Variant report

Variant	nsv437830
Chromosome Location	chr19:41408746-41515702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1229)
CpG islands
(count:915)
Chromatin interactive
region (count:33)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1229 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41426619-41427639	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:41506351-41506450	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:41410840-41411013	K562	blood:	n/a	n/a
5	ARID3A	chr19:41507311-41507499	K562	blood:	n/a	n/a
6	ATF1	chr19:41410781-41411006	K562	blood:	n/a	n/a
7	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
8	ATF1	chr19:41434897-41435097	K562	blood:	n/a	n/a
9	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
10	ATF3	chr19:41426642-41427965	A549	lung:	n/a	n/a
11	ATF3	chr19:41426280-41428001	A549	lung:	n/a	n/a
12	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
13	ATF3	chr19:41426982-41427439	HepG2	liver:	n/a	n/a
14	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
15	ATF3	chr19:41410728-41411084	K562	blood:	n/a	n/a
16	ATF3	chr19:41506069-41506786	HCT-116	colon:	n/a	n/a
17	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr19:41437946-41438301	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr19:41430483-41430507	K562	blood:	n/a	n/a
20	BACH1	chr19:41437956-41438260	K562	blood:	n/a	n/a
21	BCL3	chr19:41426105-41428005	A549	lung:	n/a	n/a
22	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
23	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
24	BCL3	chr19:41426209-41428048	A549	lung:	n/a	n/a
25	BHLHE40	chr19:41507420-41507421	K562	blood:	n/a	n/a
26	BHLHE40	chr19:41427051-41427149	K562	blood:	n/a	n/a
27	BHLHE40	chr19:41410515-41411000	K562	blood:	n/a	n/a
28	BHLHE40	chr19:41426976-41427417	HepG2	liver:	n/a	n/a
29	BHLHE40	chr19:41426865-41427680	HepG2	liver:	n/a	n/a
30	BHLHE40	chr19:41414366-41414529	K562	blood:	n/a	n/a
31	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
32	CBX3	chr19:41425461-41425971	K562	blood:	n/a	n/a
33	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
34	CBX3	chr19:41425402-41426054	K562	blood:	n/a	n/a
35	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
36	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
37	CBX3	chr19:41426983-41427522	K562	blood:	n/a	n/a
38	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
39	CCNT2	chr19:41434884-41435092	K562	blood:	n/a	n/a
40	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
41	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
42	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
43	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
44	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
45	CEBPB	chr19:41426226-41428113	A549	lung:	n/a	chr19:41427674-41427685 chr19:41427674-41427685
46	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
47	CEBPB	chr19:41434742-41435118	K562	blood:	n/a	n/a
48	CEBPB	chr19:41434826-41435086	K562	blood:	n/a	n/a
49	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
50	CEBPB	chr19:41434755-41435152	K562	blood:	n/a	n/a

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41510272-41510322	SKMC	muscle:	n/a
2	chr19:41496749-41496799	T-47D	breast:	n/a
3	chr19:41510272-41510322	GM12878	blood:	n/a
4	chr19:41496043-41496093	Hepatocyte	liver:	n/a
5	chr19:41510026-41510076	GM12892	blood:	n/a
6	chr19:41429786-41429836	HEEpiC	esophagus:	n/a
7	chr19:41430189-41430239	HIPEpiC	eye:	n/a
8	chr19:41430077-41430127	AG09309	skin:	n/a
9	chr19:41510098-41510148	SK-N-MC	brain:	n/a
10	chr19:41497222-41497272	HIPEpiC	eye:	n/a
11	chr19:41510059-41510109	AG04450	lung:	fetal
12	chr19:41429786-41429836	HRCEpiC	kidney:	n/a
13	chr19:41430077-41430127	HIPEpiC	eye:	n/a
14	chr19:41510037-41510087	Hepatocyte	liver:	n/a
15	chr19:41510243-41510293	GM19239	blood:	n/a
16	chr19:41430077-41430127	NT2-D1	testis:	n/a
17	chr19:41430189-41430239	MCF10A-Er-Src	breast:	n/a
18	chr19:41510026-41510076	HPAEpiC	pulmonary alveolar:	n/a
19	chr19:41429786-41429836	AoSMC	blood vessel:	n/a
20	chr19:41496043-41496093	HRCEpiC	kidney:	n/a
21	chr19:41495942-41495992	SAEC	small airway:	n/a
22	chr19:41510098-41510148	PFSK-1	brain:	n/a
23	chr19:41510037-41510087	BE2_C	brain:	n/a
24	chr19:41510272-41510322	SAEC	small airway:	n/a
25	chr19:41510243-41510293	MCF10A-Er-Src	breast:	n/a
26	chr19:41510059-41510109	NB4	blood:	n/a
27	chr19:41497222-41497272	AoSMC	blood vessel:	n/a
28	chr19:41510272-41510322	HAEpiC	amniotic membrane:	n/a
29	chr19:41510243-41510293	HIPEpiC	eye:	n/a
30	chr19:41510272-41510322	GM06990	blood:	n/a
31	chr19:41510285-41510335	GM12892	blood:	n/a
32	chr19:41510285-41510335	HRPEpiC	eye:	n/a
33	chr19:41429786-41429836	LNCaP	prostate:	n/a
34	chr19:41510272-41510322	HEEpiC	esophagus:	n/a
35	chr19:41510037-41510087	NT2-D1	testis:	n/a
36	chr19:41510098-41510148	BE2_C	brain:	n/a
37	chr19:41496749-41496799	Caco-2	colon:	n/a
38	chr19:41495942-41495992	AG09309	skin:	n/a
39	chr19:41510243-41510293	T-47D	breast:	n/a
40	chr19:41414353-41414403	U87	brain:	n/a
41	chr19:41510272-41510322	LNCaP	prostate:	n/a
42	chr19:41414353-41414403	Jurkat	blood:	n/a
43	chr19:41429786-41429836	IMR90	lung:	fetal
44	chr19:41510026-41510076	AG04450	lung:	fetal
45	chr19:41510037-41510087	HIPEpiC	eye:	n/a
46	chr19:41510098-41510148	GM12878	blood:	n/a
47	chr19:41495942-41495992	HCF	heart:	n/a
48	chr19:41510059-41510109	Hela-S3	cervix:	n/a
49	chr19:41430077-41430127	SK-N-SH	brain:	n/a
50	chr19:41510243-41510293	SK-N-SH_RA	brain:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
2	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
3	chr19:41429883..41432599-chr19:41435321..41438137,2	MCF-7	breast:
4	chr19:41435849..41437489-chr19:41440022..41442246,2	MCF-7	breast:
5	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
6	chr19:41444451..41445965-chr19:41446160..41448128,2	MCF-7	breast:
7	chr19:41400931..41403268-chr19:41432541..41435329,2	K562	blood:
8	chr19:41435849..41437489-chr19:41440022..41442246,2	MCF-7	breast:
9	chr19:41438993..41440711-chr19:41442295..41445002,2	MCF-7	breast:
10	chr19:41403631..41404535-chr19:41426743..41427640,3	MCF-7	breast:
11	chr19:41303143..41305588-chr19:41428304..41431722,3	MCF-7	breast:
12	chr19:40971826..40972553-chr19:41426973..41427731,2	MCF-7	breast:
13	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
14	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
15	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
16	chr19:41310513..41314653-chr19:41415794..41419669,4	K562	blood:
17	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
18	chr19:41403893..41404465-chr19:41426940..41427721,3	MCF-7	breast:
19	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
20	chr19:41303781..41306051-chr19:41433024..41435492,2	MCF-7	breast:
21	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
22	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
23	chr19:41438993..41440711-chr19:41442295..41445002,2	MCF-7	breast:
24	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
25	chr19:41220910..41226186-chr19:41426409..41429163,5	MCF-7	breast:
26	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
27	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
28	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
29	chr19:41283761..41286182-chr19:41409909..41411443,2	K562	blood:
30	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
31	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
32	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
33	chr19:41426562..41427465-chr19:41557958..41558773,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2B6-2	chr19:41453006-41453355	ENSG00000269353.1
2	lnc-CYP2B6-1	chr19:41495264-41495408	l_1687_chr19:41492503-41503928_testes
3	lnc-CYP2B6-1	chr19:41503762-41503928	l_1687_chr19:41492503-41503928_testes
4	lnc-CYP2B6-2	chr19:41452252-41452450	ENSG00000269353.1
5	lnc-CYP2B6-1	chr19:41492504-41492600	l_1687_chr19:41492503-41503928_testes
6	lnc-CYP2B6-1	chr19:41493177-41493736	l_1687_chr19:41492503-41503928_testes
7	lnc-CYP2B6-1	chr19:41493956-41494534	l_1687_chr19:41492503-41503928_testes

No data

Variant related genes	Relation type
CYP2B6	TF binding region
ENSG00000198251	TF binding region
ENSG00000269353	TF binding region
CYP2B7P	TF binding region
CYP2B6	CpG island
ENSG00000198251	CpG island
ENSG00000269353	CpG island
CYP2B7P	CpG island
ENSG00000123815	chromatin interactions
ENSG00000269858	chromatin interactions
ENSG00000256612	chromatin interactions
ENSG00000086544	chromatin interactions
ENSG00000160460	chromatin interactions
ENSG00000171570	chromatin interactions
ENSG00000167578	chromatin interactions

Extended variants
information (count: 4311 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4311 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7258728	chr19:41408746-41408747	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs569505226	chr19:41408760-41408761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12974293	chr19:41408807-41408808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs555009224	chr19:41408842-41408843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115351592	chr19:41408859-41408860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557594938	chr19:41408866-41408867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567005925	chr19:41408877-41408878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575842554	chr19:41408895-41408896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs546568661	chr19:41408897-41408898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534916054	chr19:41408959-41408960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs372005051	chr19:41409021-41409022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs117092623	chr19:41409072-41409073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188757822	chr19:41409117-41409118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs562060213	chr19:41409120-41409121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529034925	chr19:41409130-41409131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147262009	chr19:41409153-41409154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562743376	chr19:41409190-41409191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs533072576	chr19:41409191-41409192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551289370	chr19:41409199-41409200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs538920525	chr19:41409238-41409239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs71358948	chr19:41409253-41409254	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181147818	chr19:41409268-41409269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144692448	chr19:41409335-41409336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs139479118	chr19:41409388-41409389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567260347	chr19:41409395-41409396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369250194	chr19:41409402-41409403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537988853	chr19:41409414-41409415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs557272141	chr19:41409425-41409426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575824892	chr19:41409430-41409431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540123903	chr19:41409447-41409448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558500710	chr19:41409484-41409485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573244861	chr19:41409586-41409587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185989571	chr19:41409603-41409604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs148477246	chr19:41409609-41409610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76558089	chr19:41409627-41409628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544737985	chr19:41409634-41409635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562520546	chr19:41409664-41409665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs552278829	chr19:41409665-41409666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190838539	chr19:41409690-41409691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560019644	chr19:41409701-41409702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs565826038	chr19:41409749-41409750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs527252987	chr19:41409763-41409764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs142652525	chr19:41409778-41409779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567303202	chr19:41409779-41409780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs537524280	chr19:41409795-41409796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549885285	chr19:41409841-41409842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542165111	chr19:41409892-41409893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569316209	chr19:41409936-41409937	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540058891	chr19:41409960-41409961	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182550790	chr19:41409988-41409989	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:572 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41403000-41414200	Weak transcription	Lung	lung
2	chr19:41406800-41410400	Weak transcription	K562	blood
3	chr19:41408200-41410600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr19:41410000-41410600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr19:41410400-41411200	Enhancers	K562	blood
6	chr19:41410600-41411200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr19:41410600-41411200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr19:41410800-41411000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:41410800-41411200	Enhancers	A549	lung
10	chr19:41411200-41413400	Weak transcription	K562	blood
11	chr19:41411200-41414400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr19:41413400-41413800	Enhancers	K562	blood
13	chr19:41413600-41414200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr19:41413600-41414200	Enhancers	Primary B cells from peripheral blood	blood
15	chr19:41413600-41414400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr19:41413600-41414400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
17	chr19:41413600-41415400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr19:41413800-41414000	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr19:41413800-41414200	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr19:41413800-41414200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr19:41413800-41414200	Flanking Active TSS	K562	blood
22	chr19:41413800-41414400	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr19:41413800-41414400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
24	chr19:41413800-41414800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr19:41413800-41415200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr19:41414000-41414200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
27	chr19:41414000-41414200	Enhancers	Colon Smooth Muscle	Colon
28	chr19:41414000-41414200	Bivalent/Poised TSS	Monocytes-CD14+_RO01746	blood
29	chr19:41414000-41414400	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr19:41414000-41414400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr19:41414000-41414600	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr19:41414000-41414600	Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr19:41414000-41414600	Active TSS	Primary hematopoietic stem cells	blood
34	chr19:41414000-41414600	Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr19:41414000-41414800	Active TSS	HUES64 Cell Line	embryonic stem cell
36	chr19:41414200-41414400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr19:41414200-41414400	Active TSS	Primary T helper cells fromperipheralblood	blood
38	chr19:41414200-41414400	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr19:41414200-41414400	Enhancers	Adipose Nuclei	Adipose
40	chr19:41414200-41414400	Bivalent Enhancer	Fetal Brain Female	brain
41	chr19:41414200-41414400	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr19:41414200-41414400	Enhancers	K562	blood
43	chr19:41414200-41414600	Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr19:41414200-41414600	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
45	chr19:41414200-41414600	Flanking Active TSS	Primary B cells from peripheral blood	blood
46	chr19:41414200-41414600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
47	chr19:41414200-41414600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
48	chr19:41414200-41414600	Bivalent Enhancer	Colon Smooth Muscle	Colon
49	chr19:41414200-41414600	Enhancers	Lung	lung
50	chr19:41414200-41414600	Active TSS	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links