Variant report

Variant	nsv912140
Chromosome Location	chr19:45434874-45451721
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:514)
CpG islands
(count:1038)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:514 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:45439106-45439470	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:45442945-45443204	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:45449069-45449525	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:45447009-45447238	K562	blood:	n/a	n/a
5	ATF2	chr19:45447008-45447414	GM12878	blood:	n/a	n/a
6	BCL11A	chr19:45447085-45447434	GM12878	blood:	n/a	n/a
7	BCL3	chr19:45442673-45442951	GM12878	blood:	n/a	n/a
8	BCL3	chr19:45442653-45442945	GM12878	blood:	n/a	n/a
9	BCL3	chr19:45445570-45446047	GM12878	blood:	n/a	n/a
10	BCL3	chr19:45445564-45446060	GM12878	blood:	n/a	n/a
11	BCLAF1	chr19:45446954-45447451	K562	blood:	n/a	n/a
12	BHLHE40	chr19:45445771-45445868	K562	blood:	n/a	n/a
13	BHLHE40	chr19:45439108-45439520	HepG2	liver:	n/a	n/a
14	BHLHE40	chr19:45447024-45447383	GM12878	blood:	n/a	n/a
15	BHLHE40	chr19:45446997-45447412	K562	blood:	n/a	n/a
16	BRCA1	chr19:45448913-45448959	HepG2	liver:	n/a	n/a
17	CBX3	chr19:45446867-45447516	K562	blood:	n/a	n/a
18	CCNT2	chr19:45439179-45439209	K562	blood:	n/a	n/a
19	CCNT2	chr19:45447086-45447439	K562	blood:	n/a	n/a
20	CEBPB	chr19:45442927-45443180	K562	blood:	n/a	chr19:45443063-45443074
21	CEBPB	chr19:45450231-45450505	K562	blood:	n/a	chr19:45450359-45450370
22	CEBPB	chr19:45437211-45437397	HepG2	liver:	n/a	chr19:45437284-45437295
23	CEBPB	chr19:45438309-45438659	HepG2	liver:	n/a	chr19:45438482-45438493
24	CEBPB	chr19:45442821-45443308	HepG2	liver:	n/a	chr19:45443063-45443074
25	CEBPB	chr19:45442827-45443386	A549	lung:	n/a	chr19:45443063-45443074
26	CEBPB	chr19:45438321-45438627	A549	lung:	n/a	chr19:45438482-45438493
27	CEBPB	chr19:45442996-45443218	MCF-7	breast:	n/a	chr19:45443063-45443074
28	CEBPB	chr19:45439095-45439449	HepG2	liver:	n/a	n/a
29	CEBPB	chr19:45437175-45437420	HepG2	liver:	n/a	chr19:45437284-45437295
30	CEBPB	chr19:45437192-45437532	A549	lung:	n/a	chr19:45437284-45437295
31	CEBPB	chr19:45437139-45437461	A549	lung:	n/a	chr19:45437284-45437295
32	CEBPB	chr19:45443007-45443150	Hela-S3	cervix:	n/a	chr19:45443063-45443074
33	CEBPB	chr19:45438320-45438640	A549	lung:	n/a	chr19:45438482-45438493
34	CEBPB	chr19:45442914-45443217	IMR90	lung:	n/a	chr19:45443063-45443074
35	CEBPB	chr19:45440399-45440452	HepG2	liver:	n/a	n/a
36	CEBPB	chr19:45438321-45438658	K562	blood:	n/a	chr19:45438482-45438493
37	CEBPB	chr19:45450119-45450560	HepG2	liver:	n/a	chr19:45450359-45450370
38	CEBPB	chr19:45442946-45443235	HepG2	liver:	n/a	chr19:45443063-45443074
39	CEBPB	chr19:45439110-45439384	HepG2	liver:	n/a	n/a
40	CEBPB	chr19:45442933-45443262	A549	lung:	n/a	chr19:45443063-45443074
41	CEBPB	chr19:45450263-45450469	HepG2	liver:	n/a	chr19:45450359-45450370
42	CEBPB	chr19:45437122-45437466	IMR90	lung:	n/a	chr19:45437284-45437295
43	CEBPB	chr19:45437142-45437386	Hela-S3	cervix:	n/a	chr19:45437284-45437295
44	CEBPB	chr19:45437107-45437380	HepG2	liver:	n/a	chr19:45437284-45437295
45	CEBPB	chr19:45442898-45443306	HepG2	liver:	n/a	chr19:45443063-45443074
46	CEBPB	chr19:45442888-45443292	HepG2	liver:	n/a	chr19:45443063-45443074
47	CEBPB	chr19:45438339-45438548	H1-hESC	embryonic stem cell:	n/a	chr19:45438482-45438493
48	CEBPB	chr19:45437275-45437312	K562	blood:	n/a	chr19:45437284-45437295
49	CEBPB	chr19:45450203-45450519	HepG2	liver:	n/a	chr19:45450359-45450370
50	CEBPB	chr19:45450215-45450522	HepG2	liver:	n/a	chr19:45450359-45450370

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:45449006-45449056	MCF-7	breast:	n/a
2	chr19:45449006-45449056	MCF-7	breast:	n/a
3	chr19:45449301-45449351	Hela-S3	cervix:	n/a
4	chr19:45448959-45449009	NHBE	bronchial:	n/a
5	chr19:45449297-45449347	HEK293	kidney:	embryo
6	chr19:45449301-45449351	HAEpiC	amniotic membrane:	n/a
7	chr19:45449297-45449347	HRE	kidney:	n/a
8	chr19:45449006-45449056	GM06990	blood:	n/a
9	chr19:45445437-45445487	HepG2	liver:	n/a
10	chr19:45444811-45444861	HUVEC	blood vessel:	n/a
11	chr19:45445693-45445743	SAEC	small airway:	n/a
12	chr19:45444860-45444910	ProgFib	skin:	n/a
13	chr19:45448680-45448730	SK-N-MC	brain:	n/a
14	chr19:45448413-45448463	Hela-S3	cervix:	n/a
15	chr19:45444811-45444861	HepG2	liver:	n/a
16	chr19:45448413-45448463	HCPEpiC	choroid plexus:	n/a
17	chr19:45449099-45449149	HRPEpiC	eye:	n/a
18	chr19:45449297-45449347	NH-A	brain:	n/a
19	chr19:45448680-45448730	Jurkat	blood:	n/a
20	chr19:45445486-45445536	AG09309	skin:	n/a
21	chr19:45448680-45448730	PANC-1	pancreas:	n/a
22	chr19:45444199-45444249	HCPEpiC	choroid plexus:	n/a
23	chr19:45445486-45445536	HCPEpiC	choroid plexus:	n/a
24	chr19:45448413-45448463	HL-60	blood:	n/a
25	chr19:45444199-45444249	NH-A	brain:	n/a
26	chr19:45445437-45445487	T-47D	breast:	n/a
27	chr19:45444199-45444249	PrEC	prostate:	n/a
28	chr19:45445449-45445499	NHBE	bronchial:	n/a
29	chr19:45445521-45445571	H1-hESC	embryonic stem cell:	embryo
30	chr19:45444811-45444861	HEK293	kidney:	embryo
31	chr19:45449006-45449056	NHDF-neo	bronchial:	n/a
32	chr19:45449301-45449351	HCT-116	colon:	n/a
33	chr19:45444811-45444861	LNCaP	prostate:	n/a
34	chr19:45445486-45445536	HUVEC	blood vessel:	n/a
35	chr19:45444811-45444861	Jurkat	blood:	n/a
36	chr19:45445693-45445743	NHDF-neo	bronchial:	n/a
37	chr19:45449301-45449351	HCF	heart:	n/a
38	chr19:45448413-45448463	HRE	kidney:	n/a
39	chr19:45445437-45445487	ECC-1	luminal epithelium:	n/a
40	chr19:45445491-45445541	HCPEpiC	choroid plexus:	n/a
41	chr19:45445437-45445487	LNCaP	prostate:	n/a
42	chr19:45445693-45445743	ovcar-3	ovarian:	n/a
43	chr19:45448680-45448730	SK-N-SH	brain:	n/a
44	chr19:45448959-45449009	HL-60	blood:	n/a
45	chr19:45444811-45444861	BE2_C	brain:	n/a
46	chr19:45449099-45449149	HIPEpiC	eye:	n/a
47	chr19:45445521-45445571	A549	lung:	n/a
48	chr19:45449099-45449149	NB4	blood:	n/a
49	chr19:45448959-45449009	HEEpiC	esophagus:	n/a
50	chr19:45445449-45445499	PrEC	prostate:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:45406430..45407977-chr19:45445993..45448710,2	K562	blood:
2	chr19:45415569..45417963-chr19:45443014..45445506,2	K562	blood:
3	chr19:45393153..45395531-chr19:45443395..45445635,2	K562	blood:
4	chr19:45399714..45401565-chr19:45445592..45447999,2	K562	blood:
5	chr19:45444327..45448309-chr19:45456781..45460381,5	K562	blood:
6	chr19:45441969..45444512-chr19:45446313..45448953,2	K562	blood:
7	chr19:45441969..45444512-chr19:45446313..45448953,2	K562	blood:
8	chr19:45406430..45412448-chr19:45445993..45451546,6	K562	blood:
9	chr19:45428614..45431090-chr19:45445301..45448167,2	K562	blood:

No data

Variant related genes	Relation type
APOC2	TF binding region
APOC4	TF binding region
APOC4-APOC2	TF binding region
APOC2	CpG island
APOC4	CpG island
APOC4-APOC2	CpG island
ENSG00000267114	chromatin interactions
ENSG00000130208	chromatin interactions
ENSG00000214855	chromatin interactions
ENSG00000267282	chromatin interactions
ENSG00000130204	chromatin interactions
ENSG00000104853	chromatin interactions
ENSG00000130203	chromatin interactions

Extended variants
information (count: 783 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:783 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7255574	chr19:45434874-45434875	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs370625306	chr19:45434881-45434882	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7255698	chr19:45434927-45434928	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181131582	chr19:45434973-45434974	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149795159	chr19:45434976-45434977	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530696937	chr19:45435073-45435074	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550788630	chr19:45435093-45435094	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558797558	chr19:45435115-45435116	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368842910	chr19:45435135-45435136	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs527977225	chr19:45435152-45435153	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs570521790	chr19:45435191-45435192	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs533072062	chr19:45435198-45435199	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145777103	chr19:45435225-45435226	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs566486137	chr19:45435229-45435230	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535484784	chr19:45435277-45435278	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552842135	chr19:45435314-45435315	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576228775	chr19:45435358-45435359	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538005841	chr19:45435402-45435403	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34731969	chr19:45435421-45435422	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538141581	chr19:45435425-45435426	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs397758367	chr19:45435434-45435435	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185490300	chr19:45435458-45435459	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113101476	chr19:45435466-45435467	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368969130	chr19:45435489-45435490	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs578088571	chr19:45435494-45435495	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140082891	chr19:45435525-45435526	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs547591252	chr19:45435536-45435537	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553808241	chr19:45435599-45435600	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs367640933	chr19:45435631-45435632	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538466953	chr19:45435635-45435636	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542643453	chr19:45435648-45435649	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs9749443	chr19:45435661-45435662	Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs34159556	chr19:45435726-45435727	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375427001	chr19:45435748-45435749	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147722271	chr19:45435762-45435763	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564309961	chr19:45435771-45435772	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532944725	chr19:45435774-45435775	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs113110693	chr19:45435775-45435776	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111537522	chr19:45435776-45435777	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs9749609	chr19:45435813-45435814	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549033607	chr19:45435827-45435828	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs558674284	chr19:45435839-45435840	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200884687	chr19:45435876-45435877	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538551913	chr19:45435931-45435932	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150922154	chr19:45435986-45435987	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571819533	chr19:45435990-45435991	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140741671	chr19:45436010-45436011	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553939528	chr19:45436014-45436015	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74924179	chr19:45436037-45436038	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs190397429	chr19:45436065-45436066	Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	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
Adrenocortical carcinoma	18281524	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Muscular dystrophy	17160897	CNVD
Multiple myeloma	16616336	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Cancer	17440070	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Breast cancer	19602461	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:254 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45430400-45447000	Weak transcription	Right Atrium	heart
2	chr19:45430600-45449000	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr19:45431000-45454600	Weak transcription	Esophagus	oesophagus
4	chr19:45431200-45439000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr19:45431200-45439000	Weak transcription	Pancreas	Pancrea
6	chr19:45431400-45437600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr19:45431400-45437800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:45434000-45436200	Weak transcription	HepG2	liver
9	chr19:45434800-45436200	Genic enhancers	Liver	Liver
10	chr19:45435200-45437800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr19:45436200-45436600	Weak transcription	Liver	Liver
12	chr19:45436200-45439000	Enhancers	HepG2	liver
13	chr19:45436600-45440600	Enhancers	Liver	Liver
14	chr19:45437600-45437800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr19:45437600-45439400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr19:45437800-45438000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:45437800-45439600	Enhancers	Ovary	ovary
18	chr19:45437800-45440400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr19:45438000-45438200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:45438200-45439400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:45438400-45439200	Weak transcription	Brain Hippocampus Middle	brain
22	chr19:45438800-45439400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr19:45438800-45439400	Enhancers	Adipose Nuclei	Adipose
24	chr19:45438800-45439600	Enhancers	Fetal Muscle Leg	muscle
25	chr19:45439000-45439200	Weak transcription	Brain Substantia Nigra	brain
26	chr19:45439000-45439200	Enhancers	Colonic Mucosa	Colon
27	chr19:45439000-45439400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr19:45439000-45439400	Enhancers	Duodenum Mucosa	Duodenum
29	chr19:45439000-45439400	Enhancers	Fetal Heart	heart
30	chr19:45439000-45439400	Enhancers	Gastric	stomach
31	chr19:45439000-45439600	Enhancers	Fetal Intestine Large	intestine
32	chr19:45439000-45439600	Enhancers	Fetal Intestine Small	intestine
33	chr19:45439000-45439600	Enhancers	Fetal Muscle Trunk	muscle
34	chr19:45439000-45439600	Enhancers	Placenta	Placenta
35	chr19:45439000-45439600	Enhancers	Pancreas	Pancrea
36	chr19:45439000-45439600	Enhancers	Rectal Mucosa Donor 29	rectum
37	chr19:45439000-45439600	Flanking Active TSS	HepG2	liver
38	chr19:45439000-45439600	Enhancers	K562	blood
39	chr19:45439000-45440000	Enhancers	Spleen	Spleen
40	chr19:45439200-45439400	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr19:45439200-45439400	Enhancers	Brain Hippocampus Middle	brain
42	chr19:45439200-45439400	Enhancers	Brain Substantia Nigra	brain
43	chr19:45439200-45439600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
44	chr19:45439200-45456800	Weak transcription	Colonic Mucosa	Colon
45	chr19:45439400-45439600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr19:45439400-45445600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr19:45439400-45451800	Weak transcription	Brain Hippocampus Middle	brain
48	chr19:45439400-45451800	Weak transcription	Brain Substantia Nigra	brain
49	chr19:45439400-45453800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr19:45439400-45457000	Weak transcription	Gastric	stomach

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