Variant report

Variant	nsv961236
Chromosome Location	chr19:51429291-51435801
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	chr19:51433219-51433222	K562	blood:	n/a	n/a
2	ATF3	chr19:51433038-51433476	A549	lung:	n/a	n/a
3	BHLHE40	chr19:51433238-51433430	GM12878	blood:	n/a	n/a
4	BHLHE40	chr19:51433159-51433515	K562	blood:	n/a	n/a
5	CBX3	chr19:51435030-51436414	HCT-116	colon:	n/a	n/a
6	CEBPB	chr19:51429134-51429315	H1-hESC	embryonic stem cell:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
7	CEBPB	chr19:51429046-51429372	HepG2	liver:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
8	CEBPB	chr19:51429034-51429358	K562	blood:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
9	CEBPB	chr19:51433177-51433511	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr19:51429007-51429367	IMR90	lung:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
11	CEBPB	chr19:51429009-51429437	A549	lung:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
12	CEBPB	chr19:51433162-51433463	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr19:51435192-51435718	MCF-7	breast:	n/a	n/a
14	CEBPB	chr19:51428944-51429413	A549	lung:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
15	CEBPB	chr19:51429017-51429377	Hela-S3	cervix:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
16	CEBPB	chr19:51429001-51429337	A549	lung:	n/a	chr19:51429191-51429200 chr19:51429191-51429200 chr19:51429191-51429200
17	CREB1	chr19:51433043-51433512	A549	lung:	n/a	n/a
18	CTCF	chr19:51433200-51433350	RPTEC	kidney:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
19	CTCF	chr19:51432220-51432370	A549	lung:	n/a	n/a
20	CTCF	chr19:51432760-51432910	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr19:51433200-51433350	MCF-7	breast:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
22	CTCF	chr19:51433180-51433330	NHDF-neo	bronchial:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
23	CTCF	chr19:51433120-51433270	HAc	cerebellar:	n/a	n/a
24	CTCF	chr19:51433760-51433910	GM12864	blood:	n/a	n/a
25	CTCF	chr19:51433200-51433350	HEK293	kidney:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
26	CTCF	chr19:51433073-51433474	GM12878	blood:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
27	CTCF	chr19:51433160-51433392	HepG2	liver:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
28	CTCF	chr19:51433073-51433473	IMR90	lung:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
29	CTCF	chr19:51433220-51433370	K562	blood:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
30	CTCF	chr19:51433200-51433350	Hela-S3	cervix:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
31	CTCF	chr19:51433180-51433330	HL-60	blood:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
32	CTCF	chr19:51433017-51433986	A549	lung:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
33	CTCF	chr19:51432268-51432323	K562	blood:	n/a	n/a
34	CTCF	chr19:51432948-51432972	GM13976	blood:	n/a	n/a
35	CTCF	chr19:51433160-51433310	WERI-Rb-1	eye:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
36	CTCF	chr19:51432820-51432970	GM12873	blood:	n/a	n/a
37	CTCF	chr19:51433180-51433330	HMEC	breast:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
38	CTCF	chr19:51433149-51433425	ProgFib	skin:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
39	CTCF	chr19:51432200-51432350	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr19:51433200-51433350	SK-N-SH_RA	brain:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
41	CTCF	chr19:51433100-51433408	GM13977	blood:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
42	CTCF	chr19:51433158-51433481	MCF-7	breast:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
43	CTCF	chr19:51433200-51433350	GM12864	blood:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
44	CTCF	chr19:51433200-51433350	HCPEpiC	choroid plexus:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
45	CTCF	chr19:51433220-51433370	Hela-S3	cervix:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
46	CTCF	chr19:51433125-51433440	GM12892	blood:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
47	CTCF	chr19:51433121-51433401	Spleen_OC	spleen:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
48	CTCF	chr19:51433200-51433350	HCM	heart:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
49	CTCF	chr19:51433200-51433350	NHLF	lung:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280
50	CTCF	chr19:51433059-51433466	H1-hESC	embryonic stem cell:	n/a	chr19:51433263-51433279 chr19:51433265-51433278 chr19:51433264-51433285 chr19:51433262-51433280

No.	Distal block	Cell Line	Cell type
1	chr19:51434633..51437276-chr19:51470056..51473720,4	MCF-7	breast:
2	chr19:51305575..51307779-chr19:51427120..51430041,2	MCF-7	breast:
3	chr19:51432897..51433716-chr19:51502734..51503640,2	MCF-7	breast:
4	chr19:51409507..51410240-chr19:51435323..51436234,2	MCF-7	breast:
5	chr19:51306468..51309134-chr19:51431722..51433817,2	K562	blood:
6	chr19:51432828..51433754-chr19:51597689..51598455,7	K562	blood:
7	chr19:51432779..51433771-chr19:51519612..51520697,15	MCF-7	breast:
8	chr19:51432762..51433289-chr19:51599890..51600413,2	MCF-7	breast:
9	chr19:51435279..51436842-chr19:51510358..51513256,2	MCF-7	breast:
10	chr19:51427739..51428732-chr19:51435714..51436347,2	K562	blood:
11	chr19:51432884..51433525-chr19:51597706..51598661,3	MCF-7	breast:
12	chr19:51432788..51433791-chr19:51519737..51520704,6	MCF-7	breast:
13	chr19:51297794..51299902-chr19:51431890..51433458,2	K562	blood:
14	chr19:51426938..51429460-chr19:51429562..51431965,2	K562	blood:
15	chr19:51432732..51437222-chr19:51477627..51480793,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000228674	TF binding region
ENSG00000228674	chromatin interactions
ENSG00000220988	chromatin interactions
ENSG00000129451	chromatin interactions
ENSG00000167749	chromatin interactions
ENSG00000267879	chromatin interactions
ENSG00000213022	chromatin interactions
ENSG00000167755	chromatin interactions
ENSG00000167747	chromatin interactions

Extended variants
information (count: 358 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:358 , 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	rs16988213	chr19:51429298-51429299	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs28600032	chr19:51429306-51429307	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs79735327	chr19:51429332-51429333	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs16988215	chr19:51429333-51429334	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs368288880	chr19:51429353-51429354	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs555964427	chr19:51429363-51429364	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs193279648	chr19:51429419-51429420	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs17800825	chr19:51429512-51429513	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs553524339	chr19:51429521-51429522	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs7256917	chr19:51429535-51429536	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs564203541	chr19:51429560-51429561	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs576332851	chr19:51429581-51429582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs144049209	chr19:51429587-51429588	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs201212666	chr19:51429588-51429589	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs8111289	chr19:51429589-51429590	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs529058614	chr19:51429595-51429596	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs8110335	chr19:51429596-51429597	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs559040003	chr19:51429603-51429604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs146445039	chr19:51429605-51429606	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs376516562	chr19:51429606-51429607	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144627964	chr19:51429608-51429609	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs185099965	chr19:51429612-51429613	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs549412787	chr19:51429614-51429615	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs189241196	chr19:51429667-51429668	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535246653	chr19:51429696-51429697	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs553487533	chr19:51429702-51429703	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs181276920	chr19:51429703-51429704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs148193534	chr19:51429733-51429734	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs564531463	chr19:51429745-51429746	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs140396525	chr19:51429757-51429758	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs8111539	chr19:51429766-51429767	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs543655141	chr19:51429791-51429792	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs150365671	chr19:51429802-51429803	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs377189963	chr19:51429803-51429804	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs183992561	chr19:51429815-51429816	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs188723421	chr19:51429820-51429821	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs180741324	chr19:51429822-51429823	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs113281337	chr19:51429823-51429824	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs12609875	chr19:51429827-51429828	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs8113547	chr19:51429883-51429884	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs145923350	chr19:51429895-51429896	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs62115178	chr19:51429906-51429907	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530442728	chr19:51429916-51429917	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs549617519	chr19:51429949-51429950	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34461427	chr19:51429953-51429954	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs8100471	chr19:51429959-51429960	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs528673597	chr19:51429988-51429989	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs139175576	chr19:51430006-51430007	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571759562	chr19:51430007-51430008	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs539083317	chr19:51430043-51430044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Adrenocortical carcinoma	18281524	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

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:51426000-51432200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:51427600-51429800	Enhancers	HMEC	breast
3	chr19:51427800-51429800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr19:51427800-51429800	Enhancers	NHEK	skin
5	chr19:51429200-51429400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr19:51429200-51429800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr19:51429200-51429800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr19:51429800-51432000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr19:51429800-51433200	Weak transcription	HMEC	breast
10	chr19:51429800-51433200	Weak transcription	NHEK	skin
11	chr19:51429800-51433400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr19:51429800-51433400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr19:51430400-51435200	Weak transcription	Hela-S3	cervix
14	chr19:51432000-51432200	Enhancers	H9 Cell Line	embryonic stem cell
15	chr19:51432000-51432200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr19:51432000-51432200	Enhancers	Esophagus	oesophagus
17	chr19:51432200-51432400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr19:51432200-51432800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr19:51432400-51433400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr19:51432800-51433600	Enhancers	Brain Hippocampus Middle	brain
21	chr19:51432800-51435400	Weak transcription	Esophagus	oesophagus
22	chr19:51432800-51437400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr19:51433200-51433400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr19:51433200-51433400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
25	chr19:51433200-51433600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
26	chr19:51433200-51433600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
27	chr19:51433200-51433600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr19:51433200-51433600	Enhancers	A549	lung
29	chr19:51433200-51433800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
30	chr19:51433200-51434000	Enhancers	NHEK	skin
31	chr19:51433200-51437600	Enhancers	HMEC	breast
32	chr19:51433400-51433600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr19:51433400-51433600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
34	chr19:51433400-51433600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
35	chr19:51433400-51433800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
36	chr19:51433400-51433800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr19:51433400-51433800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr19:51433400-51434000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr19:51433400-51434000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr19:51433400-51435000	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr19:51433600-51435200	Weak transcription	A549	lung
42	chr19:51433800-51434200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr19:51434000-51434400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:51434000-51434400	Weak transcription	NHEK	skin
45	chr19:51434000-51453200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr19:51434200-51434600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr19:51434400-51435400	Enhancers	NHEK	skin
48	chr19:51434400-51435600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr19:51434600-51435600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr19:51435000-51436000	Weak transcription	Breast Myoepithelial Primary Cells	Breast

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