Variant report

Variant	nsv580045
Chromosome Location	chr19:53374787-53401760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:457)
CpG islands
(count:672)
Chromatin interactive
region (count:15)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:457 , 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	BACH1	chr19:53400547-53401042	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:53400452-53401079	K562	blood:	n/a	n/a
3	BHLHE40	chr19:53400368-53401093	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:53376302-53376339	K562	blood:	n/a	n/a
5	BHLHE40	chr19:53401560-53401600	K562	blood:	n/a	n/a
6	BRCA1	chr19:53400246-53400961	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr19:53400249-53401056	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr19:53400551-53400898	GM12878	blood:	n/a	n/a
9	CBX3	chr19:53399712-53400079	K562	blood:	n/a	n/a
10	CBX3	chr19:53383913-53384365	K562	blood:	n/a	n/a
11	CBX3	chr19:53376216-53376620	K562	blood:	n/a	n/a
12	CBX3	chr19:53400349-53401271	K562	blood:	n/a	n/a
13	CCNT2	chr19:53400798-53401141	K562	blood:	n/a	n/a
14	CEBPB	chr19:53400920-53401034	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr19:53400754-53401233	K562	blood:	n/a	n/a
16	CEBPB	chr19:53399436-53399442	K562	blood:	n/a	n/a
17	CEBPD	chr19:53376161-53376655	K562	blood:	n/a	n/a
18	CEBPD	chr19:53394674-53395077	K562	blood:	n/a	n/a
19	CHD1	chr19:53400535-53400920	GM12878	blood:	n/a	n/a
20	CHD2	chr19:53400483-53401264	GM12878	blood:	n/a	chr19:53401172-53401179
21	CHD2	chr19:53400275-53401144	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr19:53400465-53401290	H1-hESC	embryonic stem cell:	n/a	chr19:53401172-53401179
23	CHD2	chr19:53400155-53401050	K562	blood:	n/a	n/a
24	CTCF	chr19:53400680-53400830	SK-N-SH_RA	brain:	n/a	n/a
25	CTCF	chr19:53400420-53400570	AG09319	gingival:	n/a	n/a
26	CTCF	chr19:53400460-53400610	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr19:53400440-53400590	AG09319	gingival:	n/a	n/a
28	CTCF	chr19:53391416-53391462	GM20000	blood:	n/a	n/a
29	CTCF	chr19:53382813-53382847	GM13977	blood:	n/a	n/a
30	CTCF	chr19:53399860-53400010	GM12865	blood:	n/a	n/a
31	CTCF	chr19:53400835-53400983	K562	blood:	n/a	n/a
32	CTCF	chr19:53400788-53401009	GM12878	blood:	n/a	n/a
33	CTCF	chr19:53400844-53401078	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr19:53400440-53400590	AG04449	skin:	n/a	n/a
35	CTCF	chr19:53384676-53384683	Spleen_OC	spleen:	n/a	n/a
36	CUX1	chr19:53400707-53400913	K562	blood:	n/a	n/a
37	CUX1	chr19:53400840-53400925	GM12878	blood:	n/a	n/a
38	CUX1	chr19:53400396-53400510	GM12878	blood:	n/a	n/a
39	E2F4	chr19:53400653-53400910	GM12878	blood:	n/a	n/a
40	E2F4	chr19:53387175-53387242	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr19:53400768-53401105	MCF10A-Er-Src	breast:	n/a	chr19:53401001-53401011
42	E2F6	chr19:53400388-53400676	K562	blood:	n/a	n/a
43	E2F6	chr19:53400743-53400912	K562	blood:	n/a	n/a
44	E2F6	chr19:53400729-53401044	K562	blood:	n/a	chr19:53401001-53401011
45	E2F6	chr19:53400093-53400265	K562	blood:	n/a	n/a
46	E2F6	chr19:53400409-53401070	K562	blood:	n/a	chr19:53401001-53401011
47	EBF1	chr19:53400808-53401031	GM12878	blood:	n/a	n/a
48	EBF1	chr19:53400731-53401011	GM12878	blood:	n/a	n/a
49	EGR1	chr19:53400863-53401229	K562	blood:	n/a	chr19:53401038-53401048 chr19:53401122-53401131 chr19:53401119-53401132 chr19:53401037-53401047 chr19:53401122-53401132
50	EGR1	chr19:53400774-53401264	K562	blood:	n/a	chr19:53401038-53401048 chr19:53401122-53401131 chr19:53401119-53401132 chr19:53401037-53401047 chr19:53401122-53401132

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:53401204-53401254	NHBE	bronchial:	n/a
2	chr19:53401204-53401254	NHBE	bronchial:	n/a
3	chr19:53383549-53383599	HepG2	liver:	n/a
4	chr19:53400933-53400983	HRCEpiC	kidney:	n/a
5	chr19:53394977-53395027	AG10803	skin:	n/a
6	chr19:53394626-53394676	IMR90	lung:	fetal
7	chr19:53394977-53395027	ovcar-3	ovarian:	n/a
8	chr19:53400981-53401031	AG09319	gingival:	n/a
9	chr19:53395225-53395275	BE2_C	brain:	n/a
10	chr19:53400981-53401031	AoSMC	blood vessel:	n/a
11	chr19:53394977-53395027	HRE	kidney:	n/a
12	chr19:53394626-53394676	HEK293	kidney:	embryo
13	chr19:53400933-53400983	ProgFib	skin:	n/a
14	chr19:53400545-53400595	IMR90	lung:	fetal
15	chr19:53393512-53393562	HRCEpiC	kidney:	n/a
16	chr19:53400545-53400595	SK-N-MC	brain:	n/a
17	chr19:53401204-53401254	HIPEpiC	eye:	n/a
18	chr19:53393512-53393562	PANC-1	pancreas:	n/a
19	chr19:53400545-53400595	Jurkat	blood:	n/a
20	chr19:53401204-53401254	Jurkat	blood:	n/a
21	chr19:53393512-53393562	Jurkat	blood:	n/a
22	chr19:53400933-53400983	U87	brain:	n/a
23	chr19:53400778-53400828	HEEpiC	esophagus:	n/a
24	chr19:53394626-53394676	AG10803	skin:	n/a
25	chr19:53400778-53400828	H1-hESC	embryonic stem cell:	embryo
26	chr19:53395225-53395275	HRCEpiC	kidney:	n/a
27	chr19:53400981-53401031	NB4	blood:	n/a
28	chr19:53395225-53395275	HCM	heart:	n/a
29	chr19:53383549-53383599	GM06990	blood:	n/a
30	chr19:53394626-53394676	HepG2	liver:	n/a
31	chr19:53400933-53400983	Hepatocyte	liver:	n/a
32	chr19:53383549-53383599	HL-60	blood:	n/a
33	chr19:53401204-53401254	HAEpiC	amniotic membrane:	n/a
34	chr19:53400545-53400595	GM19239	blood:	n/a
35	chr19:53383549-53383599	GM12878	blood:	n/a
36	chr19:53400933-53400983	NH-A	brain:	n/a
37	chr19:53394977-53395027	HRCEpiC	kidney:	n/a
38	chr19:53401204-53401254	HepG2	liver:	n/a
39	chr19:53400933-53400983	HMEC	breast:	n/a
40	chr19:53401204-53401254	HPAEpiC	pulmonary alveolar:	n/a
41	chr19:53401204-53401254	HNPCEpiC	eye:	n/a
42	chr19:53383549-53383599	ProgFib	skin:	n/a
43	chr19:53394977-53395027	HCF	heart:	n/a
44	chr19:53400981-53401031	Hepatocyte	liver:	n/a
45	chr19:53395225-53395275	CMK	blood:	n/a
46	chr19:53395225-53395275	PFSK-1	brain:	n/a
47	chr19:53383549-53383599	HRCEpiC	kidney:	n/a
48	chr19:53394977-53395027	IMR90	lung:	fetal
49	chr19:53401204-53401254	NT2-D1	testis:	n/a
50	chr19:53394977-53395027	HIPEpiC	eye:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:53391514..53397028-chr19:53398889..53402751,6	K562	blood:
2	chr19:53400711..53402486-chr19:53463191..53466156,2	K562	blood:
3	chr19:53377771..53379611-chr19:53399736..53401870,2	K562	blood:
4	chr19:53398338..53401958-chr19:53425181..53428572,6	K562	blood:
5	chr19:53398338..53403121-chr19:53425170..53428184,6	K562	blood:
6	chr19:53393138..53396276-chr19:53398172..53401096,6	MCF-7	breast:
7	chr18:61637223..61637841-chr19:53397208..53398194,2	Hela-S3	cervix:
8	chr19:53397070..53398594-chr19:53398820..53400571,2	MCF-7	breast:
9	chr19:53393138..53396276-chr19:53398172..53401096,6	MCF-7	breast:
10	chr19:53398857..53399725-chr3:31226625..31227200,2	MCF-7	breast:
11	chr19:53380234..53382987-chr19:53399088..53400987,2	K562	blood:
12	chr19:53391514..53397028-chr19:53398889..53402751,6	K562	blood:
13	chr19:53390480..53393412-chr19:53415932..53418277,2	K562	blood:
14	chr19:53399773..53402425-chr19:53424830..53427617,2	MCF-7	breast:
15	chr19:53380234..53382987-chr19:53399088..53400987,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF320-2	chr19:53397032-53397109	NONHSAT067595
2	lnc-ZNF320-3	chr19:53382704-53382886	NONHSAT067592
3	lnc-ZNF320-2	chr19:53400773-53400908	NONHSAT067594
4	lnc-ZNF320-1	chr19:53398098-53398409	NONHSAT067593
5	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067591
6	lnc-ZNF320-2	chr19:53393562-53393581	NONHSAT067595
7	lnc-ZNF320-3	chr19:53377411-53377490	NONHSAT067591
8	lnc-ZNF320-2	chr19:53396637-53396872	NONHSAT067594
9	lnc-ZNF320-2	chr19:53393514-53393581	NONHSAT067594
10	lnc-ZNF320-3	chr19:53377245-53377325	NONHSAT067592
11	lnc-ZNF320-2	chr19:53398644-53399035	NONHSAT067597
12	lnc-ZNF320-2	chr19:53396637-53396872	NONHSAT067595
13	lnc-ZNF320-2	chr19:53400773-53400888	NONHSAT067597
14	lnc-ZNF320-2	chr19:53394482-53394599	NONHSAT067594
15	lnc-ZNF320-2	chr19:53394482-53394599	NONHSAT067595
16	lnc-ZNF320-2	chr19:53397032-53397174	NONHSAT067596
17	lnc-ZNF320-2	chr19:53400773-53400902	NONHSAT067595
18	lnc-ZNF320-1	chr19:53379431-53379838	NONHSAT067593
19	lnc-ZNF320-2	chr19:53394513-53394599	NONHSAT067596

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF320	hsa-miR-192-5p	chr19:53381440-53381461

Variant related genes	Relation type
ZNF320	TF binding region
ZNF320	CpG island
ENSG00000180257	chromatin interactions
ENSG00000269646	chromatin interactions
ENSG00000182986	chromatin interactions
ENSG00000221874	chromatin interactions
ENSG00000166401	chromatin interactions
ENSG00000213793	chromatin interactions

Extended variants
information (count: 1277 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1277 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8110526	chr19:53374787-53374788	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566583785	chr19:53374793-53374794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567131937	chr19:53374799-53374800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527470550	chr19:53374810-53374811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552551122	chr19:53374822-53374823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185440768	chr19:53374837-53374838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559337003	chr19:53374856-53374857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12972155	chr19:53374907-53374908	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs537885635	chr19:53374910-53374911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556584925	chr19:53374915-53374916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs550242638	chr19:53374935-53374936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374156708	chr19:53374954-53374955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373697091	chr19:53374981-53374982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12461132	chr19:53374984-53374985	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs571957538	chr19:53375044-53375045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545670472	chr19:53375097-53375098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564075838	chr19:53375124-53375125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531175518	chr19:53375160-53375161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369729985	chr19:53375161-53375162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34689635	chr19:53375181-53375182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189967794	chr19:53375207-53375208	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111460869	chr19:53375223-53375224	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528991443	chr19:53375225-53375226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs11880864	chr19:53375235-53375236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs567064824	chr19:53375285-53375286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534420926	chr19:53375354-53375355	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147080749	chr19:53375375-53375376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571174506	chr19:53375376-53375377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538208873	chr19:53375378-53375379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138487627	chr19:53375397-53375398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144029130	chr19:53375399-53375400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535568751	chr19:53375401-53375402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553877728	chr19:53375404-53375405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146897436	chr19:53375409-53375410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs545610781	chr19:53375419-53375420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564012612	chr19:53375446-53375447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs370278057	chr19:53375447-53375448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570126289	chr19:53375452-53375453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568167637	chr19:53375512-53375513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561520863	chr19:53375566-53375567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528932465	chr19:53375577-53375578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547151697	chr19:53375608-53375609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs559521931	chr19:53375626-53375627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs527850801	chr19:53375645-53375646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552823874	chr19:53375666-53375667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs571109121	chr19:53375669-53375670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs538164737	chr19:53375674-53375675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373623750	chr19:53375690-53375691	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138977544	chr19:53375694-53375695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535877541	chr19:53375700-53375701	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Melanoma	17363583	CNVD
Breast cancer	21785460	CNVD
Adrenocortical carcinoma	18281524	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1270 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:53361400-53381800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr19:53361400-53381800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr19:53361400-53381800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr19:53361400-53381800	Weak transcription	Brain Angular Gyrus	brain
5	chr19:53361400-53382000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr19:53361400-53382000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:53361600-53380400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr19:53361600-53381800	Weak transcription	Psoas Muscle	Psoas
9	chr19:53361800-53381800	Weak transcription	Brain Anterior Caudate	brain
10	chr19:53361800-53381800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr19:53361800-53381800	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr19:53361800-53383800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr19:53362000-53382000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr19:53369000-53380400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr19:53370600-53382000	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr19:53371600-53382000	Weak transcription	Stomach Smooth Muscle	stomach
17	chr19:53372000-53381800	Weak transcription	Placenta	Placenta
18	chr19:53374600-53381800	Weak transcription	Fetal Stomach	stomach
19	chr19:53374800-53381800	Weak transcription	Left Ventricle	heart
20	chr19:53374800-53382000	Weak transcription	Brain Hippocampus Middle	brain
21	chr19:53375000-53381200	Weak transcription	Primary T cells from cord blood	blood
22	chr19:53375200-53379000	Enhancers	K562	blood
23	chr19:53375400-53381800	Weak transcription	Colon Smooth Muscle	Colon
24	chr19:53375400-53381800	Weak transcription	Fetal Muscle Leg	muscle
25	chr19:53376000-53383200	Weak transcription	Brain Substantia Nigra	brain
26	chr19:53376400-53377200	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr19:53376800-53377000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr19:53377000-53377400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr19:53377000-53377800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr19:53377200-53383400	Weak transcription	Brain Germinal Matrix	brain
31	chr19:53377400-53379000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr19:53377400-53380400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr19:53377600-53382000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr19:53377800-53383600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr19:53378200-53378400	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr19:53378400-53381200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr19:53378800-53380600	Weak transcription	Fetal Brain Female	brain
38	chr19:53378800-53382000	Weak transcription	Skeletal Muscle Female	skeletal muscle
39	chr19:53379000-53380600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr19:53379000-53381800	Weak transcription	K562	blood
41	chr19:53379000-53383400	Weak transcription	Fetal Kidney	kidney
42	chr19:53379000-53383800	Weak transcription	Fetal Brain Male	brain
43	chr19:53379200-53381800	Weak transcription	HSMM	muscle
44	chr19:53379200-53382000	Weak transcription	Fetal Lung	lung
45	chr19:53379400-53381200	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr19:53379400-53381600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr19:53379800-53380000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
48	chr19:53379800-53381800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr19:53379800-53388600	ZNF genes & repeats	Liver	Liver
50	chr19:53380000-53381800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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