Variant report

Variant	nsv963024
Chromosome Location	chr19:21686690-21722618
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	ARID3A	chr19:21689384-21689643	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:21688183-21688449	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:21688150-21688402	K562	blood:	n/a	n/a
4	ATF1	chr19:21688140-21688844	K562	blood:	n/a	n/a
5	ATF2	chr19:21688277-21688624	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:21688505-21688907	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr19:21688222-21688771	GM12878	blood:	n/a	n/a
8	BHLHE40	chr19:21688144-21689372	GM12878	blood:	n/a	n/a
9	BHLHE40	chr19:21688113-21689201	K562	blood:	n/a	n/a
10	BHLHE40	chr19:21693031-21693169	K562	blood:	n/a	n/a
11	BHLHE40	chr19:21688202-21688938	HepG2	liver:	n/a	n/a
12	CBX3	chr19:21702263-21702592	K562	blood:	n/a	n/a
13	CBX3	chr19:21702289-21702654	K562	blood:	n/a	n/a
14	CCNT2	chr19:21688275-21688660	K562	blood:	n/a	chr19:21688608-21688617
15	CCNT2	chr19:21691185-21691385	K562	blood:	n/a	n/a
16	CEBPB	chr19:21689428-21689789	K562	blood:	n/a	n/a
17	CEBPB	chr19:21704016-21704332	IMR90	lung:	n/a	chr19:21704174-21704185
18	CEBPB	chr19:21715804-21716043	K562	blood:	n/a	n/a
19	CEBPB	chr19:21688274-21689053	H1-hESC	embryonic stem cell:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
20	CEBPB	chr19:21688590-21689217	MCF-7	breast:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
21	CEBPB	chr19:21688394-21689023	ECC-1	luminal epithelium:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
22	CEBPB	chr19:21704035-21704303	A549	lung:	n/a	chr19:21704174-21704185
23	CEBPB	chr19:21688302-21689099	K562	blood:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
24	CEBPB	chr19:21688289-21689034	HepG2	liver:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
25	CEBPB	chr19:21715858-21715920	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr19:21688567-21689116	MCF-7	breast:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
27	CEBPB	chr19:21688619-21689043	ECC-1	luminal epithelium:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
28	CEBPB	chr19:21688740-21688955	HepG2	liver:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
29	CEBPB	chr19:21704019-21704348	HepG2	liver:	n/a	chr19:21704174-21704185
30	CEBPB	chr19:21688461-21689067	K562	blood:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
31	CEBPB	chr19:21704026-21704273	K562	blood:	n/a	chr19:21704174-21704185
32	CEBPB	chr19:21688302-21689216	IMR90	lung:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
33	CEBPB	chr19:21688289-21689041	HepG2	liver:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
34	CEBPB	chr19:21688594-21689031	HepG2	liver:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
35	CEBPB	chr19:21688679-21689010	K562	blood:	n/a	chr19:21688851-21688862 chr19:21688852-21688863 chr19:21688851-21688864
36	CEBPD	chr19:21691055-21691459	K562	blood:	n/a	n/a
37	CEBPD	chr19:21688270-21689083	K562	blood:	n/a	n/a
38	CEBPD	chr19:21688336-21688573	HepG2	liver:	n/a	n/a
39	CEBPZ	chr19:21702442-21702596	HepG2	liver:	n/a	n/a
40	CHD1	chr19:21688440-21688838	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr19:21688171-21688912	GM12878	blood:	n/a	n/a
42	CHD2	chr19:21688223-21688824	K562	blood:	n/a	n/a
43	CHD2	chr19:21688207-21688843	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr19:21688323-21688783	HepG2	liver:	n/a	n/a
45	CREB1	chr19:21688122-21688567	HepG2	liver:	n/a	n/a
46	CREB1	chr19:21688156-21688841	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr19:21688057-21688668	GM12878	blood:	n/a	n/a
48	CREB1	chr19:21688132-21688947	GM12878	blood:	n/a	n/a
49	CREB1	chr19:21688180-21689008	HepG2	liver:	n/a	n/a
50	CREB1	chr19:21688181-21688468	ECC-1	luminal epithelium:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21690914-21690964	BE2_C	brain:	n/a
2	chr19:21690914-21690964	BE2_C	brain:	n/a
3	chr19:21688304-21688354	GM06990	blood:	n/a
4	chr19:21690914-21690964	HCF	heart:	n/a
5	chr19:21688304-21688354	H1-hESC	embryonic stem cell:	embryo
6	chr19:21688647-21688697	Caco-2	colon:	n/a
7	chr19:21687300-21687350	GM12892	blood:	n/a
8	chr19:21688263-21688313	HRE	kidney:	n/a
9	chr19:21688304-21688354	HCPEpiC	choroid plexus:	n/a
10	chr19:21688647-21688697	T-47D	breast:	n/a
11	chr19:21688739-21688789	AG04450	lung:	fetal
12	chr19:21688519-21688569	LNCaP	prostate:	n/a
13	chr19:21688397-21688447	GM19239	blood:	n/a
14	chr19:21688755-21688805	NHBE	bronchial:	n/a
15	chr19:21687792-21687842	AG10803	skin:	n/a
16	chr19:21688828-21688878	SAEC	small airway:	n/a
17	chr19:21688905-21688955	NHBE	bronchial:	n/a
18	chr19:21688905-21688955	A549	lung:	n/a
19	chr19:21688905-21688955	HMEC	breast:	n/a
20	chr19:21687792-21687842	HCM	heart:	n/a
21	chr19:21688828-21688878	GM06990	blood:	n/a
22	chr19:21687300-21687350	NHBE	bronchial:	n/a
23	chr19:21688397-21688447	SK-N-MC	brain:	n/a
24	chr19:21688304-21688354	SAEC	small airway:	n/a
25	chr19:21688905-21688955	AoSMC	blood vessel:	n/a
26	chr19:21688905-21688955	H1-hESC	embryonic stem cell:	embryo
27	chr19:21687792-21687842	HCF	heart:	n/a
28	chr19:21688647-21688697	MCF10A-Er-Src	breast:	n/a
29	chr19:21687792-21687842	NHBE	bronchial:	n/a
30	chr19:21688304-21688354	A549	lung:	n/a
31	chr19:21688905-21688955	BJ	skin:	n/a
32	chr19:21687300-21687350	Jurkat	blood:	n/a
33	chr19:21688263-21688313	SK-N-MC	brain:	n/a
34	chr19:21688263-21688313	ovcar-3	ovarian:	n/a
35	chr19:21688905-21688955	Hela-S3	cervix:	n/a
36	chr19:21690914-21690964	GM12878	blood:	n/a
37	chr19:21688304-21688354	ovcar-3	ovarian:	n/a
38	chr19:21688647-21688697	HRPEpiC	eye:	n/a
39	chr19:21688828-21688878	HCT-116	colon:	n/a
40	chr19:21688519-21688569	HIPEpiC	eye:	n/a
41	chr19:21690914-21690964	A549	lung:	n/a
42	chr19:21690914-21690964	Caco-2	colon:	n/a
43	chr19:21687792-21687842	HepG2	liver:	n/a
44	chr19:21688905-21688955	SK-N-MC	brain:	n/a
45	chr19:21688519-21688569	CMK	blood:	n/a
46	chr19:21688739-21688789	NT2-D1	testis:	n/a
47	chr19:21687792-21687842	SK-N-SH	brain:	n/a
48	chr19:21687792-21687842	SK-N-SH_RA	brain:	n/a
49	chr19:21688519-21688569	HRPEpiC	eye:	n/a
50	chr19:21688739-21688789	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:21691065..21693260-chr19:21696883..21699244,2	MCF-7	breast:
2	chr19:21691580..21693623-chr19:22017806..22019839,2	MCF-7	breast:
3	chr19:21686543..21689002-chr19:21689124..21690640,2	MCF-7	breast:
4	chr19:21691065..21693260-chr19:21696883..21699244,2	MCF-7	breast:
5	chr19:21689678..21691656-chr19:21877431..21879636,2	K562	blood:
6	chr19:21510924..21513197-chr19:21688433..21691004,2	MCF-7	breast:
7	chr19:21687904..21690838-chr19:21705351..21707923,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF429-3	chr19:21688787-21688882	NONHSAT063719
2	lnc-ZNF429-3	chr19:21688443-21688576	NONHSAT063719
3	lnc-ZNF429-3	chr19:21690322-21690466	NONHSAT063719
4	lnc-ZNF429-1	chr19:21688064-21688090	NONHSAT063713
5	lnc-ZNF708-11	chr19:21704145-21704698	NONHSAT063722

Variant related genes	Relation type
ZNF429	TF binding region
ENSG00000268705	TF binding region
ZNF429	CpG island
ENSG00000268705	CpG island
ENSG00000182141	chromatin interactions
ENSG00000198521	chromatin interactions
ENSG00000197013	chromatin interactions

Extended variants
information (count: 1747 )
Associated
traits (count: 43 )

Variant overlapped rSNPs/rCNVs (count:1747 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529209968	chr19:21686707-21686708	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs189646635	chr19:21686723-21686724	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs2650806	chr19:21686745-21686746	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs374459995	chr19:21686773-21686774	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs565489532	chr19:21686804-21686805	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs113745133	chr19:21686810-21686811	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs188846576	chr19:21686811-21686812	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs181245643	chr19:21686813-21686814	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs73017716	chr19:21686819-21686820	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
10	rs8102526	chr19:21686859-21686860	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs8102528	chr19:21686865-21686866	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs527923582	chr19:21686866-21686867	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs58222465	chr19:21686884-21686885	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148162752	chr19:21686921-21686922	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs146217883	chr19:21686941-21686942	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs375715785	chr19:21686944-21686945	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs113249059	chr19:21687009-21687010	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs567712730	chr19:21687014-21687015	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs567788098	chr19:21687018-21687019	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs535308272	chr19:21687022-21687023	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs8102699	chr19:21687049-21687050	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs546944199	chr19:21687087-21687088	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs71176890	chr19:21687158-21687159	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs386807797	chr19:21687159-21687160	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs59687008	chr19:21687160-21687161	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs71176891	chr19:21687165-21687166	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs569696812	chr19:21687175-21687176	Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs571702266	chr19:21687220-21687221	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs545397428	chr19:21687231-21687232	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs557389497	chr19:21687240-21687241	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs575747354	chr19:21687301-21687302	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs543225071	chr19:21687303-21687304	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs561899197	chr19:21687304-21687305	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs538622566	chr19:21687315-21687316	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs201819100	chr19:21687317-21687318	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs529112742	chr19:21687326-21687327	Weak transcription Enhancers Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs541310320	chr19:21687373-21687374	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs191197806	chr19:21687388-21687389	Weak transcription Enhancers Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs536402810	chr19:21687436-21687437	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs533319972	chr19:21687437-21687438	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs551812263	chr19:21687441-21687442	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570132971	chr19:21687502-21687503	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs375128797	chr19:21687551-21687552	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs7252254	chr19:21687561-21687562	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs567836571	chr19:21687568-21687569	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs73546789	chr19:21687603-21687604	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs540723265	chr19:21687614-21687615	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs553203009	chr19:21687623-21687624	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs571616094	chr19:21687666-21687667	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs539011698	chr19:21687678-21687679	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:43)

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
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1539 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21658200-21687800	Weak transcription	Brain Substantia Nigra	brain
2	chr19:21666800-21687600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr19:21669000-21687600	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr19:21673400-21687800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr19:21674800-21687800	Weak transcription	Brain Hippocampus Middle	brain
6	chr19:21675800-21687200	Weak transcription	Primary T cells from cord blood	blood
7	chr19:21676000-21688000	Weak transcription	Fetal Stomach	stomach
8	chr19:21678000-21688000	Weak transcription	Thymus	Thymus
9	chr19:21679200-21688200	Weak transcription	Brain Angular Gyrus	brain
10	chr19:21680000-21687800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr19:21680000-21688200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr19:21680200-21687600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr19:21680200-21688200	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr19:21681200-21688400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr19:21681400-21688200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr19:21681600-21688200	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr19:21681800-21687600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr19:21681800-21688000	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr19:21681800-21688000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr19:21681800-21688200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr19:21681800-21688400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:21683800-21688000	Weak transcription	Fetal Intestine Large	intestine
23	chr19:21686400-21687400	Active TSS	Liver	Liver
24	chr19:21686600-21687400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr19:21687200-21687400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr19:21687200-21687400	Enhancers	Pancreas	Pancrea
27	chr19:21687200-21687600	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr19:21687200-21687800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr19:21687200-21688200	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr19:21687200-21688200	Enhancers	Primary neutrophils fromperipheralblood	blood
31	chr19:21687200-21688200	Enhancers	Primary T cells from cord blood	blood
32	chr19:21687200-21688200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr19:21687400-21687600	Weak transcription	Liver	Liver
34	chr19:21687400-21688000	Enhancers	Primary T cells fromperipheralblood	blood
35	chr19:21687400-21688000	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr19:21687400-21688000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr19:21687400-21688000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr19:21687400-21688000	Enhancers	Dnd41	blood
39	chr19:21687400-21688200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr19:21687400-21688200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr19:21687600-21687800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr19:21687600-21687800	Enhancers	Fetal Heart	heart
43	chr19:21687600-21688000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr19:21687600-21688000	Enhancers	Brain Anterior Caudate	brain
45	chr19:21687600-21688000	Enhancers	Brain Cingulate Gyrus	brain
46	chr19:21687600-21688000	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr19:21687600-21688000	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr19:21687600-21688000	Enhancers	K562	blood
49	chr19:21687600-21688000	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr19:21687600-21688200	Enhancers	Primary B cells from peripheral blood	blood

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