Variant report

Variant	esv1800937
Chromosome Location	chr19:53514613-53573309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:917)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:53558916-53559216	K562	blood:	n/a	n/a
2	ATF3	chr19:53558902-53559223	K562	blood:	n/a	n/a
3	BACH1	chr19:53518961-53519336	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr19:53558384-53558600	K562	blood:	n/a	n/a
5	BRCA1	chr19:53548078-53548353	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr19:53572060-53572399	K562	blood:	n/a	n/a
7	CBX3	chr19:53556503-53556768	K562	blood:	n/a	n/a
8	CBX3	chr19:53571433-53572014	K562	blood:	n/a	n/a
9	CBX3	chr19:53571258-53571951	K562	blood:	n/a	n/a
10	CEBPB	chr19:53563520-53563530	HepG2	liver:	n/a	n/a
11	CEBPB	chr19:53563457-53563536	A549	lung:	n/a	chr19:53563503-53563514
12	CEBPB	chr19:53520052-53520352	K562	blood:	n/a	n/a
13	CEBPB	chr19:53563501-53563543	K562	blood:	n/a	chr19:53563503-53563514
14	CEBPB	chr19:53520162-53520365	MCF-7	breast:	n/a	n/a
15	CEBPB	chr19:53520072-53520352	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr19:53520045-53520364	IMR90	lung:	n/a	n/a
17	CEBPB	chr19:53563196-53563210	HepG2	liver:	n/a	n/a
18	CEBPB	chr19:53514645-53514955	HepG2	liver:	n/a	chr19:53514790-53514801
19	CEBPB	chr19:53559033-53559111	K562	blood:	n/a	n/a
20	CEBPB	chr19:53514709-53514946	Hela-S3	cervix:	n/a	chr19:53514790-53514801
21	CEBPB	chr19:53514622-53514961	K562	blood:	n/a	chr19:53514790-53514801
22	CEBPB	chr19:53514683-53514869	A549	lung:	n/a	chr19:53514790-53514801
23	CHD2	chr19:53571538-53571719	K562	blood:	n/a	n/a
24	CTBP2	chr19:53561350-53561890	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr19:53522935-53523279	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr19:53550380-53550387	GM20000	blood:	n/a	n/a
27	CTCF	chr19:53523000-53523150	NHEK	skin:	n/a	n/a
28	CTCF	chr19:53523000-53523150	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr19:53522961-53523288	T-47D	breast:	n/a	n/a
30	CTCF	chr19:53522996-53523308	GM12878	blood:	n/a	n/a
31	CTCF	chr19:53520160-53520310	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr19:53523060-53523210	GM12867	blood:	n/a	n/a
33	CTCF	chr19:53523060-53523210	HCFaa	heart:	n/a	n/a
34	CTCF	chr19:53523097-53523100	GM19239	blood:	n/a	n/a
35	CTCF	chr19:53523100-53523250	GM12866	blood:	n/a	n/a
36	CTCF	chr19:53522860-53523010	K562	blood:	n/a	n/a
37	CTCF	chr19:53523092-53523198	GM19238	blood:	n/a	n/a
38	CTCF	chr19:53523040-53523190	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr19:53523114-53523192	GM10266	blood:	n/a	n/a
40	CTCF	chr19:53518162-53518286	GM20000	blood:	n/a	n/a
41	CTCF	chr19:53523080-53523230	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr19:53523080-53523230	NHEK	skin:	n/a	n/a
43	CTCF	chr19:53522968-53523321	K562	blood:	n/a	n/a
44	CTCF	chr19:53523155-53523182	HepG2	liver:	n/a	n/a
45	CTCF	chr19:53538670-53538733	GM10248	blood:	n/a	n/a
46	CTCF	chr19:53523020-53523170	K562	blood:	n/a	n/a
47	CTCF	chr19:53523020-53523170	GM12874	blood:	n/a	n/a
48	CTCF	chr19:53523155-53523191	LNCaP	prostate:	n/a	n/a
49	CTCF	chr19:53522989-53523273	K562	blood:	n/a	n/a
50	CTCF	chr19:53523080-53523230	BE2_C	brain:	n/a	n/a

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53571146-53571196	ProgFib	skin:	n/a
2	chr19:53557328-53557378	PrEC	prostate:	n/a
3	chr19:53571146-53571196	ProgFib	skin:	n/a
4	chr19:53557328-53557378	PrEC	prostate:	n/a
5	chr19:53538687-53538737	AG09319	gingival:	n/a
6	chr19:53561441-53561491	HRPEpiC	eye:	n/a
7	chr19:53541287-53541337	HRPEpiC	eye:	n/a
8	chr19:53538687-53538737	HRPEpiC	eye:	n/a
9	chr19:53561973-53562023	U87	brain:	n/a
10	chr19:53561386-53561436	HepG2	liver:	n/a
11	chr19:53541287-53541337	SK-N-MC	brain:	n/a
12	chr19:53561441-53561491	HRE	kidney:	n/a
13	chr19:53538883-53538933	PFSK-1	brain:	n/a
14	chr19:53538687-53538737	HCF	heart:	n/a
15	chr19:53541186-53541236	RPTEC	kidney:	n/a
16	chr19:53561563-53561613	NHBE	bronchial:	n/a
17	chr19:53540902-53540952	HRE	kidney:	n/a
18	chr19:53538687-53538737	HUVEC	blood vessel:	n/a
19	chr19:53541287-53541337	HEEpiC	esophagus:	n/a
20	chr19:53538883-53538933	NHDF-neo	bronchial:	n/a
21	chr19:53571146-53571196	AG10803	skin:	n/a
22	chr19:53561563-53561613	HUVEC	blood vessel:	n/a
23	chr19:53540902-53540952	NB4	blood:	n/a
24	chr19:53557328-53557378	HEK293	kidney:	embryo
25	chr19:53571146-53571196	SK-N-MC	brain:	n/a
26	chr19:53564251-53564301	HEK293	kidney:	embryo
27	chr19:53541287-53541337	Caco-2	colon:	n/a
28	chr19:53540845-53540895	GM12892	blood:	n/a
29	chr19:53571146-53571196	HepG2	liver:	n/a
30	chr19:53564251-53564301	Caco-2	colon:	n/a
31	chr19:53540845-53540895	HCPEpiC	choroid plexus:	n/a
32	chr19:53561811-53561861	PrEC	prostate:	n/a
33	chr19:53571146-53571196	U87	brain:	n/a
34	chr19:53557328-53557378	GM12891	blood:	n/a
35	chr19:53538883-53538933	HCT-116	colon:	n/a
36	chr19:53559508-53559558	LNCaP	prostate:	n/a
37	chr19:53561386-53561436	BJ	skin:	n/a
38	chr19:53541186-53541236	HCM	heart:	n/a
39	chr19:53561563-53561613	BE2_C	brain:	n/a
40	chr19:53540845-53540895	K562	blood:	n/a
41	chr19:53561811-53561861	NB4	blood:	n/a
42	chr19:53538687-53538737	AG04450	lung:	fetal
43	chr19:53540845-53540895	SK-N-SH	brain:	n/a
44	chr19:53571146-53571196	MCF10A-Er-Src	breast:	n/a
45	chr19:53571146-53571196	HL-60	blood:	n/a
46	chr19:53561441-53561491	HCM	heart:	n/a
47	chr19:53571146-53571196	SKMC	muscle:	n/a
48	chr19:53561973-53562023	ovcar-3	ovarian:	n/a
49	chr19:53540902-53540952	SK-N-MC	brain:	n/a
50	chr19:53540845-53540895	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:53541069..53542606-chr19:53543581..53546044,2	K562	blood:
2	chr19:53565063..53566659-chr19:53568054..53569781,2	MCF-7	breast:
3	chr19:53191910..53193662-chr19:53562323..53563875,2	K562	blood:
4	chr19:53514929..53517284-chr19:53527300..53529548,2	MCF-7	breast:
5	chr19:53536567..53539141-chr19:53540653..53542425,2	K562	blood:
6	chr19:53571470..53573279-chr19:53575256..53577909,2	K562	blood:
7	chr19:53557284..53559670-chr19:53575484..53577211,2	K562	blood:
8	chr19:53565063..53566659-chr19:53568054..53569781,2	MCF-7	breast:
9	chr10:9353360..9353955-chr19:53525559..53526530,2	MCF-7	breast:
10	chr19:53515874..53517968-chr19:53519511..53521544,2	K562	blood:
11	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:
12	chr19:53569932..53571505-chr19:53575389..53577141,2	K562	blood:
13	chr19:53570126..53572059-chr19:53579091..53581644,2	K562	blood:
14	chr19:53569123..53571974-chr19:53605112..53607818,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF160-1	chr19:53517843-53519833	ENSG00000251255
2	lnc-ZNF415-3	chr19:53571484-53571707	NONHSAT067621
3	lnc-ZNF160-1	chr19:53517584-53517806	ENSG00000251255
4	lnc-VN1R2-9	chr19:53569945-53572927	NONHSAT067620
5	lnc-ZNF816-2	chr19:53540978-53541136	NONHSAT067613

No data

Variant related genes	Relation type
ERVV-1	TF binding region
ERVV-2	TF binding region
ZNF702P	TF binding region
ERVV-1	CpG island
ERVV-2	CpG island
ZNF702P	CpG island
ENSG00000242779	chromatin interactions
ENSG00000170949	chromatin interactions
ENSG00000213020	chromatin interactions
ENSG00000269526	chromatin interactions
RNF4	miRNA target sites
GPR107	miRNA target sites

Extended variants
information (count: 2207 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2207 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187439643	chr19:53514614-53514615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1661965	chr19:53514687-53514688	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs36080416	chr19:53514775-53514776	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112728324	chr19:53514821-53514822	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs191906327	chr19:53514850-53514851	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs558891423	chr19:53514862-53514863	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs577229767	chr19:53514898-53514899	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs1661964	chr19:53514904-53514905	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs563278640	chr19:53514969-53514970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115854033	chr19:53515001-53515002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs146251289	chr19:53515044-53515045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550132931	chr19:53515096-53515097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373808013	chr19:53515110-53515111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs115201830	chr19:53515223-53515224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs548118853	chr19:53515255-53515256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534144522	chr19:53515265-53515266	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142748110	chr19:53515266-53515267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34629444	chr19:53515290-53515291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577613474	chr19:53515297-53515298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs539887304	chr19:53515326-53515327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182081314	chr19:53515344-53515345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186063486	chr19:53515405-53515406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537229158	chr19:53515407-53515408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145202691	chr19:53515460-53515461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369887848	chr19:53515462-53515463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs370576197	chr19:53515510-53515511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555243812	chr19:53515540-53515541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs573518828	chr19:53515547-53515548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs147390260	chr19:53515548-53515549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552854694	chr19:53515553-53515554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs577217429	chr19:53515557-53515558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs577192605	chr19:53515606-53515607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563372068	chr19:53515653-53515654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369155779	chr19:53515677-53515678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112675672	chr19:53515678-53515679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575219710	chr19:53515694-53515695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542719835	chr19:53515752-53515753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556638340	chr19:53515764-53515765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562101826	chr19:53515765-53515766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529514317	chr19:53515773-53515774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111878710	chr19:53515777-53515778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182696673	chr19:53515811-53515812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560130265	chr19:53515833-53515834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs73068774	chr19:53515842-53515843	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs551513081	chr19:53515857-53515858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570054390	chr19:53515867-53515868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs8106572	chr19:53515886-53515887	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs148547435	chr19:53515975-53515976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567077949	chr19:53516015-53516016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141948399	chr19:53516067-53516068	Weak transcription Enhancers	n/a	n/a	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
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
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:565 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53512600-53518800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr19:53514000-53516600	Enhancers	Placenta	Placenta
3	chr19:53514200-53518800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:53516600-53517200	Genic enhancers	Placenta	Placenta
5	chr19:53517200-53518600	Weak transcription	Placenta	Placenta
6	chr19:53518600-53519400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr19:53518600-53519400	Genic enhancers	Placenta	Placenta
8	chr19:53518800-53519200	Genic enhancers	Placenta Amnion	Placenta Amnion
9	chr19:53518800-53519400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr19:53519200-53519400	Enhancers	Placenta Amnion	Placenta Amnion
11	chr19:53519400-53519800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr19:53519400-53520400	Weak transcription	Placenta Amnion	Placenta Amnion
13	chr19:53519400-53520600	Enhancers	Placenta	Placenta
14	chr19:53519800-53520200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr19:53520400-53520600	Enhancers	Placenta Amnion	Placenta Amnion
16	chr19:53520400-53520800	Enhancers	Osteobl	bone
17	chr19:53522600-53523400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr19:53527800-53528000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr19:53528000-53538600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:53529400-53530000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr19:53529600-53529800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr19:53530000-53540400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr19:53531000-53531200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr19:53531000-53531800	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr19:53531200-53532000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr19:53531600-53532200	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr19:53531600-53532200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr19:53531800-53532000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr19:53531800-53532200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr19:53531800-53532400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr19:53532000-53532200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr19:53532000-53532800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr19:53532200-53539600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr19:53532800-53533000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr19:53536200-53536400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr19:53536400-53536600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr19:53536400-53539600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr19:53536600-53536800	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr19:53536600-53539800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr19:53536800-53538600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr19:53537000-53538400	Weak transcription	Fetal Kidney	kidney
42	chr19:53537800-53538800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr19:53538400-53538800	Enhancers	Placenta Amnion	Placenta Amnion
44	chr19:53538400-53540400	Enhancers	Placenta	Placenta
45	chr19:53538600-53538800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:53538600-53538800	ZNF genes & repeats	Fetal Kidney	kidney
47	chr19:53538800-53539200	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr19:53538800-53539600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr19:53538800-53539600	Weak transcription	Fetal Kidney	kidney
50	chr19:53539200-53539400	Enhancers	Placenta Amnion	Placenta Amnion

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