Variant report

Variant	nsv1010895
Chromosome Location	chr1:152744949-152776743
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:1100)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr1:152751552-152751774	HepG2	liver:	n/a	chr1:152751690-152751701
2	CEBPB	chr1:152752164-152752209	K562	blood:	n/a	chr1:152752194-152752205
3	CEBPB	chr1:152752036-152752272	HepG2	liver:	n/a	chr1:152752194-152752205
4	CTCF	chr1:152750013-152750371	K562	blood:	n/a	n/a
5	CTCF	chr1:152750120-152750270	HL-60	blood:	n/a	n/a
6	CTCF	chr1:152750140-152750290	HA-sp	spinal cord:	n/a	n/a
7	CTCF	chr1:152750140-152750290	Hela-S3	cervix:	n/a	n/a
8	CTCF	chr1:152750120-152750270	HPF	lung:	n/a	n/a
9	CTCF	chr1:152750080-152750230	GM12865	blood:	n/a	n/a
10	CTCF	chr1:152750160-152750310	GM06990	blood:	n/a	n/a
11	CTCF	chr1:152747500-152747650	Caco-2	colon:	n/a	chr1:152747561-152747574
12	CTCF	chr1:152750160-152750310	GM12869	blood:	n/a	n/a
13	CTCF	chr1:152750140-152750290	GM12871	blood:	n/a	n/a
14	CTCF	chr1:152747452-152747633	MCF-7	breast:	n/a	chr1:152747561-152747574
15	CTCF	chr1:152750112-152750116	GM19240	blood:	n/a	n/a
16	CTCF	chr1:152747520-152747670	GM12873	blood:	n/a	chr1:152747561-152747574
17	CTCF	chr1:152750140-152750290	GM12872	blood:	n/a	n/a
18	CTCF	chr1:152750140-152750290	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr1:152747431-152747678	MCF-7	breast:	n/a	chr1:152747561-152747574
20	CTCF	chr1:152750126-152750327	A549	lung:	n/a	n/a
21	CTCF	chr1:152750100-152750250	GM12871	blood:	n/a	n/a
22	CTCF	chr1:152747500-152747650	HCT-116	colon:	n/a	chr1:152747561-152747574
23	CTCF	chr1:152750160-152750310	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr1:152747460-152747610	WERI-Rb-1	eye:	n/a	chr1:152747561-152747574
25	CTCF	chr1:152747440-152747590	GM12874	blood:	n/a	chr1:152747561-152747574
26	CTCF	chr1:152750156-152750286	GM12891	blood:	n/a	n/a
27	CTCF	chr1:152747480-152747630	GM12869	blood:	n/a	chr1:152747561-152747574
28	CTCF	chr1:152750119-152750279	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr1:152750160-152750310	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr1:152750140-152750290	GM12873	blood:	n/a	n/a
31	CTCF	chr1:152750094-152750339	Gliobla	brain:	n/a	n/a
32	CTCF	chr1:152747480-152747630	NHEK	skin:	n/a	chr1:152747561-152747574
33	CTCF	chr1:152750158-152750299	MCF-7	breast:	n/a	n/a
34	CTCF	chr1:152750620-152750770	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr1:152750160-152750310	GM12875	blood:	n/a	n/a
36	CTCF	chr1:152747482-152747647	Fibrobl	skin:	n/a	chr1:152747561-152747574
37	CTCF	chr1:152747453-152747635	MCF-7	breast:	n/a	chr1:152747561-152747574
38	CTCF	chr1:152750022-152750441	MCF-7	breast:	n/a	n/a
39	CTCF	chr1:152750040-152750190	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr1:152750120-152750270	HEK293	kidney:	n/a	n/a
41	CTCF	chr1:152750093-152750348	K562	blood:	n/a	n/a
42	CTCF	chr1:152750140-152750290	BE2_C	brain:	n/a	n/a
43	CTCF	chr1:152750314-152750315	GM10248	blood:	n/a	n/a
44	CTCF	chr1:152750100-152750250	NHEK	skin:	n/a	n/a
45	CTCF	chr1:152750118-152750351	GM19240	blood:	n/a	n/a
46	CTCF	chr1:152772992-152773083	GM10266	blood:	n/a	n/a
47	CTCF	chr1:152750160-152750310	GM12878	blood:	n/a	n/a
48	CTCF	chr1:152747520-152747670	HEEpiC	esophagus:	n/a	chr1:152747561-152747574
49	CTCF	chr1:152750039-152750405	HepG2	liver:	n/a	n/a
50	CTCF	chr1:152750042-152750363	IMR90	lung:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152768267-152768317	GM12878	blood:	n/a
2	chr1:152768476-152768526	NHBE	bronchial:	n/a
3	chr1:152768267-152768317	GM12878	blood:	n/a
4	chr1:152768476-152768526	NHBE	bronchial:	n/a
5	chr1:152769896-152769946	SKMC	muscle:	n/a
6	chr1:152757464-152757514	Hela-S3	cervix:	n/a
7	chr1:152770520-152770570	HNPCEpiC	eye:	n/a
8	chr1:152748838-152748888	PANC-1	pancreas:	n/a
9	chr1:152748838-152748888	NB4	blood:	n/a
10	chr1:152760341-152760391	Hela-S3	cervix:	n/a
11	chr1:152769896-152769946	T-47D	breast:	n/a
12	chr1:152770502-152770552	ECC-1	luminal epithelium:	n/a
13	chr1:152770520-152770570	H1-hESC	embryonic stem cell:	embryo
14	chr1:152757464-152757514	GM19239	blood:	n/a
15	chr1:152747562-152747612	AG04450	lung:	fetal
16	chr1:152759772-152759822	LNCaP	prostate:	n/a
17	chr1:152770502-152770552	SKMC	muscle:	n/a
18	chr1:152768476-152768526	ECC-1	luminal epithelium:	n/a
19	chr1:152757464-152757514	HCPEpiC	choroid plexus:	n/a
20	chr1:152760341-152760391	NH-A	brain:	n/a
21	chr1:152769896-152769946	AG04449	skin:	fetal
22	chr1:152757464-152757514	RPTEC	kidney:	n/a
23	chr1:152757464-152757514	AG09319	gingival:	n/a
24	chr1:152758632-152758682	AG10803	skin:	n/a
25	chr1:152768267-152768317	H1-hESC	embryonic stem cell:	embryo
26	chr1:152768727-152768777	GM12878	blood:	n/a
27	chr1:152749106-152749156	PrEC	prostate:	n/a
28	chr1:152769896-152769946	K562	blood:	n/a
29	chr1:152747562-152747612	HCT-116	colon:	n/a
30	chr1:152758453-152758503	HAEpiC	amniotic membrane:	n/a
31	chr1:152770520-152770570	Hela-S3	cervix:	n/a
32	chr1:152749106-152749156	T-47D	breast:	n/a
33	chr1:152768267-152768317	IMR90	lung:	fetal
34	chr1:152768267-152768317	K562	blood:	n/a
35	chr1:152759772-152759822	HRE	kidney:	n/a
36	chr1:152770502-152770552	HL-60	blood:	n/a
37	chr1:152768727-152768777	MCF10A-Er-Src	breast:	n/a
38	chr1:152758632-152758682	H1-hESC	embryonic stem cell:	embryo
39	chr1:152768727-152768777	SK-N-SH_RA	brain:	n/a
40	chr1:152759772-152759822	HCT-116	colon:	n/a
41	chr1:152768727-152768777	AG09309	skin:	n/a
42	chr1:152747501-152747551	NB4	blood:	n/a
43	chr1:152747472-152747522	NB4	blood:	n/a
44	chr1:152759772-152759822	HMEC	breast:	n/a
45	chr1:152757464-152757514	ovcar-3	ovarian:	n/a
46	chr1:152760341-152760391	HMEC	breast:	n/a
47	chr1:152770502-152770552	AG10803	skin:	n/a
48	chr1:152768476-152768526	HRCEpiC	kidney:	n/a
49	chr1:152769896-152769946	MCF10A-Er-Src	breast:	n/a
50	chr1:152768267-152768317	NHDF-neo	bronchial:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:152633504..152636346-chr1:152743964..152745780,2	K562	blood:
2	chr1:152745990..152747904-chr1:152750482..152752734,2	MCF-7	breast:
3	chr1:152769863..152772434-chr1:152783643..152785689,2	MCF-7	breast:
4	chr1:152775301..152777562-chr1:152781297..152783006,2	K562	blood:
5	chr1:152758579..152760547-chr1:152770579..152772468,2	MCF-7	breast:
6	chr1:152715187..152719235-chr1:152774123..152777725,4	MCF-7	breast:
7	chr1:152626437..152627174-chr1:152749824..152750672,3	MCF-7	breast:
8	chr1:152745990..152747904-chr1:152750482..152752734,2	MCF-7	breast:

No data

Variant related genes	Relation type
LCE1F	TF binding region
LCE1E	TF binding region
LCE1D	TF binding region
LCE1F	CpG island
LCE1E	CpG island
LCE1D	CpG island
ENSG00000187223	chromatin interactions
ENSG00000196734	chromatin interactions
ENSG00000186226	chromatin interactions
ENSG00000233819	chromatin interactions

Extended variants
information (count: 945 )
Associated
traits (count: 122 )

Variant overlapped rSNPs/rCNVs (count:945 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527822558	chr1:152744960-152744961	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs189194000	chr1:152744991-152744992	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs79682040	chr1:152744994-152744995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181905418	chr1:152745003-152745004	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185686433	chr1:152745013-152745014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs569486985	chr1:152745016-152745017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs192081441	chr1:152745032-152745033	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149943213	chr1:152745051-152745052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs182917483	chr1:152745063-152745064	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558968232	chr1:152745076-152745077	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs144995212	chr1:152745090-152745091	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554529952	chr1:152745153-152745154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568000521	chr1:152745228-152745229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371305239	chr1:152745281-152745282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs536921459	chr1:152745282-152745283	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375751097	chr1:152745284-152745285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556897901	chr1:152745298-152745299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576666154	chr1:152745308-152745309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs545605538	chr1:152745309-152745310	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559241314	chr1:152745323-152745324	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373608823	chr1:152745335-152745336	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs61273768	chr1:152745398-152745399	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs541199995	chr1:152745400-152745401	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs186674257	chr1:152745429-152745430	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs144675576	chr1:152745454-152745455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530063677	chr1:152745478-152745479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543267249	chr1:152745490-152745491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs563251711	chr1:152745512-152745513	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372103324	chr1:152745533-152745534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs532313784	chr1:152745537-152745538	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs551953338	chr1:152745550-152745551	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374289361	chr1:152745570-152745571	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs368457917	chr1:152745586-152745587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs371960745	chr1:152745643-152745644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191270486	chr1:152745648-152745649	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs547998353	chr1:152745671-152745672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146686140	chr1:152745684-152745685	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs143284883	chr1:152745715-152745716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
39	rs182145506	chr1:152745721-152745722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs570360225	chr1:152745741-152745742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539369042	chr1:152745764-152745765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs559178210	chr1:152745779-152745780	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs572566760	chr1:152745795-152745796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369215534	chr1:152745799-152745800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs371853600	chr1:152745824-152745825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541488577	chr1:152745834-152745835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11205101	chr1:152745858-152745859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369929328	chr1:152745860-152745861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574735079	chr1:152745874-152745875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189834491	chr1:152745893-152745894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:122)

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
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152743000-152747200	Weak transcription	NHEK	skin
2	chr1:152743400-152747000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:152746600-152747000	Weak transcription	HMEC	breast
4	chr1:152747000-152747800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:152747200-152747600	Enhancers	NHEK	skin
6	chr1:152747200-152747800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:152747200-152747800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:152747200-152747800	Enhancers	HMEC	breast
9	chr1:152747800-152755400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:152754000-152754200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr1:152754000-152754200	Enhancers	NHDF-Ad	bronchial
12	chr1:152754200-152755400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:152754200-152755400	Weak transcription	NHDF-Ad	bronchial
14	chr1:152754200-152756000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:152755400-152755800	Enhancers	NHDF-Ad	bronchial
16	chr1:152755400-152755800	Enhancers	NHEK	skin
17	chr1:152755400-152756000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:152755400-152756000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr1:152755400-152756000	Enhancers	HMEC	breast
20	chr1:152755400-152756000	Enhancers	NHLF	lung
21	chr1:152755600-152755800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:152755800-152758200	Weak transcription	NHEK	skin
23	chr1:152755800-152758400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr1:152756000-152758200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:152756000-152758200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:152756000-152758200	Weak transcription	HMEC	breast
27	chr1:152757200-152757400	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr1:152757400-152758400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr1:152758200-152758400	Enhancers	HMEC	breast
30	chr1:152758200-152758600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:152758200-152758600	Enhancers	Fetal Stomach	stomach
32	chr1:152758200-152758800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr1:152758200-152758800	Enhancers	Ovary	ovary
34	chr1:152758200-152759000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr1:152758200-152759200	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr1:152758200-152759200	Enhancers	NHEK	skin
37	chr1:152758400-152758600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:152758400-152758800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr1:152758400-152759400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr1:152758400-152759400	Flanking Active TSS	HMEC	breast
41	chr1:152758600-152758800	Bivalent Enhancer	Lung	lung
42	chr1:152758600-152759000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr1:152758600-152759200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr1:152758800-152759200	Enhancers	HepG2	liver
45	chr1:152759000-152759400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr1:152759000-152759400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:152759200-152759800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr1:152759400-152759800	Enhancers	HMEC	breast
49	chr1:152765600-152765800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr1:152765800-152766000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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