Variant report

Variant	esv3384748
Chromosome Location	chr19:56727320-56744483
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	CEBPB	chr19:56732764-56733076	HepG2	liver:	n/a	chr19:56732934-56732945
3	CEBPB	chr19:56732730-56733098	A549	lung:	n/a	chr19:56732934-56732945
4	CEBPB	chr19:56741719-56741891	K562	blood:	n/a	chr19:56741810-56741821
5	CEBPB	chr19:56741714-56741974	IMR90	lung:	n/a	chr19:56741810-56741821
6	CEBPB	chr19:56744051-56744221	K562	blood:	n/a	n/a
7	CEBPB	chr19:56736715-56737020	A549	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
8	CEBPB	chr19:56744025-56744198	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr19:56732731-56733102	K562	blood:	n/a	chr19:56732934-56732945
10	CEBPB	chr19:56732645-56733248	Hela-S3	cervix:	n/a	chr19:56732934-56732945
11	CEBPB	chr19:56741741-56741909	H1-hESC	embryonic stem cell:	n/a	chr19:56741810-56741821
12	CEBPB	chr19:56732773-56733100	IMR90	lung:	n/a	chr19:56732934-56732945
13	CEBPB	chr19:56732803-56733050	K562	blood:	n/a	chr19:56732934-56732945
14	CEBPB	chr19:56741673-56741957	K562	blood:	n/a	chr19:56741810-56741821
15	CEBPB	chr19:56741649-56741971	A549	lung:	n/a	chr19:56741810-56741821
16	CEBPB	chr19:56736709-56737013	Hela-S3	cervix:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
17	CEBPB	chr19:56732726-56733084	MCF-7	breast:	n/a	chr19:56732934-56732945
18	CEBPB	chr19:56736739-56736963	HepG2	liver:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
19	CEBPB	chr19:56732747-56733109	K562	blood:	n/a	chr19:56732934-56732945
20	CEBPB	chr19:56736713-56736976	K562	blood:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
21	CEBPB	chr19:56732796-56733078	A549	lung:	n/a	chr19:56732934-56732945
22	CEBPB	chr19:56732791-56733124	H1-hESC	embryonic stem cell:	n/a	chr19:56732934-56732945
23	CEBPB	chr19:56741646-56741970	HepG2	liver:	n/a	chr19:56741810-56741821
24	CEBPB	chr19:56736697-56737012	IMR90	lung:	n/a	chr19:56736904-56736915 chr19:56736832-56736843 chr19:56736904-56736915
25	CEBPD	chr19:56732776-56733035	K562	blood:	n/a	n/a
26	CTCF	chr19:56732858-56733182	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr19:56733200-56733350	HEK293	kidney:	n/a	n/a
28	CTCF	chr19:56728840-56728990	HMEC	breast:	n/a	n/a
29	CTCF	chr19:56733034-56733132	GM12892	blood:	n/a	n/a
30	CTCF	chr19:56732960-56733110	HVMF	connective:	n/a	n/a
31	CTCF	chr19:56732940-56733090	HMF	breast:	n/a	n/a
32	CTCF	chr19:56732975-56733113	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr19:56732940-56733090	GM12873	blood:	n/a	n/a
34	CTCF	chr19:56732979-56733180	Gliobla	brain:	n/a	n/a
35	CTCF	chr19:56732940-56733090	AG09319	gingival:	n/a	n/a
36	CTCF	chr19:56732940-56733090	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr19:56734400-56734650	GM12873	blood:	n/a	n/a
38	CTCF	chr19:56734367-56734590	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr19:56734457-56734488	GM10266	blood:	n/a	n/a
40	CTCF	chr19:56734380-56734530	GM12873	blood:	n/a	n/a
41	CTCF	chr19:56732960-56733110	A549	lung:	n/a	n/a
42	CTCF	chr19:56732940-56733090	BE2_C	brain:	n/a	n/a
43	CTCF	chr19:56732920-56733070	GM12864	blood:	n/a	n/a
44	CTCF	chr19:56732980-56733130	RPTEC	kidney:	n/a	n/a
45	CTCF	chr19:56735755-56735795	GM10248	blood:	n/a	n/a
46	CTCF	chr19:56732920-56733070	HRE	kidney:	n/a	n/a
47	CTCF	chr19:56733260-56733410	HCM	heart:	n/a	n/a
48	CTCF	chr19:56734297-56734627	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr19:56732960-56733110	HA-sp	spinal cord:	n/a	n/a
50	CTCF	chr19:56734420-56734570	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:56732932-56732982	NH-A	brain:	n/a
2	chr19:56741019-56741069	MCF10A-Er-Src	breast:	n/a
3	chr19:56732932-56732982	NH-A	brain:	n/a
4	chr19:56741019-56741069	MCF10A-Er-Src	breast:	n/a
5	chr19:56739741-56739791	AoSMC	blood vessel:	n/a
6	chr19:56739788-56739838	AG09319	gingival:	n/a
7	chr19:56739782-56739832	HRPEpiC	eye:	n/a
8	chr19:56741019-56741069	GM19239	blood:	n/a
9	chr19:56728589-56728639	GM06990	blood:	n/a
10	chr19:56738933-56738983	HMEC	breast:	n/a
11	chr19:56730494-56730544	GM06990	blood:	n/a
12	chr19:56742355-56742405	HCPEpiC	choroid plexus:	n/a
13	chr19:56738933-56738983	GM12891	blood:	n/a
14	chr19:56739782-56739832	HAEpiC	amniotic membrane:	n/a
15	chr19:56732932-56732982	SK-N-SH	brain:	n/a
16	chr19:56739731-56739781	GM12891	blood:	n/a
17	chr19:56733045-56733095	HAEpiC	amniotic membrane:	n/a
18	chr19:56732932-56732982	HEEpiC	esophagus:	n/a
19	chr19:56739573-56739623	MCF10A-Er-Src	breast:	n/a
20	chr19:56728422-56728472	MCF-7	breast:	n/a
21	chr19:56742355-56742405	HMEC	breast:	n/a
22	chr19:56739782-56739832	Caco-2	colon:	n/a
23	chr19:56740672-56740722	HIPEpiC	eye:	n/a
24	chr19:56738933-56738983	AG04450	lung:	fetal
25	chr19:56728422-56728472	NH-A	brain:	n/a
26	chr19:56728422-56728472	GM12891	blood:	n/a
27	chr19:56732932-56732982	ovcar-3	ovarian:	n/a
28	chr19:56739749-56739799	AG04450	lung:	fetal
29	chr19:56733045-56733095	ovcar-3	ovarian:	n/a
30	chr19:56739731-56739781	NB4	blood:	n/a
31	chr19:56739741-56739791	Caco-2	colon:	n/a
32	chr19:56739749-56739799	NB4	blood:	n/a
33	chr19:56739782-56739832	SKMC	muscle:	n/a
34	chr19:56733045-56733095	PrEC	prostate:	n/a
35	chr19:56739573-56739623	AG09309	skin:	n/a
36	chr19:56739731-56739781	HL-60	blood:	n/a
37	chr19:56739741-56739791	HUVEC	blood vessel:	n/a
38	chr19:56739573-56739623	NH-A	brain:	n/a
39	chr19:56728422-56728472	SAEC	small airway:	n/a
40	chr19:56732932-56732982	LNCaP	prostate:	n/a
41	chr19:56739741-56739791	SK-N-MC	brain:	n/a
42	chr19:56741019-56741069	HepG2	liver:	n/a
43	chr19:56742355-56742405	HEEpiC	esophagus:	n/a
44	chr19:56739788-56739838	SK-N-MC	brain:	n/a
45	chr19:56732932-56732982	AG09309	skin:	n/a
46	chr19:56742355-56742405	AG09309	skin:	n/a
47	chr19:56732932-56732982	HCPEpiC	choroid plexus:	n/a
48	chr19:56739868-56739918	AG09309	skin:	n/a
49	chr19:56739749-56739799	HRPEpiC	eye:	n/a
50	chr19:56728589-56728639	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:56587934..56588448-chr19:56732565..56733070,2	MCF-7	breast:
2	chr19:56717707..56719210-chr19:56732793..56735030,2	MCF-7	breast:
3	chr19:56731454..56732253-chr19:56820726..56821606,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000242411	TF binding region
ZSCAN5A	TF binding region
ENSG00000242411	CpG island
ZSCAN5A	CpG island

Extended variants
information (count: 910 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:910 , 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	rs565798546	chr19:56727323-56727324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528080589	chr19:56727371-56727372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs7247056	chr19:56727401-56727402	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs191520532	chr19:56727433-56727434	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs535524277	chr19:56727441-56727442	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs557491114	chr19:56727449-56727450	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs142551685	chr19:56727474-56727475	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs552769620	chr19:56727509-56727510	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs78714335	chr19:56727510-56727511	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs536878316	chr19:56727511-56727512	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs79851675	chr19:56727512-56727513	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs373032111	chr19:56727525-56727526	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs79574114	chr19:56727555-56727556	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs544998131	chr19:56727570-56727571	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs66649854	chr19:56727606-56727607	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs577473652	chr19:56727634-56727635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147718003	chr19:56727641-56727642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371132033	chr19:56727677-56727678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543364319	chr19:56727680-56727681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563467681	chr19:56727716-56727717	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs373815174	chr19:56727721-56727722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs12973406	chr19:56727776-56727777	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs542844508	chr19:56727782-56727783	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541277617	chr19:56727786-56727787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs113188879	chr19:56727799-56727800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs114691975	chr19:56727818-56727819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186319668	chr19:56727827-56727828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs118101022	chr19:56727844-56727845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531195401	chr19:56727921-56727922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200297202	chr19:56727955-56727956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201487013	chr19:56727957-56727958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs79906766	chr19:56727958-56727959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs10522110	chr19:56727980-56727981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs376129129	chr19:56728001-56728002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189881007	chr19:56728029-56728030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547963989	chr19:56728056-56728057	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533690720	chr19:56728068-56728069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144615042	chr19:56728115-56728116	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146863526	chr19:56728170-56728171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538754466	chr19:56728189-56728190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140721389	chr19:56728203-56728204	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs182100992	chr19:56728216-56728217	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs187585014	chr19:56728217-56728218	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs556961971	chr19:56728221-56728222	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs367880036	chr19:56728258-56728259	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs531275425	chr19:56728261-56728262	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs573921202	chr19:56728265-56728266	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs542457884	chr19:56728266-56728267	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs559594413	chr19:56728267-56728268	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs71368885	chr19:56728279-56728280	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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

Chromatin state (count:317 , 50 per page) page: 1 2 3 4 5 6 7

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

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