Variant report

Variant	nsv1063564
Chromosome Location	chr19:23898001-24029686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1259)
CpG islands
(count:1466)
Chromatin interactive
region (count:19)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1259 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:23946565-23946828	K562	blood:	n/a	n/a
2	ARID3A	chr19:23953533-23953728	K562	blood:	n/a	n/a
3	ARID3A	chr19:23941611-23941919	K562	blood:	n/a	n/a
4	ATF1	chr19:23941540-23941902	K562	blood:	n/a	n/a
5	ATF1	chr19:24006791-24007164	K562	blood:	n/a	n/a
6	ATF1	chr19:23958138-23958329	K562	blood:	n/a	n/a
7	BACH1	chr19:23922436-23922552	K562	blood:	n/a	n/a
8	BACH1	chr19:24000521-24000697	K562	blood:	n/a	n/a
9	BATF	chr19:23955417-23955716	GM12878	blood:	n/a	n/a
10	BATF	chr19:23967080-23967345	GM12878	blood:	n/a	n/a
11	BATF	chr19:23955472-23955714	GM12878	blood:	n/a	n/a
12	BATF	chr19:23967036-23967332	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:23968376-23968383	K562	blood:	n/a	n/a
14	BHLHE40	chr19:24006925-24007160	K562	blood:	n/a	n/a
15	BHLHE40	chr19:23911603-23911632	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:23945754-23945986	K562	blood:	n/a	n/a
17	BHLHE40	chr19:23943218-23943418	GM12878	blood:	n/a	n/a
18	BHLHE40	chr19:23941310-23941885	K562	blood:	n/a	n/a
19	CBX3	chr19:24006626-24007181	K562	blood:	n/a	n/a
20	CBX3	chr19:24006670-24007006	K562	blood:	n/a	n/a
21	CBX3	chr19:23941229-23941835	K562	blood:	n/a	n/a
22	CBX3	chr19:23945432-23946054	K562	blood:	n/a	n/a
23	CCNT2	chr19:23945563-23946451	K562	blood:	n/a	n/a
24	CEBPB	chr19:23945777-23946061	IMR90	lung:	n/a	n/a
25	CEBPB	chr19:24000487-24000738	K562	blood:	n/a	n/a
26	CEBPB	chr19:23966059-23966939	A549	lung:	n/a	chr19:23966205-23966216 chr19:23966237-23966248
27	CEBPB	chr19:23962499-23962745	IMR90	lung:	n/a	n/a
28	CEBPB	chr19:23992206-23992260	K562	blood:	n/a	n/a
29	CEBPB	chr19:23951625-23951915	HepG2	liver:	n/a	n/a
30	CEBPB	chr19:23965616-23965852	A549	lung:	n/a	chr19:23965729-23965740
31	CEBPB	chr19:23903502-23903839	IMR90	lung:	n/a	chr19:23903671-23903682
32	CEBPB	chr19:23957054-23957915	MCF-7	breast:	n/a	n/a
33	CEBPB	chr19:23903521-23903797	Hela-S3	cervix:	n/a	chr19:23903671-23903682
34	CEBPB	chr19:23959786-23960810	HepG2	liver:	n/a	n/a
35	CEBPB	chr19:23951627-23951924	A549	lung:	n/a	n/a
36	CEBPB	chr19:23967860-23968049	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:23969436-23970244	A549	lung:	n/a	n/a
38	CEBPB	chr19:23966086-23966642	K562	blood:	n/a	chr19:23966205-23966216 chr19:23966237-23966248
39	CEBPB	chr19:23959197-23959542	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr19:23940391-23940983	K562	blood:	n/a	n/a
41	CEBPB	chr19:23964650-23965334	A549	lung:	n/a	n/a
42	CEBPB	chr19:23971312-23971526	HepG2	liver:	n/a	chr19:23971380-23971391
43	CEBPB	chr19:23966087-23966409	IMR90	lung:	n/a	chr19:23966205-23966216 chr19:23966237-23966248
44	CEBPB	chr19:23968010-23968382	K562	blood:	n/a	n/a
45	CEBPB	chr19:23954211-23954496	A549	lung:	n/a	n/a
46	CEBPB	chr19:23969555-23969641	K562	blood:	n/a	n/a
47	CEBPB	chr19:23959151-23959571	HepG2	liver:	n/a	n/a
48	CEBPB	chr19:23952594-23952832	K562	blood:	n/a	n/a
49	CEBPB	chr19:23969813-23970335	MCF-7	breast:	n/a	n/a
50	CEBPB	chr19:23946654-23946904	K562	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23945743-23945793	HCF	heart:	n/a
2	chr19:23941408-23941458	Caco-2	colon:	n/a
3	chr19:23945743-23945793	HCF	heart:	n/a
4	chr19:23941408-23941458	Caco-2	colon:	n/a
5	chr19:23942040-23942090	HMEC	breast:	n/a
6	chr19:23946205-23946255	HepG2	liver:	n/a
7	chr19:23945996-23946046	HAEpiC	amniotic membrane:	n/a
8	chr19:23941438-23941488	NH-A	brain:	n/a
9	chr19:23941711-23941761	CMK	blood:	n/a
10	chr19:23946205-23946255	PrEC	prostate:	n/a
11	chr19:23945903-23945953	PrEC	prostate:	n/a
12	chr19:23945722-23945772	CMK	blood:	n/a
13	chr19:23942126-23942176	HAEpiC	amniotic membrane:	n/a
14	chr19:23945761-23945811	HRCEpiC	kidney:	n/a
15	chr19:23941871-23941921	SKMC	muscle:	n/a
16	chr19:23945996-23946046	T-47D	breast:	n/a
17	chr19:23945203-23945253	PFSK-1	brain:	n/a
18	chr19:23942040-23942090	NHBE	bronchial:	n/a
19	chr19:23941767-23941817	MCF10A-Er-Src	breast:	n/a
20	chr19:23941718-23941768	NHDF-neo	bronchial:	n/a
21	chr19:23941711-23941761	PFSK-1	brain:	n/a
22	chr19:23942073-23942123	MCF10A-Er-Src	breast:	n/a
23	chr19:23941859-23941909	U87	brain:	n/a
24	chr19:23941313-23941363	RPTEC	kidney:	n/a
25	chr19:23946205-23946255	HAEpiC	amniotic membrane:	n/a
26	chr19:23941859-23941909	NH-A	brain:	n/a
27	chr19:23942040-23942090	HAEpiC	amniotic membrane:	n/a
28	chr19:23941575-23941625	HCT-116	colon:	n/a
29	chr19:23941859-23941909	NHBE	bronchial:	n/a
30	chr19:23946205-23946255	ProgFib	skin:	n/a
31	chr19:23945722-23945772	HEEpiC	esophagus:	n/a
32	chr19:23945743-23945793	HCT-116	colon:	n/a
33	chr19:23941408-23941458	HNPCEpiC	eye:	n/a
34	chr19:23941438-23941488	AG09309	skin:	n/a
35	chr19:23945743-23945793	SK-N-SH	brain:	n/a
36	chr19:23945659-23945709	Caco-2	colon:	n/a
37	chr19:23941438-23941488	ECC-1	luminal epithelium:	n/a
38	chr19:23942126-23942176	HNPCEpiC	eye:	n/a
39	chr19:23945761-23945811	HPAEpiC	pulmonary alveolar:	n/a
40	chr19:23941711-23941761	Caco-2	colon:	n/a
41	chr19:23942126-23942176	GM12891	blood:	n/a
42	chr19:23946205-23946255	HRPEpiC	eye:	n/a
43	chr19:23941718-23941768	SK-N-MC	brain:	n/a
44	chr19:23941313-23941363	HRPEpiC	eye:	n/a
45	chr19:23941313-23941363	HMEC	breast:	n/a
46	chr19:23941408-23941458	ovcar-3	ovarian:	n/a
47	chr19:23945903-23945953	NHDF-neo	bronchial:	n/a
48	chr19:23941859-23941909	HCPEpiC	choroid plexus:	n/a
49	chr19:23941313-23941363	GM19239	blood:	n/a
50	chr19:23945996-23946046	HCF	heart:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:23939020..23940771-chr19:23944929..23946876,2	K562	blood:
2	chr19:23947709..23949776-chr19:23958415..23961237,2	K562	blood:
3	chr19:23934332..23937161-chr19:23938726..23941711,2	K562	blood:
4	chr19:23940633..23942866-chr19:23945047..23947463,3	K562	blood:
5	chr19:23956310..23957870-chr19:23960230..23962213,2	K562	blood:
6	chr19:23900187..23902278-chr19:23940194..23942513,2	K562	blood:
7	chr19:23941209..23941866-chr7:64126456..64127217,2	Hela-S3	cervix:
8	chr16:10416054..10418828-chr19:23906524..23908025,2	MCF-7	breast:
9	chr19:23940633..23942866-chr19:23945047..23947463,3	K562	blood:
10	chr19:24000616..24002168-chr19:24002694..24005183,2	MCF-7	breast:
11	chr19:23944623..23946640-chr19:23952768..23956450,3	MCF-7	breast:
12	chr19:23947709..23949776-chr19:23958415..23961237,2	K562	blood:
13	chr19:23990207..23992454-chr19:24002314..24004892,2	K562	blood:
14	chr19:23990207..23992454-chr19:24002314..24004892,2	K562	blood:
15	chr19:23956310..23957870-chr19:23960230..23962213,2	K562	blood:
16	chr19:23946413..23950001-chr19:23953368..23955533,3	K562	blood:
17	chr19:24000616..24002168-chr19:24002694..24005183,2	MCF-7	breast:
18	chr19:23935159..23938010-chr19:23940371..23942575,2	K562	blood:
19	chr19:23946413..23950001-chr19:23953368..23955533,3	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF675-3	chr19:23932373-23932637	l_1665_chr19:23924177-23932637_testes
2	lnc-RPSAP58-2	chr19:23991521-23991616	NONHSAT063933
3	lnc-RPSAP58-2	chr19:23964883-23965301	NONHSAT063935
4	lnc-RPSAP58-2	chr19:23945814-23945936	NONHSAT063934
5	lnc-ZNF675-3	chr19:23924178-23924868	l_1665_chr19:23924177-23932637_testes
6	lnc-RPSAP58-2	chr19:24014399-24014998	NONHSAT063934
7	lnc-RPSAP58-2	chr19:23945746-23945936	NONHSAT063933
8	lnc-RPSAP58-2	chr19:23990628-23990741	NONHSAT063933
9	lnc-ZNF726-1	chr19:23969576-23969850	ENSG00000250795
10	lnc-RPSAP58-2	chr19:23990628-23990741	NONHSAT063935
11	lnc-RPSAP58-2	chr19:23991521-23992317	NONHSAT063935
12	lnc-RPSAP58-2	chr19:24014399-24014998	NONHSAT063933
13	lnc-ZNF726-1	chr19:23969947-23970608	ENSG00000250795
14	lnc-ZNF681-3	chr19:23981726-23982279	NONHSAT063937
15	lnc-ZNF675-2	chr19:23922003-23923732	NONHSAT063932
16	lnc-ZNF726-1	chr19:23968384-23969193	ENSG00000250795
17	lnc-ZNF675-3	chr19:23926812-23927078	l_1665_chr19:23924177-23932637_testes

No data

Variant related genes	Relation type
RPSAP58	TF binding region
ENSG00000269662	TF binding region
ZNF681	TF binding region
ENSG00000233836	TF binding region
RPSAP58	CpG island
ENSG00000269662	CpG island
ZNF681	CpG island
ENSG00000233836	CpG island
ENSG00000196172	chromatin interactions
ENSG00000233836	chromatin interactions
ENSG00000196247	chromatin interactions
ENSG00000205246	chromatin interactions
GATA6	miRNA target sites
TIAL1	miRNA target sites
NOTCH2	miRNA target sites

Extended variants
information (count: 5169 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:5169 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4932913	chr19:23900196-23900197	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573661432	chr19:23900252-23900253	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs541046924	chr19:23900309-23900310	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4932914	chr19:23900328-23900329	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs62120032	chr19:23900336-23900337	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368915102	chr19:23900355-23900356	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532642523	chr19:23900448-23900449	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs184225962	chr19:23900487-23900488	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs552483603	chr19:23900545-23900546	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564122628	chr19:23900547-23900548	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs75714701	chr19:23900548-23900549	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs545937734	chr19:23900592-23900593	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs529202179	chr19:23900635-23900636	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568184224	chr19:23900641-23900642	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs12327627	chr19:23900691-23900692	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs375033016	chr19:23900721-23900722	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149432955	chr19:23900739-23900740	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs188681458	chr19:23900750-23900751	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs8106974	chr19:23900800-23900801	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs192779768	chr19:23900891-23900892	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs182258765	chr19:23900941-23900942	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs537261077	chr19:23900952-23900953	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200374659	chr19:23900954-23900955	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs75603997	chr19:23900955-23900956	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs67858059	chr19:23900956-23900957	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10682065	chr19:23900957-23900958	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs367842106	chr19:23900958-23900959	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs544076183	chr19:23900977-23900978	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs111917116	chr19:23901187-23901188	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs147546230	chr19:23901188-23901189	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573773172	chr19:23901190-23901191	Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs4932728	chr19:23901285-23901286	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs559478288	chr19:23901318-23901319	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs186568568	chr19:23901334-23901335	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs191705838	chr19:23901389-23901390	Active TSS Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs548501793	chr19:23901407-23901408	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4932915	chr19:23901409-23901410	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs531377273	chr19:23901421-23901422	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs549980107	chr19:23901433-23901434	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs373738923	chr19:23901502-23901503	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs561900072	chr19:23901503-23901504	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs183835589	chr19:23901527-23901528	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547563701	chr19:23901550-23901551	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565494931	chr19:23901552-23901553	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs539430498	chr19:23901554-23901555	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs367570742	chr19:23901595-23901596	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs190403663	chr19:23901615-23901616	Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs55936609	chr19:23901618-23901619	Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs537374672	chr19:23901643-23901644	Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555522977	chr19:23901654-23901655	Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
Ductal carcinoma	22052326	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2075 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23900200-23901000	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr19:23900200-23901200	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr19:23900600-23901000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr19:23900600-23901400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr19:23900800-23901000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr19:23900800-23901000	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr19:23901000-23901200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr19:23901000-23901200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr19:23901000-23901400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
10	chr19:23901000-23901400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr19:23901000-23901400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr19:23901200-23901400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:23901200-23901400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr19:23901200-23902000	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr19:23901200-23902400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chr19:23901200-23902600	Active TSS	iPS-18 Cell Line	embryonic stem cell
17	chr19:23901200-23902800	Active TSS	ES-I3 Cell Line	embryonic stem cell
18	chr19:23901400-23901600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr19:23901400-23902400	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr19:23901400-23902400	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr19:23901400-23902400	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr19:23901400-23902800	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr19:23901600-23902400	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr19:23901600-23902600	Active TSS	H9 Cell Line	embryonic stem cell
25	chr19:23901800-23902000	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr19:23902000-23903200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr19:23902400-23902600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr19:23902400-23902600	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr19:23902400-23902600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
30	chr19:23902400-23902600	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr19:23902400-23902600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr19:23902400-23902600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr19:23902400-23902600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:23902400-23903800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr19:23902600-23902800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr19:23902600-23905400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr19:23902600-23905600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr19:23902600-23906200	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr19:23902600-23906200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr19:23902800-23903000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
41	chr19:23902800-23904400	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chr19:23902800-23905600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr19:23903000-23905400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr19:23903200-23906400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr19:23904400-23904800	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr19:23904800-23906200	Weak transcription	HUES6 Cell Line	embryonic stem cell
47	chr19:23905400-23905600	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr19:23905400-23905600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr19:23905400-23905800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr19:23905400-23906200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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