Variant report

Variant	nsv869598
Chromosome Location	chr19:35847245-35870922
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:377)
CpG islands
(count:366)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:35865850-35866169	K562	blood:	n/a	n/a
2	ATF1	chr19:35849261-35849449	K562	blood:	n/a	n/a
3	ATF1	chr19:35865921-35866194	K562	blood:	n/a	n/a
4	ATF2	chr19:35867800-35868411	GM12878	blood:	n/a	n/a
5	ATF2	chr19:35867750-35868427	GM12878	blood:	n/a	n/a
6	ATF3	chr19:35865822-35866257	K562	blood:	n/a	n/a
7	ATF3	chr19:35865963-35866126	K562	blood:	n/a	n/a
8	BACH1	chr19:35851866-35852079	K562	blood:	n/a	n/a
9	BATF	chr19:35867870-35868281	GM12878	blood:	n/a	n/a
10	BCL11A	chr19:35867927-35868350	GM12878	blood:	n/a	n/a
11	BCL3	chr19:35867838-35868337	GM12878	blood:	n/a	n/a
12	BCL3	chr19:35867879-35868288	GM12878	blood:	n/a	n/a
13	BHLHE40	chr19:35867943-35868341	GM12878	blood:	n/a	n/a
14	BHLHE40	chr19:35865883-35866242	K562	blood:	n/a	n/a
15	BHLHE40	chr19:35865989-35866016	GM12878	blood:	n/a	n/a
16	CBX3	chr19:35865901-35866279	K562	blood:	n/a	n/a
17	CEBPB	chr19:35870554-35870680	HepG2	liver:	n/a	chr19:35870619-35870630
18	CEBPB	chr19:35870443-35870797	IMR90	lung:	n/a	chr19:35870619-35870630
19	CEBPB	chr19:35849083-35849292	H1-hESC	embryonic stem cell:	n/a	chr19:35849192-35849203
20	CEBPB	chr19:35861294-35861521	HepG2	liver:	n/a	chr19:35861400-35861411
21	CEBPB	chr19:35849039-35849353	Hela-S3	cervix:	n/a	chr19:35849192-35849203
22	CEBPB	chr19:35870455-35870720	H1-hESC	embryonic stem cell:	n/a	chr19:35870619-35870630
23	CEBPB	chr19:35868610-35868885	H1-hESC	embryonic stem cell:	n/a	chr19:35868767-35868780
24	CEBPB	chr19:35849017-35849385	IMR90	lung:	n/a	chr19:35849192-35849203
25	CEBPB	chr19:35870443-35870805	A549	lung:	n/a	chr19:35870619-35870630
26	CEBPB	chr19:35868553-35868937	HepG2	liver:	n/a	chr19:35868767-35868780
27	CEBPB	chr19:35861266-35861524	A549	lung:	n/a	chr19:35861400-35861411
28	CEBPB	chr19:35867769-35868434	GM12878	blood:	n/a	n/a
29	CEBPB	chr19:35870425-35870760	K562	blood:	n/a	chr19:35870619-35870630
30	CEBPB	chr19:35864457-35864718	HepG2	liver:	n/a	n/a
31	CEBPB	chr19:35849037-35849249	K562	blood:	n/a	chr19:35849192-35849203
32	CEBPB	chr19:35870435-35870832	MCF-7	breast:	n/a	chr19:35870619-35870630
33	CEBPB	chr19:35849025-35849368	K562	blood:	n/a	chr19:35849192-35849203
34	CEBPB	chr19:35861291-35861545	IMR90	lung:	n/a	chr19:35861400-35861411
35	CEBPB	chr19:35868648-35868878	A549	lung:	n/a	chr19:35868767-35868780
36	CEBPB	chr19:35870419-35871781	K562	blood:	n/a	chr19:35870619-35870630
37	CEBPB	chr19:35870303-35870872	A549	lung:	n/a	chr19:35870619-35870630
38	CEBPB	chr19:35868595-35868939	HepG2	liver:	n/a	chr19:35868767-35868780
39	CEBPB	chr19:35870459-35870646	Hela-S3	cervix:	n/a	chr19:35870619-35870630
40	CEBPB	chr19:35868592-35868934	A549	lung:	n/a	chr19:35868767-35868780
41	CEBPB	chr19:35866839-35866916	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr19:35868644-35868844	IMR90	lung:	n/a	chr19:35868767-35868780
43	CEBPB	chr19:35864499-35864730	K562	blood:	n/a	n/a
44	CEBPB	chr19:35868665-35868869	HepG2	liver:	n/a	chr19:35868767-35868780
45	CEBPB	chr19:35849029-35849356	A549	lung:	n/a	chr19:35849192-35849203
46	CEBPB	chr19:35870435-35870802	HepG2	liver:	n/a	chr19:35870619-35870630
47	CEBPB	chr19:35861320-35861547	K562	blood:	n/a	chr19:35861400-35861411
48	CEBPB	chr19:35868508-35868945	A549	lung:	n/a	chr19:35868767-35868780
49	CEBPB	chr19:35849027-35849357	HepG2	liver:	n/a	chr19:35849192-35849203
50	CHD2	chr19:35867926-35868275	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35848801-35848851	Caco-2	colon:	n/a
2	chr19:35861862-35861912	AG09309	skin:	n/a
3	chr19:35848801-35848851	SK-N-SH_RA	brain:	n/a
4	chr19:35849024-35849074	U87	brain:	n/a
5	chr19:35849393-35849443	HNPCEpiC	eye:	n/a
6	chr19:35849176-35849226	HIPEpiC	eye:	n/a
7	chr19:35850463-35850513	H1-hESC	embryonic stem cell:	embryo
8	chr19:35850463-35850513	IMR90	lung:	fetal
9	chr19:35861862-35861912	HEK293	kidney:	embryo
10	chr19:35848801-35848851	ECC-1	luminal epithelium:	n/a
11	chr19:35849393-35849443	T-47D	breast:	n/a
12	chr19:35850463-35850513	HRPEpiC	eye:	n/a
13	chr19:35849176-35849226	Hepatocyte	liver:	n/a
14	chr19:35848801-35848851	PrEC	prostate:	n/a
15	chr19:35849393-35849443	NB4	blood:	n/a
16	chr19:35850463-35850513	HEEpiC	esophagus:	n/a
17	chr19:35848801-35848851	Hela-S3	cervix:	n/a
18	chr19:35861862-35861912	PANC-1	pancreas:	n/a
19	chr19:35849176-35849226	ECC-1	luminal epithelium:	n/a
20	chr19:35849024-35849074	GM12892	blood:	n/a
21	chr19:35848801-35848851	NHDF-neo	bronchial:	n/a
22	chr19:35849393-35849443	HRCEpiC	kidney:	n/a
23	chr19:35850463-35850513	PANC-1	pancreas:	n/a
24	chr19:35849176-35849226	GM12878	blood:	n/a
25	chr19:35848801-35848851	HRCEpiC	kidney:	n/a
26	chr19:35849393-35849443	IMR90	lung:	fetal
27	chr19:35850463-35850513	HepG2	liver:	n/a
28	chr19:35849176-35849226	BE2_C	brain:	n/a
29	chr19:35850463-35850513	AG09319	gingival:	n/a
30	chr19:35861862-35861912	HPAEpiC	pulmonary alveolar:	n/a
31	chr19:35849393-35849443	H1-hESC	embryonic stem cell:	embryo
32	chr19:35849393-35849443	Hepatocyte	liver:	n/a
33	chr19:35850463-35850513	PrEC	prostate:	n/a
34	chr19:35849024-35849074	NH-A	brain:	n/a
35	chr19:35848801-35848851	HEK293	kidney:	embryo
36	chr19:35849024-35849074	HMEC	breast:	n/a
37	chr19:35849176-35849226	HCF	heart:	n/a
38	chr19:35849024-35849074	HCM	heart:	n/a
39	chr19:35861862-35861912	HCPEpiC	choroid plexus:	n/a
40	chr19:35849176-35849226	ProgFib	skin:	n/a
41	chr19:35849393-35849443	A549	lung:	n/a
42	chr19:35849393-35849443	AG04450	lung:	fetal
43	chr19:35861862-35861912	ovcar-3	ovarian:	n/a
44	chr19:35848801-35848851	A549	lung:	n/a
45	chr19:35848801-35848851	AoSMC	blood vessel:	n/a
46	chr19:35849176-35849226	NH-A	brain:	n/a
47	chr19:35850463-35850513	GM12892	blood:	n/a
48	chr19:35849024-35849074	HEK293	kidney:	embryo
49	chr19:35861862-35861912	SK-N-MC	brain:	n/a
50	chr19:35850463-35850513	U87	brain:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35866654..35868491-chr19:35868954..35871337,2	K562	blood:
2	chr19:35866654..35868491-chr19:35868954..35871337,2	K562	blood:
3	chr19:35847716..35849933-chr19:35855045..35856568,2	MCF-7	breast:
4	chr19:35865310..35868154-chr19:35869837..35872073,2	K562	blood:
5	chr19:35864467..35867206-chr19:35939200..35941045,2	MCF-7	breast:
6	chr19:35842321..35845191-chr19:35845202..35847710,3	MCF-7	breast:
7	chr19:35842803..35847555-chr19:35958346..35962291,5	MCF-7	breast:
8	chr19:35865310..35868154-chr19:35869837..35872073,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR42-2	chr19:35870421-35870690	NONHSAT065830

No data

Variant related genes	Relation type
FFAR3	TF binding region
EEF1A1P7	TF binding region
GPR42	TF binding region
FFAR3	CpG island
EEF1A1P7	CpG island
GPR42	CpG island
ENSG00000126262	chromatin interactions
ENSG00000126266	chromatin interactions
ENSG00000185897	chromatin interactions

Extended variants
information (count: 823 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200643639	chr19:35847250-35847251	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs534972975	chr19:35847252-35847253	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs201639426	chr19:35847253-35847254	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs113486798	chr19:35847254-35847255	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs57204311	chr19:35847258-35847259	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs113677152	chr19:35847259-35847260	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs375322004	chr19:35847263-35847264	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs200117646	chr19:35847264-35847265	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369019593	chr19:35847267-35847268	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs55921668	chr19:35847268-35847269	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs12104389	chr19:35847280-35847281	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs577472364	chr19:35847295-35847296	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs546043767	chr19:35847397-35847398	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs34425019	chr19:35847403-35847404	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531816494	chr19:35847405-35847406	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs8101157	chr19:35847436-35847437	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs74565154	chr19:35847441-35847442	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201602660	chr19:35847446-35847447	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs78768714	chr19:35847448-35847449	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs201354673	chr19:35847459-35847460	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs199503189	chr19:35847461-35847462	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs62109579	chr19:35847465-35847466	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs8101172	chr19:35847468-35847469	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs568179211	chr19:35847486-35847487	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs547772882	chr19:35847512-35847513	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75312735	chr19:35847555-35847556	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs535610450	chr19:35847571-35847572	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12104398	chr19:35847616-35847617	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577906589	chr19:35847622-35847623	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs115151742	chr19:35847686-35847687	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12104399	chr19:35847719-35847720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs569543387	chr19:35847772-35847773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs116864731	chr19:35847795-35847796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555085811	chr19:35847798-35847799	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs202085680	chr19:35847814-35847815	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143925508	chr19:35847823-35847824	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs534278553	chr19:35847835-35847836	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs8100218	chr19:35847881-35847882	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs71352978	chr19:35847893-35847894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs577434629	chr19:35847902-35847903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371513998	chr19:35847920-35847921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140491384	chr19:35847921-35847922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113586923	chr19:35847929-35847930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111491811	chr19:35847935-35847936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs557726593	chr19:35847938-35847939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75638589	chr19:35847984-35847985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190143651	chr19:35847985-35847986	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542338171	chr19:35848038-35848039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562115967	chr19:35848045-35848046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs74172721	chr19:35848058-35848059	Weak transcription	n/a	n/a	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
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
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	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
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:163 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35836800-35848000	Weak transcription	Brain Substantia Nigra	brain
2	chr19:35838200-35849200	Weak transcription	Brain Hippocampus Middle	brain
3	chr19:35839200-35848600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr19:35839200-35848800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr19:35840800-35848400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr19:35843600-35848000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr19:35843800-35848600	Weak transcription	Gastric	stomach
8	chr19:35844000-35848400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr19:35844000-35848800	Weak transcription	Primary hematopoietic stem cells	blood
10	chr19:35844000-35849000	Weak transcription	Ovary	ovary
11	chr19:35844000-35849000	Weak transcription	Spleen	Spleen
12	chr19:35844200-35848200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr19:35844200-35848400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr19:35844200-35848400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr19:35844200-35848400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr19:35844200-35848800	Weak transcription	Primary T helper cells fromperipheralblood	blood
17	chr19:35844200-35849000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr19:35844200-35849000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr19:35844600-35847400	Weak transcription	Primary B cells from cord blood	blood
20	chr19:35844600-35849000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr19:35845000-35848200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr19:35845000-35848400	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr19:35846200-35847600	Enhancers	Fetal Lung	lung
24	chr19:35846400-35847600	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr19:35846400-35848200	Weak transcription	Primary neutrophils fromperipheralblood	blood
26	chr19:35846400-35848800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr19:35846800-35847400	Enhancers	Fetal Stomach	stomach
28	chr19:35846800-35847600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr19:35847000-35847600	Enhancers	Fetal Muscle Trunk	muscle
30	chr19:35847000-35848400	Weak transcription	HepG2	liver
31	chr19:35847200-35848600	Weak transcription	Adipose Nuclei	Adipose
32	chr19:35847200-35848800	Weak transcription	Liver	Liver
33	chr19:35847200-35852000	Weak transcription	GM12878-XiMat	blood
34	chr19:35847600-35847800	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr19:35847600-35848600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr19:35847600-35848600	Weak transcription	Fetal Lung	lung
37	chr19:35847600-35848800	Weak transcription	Fetal Muscle Trunk	muscle
38	chr19:35847800-35848200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr19:35848000-35848400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr19:35848200-35848800	Enhancers	Primary neutrophils fromperipheralblood	blood
41	chr19:35848200-35849200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr19:35848200-35849400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
43	chr19:35848200-35849600	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr19:35848400-35848800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr19:35848400-35849000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr19:35848400-35849400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr19:35848400-35849400	Enhancers	Primary T helper naive cells from peripheral blood	blood
48	chr19:35848400-35849400	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr19:35848400-35849400	Enhancers	Fetal Muscle Leg	muscle
50	chr19:35848400-35849400	Enhancers	HepG2	liver

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