Variant report

Variant	esv2762041
Chromosome Location	chr19:43986023-44014457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:686)
CpG islands
(count:1283)
Chromatin interactive
region (count:24)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:686 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:44008474-44008677	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:44003276-44003523	HepG2	liver:	n/a	n/a
3	ATF1	chr19:44008295-44008600	K562	blood:	n/a	n/a
4	ATF2	chr19:43993506-43993810	GM12878	blood:	n/a	n/a
5	ATF2	chr19:43993435-43993861	GM12878	blood:	n/a	n/a
6	BACH1	chr19:44008427-44008537	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr19:44006131-44006455	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr19:43993479-43993759	GM12878	blood:	n/a	n/a
9	BCL3	chr19:44008319-44008810	A549	lung:	n/a	n/a
10	BCL3	chr19:43993535-43993783	GM12878	blood:	n/a	n/a
11	BCL3	chr19:43993454-43993846	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:44007798-44008178	K562	blood:	n/a	n/a
13	BHLHE40	chr19:43986439-43986688	K562	blood:	n/a	n/a
14	BHLHE40	chr19:44008389-44008965	K562	blood:	n/a	n/a
15	BHLHE40	chr19:43986468-43986668	GM12878	blood:	n/a	n/a
16	BHLHE40	chr19:44010124-44010324	K562	blood:	n/a	n/a
17	BHLHE40	chr19:44008093-44008212	GM12878	blood:	n/a	n/a
18	BRCA1	chr19:44003243-44003646	HepG2	liver:	n/a	n/a
19	BRCA1	chr19:44008529-44008684	HepG2	liver:	n/a	n/a
20	CCNT2	chr19:44007890-44008582	K562	blood:	n/a	chr19:44008313-44008322
21	CEBPB	chr19:44007690-44007726	HepG2	liver:	n/a	n/a
22	CEBPB	chr19:43991756-43992046	IMR90	lung:	n/a	n/a
23	CEBPB	chr19:44007592-44008085	K562	blood:	n/a	n/a
24	CEBPB	chr19:44008269-44008276	HepG2	liver:	n/a	n/a
25	CEBPB	chr19:43991760-43991983	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:44007601-44007819	A549	lung:	n/a	n/a
27	CEBPB	chr19:43991799-43991999	A549	lung:	n/a	n/a
28	CEBPB	chr19:43991705-43992024	A549	lung:	n/a	n/a
29	CEBPB	chr19:43991761-43992095	K562	blood:	n/a	n/a
30	CEBPB	chr19:44006388-44006485	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr19:44010105-44010303	K562	blood:	n/a	n/a
32	CEBPB	chr19:44007554-44007841	Hela-S3	cervix:	n/a	n/a
33	CEBPD	chr19:44007940-44008360	HepG2	liver:	n/a	n/a
34	CEBPD	chr19:44008426-44009091	HepG2	liver:	n/a	n/a
35	CHD1	chr19:44005986-44006075	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr19:44007875-44008226	GM12878	blood:	n/a	n/a
37	CHD2	chr19:44008889-44008895	K562	blood:	n/a	n/a
38	CHD2	chr19:44007878-44008574	Hela-S3	cervix:	n/a	chr19:44008357-44008367
39	CHD2	chr19:44003246-44003460	HepG2	liver:	n/a	n/a
40	CHD2	chr19:44008253-44008762	H1-hESC	embryonic stem cell:	n/a	chr19:44008657-44008667 chr19:44008357-44008367
41	CHD2	chr19:44009063-44009072	GM12878	blood:	n/a	n/a
42	CREB1	chr19:44007735-44009221	HepG2	liver:	n/a	n/a
43	CREB1	chr19:44008071-44008503	A549	lung:	n/a	n/a
44	CREB1	chr19:44008035-44008817	A549	lung:	n/a	n/a
45	CTCF	chr19:44008580-44008730	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr19:44008500-44008650	GM12874	blood:	n/a	chr19:44008517-44008533
47	CTCF	chr19:44008560-44008710	WI-38	lung:	n/a	n/a
48	CTCF	chr19:44007720-44007870	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr19:44008580-44008730	RPTEC	kidney:	n/a	n/a
50	CTCF	chr19:44007700-44007850	GM12873	blood:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:44006148-44006198	ovcar-3	ovarian:	n/a
2	chr19:44009019-44009069	LNCaP	prostate:	n/a
3	chr19:44006148-44006198	ovcar-3	ovarian:	n/a
4	chr19:44009019-44009069	LNCaP	prostate:	n/a
5	chr19:44009042-44009092	PANC-1	pancreas:	n/a
6	chr19:44002716-44002766	HRE	kidney:	n/a
7	chr19:44006148-44006198	CMK	blood:	n/a
8	chr19:44005808-44005858	SK-N-SH	brain:	n/a
9	chr19:44009429-44009479	PFSK-1	brain:	n/a
10	chr19:44009067-44009117	NHDF-neo	bronchial:	n/a
11	chr19:44009067-44009117	MCF10A-Er-Src	breast:	n/a
12	chr19:44008806-44008856	IMR90	lung:	fetal
13	chr19:44005808-44005858	K562	blood:	n/a
14	chr19:44005893-44005943	NB4	blood:	n/a
15	chr19:44010371-44010421	PFSK-1	brain:	n/a
16	chr19:44012195-44012245	BE2_C	brain:	n/a
17	chr19:44009073-44009123	HAEpiC	amniotic membrane:	n/a
18	chr19:44005808-44005858	RPTEC	kidney:	n/a
19	chr19:44008806-44008856	HCPEpiC	choroid plexus:	n/a
20	chr19:44005808-44005858	GM06990	blood:	n/a
21	chr19:44005893-44005943	HUVEC	blood vessel:	n/a
22	chr19:44009019-44009069	HEEpiC	esophagus:	n/a
23	chr19:44009073-44009123	HUVEC	blood vessel:	n/a
24	chr19:44009042-44009092	K562	blood:	n/a
25	chr19:44010371-44010421	SKMC	muscle:	n/a
26	chr19:44009429-44009479	HCT-116	colon:	n/a
27	chr19:44009049-44009099	AG10803	skin:	n/a
28	chr19:44008806-44008856	PFSK-1	brain:	n/a
29	chr19:44008145-44008195	HRCEpiC	kidney:	n/a
30	chr19:44005906-44005956	HNPCEpiC	eye:	n/a
31	chr19:44009067-44009117	HNPCEpiC	eye:	n/a
32	chr19:44005893-44005943	PrEC	prostate:	n/a
33	chr19:44008145-44008195	PFSK-1	brain:	n/a
34	chr19:44012195-44012245	MCF-7	breast:	n/a
35	chr19:44006432-44006482	K562	blood:	n/a
36	chr19:44008615-44008665	NHBE	bronchial:	n/a
37	chr19:44008145-44008195	NB4	blood:	n/a
38	chr19:44009067-44009117	MCF-7	breast:	n/a
39	chr19:44009073-44009123	HCF	heart:	n/a
40	chr19:44008476-44008526	RPTEC	kidney:	n/a
41	chr19:44005893-44005943	K562	blood:	n/a
42	chr19:44008476-44008526	AG04449	skin:	fetal
43	chr19:44009073-44009123	HRE	kidney:	n/a
44	chr19:44006148-44006198	AG10803	skin:	n/a
45	chr19:44009353-44009403	Hepatocyte	liver:	n/a
46	chr19:44012195-44012245	NB4	blood:	n/a
47	chr19:44008615-44008665	GM12878	blood:	n/a
48	chr19:44002716-44002766	AoSMC	blood vessel:	n/a
49	chr19:44006432-44006482	HL-60	blood:	n/a
50	chr19:44009049-44009099	BE2_C	brain:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:43997566..43999974-chr19:44006795..44009700,2	K562	blood:
2	chr19:44006496..44008143-chr19:44098024..44100658,2	MCF-7	breast:
3	chr19:44006689..44009864-chr19:44027261..44031051,4	MCF-7	breast:
4	chr19:43995298..43997573-chr19:44007651..44009596,2	MCF-7	breast:
5	chr19:44005667..44006443-chr6:81951149..81952062,2	MCF-7	breast:
6	chr19:43964006..43968075-chr19:43982623..43986349,3	MCF-7	breast:
7	chr19:44005750..44008125-chr19:44129589..44132282,2	K562	blood:
8	chr19:43966113..43971089-chr19:44005040..44010546,6	K562	blood:
9	chr19:43991164..43993354-chr19:44079151..44081521,2	K562	blood:
10	chr19:43965066..43971111-chr19:44006791..44009897,14	MCF-7	breast:
11	chr19:43997566..43999974-chr19:44006795..44009700,2	K562	blood:
12	chr19:43986499..43988860-chr19:43990257..43991962,2	MCF-7	breast:
13	chr19:43997566..43999110-chr19:44006795..44008578,2	K562	blood:
14	chr19:43977172..43980889-chr19:44011519..44014130,3	MCF-7	breast:
15	chr19:43966525..43969059-chr19:44008556..44010178,2	K562	blood:
16	chr19:44007568..44009583-chr19:44036201..44039639,3	MCF-7	breast:
17	chr19:44008750..44013083-chr19:44013430..44017260,4	K562	blood:
18	chr19:43979844..43983821-chr19:43985802..43988529,4	MCF-7	breast:
19	chr19:43977180..43982299-chr19:44003653..44008245,6	K562	blood:
20	chr19:43967204..43969877-chr19:44006593..44010322,9	MCF-7	breast:
21	chr19:44007345..44009870-chr19:44010620..44012235,2	K562	blood:
22	chr19:43970034..43971931-chr19:43987408..43990359,2	MCF-7	breast:
23	chr19:43997566..43999110-chr19:44006795..44008578,2	K562	blood:
24	chr19:43967644..43971432-chr19:44003665..44007669,4	K562	blood:

No data

Variant related genes	Relation type
PHLDB3	TF binding region
PHLDB3	CpG island
ENSG00000176531	chromatin interactions
ENSG00000234465	chromatin interactions
ENSG00000073050	chromatin interactions
ENSG00000176472	chromatin interactions
ENSG00000124466	chromatin interactions
ENSG00000124444	chromatin interactions
ENSG00000167378	chromatin interactions
ENSG00000105767	chromatin interactions

Extended variants
information (count: 1192 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1192 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11665812	chr19:43986023-43986024	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544968116	chr19:43986027-43986028	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141482852	chr19:43986051-43986052	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145766222	chr19:43986102-43986103	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540835331	chr19:43986110-43986111	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369765544	chr19:43986117-43986118	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs560450463	chr19:43986147-43986148	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184011332	chr19:43986229-43986230	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34020662	chr19:43986255-43986256	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs397859185	chr19:43986256-43986257	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs117076507	chr19:43986371-43986372	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561396238	chr19:43986392-43986393	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28568283	chr19:43986396-43986397	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs550497786	chr19:43986402-43986403	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190942036	chr19:43986466-43986467	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79244214	chr19:43986479-43986480	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546777327	chr19:43986497-43986498	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574288807	chr19:43986541-43986542	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs138426913	chr19:43986551-43986552	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs535985655	chr19:43986571-43986572	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs369861032	chr19:43986605-43986606	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs143017905	chr19:43986627-43986628	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182530458	chr19:43986674-43986675	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs377751350	chr19:43986683-43986684	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs548781054	chr19:43986686-43986687	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs8101223	chr19:43986737-43986738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538226112	chr19:43986747-43986748	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs541498098	chr19:43986766-43986767	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs146154288	chr19:43986771-43986772	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540521175	chr19:43986792-43986793	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559901776	chr19:43986812-43986813	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140037709	chr19:43986846-43986847	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10409591	chr19:43986855-43986856	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
34	rs143888974	chr19:43986874-43986875	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs561433350	chr19:43986878-43986879	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530489594	chr19:43986879-43986880	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs564393703	chr19:43986910-43986911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373600990	chr19:43986939-43986940	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs563693129	chr19:43986982-43986983	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs148630915	chr19:43986991-43986992	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs546569068	chr19:43987043-43987044	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs566707006	chr19:43987048-43987049	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs187183179	chr19:43987049-43987050	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142122788	chr19:43987120-43987121	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs569389178	chr19:43987243-43987244	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538311988	chr19:43987247-43987248	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs147394534	chr19:43987289-43987290	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571507550	chr19:43987291-43987292	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs534547410	chr19:43987315-43987316	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150214408	chr19:43987353-43987354	Weak transcription Strong transcription	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:1420 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43970000-43998200	Weak transcription	Gastric	stomach
2	chr19:43973800-43999800	Weak transcription	HepG2	liver
3	chr19:43979600-44005800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:43979800-43990200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr19:43979800-43992400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr19:43979800-43994800	Weak transcription	Left Ventricle	heart
7	chr19:43979800-43998400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr19:43979800-43998600	Weak transcription	Lung	lung
9	chr19:43979800-43998800	Weak transcription	Aorta	Aorta
10	chr19:43979800-43998800	Weak transcription	Pancreas	Pancrea
11	chr19:43980000-43989000	Strong transcription	Fetal Intestine Small	intestine
12	chr19:43980000-43990600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr19:43980000-43990800	Weak transcription	Colonic Mucosa	Colon
14	chr19:43980000-43994600	Weak transcription	Brain Anterior Caudate	brain
15	chr19:43980000-43994800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr19:43980000-43995000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:43980000-43998600	Weak transcription	Brain Germinal Matrix	brain
18	chr19:43980000-43998600	Weak transcription	Fetal Brain Female	brain
19	chr19:43980000-43998800	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr19:43980000-43999400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr19:43980000-43999400	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr19:43980000-43999600	Weak transcription	Brain Angular Gyrus	brain
23	chr19:43980000-43999600	Weak transcription	Colon Smooth Muscle	Colon
24	chr19:43980000-44001000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr19:43980000-44001000	Weak transcription	Fetal Lung	lung
26	chr19:43980000-44001200	Weak transcription	Brain Substantia Nigra	brain
27	chr19:43980000-44001200	Weak transcription	Rectal Smooth Muscle	rectum
28	chr19:43980000-44005600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr19:43980000-44005600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr19:43980000-44006200	Weak transcription	HMEC	breast
31	chr19:43980200-43988800	Strong transcription	Liver	Liver
32	chr19:43980200-43989800	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr19:43980200-43999600	Weak transcription	Adipose Nuclei	Adipose
34	chr19:43980200-44001000	Weak transcription	Fetal Thymus	thymus
35	chr19:43980400-43986600	Strong transcription	Fetal Stomach	stomach
36	chr19:43980400-43990800	Weak transcription	Primary B cells from cord blood	blood
37	chr19:43980400-43998200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr19:43980400-43998800	Weak transcription	Duodenum Mucosa	Duodenum
39	chr19:43980400-43999000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr19:43980400-43999200	Weak transcription	Placenta	Placenta
41	chr19:43980400-43999800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr19:43980400-44000400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr19:43980400-44001200	Weak transcription	Brain Cingulate Gyrus	brain
44	chr19:43980800-43998200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr19:43980800-44007400	Weak transcription	HSMM	muscle
46	chr19:43981000-43987000	Weak transcription	HSMMtube	muscle
47	chr19:43981000-43990400	Weak transcription	Fetal Muscle Leg	muscle
48	chr19:43981000-43998800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr19:43981200-43986200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr19:43981200-43998800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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