Variant report

Variant	nsv579594
Chromosome Location	chr19:41442165-41494891
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	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
6	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
7	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
8	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
9	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
10	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
11	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
12	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
13	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
14	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
15	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
16	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
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	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
19	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
20	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
21	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
22	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
23	CEBPB	chr19:41446714-41446729	A549	lung:	n/a	n/a
24	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
25	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
26	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
27	CEBPD	chr19:41458422-41458815	K562	blood:	n/a	n/a
28	CHD2	chr19:41465957-41466157	K562	blood:	n/a	n/a
29	CREB1	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr19:41468563-41468752	A549	lung:	n/a	n/a
31	CTCF	chr19:41480600-41480750	HA-sp	spinal cord:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
32	CTCF	chr19:41480536-41480765	MCF-7	breast:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
33	CTCF	chr19:41487408-41487461	Kidney_OC	kidney:	n/a	n/a
34	CTCF	chr19:41447302-41447411	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr19:41480476-41480870	K562	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
36	CTCF	chr19:41480530-41480795	ProgFib	skin:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
37	CTCF	chr19:41480532-41480780	GM12892	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
38	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
39	CTCF	chr19:41447051-41447156	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr19:41480500-41480650	AG04450	lung:	n/a	n/a
41	CTCF	chr19:41480252-41480373	GM13977	blood:	n/a	n/a
42	CTCF	chr19:41480520-41480670	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
43	CTCF	chr19:41480560-41480710	AG10803	skin:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
44	CTCF	chr19:41480484-41480723	T-47D	breast:	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	chr19:41480560-41480710	MCF-7	breast:	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	chr19:41448093-41448122	GM13976	blood:	n/a	n/a
47	CTCF	chr19:41480700-41480850	HAc	cerebellar:	n/a	n/a
48	CTCF	chr19:41480530-41480777	MCF-7	breast:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
49	CTCF	chr19:41480560-41480710	GM12871	blood:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660
50	CTCF	chr19:41480517-41480847	MCF-7	breast:	n/a	chr19:41480643-41480659 chr19:41480644-41480665 chr19:41480645-41480658 chr19:41480645-41480658 chr19:41480647-41480657 chr19:41480645-41480654 chr19:41480642-41480660

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

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

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

Extended variants
information (count: 1957 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11665968	chr19:41442165-41442166	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs200953890	chr19:41442177-41442178	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs570124237	chr19:41442195-41442196	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs547776425	chr19:41442198-41442199	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs536024440	chr19:41442212-41442213	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149353824	chr19:41442229-41442230	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576979675	chr19:41442244-41442245	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs193186967	chr19:41442257-41442258	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552970259	chr19:41442273-41442274	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs185074724	chr19:41442278-41442279	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541414453	chr19:41442299-41442300	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113495956	chr19:41442321-41442322	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35161018	chr19:41442325-41442326	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530473733	chr19:41442337-41442338	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545512651	chr19:41442339-41442340	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564244509	chr19:41442350-41442351	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3745219	chr19:41442352-41442353	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs189922535	chr19:41442380-41442381	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540810366	chr19:41442383-41442384	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs566233519	chr19:41442394-41442395	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530427332	chr19:41442396-41442397	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144596795	chr19:41442406-41442407	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs181138657	chr19:41442409-41442410	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199919635	chr19:41442430-41442431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533825918	chr19:41442434-41442435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558766334	chr19:41442450-41442451	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570950600	chr19:41442452-41442453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183648722	chr19:41442462-41442463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73038469	chr19:41442597-41442598	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs574349077	chr19:41442600-41442601	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs541722294	chr19:41442623-41442624	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs556507444	chr19:41442733-41442734	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs139457050	chr19:41442766-41442767	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs187963717	chr19:41442782-41442783	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs180823734	chr19:41442786-41442787	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs144084665	chr19:41442831-41442832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186422056	chr19:41442881-41442882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146009814	chr19:41442882-41442883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139926669	chr19:41442915-41442916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548914970	chr19:41442966-41442967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs564005117	chr19:41443019-41443020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs530904298	chr19:41443036-41443037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552586364	chr19:41443071-41443072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs544298976	chr19:41443095-41443096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs570845785	chr19:41443127-41443128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535126839	chr19:41443145-41443146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546428081	chr19:41443146-41443147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567933458	chr19:41443150-41443151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556814199	chr19:41443151-41443152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4803406	chr19:41443170-41443171	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41432200-41447600	Weak transcription	Liver	Liver
2	chr19:41438800-41444000	Weak transcription	Fetal Intestine Large	intestine
3	chr19:41439200-41447800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:41439200-41448000	Weak transcription	Stomach Mucosa	stomach
5	chr19:41440600-41442400	Weak transcription	Lung	lung
6	chr19:41442000-41442400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:41442000-41445400	Strong transcription	Fetal Intestine Small	intestine
8	chr19:41442400-41442600	Strong transcription	Lung	lung
9	chr19:41442400-41451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr19:41442600-41442800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
11	chr19:41442600-41450200	Weak transcription	Lung	lung
12	chr19:41444000-41444800	Strong transcription	Fetal Intestine Large	intestine
13	chr19:41444400-41445400	Bivalent Enhancer	A549	lung
14	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
15	chr19:41445400-41450200	Weak transcription	Fetal Intestine Small	intestine
16	chr19:41445800-41449200	Enhancers	HUVEC	blood vessel
17	chr19:41446400-41446600	Enhancers	A549	lung
18	chr19:41446600-41446800	Flanking Active TSS	A549	lung
19	chr19:41446800-41447200	Enhancers	A549	lung
20	chr19:41447200-41447600	Bivalent Enhancer	A549	lung
21	chr19:41447400-41448000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr19:41447600-41447800	Flanking Bivalent TSS/Enh	A549	lung
23	chr19:41447600-41448200	Strong transcription	Liver	Liver
24	chr19:41447800-41448200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr19:41447800-41448200	Bivalent Enhancer	A549	lung
26	chr19:41447800-41448200	Bivalent Enhancer	K562	blood
27	chr19:41448200-41449600	Weak transcription	Liver	Liver
28	chr19:41449600-41451800	Strong transcription	Liver	Liver
29	chr19:41450200-41450400	Bivalent Enhancer	Esophagus	oesophagus
30	chr19:41450200-41450600	ZNF genes & repeats	Lung	lung
31	chr19:41450200-41450800	Strong transcription	Fetal Intestine Small	intestine
32	chr19:41450800-41451800	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr19:41451400-41451800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:41451400-41452200	Flanking Active TSS	K562	blood
35	chr19:41451800-41452200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr19:41451800-41455200	Weak transcription	Liver	Liver
37	chr19:41451800-41456200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr19:41451800-41456200	Weak transcription	Fetal Intestine Small	intestine
39	chr19:41452200-41452400	Enhancers	K562	blood
40	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
41	chr19:41456200-41456400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
43	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
44	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
46	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
47	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
48	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
49	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
50	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell

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