Variant report

Variant	nsv978907
Chromosome Location	chr19:35987077-35993083
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:128)
CpG islands
(count:244)
Chromatin interactive
region (count:14)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:128 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr19:35989944-35990140	K562	blood:	n/a	n/a
2	BHLHE40	chr19:35991450-35991583	K562	blood:	n/a	n/a
3	CEBPB	chr19:35992792-35993090	IMR90	lung:	n/a	n/a
4	CEBPB	chr19:35992790-35993048	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr19:35992898-35993056	A549	lung:	n/a	n/a
6	CTCF	chr19:35988526-35988763	K562	blood:	n/a	n/a
7	CTCF	chr19:35988560-35988710	Caco-2	colon:	n/a	n/a
8	CTCF	chr19:35988640-35988790	HCPEpiC	choroid plexus:	n/a	n/a
9	CTCF	chr19:35988560-35988710	BJ	skin:	n/a	n/a
10	CTCF	chr19:35988634-35988710	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr19:35988580-35988730	NHDF-neo	bronchial:	n/a	n/a
12	CTCF	chr19:35988580-35988730	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr19:35988520-35988670	HEK293	kidney:	n/a	n/a
14	CTCF	chr19:35988641-35988654	MCF-7	breast:	n/a	n/a
15	CTCF	chr19:35992918-35992967	Kidney_OC	kidney:	n/a	n/a
16	CTCF	chr19:35988638-35988679	MCF-7	breast:	n/a	n/a
17	CTCF	chr19:35988560-35988710	AG09309	skin:	n/a	n/a
18	CTCF	chr19:35986960-35987110	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr19:35988560-35988710	K562	blood:	n/a	n/a
20	CTCF	chr19:35988566-35988795	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr19:35988640-35988675	MCF-7	breast:	n/a	n/a
22	CTCF	chr19:35986940-35987230	GM12868	blood:	n/a	n/a
23	CTCF	chr19:35985678-35987248	A549	lung:	n/a	n/a
24	CTCF	chr19:35986940-35987090	AG04449	skin:	n/a	n/a
25	CTCF	chr19:35988584-35988763	K562	blood:	n/a	n/a
26	CTCF	chr19:35988600-35988750	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr19:35988660-35988810	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr19:35987074-35987100	GM19240	blood:	n/a	n/a
29	CTCF	chr19:35988599-35988687	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr19:35988620-35988770	GM06990	blood:	n/a	n/a
31	CTCF	chr19:35987040-35987190	GM12873	blood:	n/a	n/a
32	CTCF	chr19:35988580-35988730	HPF	lung:	n/a	n/a
33	E2F6	chr19:35988456-35988559	K562	blood:	n/a	n/a
34	ESR1	chr19:35992213-35992526	ECC-1	luminal epithelium:	n/a	n/a
35	ESR1	chr19:35992155-35992873	ECC-1	luminal epithelium:	n/a	n/a
36	ESR1	chr19:35992128-35992892	ECC-1	luminal epithelium:	n/a	n/a
37	ESR1	chr19:35992150-35992770	ECC-1	luminal epithelium:	n/a	n/a
38	ESR1	chr19:35992242-35992539	ECC-1	luminal epithelium:	n/a	n/a
39	ESR1	chr19:35992258-35992474	ECC-1	luminal epithelium:	n/a	n/a
40	FOS	chr19:35992749-35993042	MCF10A-Er-Src	breast:	n/a	chr19:35993024-35993033
41	FOS	chr19:35992741-35993042	MCF10A-Er-Src	breast:	n/a	chr19:35993024-35993033
42	FOS	chr19:35992713-35993047	MCF10A-Er-Src	breast:	n/a	chr19:35993024-35993033
43	FOS	chr19:35992745-35993042	MCF10A-Er-Src	breast:	n/a	chr19:35993024-35993033
44	GATA1	chr19:35992923-35993396	K562	blood:	n/a	n/a
45	GATA3	chr19:35992943-35993463	MCF-7	breast:	n/a	n/a
46	GATA3	chr19:35992958-35993293	MCF-7	breast:	n/a	n/a
47	HMGN3	chr19:35992625-35992800	K562	blood:	n/a	n/a
48	JUND	chr19:35992797-35992905	K562	blood:	n/a	n/a
49	MAFK	chr19:35990172-35990303	K562	blood:	n/a	n/a
50	MAX	chr19:35988566-35988761	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35991319-35991369	SKMC	muscle:	n/a
2	chr19:35992883-35992933	HIPEpiC	eye:	n/a
3	chr19:35992791-35992841	NT2-D1	testis:	n/a
4	chr19:35992791-35992841	HL-60	blood:	n/a
5	chr19:35991319-35991369	HL-60	blood:	n/a
6	chr19:35992984-35993034	Hepatocyte	liver:	n/a
7	chr19:35992791-35992841	MCF10A-Er-Src	breast:	n/a
8	chr19:35992791-35992841	A549	lung:	n/a
9	chr19:35992791-35992841	HPAEpiC	pulmonary alveolar:	n/a
10	chr19:35992883-35992933	HCPEpiC	choroid plexus:	n/a
11	chr19:35992883-35992933	HNPCEpiC	eye:	n/a
12	chr19:35992883-35992933	SK-N-SH	brain:	n/a
13	chr19:35992883-35992933	NB4	blood:	n/a
14	chr19:35992984-35993034	A549	lung:	n/a
15	chr19:35992791-35992841	HEK293	kidney:	embryo
16	chr19:35992984-35993034	H1-hESC	embryonic stem cell:	embryo
17	chr19:35991319-35991369	GM19239	blood:	n/a
18	chr19:35992791-35992841	HCT-116	colon:	n/a
19	chr19:35991319-35991369	AG04450	lung:	fetal
20	chr19:35992791-35992841	AG04449	skin:	fetal
21	chr19:35992791-35992841	HRCEpiC	kidney:	n/a
22	chr19:35992984-35993034	MCF-7	breast:	n/a
23	chr19:35991319-35991369	AG10803	skin:	n/a
24	chr19:35991319-35991369	HCT-116	colon:	n/a
25	chr19:35992984-35993034	CMK	blood:	n/a
26	chr19:35992883-35992933	GM06990	blood:	n/a
27	chr19:35992883-35992933	GM19239	blood:	n/a
28	chr19:35992791-35992841	HCF	heart:	n/a
29	chr19:35991319-35991369	T-47D	breast:	n/a
30	chr19:35992883-35992933	T-47D	breast:	n/a
31	chr19:35992984-35993034	HRCEpiC	kidney:	n/a
32	chr19:35992791-35992841	IMR90	lung:	fetal
33	chr19:35992883-35992933	RPTEC	kidney:	n/a
34	chr19:35992984-35993034	HCM	heart:	n/a
35	chr19:35992791-35992841	NHBE	bronchial:	n/a
36	chr19:35992791-35992841	PrEC	prostate:	n/a
37	chr19:35992791-35992841	SK-N-MC	brain:	n/a
38	chr19:35992984-35993034	NHBE	bronchial:	n/a
39	chr19:35992883-35992933	ProgFib	skin:	n/a
40	chr19:35991319-35991369	PFSK-1	brain:	n/a
41	chr19:35992791-35992841	LNCaP	prostate:	n/a
42	chr19:35991319-35991369	AoSMC	blood vessel:	n/a
43	chr19:35992883-35992933	HCF	heart:	n/a
44	chr19:35992984-35993034	Hela-S3	cervix:	n/a
45	chr19:35992791-35992841	Hela-S3	cervix:	n/a
46	chr19:35992883-35992933	SK-N-MC	brain:	n/a
47	chr19:35991319-35991369	HIPEpiC	eye:	n/a
48	chr19:35992883-35992933	SAEC	small airway:	n/a
49	chr19:35992883-35992933	Hepatocyte	liver:	n/a
50	chr19:35992883-35992933	MCF-7	breast:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35989496..35991210-chr19:35992693..35995113,2	K562	blood:
2	chr19:35985467..35988273-chr19:35990400..35992597,2	K562	blood:
3	chr19:35985581..35988105-chr19:35990432..35992271,2	MCF-7	breast:
4	chr19:35991484..35996459-chr19:35997926..36003071,7	MCF-7	breast:
5	chr19:35985581..35988105-chr19:35990432..35992271,2	MCF-7	breast:
6	chr19:35990632..35993520-chr19:36000182..36002050,2	MCF-7	breast:
7	chr19:35988209..35991439-chr19:35991792..35995590,3	MCF-7	breast:
8	chr19:35991475..35994230-chr19:35996710..35999292,3	MCF-7	breast:
9	chr19:35988209..35991439-chr19:35991792..35995590,3	MCF-7	breast:
10	chr19:35979822..35982375-chr19:35989666..35992249,2	MCF-7	breast:
11	chr19:35989496..35991210-chr19:35992693..35995113,2	K562	blood:
12	chr19:35985384..35987874-chr19:36000035..36002510,2	MCF-7	breast:
13	chr19:35985467..35988273-chr19:35990400..35992597,2	K562	blood:
14	chr19:35988445..35991063-chr19:35995324..35997117,2	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMKN-1	chr19:35989776-35990184	NONHSAT065848
2	lnc-DMKN-1	chr19:35988240-35988440	NONHSAT065848
3	lnc-DMKN-1	chr19:35988240-35988440	NONHSAT065849
4	lnc-DMKN-1	chr19:35989618-35990184	NONHSAT065849
5	lnc-DMKN-1	chr19:35993038-35993085	NONHSAT065854
6	lnc-DMKN-1	chr19:35989500-35989665	NONHSAT065848
7	lnc-DMKN-1	chr19:35988240-35988440	NONHSAT065850
8	lnc-DMKN-1	chr19:35989500-35990050	NONHSAT065850
9	lnc-DMKN-1	chr19:35988549-35988835	NONHSAT065846
10	lnc-DMKN-1	chr19:35989776-35990184	NONHSAT065851
11	lnc-DMKN-1	chr19:35990860-35991331	NONHSAT065847
12	lnc-DMKN-1	chr19:35988122-35988440	NONHSAT065846
13	lnc-DMKN-1	chr19:35989776-35990040	NONHSAT065853
14	lnc-DMKN-1	chr19:35991280-35991482	NONHSAT065854
15	lnc-DMKN-1	chr19:35990867-35990931	NONHSAT065854
16	lnc-DMKN-1	chr19:35989776-35989799	NONHSAT065847
17	lnc-DMKN-1	chr19:35988240-35988440	NONHSAT065851
18	lnc-DMKN-1	chr19:35989618-35989665	NONHSAT065851
19	lnc-DMKN-1	chr19:35988213-35988440	NONHSAT065847
20	lnc-DMKN-1	chr19:35989618-35989665	NONHSAT065847
21	lnc-DMKN-1	chr19:35988549-35988583	NONHSAT065848
22	lnc-DMKN-1	chr19:35989149-35989665	NONHSAT065853

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	DMKN	hsa-miR-93-5p	chr19:35988233-35988253
2	DMKN	hsa-miR-138-5p	chr19:35988239-35988261
3	DMKN	hsa-miR-138-5p	chr19:35988257-35988281

Variant related genes	Relation type
DMKN	TF binding region
KRTDAP	TF binding region
DMKN	CpG island
KRTDAP	CpG island
ENSG00000161249	chromatin interactions
ENSG00000188508	chromatin interactions

Extended variants
information (count: 317 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:317 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538533376	chr19:35987101-35987102	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs181023740	chr19:35987128-35987129	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs114503517	chr19:35987179-35987180	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs185000694	chr19:35987213-35987214	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs553947732	chr19:35987227-35987228	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577182617	chr19:35987230-35987231	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs191570902	chr19:35987241-35987242	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs545826367	chr19:35987260-35987261	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562522005	chr19:35987263-35987264	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs575977108	chr19:35987286-35987287	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs541713964	chr19:35987308-35987309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561555473	chr19:35987341-35987342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs527450913	chr19:35987371-35987372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs561105416	chr19:35987398-35987399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs142319145	chr19:35987427-35987428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs549847027	chr19:35987432-35987433	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs181161751	chr19:35987478-35987479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs540004223	chr19:35987487-35987488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548850478	chr19:35987495-35987496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs568659512	chr19:35987519-35987520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs10401945	chr19:35987522-35987523	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs533277285	chr19:35987526-35987527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs191406130	chr19:35987536-35987537	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs539543419	chr19:35987566-35987567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555396468	chr19:35987574-35987575	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75487965	chr19:35987585-35987586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs375694739	chr19:35987606-35987607	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs575988653	chr19:35987636-35987637	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs541726557	chr19:35987650-35987651	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs563450446	chr19:35987652-35987653	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs561807871	chr19:35987674-35987675	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs144589032	chr19:35987749-35987750	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs540905272	chr19:35987763-35987764	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs138542930	chr19:35987782-35987783	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs533098140	chr19:35987852-35987853	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543501040	chr19:35987873-35987874	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs563274732	chr19:35987909-35987910	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs113295540	chr19:35987921-35987922	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77888578	chr19:35987931-35987932	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs75052630	chr19:35987933-35987934	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs115412492	chr19:35987941-35987942	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs34431859	chr19:35987953-35987954	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs550112869	chr19:35987963-35987964	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548913247	chr19:35987973-35987974	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs11671004	chr19:35987994-35987995	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs527963570	chr19:35988018-35988019	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs371809238	chr19:35988051-35988052	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs376199776	chr19:35988053-35988054	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571015833	chr19:35988054-35988055	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539555856	chr19:35988059-35988060	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Pleomorphic liposarcoma	18784837	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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35983800-35988000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr19:35984800-35987200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:35986200-35987200	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr19:35986400-35987200	Enhancers	H1 Cell Line	embryonic stem cell
5	chr19:35986400-35989400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr19:35986400-35989800	Weak transcription	Aorta	Aorta
7	chr19:35986400-35992400	Weak transcription	Brain Anterior Caudate	brain
8	chr19:35986400-35994000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr19:35986400-35999600	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr19:35986400-36000000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr19:35986400-36000600	Weak transcription	Right Atrium	heart
12	chr19:35986600-35987800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr19:35986600-35988200	Weak transcription	Fetal Intestine Small	intestine
14	chr19:35986600-35989600	Weak transcription	Fetal Intestine Large	intestine
15	chr19:35986600-35992600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr19:35986600-35993800	Weak transcription	Spleen	Spleen
17	chr19:35986800-35988000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr19:35986800-35988600	Weak transcription	Fetal Stomach	stomach
19	chr19:35986800-35988800	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr19:35986800-35989400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr19:35986800-35989400	Weak transcription	Pancreas	Pancrea
22	chr19:35986800-35989400	Weak transcription	NHEK	skin
23	chr19:35986800-35989600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr19:35986800-35989600	Weak transcription	Lung	lung
25	chr19:35986800-35989600	Weak transcription	Ovary	ovary
26	chr19:35986800-35989800	Weak transcription	Liver	Liver
27	chr19:35986800-35989800	Weak transcription	HMEC	breast
28	chr19:35986800-35991200	Weak transcription	Esophagus	oesophagus
29	chr19:35986800-35991600	Weak transcription	Fetal Lung	lung
30	chr19:35986800-35992000	Weak transcription	GM12878-XiMat	blood
31	chr19:35986800-35992600	Weak transcription	Brain Angular Gyrus	brain
32	chr19:35986800-35995200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr19:35986800-35996400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr19:35986800-36000200	Weak transcription	Gastric	stomach
35	chr19:35986800-36000400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr19:35987000-35987800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr19:35987000-35988000	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr19:35987000-35988000	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr19:35987000-35988000	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr19:35987000-35988200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:35987000-35989000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr19:35987000-35990400	Weak transcription	HepG2	liver
43	chr19:35987000-35990800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr19:35987000-35992200	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr19:35987200-35988200	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr19:35987200-35988200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr19:35987200-35988200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr19:35987800-35992200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr19:35987800-35998200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr19:35988000-35992600	Strong transcription	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links