Variant report

Variant	esv3378202
Chromosome Location	chr19:39409312-39413510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:96)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:96 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr19:39409840-39410477	A549	lung:	n/a	n/a
2	BCL3	chr19:39411538-39411870	GM12878	blood:	n/a	n/a
3	CHD2	chr19:39413212-39413471	K562	blood:	n/a	n/a
4	CTCF	chr19:39408445-39409548	A549	lung:	n/a	chr19:39408855-39408864
5	NR2F2	chr19:39408514-39409348	MCF-7	breast:	n/a	n/a
6	POLR2A	chr19:39411434-39411736	GM12891	blood:	n/a	n/a
7	POLR2A	chr19:39412800-39413078	HepG2	liver:	n/a	n/a
8	POLR2A	chr19:39408887-39409467	A549	lung:	n/a	n/a
9	POLR2A	chr19:39410022-39410161	HepG2	liver:	n/a	n/a
10	POLR2A	chr19:39411948-39412210	A549	lung:	n/a	n/a
11	POLR2A	chr19:39408945-39409414	K562	blood:	n/a	n/a
12	POLR2A	chr19:39409896-39410560	K562	blood:	n/a	n/a
13	POLR2A	chr19:39413056-39413152	GM12878	blood:	n/a	n/a
14	POLR2A	chr19:39411383-39411857	GM12891	blood:	n/a	n/a
15	POLR2A	chr19:39409885-39410854	K562	blood:	n/a	n/a
16	POLR2A	chr19:39411491-39411915	GM12891	blood:	n/a	n/a
17	POLR2A	chr19:39407758-39409703	K562	blood:	n/a	n/a
18	POLR2A	chr19:39409939-39410148	H1-hESC	embryonic stem cell:	n/a	n/a
19	POLR2A	chr19:39411580-39411837	H1-hESC	embryonic stem cell:	n/a	n/a
20	POLR2A	chr19:39411971-39412513	H1-hESC	embryonic stem cell:	n/a	n/a
21	POLR2A	chr19:39411533-39411866	H1-hESC	embryonic stem cell:	n/a	n/a
22	POLR2A	chr19:39410066-39410195	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr19:39408099-39409398	HepG2	liver:	n/a	n/a
24	POLR2A	chr19:39411195-39412000	SK-N-MC	brain:	n/a	n/a
25	POLR2A	chr19:39409472-39409564	K562	blood:	n/a	n/a
26	POLR2A	chr19:39411606-39411901	K562	blood:	n/a	n/a
27	POLR2A	chr19:39399024-39410741	PANC-1	pancreas:	n/a	n/a
28	POLR2A	chr19:39410749-39413573	PANC-1	pancreas:	n/a	n/a
29	POLR2A	chr19:39411024-39412667	GM12892	blood:	n/a	n/a
30	POLR2A	chr19:39411429-39412584	GM12878	blood:	n/a	n/a
31	POLR2A	chr19:39412418-39412575	K562	blood:	n/a	n/a
32	POLR2A	chr19:39411976-39412371	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr19:39410376-39410549	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr19:39409403-39409475	HepG2	liver:	n/a	n/a
35	POLR2A	chr19:39408330-39409602	A549	lung:	n/a	n/a
36	POLR2A	chr19:39409584-39410335	K562	blood:	n/a	n/a
37	POLR2A	chr19:39411431-39411889	GM12891	blood:	n/a	n/a
38	POLR2A	chr19:39411279-39412214	GM12892	blood:	n/a	n/a
39	POLR2A	chr19:39412436-39412457	HepG2	liver:	n/a	n/a
40	POLR2A	chr19:39412006-39412360	HL-60	blood:	n/a	n/a
41	POLR2A	chr19:39409736-39410007	HepG2	liver:	n/a	n/a
42	POLR2A	chr19:39411501-39411872	A549	lung:	n/a	n/a
43	POLR2A	chr19:39412089-39412359	A549	lung:	n/a	n/a
44	POLR2A	chr19:39411331-39412950	HepG2	liver:	n/a	n/a
45	POLR2A	chr19:39410161-39410487	H1-hESC	embryonic stem cell:	n/a	n/a
46	POLR2A	chr19:39407747-39409674	SK-N-MC	brain:	n/a	n/a
47	POLR2A	chr19:39411650-39412599	K562	blood:	n/a	n/a
48	POLR2A	chr19:39411587-39412636	K562	blood:	n/a	n/a
49	POLR2A	chr19:39411980-39412597	GM12891	blood:	n/a	n/a
50	POLR2A	chr19:39410436-39410443	HepG2	liver:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:39411214..39414705-chr19:39419221..39421908,4	MCF-7	breast:
2	chr19:39338289..39340175-chr19:39412991..39414800,2	K562	blood:
3	chr19:39411897..39413585-chr19:39419804..39422534,2	K562	blood:
4	chr19:39390485..39392144-chr19:39409724..39411734,2	MCF-7	breast:
5	chr19:39339873..39342860-chr19:39409643..39412054,2	MCF-7	breast:
6	chr19:39337019..39338579-chr19:39410355..39412359,2	MCF-7	breast:
7	chr19:39341116..39343070-chr19:39413366..39415101,2	K562	blood:
8	chr19:39340110..39342981-chr19:39406423..39409674,4	MCF-7	breast:
9	chr19:39388836..39392687-chr19:39409083..39412619,5	K562	blood:
10	chr19:39332878..39335584-chr19:39408217..39410062,2	MCF-7	breast:
11	chr19:39413074..39415034-chr19:39423613..39425226,2	K562	blood:
12	chr19:39334351..39336976-chr19:39412590..39415295,2	K562	blood:

No data

Variant related genes	Relation type
SARS2	TF binding region
ENSG00000269688	chromatin interactions
ENSG00000104835	chromatin interactions
ENSG00000128626	chromatin interactions
ENSG00000104825	chromatin interactions
ENSG00000068903	chromatin interactions
ENSG00000104824	chromatin interactions

Extended variants
information (count: 273 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:273 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531650280	chr19:39409321-39409322	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs543051739	chr19:39409323-39409324	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs561305139	chr19:39409344-39409345	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs370243513	chr19:39409355-39409356	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs374199515	chr19:39409358-39409359	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs115226793	chr19:39409379-39409380	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs375828739	chr19:39409392-39409393	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs368271481	chr19:39409415-39409416	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs372151812	chr19:39409418-39409419	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs563299553	chr19:39409436-39409437	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs147888941	chr19:39409437-39409438	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs375205027	chr19:39409441-39409442	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs533170211	chr19:39409458-39409459	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs551261504	chr19:39409466-39409467	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs367898096	chr19:39409493-39409494	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs184423391	chr19:39409501-39409502	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs533604342	chr19:39409553-39409554	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs370206445	chr19:39409569-39409570	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs561716693	chr19:39409598-39409599	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs529568983	chr19:39409623-39409624	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs547667382	chr19:39409624-39409625	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs12459197	chr19:39409637-39409638	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs566970425	chr19:39409654-39409655	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs537422575	chr19:39409669-39409670	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs73541506	chr19:39409720-39409721	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs578166641	chr19:39409759-39409760	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs11878472	chr19:39409765-39409766	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs75311574	chr19:39409767-39409768	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs539224908	chr19:39409795-39409796	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs143120174	chr19:39409805-39409806	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs371178115	chr19:39409822-39409823	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs190530313	chr19:39409826-39409827	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs572665342	chr19:39409861-39409862	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs539641811	chr19:39409897-39409898	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs192459601	chr19:39409902-39409903	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs561343966	chr19:39409904-39409905	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs138980291	chr19:39409922-39409923	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs79410427	chr19:39409945-39409946	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs531574026	chr19:39409953-39409954	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs562826044	chr19:39409993-39409994	Weak transcription Strong transcription Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs533034043	chr19:39410018-39410019	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs551564250	chr19:39410064-39410065	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs559957628	chr19:39410086-39410087	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs527480372	chr19:39410098-39410099	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs548697923	chr19:39410110-39410111	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs2099339	chr19:39410119-39410120	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs142883837	chr19:39410204-39410205	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs367652677	chr19:39410206-39410207	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs117248168	chr19:39410221-39410222	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs539002283	chr19:39410283-39410284	Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Pleomorphic liposarcoma	18784837	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
Disorders of sex development	21048976	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
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:324 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39391200-39420800	Weak transcription	Small Intestine	intestine
2	chr19:39391600-39414800	Weak transcription	HMEC	breast
3	chr19:39391600-39420600	Weak transcription	Right Atrium	heart
4	chr19:39391800-39412200	Weak transcription	Osteobl	bone
5	chr19:39392400-39414800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:39392600-39414600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr19:39392600-39418800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr19:39395600-39414800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr19:39395600-39415000	Weak transcription	Hela-S3	cervix
10	chr19:39396800-39412000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr19:39397000-39412200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr19:39398000-39412400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr19:39398000-39420600	Weak transcription	Psoas Muscle	Psoas
14	chr19:39398200-39412200	Weak transcription	Brain Angular Gyrus	brain
15	chr19:39398400-39411600	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr19:39398600-39410200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr19:39398600-39415000	Weak transcription	Brain Substantia Nigra	brain
18	chr19:39398800-39410000	Weak transcription	HSMMtube	muscle
19	chr19:39398800-39411600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:39398800-39412000	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr19:39398800-39412200	Weak transcription	NHEK	skin
22	chr19:39398800-39412400	Weak transcription	Rectal Mucosa Donor 31	rectum
23	chr19:39398800-39415000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr19:39399000-39412400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr19:39399800-39412200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr19:39399800-39412200	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr19:39399800-39414800	Weak transcription	Primary B cells from peripheral blood	blood
28	chr19:39399800-39414800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr19:39400000-39410000	Weak transcription	K562	blood
30	chr19:39400000-39412000	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr19:39400000-39412200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr19:39400000-39412200	Weak transcription	Primary T helper cells PMA-I stimulated	--
33	chr19:39400000-39412200	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr19:39400000-39412200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr19:39400000-39414200	Weak transcription	Left Ventricle	heart
36	chr19:39400200-39410000	Weak transcription	Primary T cells from cord blood	blood
37	chr19:39400200-39410000	Weak transcription	Dnd41	blood
38	chr19:39400200-39412000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr19:39400200-39412000	Weak transcription	Aorta	Aorta
40	chr19:39400200-39412600	Weak transcription	Primary B cells from cord blood	blood
41	chr19:39400200-39412800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr19:39401000-39412000	Weak transcription	Gastric	stomach
43	chr19:39402400-39412200	Weak transcription	Right Ventricle	heart
44	chr19:39402800-39420200	Weak transcription	Colon Smooth Muscle	Colon
45	chr19:39403000-39412000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr19:39403000-39412000	Weak transcription	NHLF	lung
47	chr19:39403000-39412400	Weak transcription	Fetal Thymus	thymus
48	chr19:39403000-39415000	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr19:39403400-39412000	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr19:39403400-39412200	Weak transcription	Brain Anterior Caudate	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links