Variant report

Variant	nsv960874
Chromosome Location	chr19:55713386-55721747
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:763)
CpG islands
(count:366)
Chromatin interactive
region (count:25)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:763 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:55717979-55718949	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:55721138-55721896	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:55718466-55718910	K562	blood:	n/a	n/a
4	ATF1	chr19:55718505-55718877	K562	blood:	n/a	n/a
5	ATF3	chr19:55718490-55718808	K562	blood:	n/a	n/a
6	ATF3	chr19:55721152-55721965	A549	lung:	n/a	n/a
7	ATF3	chr19:55718427-55718964	K562	blood:	n/a	n/a
8	ATF3	chr19:55721371-55721907	A549	lung:	n/a	n/a
9	BCL3	chr19:55720776-55721926	A549	lung:	n/a	chr19:55720933-55720942
10	BCL3	chr19:55721190-55722026	A549	lung:	n/a	n/a
11	BCLAF1	chr19:55718344-55718923	K562	blood:	n/a	chr19:55718825-55718834
12	BHLHE40	chr19:55720899-55721920	HepG2	liver:	n/a	n/a
13	BHLHE40	chr19:55718238-55718838	K562	blood:	n/a	n/a
14	BHLHE40	chr19:55721539-55721815	HepG2	liver:	n/a	n/a
15	BRCA1	chr19:55718354-55718858	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr19:55718059-55718826	HepG2	liver:	n/a	n/a
17	BRCA1	chr19:55721268-55721886	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr19:55721204-55721562	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:55720463-55720486	HepG2	liver:	n/a	n/a
20	CBX3	chr19:55718377-55718968	K562	blood:	n/a	n/a
21	CCNT2	chr19:55718379-55718822	K562	blood:	n/a	n/a
22	CEBPB	chr19:55718412-55718752	HepG2	liver:	n/a	n/a
23	CEBPB	chr19:55721290-55721948	A549	lung:	n/a	n/a
24	CEBPB	chr19:55718563-55718751	K562	blood:	n/a	n/a
25	CEBPB	chr19:55718480-55718903	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr19:55721436-55721836	Hela-S3	cervix:	n/a	n/a
27	CEBPD	chr19:55718488-55718957	K562	blood:	n/a	n/a
28	CEBPD	chr19:55718398-55718929	HepG2	liver:	n/a	n/a
29	CEBPD	chr19:55720271-55720527	HepG2	liver:	n/a	n/a
30	CEBPD	chr19:55718549-55718849	HepG2	liver:	n/a	n/a
31	CEBPD	chr19:55720334-55720514	HepG2	liver:	n/a	n/a
32	CHD2	chr19:55718417-55718788	K562	blood:	n/a	n/a
33	CHD2	chr19:55721144-55721780	HepG2	liver:	n/a	n/a
34	CHD2	chr19:55718388-55718867	Hela-S3	cervix:	n/a	n/a
35	CHD2	chr19:55718040-55718891	HepG2	liver:	n/a	n/a
36	CREB1	chr19:55718450-55718883	A549	lung:	n/a	n/a
37	CREB1	chr19:55717909-55719011	HepG2	liver:	n/a	n/a
38	CTCF	chr19:55713660-55713810	HCFaa	heart:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
39	CTCF	chr19:55713680-55713830	GM12870	blood:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
40	CTCF	chr19:55713649-55713908	MCF-7	breast:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
41	CTCF	chr19:55713740-55713890	NHEK	skin:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
42	CTCF	chr19:55713660-55713810	NHEK	skin:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
43	CTCF	chr19:55713660-55713810	AoAF	blood vessel:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
44	CTCF	chr19:55713660-55713810	HCM	heart:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
45	CTCF	chr19:55713640-55713790	HBMEC	blood vessel:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
46	CTCF	chr19:55713505-55713962	K562	blood:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
47	CTCF	chr19:55713680-55713830	GM12868	blood:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
48	CTCF	chr19:55713592-55713979	A549	lung:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
49	CTCF	chr19:55713760-55713910	AG04449	skin:	n/a	chr19:55713766-55713784 chr19:55713769-55713777
50	CTCF	chr19:55713660-55713810	NHLF	lung:	n/a	chr19:55713766-55713784 chr19:55713769-55713777

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:55721290-55721340	Jurkat	blood:	n/a
2	chr19:55721290-55721340	HIPEpiC	eye:	n/a
3	chr19:55721290-55721340	NH-A	brain:	n/a
4	chr19:55721638-55721688	K562	blood:	n/a
5	chr19:55718589-55718639	GM06990	blood:	n/a
6	chr19:55720737-55720787	ovcar-3	ovarian:	n/a
7	chr19:55721180-55721230	AoSMC	blood vessel:	n/a
8	chr19:55721180-55721230	GM12891	blood:	n/a
9	chr19:55721638-55721688	A549	lung:	n/a
10	chr19:55720817-55720867	U87	brain:	n/a
11	chr19:55720817-55720867	ECC-1	luminal epithelium:	n/a
12	chr19:55718589-55718639	ECC-1	luminal epithelium:	n/a
13	chr19:55720817-55720867	HIPEpiC	eye:	n/a
14	chr19:55720817-55720867	HNPCEpiC	eye:	n/a
15	chr19:55721180-55721230	NT2-D1	testis:	n/a
16	chr19:55720737-55720787	HepG2	liver:	n/a
17	chr19:55721180-55721230	HCPEpiC	choroid plexus:	n/a
18	chr19:55721180-55721230	HMEC	breast:	n/a
19	chr19:55720737-55720787	Hepatocyte	liver:	n/a
20	chr19:55720817-55720867	ovcar-3	ovarian:	n/a
21	chr19:55721638-55721688	AG04449	skin:	fetal
22	chr19:55721638-55721688	AG04450	lung:	fetal
23	chr19:55721290-55721340	MCF10A-Er-Src	breast:	n/a
24	chr19:55721638-55721688	U87	brain:	n/a
25	chr19:55721180-55721230	AG04450	lung:	fetal
26	chr19:55721290-55721340	AG04449	skin:	fetal
27	chr19:55720817-55720867	MCF10A-Er-Src	breast:	n/a
28	chr19:55720737-55720787	AG10803	skin:	n/a
29	chr19:55721180-55721230	AG10803	skin:	n/a
30	chr19:55721180-55721230	Hela-S3	cervix:	n/a
31	chr19:55718589-55718639	HCM	heart:	n/a
32	chr19:55721638-55721688	PANC-1	pancreas:	n/a
33	chr19:55718589-55718639	AG04450	lung:	fetal
34	chr19:55721638-55721688	Hela-S3	cervix:	n/a
35	chr19:55718589-55718639	NH-A	brain:	n/a
36	chr19:55720737-55720787	NT2-D1	testis:	n/a
37	chr19:55720817-55720867	T-47D	breast:	n/a
38	chr19:55720817-55720867	GM12878	blood:	n/a
39	chr19:55720737-55720787	NHBE	bronchial:	n/a
40	chr19:55721180-55721230	T-47D	breast:	n/a
41	chr19:55720817-55720867	HCPEpiC	choroid plexus:	n/a
42	chr19:55721638-55721688	HNPCEpiC	eye:	n/a
43	chr19:55720817-55720867	GM06990	blood:	n/a
44	chr19:55720817-55720867	PANC-1	pancreas:	n/a
45	chr19:55721180-55721230	Jurkat	blood:	n/a
46	chr19:55720737-55720787	HL-60	blood:	n/a
47	chr19:55720817-55720867	SKMC	muscle:	n/a
48	chr19:55721638-55721688	RPTEC	kidney:	n/a
49	chr19:55720737-55720787	GM12891	blood:	n/a
50	chr19:55720737-55720787	HUVEC	blood vessel:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:55690042..55692776-chr19:55717237..55718780,2	K562	blood:
2	chr19:55717271..55720119-chr19:55971581..55974042,2	K562	blood:
3	chr19:55712362..55714079-chr19:55717109..55720117,3	K562	blood:
4	chr19:55711425..55714079-chr19:55726624..55728744,2	K562	blood:
5	chr19:55718690..55723182-chr19:55767265..55771415,7	MCF-7	breast:
6	chr19:55710077..55713946-chr19:55715041..55719503,7	K562	blood:
7	chr19:55720076..55722268-chr19:55917409..55919415,2	MCF-7	breast:
8	chr19:55717069..55718690-chr19:55897128..55899524,2	K562	blood:
9	chr19:55716986..55718493-chr19:55791632..55793332,2	MCF-7	breast:
10	chr19:55718998..55723683-chr19:55726226..55730125,7	MCF-7	breast:
11	chr19:55720239..55723202-chr19:55851102..55853910,2	MCF-7	breast:
12	chr19:55718158..55718787-chr2:70417569..70418158,2	Hela-S3	cervix:
13	chr19:55713511..55716413-chr19:55771406..55774193,2	MCF-7	breast:
14	chr19:55704482..55706178-chr19:55716110..55717616,2	K562	blood:
15	chr19:55703436..55706560-chr19:55709695..55713857,3	K562	blood:
16	chr19:55721407..55723534-chr19:55807919..55810195,2	K562	blood:
17	chr19:55720966..55723158-chr19:55759266..55761858,2	MCF-7	breast:
18	chr19:55677672..55679195-chr19:55716116..55718159,2	MCF-7	breast:
19	chr19:55684879..55686896-chr19:55721542..55723925,2	K562	blood:
20	chr19:55711944..55714084-chr19:55716574..55718347,2	MCF-7	breast:
21	chr19:55711944..55714084-chr19:55716574..55718347,2	MCF-7	breast:
22	chr19:55690518..55692757-chr19:55718822..55720568,2	K562	blood:
23	chr19:55686310..55687891-chr19:55719950..55721494,2	K562	blood:
24	chr19:55721643..55726695-chr19:55909810..55913301,8	K562	blood:
25	chr19:55720878..55730679-chr19:55764402..55774570,47	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM86B-3	chr19:55718494-55718607	NONHSAT068004
2	lnc-TMEM86B-3	chr19:55716760-55716960	NONHSAT068004
3	lnc-TMEM86B-3	chr19:55718057-55718323	NONHSAT068004

No data

Variant related genes	Relation type
PTPRH	TF binding region
PTPRH	CpG island
ENSG00000167646	chromatin interactions
ENSG00000115998	chromatin interactions
ENSG00000080031	chromatin interactions
ENSG00000239137	chromatin interactions
ENSG00000133265	chromatin interactions
ENSG00000063241	chromatin interactions
ENSG00000267093	chromatin interactions
ENSG00000267649	chromatin interactions
ENSG00000129990	chromatin interactions
ENSG00000105063	chromatin interactions
ENSG00000108107	chromatin interactions
ENSG00000133247	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000267531	chromatin interactions

Extended variants
information (count: 558 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:558 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566026099	chr19:55713399-55713400	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs149635366	chr19:55713402-55713403	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs191528719	chr19:55713410-55713411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs144253410	chr19:55713411-55713412	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs537172387	chr19:55713416-55713417	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs139848790	chr19:55713427-55713428	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs200281532	chr19:55713439-55713440	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs199931398	chr19:55713447-55713448	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs199800897	chr19:55713456-55713457	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs35748572	chr19:55713469-55713470	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs536291307	chr19:55713470-55713471	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200768477	chr19:55713475-55713476	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs145382307	chr19:55713481-55713482	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs149061932	chr19:55713483-55713484	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147691392	chr19:55713502-55713503	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140867659	chr19:55713514-55713515	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs61734208	chr19:55713521-55713522	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs151185756	chr19:55713527-55713528	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs2288515	chr19:55713535-55713536	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs370232572	chr19:55713547-55713548	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs544465704	chr19:55713586-55713587	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs563401090	chr19:55713607-55713608	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs10416122	chr19:55713614-55713615	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs146527266	chr19:55713616-55713617	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs201141668	chr19:55713636-55713637	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs377115239	chr19:55713638-55713639	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs368421898	chr19:55713645-55713646	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs140788530	chr19:55713661-55713662	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144628967	chr19:55713666-55713667	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs372445009	chr19:55713668-55713669	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs34114816	chr19:55713725-55713726	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs200731646	chr19:55713727-55713728	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12462430	chr19:55713739-55713740	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs112947122	chr19:55713762-55713763	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs12609389	chr19:55713796-55713797	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550356008	chr19:55713811-55713812	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs372941840	chr19:55713819-55713820	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs536305793	chr19:55713821-55713822	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552951647	chr19:55713823-55713824	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs112291617	chr19:55713826-55713827	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs538977714	chr19:55713831-55713832	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs35113011	chr19:55713846-55713847	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs575826655	chr19:55713848-55713849	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs544837832	chr19:55713852-55713853	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs114329352	chr19:55713885-55713886	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs8109428	chr19:55713886-55713887	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs542700337	chr19:55713914-55713915	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs373852062	chr19:55713930-55713931	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs146718002	chr19:55713960-55713961	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs59851779	chr19:55713961-55713962	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	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
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Congenital anomalies of the kidney and urinary tract	18852474	CNVD
Glioblastoma multiforme	17002787	CNVD
Cervical cancer	21062161	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	16573809	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Breast cancer	20459607	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:55691200-55718200	Weak transcription	Right Atrium	heart
2	chr19:55691600-55718200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:55691800-55717600	Strong transcription	Fetal Intestine Small	intestine
4	chr19:55692600-55717000	Strong transcription	Duodenum Mucosa	Duodenum
5	chr19:55701200-55718000	Weak transcription	A549	lung
6	chr19:55701400-55718400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:55702600-55714800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr19:55702800-55713400	Weak transcription	Small Intestine	intestine
9	chr19:55703000-55717800	Weak transcription	Hela-S3	cervix
10	chr19:55704200-55718200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr19:55704800-55717400	Strong transcription	Rectal Mucosa Donor 29	rectum
12	chr19:55705000-55714200	Strong transcription	HepG2	liver
13	chr19:55705000-55717000	Strong transcription	Sigmoid Colon	Sigmoid Colon
14	chr19:55707000-55713600	Strong transcription	Fetal Intestine Large	intestine
15	chr19:55707200-55718400	Weak transcription	Brain Angular Gyrus	brain
16	chr19:55707800-55713800	Strong transcription	K562	blood
17	chr19:55707800-55715600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr19:55707800-55717200	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr19:55708800-55720600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr19:55709400-55715800	Weak transcription	Spleen	Spleen
21	chr19:55709600-55713800	Strong transcription	Gastric	stomach
22	chr19:55710400-55718200	Weak transcription	Stomach Mucosa	stomach
23	chr19:55711600-55717200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr19:55711800-55718200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr19:55712000-55718000	Weak transcription	Colonic Mucosa	Colon
26	chr19:55712000-55718000	Weak transcription	Pancreas	Pancrea
27	chr19:55712800-55718000	Weak transcription	NHLF	lung
28	chr19:55713000-55715200	Weak transcription	Fetal Stomach	stomach
29	chr19:55713600-55715400	Weak transcription	Fetal Intestine Large	intestine
30	chr19:55713800-55715200	Weak transcription	K562	blood
31	chr19:55713800-55716000	Weak transcription	Gastric	stomach
32	chr19:55714200-55714800	Weak transcription	HepG2	liver
33	chr19:55714800-55715200	Genic enhancers	HepG2	liver
34	chr19:55714800-55717200	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr19:55715200-55716400	Strong transcription	K562	blood
36	chr19:55715200-55716600	Strong transcription	Fetal Stomach	stomach
37	chr19:55715200-55717200	Transcr. at gene 5' and 3'	HepG2	liver
38	chr19:55715400-55717200	Strong transcription	Fetal Intestine Large	intestine
39	chr19:55715600-55717800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr19:55715800-55717000	Genic enhancers	Spleen	Spleen
41	chr19:55716000-55716600	Strong transcription	Gastric	stomach
42	chr19:55716400-55717200	Genic enhancers	K562	blood
43	chr19:55716600-55718400	Weak transcription	Gastric	stomach
44	chr19:55717000-55717800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr19:55717000-55718400	Weak transcription	Spleen	Spleen
46	chr19:55717000-55720400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr19:55717200-55717400	Transcr. at gene 5' and 3'	K562	blood
48	chr19:55717200-55717600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr19:55717200-55717600	Flanking Active TSS	HepG2	liver
50	chr19:55717200-55717800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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