Variant report

Variant	nsv912098
Chromosome Location	chr19:43629573-43806559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2377)
CpG islands
(count:1283)
Chromatin interactive
region (count:4)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2377 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr19:43733581-43733686	K562	blood:	n/a	n/a
2	ATF1	chr19:43779068-43779071	K562	blood:	n/a	n/a
3	ATF3	chr19:43686016-43686763	A549	lung:	n/a	n/a
4	BATF	chr19:43738081-43738296	GM12878	blood:	n/a	chr19:43738185-43738196
5	BATF	chr19:43711409-43711658	GM12878	blood:	n/a	n/a
6	BATF	chr19:43775309-43775522	GM12878	blood:	n/a	n/a
7	BATF	chr19:43692257-43692526	GM12878	blood:	n/a	n/a
8	BATF	chr19:43692397-43692675	GM12878	blood:	n/a	n/a
9	BATF	chr19:43798559-43798850	GM12878	blood:	n/a	chr19:43798663-43798674
10	BHLHE40	chr19:43733601-43733620	K562	blood:	n/a	n/a
11	BHLHE40	chr19:43709323-43709343	K562	blood:	n/a	n/a
12	BRCA1	chr19:43769426-43769782	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr19:43775261-43775711	HCT-116	colon:	n/a	n/a
14	CBX3	chr19:43775276-43775644	K562	blood:	n/a	n/a
15	CEBPB	chr19:43709791-43709942	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr19:43656390-43656701	K562	blood:	n/a	chr19:43656521-43656532
17	CEBPB	chr19:43668229-43668245	IMR90	lung:	n/a	n/a
18	CEBPB	chr19:43705107-43705824	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr19:43656448-43656689	HepG2	liver:	n/a	chr19:43656521-43656532
20	CEBPB	chr19:43759754-43759856	K562	blood:	n/a	n/a
21	CEBPB	chr19:43769050-43769817	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr19:43675341-43675474	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr19:43728619-43728662	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:43656349-43656822	Hela-S3	cervix:	n/a	chr19:43656521-43656532
25	CEBPB	chr19:43685985-43686627	IMR90	lung:	n/a	n/a
26	CEBPB	chr19:43686079-43686251	A549	lung:	n/a	n/a
27	CEBPB	chr19:43656366-43656852	IMR90	lung:	n/a	chr19:43656521-43656532
28	CEBPB	chr19:43676596-43676779	K562	blood:	n/a	n/a
29	CEBPB	chr19:43768999-43769727	IMR90	lung:	n/a	n/a
30	CEBPB	chr19:43685962-43686735	A549	lung:	n/a	n/a
31	CEBPB	chr19:43686010-43686301	A549	lung:	n/a	n/a
32	CEBPB	chr19:43705598-43705699	IMR90	lung:	n/a	n/a
33	CEBPB	chr19:43705122-43705386	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:43634604-43634632	HepG2	liver:	n/a	chr19:43634618-43634629 chr19:43634616-43634629 chr19:43634616-43634629 chr19:43634616-43634627
35	CEBPB	chr19:43790251-43790803	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr19:43656430-43656683	A549	lung:	n/a	chr19:43656521-43656532
37	CEBPB	chr19:43653804-43654163	IMR90	lung:	n/a	n/a
38	CEBPB	chr19:43786125-43786327	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr19:43685985-43686805	Hela-S3	cervix:	n/a	n/a
40	CHD1	chr19:43778774-43779172	IMR90	lung:	n/a	n/a
41	CHD2	chr19:43769435-43769730	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr19:43790318-43790669	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr19:43733578-43733669	A549	lung:	n/a	n/a
44	CTCF	chr19:43692252-43692429	SK-N-SH_RA	brain:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
45	CTCF	chr19:43706340-43706490	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr19:43766717-43767153	A549	lung:	n/a	chr19:43766866-43766879 chr19:43766865-43766886
47	CTCF	chr19:43775380-43775530	GM12864	blood:	n/a	chr19:43775423-43775439 chr19:43775417-43775438 chr19:43775422-43775440 chr19:43775425-43775435 chr19:43775428-43775437
48	CTCF	chr19:43692240-43692390	K562	blood:	n/a	chr19:43692365-43692386 chr19:43692376-43692385 chr19:43692370-43692388
49	CTCF	chr19:43683920-43684070	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr19:43793160-43793310	HCT-116	colon:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:43691930-43691980	K562	blood:	n/a
2	chr19:43709754-43709804	K562	blood:	n/a
3	chr19:43691930-43691980	K562	blood:	n/a
4	chr19:43709754-43709804	K562	blood:	n/a
5	chr19:43683698-43683748	SK-N-SH	brain:	n/a
6	chr19:43683698-43683748	HEEpiC	esophagus:	n/a
7	chr19:43769725-43769775	HEK293	kidney:	embryo
8	chr19:43710277-43710327	HMEC	breast:	n/a
9	chr19:43769725-43769775	AG10803	skin:	n/a
10	chr19:43710277-43710327	MCF10A-Er-Src	breast:	n/a
11	chr19:43697480-43697530	GM12878	blood:	n/a
12	chr19:43683698-43683748	HRCEpiC	kidney:	n/a
13	chr19:43690622-43690672	HMEC	breast:	n/a
14	chr19:43709360-43709410	IMR90	lung:	fetal
15	chr19:43690622-43690672	NB4	blood:	n/a
16	chr19:43691878-43691928	Hepatocyte	liver:	n/a
17	chr19:43710277-43710327	AG04450	lung:	fetal
18	chr19:43709360-43709410	HCPEpiC	choroid plexus:	n/a
19	chr19:43710277-43710327	U87	brain:	n/a
20	chr19:43774921-43774971	Caco-2	colon:	n/a
21	chr19:43711064-43711114	AG04450	lung:	fetal
22	chr19:43774982-43775032	HUVEC	blood vessel:	n/a
23	chr19:43709754-43709804	AG04449	skin:	fetal
24	chr19:43774921-43774971	HCT-116	colon:	n/a
25	chr19:43710277-43710327	RPTEC	kidney:	n/a
26	chr19:43683698-43683748	NB4	blood:	n/a
27	chr19:43709654-43709704	NB4	blood:	n/a
28	chr19:43691878-43691928	HRPEpiC	eye:	n/a
29	chr19:43691878-43691928	AoSMC	blood vessel:	n/a
30	chr19:43774982-43775032	SK-N-SH_RA	brain:	n/a
31	chr19:43709754-43709804	Hepatocyte	liver:	n/a
32	chr19:43709654-43709704	NHBE	bronchial:	n/a
33	chr19:43774921-43774971	U87	brain:	n/a
34	chr19:43774820-43774870	IMR90	lung:	fetal
35	chr19:43690996-43691046	GM06990	blood:	n/a
36	chr19:43683698-43683748	U87	brain:	n/a
37	chr19:43691878-43691928	U87	brain:	n/a
38	chr19:43774982-43775032	IMR90	lung:	fetal
39	chr19:43690996-43691046	H1-hESC	embryonic stem cell:	embryo
40	chr19:43709654-43709704	IMR90	lung:	fetal
41	chr19:43709832-43709882	HCF	heart:	n/a
42	chr19:43774820-43774870	NT2-D1	testis:	n/a
43	chr19:43711249-43711299	HL-60	blood:	n/a
44	chr19:43774893-43774943	HNPCEpiC	eye:	n/a
45	chr19:43691930-43691980	NT2-D1	testis:	n/a
46	chr19:43711064-43711114	NHBE	bronchial:	n/a
47	chr19:43774982-43775032	AG09309	skin:	n/a
48	chr19:43774982-43775032	ovcar-3	ovarian:	n/a
49	chr19:43774820-43774870	K562	blood:	n/a
50	chr19:43690622-43690672	AG10803	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
2	chr19:43265768..43266290-chr19:43769932..43770473,2	MCF-7	breast:
3	chr19:43801843..43804269-chr19:43806143..43807885,2	MCF-7	breast:
4	chr19:43678340..43681333-chr19:43698109..43700078,2	MCF-7	breast:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSG4-2	chr19:43688934-43689087	NONHSAT066587
2	lnc-CD177-1	chr19:43657665-43657763	ENSG00000227606.1
3	lnc-PSG9-2	chr19:43724783-43725023	NONHSAT066593
4	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066591
5	lnc-PSG9-2	chr19:43719405-43719531	NONHSAT066591
6	lnc-PSG4-3	chr19:43674207-43674717	NONHSAT066586
7	lnc-CD177-1	chr19:43657431-43657763	ENSG00000227606.1
8	lnc-PSG9-2	chr19:43752643-43752798	NONHSAT066591
9	lnc-PSG4-1	chr19:43710321-43711451	NONHSAT066590
10	lnc-CD177-1	chr19:43659324-43659477	ENSG00000227606.1
11	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066591
12	lnc-PSG4-2	chr19:43684499-43684748	NONHSAT066587
13	lnc-PSG4-3	chr19:43674207-43674723	NONHSAT066585
14	lnc-PSG5-1	chr19:43698107-43698746	NONHSAT066589
15	lnc-PSG9-2	chr19:43752160-43752275	NONHSAT066591
16	lnc-PSG9-2	chr19:43715943-43716627	NONHSAT066592
17	lnc-PSG9-2	chr19:43734076-43734177	NONHSAT066591
18	lnc-PSG4-3	chr19:43672274-43672355	NONHSAT066586
19	lnc-PSG9-2	chr19:43737376-43737446	NONHSAT066591
20	lnc-PSG9-2	chr19:43728324-43728464	NONHSAT066591
21	lnc-CD177-1	chr19:43665002-43665014	ENSG00000227606.1
22	lnc-CD177-1	chr19:43658863-43659311	ENSG00000227606.1
23	lnc-PSG9-2	chr19:43763009-43764898	NONHSAT066592
24	lnc-PSG4-3	chr19:43671924-43672287	NONHSAT066585
25	lnc-PSG5-1	chr19:43699147-43699301	NONHSAT066589
26	lnc-PSG9-2	chr19:43727043-43727110	NONHSAT066591
27	lnc-PSG5-1	chr19:43698492-43699038	NONHSAT066588
28	lnc-PSG5-1	chr19:43696890-43697540	NONHSAT066588
29	lnc-PSG4-1	chr19:43707241-43708403	NONHSAT066590
30	lnc-PSG9-2	chr19:43762354-43762608	NONHSAT066592
31	lnc-PSG9-2	chr19:43724140-43724394	NONHSAT066593

No data

Variant related genes	Relation type
PSG5	TF binding region
CEACAMP10	TF binding region
PSG9	TF binding region
PSG4	TF binding region
CEACAMP11	TF binding region
ENSG00000227606	TF binding region
PSG5	CpG island
CEACAMP10	CpG island
PSG9	CpG island
PSG4	CpG island
CEACAMP11	CpG island
ENSG00000227606	CpG island
ENSG00000243137	chromatin interactions

Extended variants
information (count: 8479 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:8479 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2354285	chr19:43629573-43629574	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs578102445	chr19:43629575-43629576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs185920792	chr19:43629576-43629577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs191169627	chr19:43629577-43629578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181204769	chr19:43629607-43629608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562481719	chr19:43629631-43629632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548348688	chr19:43629645-43629646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369390572	chr19:43629647-43629648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs2883407	chr19:43629658-43629659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs530528642	chr19:43629678-43629679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs3085826	chr19:43629696-43629697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs373703721	chr19:43629697-43629698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58844181	chr19:43629702-43629703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2354284	chr19:43629717-43629718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs550819660	chr19:43629732-43629733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570678740	chr19:43629745-43629746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533287899	chr19:43629764-43629765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113343959	chr19:43629773-43629774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566943225	chr19:43629774-43629775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535551129	chr19:43629778-43629779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs186657424	chr19:43629814-43629815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568872743	chr19:43629815-43629816	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150153658	chr19:43629822-43629823	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138585187	chr19:43629827-43629828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs578175655	chr19:43629829-43629830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540962000	chr19:43629901-43629902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs35916359	chr19:43629962-43629963	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs36042335	chr19:43629966-43629967	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs541903429	chr19:43629991-43629992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372057136	chr19:43629998-43629999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561780545	chr19:43630030-43630031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530492075	chr19:43630038-43630039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs376401120	chr19:43630059-43630060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs567645885	chr19:43630068-43630069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182925905	chr19:43630095-43630096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34706657	chr19:43630096-43630097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs59375866	chr19:43630117-43630118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs564146299	chr19:43630122-43630123	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs62114360	chr19:43630123-43630124	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs186085456	chr19:43630124-43630125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs566284520	chr19:43630146-43630147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs75745198	chr19:43630161-43630162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529064839	chr19:43630162-43630163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373343814	chr19:43630174-43630175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs137980932	chr19:43630279-43630280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143432319	chr19:43630282-43630283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200558125	chr19:43630299-43630300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190867892	chr19:43630309-43630310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184199794	chr19:43630310-43630311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs537983102	chr19:43630312-43630313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Astrocytoma	22246337	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	21509527	CNVD
Cancer	20164920	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	20800559	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Spondylocostal dysostosis	21085971	CNVD
Nicotine metabolism	21956041	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	20459617	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:543 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:43625200-43629600	Weak transcription	Osteobl	bone
2	chr19:43625200-43630800	Weak transcription	NHLF	lung
3	chr19:43625200-43631000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr19:43625400-43630800	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr19:43626200-43630200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr19:43626200-43630800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr19:43626200-43631000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr19:43627000-43630800	Weak transcription	NHDF-Ad	bronchial
9	chr19:43627800-43636000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr19:43628000-43630800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr19:43628400-43630000	Enhancers	Placenta	Placenta
12	chr19:43628800-43630800	Weak transcription	HMEC	breast
13	chr19:43629000-43630000	Weak transcription	NHEK	skin
14	chr19:43629400-43630800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr19:43629600-43630200	Enhancers	Osteobl	bone
16	chr19:43630000-43631400	Weak transcription	Placenta	Placenta
17	chr19:43630000-43633600	Enhancers	NHEK	skin
18	chr19:43630200-43630600	Weak transcription	Osteobl	bone
19	chr19:43630200-43636000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr19:43630600-43632600	Enhancers	Osteobl	bone
21	chr19:43630800-43631000	Enhancers	A549	lung
22	chr19:43630800-43631600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr19:43630800-43632200	Enhancers	NH-A	brain
24	chr19:43630800-43632400	Enhancers	Muscle Satellite Cultured Cells	--
25	chr19:43630800-43632600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr19:43630800-43632800	Enhancers	NHLF	lung
27	chr19:43630800-43633200	Enhancers	NHDF-Ad	bronchial
28	chr19:43630800-43636000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr19:43630800-43636200	Enhancers	HMEC	breast
30	chr19:43631000-43631200	Flanking Active TSS	A549	lung
31	chr19:43631000-43631800	Enhancers	Colon Smooth Muscle	Colon
32	chr19:43631000-43632000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr19:43631000-43632200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr19:43631000-43632200	Enhancers	HSMM	muscle
35	chr19:43631000-43632400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr19:43631000-43632600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr19:43631200-43631600	Enhancers	A549	lung
38	chr19:43631400-43631800	Enhancers	Placenta	Placenta
39	chr19:43631400-43632000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr19:43631400-43632000	Enhancers	Rectal Smooth Muscle	rectum
41	chr19:43631600-43632000	Flanking Active TSS	A549	lung
42	chr19:43631600-43637000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr19:43631800-43633000	Weak transcription	Placenta	Placenta
44	chr19:43632000-43632800	Enhancers	A549	lung
45	chr19:43632200-43636600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr19:43632400-43634000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr19:43632600-43633600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr19:43633200-43636800	Weak transcription	NHDF-Ad	bronchial
49	chr19:43633400-43633600	Enhancers	Placenta	Placenta
50	chr19:43633600-43633800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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