Variant report

Variant	nsv579534
Chromosome Location	chr19:41351267-41384578
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:341)
CpG islands
(count:368)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41370633-41370945	K562	blood:	n/a	n/a
2	ARID3A	chr19:41378197-41378436	K562	blood:	n/a	n/a
3	ATF1	chr19:41378237-41378485	K562	blood:	n/a	n/a
4	ATF1	chr19:41370536-41370948	K562	blood:	n/a	n/a
5	ATF3	chr19:41378141-41378430	K562	blood:	n/a	n/a
6	ATF3	chr19:41370620-41370877	K562	blood:	n/a	n/a
7	CBX3	chr19:41379769-41380227	K562	blood:	n/a	n/a
8	CBX3	chr19:41379821-41380148	K562	blood:	n/a	n/a
9	CBX3	chr19:41370123-41371107	K562	blood:	n/a	n/a
10	CBX3	chr19:41381255-41381833	K562	blood:	n/a	n/a
11	CCNT2	chr19:41370582-41370786	K562	blood:	n/a	n/a
12	CEBPB	chr19:41362024-41362201	K562	blood:	n/a	n/a
13	CEBPB	chr19:41378139-41378466	K562	blood:	n/a	n/a
14	CEBPB	chr19:41373834-41374300	A549	lung:	n/a	n/a
15	CEBPB	chr19:41370209-41371189	K562	blood:	n/a	chr19:41370433-41370441
16	CEBPB	chr19:41370305-41370801	K562	blood:	n/a	chr19:41370433-41370441
17	CEBPB	chr19:41368480-41368982	A549	lung:	n/a	n/a
18	CEBPB	chr19:41368761-41369068	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:41373920-41374208	K562	blood:	n/a	n/a
20	CEBPB	chr19:41370543-41370910	K562	blood:	n/a	n/a
21	CEBPB	chr19:41367289-41367476	A549	lung:	n/a	n/a
22	CEBPB	chr19:41368416-41368601	K562	blood:	n/a	n/a
23	CEBPB	chr19:41378202-41378474	K562	blood:	n/a	n/a
24	CEBPB	chr19:41374056-41374100	A549	lung:	n/a	n/a
25	CEBPD	chr19:41370661-41370862	K562	blood:	n/a	n/a
26	CEBPD	chr19:41370295-41371143	K562	blood:	n/a	n/a
27	CTCF	chr19:41368340-41368490	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr19:41354562-41354668	GM10248	blood:	n/a	n/a
29	CTCF	chr19:41367560-41367710	HEK293	kidney:	n/a	n/a
30	CTCF	chr19:41354580-41354730	BE2_C	brain:	n/a	chr19:41354699-41354709
31	CTCF	chr19:41354520-41354670	HMEC	breast:	n/a	n/a
32	CTCF	chr19:41354500-41354650	BJ	skin:	n/a	n/a
33	CTCF	chr19:41368340-41368490	AoAF	blood vessel:	n/a	n/a
34	CTCF	chr19:41354520-41354670	HRE	kidney:	n/a	n/a
35	CTCF	chr19:41354540-41354690	HPF	lung:	n/a	n/a
36	CTCF	chr19:41354437-41354750	K562	blood:	n/a	chr19:41354699-41354709
37	CTCF	chr19:41359824-41359874	LNCaP	prostate:	n/a	n/a
38	CTCF	chr19:41364147-41364298	K562	blood:	n/a	n/a
39	CTCF	chr19:41364113-41364398	K562	blood:	n/a	n/a
40	CTCF	chr19:41354500-41354650	HL-60	blood:	n/a	n/a
41	CTCF	chr19:41354540-41354690	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr19:41354510-41354631	Medullo	brain:	n/a	n/a
43	CTCF	chr19:41354333-41354798	H1-hESC	embryonic stem cell:	n/a	chr19:41354699-41354709
44	CTCF	chr19:41368540-41368690	AoAF	blood vessel:	n/a	n/a
45	CTCF	chr19:41354500-41354650	AG04449	skin:	n/a	n/a
46	CTCF	chr19:41364081-41364360	K562	blood:	n/a	n/a
47	CTCF	chr19:41354461-41354702	A549	lung:	n/a	n/a
48	CTCF	chr19:41368300-41368450	AG04450	lung:	n/a	n/a
49	CTCF	chr19:41354520-41354670	SAEC	small airway:	n/a	n/a
50	CTCF	chr19:41368380-41368530	HEK293	kidney:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41383654-41383704	SKMC	muscle:	n/a
2	chr19:41354682-41354732	HEEpiC	esophagus:	n/a
3	chr19:41383654-41383704	SKMC	muscle:	n/a
4	chr19:41354682-41354732	HEEpiC	esophagus:	n/a
5	chr19:41354553-41354603	HPAEpiC	pulmonary alveolar:	n/a
6	chr19:41354682-41354732	ECC-1	luminal epithelium:	n/a
7	chr19:41354142-41354192	NB4	blood:	n/a
8	chr19:41354142-41354192	SAEC	small airway:	n/a
9	chr19:41354142-41354192	HEK293	kidney:	embryo
10	chr19:41355973-41356023	GM06990	blood:	n/a
11	chr19:41355973-41356023	PANC-1	pancreas:	n/a
12	chr19:41354682-41354732	SK-N-SH_RA	brain:	n/a
13	chr19:41354142-41354192	BJ	skin:	n/a
14	chr19:41383654-41383704	GM19239	blood:	n/a
15	chr19:41354142-41354192	AG10803	skin:	n/a
16	chr19:41355973-41356023	HUVEC	blood vessel:	n/a
17	chr19:41354682-41354732	AG04450	lung:	fetal
18	chr19:41354553-41354603	HIPEpiC	eye:	n/a
19	chr19:41383654-41383704	HCF	heart:	n/a
20	chr19:41383654-41383704	HUVEC	blood vessel:	n/a
21	chr19:41351924-41351974	AG04450	lung:	fetal
22	chr19:41355973-41356023	GM12892	blood:	n/a
23	chr19:41354142-41354192	HRE	kidney:	n/a
24	chr19:41351924-41351974	HCF	heart:	n/a
25	chr19:41383654-41383704	HCT-116	colon:	n/a
26	chr19:41354553-41354603	AG04450	lung:	fetal
27	chr19:41354682-41354732	IMR90	lung:	fetal
28	chr19:41383654-41383704	HEK293	kidney:	embryo
29	chr19:41355973-41356023	SAEC	small airway:	n/a
30	chr19:41383654-41383704	PANC-1	pancreas:	n/a
31	chr19:41355973-41356023	MCF-7	breast:	n/a
32	chr19:41351924-41351974	RPTEC	kidney:	n/a
33	chr19:41354553-41354603	AG04449	skin:	fetal
34	chr19:41351924-41351974	Hela-S3	cervix:	n/a
35	chr19:41354553-41354603	SAEC	small airway:	n/a
36	chr19:41354142-41354192	HEEpiC	esophagus:	n/a
37	chr19:41354682-41354732	HNPCEpiC	eye:	n/a
38	chr19:41354682-41354732	H1-hESC	embryonic stem cell:	embryo
39	chr19:41354682-41354732	HIPEpiC	eye:	n/a
40	chr19:41354682-41354732	HUVEC	blood vessel:	n/a
41	chr19:41354142-41354192	HCM	heart:	n/a
42	chr19:41354682-41354732	HAEpiC	amniotic membrane:	n/a
43	chr19:41354142-41354192	U87	brain:	n/a
44	chr19:41351924-41351974	PrEC	prostate:	n/a
45	chr19:41354553-41354603	HEEpiC	esophagus:	n/a
46	chr19:41354553-41354603	NH-A	brain:	n/a
47	chr19:41351924-41351974	ProgFib	skin:	n/a
48	chr19:41383654-41383704	SK-N-SH	brain:	n/a
49	chr19:41355973-41356023	SK-N-SH_RA	brain:	n/a
50	chr19:41383654-41383704	AG10803	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
2	chr16:4474827..4477394-chr19:41351022..41353007,2	MCF-7	breast:
3	chr19:41369230..41371017-chr19:41372027..41374078,2	K562	blood:
4	chr19:41195484..41197379-chr19:41368669..41371255,2	K562	blood:

No data

Variant related genes	Relation type
CYP2A6	TF binding region
CYP2A7	TF binding region
CYP2A6	CpG island
CYP2A7	CpG island
ENSG00000105245	chromatin interactions
ENSG00000262246	chromatin interactions
ENSG00000103423	chromatin interactions

Extended variants
information (count: 1715 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1715 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28399454	chr19:41351267-41351268	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375925239	chr19:41351289-41351290	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs143841823	chr19:41351305-41351306	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs148166815	chr19:41351309-41351310	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs200267449	chr19:41351321-41351322	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs141074424	chr19:41351324-41351325	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs150247689	chr19:41351344-41351345	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs374200109	chr19:41351354-41351355	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs138932530	chr19:41351355-41351356	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs61605570	chr19:41351363-41351364	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs146206761	chr19:41351368-41351369	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs137904044	chr19:41351370-41351371	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs535231886	chr19:41351376-41351377	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546089312	chr19:41351382-41351383	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs188167379	chr19:41351393-41351394	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs28399453	chr19:41351400-41351401	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs148057229	chr19:41351429-41351430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528694759	chr19:41351436-41351437	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs577654198	chr19:41351448-41351449	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2388874	chr19:41351456-41351457	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs4001931	chr19:41351461-41351462	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs4001930	chr19:41351475-41351476	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs2302989	chr19:41351482-41351483	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs4001929	chr19:41351496-41351497	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs2388873	chr19:41351525-41351526	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs8192728	chr19:41351538-41351539	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563421126	chr19:41351544-41351545	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530503863	chr19:41351554-41351555	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs144437384	chr19:41351563-41351564	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs2316213	chr19:41351605-41351606	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs549902541	chr19:41351611-41351612	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs55971367	chr19:41351614-41351615	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs2388871	chr19:41351616-41351617	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs2316214	chr19:41351621-41351622	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2388870	chr19:41351628-41351629	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs181001074	chr19:41351632-41351633	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs528987773	chr19:41351634-41351635	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs56048590	chr19:41351651-41351652	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs567978574	chr19:41351657-41351658	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs535660414	chr19:41351682-41351683	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs72549445	chr19:41351696-41351697	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs566118912	chr19:41351736-41351737	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs149876040	chr19:41351747-41351748	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs537139773	chr19:41351755-41351756	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs558957904	chr19:41351758-41351759	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs4997555	chr19:41351771-41351772	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs185020627	chr19:41351772-41351773	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs4997556	chr19:41351788-41351789	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs553719688	chr19:41351805-41351806	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs375518878	chr19:41351831-41351832	Weak transcription Strong transcription	Chromatin interactive region	2 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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41349800-41353800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:41350000-41351400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr19:41350000-41352600	Weak transcription	Lung	lung
4	chr19:41350000-41353000	Strong transcription	Liver	Liver
5	chr19:41350600-41354400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr19:41350800-41354400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr19:41351000-41354600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr19:41351200-41354400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr19:41351200-41354400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr19:41351400-41351600	Enhancers	Esophagus	oesophagus
11	chr19:41351400-41351600	Enhancers	Right Ventricle	heart
12	chr19:41351400-41354200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr19:41352800-41353000	Enhancers	Lung	lung
14	chr19:41352800-41354400	Weak transcription	Pancreas	Pancrea
15	chr19:41353000-41353600	Weak transcription	Lung	lung
16	chr19:41353000-41354000	Weak transcription	Liver	Liver
17	chr19:41353600-41354800	Enhancers	Lung	lung
18	chr19:41353800-41354000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
19	chr19:41353800-41354200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr19:41353800-41354200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:41353800-41354800	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
22	chr19:41354000-41354200	Enhancers	Liver	Liver
23	chr19:41354000-41354800	Enhancers	Spleen	Spleen
24	chr19:41354200-41354400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
25	chr19:41354200-41354400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr19:41354200-41354400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr19:41354200-41354400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr19:41354200-41354400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr19:41354200-41354400	Enhancers	Ovary	ovary
30	chr19:41354200-41354600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr19:41354200-41354600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr19:41354200-41354600	Flanking Active TSS	Liver	Liver
33	chr19:41354200-41354800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
34	chr19:41354200-41354800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
35	chr19:41354200-41354800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
36	chr19:41354200-41354800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
37	chr19:41354200-41355000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
38	chr19:41354200-41355000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
39	chr19:41354400-41354600	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
40	chr19:41354400-41354600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr19:41354400-41354600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr19:41354400-41354600	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr19:41354400-41354600	Bivalent Enhancer	Fetal Brain Male	brain
44	chr19:41354400-41354600	Flanking Active TSS	Ovary	ovary
45	chr19:41354400-41354600	Enhancers	Rectal Smooth Muscle	rectum
46	chr19:41354400-41354600	Enhancers	Right Ventricle	heart
47	chr19:41354400-41354600	Bivalent Enhancer	Stomach Mucosa	stomach
48	chr19:41354400-41354800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
49	chr19:41354400-41354800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr19:41354400-41354800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell

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