Variant report

Variant	nsv872717
Chromosome Location	chr1:189585380-189748851
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1129)
CpG islands
(count:122)
Chromatin interactive
region (count:36)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1129 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

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	ARID3A	chr1:189743917-189744230	HepG2	liver:	n/a	n/a
3	ATF1	chr1:189692607-189692756	K562	blood:	n/a	n/a
4	ATF1	chr1:189645110-189645131	K562	blood:	n/a	n/a
5	ATF3	chr1:189624065-189624449	HCT-116	colon:	n/a	n/a
6	BACH1	chr1:189660033-189660067	K562	blood:	n/a	n/a
7	BCL3	chr1:189650561-189651101	A549	lung:	n/a	n/a
8	BCL3	chr1:189743704-189744394	A549	lung:	n/a	chr1:189744338-189744347
9	BRCA1	chr1:189588843-189589197	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr1:189640354-189640407	H1-hESC	embryonic stem cell:	n/a	n/a
11	CBX3	chr1:189631288-189631734	HCT-116	colon:	n/a	n/a
12	CBX3	chr1:189626762-189627309	HCT-116	colon:	n/a	n/a
13	CBX3	chr1:189588763-189589390	HCT-116	colon:	n/a	n/a
14	CBX3	chr1:189588801-189589528	HCT-116	colon:	n/a	n/a
15	CBX3	chr1:189631264-189631803	HCT-116	colon:	n/a	n/a
16	CBX3	chr1:189627431-189627982	HCT-116	colon:	n/a	n/a
17	CEBPB	chr1:189626895-189627312	Hela-S3	cervix:	n/a	chr1:189627200-189627217
18	CEBPB	chr1:189604520-189604793	HepG2	liver:	n/a	n/a
19	CEBPB	chr1:189688107-189688436	HepG2	liver:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
20	CEBPB	chr1:189606191-189606464	HepG2	liver:	n/a	chr1:189606323-189606334
21	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
22	CEBPB	chr1:189688106-189688428	IMR90	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
23	CEBPB	chr1:189588715-189589168	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr1:189689001-189689131	IMR90	lung:	n/a	n/a
25	CEBPB	chr1:189743808-189744409	A549	lung:	n/a	chr1:189743903-189743914
26	CEBPB	chr1:189624014-189624396	IMR90	lung:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
27	CEBPB	chr1:189688098-189688417	A549	lung:	n/a	chr1:189688274-189688285 chr1:189688275-189688286
28	CEBPB	chr1:189738620-189739003	IMR90	lung:	n/a	n/a
29	CEBPB	chr1:189631210-189631769	HCT-116	colon:	n/a	n/a
30	CEBPB	chr1:189675218-189675345	A549	lung:	n/a	chr1:189675255-189675266
31	CEBPB	chr1:189651781-189651981	A549	lung:	n/a	n/a
32	CEBPB	chr1:189624053-189624347	H1-hESC	embryonic stem cell:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
33	CEBPB	chr1:189606179-189606483	IMR90	lung:	n/a	chr1:189606323-189606334
34	CEBPB	chr1:189675215-189675438	HepG2	liver:	n/a	chr1:189675255-189675266
35	CEBPB	chr1:189586083-189586474	A549	lung:	n/a	n/a
36	CEBPB	chr1:189624035-189624369	K562	blood:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
37	CEBPB	chr1:189626911-189627214	MCF-7	breast:	n/a	n/a
38	CEBPB	chr1:189624089-189624306	MCF-7	breast:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
39	CEBPB	chr1:189626976-189627210	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:189650548-189650953	A549	lung:	n/a	n/a
41	CEBPB	chr1:189604468-189604766	A549	lung:	n/a	n/a
42	CEBPB	chr1:189626892-189627296	A549	lung:	n/a	chr1:189627200-189627217
43	CEBPB	chr1:189606174-189606516	A549	lung:	n/a	chr1:189606323-189606334
44	CEBPB	chr1:189731505-189731602	K562	blood:	n/a	chr1:189731575-189731586
45	CEBPB	chr1:189626703-189627383	HCT-116	colon:	n/a	chr1:189627200-189627217
46	CEBPB	chr1:189626736-189627414	HCT-116	colon:	n/a	chr1:189627200-189627217
47	CEBPB	chr1:189624011-189624388	Hela-S3	cervix:	n/a	chr1:189624201-189624212 chr1:189624203-189624214 chr1:189624201-189624214 chr1:189624201-189624214 chr1:189624201-189624214
48	CEBPB	chr1:189592550-189592866	A549	lung:	n/a	chr1:189592697-189592708
49	CEBPB	chr1:189606177-189606515	Hela-S3	cervix:	n/a	chr1:189606323-189606334
50	CEBPB	chr1:189646472-189646806	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:189722103-189722153	PFSK-1	brain:	n/a
2	chr1:189722103-189722153	Hela-S3	cervix:	n/a
3	chr1:189722103-189722153	AG04449	skin:	fetal
4	chr1:189722103-189722153	NHDF-neo	bronchial:	n/a
5	chr1:189722103-189722153	AG09319	gingival:	n/a
6	chr1:189722103-189722153	Hepatocyte	liver:	n/a
7	chr1:189744005-189744055	NHDF-neo	bronchial:	n/a
8	chr1:189722103-189722153	NB4	blood:	n/a
9	chr1:189722103-189722153	GM12892	blood:	n/a
10	chr1:189722103-189722153	SK-N-MC	brain:	n/a
11	chr1:189722103-189722153	HUVEC	blood vessel:	n/a
12	chr1:189744005-189744055	LNCaP	prostate:	n/a
13	chr1:189722103-189722153	H1-hESC	embryonic stem cell:	embryo
14	chr1:189744005-189744055	IMR90	lung:	fetal
15	chr1:189744005-189744055	HRPEpiC	eye:	n/a
16	chr1:189744005-189744055	BJ	skin:	n/a
17	chr1:189722103-189722153	LNCaP	prostate:	n/a
18	chr1:189744005-189744055	HUVEC	blood vessel:	n/a
19	chr1:189744005-189744055	T-47D	breast:	n/a
20	chr1:189722103-189722153	HCT-116	colon:	n/a
21	chr1:189744005-189744055	AoSMC	blood vessel:	n/a
22	chr1:189744005-189744055	SKMC	muscle:	n/a
23	chr1:189744005-189744055	MCF10A-Er-Src	breast:	n/a
24	chr1:189722103-189722153	HRE	kidney:	n/a
25	chr1:189722103-189722153	Jurkat	blood:	n/a
26	chr1:189722103-189722153	ProgFib	skin:	n/a
27	chr1:189722103-189722153	GM06990	blood:	n/a
28	chr1:189722103-189722153	HCM	heart:	n/a
29	chr1:189744005-189744055	GM12892	blood:	n/a
30	chr1:189744005-189744055	PANC-1	pancreas:	n/a
31	chr1:189744005-189744055	U87	brain:	n/a
32	chr1:189744005-189744055	HMEC	breast:	n/a
33	chr1:189744005-189744055	SAEC	small airway:	n/a
34	chr1:189744005-189744055	K562	blood:	n/a
35	chr1:189744005-189744055	HEK293	kidney:	embryo
36	chr1:189722103-189722153	HL-60	blood:	n/a
37	chr1:189722103-189722153	MCF-7	breast:	n/a
38	chr1:189722103-189722153	MCF10A-Er-Src	breast:	n/a
39	chr1:189722103-189722153	SKMC	muscle:	n/a
40	chr1:189744005-189744055	HCPEpiC	choroid plexus:	n/a
41	chr1:189722103-189722153	HRCEpiC	kidney:	n/a
42	chr1:189722103-189722153	ECC-1	luminal epithelium:	n/a
43	chr1:189722103-189722153	HepG2	liver:	n/a
44	chr1:189722103-189722153	GM19239	blood:	n/a
45	chr1:189722103-189722153	NHBE	bronchial:	n/a
46	chr1:189744005-189744055	Jurkat	blood:	n/a
47	chr1:189722103-189722153	A549	lung:	n/a
48	chr1:189722103-189722153	HNPCEpiC	eye:	n/a
49	chr1:189744005-189744055	HepG2	liver:	n/a
50	chr1:189744005-189744055	AG04450	lung:	fetal

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
2	chr1:189646033..189647879-chr5:175874488..175876371,2	MCF-7	breast:
3	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
4	chr1:189398440..189399083-chr1:189642226..189643036,4	MCF-7	breast:
5	chr1:189589226..189590045-chr1:189662088..189662866,2	MCF-7	breast:
6	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
7	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
8	chr1:189398408..189399387-chr1:189661985..189662829,2	MCF-7	breast:
9	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
10	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
11	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
12	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
13	chr1:189677502..189678569-chr1:190053452..190054228,3	MCF-7	breast:
14	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
15	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
16	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
17	chr1:189672702..189674835-chr1:189679900..189682761,2	MCF-7	breast:
18	chr1:189709848..189710556-chr1:189743646..189744501,3	MCF-7	breast:
19	chr1:189627801..189630516-chr1:189640573..189642596,2	MCF-7	breast:
20	chr1:189705345..189707314-chr1:189708117..189710746,3	MCF-7	breast:
21	chr1:189630297..189631878-chr1:189633078..189635794,2	K562	blood:
22	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
23	chr1:189589226..189590045-chr1:189662088..189662866,2	MCF-7	breast:
24	chr1:189627826..189630498-chr1:189636599..189639267,2	MCF-7	breast:
25	chr1:189617058..189619904-chr1:189621793..189623517,2	MCF-7	breast:
26	chr1:189746682..189748361-chr1:189748606..189750164,2	MCF-7	breast:
27	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
28	chr1:189624367..189627091-chr1:189650312..189652304,2	MCF-7	breast:
29	chr1:189588020..189590795-chr1:189591484..189594244,3	MCF-7	breast:
30	chr1:189581455..189584315-chr1:189585168..189587493,2	K562	blood:
31	chr1:189740038..189741669-chr1:189745873..189748337,2	K562	blood:
32	chr1:189625524..189628069-chr1:189701890..189703665,2	MCF-7	breast:
33	chr1:189705156..189706947-chr1:189708552..189710958,2	K562	blood:
34	chr1:189608651..189610421-chr1:189613616..189615684,2	K562	blood:
35	chr1:189677420..189678491-chr1:190289916..190290952,3	MCF-7	breast:
36	chr1:189398509..189399144-chr1:189660311..189661261,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS18-7	chr1:189744595-189744695	XLOC_000503
2	lnc-RGS18-7	chr1:189746390-189746467	XLOC_000503

No data

Variant related genes	Relation type
RNA5SP73	TF binding region
ENSG00000232212	TF binding region
RNA5SP73	CpG island
ENSG00000232212	CpG island
ENSG00000252553	chromatin interactions
ENSG00000113194	chromatin interactions
SOX11	miRNA target sites

Extended variants
information (count: 1999 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1999 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10922362	chr1:189585380-189585381	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371393816	chr1:189585508-189585509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs111896409	chr1:189585521-189585522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs28488254	chr1:189585540-189585541	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs376914386	chr1:189585547-189585548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559629208	chr1:189585580-189585581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs72735892	chr1:189585583-189585584	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75191574	chr1:189585584-189585585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192920727	chr1:189585689-189585690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533075538	chr1:189585776-189585777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532537316	chr1:189585781-189585782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs577703890	chr1:189585782-189585783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527610897	chr1:189585832-189585833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569913818	chr1:189585850-189585851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535139435	chr1:189585875-189585876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2902582	chr1:189585876-189585877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565686014	chr1:189585920-189585921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs184660902	chr1:189585929-189585930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370081209	chr1:189585953-189585954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs56366121	chr1:189585960-189585961	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs112240859	chr1:189585973-189585974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs578196225	chr1:189585984-189585985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs544008729	chr1:189586042-189586043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs560217738	chr1:189586043-189586044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75588390	chr1:189586045-189586046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs57523607	chr1:189586051-189586052	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs543306455	chr1:189586118-189586119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs58571092	chr1:189586121-189586122	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs528585007	chr1:189586122-189586123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs111853880	chr1:189586141-189586142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146092942	chr1:189586143-189586144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563963657	chr1:189586233-189586234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs189496506	chr1:189586253-189586254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549552781	chr1:189586258-189586259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531889678	chr1:189586279-189586280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35689319	chr1:189586287-189586288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs13374577	chr1:189586310-189586311	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs532505888	chr1:189586311-189586312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548706505	chr1:189586322-189586323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386637856	chr1:189586325-189586326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs113216346	chr1:189586326-189586327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs9287137	chr1:189586327-189586328	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs551528428	chr1:189586328-189586329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs13374026	chr1:189586353-189586354	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs572149758	chr1:189586357-189586358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13374345	chr1:189586395-189586396	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs557525857	chr1:189586398-189586399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567495556	chr1:189586439-189586440	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs112325405	chr1:189586509-189586510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs180752788	chr1:189586511-189586512	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:189585000-189587000	Enhancers	A549	lung
2	chr1:189585600-189587000	Enhancers	Muscle Satellite Cultured Cells	--
3	chr1:189586000-189586400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:189586000-189586400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr1:189586000-189586400	Enhancers	HMEC	breast
6	chr1:189586000-189586600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr1:189586400-189588800	Weak transcription	HMEC	breast
8	chr1:189586400-189589000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:189586600-189588600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr1:189587000-189588200	Weak transcription	A549	lung
11	chr1:189587000-189588600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:189588200-189588800	Enhancers	A549	lung
13	chr1:189588600-189589600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr1:189588600-189589600	Enhancers	HUVEC	blood vessel
15	chr1:189588600-189589800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:189588800-189589000	Active TSS	A549	lung
17	chr1:189588800-189589400	Enhancers	NHEK	skin
18	chr1:189588800-189589800	Enhancers	HMEC	breast
19	chr1:189589000-189589400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr1:189589000-189589400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr1:189589000-189589400	Flanking Active TSS	A549	lung
22	chr1:189589000-189589400	Enhancers	Hela-S3	cervix
23	chr1:189589000-189589400	Enhancers	NH-A	brain
24	chr1:189589000-189589400	Enhancers	Osteobl	bone
25	chr1:189589400-189589800	Enhancers	A549	lung
26	chr1:189589400-189593200	Weak transcription	Hela-S3	cervix
27	chr1:189589800-189597800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:189589800-189598000	Weak transcription	HMEC	breast
29	chr1:189596400-189597400	Enhancers	A549	lung
30	chr1:189597800-189598400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr1:189598000-189598400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr1:189598000-189598400	Enhancers	HMEC	breast
33	chr1:189599600-189600600	Enhancers	Fetal Heart	heart
34	chr1:189606000-189606800	Enhancers	A549	lung
35	chr1:189606200-189606600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr1:189606400-189606800	Enhancers	Fetal Intestine Small	intestine
37	chr1:189606800-189610400	Weak transcription	Fetal Intestine Small	intestine
38	chr1:189610400-189611000	Enhancers	Fetal Intestine Small	intestine
39	chr1:189624000-189624200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr1:189624000-189624200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr1:189624000-189624400	Enhancers	HMEC	breast
42	chr1:189624200-189624600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr1:189624200-189625000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:189624200-189626000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr1:189624400-189626000	Weak transcription	HMEC	breast
46	chr1:189624600-189626200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr1:189625000-189626000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr1:189626000-189626200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr1:189626000-189626200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:189626000-189626400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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