Variant report

Variant	esv1810349
Chromosome Location	chr19:53498380-53553963
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:274)
CpG islands
(count:428)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:274 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53518961-53519336	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:53510497-53510963	K562	blood:	n/a	n/a
3	BHLHE40	chr19:53510493-53510782	GM12878	blood:	n/a	n/a
4	BRCA1	chr19:53548078-53548353	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr19:53514645-53514955	HepG2	liver:	n/a	chr19:53514790-53514801
6	CEBPB	chr19:53503242-53503648	K562	blood:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
7	CEBPB	chr19:53514709-53514946	Hela-S3	cervix:	n/a	chr19:53514790-53514801
8	CEBPB	chr19:53503339-53503575	IMR90	lung:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
9	CEBPB	chr19:53514622-53514961	K562	blood:	n/a	chr19:53514790-53514801
10	CEBPB	chr19:53499048-53499248	K562	blood:	n/a	n/a
11	CEBPB	chr19:53520045-53520364	IMR90	lung:	n/a	n/a
12	CEBPB	chr19:53520052-53520352	K562	blood:	n/a	n/a
13	CEBPB	chr19:53514683-53514869	A549	lung:	n/a	chr19:53514790-53514801
14	CEBPB	chr19:53503344-53503663	HepG2	liver:	n/a	chr19:53503521-53503534 chr19:53503522-53503533 chr19:53503521-53503532 chr19:53503521-53503534 chr19:53503521-53503534
15	CEBPB	chr19:53520072-53520352	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr19:53520162-53520365	MCF-7	breast:	n/a	n/a
17	CTCF	chr19:53517080-53517230	GM12866	blood:	n/a	n/a
18	CTCF	chr19:53523481-53523551	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr19:53523092-53523198	GM19238	blood:	n/a	n/a
20	CTCF	chr19:53523100-53523250	HCM	heart:	n/a	n/a
21	CTCF	chr19:53522989-53523273	K562	blood:	n/a	n/a
22	CTCF	chr19:53523020-53523170	HEEpiC	esophagus:	n/a	n/a
23	CTCF	chr19:53523097-53523100	GM19239	blood:	n/a	n/a
24	CTCF	chr19:53523040-53523190	HUVEC	blood vessel:	n/a	n/a
25	CTCF	chr19:53522981-53523241	K562	blood:	n/a	n/a
26	CTCF	chr19:53522940-53523416	MCF-7	breast:	n/a	n/a
27	CTCF	chr19:53513826-53514079	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr19:53522895-53523274	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr19:53523066-53523228	Medullo	brain:	n/a	n/a
30	CTCF	chr19:53523080-53523230	GM12878	blood:	n/a	n/a
31	CTCF	chr19:53517968-53518032	K562	blood:	n/a	n/a
32	CTCF	chr19:53510840-53510990	K562	blood:	n/a	chr19:53510955-53510973 chr19:53510961-53510970
33	CTCF	chr19:53523040-53523190	BJ	skin:	n/a	n/a
34	CTCF	chr19:53523080-53523230	GM12873	blood:	n/a	n/a
35	CTCF	chr19:53523040-53523190	GM12873	blood:	n/a	n/a
36	CTCF	chr19:53523070-53523239	NHEK	skin:	n/a	n/a
37	CTCF	chr19:53522940-53523090	HCT-116	colon:	n/a	n/a
38	CTCF	chr19:53523000-53523150	NHEK	skin:	n/a	n/a
39	CTCF	chr19:53523158-53523228	GM13977	blood:	n/a	n/a
40	CTCF	chr19:53538670-53538733	GM10248	blood:	n/a	n/a
41	CTCF	chr19:53523141-53523173	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr19:53523060-53523210	HL-60	blood:	n/a	n/a
43	CTCF	chr19:53523101-53523200	GM19239	blood:	n/a	n/a
44	CTCF	chr19:53523020-53523170	RPTEC	kidney:	n/a	n/a
45	CTCF	chr19:53522996-53523308	GM12878	blood:	n/a	n/a
46	CTCF	chr19:53513900-53514050	HepG2	liver:	n/a	n/a
47	CTCF	chr19:53547820-53547970	GM12875	blood:	n/a	n/a
48	CTCF	chr19:53523020-53523170	GM12874	blood:	n/a	n/a
49	CTCF	chr19:53523140-53523202	MCF-7	breast:	n/a	n/a
50	CTCF	chr19:53523040-53523190	GM12872	blood:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53540845-53540895	H1-hESC	embryonic stem cell:	embryo
2	chr19:53540845-53540895	H1-hESC	embryonic stem cell:	embryo
3	chr19:53538883-53538933	ProgFib	skin:	n/a
4	chr19:53541287-53541337	HRE	kidney:	n/a
5	chr19:53540902-53540952	AG09309	skin:	n/a
6	chr19:53538687-53538737	IMR90	lung:	fetal
7	chr19:53538883-53538933	SK-N-SH	brain:	n/a
8	chr19:53538883-53538933	RPTEC	kidney:	n/a
9	chr19:53538687-53538737	AG10803	skin:	n/a
10	chr19:53500997-53501047	BE2_C	brain:	n/a
11	chr19:53538687-53538737	K562	blood:	n/a
12	chr19:53500997-53501047	K562	blood:	n/a
13	chr19:53540902-53540952	U87	brain:	n/a
14	chr19:53538687-53538737	HUVEC	blood vessel:	n/a
15	chr19:53540845-53540895	MCF10A-Er-Src	breast:	n/a
16	chr19:53541287-53541337	GM12892	blood:	n/a
17	chr19:53540902-53540952	GM12878	blood:	n/a
18	chr19:53538883-53538933	GM12891	blood:	n/a
19	chr19:53541287-53541337	HL-60	blood:	n/a
20	chr19:53500997-53501047	AG09319	gingival:	n/a
21	chr19:53538687-53538737	SK-N-MC	brain:	n/a
22	chr19:53541186-53541236	SK-N-MC	brain:	n/a
23	chr19:53538883-53538933	PFSK-1	brain:	n/a
24	chr19:53541186-53541236	PANC-1	pancreas:	n/a
25	chr19:53538883-53538933	HRCEpiC	kidney:	n/a
26	chr19:53500997-53501047	AoSMC	blood vessel:	n/a
27	chr19:53541287-53541337	Caco-2	colon:	n/a
28	chr19:53541186-53541236	HUVEC	blood vessel:	n/a
29	chr19:53538687-53538737	PANC-1	pancreas:	n/a
30	chr19:53541186-53541236	BE2_C	brain:	n/a
31	chr19:53538687-53538737	CMK	blood:	n/a
32	chr19:53538687-53538737	Hepatocyte	liver:	n/a
33	chr19:53538687-53538737	HCF	heart:	n/a
34	chr19:53540845-53540895	BJ	skin:	n/a
35	chr19:53538687-53538737	RPTEC	kidney:	n/a
36	chr19:53541287-53541337	NB4	blood:	n/a
37	chr19:53540845-53540895	SKMC	muscle:	n/a
38	chr19:53541287-53541337	AG09309	skin:	n/a
39	chr19:53541287-53541337	HCT-116	colon:	n/a
40	chr19:53541287-53541337	GM12891	blood:	n/a
41	chr19:53541287-53541337	LNCaP	prostate:	n/a
42	chr19:53538883-53538933	AG09309	skin:	n/a
43	chr19:53541186-53541236	Caco-2	colon:	n/a
44	chr19:53540845-53540895	AG04450	lung:	fetal
45	chr19:53541186-53541236	NHDF-neo	bronchial:	n/a
46	chr19:53538687-53538737	HCM	heart:	n/a
47	chr19:53541287-53541337	PFSK-1	brain:	n/a
48	chr19:53538883-53538933	HMEC	breast:	n/a
49	chr19:53541287-53541337	Hela-S3	cervix:	n/a
50	chr19:53500997-53501047	RPTEC	kidney:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53541069..53542606-chr19:53543581..53546044,2	K562	blood:
2	chr10:9353360..9353955-chr19:53525559..53526530,2	MCF-7	breast:
3	chr19:53536567..53539141-chr19:53540653..53542425,2	K562	blood:
4	chr19:53237008..53239147-chr19:53540786..53542527,2	MCF-7	breast:
5	chr19:53514929..53517284-chr19:53527300..53529548,2	MCF-7	breast:
6	chr14:77866421..77867168-chr19:53501795..53502295,2	MCF-7	breast:
7	chr19:53515874..53517968-chr19:53519511..53521544,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF816-2	chr19:53540978-53541136	NONHSAT067613
2	lnc-ZNF160-1	chr19:53517584-53517806	ENSG00000251255
3	lnc-ZNF160-1	chr19:53517843-53519833	ENSG00000251255

No data

Variant related genes	Relation type
ENSG00000268282	TF binding region
ENSG00000267943	TF binding region
ERVV-1	TF binding region
ERVV-2	TF binding region
ZNF702P	TF binding region
ENSG00000268282	CpG island
ENSG00000267943	CpG island
ERVV-1	CpG island
ERVV-2	CpG island
ZNF702P	CpG island
ENSG00000269526	chromatin interactions
ENSG00000242779	chromatin interactions
ENSG00000213020	chromatin interactions
GPR107	miRNA target sites
RNF4	miRNA target sites

Extended variants
information (count: 2142 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2142 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190573365	chr19:53498380-53498381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565970153	chr19:53498383-53498384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs533108871	chr19:53498403-53498404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs150741946	chr19:53498442-53498443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs376756542	chr19:53498449-53498450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs6509712	chr19:53498467-53498468	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs537059970	chr19:53498494-53498495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs554996719	chr19:53498535-53498536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs546312154	chr19:53498539-53498540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567070108	chr19:53498555-53498556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs535645037	chr19:53498583-53498584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553982197	chr19:53498622-53498623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181897720	chr19:53498632-53498633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs8106463	chr19:53498644-53498645	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs576094233	chr19:53498682-53498683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543223909	chr19:53498685-53498686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs8106476	chr19:53498690-53498691	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529199543	chr19:53498697-53498698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146235199	chr19:53498769-53498770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368763245	chr19:53498771-53498772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529446621	chr19:53498783-53498784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs386810627	chr19:53498794-53498795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559613995	chr19:53498795-53498796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533174171	chr19:53498808-53498809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77208263	chr19:53498819-53498820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577432647	chr19:53498837-53498838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs77210164	chr19:53498843-53498844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143101253	chr19:53498930-53498931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs578067161	chr19:53498982-53498983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs569936333	chr19:53498992-53498993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs66535967	chr19:53499015-53499016	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs398079949	chr19:53499016-53499017	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs397740516	chr19:53499017-53499018	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs201369200	chr19:53499018-53499019	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202203533	chr19:53499019-53499020	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553183165	chr19:53499057-53499058	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs532771832	chr19:53499062-53499063	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs534355491	chr19:53499140-53499141	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs548610146	chr19:53499152-53499153	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs7256944	chr19:53499166-53499167	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs118138724	chr19:53499200-53499201	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs546314490	chr19:53499209-53499210	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs139544699	chr19:53499242-53499243	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs181507799	chr19:53499245-53499246	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs548955400	chr19:53499258-53499259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11668512	chr19:53499275-53499276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116712152	chr19:53499294-53499295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs370060779	chr19:53499297-53499298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185754651	chr19:53499313-53499314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537039772	chr19:53499316-53499317	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:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53497600-53500800	Enhancers	Placenta	Placenta
2	chr19:53497600-53501200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr19:53497600-53502000	Weak transcription	Right Ventricle	heart
4	chr19:53497600-53509800	Weak transcription	Right Atrium	heart
5	chr19:53498000-53499000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr19:53498000-53500800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr19:53498000-53510400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr19:53498200-53498400	Enhancers	Brain Anterior Caudate	brain
9	chr19:53499000-53499200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr19:53499200-53507200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr19:53500400-53500600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
12	chr19:53500400-53500600	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr19:53500400-53501400	Active TSS	iPS-20b Cell Line	embryonic stem cell
14	chr19:53500400-53501400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
15	chr19:53500400-53501600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
16	chr19:53500400-53501600	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr19:53500400-53501600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
18	chr19:53500400-53501600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
19	chr19:53500600-53501200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr19:53500600-53501600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
21	chr19:53500800-53501000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr19:53500800-53501200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr19:53500800-53501400	Active TSS	Placenta	Placenta
24	chr19:53501000-53501400	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr19:53501200-53501400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr19:53501200-53501400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr19:53501400-53501600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
28	chr19:53501400-53501800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr19:53501400-53501800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr19:53501400-53502600	Weak transcription	Placenta	Placenta
31	chr19:53501600-53501800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
32	chr19:53501600-53501800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
33	chr19:53501600-53501800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
34	chr19:53501600-53501800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr19:53501600-53502000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
36	chr19:53501800-53505200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:53502600-53503200	Enhancers	Placenta	Placenta
38	chr19:53503200-53507000	Weak transcription	Placenta	Placenta
39	chr19:53505200-53505400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr19:53505400-53506000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr19:53505800-53506200	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr19:53505800-53506200	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chr19:53506000-53509800	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr19:53506200-53507200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr19:53507000-53507600	Active TSS	Brain Germinal Matrix	brain
46	chr19:53507000-53510400	Enhancers	Placenta	Placenta
47	chr19:53507200-53507400	Enhancers	H1 Cell Line	embryonic stem cell
48	chr19:53507200-53507400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr19:53507200-53507600	Active TSS	Brain Anterior Caudate	brain
50	chr19:53507200-53507600	Active TSS	Fetal Brain Female	brain

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