Variant report

Variant	esv2762038
Chromosome Location	chr19:39444417-39455548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:380)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:380 , 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	ARID3A	chr19:39452764-39453058	K562	blood:	n/a	n/a
2	ATF2	chr19:39452847-39453190	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr19:39452785-39453105	GM12878	blood:	n/a	n/a
4	ATF3	chr19:39452683-39453348	A549	lung:	n/a	n/a
5	BCL3	chr19:39452717-39453406	A549	lung:	n/a	n/a
6	BCL3	chr19:39444300-39444912	A549	lung:	n/a	n/a
7	BCL3	chr19:39452654-39453396	A549	lung:	n/a	n/a
8	BHLHE40	chr19:39452856-39453169	K562	blood:	n/a	n/a
9	CBX3	chr19:39452736-39453206	K562	blood:	n/a	n/a
10	CBX3	chr19:39452765-39453065	K562	blood:	n/a	n/a
11	CTCF	chr19:39452840-39452990	HFF	foreskin:	n/a	n/a
12	CTCF	chr19:39452896-39453029	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr19:39452850-39453076	GM19240	blood:	n/a	n/a
14	CTCF	chr19:39452880-39453030	NHEK	skin:	n/a	n/a
15	CTCF	chr19:39452869-39453068	Fibrobl	skin:	n/a	n/a
16	CTCF	chr19:39452860-39453010	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr19:39452838-39453048	ECC-1	luminal epithelium:	n/a	n/a
18	CTCF	chr19:39452795-39453063	HUVEC	blood vessel:	n/a	n/a
19	CTCF	chr19:39452880-39453030	HEK293	kidney:	n/a	n/a
20	CTCF	chr19:39452860-39453010	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr19:39452880-39453030	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr19:39452693-39453058	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr19:39452810-39453057	LNCaP	prostate:	n/a	n/a
24	CTCF	chr19:39452817-39453052	HepG2	liver:	n/a	n/a
25	CTCF	chr19:39452818-39453065	GM10266	blood:	n/a	n/a
26	CTCF	chr19:39452705-39453158	A549	lung:	n/a	n/a
27	CTCF	chr19:39452860-39453010	HRE	kidney:	n/a	n/a
28	CTCF	chr19:39452880-39453030	GM12873	blood:	n/a	n/a
29	CTCF	chr19:39452860-39453010	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr19:39452860-39453010	BJ	skin:	n/a	n/a
31	CTCF	chr19:39452837-39453087	Gliobla	brain:	n/a	n/a
32	CTCF	chr19:39453100-39453250	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr19:39452874-39453073	MCF-7	breast:	n/a	n/a
34	CTCF	chr19:39452834-39453191	MCF-7	breast:	n/a	n/a
35	CTCF	chr19:39452820-39452970	HCT-116	colon:	n/a	n/a
36	CTCF	chr19:39452724-39453134	IMR90	lung:	n/a	n/a
37	CTCF	chr19:39452730-39453100	ECC-1	luminal epithelium:	n/a	n/a
38	CTCF	chr19:39452578-39453363	HCT-116	colon:	n/a	n/a
39	CTCF	chr19:39452767-39453059	Lung_OC	lung:	n/a	n/a
40	CTCF	chr19:39452842-39453033	GM10248	blood:	n/a	n/a
41	CTCF	chr19:39452860-39453010	AG09319	gingival:	n/a	n/a
42	CTCF	chr19:39452880-39453030	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr19:39452860-39453010	HCFaa	heart:	n/a	n/a
44	CTCF	chr19:39452860-39453010	MCF-7	breast:	n/a	n/a
45	CTCF	chr19:39448320-39448470	NHEK	skin:	n/a	n/a
46	CTCF	chr19:39452860-39453010	AG04449	skin:	n/a	n/a
47	CTCF	chr19:39452860-39453010	GM12864	blood:	n/a	n/a
48	CTCF	chr19:39452860-39453010	HL-60	blood:	n/a	n/a
49	CTCF	chr19:39452710-39453067	A549	lung:	n/a	n/a
50	CTCF	chr19:39452820-39452970	HFF-Myc	foreskin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39444822-39444872	AG09319	gingival:	n/a
2	chr19:39444822-39444872	HepG2	liver:	n/a
3	chr19:39444822-39444872	HCPEpiC	choroid plexus:	n/a
4	chr19:39444822-39444872	HRPEpiC	eye:	n/a
5	chr19:39444822-39444872	HRE	kidney:	n/a
6	chr19:39444822-39444872	Jurkat	blood:	n/a
7	chr19:39444822-39444872	SKMC	muscle:	n/a
8	chr19:39444822-39444872	MCF10A-Er-Src	breast:	n/a
9	chr19:39444822-39444872	AG10803	skin:	n/a
10	chr19:39444822-39444872	GM19239	blood:	n/a
11	chr19:39444822-39444872	SK-N-SH_RA	brain:	n/a
12	chr19:39444822-39444872	SAEC	small airway:	n/a
13	chr19:39444822-39444872	T-47D	breast:	n/a
14	chr19:39444822-39444872	SK-N-MC	brain:	n/a
15	chr19:39444822-39444872	AG04450	lung:	fetal
16	chr19:39444822-39444872	GM12891	blood:	n/a
17	chr19:39444822-39444872	Hepatocyte	liver:	n/a
18	chr19:39444822-39444872	HL-60	blood:	n/a
19	chr19:39444822-39444872	NB4	blood:	n/a
20	chr19:39444822-39444872	BE2_C	brain:	n/a
21	chr19:39444822-39444872	MCF-7	breast:	n/a
22	chr19:39444822-39444872	PFSK-1	brain:	n/a
23	chr19:39444822-39444872	HCT-116	colon:	n/a
24	chr19:39444822-39444872	NT2-D1	testis:	n/a
25	chr19:39444822-39444872	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:39444822-39444872	AG04449	skin:	fetal
27	chr19:39444822-39444872	GM12878	blood:	n/a
28	chr19:39444822-39444872	H1-hESC	embryonic stem cell:	embryo
29	chr19:39444822-39444872	NHDF-neo	bronchial:	n/a
30	chr19:39444822-39444872	LNCaP	prostate:	n/a
31	chr19:39444822-39444872	HCM	heart:	n/a
32	chr19:39444822-39444872	HUVEC	blood vessel:	n/a
33	chr19:39444822-39444872	HMEC	breast:	n/a
34	chr19:39444822-39444872	BJ	skin:	n/a
35	chr19:39444822-39444872	HNPCEpiC	eye:	n/a
36	chr19:39444822-39444872	U87	brain:	n/a
37	chr19:39444822-39444872	GM12892	blood:	n/a
38	chr19:39444822-39444872	HEEpiC	esophagus:	n/a
39	chr19:39444822-39444872	PrEC	prostate:	n/a
40	chr19:39444822-39444872	A549	lung:	n/a
41	chr19:39444822-39444872	ECC-1	luminal epithelium:	n/a
42	chr19:39444822-39444872	AoSMC	blood vessel:	n/a
43	chr19:39444822-39444872	AG09309	skin:	n/a
44	chr19:39444822-39444872	RPTEC	kidney:	n/a
45	chr19:39444822-39444872	HEK293	kidney:	embryo
46	chr19:39444822-39444872	HRCEpiC	kidney:	n/a
47	chr19:39444822-39444872	K562	blood:	n/a
48	chr19:39444822-39444872	Hela-S3	cervix:	n/a
49	chr19:39444822-39444872	HAEpiC	amniotic membrane:	n/a
50	chr19:39444822-39444872	ovcar-3	ovarian:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39451205..39454467-chr19:39519631..39524743,4	MCF-7	breast:
2	chr19:39451089..39454157-chr19:39527302..39529882,3	MCF-7	breast:
3	chr19:39445648..39448441-chr19:39522316..39524736,2	MCF-7	breast:
4	chr19:39446984..39449185-chr19:39451380..39452922,2	K562	blood:
5	chr19:39452714..39453366-chr19:39619438..39620098,2	MCF-7	breast:
6	chr19:39450542..39452655-chr19:39464406..39466018,2	MCF-7	breast:
7	chr19:39452775..39453297-chr19:39522791..39523429,2	MCF-7	breast:
8	chr19:39450778..39452784-chr19:39902790..39905419,2	K562	blood:
9	chr19:39442111..39444861-chr19:39446173..39448020,2	K562	blood:
10	chr19:39451381..39454892-chr19:39459687..39462342,3	K562	blood:
11	chr19:39436055..39437829-chr19:39444775..39447617,2	MCF-7	breast:
12	chr14:53160999..53162843-chr19:39450717..39452706,2	MCF-7	breast:
13	chr19:39446984..39449185-chr19:39451380..39452922,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000269547	TF binding region
FBXO17	TF binding region
SARS2	TF binding region
ENSG00000269547	CpG island
FBXO17	CpG island
SARS2	CpG island
ENSG00000090924	chromatin interactions
ENSG00000197930	chromatin interactions
ENSG00000161243	chromatin interactions
ENSG00000267992	chromatin interactions
ENSG00000269190	chromatin interactions

Extended variants
information (count: 433 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:433 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11083490	chr19:39444417-39444418	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	mRNA abundance
2	rs142872979	chr19:39444426-39444427	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs553674568	chr19:39444438-39444439	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs190224693	chr19:39444458-39444459	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
5	rs552966279	chr19:39444495-39444496	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
6	rs574589175	chr19:39444499-39444500	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
7	rs181731050	chr19:39444501-39444502	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
8	rs541655621	chr19:39444515-39444516	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
9	rs138290213	chr19:39444533-39444534	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
10	rs571983831	chr19:39444534-39444535	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
11	rs372827026	chr19:39444609-39444610	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
12	rs151053998	chr19:39444610-39444611	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
13	rs538992631	chr19:39444615-39444616	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
14	rs545484285	chr19:39444620-39444621	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
15	rs186326225	chr19:39444644-39444645	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
16	rs375324602	chr19:39444724-39444725	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
17	rs142202991	chr19:39444732-39444733	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
18	rs144386251	chr19:39444734-39444735	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
19	rs529569679	chr19:39444755-39444756	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	3 gene(s)	Overlapped CNVs	n/a
20	rs551242827	chr19:39444781-39444782	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs564156174	chr19:39444786-39444787	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs375920324	chr19:39444787-39444788	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs147862338	chr19:39444822-39444823	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs190296423	chr19:39444823-39444824	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs551853605	chr19:39444874-39444875	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs368196010	chr19:39444881-39444882	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs141427904	chr19:39444914-39444915	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs549341677	chr19:39444926-39444927	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs150365043	chr19:39444994-39444995	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs182156408	chr19:39445013-39445014	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs372499374	chr19:39445044-39445045	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs137906159	chr19:39445066-39445067	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs575054314	chr19:39445095-39445096	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs149024977	chr19:39445129-39445130	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs557539645	chr19:39445130-39445131	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs367728417	chr19:39445201-39445202	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs572880190	chr19:39445205-39445206	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs368586871	chr19:39445218-39445219	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs113115937	chr19:39445220-39445221	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs34609435	chr19:39445254-39445255	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs75137525	chr19:39445265-39445266	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs12982592	chr19:39445281-39445282	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs544881514	chr19:39445282-39445283	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs185220213	chr19:39445289-39445290	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs533539264	chr19:39445334-39445335	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs551923182	chr19:39445344-39445345	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs146122738	chr19:39445364-39445365	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs527761433	chr19:39445430-39445431	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs555204228	chr19:39445435-39445436	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs567638780	chr19:39445445-39445446	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Pleomorphic liposarcoma	18784837	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
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39422600-39453000	Weak transcription	HSMMtube	muscle
2	chr19:39435800-39453000	Weak transcription	K562	blood
3	chr19:39438200-39447000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr19:39438400-39453000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr19:39439200-39452600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr19:39439600-39446200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr19:39441000-39453000	Weak transcription	Aorta	Aorta
8	chr19:39441000-39459200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr19:39441200-39446400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr19:39441200-39447600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr19:39441200-39448200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr19:39441200-39449200	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr19:39441200-39449200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr19:39441200-39450400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr19:39441200-39452800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr19:39441200-39453000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr19:39441200-39453000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr19:39441200-39453000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr19:39441200-39453000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr19:39441200-39453000	Weak transcription	Brain Hippocampus Middle	brain
21	chr19:39441200-39453000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr19:39441200-39453000	Weak transcription	Lung	lung
23	chr19:39441200-39453000	Weak transcription	Pancreas	Pancrea
24	chr19:39441200-39453000	Weak transcription	Osteobl	bone
25	chr19:39441200-39455800	Weak transcription	Psoas Muscle	Psoas
26	chr19:39441200-39459400	Weak transcription	Fetal Lung	lung
27	chr19:39441200-39465200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr19:39441200-39465200	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr19:39441200-39465200	Weak transcription	NHLF	lung
30	chr19:39441200-39465400	Weak transcription	Right Atrium	heart
31	chr19:39441400-39445800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr19:39441400-39447600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr19:39441400-39447600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr19:39441400-39452600	Weak transcription	Adipose Nuclei	Adipose
35	chr19:39441400-39452600	Weak transcription	Colon Smooth Muscle	Colon
36	chr19:39441400-39453000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr19:39441400-39453000	Weak transcription	Duodenum Smooth Muscle	Duodenum
38	chr19:39441400-39453000	Weak transcription	Fetal Brain Male	brain
39	chr19:39441400-39453000	Weak transcription	Fetal Brain Female	brain
40	chr19:39441400-39453000	Weak transcription	Ovary	ovary
41	chr19:39441400-39453000	Weak transcription	Stomach Smooth Muscle	stomach
42	chr19:39441400-39453200	Weak transcription	Fetal Heart	heart
43	chr19:39441400-39462000	Weak transcription	Small Intestine	intestine
44	chr19:39441400-39465000	Weak transcription	HUVEC	blood vessel
45	chr19:39441600-39450200	Strong transcription	Fetal Stomach	stomach
46	chr19:39441800-39444800	Strong transcription	Fetal Muscle Trunk	muscle
47	chr19:39442400-39445000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr19:39442800-39444800	Enhancers	HepG2	liver
49	chr19:39442800-39445000	Strong transcription	Fetal Muscle Leg	muscle
50	chr19:39443400-39453000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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