Variant report

Variant	nsv911767
Chromosome Location	chr19:41649516-41716271
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1512)
CpG islands
(count:980)
Chromatin interactive
region (count:47)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1512 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41672807-41673485	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41710191-41710528	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:41664953-41665409	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:41650417-41650577	K562	blood:	n/a	n/a
5	ARID3A	chr19:41682096-41682591	HepG2	liver:	n/a	n/a
6	ARID3A	chr19:41710250-41710483	K562	blood:	n/a	n/a
7	ATF1	chr19:41650377-41650629	K562	blood:	n/a	n/a
8	ATF1	chr19:41665949-41666184	K562	blood:	n/a	n/a
9	ATF2	chr19:41695217-41695700	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr19:41650238-41650641	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr19:41696179-41696649	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr19:41695148-41695700	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr19:41699149-41699377	HepG2	liver:	n/a	n/a
14	ATF3	chr19:41681806-41682604	A549	lung:	n/a	n/a
15	ATF3	chr19:41710009-41710558	A549	lung:	n/a	n/a
16	BACH1	chr19:41650392-41650566	K562	blood:	n/a	n/a
17	BATF	chr19:41706462-41706738	GM12878	blood:	n/a	chr19:41706635-41706646
18	BATF	chr19:41706506-41706767	GM12878	blood:	n/a	chr19:41706635-41706646
19	BCL3	chr19:41681572-41682628	A549	lung:	n/a	n/a
20	BCL3	chr19:41650213-41650690	A549	lung:	n/a	n/a
21	BCL3	chr19:41681514-41682747	A549	lung:	n/a	n/a
22	BCL3	chr19:41698123-41699352	A549	lung:	n/a	chr19:41698192-41698201 chr19:41699120-41699133 chr19:41698986-41698995 chr19:41698903-41698911
23	BCL3	chr19:41697854-41699470	A549	lung:	n/a	chr19:41698192-41698201 chr19:41699120-41699133 chr19:41698986-41698995 chr19:41698903-41698911
24	BCL3	chr19:41709935-41710568	A549	lung:	n/a	n/a
25	BCLAF1	chr19:41710140-41710520	GM12878	blood:	n/a	n/a
26	BHLHE40	chr19:41650454-41650612	GM12878	blood:	n/a	n/a
27	BHLHE40	chr19:41713382-41713628	K562	blood:	n/a	n/a
28	BHLHE40	chr19:41710238-41710474	K562	blood:	n/a	n/a
29	BHLHE40	chr19:41670430-41670548	K562	blood:	n/a	n/a
30	BHLHE40	chr19:41650351-41650568	K562	blood:	n/a	n/a
31	BHLHE40	chr19:41698923-41699069	K562	blood:	n/a	n/a
32	BHLHE40	chr19:41704666-41704851	K562	blood:	n/a	n/a
33	BHLHE40	chr19:41702112-41702278	GM12878	blood:	n/a	n/a
34	BRCA1	chr19:41710270-41710422	HepG2	liver:	n/a	n/a
35	BRCA1	chr19:41664942-41665424	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr19:41672882-41672907	HepG2	liver:	n/a	n/a
37	CBX3	chr19:41698667-41698955	K562	blood:	n/a	chr19:41698711-41698722
38	CBX3	chr19:41681739-41682618	HCT-116	colon:	n/a	n/a
39	CBX3	chr19:41650196-41650694	HCT-116	colon:	n/a	n/a
40	CCNT2	chr19:41698805-41699300	K562	blood:	n/a	chr19:41699012-41699032
41	CEBPB	chr19:41665817-41666220	K562	blood:	n/a	n/a
42	CEBPB	chr19:41706005-41706399	Hela-S3	cervix:	n/a	chr19:41706182-41706193
43	CEBPB	chr19:41665826-41666210	K562	blood:	n/a	n/a
44	CEBPB	chr19:41652831-41653077	K562	blood:	n/a	n/a
45	CEBPB	chr19:41693841-41694075	A549	lung:	n/a	n/a
46	CEBPB	chr19:41665004-41665316	HepG2	liver:	n/a	n/a
47	CEBPB	chr19:41706030-41706310	K562	blood:	n/a	chr19:41706182-41706193
48	CEBPB	chr19:41710238-41710551	K562	blood:	n/a	n/a
49	CEBPB	chr19:41695160-41695930	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr19:41689279-41689585	HepG2	liver:	n/a	n/a

(count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41698915-41698965	NB4	blood:	n/a
2	chr19:41698918-41698968	AG09319	gingival:	n/a
3	chr19:41698814-41698864	NT2-D1	testis:	n/a
4	chr19:41698931-41698981	AG09319	gingival:	n/a
5	chr19:41698915-41698965	NB4	blood:	n/a
6	chr19:41698918-41698968	AG09319	gingival:	n/a
7	chr19:41698814-41698864	NT2-D1	testis:	n/a
8	chr19:41698931-41698981	AG09319	gingival:	n/a
9	chr19:41713384-41713434	NHBE	bronchial:	n/a
10	chr19:41698918-41698968	NB4	blood:	n/a
11	chr19:41698906-41698956	AG04450	lung:	fetal
12	chr19:41698915-41698965	HPAEpiC	pulmonary alveolar:	n/a
13	chr19:41698918-41698968	HepG2	liver:	n/a
14	chr19:41698918-41698968	MCF-7	breast:	n/a
15	chr19:41695752-41695802	ECC-1	luminal epithelium:	n/a
16	chr19:41698915-41698965	HCM	heart:	n/a
17	chr19:41698823-41698873	HEEpiC	esophagus:	n/a
18	chr19:41699364-41699414	H1-hESC	embryonic stem cell:	embryo
19	chr19:41698987-41699037	HCF	heart:	n/a
20	chr19:41698548-41698598	HCM	heart:	n/a
21	chr19:41698548-41698598	K562	blood:	n/a
22	chr19:41698987-41699037	MCF-7	breast:	n/a
23	chr19:41698814-41698864	AG09309	skin:	n/a
24	chr19:41698823-41698873	HRE	kidney:	n/a
25	chr19:41698931-41698981	Jurkat	blood:	n/a
26	chr19:41698548-41698598	AG09319	gingival:	n/a
27	chr19:41695752-41695802	IMR90	lung:	fetal
28	chr19:41699364-41699414	LNCaP	prostate:	n/a
29	chr19:41699282-41699332	NB4	blood:	n/a
30	chr19:41695752-41695802	SK-N-SH	brain:	n/a
31	chr19:41713384-41713434	AG04450	lung:	fetal
32	chr19:41698987-41699037	HUVEC	blood vessel:	n/a
33	chr19:41699364-41699414	NT2-D1	testis:	n/a
34	chr19:41698931-41698981	K562	blood:	n/a
35	chr19:41699364-41699414	HNPCEpiC	eye:	n/a
36	chr19:41698918-41698968	RPTEC	kidney:	n/a
37	chr19:41698915-41698965	SKMC	muscle:	n/a
38	chr19:41699065-41699115	SKMC	muscle:	n/a
39	chr19:41698915-41698965	HEK293	kidney:	embryo
40	chr19:41698977-41699027	SKMC	muscle:	n/a
41	chr19:41698814-41698864	ECC-1	luminal epithelium:	n/a
42	chr19:41702153-41702203	PFSK-1	brain:	n/a
43	chr19:41698987-41699037	HAEpiC	amniotic membrane:	n/a
44	chr19:41698814-41698864	ProgFib	skin:	n/a
45	chr19:41698915-41698965	HepG2	liver:	n/a
46	chr19:41698906-41698956	CMK	blood:	n/a
47	chr19:41698915-41698965	AG09319	gingival:	n/a
48	chr19:41695752-41695802	MCF-7	breast:	n/a
49	chr19:41698814-41698864	MCF10A-Er-Src	breast:	n/a
50	chr19:41698915-41698965	AoSMC	blood vessel:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41698406..41703429-chr19:41707121..41711829,4	K562	blood:
2	chr19:41700678..41702956-chr19:41802683..41805056,2	K562	blood:
3	chr19:41708236..41711683-chr19:41767737..41770848,3	MCF-7	breast:
4	chr19:41700466..41703429-chr19:41707889..41710444,2	K562	blood:
5	chr19:41168379..41168947-chr19:41650043..41650891,2	MCF-7	breast:
6	chr19:41707770..41710442-chr19:41768632..41771124,3	K562	blood:
7	chr19:41710873..41712522-chr19:41830997..41833166,2	K562	blood:
8	chr19:41700366..41702638-chr19:41769140..41770960,2	MCF-7	breast:
9	chr19:41709766..41710945-chr19:41767825..41768718,5	MCF-7	breast:
10	chr19:41709211..41709722-chr19:41767800..41768469,2	K562	blood:
11	chr19:41709869..41710870-chr19:41767857..41768871,17	K562	blood:
12	chr19:41678854..41681708-chr19:41768595..41770762,2	MCF-7	breast:
13	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
14	chr19:41697323..41700714-chr19:41769063..41770894,3	K562	blood:
15	chr19:41711572..41712536-chr19:41767839..41768829,4	MCF-7	breast:
16	chr19:41660004..41661547-chr19:41766928..41769165,2	MCF-7	breast:
17	chr19:41698019..41700083-chr19:41767122..41769558,2	K562	blood:
18	chr19:41698406..41703429-chr19:41707121..41711829,4	K562	blood:
19	chr19:41710579..41716236-chr19:41767651..41773158,11	K562	blood:
20	chr19:41700112..41702823-chr19:41703297..41705172,2	MCF-7	breast:
21	chr19:41709626..41713446-chr19:41767553..41770209,4	MCF-7	breast:
22	chr19:41709937..41710810-chr19:41814166..41815131,2	MCF-7	breast:
23	chr19:41700466..41703429-chr19:41707889..41710444,2	K562	blood:
24	chr19:41712465..41714278-chr19:41772722..41775237,2	K562	blood:
25	chr19:41709961..41710916-chr19:41766604..41767721,3	K562	blood:
26	chr19:41710998..41712626-chr19:41765390..41767317,2	K562	blood:
27	chr19:41653070..41654935-chr19:41767041..41769003,2	MCF-7	breast:
28	chr19:41712333..41715272-chr19:41724873..41727536,3	K562	blood:
29	chr19:41676947..41678469-chr19:41769052..41771501,2	MCF-7	breast:
30	chr19:41712694..41714590-chr19:41730675..41733383,2	K562	blood:
31	chr19:41664966..41667782-chr19:41768471..41770752,2	K562	blood:
32	chr19:41700112..41702823-chr19:41703297..41705172,2	MCF-7	breast:
33	chr19:41712774..41714321-chr19:41815387..41817500,2	K562	blood:
34	chr19:41709903..41710828-chr19:41814558..41815062,3	K562	blood:
35	chr19:41698446..41700013-chr19:41702267..41703970,2	MCF-7	breast:
36	chr19:41708734..41715779-chr19:41765259..41771124,12	K562	blood:
37	chr19:41709754..41710853-chr19:41767340..41768774,11	MCF-7	breast:
38	chr19:41680953..41683356-chr19:41768146..41770884,2	MCF-7	breast:
39	chr19:41698985..41702051-chr19:41767021..41770015,3	MCF-7	breast:
40	chr19:41711877..41715272-chr19:41724756..41728311,4	K562	blood:
41	chr19:41695919..41698717-chr19:41700424..41702047,2	K562	blood:
42	chr19:41711943..41714623-chr19:41813301..41815470,3	MCF-7	breast:
43	chr19:41711670..41712535-chr19:41768074..41768746,2	MCF-7	breast:
44	chr19:41710273..41710787-chr19:41859686..41860251,2	MCF-7	breast:
45	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
46	chr19:41710333..41710841-chr19:41859735..41860515,2	K562	blood:
47	chr19:41703762..41708765-chr19:41768363..41772371,6	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TGFB1-5	chr19:41696852-41697134	NONHSAT066436

No data

Variant related genes	Relation type
RN7SL718P	TF binding region
CYP2S1	TF binding region
RPL36P16	TF binding region
RN7SL718P	CpG island
CYP2S1	CpG island
RPL36P16	CpG island
ENSG00000167600	chromatin interactions
ENSG00000105323	chromatin interactions
ENSG00000167601	chromatin interactions
ENSG00000142046	chromatin interactions
ENSG00000142039	chromatin interactions
ENSG00000269652	chromatin interactions
ENSG00000264423	chromatin interactions
ENSG00000105329	chromatin interactions

Extended variants
information (count: 2700 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2700 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182745318	chr19:41650205-41650206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147905831	chr19:41650208-41650209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs305953	chr19:41650217-41650218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547784805	chr19:41650220-41650221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs111543422	chr19:41650231-41650232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565705250	chr19:41650283-41650284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186986018	chr19:41650292-41650293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530061216	chr19:41650296-41650297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548257481	chr19:41650334-41650335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs142818356	chr19:41650335-41650336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs62119612	chr19:41650343-41650344	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs147971090	chr19:41650347-41650348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183931543	chr19:41650352-41650353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189171293	chr19:41650375-41650376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193284230	chr19:41650386-41650387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548946138	chr19:41650402-41650403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574456873	chr19:41650518-41650519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs185503714	chr19:41650553-41650554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552605897	chr19:41650558-41650559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369329667	chr19:41650562-41650563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs116171952	chr19:41650567-41650568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377238732	chr19:41650568-41650569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115386805	chr19:41650570-41650571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190308941	chr19:41650581-41650582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs375267848	chr19:41653120-41653121	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558446548	chr19:41653142-41653143	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs146760016	chr19:41653212-41653213	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs551536093	chr19:41653294-41653295	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs559193945	chr19:41653299-41653300	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140317908	chr19:41653304-41653305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574234157	chr19:41653313-41653314	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs544697595	chr19:41653336-41653337	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs112507308	chr19:41653364-41653365	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs187478089	chr19:41653365-41653366	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs144109120	chr19:41653373-41653374	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548521266	chr19:41653375-41653376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544944341	chr19:41653377-41653378	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570008464	chr19:41653388-41653389	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78017644	chr19:41653430-41653431	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191951603	chr19:41653466-41653467	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs567018510	chr19:41653505-41653506	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs531265858	chr19:41653570-41653571	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs531268491	chr19:41653590-41653591	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs58140016	chr19:41653635-41653636	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376177001	chr19:41653667-41653668	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs539150404	chr19:41653671-41653672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs369943087	chr19:41653674-41653675	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146443995	chr19:41653675-41653676	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs200120252	chr19:41653679-41653680	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs567214429	chr19:41653686-41653687	Inactive region	Chromatin interactive region	1 gene(s)	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
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
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
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1234 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41650200-41650600	Enhancers	Primary T cells fromperipheralblood	blood
2	chr19:41650400-41650600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr19:41656400-41665000	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr19:41656600-41662000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr19:41657200-41658000	Enhancers	Hela-S3	cervix
6	chr19:41658000-41660200	Weak transcription	Hela-S3	cervix
7	chr19:41660200-41660400	Enhancers	Hela-S3	cervix
8	chr19:41660400-41660800	Flanking Active TSS	Hela-S3	cervix
9	chr19:41660800-41661400	Enhancers	Hela-S3	cervix
10	chr19:41661000-41665000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr19:41661400-41663800	Weak transcription	Hela-S3	cervix
12	chr19:41662000-41662800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
13	chr19:41662200-41662600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr19:41662200-41662800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr19:41662600-41662800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
16	chr19:41662600-41678200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr19:41662800-41665000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr19:41662800-41665000	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr19:41663200-41663400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
20	chr19:41663400-41663600	Enhancers	Gastric	stomach
21	chr19:41663400-41665000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr19:41663400-41668000	Enhancers	Fetal Intestine Large	intestine
23	chr19:41663600-41665000	Weak transcription	Gastric	stomach
24	chr19:41663800-41665000	Enhancers	Hela-S3	cervix
25	chr19:41663800-41666600	Enhancers	Fetal Intestine Small	intestine
26	chr19:41664200-41675600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:41664400-41665000	Enhancers	HepG2	liver
28	chr19:41664400-41666000	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr19:41664600-41665000	Enhancers	K562	blood
30	chr19:41664600-41666600	Enhancers	Stomach Mucosa	stomach
31	chr19:41664800-41665000	Enhancers	A549	lung
32	chr19:41664800-41665800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr19:41665000-41665200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
34	chr19:41665000-41665200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr19:41665000-41665200	Enhancers	Gastric	stomach
36	chr19:41665000-41665200	Flanking Active TSS	Hela-S3	cervix
37	chr19:41665000-41665400	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr19:41665000-41665400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr19:41665000-41665400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr19:41665000-41665400	Enhancers	H9 Cell Line	embryonic stem cell
41	chr19:41665000-41665400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr19:41665000-41665400	Enhancers	Placenta	Placenta
43	chr19:41665000-41665400	Enhancers	Placenta Amnion	Placenta Amnion
44	chr19:41665000-41665400	Flanking Active TSS	A549	lung
45	chr19:41665000-41665400	Flanking Active TSS	HepG2	liver
46	chr19:41665000-41665400	Flanking Active TSS	K562	blood
47	chr19:41665000-41665800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr19:41665000-41666400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr19:41665200-41665400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr19:41665200-41665400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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