Variant report

Variant	nsv889246
Chromosome Location	chr7:139710148-139771380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1014)
CpG islands
(count:855)
Chromatin interactive
region (count:100)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1014 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:139763122-139763314	K562	blood:	n/a	n/a
2	ARID3A	chr7:139762752-139762780	K562	blood:	n/a	n/a
3	ARID3A	chr7:139762724-139763051	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:139749016-139749849	HepG2	liver:	n/a	n/a
5	ATF1	chr7:139753991-139754296	K562	blood:	n/a	n/a
6	ATF2	chr7:139762626-139763048	GM12878	blood:	n/a	n/a
7	ATF3	chr7:139762391-139763017	K562	blood:	n/a	n/a
8	ATF3	chr7:139762357-139763032	K562	blood:	n/a	n/a
9	BACH1	chr7:139762033-139762811	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr7:139762720-139763237	A549	lung:	n/a	n/a
11	BCLAF1	chr7:139762248-139763109	K562	blood:	n/a	n/a
12	BCLAF1	chr7:139762540-139762966	GM12878	blood:	n/a	n/a
13	BHLHE40	chr7:139762489-139763197	K562	blood:	n/a	chr7:139762694-139762710 chr7:139762843-139762859 chr7:139762808-139762824 chr7:139762659-139762675
14	BHLHE40	chr7:139759062-139759310	K562	blood:	n/a	n/a
15	BHLHE40	chr7:139760531-139761304	K562	blood:	n/a	n/a
16	BHLHE40	chr7:139717752-139718222	HepG2	liver:	n/a	n/a
17	BHLHE40	chr7:139753668-139754168	GM12878	blood:	n/a	n/a
18	BHLHE40	chr7:139762351-139763005	GM12878	blood:	n/a	chr7:139762694-139762710 chr7:139762843-139762859 chr7:139762808-139762824 chr7:139762659-139762675
19	BRCA1	chr7:139746328-139746482	HepG2	liver:	n/a	n/a
20	CBX3	chr7:139766378-139767595	K562	blood:	n/a	n/a
21	CBX3	chr7:139761205-139761954	K562	blood:	n/a	n/a
22	CBX3	chr7:139759912-139763802	K562	blood:	n/a	n/a
23	CBX3	chr7:139766770-139767294	K562	blood:	n/a	n/a
24	CBX3	chr7:139762445-139762994	K562	blood:	n/a	n/a
25	CCNT2	chr7:139759224-139759621	K562	blood:	n/a	n/a
26	CCNT2	chr7:139762193-139763165	K562	blood:	n/a	n/a
27	CEBPB	chr7:139723497-139723861	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:139758829-139759012	K562	blood:	n/a	n/a
29	CEBPB	chr7:139723503-139723854	IMR90	lung:	n/a	n/a
30	CEBPB	chr7:139723405-139723899	MCF-7	breast:	n/a	n/a
31	CEBPB	chr7:139723489-139723836	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr7:139758761-139759245	IMR90	lung:	n/a	n/a
33	CEBPB	chr7:139723489-139723868	K562	blood:	n/a	n/a
34	CEBPB	chr7:139762504-139762950	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr7:139723513-139723838	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr7:139723464-139723852	K562	blood:	n/a	n/a
37	CEBPB	chr7:139762542-139762658	K562	blood:	n/a	n/a
38	CEBPB	chr7:139758845-139758936	A549	lung:	n/a	n/a
39	CEBPB	chr7:139723537-139723894	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr7:139723503-139723853	A549	lung:	n/a	n/a
41	CEBPB	chr7:139723456-139723940	A549	lung:	n/a	n/a
42	CEBPB	chr7:139723575-139723749	HepG2	liver:	n/a	n/a
43	CEBPB	chr7:139759733-139759902	K562	blood:	n/a	n/a
44	CEBPB	chr7:139723501-139723836	MCF-7	breast:	n/a	n/a
45	CEBPB	chr7:139759726-139760019	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr7:139749038-139749301	HepG2	liver:	n/a	n/a
47	CHD1	chr7:139753950-139753958	GM12878	blood:	n/a	n/a
48	CHD1	chr7:139762964-139763021	GM12878	blood:	n/a	n/a
49	CHD1	chr7:139762662-139762694	GM12878	blood:	n/a	n/a
50	CHD2	chr7:139762072-139762311	GM12878	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:139723923-139723973	HCM	heart:	n/a
2	chr7:139723923-139723973	HCM	heart:	n/a
3	chr7:139763574-139763624	T-47D	breast:	n/a
4	chr7:139761087-139761137	PANC-1	pancreas:	n/a
5	chr7:139763659-139763709	AG10803	skin:	n/a
6	chr7:139760375-139760425	NH-A	brain:	n/a
7	chr7:139719913-139719963	BE2_C	brain:	n/a
8	chr7:139767162-139767212	GM19239	blood:	n/a
9	chr7:139763542-139763592	HPAEpiC	pulmonary alveolar:	n/a
10	chr7:139760671-139760721	A549	lung:	n/a
11	chr7:139763659-139763709	MCF-7	breast:	n/a
12	chr7:139723923-139723973	HRPEpiC	eye:	n/a
13	chr7:139763659-139763709	HL-60	blood:	n/a
14	chr7:139761087-139761137	GM12878	blood:	n/a
15	chr7:139763542-139763592	NHDF-neo	bronchial:	n/a
16	chr7:139762256-139762306	HNPCEpiC	eye:	n/a
17	chr7:139762806-139762856	HRPEpiC	eye:	n/a
18	chr7:139762483-139762533	Jurkat	blood:	n/a
19	chr7:139759577-139759627	Jurkat	blood:	n/a
20	chr7:139761087-139761137	Hela-S3	cervix:	n/a
21	chr7:139723923-139723973	Jurkat	blood:	n/a
22	chr7:139762806-139762856	ovcar-3	ovarian:	n/a
23	chr7:139763542-139763592	SAEC	small airway:	n/a
24	chr7:139759577-139759627	RPTEC	kidney:	n/a
25	chr7:139763574-139763624	HCM	heart:	n/a
26	chr7:139763659-139763709	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:139767162-139767212	PANC-1	pancreas:	n/a
28	chr7:139723923-139723973	PANC-1	pancreas:	n/a
29	chr7:139763659-139763709	HEEpiC	esophagus:	n/a
30	chr7:139761087-139761137	Jurkat	blood:	n/a
31	chr7:139760375-139760425	HepG2	liver:	n/a
32	chr7:139759577-139759627	GM12891	blood:	n/a
33	chr7:139719913-139719963	AoSMC	blood vessel:	n/a
34	chr7:139762806-139762856	CMK	blood:	n/a
35	chr7:139762483-139762533	ProgFib	skin:	n/a
36	chr7:139760671-139760721	GM12891	blood:	n/a
37	chr7:139719913-139719963	MCF-7	breast:	n/a
38	chr7:139762806-139762856	AoSMC	blood vessel:	n/a
39	chr7:139763773-139763823	SKMC	muscle:	n/a
40	chr7:139763773-139763823	SAEC	small airway:	n/a
41	chr7:139762256-139762306	HRCEpiC	kidney:	n/a
42	chr7:139760375-139760425	PrEC	prostate:	n/a
43	chr7:139762256-139762306	SK-N-MC	brain:	n/a
44	chr7:139760375-139760425	HL-60	blood:	n/a
45	chr7:139767162-139767212	SK-N-SH	brain:	n/a
46	chr7:139763773-139763823	HUVEC	blood vessel:	n/a
47	chr7:139762483-139762533	AG09309	skin:	n/a
48	chr7:139762483-139762533	GM12891	blood:	n/a
49	chr7:139759577-139759627	H1-hESC	embryonic stem cell:	embryo
50	chr7:139763542-139763592	MCF-7	breast:	n/a

(count:100 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:139735614..139738021-chr7:139752225..139753884,2	K562	blood:
2	chr7:139758966..139761758-chr7:139775395..139777316,2	MCF-7	breast:
3	chr7:139769866..139772271-chr7:140024148..140026188,2	K562	blood:
4	chr7:139758444..139761408-chr7:139877423..139879003,2	K562	blood:
5	chr7:139732078..139733852-chr7:139736755..139739361,2	K562	blood:
6	chr7:139735162..139737651-chr7:139749199..139752181,2	MCF-7	breast:
7	chr7:139742577..139745448-chr7:139748643..139750859,3	K562	blood:
8	chr7:139703522..139705249-chr7:139711647..139714491,2	K562	blood:
9	chr7:139731761..139735058-chr7:139738550..139741730,3	MCF-7	breast:
10	chr7:139725774..139727570-chr7:139730843..139733004,2	K562	blood:
11	chr7:139742577..139745634-chr7:139749298..139751602,3	K562	blood:
12	chr15:41221155..41221697-chr7:139762629..139763275,2	NB4	blood:
13	chr7:139718158..139721333-chr7:139723129..139725747,3	MCF-7	breast:
14	chr7:139722016..139723761-chr7:139729822..139731357,2	K562	blood:
15	chr7:139590567..139592223-chr7:139758763..139760912,2	K562	blood:
16	chr7:139736132..139738632-chr7:139742471..139744834,2	K562	blood:
17	chr7:139734783..139736677-chr7:139761911..139764455,2	K562	blood:
18	chr7:139733160..139735784-chr7:139875097..139878078,2	K562	blood:
19	chr7:139715605..139717869-chr7:139720916..139723074,2	MCF-7	breast:
20	chr7:139724174..139726340-chr7:139728064..139730717,3	K562	blood:
21	chr7:139761138..139763901-chr7:140041556..140043534,2	K562	blood:
22	chr7:139742577..139745634-chr7:139749298..139751602,3	K562	blood:
23	chr7:139726200..139730000-chr7:139733204..139736690,3	MCF-7	breast:
24	chr7:139726206..139729100-chr7:139761508..139763902,2	K562	blood:
25	chr7:139735614..139738740-chr7:139752225..139754473,3	K562	blood:
26	chr7:139762029..139764590-chr7:139764727..139766239,2	K562	blood:
27	chr7:139707115..139709190-chr7:139721974..139723889,2	MCF-7	breast:
28	chr7:139726206..139727848-chr7:139761244..139763008,2	K562	blood:
29	chr7:139722287..139723790-chr7:139727579..139729120,2	K562	blood:
30	chr7:139733438..139735417-chr7:139766650..139769549,2	K562	blood:
31	chr7:139726200..139730000-chr7:139733204..139736690,3	MCF-7	breast:
32	chr7:139739892..139744270-chr7:139755110..139759179,4	K562	blood:
33	chr7:139283433..139285754-chr7:139719509..139722219,2	K562	blood:
34	chr7:139708923..139710812-chr7:139717040..139718668,2	K562	blood:
35	chr7:139762520..139764369-chr7:139768005..139771105,3	MCF-7	breast:
36	chr7:139760670..139762884-chr7:140178073..140180883,2	K562	blood:
37	chr7:139757542..139765585-chr7:139766470..139772195,12	K562	blood:
38	chr7:139742059..139744270-chr7:139755110..139757507,2	K562	blood:
39	chr7:139750607..139753541-chr7:140178239..140180151,2	MCF-7	breast:
40	chr7:139748269..139751132-chr7:139760060..139762760,2	MCF-7	breast:
41	chr7:139736132..139738632-chr7:139742471..139744834,2	K562	blood:
42	chr7:139723860..139726293-chr7:139726640..139728763,2	MCF-7	breast:
43	chr7:139727809..139730734-chr7:139875603..139877669,2	K562	blood:
44	chr7:139716234..139719219-chr7:139738586..139740669,3	MCF-7	breast:
45	chr7:139761595..139764391-chr7:139874698..139878504,4	K562	blood:
46	chr7:139715725..139717874-chr7:139721172..139723646,2	K562	blood:
47	chr7:139735614..139738021-chr7:139752225..139753884,2	K562	blood:
48	chr7:139749557..139752257-chr7:139761402..139764057,2	MCF-7	breast:
49	chr7:139770280..139773267-chr7:139778753..139781695,3	K562	blood:
50	chr7:139765527..139767886-chr7:139876898..139879118,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-JHDM1D-1	chr7:139757699-139757834	NONHSAT123661
2	lnc-JHDM1D-1	chr7:139757207-139757573	NONHSAT123661
3	lnc-JHDM1D-1	chr7:139762322-139762351	NONHSAT123661
4	lnc-JHDM1D-2	chr7:139746605-139749091	ucscGeneNc_uc003vvq_1
5	lnc-TBXAS1-4	chr7:139723548-139724022	NONHSAT123658
6	lnc-JHDM1D-2	chr7:139750454-139750702	ucscGeneNc_uc003vvq_1

No data

Variant related genes	Relation type
PARP12	TF binding region
PARP12	CpG island
ENSG00000119403	chromatin interactions
ENSG00000128917	chromatin interactions
ENSG00000124588	chromatin interactions
ENSG00000006459	chromatin interactions
ENSG00000059378	chromatin interactions
ENSG00000133606	chromatin interactions
ENSG00000260231	chromatin interactions
ENSG00000189143	chromatin interactions
ENSG00000244041	chromatin interactions
ENSG00000157800	chromatin interactions

Extended variants
information (count: 2604 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2604 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3823715	chr7:139710148-139710149	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192702477	chr7:139710158-139710159	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs114549057	chr7:139710182-139710183	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs558318717	chr7:139710189-139710190	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs547728429	chr7:139710196-139710197	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs184351399	chr7:139710214-139710215	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs189719121	chr7:139710222-139710223	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs565954622	chr7:139710280-139710281	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs115118689	chr7:139710311-139710312	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs10480350	chr7:139710351-139710352	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs541907564	chr7:139710363-139710364	Enhancers Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs560530131	chr7:139710384-139710385	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539865838	chr7:139710395-139710396	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572309689	chr7:139710517-139710518	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs73734178	chr7:139710567-139710568	Enhancers Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs368710524	chr7:139710608-139710609	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs371418254	chr7:139710622-139710623	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114192766	chr7:139710646-139710647	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549939525	chr7:139710671-139710672	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562088418	chr7:139710694-139710695	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529580272	chr7:139710701-139710702	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs541596463	chr7:139710709-139710710	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566463374	chr7:139710711-139710712	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181360438	chr7:139710742-139710743	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs201984713	chr7:139710751-139710752	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563158104	chr7:139710755-139710756	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs149419726	chr7:139710760-139710761	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs199824152	chr7:139710769-139710770	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557900360	chr7:139710776-139710777	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143826843	chr7:139710782-139710783	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs184281573	chr7:139710825-139710826	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs148186201	chr7:139710846-139710847	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs141507456	chr7:139710879-139710880	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs572420045	chr7:139710902-139710903	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs545861870	chr7:139710933-139710934	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs116584754	chr7:139710967-139710968	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs146193019	chr7:139710968-139710969	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs139190979	chr7:139710969-139710970	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs142505991	chr7:139710973-139710974	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs368966905	chr7:139711055-139711056	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189018653	chr7:139711056-139711057	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs374045562	chr7:139711081-139711082	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148889222	chr7:139711082-139711083	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs386718442	chr7:139711084-139711085	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs201351082	chr7:139711085-139711086	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs386718443	chr7:139711097-139711098	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs545685271	chr7:139711101-139711102	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143213552	chr7:139711132-139711133	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs370105517	chr7:139711142-139711143	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs117456497	chr7:139711143-139711144	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Bladder cancer	21909424	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell acute lymphoblastic leukemia	16673021	CNVD
Cancer	21183584	CNVD
Intracranial ependymoma	16609018	CNVD
Non-small cell lung cancer	21829676	CNVD
Developmental delay	19490664	CNVD
Pancreatitis	20877625	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Low-grade astrocytoma	19016743	CNVD
Medulloblastoma	16968546	CNVD
Pilocytic astrocytoma	18408760	CNVD
Idiopathic chronic pancreatitis	19584086	CNVD
Pediatric low-grade astrocytoma	19016743	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Gastric cancer	16891809	CNVD
Cancer	17440070	CNVD
Astrocytoma	18398503	CNVD
Melanoma	19671679	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1819 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:139681000-139717800	Weak transcription	Thymus	Thymus
2	chr7:139693200-139729000	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr7:139695200-139721600	Weak transcription	Colonic Mucosa	Colon
4	chr7:139702200-139712000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:139702200-139721800	Weak transcription	Fetal Thymus	thymus
6	chr7:139702400-139722400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr7:139702600-139742200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr7:139703200-139727800	Weak transcription	Right Atrium	heart
9	chr7:139704200-139710200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr7:139704200-139728800	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr7:139705400-139722000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr7:139706000-139710400	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:139706000-139727800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:139706200-139710200	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr7:139706400-139710600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:139706400-139718400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr7:139707200-139711400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr7:139707600-139713200	Weak transcription	Lung	lung
19	chr7:139707800-139722200	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr7:139708400-139711800	Weak transcription	Primary hematopoietic stem cells	blood
21	chr7:139708600-139710600	Enhancers	Pancreas	Pancrea
22	chr7:139708600-139710600	Enhancers	Stomach Mucosa	stomach
23	chr7:139708800-139717000	Weak transcription	Esophagus	oesophagus
24	chr7:139709000-139710200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chr7:139709000-139710200	Weak transcription	Fetal Heart	heart
26	chr7:139709000-139710400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr7:139709200-139710200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr7:139709200-139713200	Weak transcription	Spleen	Spleen
29	chr7:139709200-139715200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:139709400-139710200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr7:139709400-139721400	Weak transcription	Liver	Liver
32	chr7:139709800-139710600	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
33	chr7:139709800-139711600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr7:139710000-139710800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:139710000-139711000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr7:139710000-139722000	Weak transcription	Gastric	stomach
37	chr7:139710200-139710400	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr7:139710200-139710400	Enhancers	Fetal Heart	heart
39	chr7:139710200-139710600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr7:139710200-139710600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr7:139710200-139710600	Enhancers	H9 Cell Line	embryonic stem cell
42	chr7:139710200-139710600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr7:139710200-139710600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr7:139710200-139710800	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr7:139710200-139711400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr7:139710200-139721600	Weak transcription	Fetal Intestine Small	intestine
47	chr7:139710400-139710600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr7:139710400-139710600	Enhancers	Brain Cingulate Gyrus	brain
49	chr7:139710400-139713000	Weak transcription	Primary neutrophils fromperipheralblood	blood
50	chr7:139710400-139717000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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