Variant report

Variant	nsv828552
Chromosome Location	chr19:42764336-42774166
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	ARID3A	chr19:42772016-42773501	K562	blood:	n/a	n/a
2	ARID3A	chr19:42772131-42772978	HepG2	liver:	n/a	n/a
3	ATF1	chr19:42771939-42773502	K562	blood:	n/a	n/a
4	ATF2	chr19:42771881-42773338	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr19:42772120-42773434	GM12878	blood:	n/a	n/a
6	ATF2	chr19:42771955-42773447	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr19:42772114-42773441	GM12878	blood:	n/a	n/a
8	ATF3	chr19:42772414-42773029	K562	blood:	n/a	chr19:42772602-42772615 chr19:42772828-42772836
9	ATF3	chr19:42771750-42773329	A549	lung:	n/a	chr19:42772602-42772615 chr19:42773235-42773244 chr19:42772828-42772836
10	ATF3	chr19:42771594-42773486	A549	lung:	n/a	chr19:42772602-42772615 chr19:42773461-42773470 chr19:42773235-42773244 chr19:42772828-42772836
11	ATF3	chr19:42772107-42772785	K562	blood:	n/a	chr19:42772602-42772615
12	BACH1	chr19:42772085-42772578	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr19:42772240-42772440	K562	blood:	n/a	n/a
14	BATF	chr19:42772347-42772644	GM12878	blood:	n/a	n/a
15	BCL11A	chr19:42772351-42772700	GM12878	blood:	n/a	n/a
16	BCL3	chr19:42771589-42773592	A549	lung:	n/a	chr19:42773504-42773513 chr19:42773235-42773248
17	BCL3	chr19:42771554-42773882	A549	lung:	n/a	chr19:42773504-42773513 chr19:42773235-42773248
18	BCLAF1	chr19:42772340-42773076	GM12878	blood:	n/a	n/a
19	BHLHE40	chr19:42772392-42773434	GM12878	blood:	n/a	chr19:42772619-42772635
20	BHLHE40	chr19:42771857-42773384	K562	blood:	n/a	chr19:42772619-42772635
21	BRCA1	chr19:42772319-42773452	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr19:42772472-42773396	GM12878	blood:	n/a	n/a
23	BRCA1	chr19:42772058-42772254	GM12878	blood:	n/a	n/a
24	BRCA1	chr19:42772469-42773401	HepG2	liver:	n/a	n/a
25	BRCA1	chr19:42772442-42772673	H1-hESC	embryonic stem cell:	n/a	n/a
26	CBX3	chr19:42772206-42773477	K562	blood:	n/a	n/a
27	CCNT2	chr19:42772180-42773522	K562	blood:	n/a	chr19:42772524-42772533 chr19:42773461-42773470 chr19:42772578-42772587 chr19:42773235-42773244
28	CEBPB	chr19:42771498-42772799	IMR90	lung:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
29	CEBPB	chr19:42769379-42769495	K562	blood:	n/a	chr19:42769418-42769429
30	CEBPB	chr19:42771396-42771756	K562	blood:	n/a	n/a
31	CEBPB	chr19:42769350-42769544	A549	lung:	n/a	chr19:42769418-42769429
32	CEBPB	chr19:42772097-42773410	Hela-S3	cervix:	n/a	chr19:42773027-42773035 chr19:42772634-42772642 chr19:42773367-42773375 chr19:42772483-42772491
33	CEBPB	chr19:42771417-42773461	A549	lung:	n/a	chr19:42773027-42773035 chr19:42772634-42772642 chr19:42773367-42773375 chr19:42772483-42772491
34	CEBPB	chr19:42772131-42772967	K562	blood:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
35	CEBPB	chr19:42769349-42769574	HepG2	liver:	n/a	chr19:42769418-42769429
36	CEBPB	chr19:42771385-42773002	K562	blood:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
37	CEBPB	chr19:42771394-42772789	HepG2	liver:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
38	CEBPB	chr19:42771492-42773567	A549	lung:	n/a	chr19:42773027-42773035 chr19:42772634-42772642 chr19:42773367-42773375 chr19:42772483-42772491
39	CEBPB	chr19:42772059-42772727	H1-hESC	embryonic stem cell:	n/a	chr19:42772634-42772642 chr19:42772483-42772491
40	CEBPD	chr19:42772183-42772539	HepG2	liver:	n/a	chr19:42772238-42772249
41	CEBPD	chr19:42773262-42773570	HepG2	liver:	n/a	n/a
42	CEBPZ	chr19:42772702-42773550	HepG2	liver:	n/a	n/a
43	CHD1	chr19:42773822-42774195	GM12878	blood:	n/a	n/a
44	CHD1	chr19:42772241-42772954	GM12878	blood:	n/a	n/a
45	CHD2	chr19:42772328-42773508	HepG2	liver:	n/a	chr19:42773462-42773472
46	CHD2	chr19:42772322-42773566	H1-hESC	embryonic stem cell:	n/a	chr19:42773462-42773472
47	CHD2	chr19:42772264-42773555	K562	blood:	n/a	chr19:42773462-42773472
48	CHD2	chr19:42772282-42773557	GM12878	blood:	n/a	chr19:42773462-42773472
49	CHD2	chr19:42772014-42773588	Hela-S3	cervix:	n/a	chr19:42773462-42773472
50	CREB1	chr19:42772084-42773587	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:42772446-42772496	HMEC	breast:	n/a
2	chr19:42772831-42772881	HRPEpiC	eye:	n/a
3	chr19:42772831-42772881	MCF10A-Er-Src	breast:	n/a
4	chr19:42772831-42772881	ProgFib	skin:	n/a
5	chr19:42772831-42772881	NB4	blood:	n/a
6	chr19:42772233-42772283	GM19239	blood:	n/a
7	chr19:42772233-42772283	SK-N-MC	brain:	n/a
8	chr19:42772831-42772881	SK-N-MC	brain:	n/a
9	chr19:42773364-42773414	AG04449	skin:	fetal
10	chr19:42772831-42772881	AG09309	skin:	n/a
11	chr19:42768724-42768774	NH-A	brain:	n/a
12	chr19:42772233-42772283	SK-N-SH_RA	brain:	n/a
13	chr19:42768724-42768774	HUVEC	blood vessel:	n/a
14	chr19:42772446-42772496	HIPEpiC	eye:	n/a
15	chr19:42772831-42772881	H1-hESC	embryonic stem cell:	embryo
16	chr19:42772892-42772942	BE2_C	brain:	n/a
17	chr19:42772233-42772283	Hepatocyte	liver:	n/a
18	chr19:42768724-42768774	HIPEpiC	eye:	n/a
19	chr19:42773364-42773414	HNPCEpiC	eye:	n/a
20	chr19:42772831-42772881	PrEC	prostate:	n/a
21	chr19:42772446-42772496	NT2-D1	testis:	n/a
22	chr19:42772233-42772283	AG04450	lung:	fetal
23	chr19:42772446-42772496	AG09319	gingival:	n/a
24	chr19:42772831-42772881	PANC-1	pancreas:	n/a
25	chr19:42772446-42772496	HCPEpiC	choroid plexus:	n/a
26	chr19:42772446-42772496	HRPEpiC	eye:	n/a
27	chr19:42773364-42773414	PrEC	prostate:	n/a
28	chr19:42768724-42768774	K562	blood:	n/a
29	chr19:42773364-42773414	SKMC	muscle:	n/a
30	chr19:42772892-42772942	HL-60	blood:	n/a
31	chr19:42772831-42772881	AG10803	skin:	n/a
32	chr19:42773364-42773414	NHDF-neo	bronchial:	n/a
33	chr19:42772446-42772496	GM19239	blood:	n/a
34	chr19:42772233-42772283	MCF10A-Er-Src	breast:	n/a
35	chr19:42773364-42773414	HCT-116	colon:	n/a
36	chr19:42773364-42773414	NB4	blood:	n/a
37	chr19:42772892-42772942	MCF10A-Er-Src	breast:	n/a
38	chr19:42773364-42773414	NHBE	bronchial:	n/a
39	chr19:42773364-42773414	RPTEC	kidney:	n/a
40	chr19:42772831-42772881	HepG2	liver:	n/a
41	chr19:42772831-42772881	SAEC	small airway:	n/a
42	chr19:42772233-42772283	AG09309	skin:	n/a
43	chr19:42772233-42772283	HL-60	blood:	n/a
44	chr19:42772892-42772942	HRCEpiC	kidney:	n/a
45	chr19:42773364-42773414	BE2_C	brain:	n/a
46	chr19:42772831-42772881	HPAEpiC	pulmonary alveolar:	n/a
47	chr19:42772831-42772881	Hepatocyte	liver:	n/a
48	chr19:42768724-42768774	HCF	heart:	n/a
49	chr19:42772892-42772942	HAEpiC	amniotic membrane:	n/a
50	chr19:42773364-42773414	K562	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:120729494..120731830-chr19:42774117..42775700,2	MCF-7	breast:
2	chr19:42756055..42758912-chr19:42766022..42767833,2	MCF-7	breast:
3	chr19:42764600..42766454-chr19:42770815..42772327,3	MCF-7	breast:
4	chr19:42764600..42766454-chr19:42770815..42772327,3	MCF-7	breast:
5	chr19:42720638..42724432-chr19:42771891..42775014,4	MCF-7	breast:
6	chr19:42771398..42774307-chr19:42804493..42807877,4	MCF-7	breast:
7	chr19:42763066..42765543-chr19:42786449..42790006,3	MCF-7	breast:
8	chr19:42773801..42775756-chr19:42804416..42807088,2	K562	blood:
9	chr19:42768481..42770570-chr19:42770967..42773649,2	K562	blood:
10	chr19:42774007..42775893-chr19:42829806..42832465,2	K562	blood:
11	chr19:42763894..42766848-chr19:42772974..42774684,3	MCF-7	breast:
12	chr19:42771105..42773106-chr19:42805155..42808634,5	K562	blood:
13	chr19:42747132..42763787-chr19:42768368..42776785,67	MCF-7	breast:

Variant related genes	Relation type
CIC	TF binding region
CIC	CpG island
ENSG00000200795	chromatin interactions
ENSG00000160570	chromatin interactions
ENSG00000105722	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000079432	chromatin interactions
ENSG00000268643	chromatin interactions
ENSG00000105429	chromatin interactions
ENSG00000167625	chromatin interactions
ENSG00000188368	chromatin interactions
ENSG00000079462	chromatin interactions

Extended variants
information (count: 373 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:373 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187383994	chr19:42764343-42764344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs57938324	chr19:42764352-42764353	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs552902938	chr19:42764353-42764354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs192084238	chr19:42764368-42764369	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs143034115	chr19:42764373-42764374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557085299	chr19:42764426-42764427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575346214	chr19:42764448-42764449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116228424	chr19:42764491-42764492	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs148201909	chr19:42764500-42764501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577477362	chr19:42764522-42764523	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574309965	chr19:42764537-42764538	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs184136771	chr19:42764542-42764543	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs543187337	chr19:42764546-42764547	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189514594	chr19:42764567-42764568	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141150402	chr19:42764576-42764577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs547783202	chr19:42764578-42764579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145186000	chr19:42764639-42764640	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs552306370	chr19:42764645-42764646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs377388374	chr19:42764677-42764678	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs570787441	chr19:42764687-42764688	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs534618053	chr19:42764749-42764750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs546913743	chr19:42764757-42764758	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs568304365	chr19:42764766-42764767	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs192854850	chr19:42764767-42764768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557122165	chr19:42764810-42764811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184407733	chr19:42764861-42764862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs539479793	chr19:42764886-42764887	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557470266	chr19:42764898-42764899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs189294000	chr19:42764944-42764945	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541399374	chr19:42764946-42764947	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559600874	chr19:42764950-42764951	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574717589	chr19:42764959-42764960	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373470415	chr19:42765014-42765015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs563508699	chr19:42765015-42765016	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181931951	chr19:42765016-42765017	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563049347	chr19:42765055-42765056	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533837142	chr19:42765091-42765092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186420279	chr19:42765104-42765105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs564373032	chr19:42765120-42765121	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs528478606	chr19:42765212-42765213	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs77251240	chr19:42765215-42765216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs189220104	chr19:42765256-42765257	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs138995184	chr19:42765260-42765261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181541508	chr19:42765267-42765268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185802485	chr19:42765273-42765274	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs568986713	chr19:42765289-42765290	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529577636	chr19:42765384-42765385	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539203703	chr19:42765388-42765389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376590359	chr19:42765390-42765391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs557823575	chr19:42765458-42765459	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	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
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:481 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:42760400-42771800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr19:42761200-42766000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr19:42761400-42766200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr19:42761400-42771800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr19:42761800-42771800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr19:42762600-42764600	Enhancers	Fetal Intestine Small	intestine
7	chr19:42762800-42771800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr19:42763400-42771600	Weak transcription	K562	blood
9	chr19:42763400-42771800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr19:42763800-42766000	Weak transcription	A549	lung
11	chr19:42764000-42764600	Enhancers	Duodenum Mucosa	Duodenum
12	chr19:42764600-42771800	Weak transcription	Duodenum Mucosa	Duodenum
13	chr19:42766000-42766400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr19:42766000-42767000	Enhancers	A549	lung
15	chr19:42766200-42766800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr19:42766400-42771800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr19:42766800-42771800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr19:42767000-42769800	Weak transcription	A549	lung
19	chr19:42767800-42771600	Weak transcription	Brain Angular Gyrus	brain
20	chr19:42769800-42770000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr19:42769800-42770200	Enhancers	A549	lung
22	chr19:42770000-42770200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr19:42770000-42770200	Enhancers	Brain Substantia Nigra	brain
24	chr19:42770000-42771600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr19:42770200-42770400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr19:42770200-42770400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr19:42770200-42771400	Weak transcription	A549	lung
28	chr19:42770200-42771800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr19:42770200-42771800	Weak transcription	Brain Substantia Nigra	brain
30	chr19:42770400-42771600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr19:42770400-42771800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr19:42771400-42771600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr19:42771400-42771600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr19:42771400-42771600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr19:42771400-42771600	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr19:42771400-42771600	Weak transcription	Fetal Muscle Trunk	muscle
37	chr19:42771400-42771600	Enhancers	Dnd41	blood
38	chr19:42771400-42771800	Enhancers	Fetal Muscle Leg	muscle
39	chr19:42771400-42771800	Enhancers	A549	lung
40	chr19:42771600-42771800	Enhancers	H9 Cell Line	embryonic stem cell
41	chr19:42771600-42771800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr19:42771600-42771800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr19:42771600-42771800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr19:42771600-42771800	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr19:42771600-42771800	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr19:42771600-42771800	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr19:42771600-42771800	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr19:42771600-42771800	Enhancers	Primary B cells from cord blood	blood
49	chr19:42771600-42771800	Enhancers	Primary T cells from cord blood	blood
50	chr19:42771600-42771800	Enhancers	Primary hematopoietic stem cells	blood

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