Variant report

Variant	esv3417194
Chromosome Location	chr19:43975161-44000760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:474)
CpG islands
(count:488)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:474 , 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	ATF1	chr19:43979383-43979801	K562	blood:	n/a	n/a
2	ATF2	chr19:43979343-43979791	GM12878	blood:	n/a	n/a
3	ATF2	chr19:43993506-43993810	GM12878	blood:	n/a	n/a
4	ATF2	chr19:43979424-43979742	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:43993435-43993861	GM12878	blood:	n/a	n/a
6	ATF2	chr19:43979302-43979811	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr19:43993479-43993759	GM12878	blood:	n/a	n/a
8	BCL3	chr19:43979127-43979859	A549	lung:	n/a	n/a
9	BCL3	chr19:43993454-43993846	GM12878	blood:	n/a	n/a
10	BCL3	chr19:43979179-43979909	A549	lung:	n/a	n/a
11	BCL3	chr19:43993535-43993783	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:43979469-43979678	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:43979076-43979813	K562	blood:	n/a	n/a
14	BHLHE40	chr19:43986468-43986668	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:43980375-43980426	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:43986439-43986688	K562	blood:	n/a	n/a
17	BHLHE40	chr19:43978709-43978772	K562	blood:	n/a	n/a
18	BRCA1	chr19:43979338-43979702	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr19:43979725-43979743	GM12878	blood:	n/a	n/a
20	BRCA1	chr19:43979216-43979872	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr19:43979413-43979888	K562	blood:	n/a	n/a
22	CCNT2	chr19:43979260-43979825	K562	blood:	n/a	n/a
23	CEBPB	chr19:43979283-43980162	A549	lung:	n/a	n/a
24	CEBPB	chr19:43991761-43992095	K562	blood:	n/a	n/a
25	CEBPB	chr19:43979249-43979393	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr19:43979470-43980170	K562	blood:	n/a	n/a
27	CEBPB	chr19:43979328-43979761	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr19:43991756-43992046	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:43979705-43980073	K562	blood:	n/a	n/a
30	CEBPB	chr19:43991799-43991999	A549	lung:	n/a	n/a
31	CEBPB	chr19:43991760-43991983	HepG2	liver:	n/a	n/a
32	CEBPB	chr19:43980643-43981018	IMR90	lung:	n/a	n/a
33	CEBPB	chr19:43979433-43980160	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:43991705-43992024	A549	lung:	n/a	n/a
35	CEBPB	chr19:43979938-43980140	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr19:43979527-43979550	GM12878	blood:	n/a	n/a
37	CHD2	chr19:43979079-43979810	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr19:43979195-43979724	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr19:43979455-43979799	GM12878	blood:	n/a	n/a
40	CHD2	chr19:43979321-43979813	K562	blood:	n/a	n/a
41	CREB1	chr19:43979256-43979936	ECC-1	luminal epithelium:	n/a	n/a
42	CREB1	chr19:43979334-43979881	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr19:43979341-43979754	A549	lung:	n/a	n/a
44	CREB1	chr19:43979300-43979813	ECC-1	luminal epithelium:	n/a	n/a
45	CREB1	chr19:43979218-43979988	H1-hESC	embryonic stem cell:	n/a	n/a
46	CREB1	chr19:43979297-43979900	GM12878	blood:	n/a	n/a
47	CREB1	chr19:43979186-43979819	A549	lung:	n/a	n/a
48	CREB1	chr19:43979270-43979999	K562	blood:	n/a	n/a
49	CREB1	chr19:43979208-43979956	K562	blood:	n/a	n/a
50	CREB1	chr19:43979352-43979967	GM12878	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43975664-43975714	NHBE	bronchial:	n/a
2	chr19:43979316-43979366	GM12892	blood:	n/a
3	chr19:43979500-43979550	HMEC	breast:	n/a
4	chr19:43983665-43983715	HEEpiC	esophagus:	n/a
5	chr19:43979739-43979789	Hela-S3	cervix:	n/a
6	chr19:43979372-43979422	RPTEC	kidney:	n/a
7	chr19:43975664-43975714	SK-N-SH_RA	brain:	n/a
8	chr19:43979372-43979422	ECC-1	luminal epithelium:	n/a
9	chr19:43979739-43979789	BE2_C	brain:	n/a
10	chr19:43979500-43979550	Caco-2	colon:	n/a
11	chr19:43979614-43979664	NHDF-neo	bronchial:	n/a
12	chr19:43979372-43979422	ovcar-3	ovarian:	n/a
13	chr19:43979464-43979514	PANC-1	pancreas:	n/a
14	chr19:43979316-43979366	GM12891	blood:	n/a
15	chr19:43983665-43983715	HMEC	breast:	n/a
16	chr19:43983665-43983715	Hela-S3	cervix:	n/a
17	chr19:43979372-43979422	ProgFib	skin:	n/a
18	chr19:43979464-43979514	HCPEpiC	choroid plexus:	n/a
19	chr19:43983665-43983715	GM06990	blood:	n/a
20	chr19:43983665-43983715	A549	lung:	n/a
21	chr19:43979464-43979514	NHBE	bronchial:	n/a
22	chr19:43979614-43979664	PANC-1	pancreas:	n/a
23	chr19:43979500-43979550	GM12892	blood:	n/a
24	chr19:43979739-43979789	HL-60	blood:	n/a
25	chr19:43979500-43979550	HRE	kidney:	n/a
26	chr19:43975664-43975714	T-47D	breast:	n/a
27	chr19:43979500-43979550	NT2-D1	testis:	n/a
28	chr19:43979739-43979789	RPTEC	kidney:	n/a
29	chr19:43979614-43979664	AG04449	skin:	fetal
30	chr19:43979464-43979514	GM06990	blood:	n/a
31	chr19:43979614-43979664	BJ	skin:	n/a
32	chr19:43979614-43979664	HRPEpiC	eye:	n/a
33	chr19:43979316-43979366	H1-hESC	embryonic stem cell:	embryo
34	chr19:43979464-43979514	NB4	blood:	n/a
35	chr19:43979464-43979514	A549	lung:	n/a
36	chr19:43979372-43979422	HCPEpiC	choroid plexus:	n/a
37	chr19:43983665-43983715	BE2_C	brain:	n/a
38	chr19:43979739-43979789	HCPEpiC	choroid plexus:	n/a
39	chr19:43979739-43979789	NB4	blood:	n/a
40	chr19:43979500-43979550	HCM	heart:	n/a
41	chr19:43975664-43975714	NB4	blood:	n/a
42	chr19:43979614-43979664	HUVEC	blood vessel:	n/a
43	chr19:43983665-43983715	SK-N-SH_RA	brain:	n/a
44	chr19:43979464-43979514	HCT-116	colon:	n/a
45	chr19:43979372-43979422	HCT-116	colon:	n/a
46	chr19:43979614-43979664	HEK293	kidney:	embryo
47	chr19:43979739-43979789	AoSMC	blood vessel:	n/a
48	chr19:43983665-43983715	Jurkat	blood:	n/a
49	chr19:43979372-43979422	GM12892	blood:	n/a
50	chr19:43979500-43979550	NHDF-neo	bronchial:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43966007..43969922-chr19:43972303..43976712,7	K562	blood:
2	chr19:43995298..43997573-chr19:44007651..44009596,2	MCF-7	breast:
3	chr19:43978041..43981341-chr19:43983217..43985087,4	K562	blood:
4	chr19:43967515..43971066-chr19:43978004..43981821,7	MCF-7	breast:
5	chr19:43967562..43969462-chr19:43975212..43976760,2	K562	blood:
6	chr19:43978041..43981148-chr19:43983217..43985461,3	K562	blood:
7	chr19:43979844..43983821-chr19:43985802..43988529,4	MCF-7	breast:
8	chr19:43978041..43981341-chr19:43983217..43985087,4	K562	blood:
9	chr19:43997566..43999974-chr19:44006795..44009700,2	K562	blood:
10	chr19:43973600..43975639-chr19:43977848..43979529,3	MCF-7	breast:
11	chr19:43997566..43999110-chr19:44006795..44008578,2	K562	blood:
12	chr19:43966005..43974691-chr19:43977125..43981104,12	K562	blood:
13	chr19:43966005..43970813-chr19:43978022..43981097,6	K562	blood:
14	chr19:43991164..43993354-chr19:44079151..44081521,2	K562	blood:
15	chr19:43964006..43968075-chr19:43982623..43986349,3	MCF-7	breast:
16	chr19:43973600..43975639-chr19:43977848..43979529,3	MCF-7	breast:
17	chr19:43977180..43982299-chr19:44003653..44008245,6	K562	blood:
18	chr19:43986499..43988860-chr19:43990257..43991962,2	MCF-7	breast:
19	chr19:43970034..43971931-chr19:43987408..43990359,2	MCF-7	breast:
20	chr19:43951229..43953633-chr19:43981664..43984219,2	MCF-7	breast:
21	chr19:43973013..43975341-chr19:43978151..43982026,3	K562	blood:
22	chr19:43979844..43983821-chr19:43985802..43988529,4	MCF-7	breast:
23	chr19:43973013..43975341-chr19:43978151..43982026,3	K562	blood:
24	chr19:43967220..43971779-chr19:43975734..43980942,11	MCF-7	breast:
25	chr19:43978041..43981148-chr19:43983217..43985461,3	K562	blood:
26	chr19:43977172..43980889-chr19:44011519..44014130,3	MCF-7	breast:

No data

Variant related genes	Relation type
PHLDB3	TF binding region
PHLDB3	CpG island
ENSG00000176531	chromatin interactions
ENSG00000124466	chromatin interactions
ENSG00000234465	chromatin interactions
ENSG00000073050	chromatin interactions

Extended variants
information (count: 1030 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1030 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182960093	chr19:43975188-43975189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs541410722	chr19:43975197-43975198	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs77712237	chr19:43975228-43975229	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs551337313	chr19:43975265-43975266	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186594812	chr19:43975290-43975291	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372822692	chr19:43975292-43975293	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2599435	chr19:43975299-43975300	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs557378071	chr19:43975309-43975310	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs567740374	chr19:43975369-43975370	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577410172	chr19:43975398-43975399	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs145496489	chr19:43975402-43975403	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536422218	chr19:43975406-43975407	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs80011772	chr19:43975452-43975453	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs11667573	chr19:43975470-43975471	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191391441	chr19:43975474-43975475	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs75015493	chr19:43975511-43975512	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7252512	chr19:43975513-43975514	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs572345598	chr19:43975568-43975569	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541211820	chr19:43975569-43975570	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs183754644	chr19:43975586-43975587	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs187600383	chr19:43975597-43975598	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs73549100	chr19:43975665-43975666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558601350	chr19:43975740-43975741	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562515036	chr19:43975756-43975757	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs572350845	chr19:43975767-43975768	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs138077473	chr19:43975790-43975791	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551692211	chr19:43975794-43975795	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565159725	chr19:43975844-43975845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77569962	chr19:43975864-43975865	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369461099	chr19:43975865-43975866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs527509847	chr19:43975918-43975919	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547634563	chr19:43975932-43975933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs7256104	chr19:43975938-43975939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs190823294	chr19:43975948-43975949	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs549960857	chr19:43975979-43975980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376400277	chr19:43975989-43975990	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs4803633	chr19:43976013-43976014	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs538646763	chr19:43976075-43976076	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs7256263	chr19:43976080-43976081	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs143067131	chr19:43976127-43976128	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs575525749	chr19:43976163-43976164	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs554760304	chr19:43976176-43976177	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12977939	chr19:43976214-43976215	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372415027	chr19:43976217-43976218	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs80331237	chr19:43976228-43976229	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs540677969	chr19:43976229-43976230	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs200869184	chr19:43976231-43976232	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574896594	chr19:43976264-43976265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12980473	chr19:43976426-43976427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs555974273	chr19:43976432-43976433	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	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
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43968800-43979200	Weak transcription	Right Atrium	heart
2	chr19:43969000-43979000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr19:43969000-43979000	Weak transcription	A549	lung
4	chr19:43969800-43979000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr19:43970000-43998200	Weak transcription	Gastric	stomach
6	chr19:43970200-43977800	Weak transcription	Spleen	Spleen
7	chr19:43970400-43976600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr19:43970400-43979200	Weak transcription	Lung	lung
9	chr19:43971200-43975800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr19:43971200-43975800	Enhancers	NHEK	skin
11	chr19:43971200-43977600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr19:43971400-43975800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr19:43971400-43977000	Enhancers	Primary T cells fromperipheralblood	blood
14	chr19:43971600-43975400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr19:43971600-43975800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr19:43971600-43976800	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr19:43971600-43978600	Weak transcription	Fetal Intestine Small	intestine
18	chr19:43971800-43975400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
19	chr19:43971800-43977400	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr19:43972000-43979000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr19:43972200-43979000	Weak transcription	NHLF	lung
22	chr19:43972200-43979200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr19:43972400-43975200	Weak transcription	Fetal Lung	lung
24	chr19:43972400-43978600	Weak transcription	Esophagus	oesophagus
25	chr19:43972400-43978800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr19:43972400-43979000	Weak transcription	K562	blood
27	chr19:43972400-43979000	Weak transcription	Osteobl	bone
28	chr19:43973000-43979200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:43973200-43979000	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr19:43973400-43977400	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr19:43973600-43975200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr19:43973600-43975200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr19:43973600-43975200	Weak transcription	HMEC	breast
34	chr19:43973600-43975600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr19:43973600-43975600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr19:43973600-43977600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr19:43973600-43978400	Weak transcription	Hela-S3	cervix
38	chr19:43973600-43978600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr19:43973600-43978600	Weak transcription	Adipose Nuclei	Adipose
40	chr19:43973600-43978600	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr19:43973600-43979000	Weak transcription	Rectal Mucosa Donor 31	rectum
42	chr19:43973600-43979000	Weak transcription	HUVEC	blood vessel
43	chr19:43973800-43975800	Weak transcription	Primary hematopoietic stem cells	blood
44	chr19:43973800-43999800	Weak transcription	HepG2	liver
45	chr19:43974000-43979200	Weak transcription	Thymus	Thymus
46	chr19:43974200-43977600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr19:43974200-43978800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr19:43974200-43979000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr19:43974400-43978000	Enhancers	Primary T cells from cord blood	blood
50	chr19:43974400-43978000	Enhancers	Primary T helper cells PMA-I stimulated	--

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