Variant report

Variant	nsv458571
Chromosome Location	chr19:39533754-39628050
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2287)
CpG islands
(count:1769)
Chromatin interactive
region (count:117)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2287 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:39557823-39558068	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:39616027-39616841	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:39617086-39617620	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:39612764-39612975	HepG2	liver:	n/a	n/a
5	ARID3A	chr19:39544497-39544615	HepG2	liver:	n/a	n/a
6	ATF1	chr19:39536758-39537053	K562	blood:	n/a	n/a
7	ATF2	chr19:39552082-39552557	GM12878	blood:	n/a	n/a
8	ATF2	chr19:39615987-39616329	GM12878	blood:	n/a	n/a
9	ATF3	chr19:39550881-39551248	K562	blood:	n/a	n/a
10	ATF3	chr19:39542833-39543390	A549	lung:	n/a	n/a
11	ATF3	chr19:39568916-39569709	A549	lung:	n/a	n/a
12	ATF3	chr19:39602847-39603476	A549	lung:	n/a	n/a
13	ATF3	chr19:39564200-39565314	A549	lung:	n/a	n/a
14	ATF3	chr19:39617023-39618100	A549	lung:	n/a	n/a
15	ATF3	chr19:39542898-39543549	A549	lung:	n/a	n/a
16	ATF3	chr19:39615698-39617005	A549	lung:	n/a	chr19:39616633-39616642
17	ATF3	chr19:39616005-39616771	A549	lung:	n/a	chr19:39616633-39616642
18	ATF3	chr19:39602734-39603546	A549	lung:	n/a	n/a
19	ATF3	chr19:39612563-39613247	A549	lung:	n/a	n/a
20	ATF3	chr19:39568971-39569949	A549	lung:	n/a	n/a
21	BATF	chr19:39552202-39552488	GM12878	blood:	n/a	n/a
22	BCL3	chr19:39612541-39613262	A549	lung:	n/a	n/a
23	BCL3	chr19:39564121-39565373	A549	lung:	n/a	n/a
24	BCL3	chr19:39617065-39617970	A549	lung:	n/a	n/a
25	BCL3	chr19:39552169-39552423	GM12878	blood:	n/a	n/a
26	BCL3	chr19:39616160-39616731	GM12878	blood:	n/a	chr19:39616415-39616424 chr19:39616629-39616642 chr19:39616461-39616470 chr19:39616637-39616650
27	BCL3	chr19:39602117-39603563	A549	lung:	n/a	n/a
28	BCL3	chr19:39568818-39569790	A549	lung:	n/a	n/a
29	BCL3	chr19:39602096-39603547	A549	lung:	n/a	n/a
30	BCL3	chr19:39615789-39618162	A549	lung:	n/a	chr19:39616415-39616424 chr19:39616629-39616642 chr19:39616461-39616470 chr19:39616637-39616650
31	BCL3	chr19:39615759-39617029	A549	lung:	n/a	chr19:39616415-39616424 chr19:39616629-39616642 chr19:39616461-39616470 chr19:39616637-39616650
32	BCL3	chr19:39542804-39543617	A549	lung:	n/a	n/a
33	BCLAF1	chr19:39552172-39552449	GM12878	blood:	n/a	n/a
34	BHLHE40	chr19:39542967-39543235	A549	lung:	n/a	n/a
35	BHLHE40	chr19:39544349-39544740	HepG2	liver:	n/a	n/a
36	BHLHE40	chr19:39601098-39601263	GM12878	blood:	n/a	n/a
37	BHLHE40	chr19:39536675-39536858	K562	blood:	n/a	n/a
38	BHLHE40	chr19:39612765-39612996	GM12878	blood:	n/a	n/a
39	BHLHE40	chr19:39543041-39543117	K562	blood:	n/a	n/a
40	BHLHE40	chr19:39599854-39599991	K562	blood:	n/a	n/a
41	BHLHE40	chr19:39564402-39564602	A549	lung:	n/a	n/a
42	BHLHE40	chr19:39601128-39601308	K562	blood:	n/a	n/a
43	BHLHE40	chr19:39616100-39616440	K562	blood:	n/a	n/a
44	BRCA1	chr19:39616491-39616668	HepG2	liver:	n/a	n/a
45	BRCA1	chr19:39542979-39543093	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr19:39602961-39603400	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr19:39615895-39616576	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr19:39612655-39613026	K562	blood:	n/a	n/a
49	CBX3	chr19:39615813-39616257	K562	blood:	n/a	n/a
50	CBX3	chr19:39615737-39616570	K562	blood:	n/a	n/a

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:39616476-39616526	AG09319	gingival:	n/a
2	chr19:39616476-39616526	HEEpiC	esophagus:	n/a
3	chr19:39600974-39601024	GM12892	blood:	n/a
4	chr19:39574712-39574762	NH-A	brain:	n/a
5	chr19:39574911-39574961	AG10803	skin:	n/a
6	chr19:39574878-39574928	BJ	skin:	n/a
7	chr19:39574712-39574762	GM19239	blood:	n/a
8	chr19:39616217-39616267	HMEC	breast:	n/a
9	chr19:39572000-39572050	A549	lung:	n/a
10	chr19:39616818-39616868	GM12891	blood:	n/a
11	chr19:39612741-39612791	GM06990	blood:	n/a
12	chr19:39574712-39574762	AG10803	skin:	n/a
13	chr19:39574513-39574563	SK-N-SH_RA	brain:	n/a
14	chr19:39575027-39575077	BJ	skin:	n/a
15	chr19:39616233-39616283	HAEpiC	amniotic membrane:	n/a
16	chr19:39620117-39620167	PANC-1	pancreas:	n/a
17	chr19:39574911-39574961	MCF-7	breast:	n/a
18	chr19:39575027-39575077	HCF	heart:	n/a
19	chr19:39618272-39618322	NT2-D1	testis:	n/a
20	chr19:39618272-39618322	U87	brain:	n/a
21	chr19:39572000-39572050	NHBE	bronchial:	n/a
22	chr19:39575027-39575077	GM12878	blood:	n/a
23	chr19:39616336-39616386	HCPEpiC	choroid plexus:	n/a
24	chr19:39575027-39575077	SK-N-SH_RA	brain:	n/a
25	chr19:39574483-39574533	HCF	heart:	n/a
26	chr19:39616296-39616346	ECC-1	luminal epithelium:	n/a
27	chr19:39574751-39574801	AG09309	skin:	n/a
28	chr19:39616296-39616346	PANC-1	pancreas:	n/a
29	chr19:39574483-39574533	BJ	skin:	n/a
30	chr19:39574765-39574815	NHBE	bronchial:	n/a
31	chr19:39574483-39574533	GM06990	blood:	n/a
32	chr19:39618272-39618322	PrEC	prostate:	n/a
33	chr19:39575027-39575077	HepG2	liver:	n/a
34	chr19:39600974-39601024	NT2-D1	testis:	n/a
35	chr19:39616041-39616091	SKMC	muscle:	n/a
36	chr19:39574186-39574236	SKMC	muscle:	n/a
37	chr19:39572000-39572050	PFSK-1	brain:	n/a
38	chr19:39616818-39616868	Jurkat	blood:	n/a
39	chr19:39616296-39616346	Hela-S3	cervix:	n/a
40	chr19:39616336-39616386	PANC-1	pancreas:	n/a
41	chr19:39574751-39574801	LNCaP	prostate:	n/a
42	chr19:39616352-39616402	ovcar-3	ovarian:	n/a
43	chr19:39574863-39574913	H1-hESC	embryonic stem cell:	embryo
44	chr19:39574640-39574690	SAEC	small airway:	n/a
45	chr19:39616818-39616868	PANC-1	pancreas:	n/a
46	chr19:39574513-39574563	BE2_C	brain:	n/a
47	chr19:39574765-39574815	HNPCEpiC	eye:	n/a
48	chr19:39616296-39616346	HIPEpiC	eye:	n/a
49	chr19:39612741-39612791	RPTEC	kidney:	n/a
50	chr19:39574640-39574690	MCF-7	breast:	n/a

(count:117 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr19:39612412..39613536-chr19:39677602..39678408,4	MCF-7	breast:
2	chr19:39617221..39619579-chr19:39672951..39675735,2	MCF-7	breast:
3	chr19:39572549..39576644-chr19:39655893..39659798,4	MCF-7	breast:
4	chr19:39599295..39601915-chr19:39625074..39628012,2	MCF-7	breast:
5	chr19:39600818..39603608-chr19:39896434..39898280,2	MCF-7	breast:
6	chr19:39624651..39625632-chr19:39641254..39641826,3	MCF-7	breast:
7	chr19:39616271..39616860-chr9:131938050..131938907,2	Hela-S3	cervix:
8	chr19:39616354..39616916-chr3:40565871..40566513,2	MCF-7	breast:
9	chr19:39196517..39199049-chr19:39616527..39619066,2	MCF-7	breast:
10	chr19:39602376..39603706-chr19:39620989..39621663,3	MCF-7	breast:
11	chr19:39622646..39624803-chr19:39656922..39658959,2	MCF-7	breast:
12	chr19:39614928..39617634-chr19:39831535..39834253,2	K562	blood:
13	chr19:39610539..39613482-chr19:39683239..39685361,3	MCF-7	breast:
14	chr19:39519101..39521598-chr19:39532998..39534703,2	K562	blood:
15	chr19:39599349..39603430-chr19:39902751..39905281,3	MCF-7	breast:
16	chr19:39542686..39543478-chr19:39600712..39601594,2	MCF-7	breast:
17	chr19:39602746..39603330-chr19:39621049..39621640,2	MCF-7	breast:
18	chr19:39612929..39614547-chr19:39644614..39646235,2	K562	blood:
19	chr19:39601113..39601676-chr19:39818467..39819389,3	K562	blood:
20	chr19:39620628..39623686-chr19:39793053..39797178,3	K562	blood:
21	chr19:39611154..39613169-chr19:39902607..39904497,2	MCF-7	breast:
22	chr19:39612566..39613389-chr19:39702383..39703279,2	MCF-7	breast:
23	chr19:39614607..39616195-chr19:39688104..39689659,2	K562	blood:
24	chr19:39521025..39525658-chr19:39535006..39538345,5	MCF-7	breast:
25	chr19:39619125..39620938-chr19:39926907..39929414,2	K562	blood:
26	chr19:39612804..39613333-chr19:39813351..39814182,2	MCF-7	breast:
27	chr19:39624660..39625575-chr19:39641363..39642260,4	MCF-7	breast:
28	chr19:39620754..39621927-chr19:39641354..39642257,8	MCF-7	breast:
29	chr19:39622591..39626006-chr19:39627126..39631368,3	MCF-7	breast:
30	chr19:39602746..39603330-chr19:39621049..39621640,2	MCF-7	breast:
31	chr19:39617432..39618936-chr19:39618990..39621023,2	K562	blood:
32	chr19:39522295..39523922-chr19:39537003..39539265,2	K562	blood:
33	chr19:39624151..39625876-chr19:39627199..39629585,2	K562	blood:
34	chr19:39565899..39568671-chr3:161088109..161090760,2	MCF-7	breast:
35	chr19:39615011..39617919-chr19:39686746..39689965,3	MCF-7	breast:
36	chr19:39615078..39616937-chr19:39618172..39620698,2	K562	blood:
37	chr19:39612790..39613344-chr19:39677633..39678518,3	MCF-7	breast:
38	chr19:39602907..39604847-chr19:39614570..39617359,2	K562	blood:
39	chr19:39624644..39625575-chr19:39641363..39642260,6	MCF-7	breast:
40	chr19:39624966..39625536-chr19:39678054..39678776,2	MCF-7	breast:
41	chr19:39618807..39620742-chr19:39901218..39902940,2	MCF-7	breast:
42	chr19:39522794..39525227-chr19:39570722..39573005,2	MCF-7	breast:
43	chr19:39601023..39604135-chr19:39897877..39902850,6	MCF-7	breast:
44	chr19:39340180..39342670-chr19:39622996..39625120,2	MCF-7	breast:
45	chr19:39602907..39606013-chr19:39614570..39617349,3	K562	blood:
46	chr19:39601597..39603147-chr19:39830972..39833548,2	MCF-7	breast:
47	chr19:39613427..39615810-chr19:39815780..39817351,2	K562	blood:
48	chr19:39621851..39624607-chr19:39667898..39670113,3	MCF-7	breast:
49	chr19:39527434..39530385-chr19:39532161..39533802,2	K562	blood:
50	chr19:39620627..39621754-chr19:39641343..39642307,28	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC011443.1-2	chr19:39565090-39565638	expReg_chr19_5095_+
2	lnc-AC011443.1-3	chr19:39616453-39616559	NONHSAT066274
3	lnc-AC011443.1-1	chr19:39572421-39575494	expReg_chr19_5096_+
4	lnc-SYCN-1	chr19:39625522-39625844	ENSG00000269172.1
5	lnc-SYCN-1	chr19:39627062-39627103	ENSG00000269172.1

No data

Variant related genes	Relation type
ENSG00000269172	TF binding region
PAK4	TF binding region
ENSG00000183760	TF binding region
ENSG00000251709	TF binding region
ENSG00000269172	CpG island
PAK4	CpG island
ENSG00000183760	CpG island
ENSG00000251709	CpG island
ENSG00000267992	chromatin interactions
ENSG00000254682	chromatin interactions
ENSG00000172888	chromatin interactions
ENSG00000128016	chromatin interactions
ENSG00000161243	chromatin interactions
ENSG00000130755	chromatin interactions
ENSG00000183760	chromatin interactions
ENSG00000130669	chromatin interactions
ENSG00000130402	chromatin interactions
ENSG00000268050	chromatin interactions
ENSG00000266559	chromatin interactions
ENSG00000179134	chromatin interactions
ENSG00000188505	chromatin interactions
ENSG00000090924	chromatin interactions
ENSG00000104824	chromatin interactions
ENSG00000269246	chromatin interactions
ENSG00000269172	chromatin interactions
ENSG00000196542	chromatin interactions
ENSG00000172893	chromatin interactions

Extended variants
information (count: 4484 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4484 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs473878	chr19:39533754-39533755	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs601966	chr19:39533819-39533820	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs570738477	chr19:39533852-39533853	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528680803	chr19:39533927-39533928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559642308	chr19:39533935-39533936	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs472104	chr19:39533937-39533938	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs541897021	chr19:39533983-39533984	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs541830399	chr19:39534020-39534021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs602899	chr19:39534031-39534032	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs603268	chr19:39534076-39534077	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs376956920	chr19:39534159-39534160	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557118962	chr19:39534193-39534194	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs190692784	chr19:39534208-39534209	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs60908804	chr19:39534242-39534243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140468131	chr19:39534419-39534420	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558916226	chr19:39534424-39534425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144552540	chr19:39534477-39534478	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs569394659	chr19:39534482-39534483	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374249083	chr19:39534533-39534534	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs553085912	chr19:39534572-39534573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536452881	chr19:39534576-39534577	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574496108	chr19:39534620-39534621	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371111032	chr19:39534644-39534645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541898778	chr19:39534653-39534654	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs563171834	chr19:39534659-39534660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs530502511	chr19:39534667-39534668	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs545365522	chr19:39534674-39534675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs7248416	chr19:39534708-39534709	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs528717513	chr19:39534709-39534710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554932	chr19:39534714-39534715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs568633237	chr19:39534726-39534727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs540558924	chr19:39534731-39534732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558507873	chr19:39534732-39534733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551034346	chr19:39534779-39534780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs117869534	chr19:39534810-39534811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372300586	chr19:39534811-39534812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539858889	chr19:39534816-39534817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553330	chr19:39534843-39534844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs182382833	chr19:39534852-39534853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144873030	chr19:39534854-39534855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552933579	chr19:39534889-39534890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs617085	chr19:39534891-39534892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs372511682	chr19:39534910-39534911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541589189	chr19:39534916-39534917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs186607678	chr19:39534927-39534928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201871219	chr19:39534940-39534941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73038198	chr19:39534941-39534942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199632570	chr19:39534949-39534950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574958788	chr19:39534951-39534952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56214332	chr19:39534954-39534955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Pleomorphic liposarcoma	18784837	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
Disorders of sex development	21048976	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
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Mental retardation	19951919	CNVD
19q13.11 deletion syndrome	22378287	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21240255	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1932 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39523400-39535400	Weak transcription	Right Atrium	heart
2	chr19:39530800-39543000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr19:39535400-39538800	Enhancers	Fetal Intestine Large	intestine
4	chr19:39535400-39538800	Enhancers	Fetal Intestine Small	intestine
5	chr19:39535800-39538800	Enhancers	Duodenum Mucosa	Duodenum
6	chr19:39536200-39536400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr19:39536200-39536400	Active TSS	HepG2	liver
8	chr19:39536200-39536400	Enhancers	K562	blood
9	chr19:39536200-39536600	Enhancers	A549	lung
10	chr19:39536400-39536600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr19:39536400-39536800	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr19:39536400-39536800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
13	chr19:39536400-39536800	Flanking Bivalent TSS/Enh	HepG2	liver
14	chr19:39536400-39537200	Enhancers	Placenta	Placenta
15	chr19:39536400-39537200	Enhancers	Hela-S3	cervix
16	chr19:39536400-39537400	Flanking Active TSS	K562	blood
17	chr19:39536400-39538200	Enhancers	Stomach Mucosa	stomach
18	chr19:39536600-39536800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr19:39536600-39537000	Flanking Active TSS	A549	lung
20	chr19:39536600-39537400	Enhancers	GM12878-XiMat	blood
21	chr19:39536600-39537600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr19:39536800-39537000	Bivalent Enhancer	HepG2	liver
23	chr19:39536800-39537200	Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr19:39536800-39537400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
25	chr19:39537000-39537200	Enhancers	HepG2	liver
26	chr19:39537000-39537600	Enhancers	A549	lung
27	chr19:39537200-39541800	Weak transcription	HepG2	liver
28	chr19:39537400-39538600	Enhancers	K562	blood
29	chr19:39537600-39543000	Weak transcription	A549	lung
30	chr19:39538800-39542200	Weak transcription	Fetal Intestine Large	intestine
31	chr19:39538800-39543000	Weak transcription	Fetal Intestine Small	intestine
32	chr19:39541200-39546400	Weak transcription	Right Atrium	heart
33	chr19:39541800-39542400	Enhancers	HepG2	liver
34	chr19:39541800-39543200	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr19:39542000-39542200	Enhancers	Brain Hippocampus Middle	brain
36	chr19:39542200-39543200	Weak transcription	Brain Hippocampus Middle	brain
37	chr19:39542200-39546600	Enhancers	Fetal Intestine Large	intestine
38	chr19:39542400-39542800	Weak transcription	HepG2	liver
39	chr19:39542800-39544000	Enhancers	HepG2	liver
40	chr19:39543000-39543200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr19:39543000-39543400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr19:39543000-39543400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
43	chr19:39543000-39543400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr19:39543000-39543400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr19:39543000-39543400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr19:39543000-39543400	Enhancers	HMEC	breast
47	chr19:39543000-39543400	Enhancers	NHEK	skin
48	chr19:39543000-39543800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr19:39543000-39544400	Enhancers	A549	lung
50	chr19:39543000-39544800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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