Variant report

Variant	nsv437831
Chromosome Location	chr19:41416072-41524087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1114)
CpG islands
(count:854)
Chromatin interactive
region (count:32)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1114 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41507311-41507499	K562	blood:	n/a	n/a
2	ARID3A	chr19:41506351-41506450	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:41426619-41427639	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
5	ATF1	chr19:41434897-41435097	K562	blood:	n/a	n/a
6	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
7	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
8	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
9	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
10	ATF3	chr19:41506069-41506786	HCT-116	colon:	n/a	n/a
11	ATF3	chr19:41426280-41428001	A549	lung:	n/a	n/a
12	ATF3	chr19:41426982-41427439	HepG2	liver:	n/a	n/a
13	ATF3	chr19:41426642-41427965	A549	lung:	n/a	n/a
14	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr19:41437946-41438301	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr19:41430483-41430507	K562	blood:	n/a	n/a
17	BACH1	chr19:41437956-41438260	K562	blood:	n/a	n/a
18	BCL3	chr19:41426105-41428005	A549	lung:	n/a	n/a
19	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
20	BCL3	chr19:41426209-41428048	A549	lung:	n/a	n/a
21	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
22	BHLHE40	chr19:41507420-41507421	K562	blood:	n/a	n/a
23	BHLHE40	chr19:41426865-41427680	HepG2	liver:	n/a	n/a
24	BHLHE40	chr19:41426976-41427417	HepG2	liver:	n/a	n/a
25	BHLHE40	chr19:41427051-41427149	K562	blood:	n/a	n/a
26	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
27	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
28	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
29	CBX3	chr19:41425461-41425971	K562	blood:	n/a	n/a
30	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
31	CBX3	chr19:41426983-41427522	K562	blood:	n/a	n/a
32	CBX3	chr19:41425402-41426054	K562	blood:	n/a	n/a
33	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
34	CCNT2	chr19:41434884-41435092	K562	blood:	n/a	n/a
35	CEBPB	chr19:41426651-41427921	A549	lung:	n/a	chr19:41427674-41427685 chr19:41427674-41427685
36	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
37	CEBPB	chr19:41434742-41435118	K562	blood:	n/a	n/a
38	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
39	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
40	CEBPB	chr19:41434755-41435152	K562	blood:	n/a	n/a
41	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
42	CEBPB	chr19:41430620-41430805	K562	blood:	n/a	n/a
43	CEBPB	chr19:41426984-41427798	HepG2	liver:	n/a	chr19:41427674-41427685 chr19:41427674-41427685
44	CEBPB	chr19:41434826-41435086	K562	blood:	n/a	n/a
45	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
46	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
47	CEBPB	chr19:41438733-41439296	A549	lung:	n/a	n/a
48	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
49	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
50	CEBPB	chr19:41438614-41439244	K562	blood:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41429786-41429836	PrEC	prostate:	n/a
2	chr19:41510098-41510148	HAEpiC	amniotic membrane:	n/a
3	chr19:41429786-41429836	GM12891	blood:	n/a
4	chr19:41510037-41510087	MCF10A-Er-Src	breast:	n/a
5	chr19:41430189-41430239	AG04450	lung:	fetal
6	chr19:41430077-41430127	HRPEpiC	eye:	n/a
7	chr19:41510098-41510148	HRPEpiC	eye:	n/a
8	chr19:41496749-41496799	LNCaP	prostate:	n/a
9	chr19:41510243-41510293	Jurkat	blood:	n/a
10	chr19:41510059-41510109	GM12891	blood:	n/a
11	chr19:41510059-41510109	NT2-D1	testis:	n/a
12	chr19:41510026-41510076	HRCEpiC	kidney:	n/a
13	chr19:41510059-41510109	BE2_C	brain:	n/a
14	chr19:41430189-41430239	GM06990	blood:	n/a
15	chr19:41510243-41510293	HCM	heart:	n/a
16	chr19:41510272-41510322	K562	blood:	n/a
17	chr19:41429786-41429836	PFSK-1	brain:	n/a
18	chr19:41510059-41510109	PANC-1	pancreas:	n/a
19	chr19:41496749-41496799	GM12878	blood:	n/a
20	chr19:41497222-41497272	AG10803	skin:	n/a
21	chr19:41430189-41430239	GM12878	blood:	n/a
22	chr19:41430189-41430239	AoSMC	blood vessel:	n/a
23	chr19:41510059-41510109	GM12878	blood:	n/a
24	chr19:41429786-41429836	HEK293	kidney:	embryo
25	chr19:41429786-41429836	MCF-7	breast:	n/a
26	chr19:41510285-41510335	HRPEpiC	eye:	n/a
27	chr19:41510059-41510109	HL-60	blood:	n/a
28	chr19:41510037-41510087	CMK	blood:	n/a
29	chr19:41510026-41510076	MCF10A-Er-Src	breast:	n/a
30	chr19:41496749-41496799	GM06990	blood:	n/a
31	chr19:41496749-41496799	SK-N-SH_RA	brain:	n/a
32	chr19:41510059-41510109	Jurkat	blood:	n/a
33	chr19:41510098-41510148	BJ	skin:	n/a
34	chr19:41510059-41510109	HEK293	kidney:	embryo
35	chr19:41510059-41510109	GM19239	blood:	n/a
36	chr19:41429786-41429836	A549	lung:	n/a
37	chr19:41510098-41510148	RPTEC	kidney:	n/a
38	chr19:41510026-41510076	T-47D	breast:	n/a
39	chr19:41430077-41430127	NHDF-neo	bronchial:	n/a
40	chr19:41510243-41510293	Hela-S3	cervix:	n/a
41	chr19:41510037-41510087	H1-hESC	embryonic stem cell:	embryo
42	chr19:41510098-41510148	LNCaP	prostate:	n/a
43	chr19:41496043-41496093	NT2-D1	testis:	n/a
44	chr19:41497222-41497272	NHDF-neo	bronchial:	n/a
45	chr19:41496043-41496093	HEEpiC	esophagus:	n/a
46	chr19:41510272-41510322	SKMC	muscle:	n/a
47	chr19:41497222-41497272	NB4	blood:	n/a
48	chr19:41510059-41510109	HRE	kidney:	n/a
49	chr19:41510098-41510148	K562	blood:	n/a
50	chr19:41510285-41510335	CMK	blood:	n/a

(count:32 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2B6-1	chr19:41503762-41503928	l_1687_chr19:41492503-41503928_testes
2	lnc-CYP2B6-2	chr19:41452252-41452450	ENSG00000269353.1
3	lnc-CYP2B6-1	chr19:41492504-41492600	l_1687_chr19:41492503-41503928_testes
4	lnc-CYP2B6-1	chr19:41493956-41494534	l_1687_chr19:41492503-41503928_testes
5	lnc-CYP2B6-2	chr19:41453006-41453355	ENSG00000269353.1
6	lnc-CYP2B6-1	chr19:41493177-41493736	l_1687_chr19:41492503-41503928_testes
7	lnc-CYP2B6-1	chr19:41495264-41495408	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
ENSG00000086544	chromatin interactions
ENSG00000269858	chromatin interactions
ENSG00000256612	chromatin interactions
ENSG00000160460	chromatin interactions

Extended variants
information (count: 4665 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:4665 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3892666	chr19:41416072-41416073	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532227431	chr19:41416088-41416089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs193192021	chr19:41416091-41416092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs144182308	chr19:41416119-41416120	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185099946	chr19:41416124-41416125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs3852872	chr19:41416143-41416144	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs113774550	chr19:41416153-41416154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34119790	chr19:41416180-41416181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs115790392	chr19:41416182-41416183	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542581685	chr19:41416195-41416196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs560926711	chr19:41416214-41416215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189951440	chr19:41416218-41416219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139469436	chr19:41416221-41416222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530439441	chr19:41416228-41416229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs71337211	chr19:41416260-41416261	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs199790829	chr19:41416263-41416264	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs78367667	chr19:41416264-41416265	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
18	rs113639146	chr19:41416304-41416305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560569216	chr19:41416354-41416355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527963831	chr19:41416439-41416440	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181098824	chr19:41416488-41416489	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs567293823	chr19:41416526-41416527	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537852242	chr19:41416596-41416597	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs549821144	chr19:41416599-41416600	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs375733056	chr19:41416604-41416605	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188000396	chr19:41416605-41416606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs553908396	chr19:41416625-41416626	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572178823	chr19:41416628-41416629	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536516049	chr19:41416635-41416636	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554592197	chr19:41416664-41416665	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181896296	chr19:41416725-41416726	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543453091	chr19:41416740-41416741	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs10419589	chr19:41416750-41416751	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs144896322	chr19:41416759-41416760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540797003	chr19:41416764-41416765	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs60833805	chr19:41416765-41416766	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560720950	chr19:41416779-41416780	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs557139919	chr19:41416831-41416832	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs201575230	chr19:41416834-41416835	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs527901327	chr19:41416835-41416836	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543258356	chr19:41416901-41416902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187666025	chr19:41416919-41416920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs56129017	chr19:41416948-41416949	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs531920391	chr19:41417037-41417038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549759418	chr19:41417047-41417048	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375934785	chr19:41417072-41417073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191938289	chr19:41417084-41417085	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182122581	chr19:41417094-41417095	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs570517914	chr19:41417097-41417098	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs570896780	chr19:41417122-41417123	Weak transcription	Chromatin interactive region	1 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:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41414800-41419400	Weak transcription	Pancreas	Pancrea
2	chr19:41415400-41416400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr19:41415400-41417600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr19:41416400-41416600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:41417600-41417800	ZNF genes & repeats	Primary B cells from peripheral blood	blood
6	chr19:41418400-41418600	Bivalent Enhancer	A549	lung
7	chr19:41426200-41426400	Enhancers	Colonic Mucosa	Colon
8	chr19:41426200-41426600	Flanking Bivalent TSS/Enh	A549	lung
9	chr19:41426200-41427600	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr19:41426200-41429800	Enhancers	Stomach Mucosa	stomach
11	chr19:41426400-41426600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr19:41426400-41426600	Flanking Active TSS	Liver	Liver
13	chr19:41426400-41427600	Weak transcription	Colonic Mucosa	Colon
14	chr19:41426400-41427800	Enhancers	HepG2	liver
15	chr19:41426400-41428000	Enhancers	Hela-S3	cervix
16	chr19:41426400-41429600	Enhancers	Ovary	ovary
17	chr19:41426400-41430200	Enhancers	Fetal Intestine Large	intestine
18	chr19:41426400-41430200	Enhancers	Fetal Intestine Small	intestine
19	chr19:41426600-41426800	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr19:41426600-41426800	Flanking Active TSS	A549	lung
21	chr19:41426600-41427000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr19:41426600-41427400	Enhancers	HUVEC	blood vessel
23	chr19:41426600-41428200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr19:41426600-41429000	Enhancers	K562	blood
25	chr19:41426600-41429600	Enhancers	Liver	Liver
26	chr19:41426800-41427000	Bivalent Enhancer	Esophagus	oesophagus
27	chr19:41426800-41427000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
28	chr19:41426800-41427200	Enhancers	Muscle Satellite Cultured Cells	--
29	chr19:41426800-41427400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr19:41426800-41427400	Enhancers	A549	lung
31	chr19:41426800-41427600	Enhancers	Gastric	stomach
32	chr19:41426800-41427600	Enhancers	Pancreas	Pancrea
33	chr19:41427000-41427200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr19:41427000-41427200	Weak transcription	Duodenum Mucosa	Duodenum
35	chr19:41427000-41427200	Active TSS	Rectal Mucosa Donor 29	rectum
36	chr19:41427000-41427600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr19:41427000-41428000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr19:41427000-41429200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr19:41427200-41427600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr19:41427200-41428000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
41	chr19:41427200-41428400	Enhancers	Placenta	Placenta
42	chr19:41427400-41427800	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
43	chr19:41427400-41428200	Flanking Active TSS	A549	lung
44	chr19:41427400-41428400	Enhancers	Duodenum Mucosa	Duodenum
45	chr19:41427600-41428000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr19:41427600-41428000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
47	chr19:41427600-41428200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr19:41427600-41428200	Enhancers	Colonic Mucosa	Colon
49	chr19:41427600-41428200	Weak transcription	Gastric	stomach
50	chr19:41427600-41428200	Enhancers	Small Intestine	intestine

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