Variant report

Variant	nsv68
Chromosome Location	chr1:152549956-152608472
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	chr1:152549641-152550036	GM12878	blood:	n/a	n/a
2	BACH1	chr1:152555244-152555264	K562	blood:	n/a	chr1:152555246-152555260
3	BATF	chr1:152549573-152550008	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:152595213-152595387	GM12878	blood:	n/a	n/a
5	CEBPB	chr1:152569565-152569765	HepG2	liver:	n/a	n/a
6	CTCF	chr1:152595811-152595936	GM20000	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
7	CTCF	chr1:152595820-152595970	WERI-Rb-1	eye:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
8	CTCF	chr1:152595840-152595980	H1-hESC	embryonic stem cell:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
9	CTCF	chr1:152595765-152596032	K562	blood:	n/a	chr1:152595771-152595784 chr1:152595886-152595904 chr1:152595881-152595902
10	CTCF	chr1:152595813-152595985	LNCaP	prostate:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
11	CTCF	chr1:152557900-152558050	GM12873	blood:	n/a	n/a
12	CTCF	chr1:152595800-152595950	HUVEC	blood vessel:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
13	CTCF	chr1:152558160-152558310	NB4	blood:	n/a	n/a
14	CTCF	chr1:152595800-152595950	A549	lung:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
15	CTCF	chr1:152558160-152558310	GM12874	blood:	n/a	n/a
16	CTCF	chr1:152595800-152595950	Hela-S3	cervix:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
17	CTCF	chr1:152558200-152558350	HRE	kidney:	n/a	n/a
18	CTCF	chr1:152595711-152596073	GM12878	blood:	n/a	chr1:152595771-152595784 chr1:152595886-152595904 chr1:152595881-152595902
19	CTCF	chr1:152558138-152558312	Gliobla	brain:	n/a	n/a
20	CTCF	chr1:152558140-152558290	HMEC	breast:	n/a	n/a
21	CTCF	chr1:152558166-152558276	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr1:152558240-152558390	HCT-116	colon:	n/a	n/a
23	CTCF	chr1:152595505-152596187	A549	lung:	n/a	chr1:152595771-152595784 chr1:152595886-152595904 chr1:152595881-152595902
24	CTCF	chr1:152595860-152596010	RPTEC	kidney:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
25	CTCF	chr1:152595860-152596010	GM12870	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
26	CTCF	chr1:152595792-152596026	Fibrobl	skin:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
27	CTCF	chr1:152595800-152595950	WERI-Rb-1	eye:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
28	CTCF	chr1:152595780-152595930	GM12867	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
29	CTCF	chr1:152595760-152595910	BJ	skin:	n/a	chr1:152595771-152595784 chr1:152595886-152595904 chr1:152595881-152595902
30	CTCF	chr1:152557580-152557730	GM12872	blood:	n/a	n/a
31	CTCF	chr1:152558160-152558310	Caco-2	colon:	n/a	n/a
32	CTCF	chr1:152595840-152595990	GM12869	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
33	CTCF	chr1:152558060-152558210	BE2_C	brain:	n/a	n/a
34	CTCF	chr1:152595700-152595850	AG09309	skin:	n/a	chr1:152595771-152595784
35	CTCF	chr1:152552840-152552990	HMEC	breast:	n/a	chr1:152552927-152552936 chr1:152552921-152552939
36	CTCF	chr1:152595740-152595890	HRE	kidney:	n/a	chr1:152595771-152595784
37	CTCF	chr1:152558166-152558316	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr1:152595820-152595970	GM12868	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
39	CTCF	chr1:152595920-152596070	BE2_C	brain:	n/a	n/a
40	CTCF	chr1:152595880-152596030	GM06990	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
41	CTCF	chr1:152595840-152595990	GM12864	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
42	CTCF	chr1:152558187-152558309	GM10266	blood:	n/a	n/a
43	CTCF	chr1:152558100-152558250	GM12864	blood:	n/a	n/a
44	CTCF	chr1:152595820-152595970	GM12866	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
45	CTCF	chr1:152595780-152595930	A549	lung:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
46	CTCF	chr1:152595812-152595995	MCF-7	breast:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
47	CTCF	chr1:152595796-152595995	NHEK	skin:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
48	CTCF	chr1:152595880-152596030	GM12872	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
49	CTCF	chr1:152595835-152595973	GM13976	blood:	n/a	chr1:152595886-152595904 chr1:152595881-152595902
50	CTCF	chr1:152595738-152596000	HepG2	liver:	n/a	chr1:152595771-152595784 chr1:152595886-152595904 chr1:152595881-152595902

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152596413-152596463	HepG2	liver:	n/a
2	chr1:152596413-152596463	HepG2	liver:	n/a
3	chr1:152596413-152596463	GM12878	blood:	n/a
4	chr1:152595842-152595892	HCT-116	colon:	n/a
5	chr1:152552494-152552544	A549	lung:	n/a
6	chr1:152595982-152596032	HMEC	breast:	n/a
7	chr1:152553096-152553146	AoSMC	blood vessel:	n/a
8	chr1:152596177-152596227	HUVEC	blood vessel:	n/a
9	chr1:152595322-152595372	HL-60	blood:	n/a
10	chr1:152595982-152596032	HUVEC	blood vessel:	n/a
11	chr1:152595351-152595401	SKMC	muscle:	n/a
12	chr1:152553244-152553294	AG09309	skin:	n/a
13	chr1:152596177-152596227	Hepatocyte	liver:	n/a
14	chr1:152595992-152596042	GM12878	blood:	n/a
15	chr1:152595351-152595401	AG04449	skin:	fetal
16	chr1:152595322-152595372	GM19239	blood:	n/a
17	chr1:152595351-152595401	NT2-D1	testis:	n/a
18	chr1:152595992-152596042	NB4	blood:	n/a
19	chr1:152595882-152595932	MCF10A-Er-Src	breast:	n/a
20	chr1:152595882-152595932	NB4	blood:	n/a
21	chr1:152595842-152595892	NHBE	bronchial:	n/a
22	chr1:152595322-152595372	HAEpiC	amniotic membrane:	n/a
23	chr1:152595351-152595401	A549	lung:	n/a
24	chr1:152595322-152595372	SAEC	small airway:	n/a
25	chr1:152595982-152596032	HEEpiC	esophagus:	n/a
26	chr1:152595322-152595372	SKMC	muscle:	n/a
27	chr1:152595351-152595401	NHDF-neo	bronchial:	n/a
28	chr1:152553244-152553294	AoSMC	blood vessel:	n/a
29	chr1:152552494-152552544	GM12892	blood:	n/a
30	chr1:152596177-152596227	HCPEpiC	choroid plexus:	n/a
31	chr1:152595322-152595372	K562	blood:	n/a
32	chr1:152553244-152553294	A549	lung:	n/a
33	chr1:152595982-152596032	GM12892	blood:	n/a
34	chr1:152553096-152553146	T-47D	breast:	n/a
35	chr1:152596413-152596463	HAEpiC	amniotic membrane:	n/a
36	chr1:152595992-152596042	GM12891	blood:	n/a
37	chr1:152595982-152596032	PrEC	prostate:	n/a
38	chr1:152595842-152595892	HRE	kidney:	n/a
39	chr1:152553096-152553146	LNCaP	prostate:	n/a
40	chr1:152553244-152553294	AG09319	gingival:	n/a
41	chr1:152552494-152552544	SAEC	small airway:	n/a
42	chr1:152552494-152552544	HRCEpiC	kidney:	n/a
43	chr1:152595982-152596032	AG09319	gingival:	n/a
44	chr1:152595992-152596042	GM06990	blood:	n/a
45	chr1:152552494-152552544	NHBE	bronchial:	n/a
46	chr1:152595842-152595892	GM12892	blood:	n/a
47	chr1:152596177-152596227	T-47D	breast:	n/a
48	chr1:152595982-152596032	NB4	blood:	n/a
49	chr1:152552175-152552225	HRE	kidney:	n/a
50	chr1:152595982-152596032	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:152550535..152553138-chr1:152591146..152593497,2	K562	blood:
2	chr1:152580545..152582523-chr1:152584809..152586590,2	K562	blood:

Variant related genes	Relation type
LCE3C	TF binding region
LCE3A	TF binding region
LCE3B	TF binding region
LCE3D	TF binding region
LCE3C	CpG island
LCE3A	CpG island
LCE3B	CpG island
LCE3D	CpG island
ENSG00000163202	chromatin interactions
ENSG00000187238	chromatin interactions

Extended variants
information (count: 807 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376132932	chr1:152549988-152549989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4085613	chr1:152550018-152550019	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
3	rs548808858	chr1:152550020-152550021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs56038709	chr1:152550103-152550104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs370857676	chr1:152550120-152550121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182756924	chr1:152550131-152550132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs534506208	chr1:152550140-152550141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186662580	chr1:152550174-152550175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs202121532	chr1:152550175-152550176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs11333062	chr1:152550178-152550179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192354860	chr1:152550240-152550241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79566054	chr1:152550300-152550301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543671039	chr1:152550344-152550345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557032421	chr1:152550377-152550378	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75503085	chr1:152550415-152550416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185494292	chr1:152550423-152550424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559482942	chr1:152550436-152550437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144719492	chr1:152550446-152550447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541268620	chr1:152550458-152550459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs7414804	chr1:152550468-152550469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147884930	chr1:152550470-152550471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs59861223	chr1:152550559-152550560	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs140436664	chr1:152550616-152550617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190571123	chr1:152550667-152550668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569742383	chr1:152550687-152550688	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532366853	chr1:152550736-152550737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs150392918	chr1:152550744-152550745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs373804312	chr1:152550768-152550769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565842241	chr1:152550796-152550797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535067915	chr1:152550816-152550817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377577401	chr1:152550823-152550824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534745778	chr1:152550826-152550827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568232185	chr1:152550842-152550843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369857105	chr1:152550913-152550914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs61813876	chr1:152550950-152550951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs536975816	chr1:152550957-152550958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138656560	chr1:152551085-152551086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78913685	chr1:152551116-152551117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573055959	chr1:152551117-152551118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs397977557	chr1:152551128-152551129	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117265068	chr1:152551129-152551130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576954951	chr1:152551153-152551154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536976004	chr1:152551183-152551184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148890332	chr1:152551237-152551238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs4112788	chr1:152551276-152551277	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
46	rs571515447	chr1:152551308-152551309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs114593512	chr1:152551310-152551311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4112787	chr1:152551325-152551326	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs561356142	chr1:152551364-152551365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193085846	chr1:152551420-152551421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152543000-152552600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr1:152547000-152552400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr1:152549400-152550800	Enhancers	Muscle Satellite Cultured Cells	--
4	chr1:152549400-152551400	Enhancers	HSMMtube	muscle
5	chr1:152549400-152551600	Enhancers	HSMM	muscle
6	chr1:152549800-152551400	Weak transcription	GM12878-XiMat	blood
7	chr1:152550800-152555200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr1:152551400-152552600	Enhancers	GM12878-XiMat	blood
9	chr1:152551600-152552800	Weak transcription	HSMM	muscle
10	chr1:152552400-152553200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr1:152552400-152553400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:152552600-152553200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:152552600-152553200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:152552600-152553400	Enhancers	HMEC	breast
15	chr1:152552800-152553200	Enhancers	HSMM	muscle
16	chr1:152552800-152553400	Enhancers	NHEK	skin
17	chr1:152553400-152555000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:152553400-152555000	Weak transcription	HMEC	breast
19	chr1:152553400-152555200	Weak transcription	NHEK	skin
20	chr1:152555000-152555600	Flanking Active TSS	A549	lung
21	chr1:152555000-152555600	Enhancers	HMEC	breast
22	chr1:152555000-152555800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:152555200-152555600	Enhancers	NHEK	skin
24	chr1:152555400-152555600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr1:152555400-152555800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr1:152569600-152570200	Enhancers	Liver	Liver
27	chr1:152591000-152592600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:152591000-152592600	ZNF genes & repeats	Adipose Nuclei	Adipose
29	chr1:152592600-152594600	Weak transcription	Adipose Nuclei	Adipose
30	chr1:152592600-152595200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:152594400-152595000	Enhancers	HSMM	muscle
32	chr1:152594600-152595400	Enhancers	Adipose Nuclei	Adipose
33	chr1:152594600-152595600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr1:152594600-152596200	Enhancers	Ovary	ovary
35	chr1:152594800-152595600	Enhancers	Muscle Satellite Cultured Cells	--
36	chr1:152595000-152596400	Enhancers	Liver	Liver
37	chr1:152595000-152596400	Flanking Active TSS	HSMM	muscle
38	chr1:152595000-152596400	Enhancers	HSMMtube	muscle
39	chr1:152595200-152596000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr1:152595200-152596600	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr1:152595400-152595600	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr1:152595400-152596000	Enhancers	Thymus	Thymus
43	chr1:152595600-152595800	Enhancers	Adipose Nuclei	Adipose
44	chr1:152595600-152596000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:152595600-152596000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr1:152595600-152596200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr1:152595600-152596200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr1:152595600-152596200	Active TSS	Brain Anterior Caudate	brain
49	chr1:152595600-152596200	Enhancers	Esophagus	oesophagus
50	chr1:152595600-152596400	Enhancers	Primary monocytes fromperipheralblood	blood

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