Variant report

Variant	esv3399352
Chromosome Location	chr19:21232738-21423323
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1778)
CpG islands
(count:1342)
Chromatin interactive
region (count:45)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:21324594-21324991	K562	blood:	n/a	n/a
2	ARID3A	chr19:21380495-21380772	K562	blood:	n/a	n/a
3	ARID3A	chr19:21298266-21298592	K562	blood:	n/a	n/a
4	ARID3A	chr19:21264624-21264646	K562	blood:	n/a	n/a
5	ARID3A	chr19:21310732-21311042	K562	blood:	n/a	n/a
6	ARID3A	chr19:21317764-21318041	HepG2	liver:	n/a	n/a
7	ARID3A	chr19:21326481-21326923	K562	blood:	n/a	n/a
8	ARID3A	chr19:21311642-21311836	K562	blood:	n/a	n/a
9	ARID3A	chr19:21320974-21321431	HepG2	liver:	n/a	n/a
10	ARID3A	chr19:21264926-21265138	K562	blood:	n/a	n/a
11	ARID3A	chr19:21309568-21309872	K562	blood:	n/a	n/a
12	ARID3A	chr19:21324511-21325033	HepG2	liver:	n/a	n/a
13	ARID3A	chr19:21385779-21386015	K562	blood:	n/a	n/a
14	ARID3A	chr19:21392842-21393238	HepG2	liver:	n/a	n/a
15	ARID3A	chr19:21264757-21265267	HepG2	liver:	n/a	n/a
16	ARID3A	chr19:21334536-21334657	HepG2	liver:	n/a	n/a
17	ATF1	chr19:21323783-21324152	K562	blood:	n/a	n/a
18	ATF1	chr19:21324532-21324958	K562	blood:	n/a	n/a
19	ATF1	chr19:21264742-21265106	K562	blood:	n/a	n/a
20	ATF1	chr19:21311655-21311901	K562	blood:	n/a	n/a
21	ATF1	chr19:21309871-21310055	K562	blood:	n/a	n/a
22	ATF1	chr19:21380399-21380892	K562	blood:	n/a	n/a
23	ATF2	chr19:21405239-21405611	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr19:21264842-21265261	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr19:21380345-21380653	K562	blood:	n/a	n/a
26	BACH1	chr19:21369719-21369791	K562	blood:	n/a	n/a
27	BACH1	chr19:21377763-21378071	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr19:21264961-21264962	K562	blood:	n/a	n/a
29	BACH1	chr19:21334389-21334437	K562	blood:	n/a	n/a
30	BATF	chr19:21284292-21284552	GM12878	blood:	n/a	chr19:21284437-21284448
31	BATF	chr19:21267212-21267440	GM12878	blood:	n/a	n/a
32	BATF	chr19:21284333-21284518	GM12878	blood:	n/a	chr19:21284437-21284448
33	BCL11A	chr19:21405281-21405550	H1-hESC	embryonic stem cell:	n/a	n/a
34	BHLHE40	chr19:21367203-21367237	K562	blood:	n/a	n/a
35	BHLHE40	chr19:21324578-21325040	K562	blood:	n/a	n/a
36	BHLHE40	chr19:21264786-21265371	K562	blood:	n/a	n/a
37	BHLHE40	chr19:21325755-21325765	K562	blood:	n/a	n/a
38	BHLHE40	chr19:21324647-21325001	GM12878	blood:	n/a	n/a
39	BHLHE40	chr19:21380546-21381220	K562	blood:	n/a	n/a
40	BHLHE40	chr19:21266686-21266689	GM12878	blood:	n/a	n/a
41	BHLHE40	chr19:21277600-21277808	GM12878	blood:	n/a	n/a
42	BHLHE40	chr19:21388606-21388806	GM12878	blood:	n/a	n/a
43	BHLHE40	chr19:21264737-21264982	GM12878	blood:	n/a	n/a
44	BRCA1	chr19:21264777-21265222	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr19:21264928-21265203	HepG2	liver:	n/a	n/a
46	CBX3	chr19:21412789-21413093	K562	blood:	n/a	n/a
47	CBX3	chr19:21324429-21325106	K562	blood:	n/a	n/a
48	CBX3	chr19:21264674-21265389	K562	blood:	n/a	n/a
49	CBX3	chr19:21412796-21413087	K562	blood:	n/a	n/a
50	CBX3	chr19:21311545-21312525	K562	blood:	n/a	n/a

(count:1342 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:21324782-21324832	AG09319	gingival:	n/a
2	chr19:21264131-21264181	AoSMC	blood vessel:	n/a
3	chr19:21324444-21324494	SK-N-SH	brain:	n/a
4	chr19:21305635-21305685	U87	brain:	n/a
5	chr19:21324782-21324832	NHBE	bronchial:	n/a
6	chr19:21264131-21264181	HPAEpiC	pulmonary alveolar:	n/a
7	chr19:21324750-21324800	GM06990	blood:	n/a
8	chr19:21324750-21324800	NB4	blood:	n/a
9	chr19:21324833-21324883	NB4	blood:	n/a
10	chr19:21264131-21264181	AG04449	skin:	fetal
11	chr19:21324130-21324180	HRPEpiC	eye:	n/a
12	chr19:21324130-21324180	A549	lung:	n/a
13	chr19:21324707-21324757	SAEC	small airway:	n/a
14	chr19:21324807-21324857	AG04450	lung:	fetal
15	chr19:21324782-21324832	HCM	heart:	n/a
16	chr19:21264982-21265032	HAEpiC	amniotic membrane:	n/a
17	chr19:21265364-21265414	GM06990	blood:	n/a
18	chr19:21324782-21324832	AG09309	skin:	n/a
19	chr19:21262035-21262085	AG10803	skin:	n/a
20	chr19:21324750-21324800	Jurkat	blood:	n/a
21	chr19:21305635-21305685	MCF10A-Er-Src	breast:	n/a
22	chr19:21323534-21323584	HIPEpiC	eye:	n/a
23	chr19:21269097-21269147	PrEC	prostate:	n/a
24	chr19:21324796-21324846	ovcar-3	ovarian:	n/a
25	chr19:21264371-21264421	SK-N-SH_RA	brain:	n/a
26	chr19:21324807-21324857	NHBE	bronchial:	n/a
27	chr19:21324796-21324846	NH-A	brain:	n/a
28	chr19:21265264-21265314	Jurkat	blood:	n/a
29	chr19:21265421-21265471	HIPEpiC	eye:	n/a
30	chr19:21265264-21265314	HepG2	liver:	n/a
31	chr19:21324750-21324800	GM12892	blood:	n/a
32	chr19:21324444-21324494	HCM	heart:	n/a
33	chr19:21323534-21323584	HCPEpiC	choroid plexus:	n/a
34	chr19:21324707-21324757	HRE	kidney:	n/a
35	chr19:21324833-21324883	NHBE	bronchial:	n/a
36	chr19:21324796-21324846	HNPCEpiC	eye:	n/a
37	chr19:21324833-21324883	SK-N-MC	brain:	n/a
38	chr19:21240978-21241028	GM12891	blood:	n/a
39	chr19:21265364-21265414	AoSMC	blood vessel:	n/a
40	chr19:21264371-21264421	SK-N-SH	brain:	n/a
41	chr19:21264371-21264421	GM12892	blood:	n/a
42	chr19:21264896-21264946	AG04450	lung:	fetal
43	chr19:21366880-21366930	HRPEpiC	eye:	n/a
44	chr19:21324707-21324757	CMK	blood:	n/a
45	chr19:21324807-21324857	CMK	blood:	n/a
46	chr19:21262035-21262085	HRPEpiC	eye:	n/a
47	chr19:21324750-21324800	HEK293	kidney:	embryo
48	chr19:21325005-21325055	HNPCEpiC	eye:	n/a
49	chr19:21265421-21265471	AG04450	lung:	fetal
50	chr19:21324707-21324757	PrEC	prostate:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:41398648..41400647-chr19:21234769..21236289,5	MCF-7	breast:
2	chr19:21246343..21248444-chr19:21263959..21266875,2	K562	blood:
3	chr19:21268071..21270842-chr19:21283139..21285114,2	K562	blood:
4	chr19:21246343..21248444-chr19:21263959..21266875,2	K562	blood:
5	chr19:21268071..21270842-chr19:21283139..21285114,2	K562	blood:
6	chr19:21392274..21393855-chr19:21395475..21398127,2	K562	blood:
7	chr19:21324747..21325334-chr19:21541551..21542092,2	Hela-S3	cervix:
8	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
9	chr19:21257717..21259573-chr19:21372943..21374798,2	K562	blood:
10	chr19:21276747..21278755-chr19:21280292..21281905,2	K562	blood:
11	chr19:21264733..21265247-chr19:21541544..21542206,2	NB4	blood:
12	chr19:21392274..21393855-chr19:21395475..21398127,2	K562	blood:
13	chr19:21325138..21326653-chr19:21327405..21328910,2	K562	blood:
14	chr19:21264288..21266539-chr19:21271478..21272991,2	MCF-7	breast:
15	chr19:21267358..21270716-chr19:21272495..21275149,3	MCF-7	breast:
16	chr19:21264715..21265215-chrX:53710755..53711257,2	NB4	blood:
17	chr17:41381905..41383742-chr19:21236269..21237789,3	K562	blood:
18	chr19:21267358..21270716-chr19:21272495..21275149,3	MCF-7	breast:
19	chr14:39639460..39640068-chr19:21325033..21325860,2	Hela-S3	cervix:
20	chr19:21327774..21330342-chr19:21332349..21334379,2	MCF-7	breast:
21	chr19:21203269..21205162-chr19:21263863..21266449,2	MCF-7	breast:
22	chr19:21325138..21326653-chr19:21327405..21328910,2	K562	blood:
23	chr19:21329795..21332186-chr19:21344748..21346568,2	K562	blood:
24	chr19:21260366..21262135-chr19:21263416..21265253,2	K562	blood:
25	chr19:21263410..21266735-chr19:21269462..21274138,5	K562	blood:
26	chr17:57969004..57971186-chr19:21264179..21266125,2	MCF-7	breast:
27	chr19:21268213..21268800-chr19:21327512..21328424,2	MCF-7	breast:
28	chr17:41381927..41383535-chr19:21236269..21237789,2	MCF-7	breast:
29	chr19:21319136..21321232-chr19:21323817..21326389,2	K562	blood:
30	chr19:21328122..21331831-chr19:21332882..21335579,3	K562	blood:
31	chr19:21329795..21332186-chr19:21344748..21346568,2	K562	blood:
32	chr19:21236568..21238876-chr19:21241377..21243478,2	K562	blood:
33	chr19:21264016..21266575-chr19:21326485..21328797,2	MCF-7	breast:
34	chr19:21324608..21326238-chr19:21328530..21331210,2	MCF-7	breast:
35	chr19:21264764..21267719-chr19:21267936..21273188,6	K562	blood:
36	chr19:21366435..21372841-chr19:21372957..21377596,6	K562	blood:
37	chr19:21230722..21233642-chr19:21264436..21267129,2	K562	blood:
38	chr19:21260635..21262427-chr19:21263416..21266258,2	K562	blood:
39	chr19:21238270..21239771-chr19:21264302..21266943,2	K562	blood:
40	chr19:21238270..21239771-chr19:21264302..21266943,2	K562	blood:
41	chr19:21312896..21314771-chr19:21323680..21326350,2	K562	blood:
42	chr19:21266339..21268600-chr19:21281169..21284066,2	MCF-7	breast:
43	chr19:21268213..21268800-chr19:21327512..21328424,2	MCF-7	breast:
44	chr19:21264345..21264942-chr7:89975847..89976737,2	Hela-S3	cervix:
45	chr19:21257717..21259573-chr19:21372943..21374798,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF431-2	chr19:21367295-21367400	NONHSAT063688
2	lnc-ZNF431-2	chr19:21372668-21373029	NONHSAT063688
3	lnc-ZNF431-1	chr19:21371401-21371756	NONHSAT063690
4	lnc-ZNF714-1	chr19:21264971-21265154	NONHSAT063683
5	lnc-ZNF430-2	chr19:21273717-21274564	NONHSAT063684
6	lnc-ZNF431-2	chr19:21368747-21369090	NONHSAT063689
7	lnc-ZNF431-2	chr19:21372668-21372801	NONHSAT063689
8	lnc-ZNF430-1	chr19:21246730-21247067	NONHSAT063682
9	lnc-ZNF714-1	chr19:21307764-21307881	NONHSAT063683
10	lnc-ZNF714-2	chr19:21306620-21306991	NONHSAT063687
11	lnc-ZNF430-2	chr19:21266826-21266875	NONHSAT063684
12	lnc-ZNF431-3	chr19:21301321-21301529	NONHSAT063686
13	lnc-ZNF708-10	chr19:21404447-21405548	NONHSAT063691
14	lnc-ZNF708-9	chr19:21407900-21407987	NONHSAT063692

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ZNF714	hsa-miR-222-3p	chr19:21304966-21304986

Variant related genes	Relation type
RPL36AP51	TF binding region
ENSG00000268892	TF binding region
VN1R81P	TF binding region
VN1R80P	TF binding region
VN1R82P	TF binding region
ZNF431	TF binding region
RNA5SP469	TF binding region
ZNF714	TF binding region
ENSG00000265650	TF binding region
ENSG00000256240	TF binding region
RPL7AP10	TF binding region
ZNF430	TF binding region
RPL36AP51	CpG island
ENSG00000268892	CpG island
VN1R81P	CpG island
VN1R80P	CpG island
VN1R82P	CpG island
ZNF431	CpG island
RNA5SP469	CpG island
ZNF714	CpG island
ENSG00000265650	CpG island
ENSG00000256240	CpG island
RPL7AP10	CpG island
ZNF430	CpG island
ENSG00000236383	chromatin interactions
ENSG00000118620	chromatin interactions
ENSG00000268598	chromatin interactions
ENSG00000086758	chromatin interactions
ENSG00000182400	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000172687	chromatin interactions
ENSG00000196705	chromatin interactions
ENSG00000160352	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000265650	chromatin interactions
ENSG00000268995	chromatin interactions
ENSG00000105793	chromatin interactions
ENSG00000240522	chromatin interactions

Extended variants
information (count: 7459 )
Associated
traits (count: 42 )

Variant overlapped rSNPs/rCNVs (count:7459 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548098589	chr19:21232738-21232739	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs568217592	chr19:21232739-21232740	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs113354732	chr19:21232767-21232768	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113106828	chr19:21232794-21232795	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs35700556	chr19:21232802-21232803	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs1971815	chr19:21232813-21232814	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs539090722	chr19:21232892-21232893	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371155803	chr19:21232905-21232906	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs376213319	chr19:21232911-21232912	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs62122605	chr19:21232912-21232913	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs535301981	chr19:21232932-21232933	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554945333	chr19:21232933-21232934	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs201686362	chr19:21232997-21232998	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs34194227	chr19:21232998-21232999	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs148580695	chr19:21233002-21233003	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs72532379	chr19:21233003-21233004	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs3047784	chr19:21233004-21233005	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373219333	chr19:21233005-21233006	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs376161364	chr19:21233006-21233007	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371554115	chr19:21233007-21233008	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575121169	chr19:21233011-21233012	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs111713598	chr19:21233103-21233104	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs34643309	chr19:21233142-21233143	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs13345915	chr19:21233245-21233246	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs150388609	chr19:21233301-21233302	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs12609167	chr19:21233388-21233389	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs190936155	chr19:21233406-21233407	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs141576246	chr19:21233409-21233410	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528397507	chr19:21233410-21233411	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs73531882	chr19:21233429-21233430	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs111276502	chr19:21233503-21233504	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547225742	chr19:21233525-21233526	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs530656697	chr19:21233618-21233619	Weak transcription Strong transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs10416383	chr19:21233662-21233663	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs35781160	chr19:21233673-21233674	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs375514629	chr19:21233702-21233703	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs138029563	chr19:21233750-21233751	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs182821728	chr19:21233758-21233759	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs369493354	chr19:21233817-21233818	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs187778569	chr19:21233826-21233827	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs546303476	chr19:21233828-21233829	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs562214087	chr19:21233882-21233883	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs149499700	chr19:21233911-21233912	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs192872949	chr19:21233958-21233959	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs183142742	chr19:21233959-21233960	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs568768457	chr19:21233963-21233964	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs537645650	chr19:21233995-21233996	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs12052091	chr19:21234122-21234123	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs577429077	chr19:21234125-21234126	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs200351502	chr19:21234151-21234152	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:42)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	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
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:4493 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:21204400-21264800	Weak transcription	Right Ventricle	heart
2	chr19:21204600-21239800	Weak transcription	Colon Smooth Muscle	Colon
3	chr19:21206200-21241600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr19:21207200-21239400	Weak transcription	Hela-S3	cervix
5	chr19:21209200-21235600	Weak transcription	Stomach Smooth Muscle	stomach
6	chr19:21211400-21235400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr19:21212000-21241400	Weak transcription	Fetal Heart	heart
8	chr19:21220400-21235200	Weak transcription	NHDF-Ad	bronchial
9	chr19:21221400-21242000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr19:21222400-21242200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr19:21223000-21244200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr19:21223400-21235600	Weak transcription	NH-A	brain
13	chr19:21224400-21232800	ZNF genes & repeats	Dnd41	blood
14	chr19:21225200-21234200	Weak transcription	A549	lung
15	chr19:21225600-21237200	Weak transcription	HUVEC	blood vessel
16	chr19:21227400-21241400	ZNF genes & repeats	GM12878-XiMat	blood
17	chr19:21227800-21247200	Weak transcription	HepG2	liver
18	chr19:21228000-21233600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr19:21228800-21235400	Weak transcription	Muscle Satellite Cultured Cells	--
20	chr19:21229600-21235600	Weak transcription	Brain Substantia Nigra	brain
21	chr19:21229800-21235400	Weak transcription	Brain Anterior Caudate	brain
22	chr19:21230600-21235600	Weak transcription	Brain Cingulate Gyrus	brain
23	chr19:21230600-21248400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr19:21230800-21232800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr19:21230800-21232800	Weak transcription	Fetal Thymus	thymus
26	chr19:21230800-21233200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr19:21230800-21233400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr19:21230800-21233400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr19:21230800-21233400	Weak transcription	Fetal Muscle Leg	muscle
30	chr19:21230800-21233600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr19:21230800-21233600	Weak transcription	Esophagus	oesophagus
32	chr19:21230800-21234000	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr19:21230800-21234200	Weak transcription	Fetal Muscle Trunk	muscle
34	chr19:21230800-21234600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
35	chr19:21230800-21235200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr19:21230800-21235400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr19:21230800-21235400	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr19:21230800-21235400	Weak transcription	Rectal Smooth Muscle	rectum
39	chr19:21230800-21235400	Weak transcription	HSMM	muscle
40	chr19:21230800-21235600	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr19:21230800-21235600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr19:21230800-21235600	Weak transcription	Brain Angular Gyrus	brain
43	chr19:21230800-21235600	Weak transcription	Left Ventricle	heart
44	chr19:21230800-21235600	Weak transcription	NHEK	skin
45	chr19:21230800-21235800	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr19:21230800-21237000	Weak transcription	Brain Hippocampus Middle	brain
47	chr19:21230800-21238600	Weak transcription	NHLF	lung
48	chr19:21230800-21240400	Weak transcription	HSMMtube	muscle
49	chr19:21230800-21243000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr19:21231000-21235600	Weak transcription	HMEC	breast

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