Variant report

Variant	nsv1063042
Chromosome Location	chr19:43139043-43175294
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	chr19:43139260-43139326	K562	blood:	n/a	n/a
2	BHLHE40	chr19:43138971-43139294	HepG2	liver:	n/a	n/a
3	BHLHE40	chr19:43139176-43139401	K562	blood:	n/a	n/a
4	BRCA1	chr19:43168346-43168356	GM12878	blood:	n/a	n/a
5	CBX3	chr19:43156238-43156476	K562	blood:	n/a	n/a
6	CEBPB	chr19:43150294-43150473	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr19:43156216-43156522	HepG2	liver:	n/a	chr19:43156349-43156360
8	CEBPB	chr19:43156174-43156554	A549	lung:	n/a	chr19:43156349-43156360
9	CEBPB	chr19:43139178-43139417	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr19:43139258-43139346	K562	blood:	n/a	n/a
11	CEBPB	chr19:43152306-43152361	IMR90	lung:	n/a	n/a
12	CHD2	chr19:43139100-43139262	K562	blood:	n/a	n/a
13	CTCF	chr19:43139180-43139330	WERI-Rb-1	eye:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
14	CTCF	chr19:43139124-43139402	MCF-7	breast:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
15	CTCF	chr19:43139180-43139330	HEEpiC	esophagus:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
16	CTCF	chr19:43139160-43139310	GM12869	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
17	CTCF	chr19:43139050-43139563	MCF-7	breast:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
18	CTCF	chr19:43139498-43139611	GM19238	blood:	n/a	n/a
19	CTCF	chr19:43139200-43139350	HFF-Myc	foreskin:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
20	CTCF	chr19:43174820-43174970	K562	blood:	n/a	n/a
21	CTCF	chr19:43174812-43174911	HepG2	liver:	n/a	n/a
22	CTCF	chr19:43139140-43139290	HCM	heart:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
23	CTCF	chr19:43139440-43139590	GM12866	blood:	n/a	n/a
24	CTCF	chr19:43139180-43139330	SK-N-SH_RA	brain:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
25	CTCF	chr19:43139580-43139730	GM12871	blood:	n/a	n/a
26	CTCF	chr19:43166900-43167050	A549	lung:	n/a	n/a
27	CTCF	chr19:43139200-43139350	HL-60	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
28	CTCF	chr19:43139180-43139330	GM12872	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
29	CTCF	chr19:43139200-43139350	GM12866	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
30	CTCF	chr19:43139200-43139350	MCF-7	breast:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
31	CTCF	chr19:43174780-43174930	HEK293	kidney:	n/a	n/a
32	CTCF	chr19:43139180-43139330	AG10803	skin:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
33	CTCF	chr19:43167043-43167084	A549	lung:	n/a	n/a
34	CTCF	chr19:43160200-43160350	NHEK	skin:	n/a	n/a
35	CTCF	chr19:43139180-43139330	HBMEC	blood vessel:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
36	CTCF	chr19:43139200-43139350	GM12867	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
37	CTCF	chr19:43139128-43139410	A549	lung:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
38	CTCF	chr19:43139525-43139584	GM12892	blood:	n/a	n/a
39	CTCF	chr19:43139140-43139290	HRE	kidney:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
40	CTCF	chr19:43139080-43139230	WI-38	lung:	n/a	n/a
41	CTCF	chr19:43139154-43139438	Lung_OC	lung:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
42	CTCF	chr19:43139114-43139409	NHEK	skin:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
43	CTCF	chr19:43167020-43167170	MCF-7	breast:	n/a	n/a
44	CTCF	chr19:43139200-43139350	WERI-Rb-1	eye:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
45	CTCF	chr19:43139057-43139454	K562	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
46	CTCF	chr19:43139220-43139370	HRE	kidney:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
47	CTCF	chr19:43139220-43139370	HVMF	connective:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
48	CTCF	chr19:43167040-43167190	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr19:43139200-43139350	GM12871	blood:	n/a	chr19:43139262-43139270 chr19:43139259-43139280 chr19:43139260-43139273 chr19:43139258-43139274 chr19:43139257-43139275
50	CTCF	chr19:43139488-43139630	GM19240	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
2	chr19:43110921..43111495-chr19:43166501..43167328,2	MCF-7	breast:
3	chr19:43139185..43139985-chr19:43166999..43167914,2	MCF-7	breast:
4	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
5	chr19:43167897..43169449-chr19:43169988..43172834,2	MCF-7	breast:
6	chr19:43139154..43139986-chr19:43246322..43246897,2	MCF-7	breast:
7	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
8	chr19:43149390..43151656-chr19:43158079..43159963,2	MCF-7	breast:
9	chr19:43138891..43139734-chr19:43166436..43166942,2	MCF-7	breast:
10	chr19:43148558..43149434-chr20:53015100..53015659,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011497.1-2	chr19:43155869-43156816	NONHSAT066564
2	lnc-AC011497.1-2	chr19:43155239-43156507	ENSG00000213904.4
3	lnc-AC011497.1-2	chr19:43155239-43156171	ENSG00000213904.4
4	lnc-AC011497.1-2	chr19:43155388-43155602	NONHSAT066564
5	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066548
6	lnc-AC011497.1-2	chr19:43155239-43156507	NONHSAT066551

Variant related genes	Relation type
CEACAMP1	TF binding region
RPS10P28	TF binding region
CEACAMP5	TF binding region
ENSG00000231561	chromatin interactions

Extended variants
information (count: 864 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:864 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190081311	chr19:43139065-43139066	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs555827372	chr19:43139078-43139079	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs182354542	chr19:43139109-43139110	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs574481182	chr19:43139172-43139173	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs543444824	chr19:43139189-43139190	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs563331425	chr19:43139228-43139229	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs377593312	chr19:43139255-43139256	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs141095789	chr19:43139260-43139261	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs545991143	chr19:43139280-43139281	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs10402401	chr19:43139284-43139285	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs370751840	chr19:43139320-43139321	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs548453034	chr19:43139350-43139351	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs11669892	chr19:43139352-43139353	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs530776563	chr19:43139354-43139355	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs117317718	chr19:43139357-43139358	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs570584826	chr19:43139451-43139452	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs533232825	chr19:43139511-43139512	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs10404509	chr19:43139521-43139522	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs185870089	chr19:43139534-43139535	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs192446357	chr19:43139545-43139546	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs118061874	chr19:43139569-43139570	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs183951013	chr19:43139587-43139588	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188863709	chr19:43139589-43139590	Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs537008965	chr19:43139668-43139669	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs78667178	chr19:43139697-43139698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs150255517	chr19:43139698-43139699	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs545865619	chr19:43139700-43139701	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs552829630	chr19:43139751-43139752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs572989176	chr19:43139768-43139769	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs370091549	chr19:43139770-43139771	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs541671122	chr19:43139861-43139862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs561617549	chr19:43139891-43139892	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs545947048	chr19:43139915-43139916	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs544129554	chr19:43139937-43139938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs138868172	chr19:43139957-43139958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs192188598	chr19:43139968-43139969	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs138111763	chr19:43149434-43149435	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs386809437	chr19:43149435-43149436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78857130	chr19:43149436-43149437	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545088133	chr19:43149437-43149438	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375538841	chr19:43149462-43149463	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs372189545	chr19:43149494-43149495	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575299822	chr19:43149593-43149594	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs370622175	chr19:43149604-43149605	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs116359333	chr19:43149613-43149614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs551222560	chr19:43149616-43149617	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565080588	chr19:43149621-43149622	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527528823	chr19:43149726-43149727	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs542690231	chr19:43149761-43149762	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs143719983	chr19:43149775-43149776	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
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
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43139000-43139600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr19:43139400-43139600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr19:43150400-43150600	ZNF genes & repeats	Brain Hippocampus Middle	brain
4	chr19:43150600-43159800	Weak transcription	Brain Hippocampus Middle	brain
5	chr19:43153200-43158000	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr19:43154000-43154200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr19:43154400-43156000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr19:43154800-43159800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr19:43155200-43155400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr19:43155400-43156000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr19:43155400-43157600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr19:43155800-43157800	Weak transcription	Adipose Nuclei	Adipose
13	chr19:43156000-43156600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr19:43156000-43156600	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr19:43156000-43162000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr19:43156400-43156800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr19:43156600-43159800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr19:43156800-43157800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr19:43157200-43158000	Enhancers	Esophagus	oesophagus
20	chr19:43157400-43157800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:43157400-43158600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr19:43157600-43160000	Weak transcription	Brain Angular Gyrus	brain
23	chr19:43157600-43160200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr19:43157800-43158000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr19:43157800-43158000	Enhancers	Pancreas	Pancrea
26	chr19:43157800-43158600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr19:43157800-43163000	Enhancers	Adipose Nuclei	Adipose
28	chr19:43158000-43158600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr19:43158200-43159800	Weak transcription	Pancreas	Pancrea
30	chr19:43158600-43162400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr19:43159200-43163000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr19:43159400-43162000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr19:43159600-43159800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr19:43159800-43160000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
35	chr19:43159800-43160600	Enhancers	Pancreas	Pancrea
36	chr19:43159800-43161800	Enhancers	Brain Inferior Temporal Lobe	brain
37	chr19:43159800-43161800	Enhancers	Brain Substantia Nigra	brain
38	chr19:43159800-43162000	Enhancers	Brain Hippocampus Middle	brain
39	chr19:43160000-43160400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:43160000-43160600	Enhancers	Gastric	stomach
41	chr19:43160000-43161400	Enhancers	Brain Anterior Caudate	brain
42	chr19:43160000-43161600	Enhancers	Brain Cingulate Gyrus	brain
43	chr19:43160000-43162000	Enhancers	Brain Angular Gyrus	brain
44	chr19:43160200-43161800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr19:43160200-43174800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr19:43160400-43161200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr19:43160800-43161000	Enhancers	Left Ventricle	heart
48	chr19:43161000-43161400	Enhancers	Colon Smooth Muscle	Colon
49	chr19:43161400-43161800	Weak transcription	Colon Smooth Muscle	Colon
50	chr19:43161400-43163000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links