-153080200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:153085000-153086400	Enhancers	Ovary	ovary
48	chr1:153086000-153086200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr1:153086000-153086400	Enhancers	K562	blood
50	chr1:153086400-153087400	Weak transcription	K562	blood

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