Variant report

Variant	esv3415719
Chromosome Location	chr19:21511760-21519079
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:480)
CpG islands
(count:612)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21511981-21512446	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:21511352-21511789	K562	blood:	n/a	n/a
3	ATF1	chr19:21512075-21512439	K562	blood:	n/a	n/a
4	ATF1	chr19:21516826-21516854	K562	blood:	n/a	n/a
5	ATF2	chr19:21512025-21512405	GM12878	blood:	n/a	n/a
6	BATF	chr19:21512047-21512392	GM12878	blood:	n/a	n/a
7	BCLAF1	chr19:21511741-21512420	GM12878	blood:	n/a	chr19:21511749-21511762
8	BCLAF1	chr19:21511700-21512480	GM12878	blood:	n/a	chr19:21511749-21511762
9	BHLHE40	chr19:21511934-21512494	GM12878	blood:	n/a	n/a
10	BHLHE40	chr19:21511805-21512401	K562	blood:	n/a	n/a
11	BRCA1	chr19:21512062-21512389	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr19:21511953-21512347	GM12878	blood:	n/a	n/a
13	CBX3	chr19:21511688-21512473	K562	blood:	n/a	n/a
14	CBX3	chr19:21518494-21518875	K562	blood:	n/a	n/a
15	CBX3	chr19:21512080-21512432	K562	blood:	n/a	n/a
16	CBX3	chr19:21518473-21518918	K562	blood:	n/a	n/a
17	CCNT2	chr19:21511735-21512332	K562	blood:	n/a	n/a
18	CEBPD	chr19:21511872-21512210	HepG2	liver:	n/a	n/a
19	CEBPD	chr19:21511987-21512428	K562	blood:	n/a	n/a
20	CHD1	chr19:21511152-21512118	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD1	chr19:21511315-21512402	GM12878	blood:	n/a	n/a
22	CHD2	chr19:21511775-21512315	K562	blood:	n/a	n/a
23	CHD2	chr19:21511911-21512374	GM12878	blood:	n/a	n/a
24	CHD2	chr19:21511821-21512364	Hela-S3	cervix:	n/a	n/a
25	CREB1	chr19:21511863-21512550	HepG2	liver:	n/a	n/a
26	CREB1	chr19:21511953-21512389	A549	lung:	n/a	n/a
27	CTCF	chr19:21518700-21518850	HPF	lung:	n/a	n/a
28	CTCF	chr19:21511620-21511770	AG09319	gingival:	n/a	n/a
29	CTCF	chr19:21518680-21518830	BE2_C	brain:	n/a	n/a
30	CTCF	chr19:21511660-21511810	HVMF	connective:	n/a	n/a
31	CTCF	chr19:21518660-21518810	HMF	breast:	n/a	n/a
32	CTCF	chr19:21518789-21518869	Gliobla	brain:	n/a	n/a
33	CTCF	chr19:21511640-21511790	GM06990	blood:	n/a	n/a
34	CTCF	chr19:21512212-21512309	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr19:21518700-21518850	HEK293	kidney:	n/a	n/a
36	CTCF	chr19:21518720-21518870	GM12864	blood:	n/a	n/a
37	CTCF	chr19:21518700-21518850	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr19:21511680-21511830	AG09319	gingival:	n/a	n/a
39	CTCF	chr19:21518776-21518842	MCF-7	breast:	n/a	n/a
40	CTCF	chr19:21511620-21511770	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr19:21518820-21518970	RPTEC	kidney:	n/a	n/a
42	CTCF	chr19:21518803-21518834	GM13977	blood:	n/a	n/a
43	CTCF	chr19:21518700-21518850	GM12873	blood:	n/a	n/a
44	CTCF	chr19:21511694-21511799	MCF-7	breast:	n/a	n/a
45	CTCF	chr19:21511640-21511790	AG10803	skin:	n/a	n/a
46	CTCF	chr19:21511747-21511772	MCF-7	breast:	n/a	n/a
47	CTCF	chr19:21512000-21512150	Caco-2	colon:	n/a	chr19:21512064-21512072 chr19:21512063-21512071
48	CTCF	chr19:21518660-21518810	HCT-116	colon:	n/a	n/a
49	CTCF	chr19:21518660-21518810	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr19:21511680-21511830	HBMEC	blood vessel:	n/a	n/a

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21512191-21512241	AG04450	lung:	fetal
2	chr19:21512202-21512252	U87	brain:	n/a
3	chr19:21512191-21512241	AG04450	lung:	fetal
4	chr19:21512202-21512252	U87	brain:	n/a
5	chr19:21512258-21512308	GM12878	blood:	n/a
6	chr19:21512258-21512308	AoSMC	blood vessel:	n/a
7	chr19:21513138-21513188	HRPEpiC	eye:	n/a
8	chr19:21513650-21513700	A549	lung:	n/a
9	chr19:21513650-21513700	ProgFib	skin:	n/a
10	chr19:21513138-21513188	HepG2	liver:	n/a
11	chr19:21512378-21512428	PANC-1	pancreas:	n/a
12	chr19:21512202-21512252	Hela-S3	cervix:	n/a
13	chr19:21513650-21513700	Jurkat	blood:	n/a
14	chr19:21512378-21512428	AG09319	gingival:	n/a
15	chr19:21512378-21512428	NHDF-neo	bronchial:	n/a
16	chr19:21512378-21512428	AoSMC	blood vessel:	n/a
17	chr19:21512141-21512191	U87	brain:	n/a
18	chr19:21512141-21512191	HCT-116	colon:	n/a
19	chr19:21512127-21512177	HCM	heart:	n/a
20	chr19:21512166-21512216	SK-N-SH_RA	brain:	n/a
21	chr19:21512141-21512191	HRE	kidney:	n/a
22	chr19:21512127-21512177	HEK293	kidney:	embryo
23	chr19:21512202-21512252	NH-A	brain:	n/a
24	chr19:21513138-21513188	NT2-D1	testis:	n/a
25	chr19:21512258-21512308	HAEpiC	amniotic membrane:	n/a
26	chr19:21512191-21512241	BJ	skin:	n/a
27	chr19:21512202-21512252	ovcar-3	ovarian:	n/a
28	chr19:21511996-21512046	AG04450	lung:	fetal
29	chr19:21512191-21512241	AG09309	skin:	n/a
30	chr19:21511996-21512046	U87	brain:	n/a
31	chr19:21512141-21512191	BE2_C	brain:	n/a
32	chr19:21512141-21512191	MCF10A-Er-Src	breast:	n/a
33	chr19:21511996-21512046	HAEpiC	amniotic membrane:	n/a
34	chr19:21512202-21512252	HCT-116	colon:	n/a
35	chr19:21512166-21512216	MCF-7	breast:	n/a
36	chr19:21512202-21512252	HEEpiC	esophagus:	n/a
37	chr19:21512258-21512308	HRCEpiC	kidney:	n/a
38	chr19:21512202-21512252	HCM	heart:	n/a
39	chr19:21512166-21512216	HNPCEpiC	eye:	n/a
40	chr19:21512191-21512241	NHBE	bronchial:	n/a
41	chr19:21512202-21512252	AG09319	gingival:	n/a
42	chr19:21513650-21513700	GM12878	blood:	n/a
43	chr19:21512166-21512216	GM06990	blood:	n/a
44	chr19:21511996-21512046	HCF	heart:	n/a
45	chr19:21513650-21513700	SK-N-SH	brain:	n/a
46	chr19:21513650-21513700	IMR90	lung:	fetal
47	chr19:21512202-21512252	PANC-1	pancreas:	n/a
48	chr19:21512378-21512428	NH-A	brain:	n/a
49	chr19:21512127-21512177	CMK	blood:	n/a
50	chr19:21512166-21512216	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:21509704..21512429-chr19:21517111..21519937,3	K562	blood:
2	chr19:21501353..21503397-chr19:21510480..21512126,2	MCF-7	breast:
3	chr19:21511256..21513599-chr19:21513725..21515814,2	MCF-7	breast:
4	chr19:21511427..21512224-chr9:140135317..140136194,2	Hela-S3	cervix:
5	chr19:21510924..21513197-chr19:21688433..21691004,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF708	TF binding region
ZNF708	CpG island
ENSG00000197013	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000182141	chromatin interactions

Extended variants
information (count: 255 )
Associated
traits (count: 41 )

Variant overlapped rSNPs/rCNVs (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11669790	chr19:21511782-21511783	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs11085443	chr19:21511784-21511785	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs146475311	chr19:21511785-21511786	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs566550223	chr19:21511809-21511810	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs534039372	chr19:21511818-21511819	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs558562384	chr19:21511834-21511835	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs537685150	chr19:21511909-21511910	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs34499034	chr19:21511913-21511914	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs112172046	chr19:21511915-21511916	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs2968051	chr19:21511975-21511976	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543198571	chr19:21511976-21511977	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs376603584	chr19:21512009-21512010	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs370678667	chr19:21512057-21512058	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs556613713	chr19:21512139-21512140	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs574945203	chr19:21512184-21512185	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs2997212	chr19:21512188-21512189	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs62107534	chr19:21512191-21512192	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs572540296	chr19:21512198-21512199	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs75175775	chr19:21512201-21512202	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs564605121	chr19:21512211-21512212	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs543486980	chr19:21512222-21512223	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs558598494	chr19:21512241-21512242	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs375028787	chr19:21512242-21512243	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs368427317	chr19:21512243-21512244	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs61035285	chr19:21512277-21512278	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs562151869	chr19:21512285-21512286	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs529692051	chr19:21512300-21512301	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547877038	chr19:21512301-21512302	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs12461384	chr19:21512321-21512322	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs533730868	chr19:21512362-21512363	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs57626552	chr19:21512369-21512370	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs559562090	chr19:21512471-21512472	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs570626856	chr19:21512492-21512493	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113403213	chr19:21512493-21512494	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs556550995	chr19:21512514-21512515	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs574883876	chr19:21512538-21512539	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs535892882	chr19:21512577-21512578	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs12461812	chr19:21512595-21512596	Active TSS Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs190321065	chr19:21512646-21512647	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527889737	chr19:21512676-21512677	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs62107536	chr19:21512677-21512678	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs368941107	chr19:21512694-21512695	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192313874	chr19:21512739-21512740	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1678832	chr19:21512782-21512783	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184745552	chr19:21512784-21512785	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188117980	chr19:21512806-21512807	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs530105108	chr19:21512837-21512838	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs79016982	chr19:21512859-21512860	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs76032627	chr19:21512865-21512866	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557792775	chr19:21512884-21512885	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:41)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
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
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:200 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21509800-21512600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr19:21510400-21512600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr19:21510400-21512600	Active TSS	Fetal Brain Female	brain
4	chr19:21510600-21511800	Flanking Active TSS	Primary B cells from cord blood	blood
5	chr19:21510600-21512400	Active TSS	Ovary	ovary
6	chr19:21510600-21512400	Active TSS	Hela-S3	cervix
7	chr19:21510800-21511800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr19:21510800-21512200	Active TSS	HMEC	breast
9	chr19:21510800-21512400	Active TSS	H1 Cell Line	embryonic stem cell
10	chr19:21510800-21512400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr19:21510800-21512400	Active TSS	iPS-15b Cell Line	embryonic stem cell
12	chr19:21510800-21512400	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr19:21510800-21512400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr19:21510800-21512400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr19:21510800-21512400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
16	chr19:21510800-21512400	Active TSS	Right Atrium	heart
17	chr19:21510800-21512400	Active TSS	A549	lung
18	chr19:21510800-21512400	Active TSS	GM12878-XiMat	blood
19	chr19:21510800-21512400	Active TSS	NHDF-Ad	bronchial
20	chr19:21510800-21512400	Active TSS	NHLF	lung
21	chr19:21510800-21512600	Active TSS	ES-I3 Cell Line	embryonic stem cell
22	chr19:21510800-21512600	Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr19:21510800-21512600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr19:21510800-21512600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr19:21510800-21512600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr19:21510800-21512600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr19:21510800-21512600	Active TSS	Brain Cingulate Gyrus	brain
28	chr19:21510800-21512600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr19:21510800-21512600	Active TSS	Fetal Brain Male	brain
30	chr19:21511000-21511800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr19:21511000-21511800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:21511000-21512200	Active TSS	Fetal Muscle Trunk	muscle
33	chr19:21511000-21512400	Active TSS	H9 Cell Line	embryonic stem cell
34	chr19:21511000-21512400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr19:21511000-21512400	Active TSS	Primary hematopoietic stem cells short term culture	blood
36	chr19:21511000-21512400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr19:21511000-21512400	Active TSS	Brain Angular Gyrus	brain
38	chr19:21511000-21512400	Active TSS	Colon Smooth Muscle	Colon
39	chr19:21511000-21512400	Active TSS	Fetal Intestine Large	intestine
40	chr19:21511000-21512600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr19:21511000-21512600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr19:21511000-21512600	Active TSS	HUES6 Cell Line	embryonic stem cell
43	chr19:21511000-21512600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr19:21511000-21512600	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr19:21511000-21512600	Active TSS	Stomach Smooth Muscle	stomach
46	chr19:21511000-21512600	Active TSS	HSMM	muscle
47	chr19:21511000-21512600	Active TSS	HSMMtube	muscle
48	chr19:21511000-21512600	Active TSS	K562	blood
49	chr19:21511200-21512200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
50	chr19:21511200-21512200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links