Variant report

Variant	nsv946307
Chromosome Location	chr1:146982909-147012496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:305)
Chromatin interactive
region (count:50)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:147010941-147011203	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:146987133-146987696	HepG2	liver:	n/a	n/a
3	BACH1	chr1:147011926-147012361	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:147012073-147012157	HepG2	liver:	n/a	n/a
5	BRCA1	chr1:146986633-146987703	Hela-S3	cervix:	n/a	n/a
6	BRCA1	chr1:146997582-146997667	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr1:146987295-146987568	H1-hESC	embryonic stem cell:	n/a	n/a
8	CBX3	chr1:147010885-147011307	K562	blood:	n/a	n/a
9	CBX3	chr1:147010742-147011440	HCT-116	colon:	n/a	n/a
10	CEBPB	chr1:147010860-147011404	HCT-116	colon:	n/a	n/a
11	CEBPB	chr1:147010799-147011472	IMR90	lung:	n/a	n/a
12	CEBPB	chr1:147006344-147006388	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:146986892-146987191	K562	blood:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
14	CEBPB	chr1:147010915-147011101	K562	blood:	n/a	n/a
15	CEBPB	chr1:147009511-147009761	HepG2	liver:	n/a	chr1:147009594-147009607 chr1:147009595-147009606
16	CEBPB	chr1:147010829-147011347	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:146986906-146987186	IMR90	lung:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
18	CEBPB	chr1:147010825-147011317	A549	lung:	n/a	n/a
19	CEBPB	chr1:147010870-147011418	MCF-7	breast:	n/a	n/a
20	CEBPB	chr1:146986863-146987704	HepG2	liver:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
21	CEBPB	chr1:147010863-147011210	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr1:147010829-147011350	ECC-1	luminal epithelium:	n/a	n/a
23	CEBPB	chr1:147010692-147011361	HCT-116	colon:	n/a	n/a
24	CEBPB	chr1:147010786-147011365	A549	lung:	n/a	n/a
25	CEBPB	chr1:147010893-147011127	K562	blood:	n/a	n/a
26	CEBPB	chr1:146986812-146987792	MCF-7	breast:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
27	CEBPB	chr1:146999121-146999462	HepG2	liver:	n/a	n/a
28	CEBPB	chr1:147009485-147009687	A549	lung:	n/a	chr1:147009594-147009607 chr1:147009595-147009606
29	CEBPB	chr1:147009452-147009747	IMR90	lung:	n/a	chr1:147009594-147009607 chr1:147009595-147009606
30	CEBPB	chr1:146986819-146987756	MCF-7	breast:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
31	CEBPB	chr1:147010812-147011225	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr1:147009429-147009723	K562	blood:	n/a	chr1:147009594-147009607 chr1:147009595-147009606
33	CEBPB	chr1:146986922-146987694	A549	lung:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
34	CEBPB	chr1:146987375-146987707	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr1:146986943-146987120	HepG2	liver:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
36	CEBPB	chr1:146986814-146987723	Hela-S3	cervix:	n/a	chr1:146987032-146987043 chr1:146987068-146987079
37	CEBPB	chr1:147010817-147011236	A549	lung:	n/a	n/a
38	CHD1	chr1:147011883-147015001	IMR90	lung:	n/a	n/a
39	CHD1	chr1:147011256-147011279	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD1	chr1:147012277-147012760	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr1:146986874-146987634	Hela-S3	cervix:	n/a	n/a
42	CHD2	chr1:147011598-147011687	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr1:146987167-146987562	HepG2	liver:	n/a	n/a
44	CTCF	chr1:146987320-146987470	Caco-2	colon:	n/a	n/a
45	CTCF	chr1:146987280-146987430	HepG2	liver:	n/a	n/a
46	CTCF	chr1:146987320-146987470	HRE	kidney:	n/a	n/a
47	CTCF	chr1:146987042-146987883	A549	lung:	n/a	n/a
48	CTCF	chr1:146987121-146987731	HCT-116	colon:	n/a	n/a
49	CTCF	chr1:146987340-146987490	HPF	lung:	n/a	n/a
50	CTCF	chr1:146987280-146987430	HPAF	blood vessel:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:146990815-146990865	HEK293	kidney:	embryo
2	chr1:146989936-146989986	HNPCEpiC	eye:	n/a
3	chr1:146990815-146990865	NHDF-neo	bronchial:	n/a
4	chr1:147011226-147011276	BJ	skin:	n/a
5	chr1:146989469-146989519	GM06990	blood:	n/a
6	chr1:146990815-146990865	Jurkat	blood:	n/a
7	chr1:146989469-146989519	HepG2	liver:	n/a
8	chr1:146989524-146989574	NT2-D1	testis:	n/a
9	chr1:146989469-146989519	SK-N-SH_RA	brain:	n/a
10	chr1:146990815-146990865	AG04449	skin:	fetal
11	chr1:146989469-146989519	HRPEpiC	eye:	n/a
12	chr1:146990815-146990865	HCF	heart:	n/a
13	chr1:147011226-147011276	HAEpiC	amniotic membrane:	n/a
14	chr1:146989469-146989519	HRCEpiC	kidney:	n/a
15	chr1:146989524-146989574	SK-N-MC	brain:	n/a
16	chr1:146989524-146989574	HMEC	breast:	n/a
17	chr1:146990815-146990865	IMR90	lung:	fetal
18	chr1:146989524-146989574	HepG2	liver:	n/a
19	chr1:146989936-146989986	HEEpiC	esophagus:	n/a
20	chr1:146989469-146989519	MCF10A-Er-Src	breast:	n/a
21	chr1:146989524-146989574	Caco-2	colon:	n/a
22	chr1:146989936-146989986	PFSK-1	brain:	n/a
23	chr1:147011226-147011276	GM19239	blood:	n/a
24	chr1:146990815-146990865	GM12891	blood:	n/a
25	chr1:146990815-146990865	HUVEC	blood vessel:	n/a
26	chr1:146990815-146990865	HepG2	liver:	n/a
27	chr1:146989524-146989574	SK-N-SH_RA	brain:	n/a
28	chr1:146990815-146990865	HL-60	blood:	n/a
29	chr1:146990815-146990865	AG04450	lung:	fetal
30	chr1:146989524-146989574	AG09309	skin:	n/a
31	chr1:146990815-146990865	Caco-2	colon:	n/a
32	chr1:146989469-146989519	SK-N-SH	brain:	n/a
33	chr1:146989469-146989519	Jurkat	blood:	n/a
34	chr1:147011226-147011276	Hepatocyte	liver:	n/a
35	chr1:146989469-146989519	NH-A	brain:	n/a
36	chr1:146989469-146989519	NHBE	bronchial:	n/a
37	chr1:146989936-146989986	PANC-1	pancreas:	n/a
38	chr1:146989469-146989519	ECC-1	luminal epithelium:	n/a
39	chr1:147011226-147011276	HMEC	breast:	n/a
40	chr1:146989469-146989519	HCM	heart:	n/a
41	chr1:146989524-146989574	H1-hESC	embryonic stem cell:	embryo
42	chr1:146989524-146989574	NHDF-neo	bronchial:	n/a
43	chr1:146990815-146990865	GM12892	blood:	n/a
44	chr1:146989524-146989574	HEEpiC	esophagus:	n/a
45	chr1:146990815-146990865	K562	blood:	n/a
46	chr1:146989936-146989986	A549	lung:	n/a
47	chr1:146989936-146989986	CMK	blood:	n/a
48	chr1:146989469-146989519	HCPEpiC	choroid plexus:	n/a
49	chr1:146989936-146989986	AG09309	skin:	n/a
50	chr1:147011226-147011276	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:146968561..146971341-chr1:146981220..146982910,2	MCF-7	breast:
2	chr1:146994684..146995210-chr1:147006230..147006786,2	MCF-7	breast:
3	chr1:146986889..146987662-chr1:147362069..147363051,2	MCF-7	breast:
4	chr1:146971936..146975765-chr1:146987041..146989232,3	MCF-7	breast:
5	chr1:146986145..146988863-chr1:147011091..147013221,2	MCF-7	breast:
6	chr1:146996649..146997529-chr1:147362466..147363022,2	K562	blood:
7	chr1:146966752..146967334-chr1:146986997..146987720,2	MCF-7	breast:
8	chr1:147006182..147008463-chr1:147080734..147083235,2	MCF-7	breast:
9	chr1:147006568..147008358-chr1:147009554..147011067,2	MCF-7	breast:
10	chr1:147004851..147006517-chr1:147008746..147011702,2	MCF-7	breast:
11	chr1:146986955..146987827-chr1:147098997..147099915,7	MCF-7	breast:
12	chr1:146994684..146995210-chr1:147006230..147006786,2	MCF-7	breast:
13	chr1:146987051..146989326-chr1:147069871..147072582,3	MCF-7	breast:
14	chr1:147008618..147011767-chr1:147071183..147073263,3	MCF-7	breast:
15	chr1:146992617..146995509-chr1:147005022..147006656,2	MCF-7	breast:
16	chr1:147004459..147006427-chr1:147014371..147016886,2	MCF-7	breast:
17	chr1:146986046..146988556-chr1:147100242..147102169,2	MCF-7	breast:
18	chr1:146986713..146988277-chr1:147098562..147099908,8	MCF-7	breast:
19	chr1:146987573..146989081-chr1:147113048..147114594,2	MCF-7	breast:
20	chr1:146985676..146987610-chr1:147082918..147084477,2	MCF-7	breast:
21	chr1:147010058..147012645-chr11:64784779..64787267,2	MCF-7	breast:
22	chr1:147008733..147014706-chr1:147069097..147075030,9	MCF-7	breast:
23	chr1:146986728..146991074-chr1:147083227..147087036,4	MCF-7	breast:
24	chr1:147004851..147006517-chr1:147008746..147011702,2	MCF-7	breast:
25	chr1:146996064..146997703-chr1:147107073..147109998,2	MCF-7	breast:
26	chr1:146981408..146984046-chr1:147070752..147072331,2	MCF-7	breast:
27	chr1:146983972..146986124-chr1:146986204..146988223,2	MCF-7	breast:
28	chr1:147000909..147003597-chr1:147005388..147008188,3	MCF-7	breast:
29	chr1:146983972..146986124-chr1:146986204..146988223,2	MCF-7	breast:
30	chr1:146990186..146991720-chr1:147111335..147114236,2	MCF-7	breast:
31	chr1:146986996..146987846-chr1:147112070..147113158,7	MCF-7	breast:
32	chr1:146986878..146987825-chr1:147113615..147114624,5	MCF-7	breast:
33	chr1:146987141..146987649-chr1:147112117..147112847,2	MCF-7	breast:
34	chr1:146995227..146997414-chr1:147002514..147004607,2	MCF-7	breast:
35	chr1:146981290..146983295-chr1:146984473..146987366,3	MCF-7	breast:
36	chr1:147011744..147014234-chr1:147070783..147072314,2	K562	blood:
37	chr1:146975932..146978497-chr1:146987460..146989632,2	MCF-7	breast:
38	chr1:147009579..147011670-chr1:147058912..147061214,2	MCF-7	breast:
39	chr1:147000909..147003597-chr1:147005388..147008188,3	MCF-7	breast:
40	chr1:146992617..146995509-chr1:147005022..147006656,2	MCF-7	breast:
41	chr1:147011744..147014234-chr1:147070783..147073063,3	K562	blood:
42	chr1:146978011..146980028-chr1:146980271..146983213,3	K562	blood:
43	chr1:146981290..146983295-chr1:146984473..146987366,3	MCF-7	breast:
44	chr1:146985951..146991555-chr1:147068919..147074935,7	MCF-7	breast:
45	chr1:147010483..147014086-chr1:147140786..147143809,3	MCF-7	breast:
46	chr1:146980604..146983264-chr1:146987752..146989754,2	K562	blood:
47	chr1:147008218..147010521-chr1:147012000..147014788,2	K562	blood:
48	chr1:147006568..147008358-chr1:147009554..147011067,2	MCF-7	breast:
49	chr1:147009715..147011902-chr1:147032676..147034909,2	MCF-7	breast:
50	chr1:146995227..146997414-chr1:147002514..147004607,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACP6-1	chr1:146986158-146986268	NONHSAT139896
2	lnc-ACP6-1	chr1:146986158-146986268	NONHSAT006035
3	lnc-ACP6-1	chr1:146986158-146986268	ENSG00000234610
4	lnc-ACP6-1	chr1:146987344-146987499	NONHSAT006037
5	lnc-ACP6-1	chr1:146989266-146989699	ENSG00000234610
6	lnc-ACP6-1	chr1:146989266-146989699	NONHSAT006032
7	lnc-ACP6-1	chr1:146985961-146986268	NONHSAT006037
8	lnc-ACP6-1	chr1:146986158-146986268	NONHSAT006032
9	lnc-ACP6-1	chr1:146987344-146987499	ENSG00000234610
10	lnc-ACP6-1	chr1:146989266-146989699	NONHSAT006008
11	lnc-ACP6-1	chr1:146987344-146987499	NONHSAT006008
12	lnc-ACP6-1	chr1:146987344-146987499	NONHSAT006032
13	lnc-ACP6-1	chr1:146987344-146987591	NONHSAT006035
14	lnc-ACP6-1	chr1:146989266-146989686	NONHSAT139896
15	lnc-ACP6-1	chr1:146987344-146987499	NONHSAT139896
16	lnc-ACP6-1	chr1:146986158-146986268	NONHSAT006008
17	lnc-ACP6-1	chr1:146989266-146989686	NONHSAT006037

No data

Variant related genes	Relation type
LINC00624	TF binding region
BCL9	TF binding region
LINC00624	CpG island
BCL9	CpG island
ENSG00000162836	chromatin interactions
ENSG00000116128	chromatin interactions
ENSG00000234610	chromatin interactions
ENSG00000213465	chromatin interactions

Extended variants
information (count: 1171 )
Associated
traits (count: 157 )

Variant overlapped rSNPs/rCNVs (count:1171 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587741419	chr1:146982942-146982943	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs184816100	chr1:146982954-146982955	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189673737	chr1:146982958-146982959	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373517778	chr1:146982970-146982971	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs587770926	chr1:146982997-146982998	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370297171	chr1:146982998-146982999	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs369086618	chr1:146983014-146983015	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs59217751	chr1:146983015-146983016	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs587702855	chr1:146983051-146983052	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146482743	chr1:146983074-146983075	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs10494254	chr1:146983083-146983084	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs587707804	chr1:146983098-146983099	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs587637688	chr1:146983105-146983106	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs6695904	chr1:146983115-146983116	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs192704033	chr1:146983127-146983128	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs587644653	chr1:146983162-146983163	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs184701069	chr1:146983191-146983192	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs587601241	chr1:146983211-146983212	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587675666	chr1:146983220-146983221	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs587708527	chr1:146983245-146983246	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587603031	chr1:146983292-146983293	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs141159366	chr1:146983313-146983314	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs74125714	chr1:146983314-146983315	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs189022477	chr1:146983395-146983396	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs181979293	chr1:146983407-146983408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587748233	chr1:146983412-146983413	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs186315941	chr1:146983423-146983424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376392428	chr1:146983427-146983428	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150167701	chr1:146983437-146983438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs587719283	chr1:146983455-146983456	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs371133654	chr1:146983463-146983464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587759207	chr1:146983465-146983466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs587626967	chr1:146983504-146983505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs189201371	chr1:146983595-146983596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs180674996	chr1:146983700-146983701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs587642994	chr1:146983705-146983706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs587722627	chr1:146983706-146983707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs587757589	chr1:146983736-146983737	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587653022	chr1:146983754-146983755	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs112691083	chr1:146983770-146983771	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185936868	chr1:146983790-146983791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs587607292	chr1:146983843-146983844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370255142	chr1:146983885-146983886	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs145595861	chr1:146983929-146983930	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs77570052	chr1:146984000-146984001	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs587594711	chr1:146984039-146984040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2353547	chr1:146984062-146984063	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs6699275	chr1:146984075-146984076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs143434916	chr1:146984115-146984116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs587678129	chr1:146984129-146984130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:157)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146978200-146987400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:146978200-146987400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:146978400-146987200	Weak transcription	Fetal Kidney	kidney
4	chr1:146979800-146989400	Weak transcription	Aorta	Aorta
5	chr1:146980400-146983000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr1:146981200-146987400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr1:146981400-146983000	Enhancers	Left Ventricle	heart
8	chr1:146981400-146983000	Enhancers	Right Atrium	heart
9	chr1:146981400-146983400	Enhancers	Fetal Lung	lung
10	chr1:146981600-146983000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr1:146981600-146984000	Enhancers	Liver	Liver
12	chr1:146981800-146983000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr1:146982000-146983200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr1:146982200-146983200	Weak transcription	Fetal Brain Female	brain
15	chr1:146982200-146983600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr1:146982200-146985800	Weak transcription	Hela-S3	cervix
17	chr1:146982200-146987400	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr1:146982400-146987200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr1:146982400-146988600	Weak transcription	Placenta	Placenta
20	chr1:146982600-146983000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr1:146982800-146983000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr1:146982800-146983000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr1:146982800-146983000	Flanking Active TSS	Fetal Heart	heart
24	chr1:146983000-146983200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr1:146983000-146983200	Enhancers	Fetal Heart	heart
26	chr1:146983000-146985800	Weak transcription	Right Atrium	heart
27	chr1:146983000-146986000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:146983000-146987400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr1:146983000-146987400	Weak transcription	Left Ventricle	heart
30	chr1:146983200-146983400	Flanking Active TSS	Fetal Heart	heart
31	chr1:146983200-146983800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr1:146983400-146985000	Enhancers	Fetal Heart	heart
33	chr1:146983400-146985800	Weak transcription	Fetal Lung	lung
34	chr1:146983600-146984200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr1:146983800-146984000	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr1:146983800-146984000	Enhancers	Fetal Brain Female	brain
37	chr1:146984000-146985600	Weak transcription	Liver	Liver
38	chr1:146985000-146987000	Weak transcription	Fetal Heart	heart
39	chr1:146985600-146987000	Enhancers	Liver	Liver
40	chr1:146985600-146988200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:146985800-146986200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:146985800-146986200	Enhancers	Right Atrium	heart
43	chr1:146985800-146986400	Enhancers	Spleen	Spleen
44	chr1:146985800-146987000	Enhancers	Fetal Lung	lung
45	chr1:146985800-146988800	Enhancers	Hela-S3	cervix
46	chr1:146986000-146987000	Weak transcription	Fetal Intestine Small	intestine
47	chr1:146986200-146987200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:146986200-146987400	Weak transcription	Right Atrium	heart
49	chr1:146986200-146990600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr1:146986400-146988000	Weak transcription	Spleen	Spleen

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