Variant report

Variant	esv3345953
Chromosome Location	chr19:56702268-56734127
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:56732773-56733067	K562	blood:	n/a	n/a
2	BRCA1	chr19:56720561-56720808	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr19:56711141-56711460	HepG2	liver:	n/a	chr19:56711325-56711336
4	CEBPB	chr19:56711237-56711378	HepG2	liver:	n/a	chr19:56711325-56711336
5	CEBPB	chr19:56720517-56720847	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr19:56732730-56733098	A549	lung:	n/a	chr19:56732934-56732945
7	CEBPB	chr19:56711145-56711495	H1-hESC	embryonic stem cell:	n/a	chr19:56711325-56711336
8	CEBPB	chr19:56707830-56708066	K562	blood:	n/a	n/a
9	CEBPB	chr19:56711153-56711485	Hela-S3	cervix:	n/a	chr19:56711325-56711336
10	CEBPB	chr19:56716510-56716908	K562	blood:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
11	CEBPB	chr19:56732773-56733100	IMR90	lung:	n/a	chr19:56732934-56732945
12	CEBPB	chr19:56732796-56733078	A549	lung:	n/a	chr19:56732934-56732945
13	CEBPB	chr19:56732726-56733084	MCF-7	breast:	n/a	chr19:56732934-56732945
14	CEBPB	chr19:56716429-56716798	A549	lung:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
15	CEBPB	chr19:56709309-56709335	K562	blood:	n/a	n/a
16	CEBPB	chr19:56711122-56711514	HepG2	liver:	n/a	chr19:56711325-56711336
17	CEBPB	chr19:56711161-56711465	K562	blood:	n/a	chr19:56711325-56711336
18	CEBPB	chr19:56705321-56705483	K562	blood:	n/a	chr19:56705438-56705449
19	CEBPB	chr19:56711177-56711471	IMR90	lung:	n/a	chr19:56711325-56711336
20	CEBPB	chr19:56732791-56733124	H1-hESC	embryonic stem cell:	n/a	chr19:56732934-56732945
21	CEBPB	chr19:56732731-56733102	K562	blood:	n/a	chr19:56732934-56732945
22	CEBPB	chr19:56732764-56733076	HepG2	liver:	n/a	chr19:56732934-56732945
23	CEBPB	chr19:56711159-56711500	A549	lung:	n/a	chr19:56711325-56711336
24	CEBPB	chr19:56711156-56711414	HepG2	liver:	n/a	chr19:56711325-56711336
25	CEBPB	chr19:56732645-56733248	Hela-S3	cervix:	n/a	chr19:56732934-56732945
26	CEBPB	chr19:56732803-56733050	K562	blood:	n/a	chr19:56732934-56732945
27	CEBPB	chr19:56723261-56723384	K562	blood:	n/a	n/a
28	CEBPB	chr19:56705349-56705533	A549	lung:	n/a	chr19:56705438-56705449
29	CEBPB	chr19:56716455-56716760	IMR90	lung:	n/a	chr19:56716533-56716544
30	CEBPB	chr19:56705414-56705462	HepG2	liver:	n/a	chr19:56705438-56705449
31	CEBPB	chr19:56716430-56716674	HepG2	liver:	n/a	chr19:56716533-56716544
32	CEBPB	chr19:56716360-56717024	Hela-S3	cervix:	n/a	chr19:56716763-56716774 chr19:56716533-56716544 chr19:56716763-56716774 chr19:56716761-56716774 chr19:56716761-56716774
33	CEBPB	chr19:56732747-56733109	K562	blood:	n/a	chr19:56732934-56732945
34	CEBPD	chr19:56732776-56733035	K562	blood:	n/a	n/a
35	CHD2	chr19:56720635-56720730	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr19:56720040-56720297	K562	blood:	n/a	n/a
37	CTCF	chr19:56733220-56733370	NHEK	skin:	n/a	n/a
38	CTCF	chr19:56732877-56733269	K562	blood:	n/a	n/a
39	CTCF	chr19:56732960-56733110	HMEC	breast:	n/a	n/a
40	CTCF	chr19:56733058-56733095	GM19240	blood:	n/a	n/a
41	CTCF	chr19:56719082-56719218	MCF-7	breast:	n/a	n/a
42	CTCF	chr19:56702660-56702810	GM06990	blood:	n/a	n/a
43	CTCF	chr19:56732920-56733070	WI-38	lung:	n/a	n/a
44	CTCF	chr19:56732940-56733090	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr19:56720375-56720428	K562	blood:	n/a	n/a
46	CTCF	chr19:56719180-56719330	HEK293	kidney:	n/a	n/a
47	CTCF	chr19:56723148-56723376	HepG2	liver:	n/a	n/a
48	CTCF	chr19:56732960-56733110	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr19:56723166-56723425	K562	blood:	n/a	n/a
50	CTCF	chr19:56732920-56733070	AG04449	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56707808-56707858	HAEpiC	amniotic membrane:	n/a
2	chr19:56709655-56709705	HCPEpiC	choroid plexus:	n/a
3	chr19:56707808-56707858	HAEpiC	amniotic membrane:	n/a
4	chr19:56709655-56709705	HCPEpiC	choroid plexus:	n/a
5	chr19:56705433-56705483	HMEC	breast:	n/a
6	chr19:56705433-56705483	HCM	heart:	n/a
7	chr19:56733045-56733095	U87	brain:	n/a
8	chr19:56709056-56709106	HRE	kidney:	n/a
9	chr19:56728589-56728639	PFSK-1	brain:	n/a
10	chr19:56730494-56730544	HMEC	breast:	n/a
11	chr19:56704341-56704391	SK-N-MC	brain:	n/a
12	chr19:56704341-56704391	BE2_C	brain:	n/a
13	chr19:56726303-56726353	GM06990	blood:	n/a
14	chr19:56730494-56730544	GM06990	blood:	n/a
15	chr19:56707808-56707858	HRCEpiC	kidney:	n/a
16	chr19:56726303-56726353	AG10803	skin:	n/a
17	chr19:56709228-56709278	CMK	blood:	n/a
18	chr19:56705433-56705483	HUVEC	blood vessel:	n/a
19	chr19:56732932-56732982	Hela-S3	cervix:	n/a
20	chr19:56707808-56707858	BJ	skin:	n/a
21	chr19:56705433-56705483	HAEpiC	amniotic membrane:	n/a
22	chr19:56705433-56705483	HEK293	kidney:	embryo
23	chr19:56705433-56705483	PFSK-1	brain:	n/a
24	chr19:56707808-56707858	GM12878	blood:	n/a
25	chr19:56730494-56730544	U87	brain:	n/a
26	chr19:56726303-56726353	MCF10A-Er-Src	breast:	n/a
27	chr19:56728589-56728639	BJ	skin:	n/a
28	chr19:56728422-56728472	ovcar-3	ovarian:	n/a
29	chr19:56728422-56728472	GM19239	blood:	n/a
30	chr19:56730494-56730544	AoSMC	blood vessel:	n/a
31	chr19:56705497-56705547	MCF-7	breast:	n/a
32	chr19:56704341-56704391	ECC-1	luminal epithelium:	n/a
33	chr19:56709655-56709705	HNPCEpiC	eye:	n/a
34	chr19:56705433-56705483	AoSMC	blood vessel:	n/a
35	chr19:56707808-56707858	AG10803	skin:	n/a
36	chr19:56728422-56728472	HNPCEpiC	eye:	n/a
37	chr19:56709056-56709106	GM12891	blood:	n/a
38	chr19:56732932-56732982	NH-A	brain:	n/a
39	chr19:56709056-56709106	BE2_C	brain:	n/a
40	chr19:56709228-56709278	NH-A	brain:	n/a
41	chr19:56732932-56732982	AG09309	skin:	n/a
42	chr19:56707808-56707858	SK-N-SH	brain:	n/a
43	chr19:56707808-56707858	LNCaP	prostate:	n/a
44	chr19:56733045-56733095	ProgFib	skin:	n/a
45	chr19:56726303-56726353	HL-60	blood:	n/a
46	chr19:56733045-56733095	SAEC	small airway:	n/a
47	chr19:56705433-56705483	HIPEpiC	eye:	n/a
48	chr19:56709228-56709278	IMR90	lung:	fetal
49	chr19:56705386-56705436	NT2-D1	testis:	n/a
50	chr19:56709228-56709278	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56731454..56732253-chr19:56820726..56821606,2	MCF-7	breast:
2	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
3	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
4	chr19:56706835..56708923-chr19:56717136..56719247,2	K562	blood:
5	chr19:56587934..56588448-chr19:56732565..56733070,2	MCF-7	breast:

Variant related genes	Relation type
ZSCAN5B	TF binding region
ZSCAN5C	TF binding region
ENSG00000242411	TF binding region
ZSCAN5B	CpG island
ZSCAN5C	CpG island
ENSG00000242411	CpG island
ENSG00000204532	chromatin interactions

Extended variants
information (count: 913 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:913 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182542443	chr19:56702286-56702287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs371929091	chr19:56702289-56702290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374861595	chr19:56702300-56702301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370187858	chr19:56702301-56702302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4801296	chr19:56702323-56702324	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs375207851	chr19:56702335-56702336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs187117582	chr19:56702353-56702354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs369380934	chr19:56702389-56702390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576182410	chr19:56702412-56702413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs112013480	chr19:56702440-56702441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555407376	chr19:56702469-56702470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs572193557	chr19:56702472-56702473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs541543442	chr19:56702515-56702516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564322695	chr19:56702540-56702541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533405892	chr19:56702577-56702578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74989446	chr19:56702589-56702590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191120313	chr19:56702605-56702606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146951416	chr19:56702617-56702618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs531496852	chr19:56702647-56702648	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs13345242	chr19:56702649-56702650	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs13343392	chr19:56702666-56702667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116689828	chr19:56702686-56702687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs114389602	chr19:56702690-56702691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570310317	chr19:56702701-56702702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539422175	chr19:56702714-56702715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556551395	chr19:56702726-56702727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs570030595	chr19:56702773-56702774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34181873	chr19:56705325-56705326	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs569501010	chr19:56705326-56705327	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs569320789	chr19:56705342-56705343	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs60591854	chr19:56705343-56705344	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs71184332	chr19:56705344-56705345	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs191925232	chr19:56705360-56705361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs572768183	chr19:56705363-56705364	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs373534845	chr19:56705387-56705388	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs544692879	chr19:56705442-56705443	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs78444867	chr19:56705469-56705470	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs564907861	chr19:56705480-56705481	Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs575986267	chr19:56705554-56705555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544968208	chr19:56705617-56705618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376547538	chr19:56705690-56705691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs184110508	chr19:56705742-56705743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560405648	chr19:56705769-56705770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375994236	chr19:56705785-56705786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190360681	chr19:56705787-56705788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375180794	chr19:56705788-56705789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369772972	chr19:56705790-56705791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568993880	chr19:56706753-56706754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs537965813	chr19:56706807-56706808	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs554587563	chr19:56706811-56706812	Inactive region	TF binding region	1 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
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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:56688600-56702400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:56702400-56702800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:56705400-56705800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr19:56710800-56712400	Enhancers	Liver	Liver
5	chr19:56711000-56711200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr19:56711000-56711800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr19:56711600-56711800	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr19:56716600-56717200	Bivalent Enhancer	Hela-S3	cervix
9	chr19:56723600-56727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr19:56724400-56728400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr19:56725000-56725200	Active TSS	A549	lung
12	chr19:56725200-56727400	Weak transcription	A549	lung
13	chr19:56727400-56727600	ZNF genes & repeats	A549	lung
14	chr19:56727400-56727800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr19:56727400-56728200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr19:56727600-56735800	Weak transcription	A549	lung
17	chr19:56727800-56728000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr19:56727800-56729000	Enhancers	Dnd41	blood
19	chr19:56728000-56728400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr19:56728000-56728400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr19:56728000-56728400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr19:56728000-56728400	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr19:56728000-56728400	Enhancers	Esophagus	oesophagus
25	chr19:56728000-56728800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:56728000-56729400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr19:56728200-56728400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr19:56728200-56728400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr19:56728200-56728400	Enhancers	Primary hematopoietic stem cells	blood
30	chr19:56728200-56728400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:56728200-56728400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr19:56728200-56728400	Enhancers	HMEC	breast
34	chr19:56728200-56728400	Enhancers	HUVEC	blood vessel
35	chr19:56728200-56728600	Bivalent Enhancer	Thymus	Thymus
36	chr19:56728200-56728800	Bivalent Enhancer	Placenta	Placenta
37	chr19:56728200-56728800	Bivalent Enhancer	Fetal Thymus	thymus
38	chr19:56728200-56729200	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr19:56728200-56729400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr19:56728200-56729400	Enhancers	Fetal Heart	heart
41	chr19:56728400-56728600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
42	chr19:56728400-56728600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr19:56728400-56728600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr19:56728400-56728600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
45	chr19:56728400-56728600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr19:56728400-56728600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr19:56728400-56728600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr19:56728400-56728600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr19:56728400-56728600	Bivalent/Poised TSS	Brain Angular Gyrus	brain
50	chr19:56728400-56728600	Bivalent Enhancer	Brain Germinal Matrix	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links