Variant report

Variant	nsv963055
Chromosome Location	chr19:43096862-43101157
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	BACH1	chr19:43100672-43101041	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:43100628-43100974	K562	blood:	n/a	n/a
3	CEBPB	chr19:43097979-43098209	K562	blood:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
4	CEBPB	chr19:43098008-43098186	IMR90	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
5	CEBPB	chr19:43097919-43098273	A549	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
6	CEBPB	chr19:43097951-43098246	HepG2	liver:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
7	CTCF	chr19:43100693-43100964	Kidney_OC	kidney:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
8	CTCF	chr19:43100220-43100317	MCF-7	breast:	n/a	chr19:43100260-43100273 chr19:43100257-43100275
9	CTCF	chr19:43100760-43100910	HPAF	blood vessel:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
10	CTCF	chr19:43100740-43100890	GM12869	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
11	CTCF	chr19:43100780-43100930	AG10803	skin:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
12	CTCF	chr19:43100740-43100890	HBMEC	blood vessel:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
13	CTCF	chr19:43100245-43100255	Fibrobl	skin:	n/a	n/a
14	CTCF	chr19:43100760-43100910	NHEK	skin:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
15	CTCF	chr19:43100300-43100450	SK-N-SH_RA	brain:	n/a	n/a
16	CTCF	chr19:43100740-43100890	Hela-S3	cervix:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
17	CTCF	chr19:43099558-43101443	A549	lung:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100260-43100273 chr19:43100257-43100275 chr19:43100809-43100827 chr19:43100812-43100822
18	CTCF	chr19:43100740-43100890	HCT-116	colon:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
19	CTCF	chr19:43100740-43100890	HPF	lung:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
20	CTCF	chr19:43100619-43100622	Gliobla	brain:	n/a	n/a
21	CTCF	chr19:43098840-43099095	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr19:43100760-43100910	GM12873	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
23	CTCF	chr19:43098900-43099050	Caco-2	colon:	n/a	n/a
24	CTCF	chr19:43100760-43100910	MCF-7	breast:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
25	CTCF	chr19:43098900-43099050	K562	blood:	n/a	n/a
26	CTCF	chr19:43100660-43100982	A549	lung:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
27	CTCF	chr19:43100486-43101071	A549	lung:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
28	CTCF	chr19:43100760-43100910	HBMEC	blood vessel:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
29	CTCF	chr19:43100720-43100870	HUVEC	blood vessel:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
30	CTCF	chr19:43098820-43098970	HEK293	kidney:	n/a	n/a
31	CTCF	chr19:43100780-43100930	K562	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
32	CTCF	chr19:43100740-43100890	WERI-Rb-1	eye:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
33	CTCF	chr19:43100610-43101074	K562	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
34	CTCF	chr19:43101107-43101161	GM13977	blood:	n/a	n/a
35	CTCF	chr19:43098840-43098990	GM06990	blood:	n/a	n/a
36	CTCF	chr19:43100760-43100910	HVMF	connective:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
37	CTCF	chr19:43098660-43098810	SAEC	small airway:	n/a	n/a
38	CTCF	chr19:43100780-43100930	SK-N-SH_RA	brain:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
39	CTCF	chr19:43100800-43100950	HFF-Myc	foreskin:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
40	CTCF	chr19:43100740-43100890	HVMF	connective:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
41	CTCF	chr19:43100740-43100890	GM12867	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
42	CTCF	chr19:43100280-43100430	AG09309	skin:	n/a	n/a
43	CTCF	chr19:43100760-43100910	RPTEC	kidney:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
44	CTCF	chr19:43100626-43100995	GM12878	blood:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
45	CTCF	chr19:43098888-43099051	MCF-7	breast:	n/a	n/a
46	CTCF	chr19:43100780-43100930	GM12875	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
47	CTCF	chr19:43101062-43101178	Gliobla	brain:	n/a	n/a
48	CTCF	chr19:43100722-43100943	LNCaP	prostate:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
49	CTCF	chr19:43100488-43101046	HepG2	liver:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
50	CTCF	chr19:43100740-43100890	HMF	breast:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43099124-43099174	HRPEpiC	eye:	n/a
2	chr19:43099795-43099845	IMR90	lung:	fetal
3	chr19:43099124-43099174	LNCaP	prostate:	n/a
4	chr19:43099845-43099895	HUVEC	blood vessel:	n/a
5	chr19:43099124-43099174	Jurkat	blood:	n/a
6	chr19:43099124-43099174	HCM	heart:	n/a
7	chr19:43099795-43099845	BJ	skin:	n/a
8	chr19:43099124-43099174	HIPEpiC	eye:	n/a
9	chr19:43099046-43099096	HAEpiC	amniotic membrane:	n/a
10	chr19:43099845-43099895	HCPEpiC	choroid plexus:	n/a
11	chr19:43099046-43099096	GM06990	blood:	n/a
12	chr19:43099845-43099895	MCF10A-Er-Src	breast:	n/a
13	chr19:43099124-43099174	NHBE	bronchial:	n/a
14	chr19:43099845-43099895	SKMC	muscle:	n/a
15	chr19:43099046-43099096	SAEC	small airway:	n/a
16	chr19:43099795-43099845	HL-60	blood:	n/a
17	chr19:43099482-43099532	U87	brain:	n/a
18	chr19:43099046-43099096	Caco-2	colon:	n/a
19	chr19:43099482-43099532	HRCEpiC	kidney:	n/a
20	chr19:43099124-43099174	HNPCEpiC	eye:	n/a
21	chr19:43099845-43099895	NT2-D1	testis:	n/a
22	chr19:43099845-43099895	SAEC	small airway:	n/a
23	chr19:43099482-43099532	GM12891	blood:	n/a
24	chr19:43099046-43099096	Hela-S3	cervix:	n/a
25	chr19:43099795-43099845	AoSMC	blood vessel:	n/a
26	chr19:43099845-43099895	SK-N-MC	brain:	n/a
27	chr19:43099046-43099096	HNPCEpiC	eye:	n/a
28	chr19:43099795-43099845	NHDF-neo	bronchial:	n/a
29	chr19:43099046-43099096	SK-N-SH_RA	brain:	n/a
30	chr19:43099124-43099174	HCF	heart:	n/a
31	chr19:43099046-43099096	IMR90	lung:	fetal
32	chr19:43099845-43099895	LNCaP	prostate:	n/a
33	chr19:43099482-43099532	AG04449	skin:	fetal
34	chr19:43099795-43099845	AG09319	gingival:	n/a
35	chr19:43099124-43099174	RPTEC	kidney:	n/a
36	chr19:43099124-43099174	GM12891	blood:	n/a
37	chr19:43099046-43099096	HIPEpiC	eye:	n/a
38	chr19:43099124-43099174	AG09309	skin:	n/a
39	chr19:43099482-43099532	Hela-S3	cervix:	n/a
40	chr19:43099124-43099174	HEK293	kidney:	embryo
41	chr19:43099845-43099895	H1-hESC	embryonic stem cell:	embryo
42	chr19:43099046-43099096	AoSMC	blood vessel:	n/a
43	chr19:43099046-43099096	HCM	heart:	n/a
44	chr19:43099124-43099174	H1-hESC	embryonic stem cell:	embryo
45	chr19:43099046-43099096	HRCEpiC	kidney:	n/a
46	chr19:43099845-43099895	BJ	skin:	n/a
47	chr19:43099046-43099096	HCPEpiC	choroid plexus:	n/a
48	chr19:43099845-43099895	AG09309	skin:	n/a
49	chr19:43099046-43099096	AG10803	skin:	n/a
50	chr19:43099046-43099096	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:43067242..43067993-chr19:43100482..43101078,2	MCF-7	breast:
2	chr19:43070688..43071772-chr19:43100056..43100921,4	MCF-7	breast:
3	chr19:42954441..42955205-chr19:43100309..43101289,2	MCF-7	breast:
4	chr19:43070787..43071783-chr19:43100383..43100953,3	MCF-7	breast:

Variant related genes	Relation type
CEACAM8	TF binding region
CEACAM8	CpG island

Extended variants
information (count: 172 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:172 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191143578	chr19:43096874-43096875	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553790306	chr19:43096891-43096892	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573759506	chr19:43096908-43096909	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs542719149	chr19:43096915-43096916	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs562915275	chr19:43096995-43096996	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531950129	chr19:43097086-43097087	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs76348564	chr19:43097130-43097131	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs36063173	chr19:43097165-43097166	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs528036500	chr19:43097219-43097220	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546607415	chr19:43097292-43097293	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566484122	chr19:43097300-43097301	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs528949500	chr19:43097301-43097302	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs73932734	chr19:43097335-43097336	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568924192	chr19:43097370-43097371	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538023816	chr19:43097410-43097411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557716857	chr19:43097422-43097423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10416108	chr19:43097434-43097435	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs533844792	chr19:43097453-43097454	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553706217	chr19:43097477-43097478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542114431	chr19:43097480-43097481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573722493	chr19:43097487-43097488	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542680216	chr19:43097488-43097489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10416322	chr19:43097525-43097526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554032575	chr19:43097554-43097555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576486525	chr19:43097578-43097579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545579185	chr19:43097602-43097603	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565376079	chr19:43097613-43097614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs527946234	chr19:43097629-43097630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368456128	chr19:43097641-43097642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374154052	chr19:43097658-43097659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199757751	chr19:43097692-43097693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs146875157	chr19:43097693-43097694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377727534	chr19:43097699-43097700	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371423676	chr19:43097700-43097701	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140735487	chr19:43097703-43097704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560162763	chr19:43097716-43097717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199506812	chr19:43097720-43097721	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528910642	chr19:43097728-43097729	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200817725	chr19:43097750-43097751	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572450516	chr19:43097753-43097754	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145626522	chr19:43097755-43097756	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs202165154	chr19:43097756-43097757	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1041997	chr19:43097776-43097777	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146553721	chr19:43097787-43097788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs45440298	chr19:43097788-43097789	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs201132231	chr19:43097789-43097790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551513615	chr19:43097806-43097807	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571360079	chr19:43097824-43097825	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367810787	chr19:43097827-43097828	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs200202664	chr19:43097828-43097829	Flanking Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43081400-43100600	Weak transcription	Spleen	Spleen
2	chr19:43094400-43100200	Weak transcription	Primary B cells from cord blood	blood
3	chr19:43096800-43097400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
4	chr19:43096800-43099000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr19:43097400-43097800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr19:43097800-43099200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr19:43099200-43099600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr19:43099600-43100800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
9	chr19:43099800-43100200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr19:43100200-43100800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr19:43100200-43100800	Enhancers	Primary B cells from cord blood	blood
12	chr19:43100400-43100800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr19:43100400-43101000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
14	chr19:43100400-43101000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
15	chr19:43100400-43101200	Enhancers	Adipose Nuclei	Adipose
16	chr19:43100600-43100800	Bivalent Enhancer	Placenta	Placenta
17	chr19:43100600-43101000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:43100600-43101000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr19:43100600-43101000	Enhancers	Right Ventricle	heart
20	chr19:43100600-43101000	Enhancers	Spleen	Spleen
21	chr19:43100600-43101200	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
22	chr19:43100600-43101200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr19:43100600-43101200	Enhancers	Brain Cingulate Gyrus	brain
24	chr19:43100600-43101200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr19:43100600-43101200	Bivalent Enhancer	HepG2	liver
26	chr19:43100800-43101000	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr19:43100800-43101000	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr19:43100800-43101000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr19:43100800-43101200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr19:43100800-43101200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr19:43100800-43101200	Bivalent Enhancer	Duodenum Mucosa	Duodenum
32	chr19:43100800-43101200	Enhancers	Esophagus	oesophagus
33	chr19:43100800-43101200	Enhancers	Pancreas	Pancrea
34	chr19:43100800-43101200	Enhancers	K562	blood
35	chr19:43100800-43105800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr19:43101000-43101200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
37	chr19:43101000-43101200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr19:43101000-43101200	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
39	chr19:43101000-43101200	Bivalent Enhancer	Fetal Intestine Small	intestine
40	chr19:43101000-43101200	Bivalent Enhancer	Stomach Mucosa	stomach

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