Variant report

Variant	nsv1064734
Chromosome Location	chr19:43076046-43182478
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	BACH1	chr19:43139260-43139326	K562	blood:	n/a	n/a
3	BACH1	chr19:43082922-43083098	K562	blood:	n/a	n/a
4	BATF	chr19:43179178-43179402	GM12878	blood:	n/a	n/a
5	BATF	chr19:43132976-43133178	GM12878	blood:	n/a	chr19:43133094-43133104
6	BCL11A	chr19:43179101-43179287	GM12878	blood:	n/a	n/a
7	BHLHE40	chr19:43106732-43106880	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:43110883-43111176	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:43138971-43139294	HepG2	liver:	n/a	n/a
10	BHLHE40	chr19:43110839-43111090	K562	blood:	n/a	n/a
11	BHLHE40	chr19:43139176-43139401	K562	blood:	n/a	n/a
12	BHLHE40	chr19:43100628-43100974	K562	blood:	n/a	n/a
13	BRCA1	chr19:43111388-43111484	GM12878	blood:	n/a	n/a
14	BRCA1	chr19:43168346-43168356	GM12878	blood:	n/a	n/a
15	CBX3	chr19:43156238-43156476	K562	blood:	n/a	n/a
16	CEBPB	chr19:43110761-43111081	HepG2	liver:	n/a	n/a
17	CEBPB	chr19:43097919-43098273	A549	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
18	CEBPB	chr19:43128989-43129127	K562	blood:	n/a	n/a
19	CEBPB	chr19:43098008-43098186	IMR90	lung:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
20	CEBPB	chr19:43097951-43098246	HepG2	liver:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
21	CEBPB	chr19:43139178-43139417	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:43156174-43156554	A549	lung:	n/a	chr19:43156349-43156360
23	CEBPB	chr19:43152306-43152361	IMR90	lung:	n/a	n/a
24	CEBPB	chr19:43076011-43076056	HepG2	liver:	n/a	chr19:43076033-43076044
25	CEBPB	chr19:43156216-43156522	HepG2	liver:	n/a	chr19:43156349-43156360
26	CEBPB	chr19:43127742-43127805	HepG2	liver:	n/a	chr19:43127762-43127773
27	CEBPB	chr19:43075958-43076158	A549	lung:	n/a	chr19:43076033-43076044
28	CEBPB	chr19:43097979-43098209	K562	blood:	n/a	chr19:43098079-43098092 chr19:43098079-43098090
29	CEBPB	chr19:43150294-43150473	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr19:43139258-43139346	K562	blood:	n/a	n/a
31	CHD2	chr19:43139100-43139262	K562	blood:	n/a	n/a
32	CTCF	chr19:43167040-43167190	NHEK	skin:	n/a	n/a
33	CTCF	chr19:43110920-43111070	GM12864	blood:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
34	CTCF	chr19:43110850-43111089	A549	lung:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
35	CTCF	chr19:43110920-43111070	MCF-7	breast:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
36	CTCF	chr19:43100760-43100910	NB4	blood:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
37	CTCF	chr19:43110940-43111090	HPAF	blood vessel:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
38	CTCF	chr19:43110920-43111070	HepG2	liver:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
39	CTCF	chr19:43110900-43111050	GM12865	blood:	n/a	chr19:43111005-43111013 chr19:43111003-43111016 chr19:43111002-43111023 chr19:43111000-43111018 chr19:43111003-43111016 chr19:43111001-43111017
40	CTCF	chr19:43166993-43167137	MCF-7	breast:	n/a	n/a
41	CTCF	chr19:43100240-43100390	WI-38	lung:	n/a	chr19:43100260-43100273 chr19:43100257-43100275
42	CTCF	chr19:43100623-43101013	Gliobla	brain:	n/a	chr19:43100804-43100825 chr19:43100656-43100669 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
43	CTCF	chr19:43139200-43139350	NHDF-neo	bronchial:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
44	CTCF	chr19:43139160-43139310	GM12869	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
45	CTCF	chr19:43139180-43139330	AG04449	skin:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
46	CTCF	chr19:43098883-43099054	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr19:43100780-43100930	HAc	cerebellar:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
48	CTCF	chr19:43166900-43167050	A549	lung:	n/a	n/a
49	CTCF	chr19:43100760-43100910	HAc	cerebellar:	n/a	chr19:43100804-43100825 chr19:43100810-43100826 chr19:43100815-43100824 chr19:43100809-43100827 chr19:43100812-43100822
50	CTCF	chr19:43139200-43139350	HFF-Myc	foreskin:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43099795-43099845	AG09309	skin:	n/a
2	chr19:43099845-43099895	BJ	skin:	n/a
3	chr19:43099795-43099845	NT2-D1	testis:	n/a
4	chr19:43099795-43099845	AG09309	skin:	n/a
5	chr19:43099845-43099895	BJ	skin:	n/a
6	chr19:43099795-43099845	NT2-D1	testis:	n/a
7	chr19:43099124-43099174	HUVEC	blood vessel:	n/a
8	chr19:43085416-43085466	Caco-2	colon:	n/a
9	chr19:43099124-43099174	SK-N-MC	brain:	n/a
10	chr19:43099845-43099895	HCM	heart:	n/a
11	chr19:43099845-43099895	NHDF-neo	bronchial:	n/a
12	chr19:43099845-43099895	HRE	kidney:	n/a
13	chr19:43099482-43099532	AG04450	lung:	fetal
14	chr19:43099845-43099895	AG04450	lung:	fetal
15	chr19:43099046-43099096	GM12891	blood:	n/a
16	chr19:43099795-43099845	HAEpiC	amniotic membrane:	n/a
17	chr19:43099482-43099532	H1-hESC	embryonic stem cell:	embryo
18	chr19:43099124-43099174	HEEpiC	esophagus:	n/a
19	chr19:43099046-43099096	IMR90	lung:	fetal
20	chr19:43099795-43099845	H1-hESC	embryonic stem cell:	embryo
21	chr19:43099845-43099895	HPAEpiC	pulmonary alveolar:	n/a
22	chr19:43099845-43099895	MCF-7	breast:	n/a
23	chr19:43099845-43099895	AoSMC	blood vessel:	n/a
24	chr19:43099124-43099174	HEK293	kidney:	embryo
25	chr19:43085416-43085466	ovcar-3	ovarian:	n/a
26	chr19:43085416-43085466	U87	brain:	n/a
27	chr19:43099795-43099845	MCF10A-Er-Src	breast:	n/a
28	chr19:43099482-43099532	NB4	blood:	n/a
29	chr19:43085416-43085466	Hela-S3	cervix:	n/a
30	chr19:43099124-43099174	H1-hESC	embryonic stem cell:	embryo
31	chr19:43099046-43099096	AG09319	gingival:	n/a
32	chr19:43099795-43099845	SK-N-MC	brain:	n/a
33	chr19:43099795-43099845	SAEC	small airway:	n/a
34	chr19:43099482-43099532	RPTEC	kidney:	n/a
35	chr19:43099124-43099174	GM12892	blood:	n/a
36	chr19:43099124-43099174	GM12878	blood:	n/a
37	chr19:43099795-43099845	GM19239	blood:	n/a
38	chr19:43099482-43099532	SK-N-MC	brain:	n/a
39	chr19:43099795-43099845	ovcar-3	ovarian:	n/a
40	chr19:43099124-43099174	HNPCEpiC	eye:	n/a
41	chr19:43099482-43099532	HPAEpiC	pulmonary alveolar:	n/a
42	chr19:43099046-43099096	HRCEpiC	kidney:	n/a
43	chr19:43099845-43099895	SK-N-SH	brain:	n/a
44	chr19:43099845-43099895	GM12878	blood:	n/a
45	chr19:43099482-43099532	ovcar-3	ovarian:	n/a
46	chr19:43099046-43099096	Caco-2	colon:	n/a
47	chr19:43099124-43099174	Jurkat	blood:	n/a
48	chr19:43085416-43085466	NHBE	bronchial:	n/a
49	chr19:43099795-43099845	LNCaP	prostate:	n/a
50	chr19:43099482-43099532	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
2	chr19:43067242..43067993-chr19:43100482..43101078,2	MCF-7	breast:
3	chr19:43139154..43139986-chr19:43246322..43246897,2	MCF-7	breast:
4	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
5	chr19:43070688..43071772-chr19:43100056..43100921,4	MCF-7	breast:
6	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
7	chr19:42954441..42955205-chr19:43100309..43101289,2	MCF-7	breast:
8	chr19:43092830..43095599-chr19:43097248..43100120,2	K562	blood:
9	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
10	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
11	chr19:43149390..43151656-chr19:43158079..43159963,2	MCF-7	breast:
12	chr19:42633464..42636070-chr19:43108015..43110975,2	K562	blood:
13	chr19:43068393..43071134-chr19:43075524..43077066,2	MCF-7	breast:
14	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:
15	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
16	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
17	chr19:43118862..43121094-chr19:43122600..43124613,2	K562	blood:
18	chr19:43110594..43111450-chr19:43197610..43198160,2	MCF-7	breast:
19	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
20	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
21	chr19:42965246..42967758-chr19:43079335..43081443,2	MCF-7	breast:
22	chr19:43148558..43149434-chr20:53015100..53015659,2	MCF-7	breast:
23	chr19:43086009..43087735-chr19:43091658..43093226,2	MCF-7	breast:
24	chr19:43070787..43071783-chr19:43100383..43100953,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011497.1-2	chr19:43155869-43156816	NONHSAT066564
2	lnc-AC011497.1-2	chr19:43155388-43155602	NONHSAT066564
3	lnc-AC011497.1-2	chr19:43155239-43156507	ENSG00000213904.4
4	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066548
5	lnc-AC011497.1-2	chr19:43155239-43156171	ENSG00000213904.4
6	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066551

Variant related genes	Relation type
CEACAMP1	TF binding region
RPS10P28	TF binding region
CEACAM8	TF binding region
CEACAMP5	TF binding region
CEACAMP1	CpG island
RPS10P28	CpG island
CEACAM8	CpG island
CEACAMP5	CpG island
ENSG00000124469	chromatin interactions
ENSG00000231561	chromatin interactions

Extended variants
information (count: 3014 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3014 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532775037	chr19:43076110-43076111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552856515	chr19:43076171-43076172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148844761	chr19:43076187-43076188	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs528834979	chr19:43076205-43076206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs77064880	chr19:43076219-43076220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs77704314	chr19:43076220-43076221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560222942	chr19:43076224-43076225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547075864	chr19:43076250-43076251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376509153	chr19:43076263-43076264	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567282733	chr19:43076271-43076272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191269419	chr19:43076305-43076306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182735243	chr19:43076306-43076307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs143471828	chr19:43076341-43076342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs186074844	chr19:43076435-43076436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560786459	chr19:43076439-43076440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs192054359	chr19:43076481-43076482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs7255271	chr19:43076494-43076495	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs370139236	chr19:43076500-43076501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183317470	chr19:43076552-43076553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs374903997	chr19:43076564-43076565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574790203	chr19:43076610-43076611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs543522993	chr19:43076634-43076635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs11668460	chr19:43076647-43076648	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs577472854	chr19:43076648-43076649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs3997125	chr19:43076656-43076657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs146781335	chr19:43076681-43076682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs60716283	chr19:43076685-43076686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546403242	chr19:43076707-43076708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs560016112	chr19:43076731-43076732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78372099	chr19:43076768-43076769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs113241728	chr19:43076803-43076804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187782721	chr19:43076815-43076816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144027043	chr19:43076875-43076876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs192163904	chr19:43076883-43076884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549580133	chr19:43076944-43076945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs376526223	chr19:43076958-43076959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569424354	chr19:43077029-43077030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532107666	chr19:43077060-43077061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551953366	chr19:43077117-43077118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565582177	chr19:43077154-43077155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs534575733	chr19:43077155-43077156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs573787566	chr19:43077220-43077221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569233506	chr19:43077257-43077258	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548946981	chr19:43077313-43077314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs568336186	chr19:43077330-43077331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112233547	chr19:43077357-43077358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537469693	chr19:43077391-43077392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs147292606	chr19:43077404-43077405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182883853	chr19:43077425-43077426	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188135165	chr19:43077448-43077449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD

Chromatin state (count:197 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43071000-43076200	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr19:43072400-43084200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr19:43073600-43078800	Weak transcription	Primary B cells from cord blood	blood
4	chr19:43074600-43076200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr19:43075600-43076200	Enhancers	Primary hematopoietic stem cells	blood
6	chr19:43076200-43080400	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr19:43076200-43080600	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr19:43077000-43077800	Weak transcription	Small Intestine	intestine
9	chr19:43077400-43078400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr19:43077600-43077800	Enhancers	Colonic Mucosa	Colon
11	chr19:43077600-43078200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr19:43077600-43078200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr19:43077600-43078200	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr19:43077600-43078200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr19:43077600-43078400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr19:43077600-43079400	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr19:43077800-43078200	Enhancers	Small Intestine	intestine
18	chr19:43078000-43078200	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr19:43078200-43080200	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr19:43078800-43081800	Enhancers	Primary B cells from peripheral blood	blood
21	chr19:43078800-43082400	Enhancers	Primary B cells from cord blood	blood
22	chr19:43079400-43079800	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr19:43079800-43081000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr19:43080200-43081800	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr19:43080400-43081600	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr19:43080600-43080800	Enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr19:43080600-43081800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr19:43081000-43081200	Enhancers	Sigmoid Colon	Sigmoid Colon
29	chr19:43081000-43081200	Enhancers	Small Intestine	intestine
30	chr19:43081000-43081400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr19:43081000-43081400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr19:43081000-43081400	Enhancers	Spleen	Spleen
33	chr19:43081000-43081800	Enhancers	Adipose Nuclei	Adipose
34	chr19:43081000-43081800	Enhancers	Colonic Mucosa	Colon
35	chr19:43081000-43081800	Enhancers	Fetal Intestine Large	intestine
36	chr19:43081200-43081600	Enhancers	Primary hematopoietic stem cells	blood
37	chr19:43081400-43082600	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr19:43081400-43100600	Weak transcription	Spleen	Spleen
39	chr19:43081600-43081800	Enhancers	Small Intestine	intestine
40	chr19:43081600-43082200	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr19:43082200-43082600	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr19:43082600-43083600	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr19:43083600-43083800	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr19:43084200-43084800	Genic enhancers	Primary neutrophils fromperipheralblood	blood
45	chr19:43084800-43085400	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr19:43085400-43086200	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr19:43086200-43088000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
48	chr19:43088000-43092200	Enhancers	Primary neutrophils fromperipheralblood	blood
49	chr19:43088400-43088800	Bivalent Enhancer	Primary B cells from cord blood	blood
50	chr19:43088400-43089400	Enhancers	Primary monocytes fromperipheralblood	blood

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