Variant report

Variant	nsv569090
Chromosome Location	chr15:34736508-34982384
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3268)
CpG islands
(count:2506)
Chromatin interactive
region (count:113)
LncRNA
region (count:24)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:3268 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34869965-34870045	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:34905532-34905838	K562	blood:	n/a	n/a
3	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
4	ARID3A	chr15:34880209-34880840	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
6	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
7	ARID3A	chr15:34908827-34909205	K562	blood:	n/a	n/a
8	ARID3A	chr15:34875226-34875237	K562	blood:	n/a	n/a
9	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
10	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
11	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
12	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
13	ARID3A	chr15:34781246-34781587	K562	blood:	n/a	n/a
14	ARID3A	chr15:34902659-34902943	K562	blood:	n/a	n/a
15	ARID3A	chr15:34886706-34886742	K562	blood:	n/a	n/a
16	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
17	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
18	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
19	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
20	ARID3A	chr15:34880295-34880915	K562	blood:	n/a	n/a
21	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
22	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
23	ATF1	chr15:34870112-34870339	K562	blood:	n/a	n/a
24	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
25	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
26	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
27	ATF1	chr15:34807442-34807640	K562	blood:	n/a	n/a
28	ATF1	chr15:34808283-34808324	K562	blood:	n/a	n/a
29	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
30	ATF1	chr15:34761374-34761389	K562	blood:	n/a	n/a
31	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
32	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
33	ATF1	chr15:34896856-34896884	K562	blood:	n/a	n/a
34	ATF1	chr15:34905714-34905797	K562	blood:	n/a	n/a
35	ATF1	chr15:34880295-34880819	K562	blood:	n/a	n/a
36	ATF1	chr15:34908847-34909148	K562	blood:	n/a	n/a
37	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
38	ATF2	chr15:34880257-34880906	GM12878	blood:	n/a	n/a
39	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
40	ATF2	chr15:34880089-34880894	GM12878	blood:	n/a	n/a
41	ATF2	chr15:34880485-34880875	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF3	chr15:34908811-34909131	K562	blood:	n/a	n/a
43	ATF3	chr15:34781262-34781502	K562	blood:	n/a	n/a
44	BACH1	chr15:34806578-34807213	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
46	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
47	BACH1	chr15:34876822-34876846	K562	blood:	n/a	n/a
48	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
49	BATF	chr15:34842238-34842949	GM12878	blood:	n/a	n/a
50	BATF	chr15:34842337-34842744	GM12878	blood:	n/a	n/a

(count:2506 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:34807679-34807729	RPTEC	kidney:	n/a
2	chr15:34874862-34874912	Hepatocyte	liver:	n/a
3	chr15:34876347-34876397	GM12891	blood:	n/a
4	chr15:34875325-34875375	HRCEpiC	kidney:	n/a
5	chr15:34807221-34807271	SAEC	small airway:	n/a
6	chr15:34807679-34807729	RPTEC	kidney:	n/a
7	chr15:34874862-34874912	Hepatocyte	liver:	n/a
8	chr15:34876347-34876397	GM12891	blood:	n/a
9	chr15:34875325-34875375	HRCEpiC	kidney:	n/a
10	chr15:34807221-34807271	SAEC	small airway:	n/a
11	chr15:34875117-34875167	HRE	kidney:	n/a
12	chr15:34875891-34875941	HAEpiC	amniotic membrane:	n/a
13	chr15:34875930-34875980	RPTEC	kidney:	n/a
14	chr15:34875138-34875188	AG04449	skin:	fetal
15	chr15:34817982-34818032	AG09319	gingival:	n/a
16	chr15:34791564-34791614	HCPEpiC	choroid plexus:	n/a
17	chr15:34876471-34876521	HMEC	breast:	n/a
18	chr15:34788847-34788897	SK-N-MC	brain:	n/a
19	chr15:34788017-34788067	HEEpiC	esophagus:	n/a
20	chr15:34806349-34806399	HUVEC	blood vessel:	n/a
21	chr15:34875937-34875987	IMR90	lung:	fetal
22	chr15:34876347-34876397	NHDF-neo	bronchial:	n/a
23	chr15:34782167-34782217	T-47D	breast:	n/a
24	chr15:34876347-34876397	HNPCEpiC	eye:	n/a
25	chr15:34807221-34807271	NHBE	bronchial:	n/a
26	chr15:34781705-34781755	NHDF-neo	bronchial:	n/a
27	chr15:34807050-34807100	HIPEpiC	eye:	n/a
28	chr15:34875250-34875300	AoSMC	blood vessel:	n/a
29	chr15:34876347-34876397	NHBE	bronchial:	n/a
30	chr15:34874183-34874233	MCF-7	breast:	n/a
31	chr15:34782820-34782870	Jurkat	blood:	n/a
32	chr15:34806592-34806642	Hela-S3	cervix:	n/a
33	chr15:34787400-34787450	NB4	blood:	n/a
34	chr15:34806349-34806399	HMEC	breast:	n/a
35	chr15:34788017-34788067	HAEpiC	amniotic membrane:	n/a
36	chr15:34875937-34875987	HPAEpiC	pulmonary alveolar:	n/a
37	chr15:34787400-34787450	ovcar-3	ovarian:	n/a
38	chr15:34788017-34788067	LNCaP	prostate:	n/a
39	chr15:34781891-34781941	BE2_C	brain:	n/a
40	chr15:34807050-34807100	IMR90	lung:	fetal
41	chr15:34874862-34874912	U87	brain:	n/a
42	chr15:34807050-34807100	NHBE	bronchial:	n/a
43	chr15:34788847-34788897	AG04450	lung:	fetal
44	chr15:34787920-34787970	AoSMC	blood vessel:	n/a
45	chr15:34806592-34806642	Caco-2	colon:	n/a
46	chr15:34875138-34875188	HRE	kidney:	n/a
47	chr15:34785380-34785430	HIPEpiC	eye:	n/a
48	chr15:34876471-34876521	HRPEpiC	eye:	n/a
49	chr15:34877407-34877457	HEEpiC	esophagus:	n/a
50	chr15:34782820-34782870	HRE	kidney:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:34879223..34881623-chr15:34893177..34895546,2	K562	blood:
2	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
3	chr15:34726561..34729987-chr15:34871215..34874723,3	K562	blood:
4	chr15:34518743..34520763-chr15:34876016..34878611,2	MCF-7	breast:
5	chr15:34867657..34871070-chr15:34876144..34878325,3	K562	blood:
6	chr15:34774551..34776237-chr15:34779411..34782082,2	K562	blood:
7	chr15:34728131..34733225-chr15:34735717..34740218,7	K562	blood:
8	chr15:34790342..34793794-chr15:34793900..34797346,3	K562	blood:
9	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
10	chr15:34949722..34952645-chr15:34986997..34989606,2	K562	blood:
11	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
12	chr15:34728587..34731061-chr15:34780506..34783189,3	K562	blood:
13	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
14	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
15	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
16	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
17	chr15:34769198..34772919-chr15:34774454..34777192,3	K562	blood:
18	chr15:34898803..34900649-chr15:34905656..34908079,2	K562	blood:
19	chr15:34875152..34877762-chr15:34886558..34889393,2	MCF-7	breast:
20	chr15:34513565..34517614-chr15:34877827..34881077,3	K562	blood:
21	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
22	chr15:34875762..34878300-chr15:34879087..34881803,6	K562	blood:
23	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
24	chr15:34728587..34731061-chr15:34780506..34783189,2	K562	blood:
25	chr15:34868472..34871070-chr15:34876144..34878325,2	K562	blood:
26	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
27	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
28	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
29	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
30	chr15:34892499..34894333-chr15:34896967..34899231,2	K562	blood:
31	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
32	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
33	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
34	chr15:34931128..34933994-chr15:34934903..34936649,2	K562	blood:
35	chr15:34873722..34878608-chr15:34878671..34882990,11	K562	blood:
36	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
37	chr15:34934825..34936603-chr15:34945044..34948146,4	K562	blood:
38	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
39	chr15:34330963..34332496-chr15:34876229..34877827,2	K562	blood:
40	chr15:34790196..34793794-chr15:34794467..34797662,3	K562	blood:
41	chr15:34659441..34662117-chr15:34875107..34877933,3	K562	blood:
42	chr15:34980841..34982732-chr15:34984201..34987180,2	K562	blood:
43	chr15:34937548..34939695-chr15:34950801..34953012,2	K562	blood:
44	chr15:34869058..34871895-chr15:34873883..34875893,3	K562	blood:
45	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
46	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
47	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
48	chr15:34941344..34943269-chr15:34977002..34979213,2	K562	blood:
49	chr15:34728066..34730668-chr15:34791069..34792682,2	K562	blood:
50	chr15:34664329..34667047-chr15:34894143..34895743,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
2	lnc-GJD2-4	chr15:34875717-34875835	NONHSAT041596
3	lnc-C15orf55-4	chr15:34752685-34752950	uc_384_+
4	lnc-GJD2-4	chr15:34843392-34843477	NONHSAT140232
5	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
6	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
7	lnc-GOLGA8B-1	chr15:34752685-34752950	uc_384_-
8	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
9	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
10	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
11	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
12	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT041596
13	lnc-GJD2-4	chr15:34845096-34845292	NONHSAT140232
14	lnc-GJD2-4	chr15:34867026-34867115	NONHSAT041596
15	lnc-GJD2-4	chr15:34845174-34845292	NONHSAT041596
16	lnc-GJD2-3	chr15:34858091-34858674	NONHSAT041597
17	lnc-GJD2-4	chr15:34845946-34846157	NONHSAT140232
18	lnc-GJD2-3	chr15:34874951-34875061	NONHSAT041597
19	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
20	lnc-GJD2-4	chr15:34873667-34873700	NONHSAT140232
21	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
22	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
23	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
24	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1233-5p	chr15:34820548-34820569	MIMAT0022943_1
hsa-miR-1233-3p	chr15:34820491-34820510	MIMAT0005588_1

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GOLGA8B	hsa-miR-15a-5p	chr15:34817527-34817548
2	GOLGA8B	hsa-miR-32-5p	chr15:34818291-34818311

Variant related genes	Relation type
ENSG00000261304	TF binding region
ENSG00000261559	TF binding region
MIR1233-2	TF binding region
ENSG00000259892	TF binding region
GOLGA8A	TF binding region
HNRNPLP2	TF binding region
ENSG00000252425	TF binding region
GOLGA8B	TF binding region
ENSG00000261304	CpG island
ENSG00000261559	CpG island
MIR1233-2	CpG island
ENSG00000259892	CpG island
GOLGA8A	CpG island
HNRNPLP2	CpG island
ENSG00000252425	CpG island
GOLGA8B	CpG island
ENSG00000128463	chromatin interactions
ENSG00000175265	chromatin interactions
ENSG00000075618	chromatin interactions
ENSG00000140199	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000215252	chromatin interactions
ENSG00000266205	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000198146	chromatin interactions
ENSG00000182117	chromatin interactions
ENSG00000259904	chromatin interactions
NEK9	miRNA target sites
NEK7	miRNA target sites

Extended variants
information (count: 6802 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:6802 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8024012	chr15:34736508-34736509	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs185302112	chr15:34736585-34736586	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs73378028	chr15:34736593-34736594	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs115143568	chr15:34736715-34736716	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571030726	chr15:34736792-34736793	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs545677531	chr15:34736794-34736795	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs190175078	chr15:34736830-34736831	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575544101	chr15:34736854-34736855	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542580643	chr15:34736913-34736914	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560970203	chr15:34736923-34736924	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113769745	chr15:34736932-34736933	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs77115468	chr15:34736934-34736935	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559489949	chr15:34736962-34736963	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs533026189	chr15:34736989-34736990	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs181534732	chr15:34737051-34737052	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs8043533	chr15:34737108-34737109	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs8023257	chr15:34737129-34737130	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs184120707	chr15:34737130-34737131	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs8023260	chr15:34737135-34737136	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs143814251	chr15:34737143-34737144	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs376437402	chr15:34737144-34737145	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs199950591	chr15:34737145-34737146	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs75583176	chr15:34737162-34737163	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs12595126	chr15:34737211-34737212	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs552837468	chr15:34737253-34737254	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs571319130	chr15:34737303-34737304	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538819673	chr15:34737324-34737325	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576704529	chr15:34737345-34737346	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs73378030	chr15:34737444-34737445	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs575506981	chr15:34737486-34737487	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114241511	chr15:34737489-34737490	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555372507	chr15:34737495-34737496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs7173792	chr15:34737496-34737497	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs150823634	chr15:34737501-34737502	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188471528	chr15:34737562-34737563	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs1826780	chr15:34737567-34737568	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs1826779	chr15:34737584-34737585	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs180931311	chr15:34737600-34737601	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs139656614	chr15:34737613-34737614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs1826778	chr15:34737622-34737623	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs550353089	chr15:34737663-34737664	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2879471	chr15:34737697-34737698	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs528025440	chr15:34737725-34737726	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546587952	chr15:34737778-34737779	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs114873407	chr15:34737813-34737814	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs538750698	chr15:34737818-34737819	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs116641563	chr15:34737819-34737820	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs569143251	chr15:34737853-34737854	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536539746	chr15:34737855-34737856	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs77762751	chr15:34737908-34737909	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34736800-34737000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr15:34738000-34738200	Bivalent Enhancer	Placenta	Placenta
3	chr15:34740000-34740600	Bivalent/Poised TSS	A549	lung
4	chr15:34749200-34749600	Enhancers	Fetal Lung	lung
5	chr15:34749600-34750400	Weak transcription	Fetal Lung	lung
6	chr15:34750400-34750600	Enhancers	Fetal Lung	lung
7	chr15:34750600-34750800	Weak transcription	Fetal Lung	lung
8	chr15:34753600-34754200	Enhancers	HepG2	liver
9	chr15:34753800-34754000	Enhancers	Fetal Lung	lung
10	chr15:34759000-34759400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:34761000-34762800	Enhancers	HepG2	liver
12	chr15:34768400-34769000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr15:34772600-34773200	Enhancers	Fetal Brain Male	brain
14	chr15:34773200-34775000	Weak transcription	Fetal Brain Male	brain
15	chr15:34775200-34775400	Enhancers	Fetal Brain Male	brain
16	chr15:34780400-34781600	Active TSS	K562	blood
17	chr15:34780800-34781600	Bivalent/Poised TSS	A549	lung
18	chr15:34781000-34781600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr15:34781600-34781800	Flanking Active TSS	K562	blood
20	chr15:34782000-34786600	Weak transcription	Right Ventricle	heart
21	chr15:34782200-34783200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
22	chr15:34782400-34782600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr15:34782400-34782600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
24	chr15:34782400-34782800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr15:34782400-34783000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:34782400-34783200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
27	chr15:34782400-34783200	Active TSS	H9 Cell Line	embryonic stem cell
28	chr15:34782400-34783200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
29	chr15:34782400-34783400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
30	chr15:34782600-34783000	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:34782600-34783200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:34782800-34783000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
33	chr15:34782800-34783000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr15:34782800-34783000	Bivalent/Poised TSS	HSMM	muscle
35	chr15:34782800-34783200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr15:34782800-34783200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
37	chr15:34782800-34783200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
38	chr15:34782800-34783200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr15:34782800-34783200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:34782800-34783400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr15:34783000-34783200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
42	chr15:34783000-34783200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr15:34783000-34783200	Bivalent Enhancer	Fetal Heart	heart
44	chr15:34783000-34783400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr15:34783000-34783400	Bivalent Enhancer	Fetal Lung	lung
46	chr15:34783200-34783400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
47	chr15:34783200-34783400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
48	chr15:34783200-34783400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
49	chr15:34783600-34783800	Bivalent/Poised TSS	Primary T cells from cord blood	blood
50	chr15:34784200-34784400	Bivalent/Poised TSS	Primary T cells from cord blood	blood

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