Variant report

Variant	esv3498662
Chromosome Location	chr19:53322552-53359131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:672)
Chromatin interactive
region (count:11)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:53324738-53324945	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr19:53336721-53337013	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
3	BATF	chr19:53336688-53337003	GM12878	blood:	n/a	chr19:53336917-53336927 chr19:53336913-53336923 chr19:53336723-53336732 chr19:53336898-53336906
4	BHLHE40	chr19:53324867-53324898	K562	blood:	n/a	n/a
5	CBX3	chr19:53324640-53325255	K562	blood:	n/a	n/a
6	CEBPB	chr19:53329098-53329325	K562	blood:	n/a	n/a
7	CEBPB	chr19:53329012-53329572	K562	blood:	n/a	n/a
8	CEBPB	chr19:53329163-53329370	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr19:53345865-53346133	HepG2	liver:	n/a	chr19:53346019-53346030
10	CEBPB	chr19:53328995-53329384	K562	blood:	n/a	n/a
11	CEBPB	chr19:53345961-53346152	A549	lung:	n/a	chr19:53346019-53346030
12	CEBPB	chr19:53345864-53346169	IMR90	lung:	n/a	chr19:53346019-53346030
13	CEBPB	chr19:53329092-53329271	MCF-7	breast:	n/a	n/a
14	CEBPD	chr19:53329085-53329417	K562	blood:	n/a	n/a
15	CTCF	chr19:53324960-53325034	MCF-7	breast:	n/a	chr19:53325004-53325017
16	CTCF	chr19:53324899-53325011	GM13976	blood:	n/a	n/a
17	CTCF	chr19:53324543-53324634	Lung_OC	lung:	n/a	n/a
18	CTCF	chr19:53328417-53328457	K562	blood:	n/a	n/a
19	CTCF	chr19:53324949-53325037	LNCaP	prostate:	n/a	chr19:53325004-53325017
20	CTCF	chr19:53324966-53325041	Kidney_OC	kidney:	n/a	chr19:53325004-53325017
21	CTCF	chr19:53325872-53325890	LNCaP	prostate:	n/a	n/a
22	CTCF	chr19:53346656-53346707	GM13976	blood:	n/a	n/a
23	CTCF	chr19:53324980-53325130	SAEC	small airway:	n/a	chr19:53325004-53325017
24	CTCF	chr19:53324938-53325019	MCF-7	breast:	n/a	chr19:53325004-53325017
25	CTCF	chr19:53324761-53325046	K562	blood:	n/a	chr19:53325004-53325017
26	CTCF	chr19:53352092-53352147	GM13976	blood:	n/a	n/a
27	CTCF	chr19:53333123-53333177	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr19:53324920-53325004	Pancreas_OC	pancreas:	n/a	n/a
29	CTCF	chr19:53325357-53325460	LNCaP	prostate:	n/a	n/a
30	CTCF	chr19:53324904-53325077	GM19240	blood:	n/a	chr19:53325004-53325017
31	CTCF	chr19:53324891-53325076	GM19238	blood:	n/a	chr19:53325004-53325017
32	CTCF	chr19:53324925-53325031	MCF-7	breast:	n/a	chr19:53325004-53325017
33	CTCF	chr19:53324864-53325078	Lung_OC	lung:	n/a	chr19:53325004-53325017
34	CTCF	chr19:53324785-53325148	K562	blood:	n/a	chr19:53325004-53325017
35	CTCF	chr19:53325000-53325150	HBMEC	blood vessel:	n/a	chr19:53325004-53325017
36	CTCF	chr19:53324980-53325130	SK-N-SH_RA	brain:	n/a	chr19:53325004-53325017
37	CTCF	chr19:53324879-53325039	GM12891	blood:	n/a	chr19:53325004-53325017
38	CTCF	chr19:53325011-53325045	GM12878	blood:	n/a	n/a
39	CTCF	chr19:53324895-53325063	K562	blood:	n/a	chr19:53325004-53325017
40	CTCF	chr19:53328020-53328170	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr19:53324980-53325130	AoAF	blood vessel:	n/a	chr19:53325004-53325017
42	CTCF	chr19:53324957-53324996	GM13977	blood:	n/a	n/a
43	CTCF	chr19:53343023-53343127	GM20000	blood:	n/a	n/a
44	CTCF	chr19:53324779-53325090	Spleen_OC	spleen:	n/a	chr19:53325004-53325017
45	CTCF	chr19:53324957-53325018	GM12892	blood:	n/a	chr19:53325004-53325017
46	CTCF	chr19:53325000-53325150	HCPEpiC	choroid plexus:	n/a	chr19:53325004-53325017
47	CTCF	chr19:53324966-53325041	GM19239	blood:	n/a	chr19:53325004-53325017
48	CTCF	chr19:53324945-53324956	GM12892	blood:	n/a	n/a
49	CTCF	chr19:53324940-53325090	AG04449	skin:	n/a	chr19:53325004-53325017
50	CTCF	chr19:53324960-53325110	HMEC	breast:	n/a	chr19:53325004-53325017

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53357134-53357184	GM06990	blood:	n/a
2	chr19:53357134-53357184	GM06990	blood:	n/a
3	chr19:53324278-53324328	ECC-1	luminal epithelium:	n/a
4	chr19:53324198-53324248	IMR90	lung:	fetal
5	chr19:53324732-53324782	HEEpiC	esophagus:	n/a
6	chr19:53324732-53324782	PrEC	prostate:	n/a
7	chr19:53324732-53324782	SK-N-SH_RA	brain:	n/a
8	chr19:53357134-53357184	CMK	blood:	n/a
9	chr19:53325080-53325130	HEK293	kidney:	embryo
10	chr19:53326219-53326269	HCPEpiC	choroid plexus:	n/a
11	chr19:53324732-53324782	NT2-D1	testis:	n/a
12	chr19:53357134-53357184	K562	blood:	n/a
13	chr19:53326219-53326269	RPTEC	kidney:	n/a
14	chr19:53326219-53326269	HMEC	breast:	n/a
15	chr19:53324198-53324248	HMEC	breast:	n/a
16	chr19:53326219-53326269	HPAEpiC	pulmonary alveolar:	n/a
17	chr19:53324198-53324248	GM06990	blood:	n/a
18	chr19:53324732-53324782	NH-A	brain:	n/a
19	chr19:53324278-53324328	MCF10A-Er-Src	breast:	n/a
20	chr19:53344366-53344416	AG09309	skin:	n/a
21	chr19:53357134-53357184	NHDF-neo	bronchial:	n/a
22	chr19:53357134-53357184	A549	lung:	n/a
23	chr19:53324198-53324248	HCT-116	colon:	n/a
24	chr19:53326091-53326141	HL-60	blood:	n/a
25	chr19:53324198-53324248	Hela-S3	cervix:	n/a
26	chr19:53344366-53344416	GM12892	blood:	n/a
27	chr19:53326219-53326269	Hela-S3	cervix:	n/a
28	chr19:53324198-53324248	SK-N-SH	brain:	n/a
29	chr19:53357134-53357184	AG04450	lung:	fetal
30	chr19:53326091-53326141	HRE	kidney:	n/a
31	chr19:53326219-53326269	AoSMC	blood vessel:	n/a
32	chr19:53324198-53324248	CMK	blood:	n/a
33	chr19:53357134-53357184	U87	brain:	n/a
34	chr19:53325913-53325963	PrEC	prostate:	n/a
35	chr19:53326219-53326269	Hepatocyte	liver:	n/a
36	chr19:53324732-53324782	HPAEpiC	pulmonary alveolar:	n/a
37	chr19:53325913-53325963	HepG2	liver:	n/a
38	chr19:53324198-53324248	PrEC	prostate:	n/a
39	chr19:53324732-53324782	HEK293	kidney:	embryo
40	chr19:53344366-53344416	AoSMC	blood vessel:	n/a
41	chr19:53324198-53324248	NT2-D1	testis:	n/a
42	chr19:53342580-53342630	NHDF-neo	bronchial:	n/a
43	chr19:53342580-53342630	RPTEC	kidney:	n/a
44	chr19:53325104-53325154	GM06990	blood:	n/a
45	chr19:53324278-53324328	Hepatocyte	liver:	n/a
46	chr19:53326219-53326269	IMR90	lung:	fetal
47	chr19:53325080-53325130	GM12891	blood:	n/a
48	chr19:53325913-53325963	AG04450	lung:	fetal
49	chr19:53325104-53325154	HRPEpiC	eye:	n/a
50	chr19:53326091-53326141	HCPEpiC	choroid plexus:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53322321..53326212-chr19:53359321..53361245,3	K562	blood:
2	chr19:53324392..53324894-chr19:53934932..53935516,2	MCF-7	breast:
3	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
4	chr19:53322321..53326212-chr19:53359240..53361245,4	K562	blood:
5	chr19:53339213..53341134-chr20:46203984..46206130,2	MCF-7	breast:
6	chr19:53338835..53341536-chr19:53343202..53344870,2	K562	blood:
7	chr19:53324497..53325251-chr19:53360339..53360857,4	MCF-7	breast:
8	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:
9	chr19:53357060..53358583-chr19:53400479..53402706,2	MCF-7	breast:
10	chr19:53193532..53195862-chr19:53359115..53361191,3	K562	blood:
11	chr19:53335113..53339470-chr19:53340101..53344099,5	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF468-1	chr19:53357511-53357598	NR_102300
2	lnc-ZNF468-1	chr19:53357125-53357379	NR_102299
3	lnc-ZNF468-1	chr19:53357125-53357360	NR_102300
4	lnc-ZNF468-1	chr19:53341785-53345404	NR_102301
5	lnc-ZNF468-1	chr19:53357125-53357379	NR_102301
6	lnc-ZNF701-2	chr19:53342913-53343520	NONHSAT067585
7	lnc-ZNF468-1	chr19:53348432-53348549	NR_102299
8	lnc-ZNF468-1	chr19:53357511-53357598	NR_102299
9	lnc-ZNF468-3	chr19:53324839-53324886	NONHSAT067588
10	lnc-ZNF468-1	chr19:53348432-53348549	NR_102300
11	lnc-ZNF468-1	chr19:53352340-53352466	NR_102301
12	lnc-ZNF468-1	chr19:53352340-53352466	NR_102299
13	lnc-ZNF468-1	chr19:53341785-53345404	NR_102300
14	lnc-ZNF468-1	chr19:53341785-53345404	NR_102299
15	lnc-ZNF468-1	chr19:53352340-53352466	NR_102300
16	lnc-ZNF468-1	chr19:53357511-53357598	NR_102301

No data

Variant related genes	Relation type
ZNF28	TF binding region
ZNF468	TF binding region
ZNF28	CpG island
ZNF468	CpG island
ENSG00000182986	chromatin interactions
ENSG00000167766	chromatin interactions
ENSG00000204604	chromatin interactions
ENSG00000160336	chromatin interactions
ENSG00000198538	chromatin interactions
ENSG00000241015	chromatin interactions

Extended variants
information (count: 2071 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2071 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111883666	chr19:53322565-53322566	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs28669963	chr19:53322594-53322595	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs183766572	chr19:53322599-53322600	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs150399876	chr19:53322606-53322607	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs188199747	chr19:53322607-53322608	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs190130797	chr19:53322613-53322614	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs545833588	chr19:53322623-53322624	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs374206273	chr19:53322628-53322629	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs182485504	chr19:53322629-53322630	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs368471493	chr19:53322633-53322634	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs138200021	chr19:53322651-53322652	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs149835076	chr19:53322662-53322663	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs543553053	chr19:53322663-53322664	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs111234956	chr19:53322685-53322686	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs530353548	chr19:53322703-53322704	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs149152297	chr19:53322714-53322715	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs386810564	chr19:53322748-53322749	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs4803003	chr19:53322749-53322750	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs62120977	chr19:53322773-53322774	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs570563691	chr19:53322775-53322776	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs62120978	chr19:53322776-53322777	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs62120979	chr19:53322781-53322782	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs62120980	chr19:53322788-53322789	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs375182628	chr19:53322806-53322807	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs62120981	chr19:53322813-53322814	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs62120982	chr19:53322816-53322817	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs62120983	chr19:53322819-53322820	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs62120984	chr19:53322821-53322822	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs62120985	chr19:53322825-53322826	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189951046	chr19:53322826-53322827	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs565858669	chr19:53322830-53322831	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs62120986	chr19:53322837-53322838	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555468457	chr19:53322847-53322848	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs13345569	chr19:53322870-53322871	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs542424766	chr19:53322871-53322872	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs181430049	chr19:53322874-53322875	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs141360897	chr19:53322895-53322896	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs546133816	chr19:53322906-53322907	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs564129023	chr19:53322950-53322951	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs150707390	chr19:53322953-53322954	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs73592049	chr19:53322954-53322955	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs567509302	chr19:53322956-53322957	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs116295481	chr19:53322972-53322973	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs112181154	chr19:53322992-53322993	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs13343698	chr19:53323004-53323005	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs199560504	chr19:53323043-53323044	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs568687929	chr19:53323131-53323132	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs535276767	chr19:53323145-53323146	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs139879581	chr19:53323153-53323154	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs74200825	chr19:53323191-53323192	Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Cancer	20164920	CNVD
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53296200-53324000	Weak transcription	Fetal Brain Male	brain
2	chr19:53306000-53324000	Weak transcription	Colon Smooth Muscle	Colon
3	chr19:53306600-53324000	Weak transcription	Psoas Muscle	Psoas
4	chr19:53308200-53324000	Weak transcription	Fetal Kidney	kidney
5	chr19:53311000-53323600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr19:53311400-53323600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr19:53311400-53324000	Weak transcription	NHDF-Ad	bronchial
8	chr19:53313600-53324000	Weak transcription	Fetal Lung	lung
9	chr19:53313600-53324000	Weak transcription	Right Ventricle	heart
10	chr19:53313600-53324200	Weak transcription	Brain Substantia Nigra	brain
11	chr19:53313800-53323600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr19:53313800-53323800	Weak transcription	Stomach Mucosa	stomach
13	chr19:53313800-53324000	Weak transcription	Brain Angular Gyrus	brain
14	chr19:53313800-53324000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr19:53313800-53324000	Weak transcription	HSMM	muscle
16	chr19:53313800-53324000	Weak transcription	NHLF	lung
17	chr19:53313800-53324200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr19:53314000-53323600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr19:53314000-53323600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:53314000-53323600	Weak transcription	K562	blood
21	chr19:53314000-53323800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr19:53314000-53323800	Weak transcription	Brain Germinal Matrix	brain
23	chr19:53314000-53323800	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr19:53314000-53323800	Weak transcription	Small Intestine	intestine
25	chr19:53314000-53324000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr19:53314000-53324000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr19:53314000-53324000	Weak transcription	Fetal Brain Female	brain
28	chr19:53314000-53324200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr19:53314000-53324200	Weak transcription	Aorta	Aorta
30	chr19:53319200-53324000	Weak transcription	Osteobl	bone
31	chr19:53319600-53323600	Weak transcription	Gastric	stomach
32	chr19:53319600-53324200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr19:53320400-53323800	Weak transcription	HUVEC	blood vessel
34	chr19:53320600-53323800	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr19:53321000-53323600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr19:53321000-53323800	Weak transcription	Primary B cells from peripheral blood	blood
37	chr19:53321200-53323600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr19:53321200-53323600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr19:53321200-53323600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr19:53321200-53323600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr19:53321200-53323600	Weak transcription	Primary hematopoietic stem cells	blood
42	chr19:53321200-53323600	Weak transcription	Placenta	Placenta
43	chr19:53321200-53323600	Weak transcription	Thymus	Thymus
44	chr19:53321200-53323800	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr19:53321200-53323800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr19:53321200-53323800	Weak transcription	Primary neutrophils fromperipheralblood	blood
47	chr19:53321200-53323800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr19:53321200-53323800	Weak transcription	Adipose Nuclei	Adipose
49	chr19:53321200-53323800	Weak transcription	Brain Hippocampus Middle	brain
50	chr19:53321200-53323800	Weak transcription	Rectal Mucosa Donor 31	rectum

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