Variant report

Variant	nsv882394
Chromosome Location	chr5:96538585-97108559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2185)
CpG islands
(count:610)
Chromatin interactive
region (count:53)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2185 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:96869893-96870174	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:96632846-96633044	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:96559836-96560263	HepG2	liver:	n/a	n/a
4	ATF1	chr5:96566806-96567076	K562	blood:	n/a	n/a
5	ATF1	chr5:96925354-96925372	K562	blood:	n/a	n/a
6	ATF2	chr5:96883636-96884569	GM12878	blood:	n/a	n/a
7	ATF2	chr5:96736132-96736743	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr5:96691322-96691778	GM12878	blood:	n/a	n/a
9	ATF2	chr5:96883703-96884520	GM12878	blood:	n/a	n/a
10	ATF2	chr5:96736083-96736724	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr5:96885956-96886136	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:96600161-96600267	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:96861461-96861877	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr5:96883695-96884539	GM12878	blood:	n/a	chr5:96884341-96884350
15	BATF	chr5:96884044-96884526	GM12878	blood:	n/a	chr5:96884341-96884350
16	BATF	chr5:96872418-96872668	GM12878	blood:	n/a	chr5:96872552-96872563
17	BATF	chr5:96713332-96713631	GM12878	blood:	n/a	n/a
18	BATF	chr5:96872429-96872695	GM12878	blood:	n/a	chr5:96872552-96872563
19	BATF	chr5:96883741-96884022	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:96883801-96884003	GM12878	blood:	n/a	chr5:96883828-96883837
21	BCL11A	chr5:96713335-96713673	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:96736211-96736597	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr5:96736252-96736517	H1-hESC	embryonic stem cell:	n/a	n/a
24	BCL11A	chr5:96884033-96884506	GM12878	blood:	n/a	n/a
25	BCL11A	chr5:96884015-96884504	GM12878	blood:	n/a	n/a
26	BCL3	chr5:96928285-96928637	GM12878	blood:	n/a	n/a
27	BCL3	chr5:96831847-96832152	GM12878	blood:	n/a	n/a
28	BCLAF1	chr5:96691310-96691873	GM12878	blood:	n/a	n/a
29	BCLAF1	chr5:96632712-96633177	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:96883684-96884500	GM12878	blood:	n/a	n/a
31	BHLHE40	chr5:96869825-96870150	GM12878	blood:	n/a	n/a
32	BHLHE40	chr5:96830650-96830767	GM12878	blood:	n/a	n/a
33	BHLHE40	chr5:96691380-96691821	GM12878	blood:	n/a	n/a
34	BRCA1	chr5:96675145-96675188	GM12878	blood:	n/a	n/a
35	BRCA1	chr5:96761275-96761538	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr5:97092073-97092104	GM12878	blood:	n/a	n/a
37	CBX3	chr5:96632687-96633278	HCT-116	colon:	n/a	n/a
38	CCNT2	chr5:96633727-96633849	K562	blood:	n/a	n/a
39	CCNT2	chr5:96691691-96691850	K562	blood:	n/a	n/a
40	CEBPB	chr5:96728466-96728767	HepG2	liver:	n/a	chr5:96728592-96728603
41	CEBPB	chr5:96566720-96567131	HCT-116	colon:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
42	CEBPB	chr5:96984131-96984412	HepG2	liver:	n/a	chr5:96984229-96984240
43	CEBPB	chr5:97070883-97071301	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:96928194-96928475	HepG2	liver:	n/a	chr5:96928315-96928326
45	CEBPB	chr5:96769639-96770035	MCF-7	breast:	n/a	n/a
46	CEBPB	chr5:96869955-96870234	K562	blood:	n/a	chr5:96870105-96870116
47	CEBPB	chr5:96658376-96658678	IMR90	lung:	n/a	chr5:96658532-96658543
48	CEBPB	chr5:96566712-96567106	ECC-1	luminal epithelium:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
49	CEBPB	chr5:96566708-96567106	H1-hESC	embryonic stem cell:	n/a	chr5:96566892-96566903 chr5:96566891-96566902
50	CEBPB	chr5:96767484-96767678	Hela-S3	cervix:	n/a	chr5:96767561-96767572

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:96742935-96742985	AG10803	skin:	n/a
2	chr5:96742935-96742985	AG04449	skin:	fetal
3	chr5:96742935-96742985	Hepatocyte	liver:	n/a
4	chr5:96742935-96742985	AoSMC	blood vessel:	n/a
5	chr5:96915770-96915820	HL-60	blood:	n/a
6	chr5:96742935-96742985	HUVEC	blood vessel:	n/a
7	chr5:96789385-96789435	PANC-1	pancreas:	n/a
8	chr5:96876834-96876884	NH-A	brain:	n/a
9	chr5:96881859-96881909	AG04450	lung:	fetal
10	chr5:96747223-96747273	NHDF-neo	bronchial:	n/a
11	chr5:96876834-96876884	SK-N-SH_RA	brain:	n/a
12	chr5:96876834-96876884	GM06990	blood:	n/a
13	chr5:96876834-96876884	BJ	skin:	n/a
14	chr5:96881859-96881909	HAEpiC	amniotic membrane:	n/a
15	chr5:96743054-96743104	CMK	blood:	n/a
16	chr5:96845117-96845167	LNCaP	prostate:	n/a
17	chr5:96743054-96743104	GM12878	blood:	n/a
18	chr5:96742935-96742985	Jurkat	blood:	n/a
19	chr5:96747223-96747273	HAEpiC	amniotic membrane:	n/a
20	chr5:96845117-96845167	HepG2	liver:	n/a
21	chr5:96789385-96789435	AoSMC	blood vessel:	n/a
22	chr5:96855476-96855526	Hela-S3	cervix:	n/a
23	chr5:96743054-96743104	HCM	heart:	n/a
24	chr5:96915770-96915820	AoSMC	blood vessel:	n/a
25	chr5:96743054-96743104	HCF	heart:	n/a
26	chr5:96743054-96743104	NB4	blood:	n/a
27	chr5:96789385-96789435	HEK293	kidney:	embryo
28	chr5:96747223-96747273	Hepatocyte	liver:	n/a
29	chr5:96742935-96742985	HEEpiC	esophagus:	n/a
30	chr5:96915770-96915820	ECC-1	luminal epithelium:	n/a
31	chr5:96855476-96855526	Caco-2	colon:	n/a
32	chr5:96876834-96876884	SAEC	small airway:	n/a
33	chr5:96855476-96855526	BJ	skin:	n/a
34	chr5:96876834-96876884	HCT-116	colon:	n/a
35	chr5:96845117-96845167	GM12891	blood:	n/a
36	chr5:96881859-96881909	NHDF-neo	bronchial:	n/a
37	chr5:96881859-96881909	PrEC	prostate:	n/a
38	chr5:96747223-96747273	HepG2	liver:	n/a
39	chr5:96915770-96915820	HUVEC	blood vessel:	n/a
40	chr5:96915770-96915820	GM12878	blood:	n/a
41	chr5:96876834-96876884	HL-60	blood:	n/a
42	chr5:96915770-96915820	SKMC	muscle:	n/a
43	chr5:96915770-96915820	AG09309	skin:	n/a
44	chr5:96743054-96743104	HEEpiC	esophagus:	n/a
45	chr5:96855476-96855526	MCF10A-Er-Src	breast:	n/a
46	chr5:96747223-96747273	PFSK-1	brain:	n/a
47	chr5:96855476-96855526	ProgFib	skin:	n/a
48	chr5:96855476-96855526	NH-A	brain:	n/a
49	chr5:96747223-96747273	HCM	heart:	n/a
50	chr5:96876834-96876884	GM12892	blood:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:96518180..96520707-chr5:96752048..96753718,2	K562	blood:
2	chr5:96735260..96736761-chr7:31786509..31788468,2	MCF-7	breast:
3	chr17:41380186..41382311-chr5:96695804..96697321,3	MCF-7	breast:
4	chr17:41463734..41465366-chr5:96695802..96697324,2	MCF-7	breast:
5	chr5:96706066..96707837-chr5:96722435..96724433,2	K562	blood:
6	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:
7	chr5:96549287..96551402-chr5:96556377..96559080,2	K562	blood:
8	chr17:41398605..41400432-chr5:96695803..96698802,4	MCF-7	breast:
9	chr5:96534501..96536985-chr5:96538534..96540888,2	MCF-7	breast:
10	chr17:41398860..41401971-chr5:96695801..96698802,6	K562	blood:
11	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:
12	chr3:73159507..73161444-chr5:96697302..96698824,2	K562	blood:
13	chr17:41464548..41466257-chr5:96697324..96698824,2	MCF-7	breast:
14	chr5:96533022..96535910-chr5:96537589..96540065,2	K562	blood:
15	chr5:96757244..96760010-chr5:96764877..96766486,2	MCF-7	breast:
16	chr5:96517922..96519748-chr5:96562831..96564407,2	MCF-7	breast:
17	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
18	chr5:97027188..97030158-chr5:97031253..97033564,2	K562	blood:
19	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
20	chr5:96711348..96714233-chr5:96714673..96716999,2	MCF-7	breast:
21	chr5:96757244..96760010-chr5:96764877..96766486,2	MCF-7	breast:
22	chr5:96517839..96519465-chr5:96545763..96548016,2	K562	blood:
23	chr5:96632616..96633407-chr5:96869853..96870506,3	MCF-7	breast:
24	chr5:97063042..97065906-chr5:97067363..97069421,2	MCF-7	breast:
25	chr5:96566532..96567370-chr5:96632847..96633430,3	MCF-7	breast:
26	chr5:96706066..96707837-chr5:96722435..96724433,2	K562	blood:
27	chr5:96865281..96867677-chr5:96867921..96869530,2	K562	blood:
28	chr5:96632479..96633406-chr5:96869339..96870359,6	MCF-7	breast:
29	chr5:97027188..97030158-chr5:97031253..97033564,2	K562	blood:
30	chr5:96987103..96987619-chr5:97253568..97254119,2	MCF-7	breast:
31	chr17:41462273..41467084-chr5:96695804..96698803,5	K562	blood:
32	chr17:41380182..41383606-chr5:96695801..96698822,3	K562	blood:
33	chr5:96517585..96519769-chr5:96537536..96540052,2	MCF-7	breast:
34	chr5:96632616..96633407-chr5:96869853..96870506,3	MCF-7	breast:
35	chr5:96695823..96698804-chr6:142366314..142367822,2	K562	blood:
36	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
37	chr5:96566532..96567370-chr5:96632847..96633430,3	MCF-7	breast:
38	chr5:96869180..96869850-chr5:98103055..98104021,2	MCF-7	breast:
39	chr17:41398650..41400853-chr5:96695801..96698804,5	K562	blood:
40	chr5:96720114..96721922-chr5:96728191..96729748,2	MCF-7	breast:
41	chr5:96656999..96658653-chr5:96658674..96662108,3	K562	blood:
42	chr5:96687334..96689961-chr5:96691050..96693898,2	MCF-7	breast:
43	chr5:96566460..96567205-chr5:96869494..96870442,2	MCF-7	breast:
44	chr5:96549287..96551402-chr5:96556377..96559080,2	K562	blood:
45	chr5:96697302..96697824-chr5:146587593..146588113,2	Hela-S3	cervix:
46	chr5:96711348..96714233-chr5:96714673..96716999,2	MCF-7	breast:
47	chr5:96656999..96658653-chr5:96658674..96662108,3	K562	blood:
48	chr5:96720114..96721922-chr5:96728191..96729748,2	MCF-7	breast:
49	chr5:96902855..96905560-chr5:96907320..96909656,2	K562	blood:
50	chr5:96898495..96900851-chr5:96905056..96906917,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	XLOC_004483
2	lnc-RIOK2-3	chr5:96785062-96785445	NONHSAT102929
3	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	XLOC_004483
4	lnc-CTD-2215E18.1.1-2	chr5:96856933-96856994	NR_105028
5	lnc-RIOK2-2	chr5:96563572-96563661	XLOC_004934
6	lnc-CTD-2215E18.1.1-2	chr5:96840399-96840496	NONHSAT102931
7	lnc-CTD-2215E18.1.1-1	chr5:96767448-96767604	ENSG00000251513.1
8	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006750	XLOC_004483
9	lnc-CTD-2215E18.1.1-1	chr5:96772257-96772921	ENSG00000251513.1
10	lnc-CTD-2215E18.1.1-2	chr5:96856932-96856994	NONHSAT102931
11	lnc-CTD-2215E18.1.1-2	chr5:96840400-96840496	NR_105028
12	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	NR_105028
13	lnc-CTD-2215E18.1.1-5	chr5:96704480-96706125	NONHSAT102928
14	lnc-RIOK2-4	chr5:96786031-96786319	NONHSAT102930
15	lnc-CTD-2215E18.1.1-2	chr5:97006298-97006755	NR_105028
16	lnc-CTD-2215E18.1.1-2	chr5:97004255-97004366	XLOC_004483
17	lnc-RIOK2-2	chr5:96559075-96559398	XLOC_004934
18	lnc-CTD-2215E18.1.1-6	chr5:97073598-97074617	NONHSAT102935
19	lnc-CTD-2215E18.1.1-2	chr5:97004254-97004366	NONHSAT102931
20	lnc-CTD-2215E18.1.1-2	chr5:97006297-97006750	NONHSAT102931

No data

Variant related genes	Relation type
ENSG00000251054	TF binding region
ENSG00000249761	TF binding region
ENSG00000248931	TF binding region
ENSG00000250331	TF binding region
ENSG00000251193	TF binding region
YTHDF1P1	TF binding region
ENSG00000248758	TF binding region
ENSG00000249977	TF binding region
ENSG00000251054	CpG island
ENSG00000249761	CpG island
ENSG00000248931	CpG island
ENSG00000250331	CpG island
ENSG00000251193	CpG island
YTHDF1P1	CpG island
ENSG00000248758	CpG island
ENSG00000249977	CpG island
ENSG00000188825	chromatin interactions
ENSG00000251513	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000058729	chromatin interactions

Extended variants
information (count: 11497 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:11497 , 50 per page) page: 1 2 3 4 5 6 7 ... 230

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12656965	chr5:96538585-96538586	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs547885378	chr5:96538601-96538602	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566104409	chr5:96538679-96538680	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs527306622	chr5:96538681-96538682	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551790685	chr5:96538703-96538704	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs570633935	chr5:96538721-96538722	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs77114433	chr5:96538735-96538736	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs556076049	chr5:96538779-96538780	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs572780261	chr5:96538810-96538811	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs138768624	chr5:96538811-96538812	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs535902775	chr5:96538839-96538840	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs554326237	chr5:96538881-96538882	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs573229315	chr5:96538909-96538910	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs572434408	chr5:96538936-96538937	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs370040957	chr5:96538954-96538955	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs191685986	chr5:96538978-96538979	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs75664065	chr5:96538979-96538980	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs548827493	chr5:96538992-96538993	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576657155	chr5:96539101-96539102	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs544107929	chr5:96539233-96539234	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs376295868	chr5:96539278-96539279	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs541351125	chr5:96539296-96539297	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs538014045	chr5:96539311-96539312	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs141888969	chr5:96539319-96539320	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs184236832	chr5:96539331-96539332	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs559612937	chr5:96539351-96539352	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs189018762	chr5:96539371-96539372	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs551880990	chr5:96539373-96539374	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs5869745	chr5:96539399-96539400	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs397998811	chr5:96539408-96539409	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs564148473	chr5:96539462-96539463	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs1423500	chr5:96539479-96539480	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs560354275	chr5:96539494-96539495	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs531464739	chr5:96539496-96539497	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs76489384	chr5:96539500-96539501	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs550049999	chr5:96539510-96539511	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs1423501	chr5:96539651-96539652	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs577277648	chr5:96539697-96539698	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs73779847	chr5:96539852-96539853	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs181695272	chr5:96539871-96539872	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs566177221	chr5:96539872-96539873	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs185554665	chr5:96539940-96539941	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs190809494	chr5:96539948-96539949	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs562597697	chr5:96539987-96539988	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs113716891	chr5:96540013-96540014	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs537318441	chr5:96540018-96540019	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs556041842	chr5:96540039-96540040	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574030189	chr5:96540096-96540097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182151675	chr5:96540101-96540102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576324493	chr5:96540102-96540103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Mental retardation	19471318	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19214233	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1079 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96534800-96542400	Weak transcription	Primary B cells from cord blood	blood
2	chr5:96534800-96543400	Weak transcription	Dnd41	blood
3	chr5:96543400-96544000	Enhancers	Dnd41	blood
4	chr5:96544000-96544400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:96544000-96545000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:96544000-96545000	Flanking Active TSS	Dnd41	blood
7	chr5:96545000-96545600	Enhancers	Dnd41	blood
8	chr5:96549800-96550200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr5:96554400-96565400	Weak transcription	Primary B cells from peripheral blood	blood
10	chr5:96556600-96559400	Weak transcription	NHDF-Ad	bronchial
11	chr5:96558800-96560000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:96559200-96560000	Enhancers	HSMMtube	muscle
13	chr5:96559200-96560200	Enhancers	HSMM	muscle
14	chr5:96559200-96560400	Enhancers	Fetal Intestine Large	intestine
15	chr5:96559400-96560000	Enhancers	NHDF-Ad	bronchial
16	chr5:96559400-96560200	Enhancers	Muscle Satellite Cultured Cells	--
17	chr5:96559400-96560400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr5:96559400-96560400	Enhancers	Liver	Liver
19	chr5:96559600-96560000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:96559600-96560200	Enhancers	NH-A	brain
21	chr5:96559600-96560200	Enhancers	Osteobl	bone
22	chr5:96559600-96560600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:96560000-96560400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:96560000-96560400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr5:96560000-96560400	Enhancers	HepG2	liver
26	chr5:96560000-96565000	Weak transcription	NHDF-Ad	bronchial
27	chr5:96560400-96561000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr5:96562400-96565400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr5:96564800-96565200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:96565000-96565200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr5:96565000-96565600	Enhancers	Placenta Amnion	Placenta Amnion
32	chr5:96565000-96566000	Enhancers	NHDF-Ad	bronchial
33	chr5:96565200-96565400	Enhancers	HUVEC	blood vessel
34	chr5:96565200-96566000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr5:96565200-96566200	Enhancers	Fetal Heart	heart
36	chr5:96565400-96565600	Enhancers	Primary B cells from peripheral blood	blood
37	chr5:96565400-96565800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr5:96565400-96565800	Flanking Active TSS	HUVEC	blood vessel
39	chr5:96565400-96566000	Enhancers	Fetal Lung	lung
40	chr5:96565400-96566000	Active TSS	Right Atrium	heart
41	chr5:96565600-96566000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr5:96565600-96571200	Weak transcription	Placenta Amnion	Placenta Amnion
43	chr5:96565800-96566000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr5:96565800-96566000	Enhancers	HUVEC	blood vessel
45	chr5:96566000-96567000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr5:96566000-96567000	Weak transcription	NHDF-Ad	bronchial
47	chr5:96566600-96567200	Enhancers	Liver	Liver
48	chr5:96566800-96567200	Active TSS	Brain Angular Gyrus	brain
49	chr5:96566800-96567200	Enhancers	Colon Smooth Muscle	Colon
50	chr5:96566800-96567400	Enhancers	Dnd41	blood

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