Variant report

Variant	nsv872718
Chromosome Location	chr1:189589339-189731048
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	chr1:189655218-189655237	K562	blood:	n/a	n/a
2	ATF1	chr1:189645110-189645131	K562	blood:	n/a	n/a
3	ATF1	chr1:189692607-189692756	K562	blood:	n/a	n/a
4	ATF3	chr1:189624065-189624449	HCT-116	colon:	n/a	n/a
5	BACH1	chr1:189660033-189660067	K562	blood:	n/a	n/a
6	BCL3	chr1:189650561-189651101	A549	lung:	n/a	n/a
7	BRCA1	chr1:189640354-189640407	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr1:189627431-189627982	HCT-116	colon:	n/a	n/a
9	CBX3	chr1:189588763-189589390	HCT-116	colon:	n/a	n/a
10	CBX3	chr1:189626762-189627309	HCT-116	colon:	n/a	n/a
11	CBX3	chr1:189588801-189589528	HCT-116	colon:	n/a	n/a
12	CBX3	chr1:189631264-189631803	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:189631288-189631734	HCT-116	colon:	n/a	n/a
14	CEBPB	chr1:189606179-189606483	IMR90	lung:	n/a	chr1:189606323-189606334
15	CEBPB	chr1:189624017-189624416	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
16	CEBPB	chr1:189624089-189624306	MCF-7	breast:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
17	CEBPB	chr1:189718442-189718647	HepG2	liver:	n/a	chr1:189718486-189718497
18	CEBPB	chr1:189650548-189650953	A549	lung:	n/a	n/a
19	CEBPB	chr1:189624086-189624348	ECC-1	luminal epithelium:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
20	CEBPB	chr1:189624035-189624369	K562	blood:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
21	CEBPB	chr1:189606177-189606515	Hela-S3	cervix:	n/a	chr1:189606323-189606334
22	CEBPB	chr1:189624011-189624388	Hela-S3	cervix:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
23	CEBPB	chr1:189623883-189624474	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
24	CEBPB	chr1:189626976-189627210	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:189689001-189689131	IMR90	lung:	n/a	n/a
26	CEBPB	chr1:189718405-189718652	A549	lung:	n/a	chr1:189718486-189718497
27	CEBPB	chr1:189606174-189606516	A549	lung:	n/a	chr1:189606323-189606334
28	CEBPB	chr1:189626895-189627312	Hela-S3	cervix:	n/a	chr1:189627200-189627217
29	CEBPB	chr1:189623967-189624524	HCT-116	colon:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
30	CEBPB	chr1:189624041-189624385	HepG2	liver:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
31	CEBPB	chr1:189626911-189627214	MCF-7	breast:	n/a	n/a
32	CEBPB	chr1:189592550-189592866	A549	lung:	n/a	chr1:189592697-189592708
33	CEBPB	chr1:189675218-189675345	A549	lung:	n/a	chr1:189675255-189675266
34	CEBPB	chr1:189624021-189624372	A549	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
35	CEBPB	chr1:189651781-189651981	A549	lung:	n/a	n/a
36	CEBPB	chr1:189672613-189673256	IMR90	lung:	n/a	n/a
37	CEBPB	chr1:189623953-189624457	MCF-7	breast:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
38	CEBPB	chr1:189626830-189627327	MCF-7	breast:	n/a	chr1:189627200-189627217
39	CEBPB	chr1:189688107-189688436	HepG2	liver:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
40	CEBPB	chr1:189606191-189606464	HepG2	liver:	n/a	chr1:189606323-189606334
41	CEBPB	chr1:189675215-189675438	HepG2	liver:	n/a	chr1:189675255-189675266
42	CEBPB	chr1:189626898-189627277	HepG2	liver:	n/a	chr1:189627200-189627217
43	CEBPB	chr1:189631210-189631769	HCT-116	colon:	n/a	n/a
44	CEBPB	chr1:189604468-189604766	A549	lung:	n/a	n/a
45	CEBPB	chr1:189688098-189688417	A549	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
46	CEBPB	chr1:189624014-189624396	IMR90	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
47	CEBPB	chr1:189606035-189606521	A549	lung:	n/a	chr1:189606323-189606334
48	CEBPB	chr1:189626703-189627383	HCT-116	colon:	n/a	chr1:189627200-189627217
49	CEBPB	chr1:189592545-189592812	HepG2	liver:	n/a	chr1:189592697-189592708
50	CEBPB	chr1:189604520-189604793	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189722103-189722153	BJ	skin:	n/a
2	chr1:189722103-189722153	ECC-1	luminal epithelium:	n/a
3	chr1:189722103-189722153	GM12878	blood:	n/a
4	chr1:189722103-189722153	GM19239	blood:	n/a
5	chr1:189722103-189722153	NHDF-neo	bronchial:	n/a
6	chr1:189722103-189722153	LNCaP	prostate:	n/a
7	chr1:189722103-189722153	HRE	kidney:	n/a
8	chr1:189722103-189722153	MCF-7	breast:	n/a
9	chr1:189722103-189722153	K562	blood:	n/a
10	chr1:189722103-189722153	AG09309	skin:	n/a
11	chr1:189722103-189722153	HEK293	kidney:	embryo
12	chr1:189722103-189722153	GM06990	blood:	n/a
13	chr1:189722103-189722153	SKMC	muscle:	n/a
14	chr1:189722103-189722153	HRCEpiC	kidney:	n/a
15	chr1:189722103-189722153	H1-hESC	embryonic stem cell:	embryo
16	chr1:189722103-189722153	HPAEpiC	pulmonary alveolar:	n/a
17	chr1:189722103-189722153	AG04450	lung:	fetal
18	chr1:189722103-189722153	HAEpiC	amniotic membrane:	n/a
19	chr1:189722103-189722153	SAEC	small airway:	n/a
20	chr1:189722103-189722153	MCF10A-Er-Src	breast:	n/a
21	chr1:189722103-189722153	GM12891	blood:	n/a
22	chr1:189722103-189722153	IMR90	lung:	fetal
23	chr1:189722103-189722153	Jurkat	blood:	n/a
24	chr1:189722103-189722153	Hela-S3	cervix:	n/a
25	chr1:189722103-189722153	PrEC	prostate:	n/a
26	chr1:189722103-189722153	HMEC	breast:	n/a
27	chr1:189722103-189722153	ProgFib	skin:	n/a
28	chr1:189722103-189722153	AG09319	gingival:	n/a
29	chr1:189722103-189722153	PFSK-1	brain:	n/a
30	chr1:189722103-189722153	NH-A	brain:	n/a
31	chr1:189722103-189722153	HL-60	blood:	n/a
32	chr1:189722103-189722153	NHBE	bronchial:	n/a
33	chr1:189722103-189722153	HEEpiC	esophagus:	n/a
34	chr1:189722103-189722153	HCM	heart:	n/a
35	chr1:189722103-189722153	T-47D	breast:	n/a
36	chr1:189722103-189722153	PANC-1	pancreas:	n/a
37	chr1:189722103-189722153	HRPEpiC	eye:	n/a
38	chr1:189722103-189722153	CMK	blood:	n/a
39	chr1:189722103-189722153	HepG2	liver:	n/a
40	chr1:189722103-189722153	RPTEC	kidney:	n/a
41	chr1:189722103-189722153	A549	lung:	n/a
42	chr1:189722103-189722153	NT2-D1	testis:	n/a
43	chr1:189722103-189722153	Hepatocyte	liver:	n/a
44	chr1:189722103-189722153	BE2_C	brain:	n/a
45	chr1:189722103-189722153	HNPCEpiC	eye:	n/a
46	chr1:189722103-189722153	U87	brain:	n/a
47	chr1:189722103-189722153	SK-N-SH_RA	brain:	n/a
48	chr1:189722103-189722153	HCPEpiC	choroid plexus:	n/a
49	chr1:189722103-189722153	SK-N-SH	brain:	n/a
50	chr1:189722103-189722153	HIPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
2	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
3	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
4	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
5	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
6	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
7	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
8	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
9	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
10	chr1:189589226..189590045-chr1:189662088..189662866,2	MCF-7	breast:
11	chr1:189677502..189678569-chr1:190053452..190054228,3	MCF-7	breast:
12	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
13	chr1:189589226..189590045-chr1:189662088..189662866,2	MCF-7	breast:
14	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
15	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
16	chr1:189646033..189647879-chr5:175874488..175876371,2	MCF-7	breast:
17	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
18	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
19	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
20	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
21	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
22	chr1:189398408..189399387-chr1:189661985..189662829,2	MCF-7	breast:
23	chr1:189677420..189678491-chr1:190289916..190290952,3	MCF-7	breast:
24	chr1:189630297..189631878-chr1:189633078..189635794,2	K562	blood:
25	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
26	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
27	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
28	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
29	chr1:189398509..189399144-chr1:189660311..189661261,2	MCF-7	breast:
30	chr1:189398440..189399083-chr1:189642226..189643036,4	MCF-7	breast:

Variant related genes	Relation type
RNA5SP73	TF binding region
RNA5SP73	CpG island
ENSG00000113194	chromatin interactions
ENSG00000252553	chromatin interactions

Extended variants
information (count: 1660 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10489759	chr1:189589339-189589340	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
2	rs539895528	chr1:189589370-189589371	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs80295109	chr1:189589407-189589408	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs2038651	chr1:189589427-189589428	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538164383	chr1:189589429-189589430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148697679	chr1:189589433-189589434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554598340	chr1:189589440-189589441	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs16829235	chr1:189589442-189589443	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533588103	chr1:189589450-189589451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16829236	chr1:189589468-189589469	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs184786768	chr1:189589512-189589513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113379736	chr1:189589555-189589556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs111987603	chr1:189589568-189589569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs16830968	chr1:189589570-189589571	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs10489758	chr1:189589594-189589595	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs113385776	chr1:189589597-189589598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116620886	chr1:189589607-189589608	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs563505177	chr1:189589626-189589627	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73049572	chr1:189589634-189589635	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs527988824	chr1:189589639-189589640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189281656	chr1:189589712-189589713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571566492	chr1:189589728-189589729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs2839903	chr1:189589737-189589738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs564432853	chr1:189589739-189589740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs116480524	chr1:189589762-189589763	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549981242	chr1:189589801-189589802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570114163	chr1:189589804-189589805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375611556	chr1:189589851-189589852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538831431	chr1:189589853-189589854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531442103	chr1:189589866-189589867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147557965	chr1:189589886-189589887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115815407	chr1:189589891-189589892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533793747	chr1:189589892-189589893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547656313	chr1:189589908-189589909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570085980	chr1:189589914-189589915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565766914	chr1:189589955-189589956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539023707	chr1:189589979-189589980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35560002	chr1:189590000-189590001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs16830972	chr1:189590026-189590027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs576078599	chr1:189590037-189590038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542106191	chr1:189590039-189590040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs80009255	chr1:189590045-189590046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs140345214	chr1:189590067-189590068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs148645270	chr1:189590129-189590130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541714912	chr1:189590178-189590179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs180903426	chr1:189590179-189590180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72735896	chr1:189590210-189590211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186495069	chr1:189590224-189590225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543786733	chr1:189590252-189590253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563676029	chr1:189590308-189590309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
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
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	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
Trisomy 5 syndrome	21098271	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	17086460	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189588600-189589600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr1:189588600-189589600	Enhancers	HUVEC	blood vessel
3	chr1:189588600-189589800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:189588800-189589400	Enhancers	NHEK	skin
5	chr1:189588800-189589800	Enhancers	HMEC	breast
6	chr1:189589000-189589400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr1:189589000-189589400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr1:189589000-189589400	Flanking Active TSS	A549	lung
9	chr1:189589000-189589400	Enhancers	Hela-S3	cervix
10	chr1:189589000-189589400	Enhancers	NH-A	brain
11	chr1:189589000-189589400	Enhancers	Osteobl	bone
12	chr1:189589400-189589800	Enhancers	A549	lung
13	chr1:189589400-189593200	Weak transcription	Hela-S3	cervix
14	chr1:189589800-189597800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:189589800-189598000	Weak transcription	HMEC	breast
16	chr1:189596400-189597400	Enhancers	A549	lung
17	chr1:189597800-189598400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:189598000-189598400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:189598000-189598400	Enhancers	HMEC	breast
20	chr1:189599600-189600600	Enhancers	Fetal Heart	heart
21	chr1:189606000-189606800	Enhancers	A549	lung
22	chr1:189606200-189606600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:189606400-189606800	Enhancers	Fetal Intestine Small	intestine
24	chr1:189606800-189610400	Weak transcription	Fetal Intestine Small	intestine
25	chr1:189610400-189611000	Enhancers	Fetal Intestine Small	intestine
26	chr1:189624000-189624200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:189624000-189624200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:189624000-189624400	Enhancers	HMEC	breast
29	chr1:189624200-189624600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr1:189624200-189625000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr1:189624200-189626000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:189624400-189626000	Weak transcription	HMEC	breast
33	chr1:189624600-189626200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:189625000-189626000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr1:189626000-189626200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr1:189626000-189626200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr1:189626000-189626400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:189626000-189629200	Enhancers	HMEC	breast
39	chr1:189626200-189626800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:189626200-189627000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr1:189626200-189629400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:189626400-189628200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:189626600-189626800	Enhancers	A549	lung
44	chr1:189626800-189627200	Flanking Active TSS	A549	lung
45	chr1:189626800-189628800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr1:189627000-189628000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:189627000-189628000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:189627000-189628000	Enhancers	NHEK	skin
49	chr1:189627200-189628200	Enhancers	A549	lung
50	chr1:189627600-189628000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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