Variant report

Variant	nsv2483
Chromosome Location	chr19:40340641-40435505
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1385)
CpG islands
(count:2868)
Chromatin interactive
region (count:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1385 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:40388564-40388584	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:40372209-40372386	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:40377903-40377918	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:40415611-40415775	HepG2	liver:	n/a	n/a
5	ATF1	chr19:40372283-40372483	K562	blood:	n/a	n/a
6	ATF2	chr19:40372203-40372491	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr19:40372199-40372449	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr19:40415366-40416097	A549	lung:	n/a	n/a
9	ATF3	chr19:40415390-40416029	A549	lung:	n/a	n/a
10	BCL11A	chr19:40404210-40404647	GM12878	blood:	n/a	chr19:40404401-40404414
11	BCL11A	chr19:40372229-40372663	GM12878	blood:	n/a	chr19:40372417-40372430
12	BCL3	chr19:40412323-40412529	GM12878	blood:	n/a	n/a
13	BCL3	chr19:40411970-40412242	GM12878	blood:	n/a	n/a
14	BCL3	chr19:40414546-40416122	A549	lung:	n/a	n/a
15	BCL3	chr19:40415371-40416066	A549	lung:	n/a	n/a
16	BCL3	chr19:40412032-40412240	GM12878	blood:	n/a	n/a
17	BCL3	chr19:40412289-40412518	GM12878	blood:	n/a	n/a
18	BHLHE40	chr19:40372341-40372378	HepG2	liver:	n/a	n/a
19	BHLHE40	chr19:40404194-40404362	GM12878	blood:	n/a	n/a
20	BHLHE40	chr19:40393689-40394027	HepG2	liver:	n/a	n/a
21	BHLHE40	chr19:40378004-40378342	HepG2	liver:	n/a	n/a
22	BHLHE40	chr19:40372310-40372375	K562	blood:	n/a	n/a
23	BHLHE40	chr19:40353783-40353941	K562	blood:	n/a	chr19:40353876-40353885 chr19:40353876-40353885 chr19:40353874-40353887 chr19:40353870-40353891 chr19:40353877-40353886
24	BHLHE40	chr19:40372174-40372382	GM12878	blood:	n/a	n/a
25	CBX3	chr19:40372094-40372533	K562	blood:	n/a	n/a
26	CBX3	chr19:40404078-40404473	K562	blood:	n/a	n/a
27	CEBPB	chr19:40388532-40388555	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:40432285-40432601	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr19:40354870-40355111	IMR90	lung:	n/a	n/a
30	CEBPB	chr19:40415560-40415709	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:40415296-40415956	A549	lung:	n/a	n/a
32	CEBPB	chr19:40432352-40432552	K562	blood:	n/a	n/a
33	CEBPB	chr19:40354824-40355043	K562	blood:	n/a	n/a
34	CEBPB	chr19:40402641-40402841	A549	lung:	n/a	chr19:40402707-40402718
35	CEBPB	chr19:40415310-40416215	A549	lung:	n/a	n/a
36	CEBPB	chr19:40354843-40355101	A549	lung:	n/a	n/a
37	CEBPB	chr19:40353775-40353778	K562	blood:	n/a	n/a
38	CEBPB	chr19:40369307-40369516	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:40425680-40425779	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:40415410-40415896	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr19:40354800-40355128	K562	blood:	n/a	n/a
42	CEBPB	chr19:40402564-40402888	HepG2	liver:	n/a	chr19:40402707-40402718
43	CEBPB	chr19:40402580-40402849	IMR90	lung:	n/a	chr19:40402707-40402718
44	CEBPB	chr19:40354817-40355067	K562	blood:	n/a	n/a
45	CEBPB	chr19:40413769-40413876	A549	lung:	n/a	n/a
46	CEBPB	chr19:40402703-40402726	H1-hESC	embryonic stem cell:	n/a	chr19:40402707-40402718
47	CEBPB	chr19:40415381-40416017	A549	lung:	n/a	n/a
48	CEBPB	chr19:40402571-40402768	K562	blood:	n/a	chr19:40402707-40402718
49	CHD2	chr19:40349294-40349313	K562	blood:	n/a	n/a
50	CHD2	chr19:40388541-40388748	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2868 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40364151-40364201	BE2_C	brain:	n/a
2	chr19:40364151-40364201	BE2_C	brain:	n/a
3	chr19:40366607-40366657	HCT-116	colon:	n/a
4	chr19:40396538-40396588	HAEpiC	amniotic membrane:	n/a
5	chr19:40359249-40359299	HUVEC	blood vessel:	n/a
6	chr19:40408707-40408757	T-47D	breast:	n/a
7	chr19:40375973-40376023	HRE	kidney:	n/a
8	chr19:40364151-40364201	U87	brain:	n/a
9	chr19:40366088-40366138	AG04450	lung:	fetal
10	chr19:40420037-40420087	SK-N-SH	brain:	n/a
11	chr19:40408707-40408757	AG09309	skin:	n/a
12	chr19:40398384-40398434	PFSK-1	brain:	n/a
13	chr19:40380319-40380369	RPTEC	kidney:	n/a
14	chr19:40380319-40380369	HRCEpiC	kidney:	n/a
15	chr19:40391320-40391370	AG04450	lung:	fetal
16	chr19:40391320-40391370	HEEpiC	esophagus:	n/a
17	chr19:40360856-40360906	HL-60	blood:	n/a
18	chr19:40408707-40408757	HMEC	breast:	n/a
19	chr19:40372977-40373027	GM12891	blood:	n/a
20	chr19:40379680-40379730	HCF	heart:	n/a
21	chr19:40362773-40362823	HepG2	liver:	n/a
22	chr19:40421700-40421750	U87	brain:	n/a
23	chr19:40392568-40392618	PANC-1	pancreas:	n/a
24	chr19:40392568-40392618	HMEC	breast:	n/a
25	chr19:40363285-40363335	H1-hESC	embryonic stem cell:	embryo
26	chr19:40364151-40364201	AG04449	skin:	fetal
27	chr19:40431111-40431161	SK-N-SH	brain:	n/a
28	chr19:40376883-40376933	Hela-S3	cervix:	n/a
29	chr19:40391320-40391370	U87	brain:	n/a
30	chr19:40399454-40399504	GM19239	blood:	n/a
31	chr19:40359249-40359299	HCF	heart:	n/a
32	chr19:40362773-40362823	T-47D	breast:	n/a
33	chr19:40411970-40412020	Caco-2	colon:	n/a
34	chr19:40399454-40399504	BE2_C	brain:	n/a
35	chr19:40420037-40420087	SK-N-MC	brain:	n/a
36	chr19:40393119-40393169	HNPCEpiC	eye:	n/a
37	chr19:40376883-40376933	NT2-D1	testis:	n/a
38	chr19:40364151-40364201	HEEpiC	esophagus:	n/a
39	chr19:40396032-40396082	SAEC	small airway:	n/a
40	chr19:40340835-40340885	AG09309	skin:	n/a
41	chr19:40430433-40430483	NT2-D1	testis:	n/a
42	chr19:40380319-40380369	HCT-116	colon:	n/a
43	chr19:40380853-40380903	A549	lung:	n/a
44	chr19:40429988-40430038	AG09309	skin:	n/a
45	chr19:40368363-40368413	ovcar-3	ovarian:	n/a
46	chr19:40391320-40391370	PrEC	prostate:	n/a
47	chr19:40377434-40377484	MCF10A-Er-Src	breast:	n/a
48	chr19:40410325-40410375	A549	lung:	n/a
49	chr19:40377434-40377484	HRPEpiC	eye:	n/a
50	chr19:40421453-40421503	Hela-S3	cervix:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40419026..40420915-chr19:40421238..40424178,2	K562	blood:
2	chr19:40327985..40330266-chr19:40338198..40340868,2	MCF-7	breast:
3	chr19:40337506..40339114-chr19:40356435..40358897,2	MCF-7	breast:
4	chr19:40424412..40427269-chr19:40428969..40431145,2	K562	blood:
5	chr19:40338036..40340893-chr19:40348527..40351769,3	MCF-7	breast:
6	chr19:40335743..40338422-chr19:40339936..40343829,5	MCF-7	breast:
7	chr19:40350892..40352430-chr19:40476216..40478037,2	K562	blood:
8	chr19:40337132..40339013-chr19:40340235..40342919,2	MCF-7	breast:
9	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:
10	chr19:40333922..40335627-chr19:40352940..40355252,2	K562	blood:
11	chr19:40371880..40372846-chr19:40476486..40477439,2	MCF-7	breast:
12	chr19:40345236..40348068-chr19:40350382..40353367,3	K562	blood:
13	chr19:40322768..40325198-chr19:40344061..40345998,2	K562	blood:
14	chr19:40335929..40339892-chr19:40340090..40345342,6	K562	blood:
15	chr19:40417302..40418803-chr19:40438310..40440290,2	K562	blood:
16	chr19:40345236..40348068-chr19:40350382..40353367,3	K562	blood:
17	chr19:40337126..40339206-chr19:40352976..40355937,2	K562	blood:
18	chr19:40414305..40416214-chr19:40418924..40420802,2	K562	blood:
19	chr19:40335567..40338351-chr19:40347856..40350907,4	MCF-7	breast:
20	chr19:40419026..40420915-chr19:40421238..40424178,2	K562	blood:
21	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
22	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
23	chr19:40403844..40404724-chr19:40476336..40477181,3	MCF-7	breast:
24	chr19:40430563..40432420-chr19:40476488..40478585,2	K562	blood:
25	chr19:40414305..40416214-chr19:40418924..40420802,2	K562	blood:
26	chr19:40338036..40340893-chr19:40348527..40351769,3	MCF-7	breast:
27	chr19:40371890..40372866-chr19:40388384..40389142,3	MCF-7	breast:
28	chr19:40343735..40346295-chr19:40347078..40349470,2	MCF-7	breast:
29	chr19:40413091..40415843-chr19:40476143..40478695,2	K562	blood:
30	chr19:40340776..40343743-chr19:40345587..40347160,2	K562	blood:
31	chr19:40335334..40338693-chr19:40343842..40347781,4	K562	blood:
32	chr19:40357371..40360227-chr19:40360263..40362766,2	MCF-7	breast:
33	chr19:40343735..40346295-chr19:40347078..40349470,2	MCF-7	breast:
34	chr19:40424412..40427269-chr19:40428969..40431145,2	K562	blood:
35	chr19:40340776..40343743-chr19:40345587..40347160,2	K562	blood:
36	chr19:40432414..40434132-chr19:40502600..40505156,2	K562	blood:
37	chr19:40351689..40354731-chr19:40355566..40357616,3	K562	blood:

No data

Variant related genes	Relation type
FBL	TF binding region
FCGBP	TF binding region
FBL	CpG island
FCGBP	CpG island
ENSG00000187187	chromatin interactions
ENSG00000105202	chromatin interactions
ENSG00000013275	chromatin interactions
ENSG00000105204	chromatin interactions

Extended variants
information (count: 4195 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4195 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371096979	chr19:40340643-40340644	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs191867845	chr19:40340676-40340677	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs59576508	chr19:40340687-40340688	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs536637226	chr19:40340688-40340689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs530278231	chr19:40340698-40340699	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs548902973	chr19:40340701-40340702	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184225558	chr19:40340702-40340703	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537092426	chr19:40340724-40340725	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs372898505	chr19:40340728-40340729	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs558254961	chr19:40340809-40340810	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145307100	chr19:40340819-40340820	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568691064	chr19:40340823-40340824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564774969	chr19:40340835-40340836	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs62106887	chr19:40340885-40340886	Weak transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs574293257	chr19:40340890-40340891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541619054	chr19:40340897-40340898	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs137862283	chr19:40340909-40340910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs368832428	chr19:40340933-40340934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs575431923	chr19:40340958-40340959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs79407257	chr19:40340962-40340963	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs371436528	chr19:40340967-40340968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs189588070	chr19:40341035-40341036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs180914704	chr19:40341036-40341037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113760642	chr19:40341056-40341057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10048486	chr19:40341110-40341111	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs200017708	chr19:40341111-40341112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs113869684	chr19:40341147-40341148	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564044905	chr19:40341148-40341149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372178436	chr19:40341153-40341154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs185580086	chr19:40341155-40341156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376856328	chr19:40341187-40341188	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs145511552	chr19:40341249-40341250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs148437026	chr19:40341258-40341259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs567803327	chr19:40341266-40341267	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373443784	chr19:40341295-40341296	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558286717	chr19:40341306-40341307	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs34856063	chr19:40341368-40341369	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs397796333	chr19:40341383-40341384	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189480427	chr19:40341388-40341389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374659873	chr19:40341477-40341478	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs575366952	chr19:40341507-40341508	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201571791	chr19:40341514-40341515	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs544133642	chr19:40341515-40341516	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs74487670	chr19:40341527-40341528	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75991463	chr19:40341529-40341530	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs368436730	chr19:40341559-40341560	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs539366284	chr19:40341566-40341567	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs181472381	chr19:40341571-40341572	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs369372876	chr19:40341625-40341626	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs557991481	chr19:40341627-40341628	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
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
Lung cancer	21569311	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
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40338000-40341400	Weak transcription	Hela-S3	cervix
2	chr19:40338400-40341400	Weak transcription	A549	lung
3	chr19:40339800-40341600	Weak transcription	K562	blood
4	chr19:40340400-40340800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr19:40341400-40341800	Enhancers	Hela-S3	cervix
6	chr19:40341400-40342400	Enhancers	A549	lung
7	chr19:40341600-40342000	Enhancers	K562	blood
8	chr19:40341800-40342000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr19:40348600-40348800	Enhancers	Primary T cells from cord blood	blood
10	chr19:40348600-40348800	Enhancers	Dnd41	blood
11	chr19:40348800-40349000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:40348800-40349200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
13	chr19:40348800-40349200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
14	chr19:40348800-40349200	Flanking Active TSS	Primary T cells from cord blood	blood
15	chr19:40348800-40349800	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr19:40348800-40349800	Flanking Active TSS	Dnd41	blood
17	chr19:40348800-40349800	Active TSS	K562	blood
18	chr19:40349000-40349200	Active TSS	Brain Angular Gyrus	brain
19	chr19:40349000-40349400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr19:40349000-40349400	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
21	chr19:40349000-40349400	Active TSS	Right Atrium	heart
22	chr19:40349000-40349800	Active TSS	H9 Cell Line	embryonic stem cell
23	chr19:40349000-40349800	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
24	chr19:40349000-40349800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr19:40349000-40349800	Active TSS	Brain Anterior Caudate	brain
26	chr19:40349200-40349400	Flanking Active TSS	Brain Angular Gyrus	brain
27	chr19:40349200-40349400	Active TSS	Colonic Mucosa	Colon
28	chr19:40349200-40349400	Enhancers	Placenta	Placenta
29	chr19:40349200-40349800	Active TSS	iPS-15b Cell Line	embryonic stem cell
30	chr19:40349200-40349800	Enhancers	Primary T cells from cord blood	blood
31	chr19:40349400-40349800	Active TSS	Primary T cells fromperipheralblood	blood
32	chr19:40349400-40350000	Weak transcription	Placenta	Placenta
33	chr19:40349400-40354400	Weak transcription	Colonic Mucosa	Colon
34	chr19:40349800-40350400	Enhancers	Dnd41	blood
35	chr19:40349800-40353600	Weak transcription	Primary T cells from cord blood	blood
36	chr19:40349800-40356000	Weak transcription	Primary T cells fromperipheralblood	blood
37	chr19:40349800-40357400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:40349800-40369000	Weak transcription	Brain Anterior Caudate	brain
39	chr19:40350000-40350600	Enhancers	Placenta	Placenta
40	chr19:40350200-40353400	Weak transcription	Fetal Intestine Small	intestine
41	chr19:40350400-40372200	Weak transcription	Dnd41	blood
42	chr19:40350600-40365200	Weak transcription	Placenta	Placenta
43	chr19:40350800-40351000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr19:40350800-40353400	Weak transcription	Fetal Stomach	stomach
45	chr19:40351000-40361000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr19:40351200-40353600	Weak transcription	Rectal Mucosa Donor 31	rectum
47	chr19:40351400-40353400	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr19:40351600-40353400	Weak transcription	Stomach Mucosa	stomach
49	chr19:40351600-40353800	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr19:40351600-40357200	Weak transcription	Primary B cells from cord blood	blood

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