Variant report

Variant	esv3380662
Chromosome Location	chr19:41436058-41502855
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
2	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
3	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
4	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr19:41437946-41438301	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr19:41437956-41438260	K562	blood:	n/a	n/a
7	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
8	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
9	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
10	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
11	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
12	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
13	CEBPB	chr19:41438733-41439296	A549	lung:	n/a	n/a
14	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
15	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
16	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
17	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
18	CEBPB	chr19:41446714-41446729	A549	lung:	n/a	n/a
19	CEBPB	chr19:41438908-41439279	K562	blood:	n/a	n/a
20	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
21	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
22	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
23	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
24	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
25	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:41438982-41439268	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
28	CEBPB	chr19:41438614-41439244	K562	blood:	n/a	n/a
29	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
30	CEBPB	chr19:41488440-41489019	H1-hESC	embryonic stem cell:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
31	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
32	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
33	CEBPD	chr19:41458422-41458815	K562	blood:	n/a	n/a
34	CHD2	chr19:41465957-41466157	K562	blood:	n/a	n/a
35	CREB1	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr19:41468563-41468752	A549	lung:	n/a	n/a
37	CTCF	chr19:41447302-41447411	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr19:41439023-41439241	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr19:41480500-41480650	AG04450	lung:	n/a	n/a
40	CTCF	chr19:41480526-41480842	GM13977	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
41	CTCF	chr19:41480533-41480776	GM12891	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
42	CTCF	chr19:41438972-41439283	K562	blood:	n/a	n/a
43	CTCF	chr19:41450720-41450870	A549	lung:	n/a	chr19:41450789-41450799 chr19:41450784-41450802 chr19:41450787-41450800
44	CTCF	chr19:41480580-41480730	GM12878	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
45	CTCF	chr19:41480498-41480741	SK-N-SH_RA	brain:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
46	CTCF	chr19:41438960-41439110	GM12865	blood:	n/a	n/a
47	CTCF	chr19:41480507-41480786	HUVEC	blood vessel:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
48	CTCF	chr19:41439091-41439167	Fibrobl	skin:	n/a	n/a
49	CTCF	chr19:41439140-41439290	NHEK	skin:	n/a	n/a
50	CTCF	chr19:41480760-41480910	WERI-Rb-1	eye:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41496043-41496093	GM12892	blood:	n/a
2	chr19:41496749-41496799	SKMC	muscle:	n/a
3	chr19:41496749-41496799	U87	brain:	n/a
4	chr19:41496749-41496799	ECC-1	luminal epithelium:	n/a
5	chr19:41496749-41496799	HRCEpiC	kidney:	n/a
6	chr19:41495942-41495992	SAEC	small airway:	n/a
7	chr19:41497222-41497272	NB4	blood:	n/a
8	chr19:41496749-41496799	ProgFib	skin:	n/a
9	chr19:41495942-41495992	PrEC	prostate:	n/a
10	chr19:41495942-41495992	HMEC	breast:	n/a
11	chr19:41497222-41497272	HRE	kidney:	n/a
12	chr19:41496043-41496093	HIPEpiC	eye:	n/a
13	chr19:41497222-41497272	HCM	heart:	n/a
14	chr19:41497222-41497272	Jurkat	blood:	n/a
15	chr19:41496749-41496799	HCPEpiC	choroid plexus:	n/a
16	chr19:41495942-41495992	U87	brain:	n/a
17	chr19:41497222-41497272	HUVEC	blood vessel:	n/a
18	chr19:41497222-41497272	AoSMC	blood vessel:	n/a
19	chr19:41496043-41496093	LNCaP	prostate:	n/a
20	chr19:41497222-41497272	HCF	heart:	n/a
21	chr19:41495942-41495992	HUVEC	blood vessel:	n/a
22	chr19:41496749-41496799	AG04450	lung:	fetal
23	chr19:41496749-41496799	IMR90	lung:	fetal
24	chr19:41495942-41495992	AG09319	gingival:	n/a
25	chr19:41496043-41496093	HCT-116	colon:	n/a
26	chr19:41496043-41496093	MCF-7	breast:	n/a
27	chr19:41496749-41496799	HCM	heart:	n/a
28	chr19:41496749-41496799	CMK	blood:	n/a
29	chr19:41497222-41497272	HIPEpiC	eye:	n/a
30	chr19:41496043-41496093	Hela-S3	cervix:	n/a
31	chr19:41496749-41496799	GM12892	blood:	n/a
32	chr19:41497222-41497272	HPAEpiC	pulmonary alveolar:	n/a
33	chr19:41496043-41496093	GM06990	blood:	n/a
34	chr19:41495942-41495992	NHBE	bronchial:	n/a
35	chr19:41497222-41497272	GM12892	blood:	n/a
36	chr19:41495942-41495992	GM12892	blood:	n/a
37	chr19:41497222-41497272	IMR90	lung:	fetal
38	chr19:41496043-41496093	HL-60	blood:	n/a
39	chr19:41495942-41495992	AG04449	skin:	fetal
40	chr19:41495942-41495992	IMR90	lung:	fetal
41	chr19:41495942-41495992	K562	blood:	n/a
42	chr19:41496043-41496093	PANC-1	pancreas:	n/a
43	chr19:41497222-41497272	MCF10A-Er-Src	breast:	n/a
44	chr19:41496043-41496093	NH-A	brain:	n/a
45	chr19:41497222-41497272	Hela-S3	cervix:	n/a
46	chr19:41496749-41496799	Hela-S3	cervix:	n/a
47	chr19:41496043-41496093	ECC-1	luminal epithelium:	n/a
48	chr19:41496043-41496093	U87	brain:	n/a
49	chr19:41496043-41496093	GM12878	blood:	n/a
50	chr19:41495942-41495992	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
2	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
3	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
4	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
5	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
6	chr19:41429883..41432599-chr19:41435321..41438137,2	MCF-7	breast:
7	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
8	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
9	chr19:41435849..41437489-chr19:41440022..41442246,2	MCF-7	breast:
10	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
11	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
12	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
13	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
14	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
15	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
16	chr19:41438993..41440711-chr19:41442295..41445002,2	MCF-7	breast:
17	chr19:41435849..41437489-chr19:41440022..41442246,2	MCF-7	breast:
18	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
19	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
20	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
21	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
22	chr19:41438993..41440711-chr19:41442295..41445002,2	MCF-7	breast:
23	chr19:41444451..41445965-chr19:41446160..41448128,2	MCF-7	breast:

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

Variant related genes	Relation type
CYP2B6	TF binding region
ENSG00000269353	TF binding region
CYP2B7P	TF binding region
CYP2B6	CpG island
ENSG00000269353	CpG island
CYP2B7P	CpG island
ENSG00000256612	chromatin interactions

Extended variants
information (count: 2586 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2586 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566345002	chr19:41436066-41436067	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536558297	chr19:41436068-41436069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs554919510	chr19:41436105-41436106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187101393	chr19:41436144-41436145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537501457	chr19:41436200-41436201	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs67301696	chr19:41436216-41436217	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs199654897	chr19:41436228-41436229	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116523176	chr19:41436267-41436268	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191564458	chr19:41436326-41436327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541206830	chr19:41436382-41436383	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184408030	chr19:41436398-41436399	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536788287	chr19:41436428-41436429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs574643087	chr19:41436479-41436480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs541782942	chr19:41436490-41436491	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141115441	chr19:41436540-41436541	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs1820025	chr19:41436546-41436547	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs34207755	chr19:41436569-41436570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536692549	chr19:41436577-41436578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369797583	chr19:41436599-41436600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551798925	chr19:41436619-41436620	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs150274956	chr19:41436672-41436673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs528203528	chr19:41436712-41436713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547935338	chr19:41436727-41436728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566162072	chr19:41436734-41436735	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs536902602	chr19:41436739-41436740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12459233	chr19:41436785-41436786	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs77573739	chr19:41436814-41436815	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566863631	chr19:41436817-41436818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs143215384	chr19:41436820-41436821	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs147481109	chr19:41436845-41436846	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534824882	chr19:41436881-41436882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs553106449	chr19:41436960-41436961	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189291945	chr19:41436985-41436986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs193099296	chr19:41436997-41436998	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185880518	chr19:41437010-41437011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs190353143	chr19:41437029-41437030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs181710516	chr19:41437035-41437036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs542070229	chr19:41437065-41437066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs556831506	chr19:41437102-41437103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575187262	chr19:41437137-41437138	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545376061	chr19:41437176-41437177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs534253240	chr19:41437253-41437254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs186010610	chr19:41437369-41437370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7248187	chr19:41437426-41437427	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs539953939	chr19:41437428-41437429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs7247910	chr19:41437440-41437441	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs77043975	chr19:41437454-41437455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538429036	chr19:41437455-41437456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556862272	chr19:41437472-41437473	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs114675593	chr19:41437495-41437496	Weak transcription	Chromatin interactive region	1 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	17431168	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:265 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41432200-41447600	Weak transcription	Liver	Liver
2	chr19:41433000-41437800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr19:41434800-41436200	Enhancers	Fetal Intestine Large	intestine
4	chr19:41435400-41436200	Enhancers	Fetal Intestine Small	intestine
5	chr19:41436000-41437600	Weak transcription	K562	blood
6	chr19:41436200-41436600	Weak transcription	Fetal Intestine Small	intestine
7	chr19:41436200-41437800	Weak transcription	Fetal Intestine Large	intestine
8	chr19:41436600-41437000	Strong transcription	Fetal Intestine Small	intestine
9	chr19:41437000-41437800	Weak transcription	Fetal Intestine Small	intestine
10	chr19:41437600-41438000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr19:41437600-41439800	Enhancers	K562	blood
12	chr19:41437800-41438000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr19:41437800-41438000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr19:41437800-41438200	Genic enhancers	Fetal Intestine Small	intestine
15	chr19:41437800-41438600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr19:41437800-41438800	Enhancers	Fetal Intestine Large	intestine
17	chr19:41438000-41439400	Bivalent Enhancer	A549	lung
18	chr19:41438200-41438400	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr19:41438200-41438600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr19:41438200-41442000	Weak transcription	Fetal Intestine Small	intestine
21	chr19:41438400-41438800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr19:41438400-41439000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr19:41438400-41439000	Enhancers	Placenta	Placenta
24	chr19:41438600-41439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr19:41438600-41439600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chr19:41438800-41444000	Weak transcription	Fetal Intestine Large	intestine
27	chr19:41439000-41439200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:41439000-41439200	Enhancers	Stomach Mucosa	stomach
29	chr19:41439000-41439800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr19:41439200-41447800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr19:41439200-41448000	Weak transcription	Stomach Mucosa	stomach
32	chr19:41439600-41439800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chr19:41439800-41441600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr19:41440600-41442400	Weak transcription	Lung	lung
35	chr19:41441600-41441800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr19:41442000-41442400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr19:41442000-41445400	Strong transcription	Fetal Intestine Small	intestine
38	chr19:41442400-41442600	Strong transcription	Lung	lung
39	chr19:41442400-41451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr19:41442600-41442800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
41	chr19:41442600-41450200	Weak transcription	Lung	lung
42	chr19:41444000-41444800	Strong transcription	Fetal Intestine Large	intestine
43	chr19:41444400-41445400	Bivalent Enhancer	A549	lung
44	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
45	chr19:41445400-41450200	Weak transcription	Fetal Intestine Small	intestine
46	chr19:41445800-41449200	Enhancers	HUVEC	blood vessel
47	chr19:41446400-41446600	Enhancers	A549	lung
48	chr19:41446600-41446800	Flanking Active TSS	A549	lung
49	chr19:41446800-41447200	Enhancers	A549	lung
50	chr19:41447200-41447600	Bivalent Enhancer	A549	lung

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