Variant report

Variant	nsv912519
Chromosome Location	chr19:57020754-57065189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr19:57050354-57050813	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr19:57050358-57050446	GM12878	blood:	n/a	n/a
3	BRCA1	chr19:57050604-57050791	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr19:57055126-57055622	A549	lung:	n/a	chr19:57055337-57055348
5	CEBPB	chr19:57055148-57055531	A549	lung:	n/a	chr19:57055337-57055348
6	CEBPB	chr19:57055163-57055521	HepG2	liver:	n/a	chr19:57055337-57055348
7	CEBPB	chr19:57055209-57055487	H1-hESC	embryonic stem cell:	n/a	chr19:57055337-57055348
8	CEBPB	chr19:57055143-57055580	A549	lung:	n/a	chr19:57055337-57055348
9	CEBPB	chr19:57055191-57055492	K562	blood:	n/a	chr19:57055337-57055348
10	CEBPB	chr19:57055151-57055530	IMR90	lung:	n/a	chr19:57055337-57055348
11	CEBPB	chr19:57034280-57034480	HepG2	liver:	n/a	chr19:57034405-57034416
12	CEBPB	chr19:57055211-57055572	MCF-7	breast:	n/a	chr19:57055337-57055348
13	CEBPB	chr19:57034299-57034494	A549	lung:	n/a	chr19:57034405-57034416
14	CHD1	chr19:57050277-57050612	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr19:57050629-57050805	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr19:57049739-57050064	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr19:57049532-57050520	A549	lung:	n/a	n/a
18	CREB1	chr19:57049461-57050173	H1-hESC	embryonic stem cell:	n/a	n/a
19	CREB1	chr19:57049572-57050152	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr19:57049612-57050035	ECC-1	luminal epithelium:	n/a	n/a
21	CREB1	chr19:57049922-57050115	A549	lung:	n/a	n/a
22	CTCF	chr19:57059040-57059190	SAEC	small airway:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
23	CTCF	chr19:57059040-57059190	NHLF	lung:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
24	CTCF	chr19:57058960-57059110	GM12872	blood:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
25	CTCF	chr19:57059294-57059306	GM10266	blood:	n/a	n/a
26	CTCF	chr19:57059030-57059183	Hela-S3	cervix:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
27	CTCF	chr19:57059020-57059170	HBMEC	blood vessel:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
28	CTCF	chr19:57059220-57059370	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr19:57059060-57059210	HBMEC	blood vessel:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
30	CTCF	chr19:57058980-57059130	HPF	lung:	n/a	chr19:57059091-57059107 chr19:57059090-57059108 chr19:57059085-57059106
31	CTCF	chr19:57059060-57059210	HRPEpiC	eye:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
32	CTCF	chr19:57059105-57059139	GM13976	blood:	n/a	n/a
33	CTCF	chr19:57059000-57059150	HepG2	liver:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
34	CTCF	chr19:57059040-57059190	HPAF	blood vessel:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
35	CTCF	chr19:57059080-57059230	GM12872	blood:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
36	CTCF	chr19:57059020-57059170	MCF-7	breast:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
37	CTCF	chr19:57050460-57050610	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr19:57059015-57059248	MCF-7	breast:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
39	CTCF	chr19:57059057-57059157	GM19240	blood:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
40	CTCF	chr19:57059020-57059170	HA-sp	spinal cord:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
41	CTCF	chr19:57059040-57059190	HEEpiC	esophagus:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
42	CTCF	chr19:57059000-57059150	GM12875	blood:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
43	CTCF	chr19:57059140-57059290	GM12872	blood:	n/a	n/a
44	CTCF	chr19:57059276-57059323	MCF-7	breast:	n/a	n/a
45	CTCF	chr19:57059100-57059250	NHEK	skin:	n/a	n/a
46	CTCF	chr19:57059046-57059159	A549	lung:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
47	CTCF	chr19:57058989-57059171	HepG2	liver:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
48	CTCF	chr19:57059000-57059150	HPAF	blood vessel:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106
49	CTCF	chr19:57059311-57059317	GM10266	blood:	n/a	n/a
50	CTCF	chr19:57059050-57059193	HUVEC	blood vessel:	n/a	chr19:57059090-57059108 chr19:57059091-57059107 chr19:57059085-57059106

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:57049857-57049907	CMK	blood:	n/a
2	chr19:57052834-57052884	HL-60	blood:	n/a
3	chr19:57049695-57049745	HNPCEpiC	eye:	n/a
4	chr19:57050620-57050670	HAEpiC	amniotic membrane:	n/a
5	chr19:57049530-57049580	NB4	blood:	n/a
6	chr19:57049777-57049827	GM19239	blood:	n/a
7	chr19:57050367-57050417	HRE	kidney:	n/a
8	chr19:57050834-57050884	Caco-2	colon:	n/a
9	chr19:57050359-57050409	HPAEpiC	pulmonary alveolar:	n/a
10	chr19:57046713-57046763	Jurkat	blood:	n/a
11	chr19:57050367-57050417	SK-N-SH	brain:	n/a
12	chr19:57046713-57046763	Hela-S3	cervix:	n/a
13	chr19:57049777-57049827	GM12892	blood:	n/a
14	chr19:57046713-57046763	ovcar-3	ovarian:	n/a
15	chr19:57049777-57049827	HEEpiC	esophagus:	n/a
16	chr19:57050620-57050670	NHDF-neo	bronchial:	n/a
17	chr19:57050359-57050409	HNPCEpiC	eye:	n/a
18	chr19:57046713-57046763	MCF10A-Er-Src	breast:	n/a
19	chr19:57049777-57049827	SK-N-SH	brain:	n/a
20	chr19:57052834-57052884	HCM	heart:	n/a
21	chr19:57049777-57049827	HRPEpiC	eye:	n/a
22	chr19:57049695-57049745	T-47D	breast:	n/a
23	chr19:57050620-57050670	A549	lung:	n/a
24	chr19:57050370-57050420	HCF	heart:	n/a
25	chr19:57049530-57049580	HepG2	liver:	n/a
26	chr19:57049530-57049580	HCM	heart:	n/a
27	chr19:57049777-57049827	CMK	blood:	n/a
28	chr19:57049857-57049907	Caco-2	colon:	n/a
29	chr19:57049695-57049745	NHBE	bronchial:	n/a
30	chr19:57046713-57046763	GM19239	blood:	n/a
31	chr19:57050370-57050420	MCF10A-Er-Src	breast:	n/a
32	chr19:57050370-57050420	GM19239	blood:	n/a
33	chr19:57049777-57049827	NH-A	brain:	n/a
34	chr19:57049777-57049827	BJ	skin:	n/a
35	chr19:57052834-57052884	SK-N-SH	brain:	n/a
36	chr19:57050834-57050884	CMK	blood:	n/a
37	chr19:57050359-57050409	ovcar-3	ovarian:	n/a
38	chr19:57049530-57049580	HRPEpiC	eye:	n/a
39	chr19:57050359-57050409	HAEpiC	amniotic membrane:	n/a
40	chr19:57049857-57049907	HNPCEpiC	eye:	n/a
41	chr19:57046713-57046763	AG10803	skin:	n/a
42	chr19:57049530-57049580	GM19239	blood:	n/a
43	chr19:57050367-57050417	HRCEpiC	kidney:	n/a
44	chr19:57050834-57050884	HEEpiC	esophagus:	n/a
45	chr19:57049695-57049745	GM06990	blood:	n/a
46	chr19:57050359-57050409	AG09319	gingival:	n/a
47	chr19:57046713-57046763	HCT-116	colon:	n/a
48	chr19:57050370-57050420	NHDF-neo	bronchial:	n/a
49	chr19:57049857-57049907	PANC-1	pancreas:	n/a
50	chr19:57049777-57049827	HCT-116	colon:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF667-2	chr19:57056935-57058640	ENSG00000269696.1
2	lnc-ZNF667-3	chr19:57049020-57049106	ENSG00000267421.2
3	lnc-ZNF471-1	chr19:57055905-57056106	NONHSAT068172
4	lnc-ZNF667-3	chr19:57049794-57049944	ENSG00000267421.2
5	lnc-ZNF667-3	chr19:57047527-57047701	ENSG00000267421.2
6	lnc-ZNF667-3	chr19:57047527-57047701	ENSG00000267421.2
7	lnc-ZNF667-3	chr19:57049020-57049106	ENSG00000267421.2
8	lnc-ZNF667-2	chr19:57056935-57058640	ENSG00000245443
9	lnc-ZNF667-3	chr19:57049020-57049106	ENSG00000267421.2
10	lnc-ZFP28-2	chr19:57021466-57021682	NONHSAT068165
11	lnc-ZNF667-3	chr19:57047525-57047701	ENSG00000267421.2
12	lnc-ZNF667-3	chr19:57049726-57049787	ENSG00000267421.2
13	lnc-ZNF470-2	chr19:57061815-57062398	NONHSAT068174
14	lnc-ZNF667-2	chr19:57056297-57058640	NONHSAT068173
15	lnc-ZNF667-3	chr19:57049017-57049800	ENSG00000267421.2
16	lnc-ZNF667-3	chr19:57049617-57049684	ENSG00000267421.2
17	lnc-ZFP28-1	chr19:57046668-57047132	ENSG00000267224.1
18	lnc-ZFP28-2	chr19:57037069-57037390	NONHSAT068165
19	lnc-ZNF667-3	chr19:57049622-57049744	ENSG00000267421.2
20	lnc-ZNF667-3	chr19:57049020-57049106	ENSG00000267421.2
21	lnc-ZNF471-1	chr19:57050994-57051085	NONHSAT068172
22	lnc-ZNF667-3	chr19:57047527-57047701	ENSG00000267421.2
23	lnc-ZNF471-1	chr19:57050438-57050595	NONHSAT068172

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZFP28	hsa-miR-335-5p	chr19:57063009-57063035

Variant related genes	Relation type
ENSG00000267421	TF binding region
ENSG00000267224	TF binding region
ZFP28	TF binding region
ZNF471	TF binding region
ENSG00000267421	CpG island
ENSG00000267224	CpG island
ZFP28	CpG island
ZNF471	CpG island
IKBIP	miRNA target sites
TMEM194A	miRNA target sites
BRCA1	miRNA target sites

Extended variants
information (count: 1699 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1699 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12978999	chr19:57020754-57020755	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs57700534	chr19:57020767-57020768	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs397975575	chr19:57020768-57020769	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs185831262	chr19:57020786-57020787	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs570092985	chr19:57020825-57020826	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs529386511	chr19:57020830-57020831	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs549138705	chr19:57020831-57020832	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs566052090	chr19:57020855-57020856	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs148999155	chr19:57020856-57020857	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs554082840	chr19:57020872-57020873	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs143825873	chr19:57020874-57020875	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs368776206	chr19:57020922-57020923	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs75118800	chr19:57020948-57020949	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs148175716	chr19:57020983-57020984	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs377105573	chr19:57020992-57020993	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs111314766	chr19:57021026-57021027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs58900821	chr19:57021029-57021030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs58693902	chr19:57021030-57021031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191444720	chr19:57021041-57021042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61412846	chr19:57021058-57021059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs61284376	chr19:57021060-57021061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs61168642	chr19:57021064-57021065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs59283540	chr19:57021067-57021068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57276377	chr19:57021072-57021073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61139704	chr19:57021074-57021075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs61518352	chr19:57021076-57021077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555102959	chr19:57021079-57021080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61196872	chr19:57021080-57021081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs34707423	chr19:57021083-57021084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370557480	chr19:57021084-57021085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs71184367	chr19:57021103-57021104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571671562	chr19:57021189-57021190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146870510	chr19:57021192-57021193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182816263	chr19:57021199-57021200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533438794	chr19:57021314-57021315	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs188235079	chr19:57021364-57021365	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs563885786	chr19:57021503-57021504	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
38	rs58408676	chr19:57021695-57021696	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs560416288	chr19:57021700-57021701	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs549425641	chr19:57021742-57021743	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs559809614	chr19:57021795-57021796	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs139133788	chr19:57021805-57021806	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs547721480	chr19:57021806-57021807	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs532843149	chr19:57021832-57021833	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs192999385	chr19:57021911-57021912	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs79010642	chr19:57021912-57021913	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs76038009	chr19:57021921-57021922	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs569816674	chr19:57021933-57021934	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs12979404	chr19:57021936-57021937	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs552547529	chr19:57021953-57021954	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Alzheimer''s disease	22166940	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Glioblastoma multiforme	21922591	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
early-passage human iPS cells	21368824	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
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1442 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:57020200-57021000	Active TSS	HSMM	muscle
2	chr19:57020200-57021200	Enhancers	Lung	lung
3	chr19:57020200-57021200	Enhancers	Pancreas	Pancrea
4	chr19:57020200-57021800	Weak transcription	Aorta	Aorta
5	chr19:57020200-57024200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr19:57020200-57025400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr19:57020200-57025400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr19:57020200-57025600	Weak transcription	Left Ventricle	heart
9	chr19:57020200-57025800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr19:57020200-57027200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr19:57020200-57029800	Weak transcription	Gastric	stomach
12	chr19:57020400-57021000	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr19:57020400-57021400	Enhancers	Brain Germinal Matrix	brain
14	chr19:57020400-57021400	Weak transcription	Rectal Smooth Muscle	rectum
15	chr19:57020400-57021600	Weak transcription	Fetal Kidney	kidney
16	chr19:57020400-57021800	Weak transcription	Adipose Nuclei	Adipose
17	chr19:57020400-57021800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr19:57020400-57022200	Weak transcription	Psoas Muscle	Psoas
19	chr19:57020400-57022800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr19:57020400-57022800	Weak transcription	Brain Hippocampus Middle	brain
21	chr19:57020400-57022800	Weak transcription	Brain Substantia Nigra	brain
22	chr19:57020400-57022800	Weak transcription	Ovary	ovary
23	chr19:57020400-57022800	Weak transcription	NHDF-Ad	bronchial
24	chr19:57020400-57023000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr19:57020400-57024400	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr19:57020400-57024600	Weak transcription	Fetal Heart	heart
27	chr19:57020400-57024600	Weak transcription	HSMMtube	muscle
28	chr19:57020400-57025200	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr19:57020400-57025400	Weak transcription	Fetal Muscle Leg	muscle
30	chr19:57020400-57025600	Weak transcription	Brain Cingulate Gyrus	brain
31	chr19:57020400-57027600	Weak transcription	Osteobl	bone
32	chr19:57020400-57030400	Weak transcription	Right Ventricle	heart
33	chr19:57020600-57020800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr19:57020600-57020800	Active TSS	Stomach Smooth Muscle	stomach
35	chr19:57020600-57021200	Enhancers	Fetal Brain Female	brain
36	chr19:57020600-57021200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr19:57020600-57021400	Enhancers	Fetal Brain Male	brain
38	chr19:57020600-57021800	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr19:57020600-57022800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr19:57020600-57023800	Weak transcription	Placenta	Placenta
41	chr19:57020600-57024200	Weak transcription	Brain Angular Gyrus	brain
42	chr19:57020600-57025600	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr19:57020600-57025600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr19:57020600-57025600	Weak transcription	Brain Anterior Caudate	brain
45	chr19:57020600-57028800	Weak transcription	Fetal Stomach	stomach
46	chr19:57020800-57024400	Weak transcription	Stomach Smooth Muscle	stomach
47	chr19:57021000-57022800	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr19:57021000-57027400	Weak transcription	HSMM	muscle
49	chr19:57021200-57022400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
50	chr19:57021200-57026000	Weak transcription	Fetal Brain Female	brain

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