Variant report

Variant	nsv584030
Chromosome Location	chr2:186915437-187001076
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	chr2:186933182-186933390	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:186994689-186995458	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:186973201-186973628	HepG2	liver:	n/a	n/a
4	BACH1	chr2:186917756-186918018	H1-hESC	embryonic stem cell:	n/a	chr2:186917846-186917860
5	BHLHE40	chr2:186929279-186929572	GM12878	blood:	n/a	n/a
6	CCNT2	chr2:186966417-186966617	K562	blood:	n/a	n/a
7	CCNT2	chr2:186984780-186984935	K562	blood:	n/a	n/a
8	CEBPB	chr2:186994884-186995064	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:186918854-186919223	HepG2	liver:	n/a	chr2:186919035-186919044 chr2:186919033-186919044 chr2:186919034-186919045
10	CEBPB	chr2:186994672-186995576	Hela-S3	cervix:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
11	CEBPB	chr2:186973189-186973514	Hela-S3	cervix:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
12	CEBPB	chr2:186994842-186995446	HepG2	liver:	n/a	n/a
13	CEBPB	chr2:186995026-186995183	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:186994724-186995491	HCT-116	colon:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
15	CEBPB	chr2:186918858-186919191	IMR90	lung:	n/a	chr2:186919035-186919044 chr2:186919033-186919044 chr2:186919034-186919045
16	CEBPB	chr2:186973165-186973556	HepG2	liver:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
17	CEBPB	chr2:186994796-186995845	ECC-1	luminal epithelium:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
18	CEBPB	chr2:186994808-186995412	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:186973206-186973512	K562	blood:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
20	CEBPB	chr2:186973240-186973488	HepG2	liver:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
21	CEBPB	chr2:186923368-186923898	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr2:186973259-186973459	H1-hESC	embryonic stem cell:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
23	CEBPB	chr2:186954617-186954851	HepG2	liver:	n/a	chr2:186954740-186954751
24	CEBPB	chr2:186973188-186973509	A549	lung:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
25	CEBPB	chr2:186995329-186995732	ECC-1	luminal epithelium:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
26	CEBPB	chr2:186973209-186973488	HepG2	liver:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
27	CEBPB	chr2:186973194-186973541	IMR90	lung:	n/a	chr2:186973313-186973324 chr2:186973356-186973367
28	CEBPB	chr2:186994645-186995518	HCT-116	colon:	n/a	chr2:186995442-186995455 chr2:186995444-186995455 chr2:186995444-186995455 chr2:186995442-186995455
29	CEBPB	chr2:186987162-186987415	HepG2	liver:	n/a	chr2:186987233-186987244
30	CEBPB	chr2:186988737-186988903	A549	lung:	n/a	n/a
31	CEBPD	chr2:186973274-186973494	HepG2	liver:	n/a	n/a
32	CTCF	chr2:186954200-186954350	MCF-7	breast:	n/a	n/a
33	CTCF	chr2:186955790-186955928	GM10248	blood:	n/a	n/a
34	CTCF	chr2:186954240-186954390	HepG2	liver:	n/a	n/a
35	CTCF	chr2:186954180-186954330	MCF-7	breast:	n/a	n/a
36	CTCF	chr2:186954213-186954310	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:186954242-186954328	HepG2	liver:	n/a	n/a
38	CTCF	chr2:186955769-186955930	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr2:186954160-186954310	HepG2	liver:	n/a	n/a
40	CTCF	chr2:186979460-186979610	HepG2	liver:	n/a	chr2:186979601-186979610
41	CTCF	chr2:186954256-186954300	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr2:186994680-186994830	GM12866	blood:	n/a	n/a
43	E2F4	chr2:186925532-186925809	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr2:186977298-186977498	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr2:186969786-186969986	MCF10A-Er-Src	breast:	n/a	n/a
46	ELK1	chr2:186997635-186997638	GM12878	blood:	n/a	n/a
47	ELK4	chr2:186994457-186994845	Hela-S3	cervix:	n/a	chr2:186994539-186994550
48	EP300	chr2:186994448-186996010	ECC-1	luminal epithelium:	n/a	chr2:186995784-186995798
49	EP300	chr2:186932207-186934119	SK-N-SH	brain:	n/a	chr2:186932821-186932835 chr2:186933640-186933654 chr2:186932819-186932833 chr2:186934089-186934103 chr2:186932820-186932834 chr2:186932818-186932832
50	EP300	chr2:186973247-186973656	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186988953-186989003	NH-A	brain:	n/a
2	chr2:186988953-186989003	HepG2	liver:	n/a
3	chr2:186924071-186924121	Caco-2	colon:	n/a
4	chr2:186968467-186968517	Hela-S3	cervix:	n/a
5	chr2:186968467-186968517	Hepatocyte	liver:	n/a
6	chr2:186924071-186924121	HNPCEpiC	eye:	n/a
7	chr2:186968467-186968517	ProgFib	skin:	n/a
8	chr2:186924071-186924121	NHBE	bronchial:	n/a
9	chr2:186988953-186989003	HNPCEpiC	eye:	n/a
10	chr2:186924071-186924121	HEEpiC	esophagus:	n/a
11	chr2:186968467-186968517	HCM	heart:	n/a
12	chr2:186988953-186989003	HCPEpiC	choroid plexus:	n/a
13	chr2:186924071-186924121	U87	brain:	n/a
14	chr2:186924071-186924121	K562	blood:	n/a
15	chr2:186988953-186989003	HPAEpiC	pulmonary alveolar:	n/a
16	chr2:186968467-186968517	ECC-1	luminal epithelium:	n/a
17	chr2:186968467-186968517	HRE	kidney:	n/a
18	chr2:186988953-186989003	MCF10A-Er-Src	breast:	n/a
19	chr2:186968467-186968517	BJ	skin:	n/a
20	chr2:186968467-186968517	NB4	blood:	n/a
21	chr2:186988953-186989003	HIPEpiC	eye:	n/a
22	chr2:186968467-186968517	AoSMC	blood vessel:	n/a
23	chr2:186924071-186924121	RPTEC	kidney:	n/a
24	chr2:186924071-186924121	Hepatocyte	liver:	n/a
25	chr2:186968467-186968517	AG04450	lung:	fetal
26	chr2:186924071-186924121	BJ	skin:	n/a
27	chr2:186968467-186968517	HPAEpiC	pulmonary alveolar:	n/a
28	chr2:186924071-186924121	HIPEpiC	eye:	n/a
29	chr2:186988953-186989003	GM19239	blood:	n/a
30	chr2:186968467-186968517	SK-N-SH_RA	brain:	n/a
31	chr2:186968467-186968517	AG09309	skin:	n/a
32	chr2:186968467-186968517	SKMC	muscle:	n/a
33	chr2:186988953-186989003	AG09319	gingival:	n/a
34	chr2:186968467-186968517	K562	blood:	n/a
35	chr2:186968467-186968517	HRCEpiC	kidney:	n/a
36	chr2:186988953-186989003	GM12892	blood:	n/a
37	chr2:186924071-186924121	ovcar-3	ovarian:	n/a
38	chr2:186924071-186924121	AG04449	skin:	fetal
39	chr2:186988953-186989003	SAEC	small airway:	n/a
40	chr2:186988953-186989003	GM06990	blood:	n/a
41	chr2:186968467-186968517	HAEpiC	amniotic membrane:	n/a
42	chr2:186924071-186924121	AG04450	lung:	fetal
43	chr2:186988953-186989003	HUVEC	blood vessel:	n/a
44	chr2:186968467-186968517	AG09319	gingival:	n/a
45	chr2:186924071-186924121	HEK293	kidney:	embryo
46	chr2:186924071-186924121	T-47D	breast:	n/a
47	chr2:186924071-186924121	AG09309	skin:	n/a
48	chr2:186988953-186989003	SKMC	muscle:	n/a
49	chr2:186968467-186968517	GM19239	blood:	n/a
50	chr2:186988953-186989003	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:186994332..186996558-chr2:186996994..186999214,2	MCF-7	breast:
2	chr2:186966503..186967236-chr4:21954917..21955427,2	MCF-7	breast:
3	chr2:186983605..186985165-chr2:186986733..186988771,2	MCF-7	breast:
4	chr2:186948418..186950441-chr2:187047439..187049579,2	K562	blood:
5	chr2:186905396..186906984-chr2:186927102..186929134,2	K562	blood:
6	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
7	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:
8	chr2:43453747..43454591-chr2:186974749..186975692,2	HCT-116	colon:
9	chr2:186953883..186956490-chr2:186957329..186960004,2	K562	blood:
10	chr2:186994332..186996558-chr2:186996994..186999214,2	MCF-7	breast:
11	chr2:186943617..186946004-chr2:186946269..186949362,3	K562	blood:
12	chr2:186983605..186985165-chr2:186986733..186988771,2	MCF-7	breast:
13	chr2:186913950..186916894-chr2:186919637..186921761,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877.2
2	lnc-FSIP2-3	chr2:186963163-186964146	NONHSAT075986
3	lnc-ZSWIM2-3	chr2:186947881-186947951	NONHSAT075981
4	lnc-FSIP2-2	chr2:186953806-186955337	NONHSAT075985
5	lnc-ZSWIM2-3	chr2:186946057-186946143	NONHSAT075981
6	lnc-FSIP2-4	chr2:186947780-186951158	NONHSAT075984
7	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
8	lnc-FSIP2-4	chr2:186923254-186923714	NONHSAT075984
9	lnc-FSIP2-1	chr2:186999554-187000911	XLOC_001781
10	lnc-ZSWIM2-3	chr2:186947881-186947950	ENSG00000237877
11	lnc-ZSWIM2-3	chr2:186951028-186951044	NR_110218
12	lnc-FSIP2-4	chr2:186964372-186965726	NONHSAT075984
13	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877.2
14	lnc-FSIP2-4	chr2:186946053-186946143	NONHSAT075984
15	lnc-ZSWIM2-3	chr2:186947881-186947948	NR_110218
16	lnc-ZSWIM2-3	chr2:186946057-186946143	NR_110218
17	lnc-FSIP2-4	chr2:186932840-186933840	NONHSAT075984
18	lnc-ZSWIM2-3	chr2:186946057-186946143	ENSG00000237877
19	lnc-ZSWIM2-3	chr2:186947881-186947960	ENSG00000237877

Variant related genes	Relation type
ENSG00000237877	TF binding region
ENSG00000237877	CpG island
ENSG00000152518	chromatin interactions
ENSG00000237877	chromatin interactions
SNAI2	miRNA target sites

Extended variants
information (count: 2719 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:2719 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6434159	chr2:186915437-186915438	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs371373967	chr2:186915482-186915483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs530002050	chr2:186915491-186915492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181631316	chr2:186915526-186915527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs374631139	chr2:186915596-186915597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557042210	chr2:186915610-186915611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs148909243	chr2:186915630-186915631	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537160007	chr2:186915642-186915643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112003409	chr2:186915650-186915651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552681178	chr2:186915668-186915669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs571352779	chr2:186915764-186915765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572324592	chr2:186915786-186915787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs538857521	chr2:186915855-186915856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554095274	chr2:186915857-186915858	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143533383	chr2:186915862-186915863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536205348	chr2:186915886-186915887	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539867800	chr2:186915896-186915897	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554612075	chr2:186915912-186915913	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576027170	chr2:186915919-186915920	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543146575	chr2:186915922-186915923	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539319940	chr2:186915935-186915936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565017991	chr2:186915960-186915961	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs185963909	chr2:186916019-186916020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541241918	chr2:186916087-186916088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs559589839	chr2:186916103-186916104	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551293068	chr2:186916114-186916115	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191125957	chr2:186916141-186916142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183305175	chr2:186916149-186916150	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563525190	chr2:186916169-186916170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368218068	chr2:186916236-186916237	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs370731008	chr2:186916309-186916310	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111757692	chr2:186916364-186916365	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs115631180	chr2:186916382-186916383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558143041	chr2:186916425-186916426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs570960712	chr2:186916428-186916429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569291010	chr2:186916454-186916455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140846441	chr2:186916492-186916493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs565937591	chr2:186916508-186916509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186100229	chr2:186916595-186916596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554948862	chr2:186916600-186916601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569526049	chr2:186916620-186916621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537082673	chr2:186916699-186916700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372057360	chr2:186916707-186916708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs13014905	chr2:186916788-186916789	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs191004078	chr2:186916942-186916943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs541181514	chr2:186916952-186916953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367931928	chr2:186917023-186917024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574733406	chr2:186917033-186917034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10048680	chr2:186917096-186917097	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs183203655	chr2:186917161-186917162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164919	CNVD

Chromatin state (count:393 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186906600-186923800	Weak transcription	Ovary	ovary
2	chr2:186907400-186933200	Weak transcription	Pancreas	Pancrea
3	chr2:186911400-186933000	Weak transcription	Psoas Muscle	Psoas
4	chr2:186915600-186916400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr2:186917800-186918200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:186918000-186918400	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:186918200-186923000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:186918400-186923000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr2:186920000-186925200	Weak transcription	HSMM	muscle
10	chr2:186923000-186923800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr2:186923000-186924000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:186923000-186924200	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr2:186923000-186924200	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:186923000-186924200	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr2:186923000-186924200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr2:186923400-186923600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr2:186923400-186923600	Enhancers	Brain Substantia Nigra	brain
18	chr2:186923400-186923800	Enhancers	Brain Cingulate Gyrus	brain
19	chr2:186923400-186924000	Enhancers	Brain Germinal Matrix	brain
20	chr2:186923400-186924200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:186923400-186924200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr2:186923400-186924200	Enhancers	Fetal Brain Female	brain
23	chr2:186923400-186924200	Enhancers	Fetal Lung	lung
24	chr2:186923400-186924200	Enhancers	Fetal Stomach	stomach
25	chr2:186923400-186924200	Enhancers	Right Atrium	heart
26	chr2:186923400-186924400	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr2:186923600-186923800	Enhancers	Brain Hippocampus Middle	brain
28	chr2:186923600-186924200	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr2:186923600-186924200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr2:186923600-186924200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr2:186923600-186924200	Enhancers	Liver	Liver
32	chr2:186923600-186924200	Enhancers	Brain Angular Gyrus	brain
33	chr2:186923600-186924200	Flanking Active TSS	Brain Substantia Nigra	brain
34	chr2:186923600-186924200	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr2:186923600-186924400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr2:186923600-186924400	Enhancers	Fetal Heart	heart
37	chr2:186923600-186924800	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr2:186923600-186925000	Enhancers	Brain Anterior Caudate	brain
39	chr2:186923600-186926600	Enhancers	Muscle Satellite Cultured Cells	--
40	chr2:186923800-186924200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr2:186923800-186924200	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr2:186923800-186924200	Enhancers	Adipose Nuclei	Adipose
43	chr2:186923800-186924200	Flanking Active TSS	Brain Cingulate Gyrus	brain
44	chr2:186923800-186924200	Flanking Active TSS	Brain Hippocampus Middle	brain
45	chr2:186923800-186924200	Enhancers	Duodenum Smooth Muscle	Duodenum
46	chr2:186923800-186924200	Enhancers	Ovary	ovary
47	chr2:186923800-186924200	Enhancers	Rectal Smooth Muscle	rectum
48	chr2:186923800-186924200	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr2:186923800-186924200	Enhancers	HUVEC	blood vessel
50	chr2:186923800-186924800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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