Variant report

Variant	esv3336214
Chromosome Location	chr19:51858913-51861611
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:60)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:60 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr19:51859414-51859776	HepG2	liver:	n/a	n/a
2	CEBPB	chr19:51859389-51859870	HepG2	liver:	n/a	n/a
3	CEBPB	chr19:51859388-51859744	HepG2	liver:	n/a	n/a
4	CEBPB	chr19:51860142-51860144	HepG2	liver:	n/a	n/a
5	CEBPB	chr19:51859391-51859646	HepG2	liver:	n/a	n/a
6	CEBPB	chr19:51859347-51859773	HepG2	liver:	n/a	n/a
7	CEBPD	chr19:51859459-51859821	HepG2	liver:	n/a	n/a
8	CHD2	chr19:51859489-51859869	HepG2	liver:	n/a	n/a
9	EP300	chr19:51859315-51859771	HepG2	liver:	n/a	n/a
10	EP300	chr19:51859369-51859937	HepG2	liver:	n/a	n/a
11	EP300	chr19:51859426-51859744	HepG2	liver:	n/a	n/a
12	FOSL2	chr19:51859350-51859815	HepG2	liver:	n/a	n/a
13	FOXA1	chr19:51859418-51859837	HepG2	liver:	n/a	n/a
14	FOXA1	chr19:51859320-51859804	HepG2	liver:	n/a	n/a
15	FOXA1	chr19:51859355-51859867	HepG2	liver:	n/a	n/a
16	FOXA2	chr19:51859412-51859787	HepG2	liver:	n/a	n/a
17	HDAC2	chr19:51859340-51859791	HepG2	liver:	n/a	n/a
18	HDAC2	chr19:51859366-51859748	HepG2	liver:	n/a	n/a
19	HEY1	chr19:51859360-51860042	HepG2	liver:	n/a	n/a
20	HEY1	chr19:51859385-51859733	HepG2	liver:	n/a	n/a
21	HNF4A	chr19:51859341-51859761	HepG2	liver:	n/a	chr19:51859593-51859606 chr19:51859593-51859606
22	HNF4A	chr19:51859954-51860139	HepG2	liver:	n/a	n/a
23	HNF4A	chr19:51859361-51859753	HepG2	liver:	n/a	chr19:51859593-51859606 chr19:51859593-51859606
24	HNF4A	chr19:51859396-51860164	HepG2	liver:	n/a	chr19:51859593-51859606 chr19:51859593-51859606
25	HNF4G	chr19:51859401-51859753	HepG2	liver:	n/a	chr19:51859593-51859606 chr19:51859593-51859606
26	HNF4G	chr19:51859316-51859866	HepG2	liver:	n/a	chr19:51859593-51859606 chr19:51859593-51859606
27	JUND	chr19:51859444-51859826	HepG2	liver:	n/a	n/a
28	MBD4	chr19:51859328-51860000	HepG2	liver:	n/a	n/a
29	MYBL2	chr19:51859253-51859930	HepG2	liver:	n/a	n/a
30	MYBL2	chr19:51859321-51860039	HepG2	liver:	n/a	n/a
31	MYC	chr19:51859553-51859775	HepG2	liver:	n/a	n/a
32	NFIC	chr19:51859351-51859799	HepG2	liver:	n/a	chr19:51859720-51859748
33	NFIC	chr19:51859357-51859777	HepG2	liver:	n/a	chr19:51859720-51859748
34	NR2F2	chr19:51859348-51859924	HepG2	liver:	n/a	n/a
35	NR2F2	chr19:51859373-51860105	HepG2	liver:	n/a	n/a
36	POLR2A	chr19:51860069-51860211	K562	blood:	n/a	n/a
37	POLR2A	chr19:51859411-51860225	HepG2	liver:	n/a	n/a
38	POLR2A	chr19:51859531-51860158	K562	blood:	n/a	n/a
39	POLR2A	chr19:51859315-51860002	HepG2	liver:	n/a	n/a
40	POLR2A	chr19:51859493-51860222	HepG2	liver:	n/a	n/a
41	POLR2A	chr19:51859486-51860017	K562	blood:	n/a	n/a
42	POLR2A	chr19:51859373-51859906	HepG2	liver:	n/a	n/a
43	POLR2A	chr19:51860223-51860268	K562	blood:	n/a	n/a
44	POLR2A	chr19:51859539-51860069	HepG2	liver:	n/a	n/a
45	POLR2A	chr19:51860057-51860113	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr19:51859910-51860174	K562	blood:	n/a	n/a
47	POLR2A	chr19:51860035-51860068	K562	blood:	n/a	n/a
48	RCOR1	chr19:51859455-51860099	HepG2	liver:	n/a	n/a
49	RXRA	chr19:51859311-51859965	HepG2	liver:	n/a	n/a
50	RXRA	chr19:51859424-51859834	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:51859473-51859523	GM12891	blood:	n/a
2	chr19:51859529-51859579	K562	blood:	n/a
3	chr19:51859529-51859579	GM19239	blood:	n/a
4	chr19:51859529-51859579	PANC-1	pancreas:	n/a
5	chr19:51859473-51859523	SK-N-SH	brain:	n/a
6	chr19:51859529-51859579	HUVEC	blood vessel:	n/a
7	chr19:51859473-51859523	AG10803	skin:	n/a
8	chr19:51859473-51859523	SAEC	small airway:	n/a
9	chr19:51859473-51859523	HCT-116	colon:	n/a
10	chr19:51859529-51859579	A549	lung:	n/a
11	chr19:51859473-51859523	GM12892	blood:	n/a
12	chr19:51859529-51859579	HCM	heart:	n/a
13	chr19:51859529-51859579	HAEpiC	amniotic membrane:	n/a
14	chr19:51859529-51859579	AG04450	lung:	fetal
15	chr19:51859473-51859523	HepG2	liver:	n/a
16	chr19:51859529-51859579	Jurkat	blood:	n/a
17	chr19:51859529-51859579	HL-60	blood:	n/a
18	chr19:51859529-51859579	T-47D	breast:	n/a
19	chr19:51859473-51859523	HUVEC	blood vessel:	n/a
20	chr19:51859473-51859523	NB4	blood:	n/a
21	chr19:51859529-51859579	NHDF-neo	bronchial:	n/a
22	chr19:51859473-51859523	AoSMC	blood vessel:	n/a
23	chr19:51859529-51859579	SK-N-MC	brain:	n/a
24	chr19:51859529-51859579	SAEC	small airway:	n/a
25	chr19:51859473-51859523	HEEpiC	esophagus:	n/a
26	chr19:51859473-51859523	PrEC	prostate:	n/a
27	chr19:51859473-51859523	MCF-7	breast:	n/a
28	chr19:51859529-51859579	AG04449	skin:	fetal
29	chr19:51859529-51859579	HIPEpiC	eye:	n/a
30	chr19:51859473-51859523	GM06990	blood:	n/a
31	chr19:51859529-51859579	HEEpiC	esophagus:	n/a
32	chr19:51859529-51859579	NT2-D1	testis:	n/a
33	chr19:51859473-51859523	SKMC	muscle:	n/a
34	chr19:51859529-51859579	SK-N-SH	brain:	n/a
35	chr19:51859529-51859579	RPTEC	kidney:	n/a
36	chr19:51859529-51859579	AG09309	skin:	n/a
37	chr19:51859529-51859579	HNPCEpiC	eye:	n/a
38	chr19:51859473-51859523	AG04450	lung:	fetal
39	chr19:51859529-51859579	HCT-116	colon:	n/a
40	chr19:51859473-51859523	HRPEpiC	eye:	n/a
41	chr19:51859529-51859579	PFSK-1	brain:	n/a
42	chr19:51859529-51859579	HEK293	kidney:	embryo
43	chr19:51859529-51859579	ProgFib	skin:	n/a
44	chr19:51859473-51859523	HL-60	blood:	n/a
45	chr19:51859529-51859579	Caco-2	colon:	n/a
46	chr19:51859529-51859579	GM12891	blood:	n/a
47	chr19:51859473-51859523	U87	brain:	n/a
48	chr19:51859529-51859579	SKMC	muscle:	n/a
49	chr19:51859529-51859579	GM12892	blood:	n/a
50	chr19:51859529-51859579	NB4	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:51861247..51863236-chr19:51869920..51872324,2	MCF-7	breast:
2	chr19:51859965..51862618-chr19:51891276..51893885,2	K562	blood:
3	chr19:51842358..51844752-chr19:51861235..51862876,2	MCF-7	breast:
4	chr19:51857894..51859596-chr19:51867682..51869323,2	MCF-7	breast:
5	chr19:51846273..51849020-chr19:51857780..51860916,3	K562	blood:
6	chr19:51856394..51859731-chr19:51867776..51870627,3	MCF-7	breast:
7	chr19:51858074..51859587-chr19:51869492..51871118,2	MCF-7	breast:

No data

Variant related genes	Relation type
ETFB	TF binding region
ETFB	CpG island
ENSG00000262874	chromatin interactions
ENSG00000267905	chromatin interactions
ENSG00000105379	chromatin interactions
ENSG00000269403	chromatin interactions
ENSG00000268520	chromatin interactions
ENSG00000186806	chromatin interactions
ENSG00000160318	chromatin interactions
ENSG00000267984	chromatin interactions

Extended variants
information (count: 109 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:109 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199608913	chr19:51858920-51858921	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs544248640	chr19:51858965-51858966	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs563625179	chr19:51858998-51858999	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs80143357	chr19:51859051-51859052	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs545575230	chr19:51859090-51859091	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs11880444	chr19:51859111-51859112	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs11880473	chr19:51859112-51859113	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs55996055	chr19:51859131-51859132	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs192498801	chr19:51859195-51859196	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs184632388	chr19:51859210-51859211	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs373759468	chr19:51859241-51859242	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs532154885	chr19:51859242-51859243	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs550284328	chr19:51859264-51859265	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs11880489	chr19:51859287-51859288	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs536536163	chr19:51859326-51859327	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs554790944	chr19:51859352-51859353	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs201352066	chr19:51859371-51859372	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs66679413	chr19:51859374-51859375	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs34601865	chr19:51859375-51859376	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs61433337	chr19:51859376-51859377	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs114693949	chr19:51859377-51859378	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs544625614	chr19:51859417-51859418	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs150942910	chr19:51859418-51859419	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs192733404	chr19:51859425-51859426	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542943789	chr19:51859487-51859488	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs55861850	chr19:51859511-51859512	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs563519688	chr19:51859532-51859533	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs532284619	chr19:51859533-51859534	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs184711761	chr19:51859554-51859555	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs546735408	chr19:51859559-51859560	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs528309179	chr19:51859613-51859614	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs540399869	chr19:51859649-51859650	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs536146190	chr19:51859657-51859658	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs117488111	chr19:51859666-51859667	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs552481166	chr19:51859792-51859793	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs532093478	chr19:51859802-51859803	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs11881186	chr19:51859847-51859848	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs58800456	chr19:51859866-51859867	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs529647173	chr19:51859880-51859881	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548483656	chr19:51859888-51859889	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566791050	chr19:51859903-51859904	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534147412	chr19:51859936-51859937	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558707442	chr19:51859938-51859939	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570962578	chr19:51859965-51859966	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs57439176	chr19:51859978-51859979	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs556372280	chr19:51859986-51859987	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369540810	chr19:51859996-51859997	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs550727056	chr19:51860052-51860053	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs116029153	chr19:51860058-51860059	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs117447999	chr19:51860063-51860064	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Adrenocortical carcinoma	18281524	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD

Chromatin state (count:151 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51844000-51865800	Weak transcription	Small Intestine	intestine
2	chr19:51844000-51866400	Weak transcription	Right Atrium	heart
3	chr19:51847200-51868600	Weak transcription	Fetal Lung	lung
4	chr19:51849000-51862400	Weak transcription	NHDF-Ad	bronchial
5	chr19:51850600-51862400	Weak transcription	NHEK	skin
6	chr19:51851000-51861600	Weak transcription	Primary B cells from cord blood	blood
7	chr19:51852400-51865200	Weak transcription	Fetal Heart	heart
8	chr19:51853600-51868600	Weak transcription	Aorta	Aorta
9	chr19:51853800-51868600	Weak transcription	HSMM	muscle
10	chr19:51854400-51862800	Weak transcription	HMEC	breast
11	chr19:51854600-51867800	Weak transcription	Psoas Muscle	Psoas
12	chr19:51854800-51862200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr19:51855200-51866000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr19:51855400-51867600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr19:51855600-51865400	Weak transcription	GM12878-XiMat	blood
16	chr19:51856400-51862200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr19:51856400-51862200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr19:51856400-51862400	Weak transcription	Placenta	Placenta
19	chr19:51856400-51865200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr19:51856400-51866000	Weak transcription	Lung	lung
21	chr19:51856600-51859600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr19:51856600-51861200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr19:51856600-51861200	Weak transcription	Adipose Nuclei	Adipose
24	chr19:51856600-51862000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr19:51856600-51862200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr19:51856600-51862200	Weak transcription	Osteobl	bone
27	chr19:51856600-51862600	Weak transcription	Stomach Smooth Muscle	stomach
28	chr19:51856600-51865600	Weak transcription	Colonic Mucosa	Colon
29	chr19:51856600-51866000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr19:51856600-51866000	Weak transcription	Gastric	stomach
31	chr19:51856600-51867000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr19:51856600-51868600	Weak transcription	Ovary	ovary
33	chr19:51856800-51866000	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr19:51857800-51859600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr19:51857800-51859600	Weak transcription	Esophagus	oesophagus
36	chr19:51857800-51859600	Weak transcription	Pancreas	Pancrea
37	chr19:51857800-51865600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr19:51857800-51865600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr19:51857800-51865800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr19:51857800-51865800	Weak transcription	Sigmoid Colon	Sigmoid Colon
41	chr19:51857800-51865800	Weak transcription	NHLF	lung
42	chr19:51857800-51866000	Weak transcription	Primary monocytes fromperipheralblood	blood
43	chr19:51857800-51866000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr19:51857800-51866000	Weak transcription	Spleen	Spleen
45	chr19:51857800-51867600	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr19:51857800-51868400	Weak transcription	Primary hematopoietic stem cells	blood
47	chr19:51858000-51859400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr19:51858000-51859800	Weak transcription	Fetal Stomach	stomach
49	chr19:51858000-51861800	Weak transcription	Fetal Muscle Trunk	muscle
50	chr19:51858000-51862800	Weak transcription	NH-A	brain

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