Variant report

Variant	nsv963031
Chromosome Location	chr19:23297529-23301004
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	BACH1	chr19:23299870-23300328	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr19:23300598-23300786	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr19:23300598-23300666	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chr19:23299891-23301413	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr19:23299685-23299854	GM12878	blood:	n/a	n/a
6	CHD2	chr19:23299572-23300608	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr19:23300140-23300290	GM06990	blood:	n/a	n/a
8	CTCF	chr19:23300127-23300260	MCF-7	breast:	n/a	n/a
9	CTCF	chr19:23300040-23300190	SAEC	small airway:	n/a	n/a
10	CTCF	chr19:23300020-23300170	AG04449	skin:	n/a	n/a
11	CTCF	chr19:23300100-23300250	AG04449	skin:	n/a	n/a
12	CTCF	chr19:23300155-23300262	ProgFib	skin:	n/a	n/a
13	CTCF	chr19:23300140-23300290	HCPEpiC	choroid plexus:	n/a	n/a
14	CTCF	chr19:23300200-23300350	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr19:23300220-23300370	HPAF	blood vessel:	n/a	n/a
16	CTCF	chr19:23299800-23299950	HRE	kidney:	n/a	n/a
17	CTCF	chr19:23300140-23300290	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr19:23300044-23300133	Fibrobl	skin:	n/a	n/a
19	CTCF	chr19:23300147-23300286	MCF-7	breast:	n/a	n/a
20	CTCF	chr19:23300145-23300146	MCF-7	breast:	n/a	n/a
21	E2F6	chr19:23299790-23300248	H1-hESC	embryonic stem cell:	n/a	chr19:23299818-23299826 chr19:23299818-23299825 chr19:23299817-23299827 chr19:23299818-23299826
22	EGR1	chr19:23299553-23299856	H1-hESC	embryonic stem cell:	n/a	chr19:23299717-23299732 chr19:23299723-23299733 chr19:23299718-23299731 chr19:23299718-23299731
23	ELF1	chr19:23299636-23299907	K562	blood:	n/a	chr19:23299808-23299817 chr19:23299806-23299819 chr19:23299807-23299818 chr19:23299839-23299848
24	ELF1	chr19:23299541-23300153	MCF-7	breast:	n/a	chr19:23299808-23299817 chr19:23299806-23299819 chr19:23299807-23299818 chr19:23299839-23299848 chr19:23300042-23300054
25	ELF1	chr19:23299543-23300030	MCF-7	breast:	n/a	chr19:23299808-23299817 chr19:23299806-23299819 chr19:23299807-23299818 chr19:23299839-23299848
26	ELF1	chr19:23299691-23299916	K562	blood:	n/a	chr19:23299808-23299817 chr19:23299806-23299819 chr19:23299807-23299818 chr19:23299839-23299848
27	ELF1	chr19:23299591-23300002	GM12878	blood:	n/a	chr19:23299808-23299817 chr19:23299806-23299819 chr19:23299807-23299818 chr19:23299839-23299848
28	GABPA	chr19:23299604-23299897	K562	blood:	n/a	chr19:23299723-23299732
29	GABPA	chr19:23299457-23300060	MCF-7	breast:	n/a	chr19:23299723-23299732
30	GATA2	chr19:23299554-23300304	SH-SY5Y	brain:	n/a	chr19:23300069-23300076
31	GATA3	chr19:23298924-23299184	SH-SY5Y	brain:	n/a	chr19:23298936-23298947
32	GATA3	chr19:23299488-23299876	T-47D	breast:	n/a	n/a
33	GTF2F1	chr19:23299716-23300493	H1-hESC	embryonic stem cell:	n/a	n/a
34	HA-E2F1	chr19:23299520-23300089	MCF-7	breast:	n/a	chr19:23299818-23299826 chr19:23299818-23299825 chr19:23299723-23299732 chr19:23299817-23299827 chr19:23299818-23299826
35	HEY1	chr19:23299835-23300010	HepG2	liver:	n/a	n/a
36	HEY1	chr19:23299871-23299975	HepG2	liver:	n/a	n/a
37	HEY1	chr19:23299758-23300036	K562	blood:	n/a	n/a
38	HEY1	chr19:23299832-23300044	K562	blood:	n/a	n/a
39	JUN	chr19:23299895-23300183	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr19:23300186-23300386	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAX	chr19:23298241-23298579	NB4	blood:	n/a	chr19:23298402-23298412
42	MAX	chr19:23299570-23300152	NB4	blood:	n/a	chr19:23299721-23299731 chr19:23299759-23299769
43	MAX	chr19:23298106-23298392	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAZ	chr19:23299564-23300470	IMR90	lung:	n/a	chr19:23299721-23299731 chr19:23299759-23299769
45	MXI1	chr19:23300539-23300668	H1-hESC	embryonic stem cell:	n/a	n/a
46	MXI1	chr19:23299693-23300267	H1-hESC	embryonic stem cell:	n/a	n/a
47	MXI1	chr19:23299311-23301143	SK-N-SH	brain:	n/a	n/a
48	MXI1	chr19:23299508-23300386	IMR90	lung:	n/a	n/a
49	MYC	chr19:23299661-23300062	NB4	blood:	n/a	chr19:23299721-23299731 chr19:23299759-23299769
50	MYC	chr19:23300376-23300576	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:23300066-23300116	AG10803	skin:	n/a
2	chr19:23299728-23299778	HPAEpiC	pulmonary alveolar:	n/a
3	chr19:23299889-23299939	GM19239	blood:	n/a
4	chr19:23300066-23300116	HRE	kidney:	n/a
5	chr19:23299728-23299778	HRE	kidney:	n/a
6	chr19:23299728-23299778	AG09309	skin:	n/a
7	chr19:23300066-23300116	HRCEpiC	kidney:	n/a
8	chr19:23300243-23300293	AG09319	gingival:	n/a
9	chr19:23299728-23299778	NHDF-neo	bronchial:	n/a
10	chr19:23299728-23299778	GM12892	blood:	n/a
11	chr19:23299889-23299939	HepG2	liver:	n/a
12	chr19:23300066-23300116	Jurkat	blood:	n/a
13	chr19:23300066-23300116	AG04450	lung:	fetal
14	chr19:23300066-23300116	H1-hESC	embryonic stem cell:	embryo
15	chr19:23299889-23299939	Hepatocyte	liver:	n/a
16	chr19:23299889-23299939	K562	blood:	n/a
17	chr19:23300243-23300293	HEEpiC	esophagus:	n/a
18	chr19:23299889-23299939	NHBE	bronchial:	n/a
19	chr19:23300066-23300116	ovcar-3	ovarian:	n/a
20	chr19:23299649-23299699	SKMC	muscle:	n/a
21	chr19:23299889-23299939	IMR90	lung:	fetal
22	chr19:23299649-23299699	Jurkat	blood:	n/a
23	chr19:23299649-23299699	SK-N-SH	brain:	n/a
24	chr19:23299649-23299699	HCT-116	colon:	n/a
25	chr19:23300066-23300116	GM19239	blood:	n/a
26	chr19:23299889-23299939	NB4	blood:	n/a
27	chr19:23299889-23299939	BE2_C	brain:	n/a
28	chr19:23300066-23300116	RPTEC	kidney:	n/a
29	chr19:23300243-23300293	BE2_C	brain:	n/a
30	chr19:23300066-23300116	BE2_C	brain:	n/a
31	chr19:23299889-23299939	MCF10A-Er-Src	breast:	n/a
32	chr19:23299728-23299778	ECC-1	luminal epithelium:	n/a
33	chr19:23300066-23300116	A549	lung:	n/a
34	chr19:23299649-23299699	GM19239	blood:	n/a
35	chr19:23299649-23299699	HEEpiC	esophagus:	n/a
36	chr19:23300243-23300293	HIPEpiC	eye:	n/a
37	chr19:23299649-23299699	AG10803	skin:	n/a
38	chr19:23300243-23300293	HepG2	liver:	n/a
39	chr19:23299649-23299699	HRE	kidney:	n/a
40	chr19:23300066-23300116	CMK	blood:	n/a
41	chr19:23299889-23299939	HIPEpiC	eye:	n/a
42	chr19:23299649-23299699	RPTEC	kidney:	n/a
43	chr19:23299649-23299699	PrEC	prostate:	n/a
44	chr19:23300066-23300116	T-47D	breast:	n/a
45	chr19:23300243-23300293	U87	brain:	n/a
46	chr19:23299889-23299939	HCT-116	colon:	n/a
47	chr19:23299649-23299699	AoSMC	blood vessel:	n/a
48	chr19:23299728-23299778	HMEC	breast:	n/a
49	chr19:23299728-23299778	AG10803	skin:	n/a
50	chr19:23299889-23299939	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:23299713..23300295-chr19:24269911..24270643,3	Hela-S3	cervix:
2	chr19:23256417..23259218-chr19:23299816..23301387,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF730-5	chr19:23299777-23299978	NONHSAT063860

Variant related genes	Relation type
ZNF730	TF binding region
ZNF730	CpG island
ENSG00000183850	chromatin interactions
ENSG00000213096	chromatin interactions
ENSG00000267886	chromatin interactions

Extended variants
information (count: 164 )
Associated
traits (count: 40 )

Variant overlapped rSNPs/rCNVs (count:164 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545774167	chr19:23297595-23297596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565316914	chr19:23297602-23297603	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs34572247	chr19:23297611-23297612	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs577414144	chr19:23297663-23297664	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs559526470	chr19:23297666-23297667	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531854700	chr19:23297721-23297722	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs544569888	chr19:23297786-23297787	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs12977913	chr19:23297793-23297794	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530421187	chr19:23297852-23297853	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs146417215	chr19:23297877-23297878	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs10716674	chr19:23297939-23297940	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs11311698	chr19:23297952-23297953	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs571115645	chr19:23298116-23298117	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs186383297	chr19:23298175-23298176	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs547884558	chr19:23298213-23298214	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs548568426	chr19:23298218-23298219	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs139542881	chr19:23298234-23298235	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs527762254	chr19:23298252-23298253	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs552685433	chr19:23298322-23298323	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs189973077	chr19:23298406-23298407	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs112142920	chr19:23298490-23298491	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs57651829	chr19:23298503-23298504	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs8107286	chr19:23298509-23298510	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs538783418	chr19:23298520-23298521	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs550362501	chr19:23298521-23298522	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs182970253	chr19:23298567-23298568	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs185985596	chr19:23298582-23298583	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs190445212	chr19:23298585-23298586	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs36096990	chr19:23298588-23298589	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs372216395	chr19:23298603-23298604	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs80103519	chr19:23298614-23298615	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572826989	chr19:23298627-23298628	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs184072096	chr19:23298683-23298684	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs188861637	chr19:23298724-23298725	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs576875392	chr19:23298730-23298731	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs374873275	chr19:23298732-23298733	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs141651881	chr19:23298734-23298735	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs79094894	chr19:23298755-23298756	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs35882915	chr19:23298773-23298774	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs76964790	chr19:23298844-23298845	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs192350760	chr19:23298849-23298850	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs560489421	chr19:23298856-23298857	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs527722952	chr19:23298857-23298858	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs2085999	chr19:23298866-23298867	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs564556232	chr19:23298907-23298908	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs564936891	chr19:23298908-23298909	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs531732224	chr19:23298910-23298911	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs550329428	chr19:23298922-23298923	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs372751074	chr19:23298923-23298924	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs7507929	chr19:23298976-23298977	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:40)

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
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:23274600-23299800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr19:23276800-23299400	Weak transcription	Right Ventricle	heart
3	chr19:23278800-23299400	Weak transcription	Primary B cells from cord blood	blood
4	chr19:23279200-23299400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr19:23282000-23299600	Weak transcription	Fetal Kidney	kidney
6	chr19:23282200-23299800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:23283000-23299600	Weak transcription	NHLF	lung
8	chr19:23283400-23299400	Weak transcription	Fetal Muscle Leg	muscle
9	chr19:23284400-23299400	Weak transcription	Fetal Lung	lung
10	chr19:23285000-23299200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr19:23285200-23299400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr19:23285200-23299600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr19:23285200-23299600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr19:23285600-23299600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr19:23285600-23299600	Weak transcription	Fetal Stomach	stomach
16	chr19:23285600-23299800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:23285600-23299800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:23285800-23299200	Weak transcription	Fetal Muscle Trunk	muscle
19	chr19:23285800-23299800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr19:23286000-23299600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr19:23286000-23299600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr19:23287800-23299400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr19:23288400-23299400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr19:23289000-23298800	Weak transcription	Dnd41	blood
25	chr19:23291000-23299400	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr19:23291200-23299400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr19:23291400-23299800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:23291800-23299400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
29	chr19:23291800-23299600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
30	chr19:23292000-23299600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr19:23292400-23299400	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr19:23293400-23298600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr19:23293800-23298200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr19:23295000-23299400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr19:23295800-23299000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr19:23298200-23298600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr19:23298600-23299400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr19:23298600-23299400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr19:23298800-23299400	Enhancers	Dnd41	blood
40	chr19:23299000-23299600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr19:23299200-23299400	Enhancers	Fetal Muscle Trunk	muscle
42	chr19:23299200-23299400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr19:23299200-23300400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr19:23299200-23301000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr19:23299400-23299600	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr19:23299400-23299600	Flanking Active TSS	Primary B cells from cord blood	blood
47	chr19:23299400-23299600	Enhancers	Primary B cells from peripheral blood	blood
48	chr19:23299400-23299600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
49	chr19:23299400-23299600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr19:23299400-23299600	Enhancers	Placenta Amnion	Placenta Amnion

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