Variant report

Variant	nsv904269
Chromosome Location	chr15:58906145-58992591
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:122)
Chromatin interactive
region (count:48)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:58918774-58919007	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:58976439-58976703	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:58992197-58992203	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:58961444-58961957	K562	blood:	n/a	chr15:58961720-58961736
5	ATF1	chr15:58970892-58971247	K562	blood:	n/a	n/a
6	ATF1	chr15:58961450-58961769	K562	blood:	n/a	n/a
7	BACH1	chr15:58992076-58992172	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr15:58992016-58992193	K562	blood:	n/a	n/a
9	CBX3	chr15:58991035-58991481	K562	blood:	n/a	n/a
10	CBX3	chr15:58949525-58949776	K562	blood:	n/a	n/a
11	CBX3	chr15:58906522-58906965	K562	blood:	n/a	n/a
12	CBX3	chr15:58906532-58906857	K562	blood:	n/a	n/a
13	CBX3	chr15:58991119-58991420	K562	blood:	n/a	n/a
14	CCNT2	chr15:58919885-58919962	K562	blood:	n/a	n/a
15	CCNT2	chr15:58961404-58961791	K562	blood:	n/a	chr15:58961565-58961585
16	CEBPB	chr15:58971027-58971233	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr15:58918503-58918845	HepG2	liver:	n/a	n/a
18	CEBPB	chr15:58992143-58992452	HepG2	liver:	n/a	n/a
19	CEBPB	chr15:58980127-58980345	HepG2	liver:	n/a	n/a
20	CEBPB	chr15:58912637-58912708	A549	lung:	n/a	chr15:58912684-58912695
21	CEBPB	chr15:58936462-58936497	IMR90	lung:	n/a	n/a
22	CEBPB	chr15:58980088-58980346	A549	lung:	n/a	n/a
23	CEBPB	chr15:58985022-58985345	A549	lung:	n/a	chr15:58985325-58985336 chr15:58985325-58985336
24	CEBPB	chr15:58992110-58992478	A549	lung:	n/a	n/a
25	CEBPB	chr15:58990795-58990995	HepG2	liver:	n/a	chr15:58990932-58990943 chr15:58990909-58990920
26	CEBPB	chr15:58987376-58987544	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr15:58992149-58992358	K562	blood:	n/a	n/a
28	CEBPB	chr15:58992098-58992475	MCF-7	breast:	n/a	n/a
29	CEBPD	chr15:58961329-58961797	K562	blood:	n/a	n/a
30	CHD2	chr15:58983000-58983009	GM12878	blood:	n/a	n/a
31	CTCF	chr15:58969661-58970003	GM12878	blood:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
32	CTCF	chr15:58969760-58969910	HPAF	blood vessel:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
33	CTCF	chr15:58983060-58983210	GM12872	blood:	n/a	n/a
34	CTCF	chr15:58969765-58969879	LNCaP	prostate:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
35	CTCF	chr15:58983071-58983118	GM12878	blood:	n/a	n/a
36	CTCF	chr15:58969773-58969867	K562	blood:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
37	CTCF	chr15:58969736-58969904	Medullo	brain:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
38	CTCF	chr15:58986558-58986661	GM10266	blood:	n/a	n/a
39	CTCF	chr15:58969768-58969851	Kidney_OC	kidney:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
40	CTCF	chr15:58958460-58958610	HRE	kidney:	n/a	n/a
41	CTCF	chr15:58983000-58983150	GM12874	blood:	n/a	n/a
42	CTCF	chr15:58983053-58983169	GM12892	blood:	n/a	n/a
43	CTCF	chr15:58969757-58969860	GM10266	blood:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
44	CTCF	chr15:58916726-58916793	Spleen_OC	spleen:	n/a	n/a
45	CTCF	chr15:58989640-58989790	HFF-Myc	foreskin:	n/a	n/a
46	CTCF	chr15:58969740-58969890	HMF	breast:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
47	CTCF	chr15:58983053-58983164	GM19240	blood:	n/a	n/a
48	CTCF	chr15:58969840-58969990	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr15:58969780-58969930	BE2_C	brain:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848
50	CTCF	chr15:58969802-58969853	GM10248	blood:	n/a	chr15:58969825-58969843 chr15:58969826-58969842 chr15:58969827-58969848

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:58985459-58985509	AG09309	skin:	n/a
2	chr15:58960059-58960109	A549	lung:	n/a
3	chr15:58960059-58960109	GM19239	blood:	n/a
4	chr15:58985459-58985509	Hepatocyte	liver:	n/a
5	chr15:58960059-58960109	K562	blood:	n/a
6	chr15:58985459-58985509	NHDF-neo	bronchial:	n/a
7	chr15:58960059-58960109	LNCaP	prostate:	n/a
8	chr15:58960059-58960109	GM06990	blood:	n/a
9	chr15:58985459-58985509	HCM	heart:	n/a
10	chr15:58960059-58960109	GM12892	blood:	n/a
11	chr15:58960059-58960109	AG04449	skin:	fetal
12	chr15:58985459-58985509	MCF10A-Er-Src	breast:	n/a
13	chr15:58985459-58985509	AoSMC	blood vessel:	n/a
14	chr15:58960059-58960109	HMEC	breast:	n/a
15	chr15:58960059-58960109	Hela-S3	cervix:	n/a
16	chr15:58985459-58985509	HIPEpiC	eye:	n/a
17	chr15:58985459-58985509	GM12891	blood:	n/a
18	chr15:58985459-58985509	HRE	kidney:	n/a
19	chr15:58960059-58960109	ovcar-3	ovarian:	n/a
20	chr15:58985459-58985509	Jurkat	blood:	n/a
21	chr15:58960059-58960109	MCF-7	breast:	n/a
22	chr15:58960059-58960109	HEEpiC	esophagus:	n/a
23	chr15:58985459-58985509	Caco-2	colon:	n/a
24	chr15:58960059-58960109	Jurkat	blood:	n/a
25	chr15:58985459-58985509	ProgFib	skin:	n/a
26	chr15:58960059-58960109	PrEC	prostate:	n/a
27	chr15:58960059-58960109	HEK293	kidney:	embryo
28	chr15:58985459-58985509	NB4	blood:	n/a
29	chr15:58985459-58985509	HL-60	blood:	n/a
30	chr15:58985459-58985509	MCF-7	breast:	n/a
31	chr15:58985459-58985509	SKMC	muscle:	n/a
32	chr15:58985459-58985509	HCT-116	colon:	n/a
33	chr15:58985459-58985509	T-47D	breast:	n/a
34	chr15:58960059-58960109	H1-hESC	embryonic stem cell:	embryo
35	chr15:58960059-58960109	HepG2	liver:	n/a
36	chr15:58960059-58960109	HAEpiC	amniotic membrane:	n/a
37	chr15:58985459-58985509	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:58960059-58960109	BJ	skin:	n/a
39	chr15:58960059-58960109	Caco-2	colon:	n/a
40	chr15:58985459-58985509	HEEpiC	esophagus:	n/a
41	chr15:58985459-58985509	AG04450	lung:	fetal
42	chr15:58960059-58960109	MCF10A-Er-Src	breast:	n/a
43	chr15:58960059-58960109	SKMC	muscle:	n/a
44	chr15:58960059-58960109	AG04450	lung:	fetal
45	chr15:58960059-58960109	HRPEpiC	eye:	n/a
46	chr15:58960059-58960109	U87	brain:	n/a
47	chr15:58960059-58960109	CMK	blood:	n/a
48	chr15:58985459-58985509	HAEpiC	amniotic membrane:	n/a
49	chr15:58985459-58985509	HUVEC	blood vessel:	n/a
50	chr15:58985459-58985509	PrEC	prostate:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:58909393..58911330-chr15:58917319..58918979,2	K562	blood:
2	chr15:58980214..58981902-chr15:58985370..58987156,2	K562	blood:
3	chr15:58903672..58906413-chr15:58914641..58916719,2	K562	blood:
4	chr15:58932722..58935543-chr15:58957168..58958694,2	K562	blood:
5	chr15:58956671..58958559-chr15:58959977..58961761,2	K562	blood:
6	chr15:58957306..58961861-chr15:58967060..58970416,4	K562	blood:
7	chr15:58945480..58947689-chr15:59040936..59043629,2	K562	blood:
8	chr15:58974278..58977039-chr15:58978595..58981232,2	K562	blood:
9	chr15:58909393..58911330-chr15:58917319..58918979,2	K562	blood:
10	chr15:58915714..58921238-chr15:58922986..58925558,6	K562	blood:
11	chr15:58953177..58955880-chr15:58958454..58961862,3	K562	blood:
12	chr15:58980214..58981902-chr15:58985370..58987156,2	K562	blood:
13	chr15:58953177..58955880-chr15:58958454..58961862,3	K562	blood:
14	chr15:58949134..58952311-chr15:58956735..58961509,4	K562	blood:
15	chr15:58932722..58935543-chr15:58957168..58958694,2	K562	blood:
16	chr15:58939363..58941206-chr15:59062666..59064194,2	MCF-7	breast:
17	chr15:58938038..58940430-chr15:58949050..58951838,2	K562	blood:
18	chr15:58959008..58961763-chr15:58963675..58966633,2	K562	blood:
19	chr15:58928689..58931025-chr15:60688699..60690909,2	K562	blood:
20	chr15:58967419..58970451-chr15:59040340..59042776,3	K562	blood:
21	chr15:58950082..58952311-chr15:58956735..58959470,2	K562	blood:
22	chr15:58960075..58965033-chr15:58965459..58970416,5	K562	blood:
23	chr15:58919916..58921624-chr15:58929696..58932530,2	K562	blood:
24	chr15:58957306..58961861-chr15:58967060..58970416,4	K562	blood:
25	chr15:58958405..58960158-chr15:58960218..58962844,2	MCF-7	breast:
26	chr15:58919916..58921624-chr15:58929696..58932530,2	K562	blood:
27	chr15:58915714..58920888-chr15:58922126..58927407,8	K562	blood:
28	chr15:58903672..58906413-chr15:58914641..58916719,2	K562	blood:
29	chr15:58950082..58952311-chr15:58956735..58959470,2	K562	blood:
30	chr15:58906314..58907814-chr15:99432678..99434601,2	MCF-7	breast:
31	chr15:58927036..58929525-chr15:58931244..58932793,2	K562	blood:
32	chr15:58915714..58921238-chr15:58922986..58925558,6	K562	blood:
33	chr15:58898609..58900839-chr15:58904046..58906383,2	K562	blood:
34	chr15:58944978..58947722-chr15:58953875..58956765,2	K562	blood:
35	chr15:58938038..58940430-chr15:58949050..58951838,2	K562	blood:
36	chr15:58915714..58920888-chr15:58922126..58927407,8	K562	blood:
37	chr15:58985652..58987532-chr15:59040716..59043625,2	K562	blood:
38	chr15:58941689..58944037-chr15:58949556..58952654,3	K562	blood:
39	chr15:58967565..58969192-chr15:58971204..58974095,2	K562	blood:
40	chr15:58919702..58922554-chr15:58940056..58942110,2	K562	blood:
41	chr15:58958405..58960158-chr15:58960218..58962844,2	MCF-7	breast:
42	chr15:58941689..58944037-chr15:58949556..58952654,3	K562	blood:
43	chr15:58944978..58947722-chr15:58953875..58956765,2	K562	blood:
44	chr15:58956671..58958559-chr15:58959977..58961761,2	K562	blood:
45	chr15:58927036..58929525-chr15:58931244..58932793,2	K562	blood:
46	chr15:58982751..58984795-chr15:59030172..59031707,2	K562	blood:
47	chr15:58949134..58952311-chr15:58956735..58961509,4	K562	blood:
48	chr15:58990755..58993550-chr15:58994892..58997699,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLTM-6	chr15:58982672-58985806	NR_073415
2	lnc-FAM63B-5	chr15:58964495-58965132	NONHSAT044121

No data

Variant related genes	Relation type
ENSG00000270986	TF binding region
ENSG00000182625	TF binding region
ADAM10	TF binding region
ENSG00000270986	CpG island
ENSG00000182625	CpG island
ADAM10	CpG island
ENSG00000137845	chromatin interactions
ENSG00000270986	chromatin interactions
ENSG00000140443	chromatin interactions
ENSG00000182625	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000182718	chromatin interactions
ENSG00000199730	chromatin interactions

Extended variants
information (count: 3557 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:3557 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4275799	chr15:58906145-58906146	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369021003	chr15:58906176-58906177	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117373644	chr15:58906207-58906208	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576173788	chr15:58906215-58906216	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544818221	chr15:58906309-58906310	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372695725	chr15:58906310-58906311	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs180835143	chr15:58906311-58906312	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540585313	chr15:58906318-58906319	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs542358287	chr15:58906354-58906355	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560433310	chr15:58906379-58906380	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs563805760	chr15:58906383-58906384	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529569415	chr15:58906401-58906402	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs8035373	chr15:58906433-58906434	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs562980867	chr15:58906440-58906441	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs531927006	chr15:58906453-58906454	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs551585374	chr15:58906457-58906458	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs142238096	chr15:58906490-58906491	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs199798161	chr15:58906499-58906500	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs200623728	chr15:58906500-58906501	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs78604572	chr15:58906506-58906507	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs186075882	chr15:58906543-58906544	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544979523	chr15:58906558-58906559	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527700840	chr15:58906578-58906579	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547785907	chr15:58906581-58906582	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs567645674	chr15:58906584-58906585	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536587587	chr15:58906599-58906600	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs552946174	chr15:58906613-58906614	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189793588	chr15:58906634-58906635	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs8036005	chr15:58906635-58906636	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs538779601	chr15:58906658-58906659	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs558379393	chr15:58906686-58906687	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs181346353	chr15:58906711-58906712	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571986333	chr15:58906719-58906720	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs540702627	chr15:58906745-58906746	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs147780083	chr15:58906762-58906763	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141140090	chr15:58906774-58906775	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569569206	chr15:58906795-58906796	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186773310	chr15:58906831-58906832	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs190662645	chr15:58906833-58906834	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs531819210	chr15:58906847-58906848	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545546841	chr15:58906920-58906921	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs200340236	chr15:58906959-58906960	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs62002361	chr15:58906970-58906971	Weak transcription ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142239924	chr15:58907029-58907030	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs112261887	chr15:58907032-58907033	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527817382	chr15:58907087-58907088	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs78921529	chr15:58907098-58907099	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186427913	chr15:58907110-58907111	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs564761224	chr15:58907143-58907144	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs11638244	chr15:58907151-58907152	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2740 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58880600-58920600	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr15:58882600-58907600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr15:58885800-58906800	Weak transcription	Fetal Brain Male	brain
4	chr15:58887200-58906600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:58888000-58906200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr15:58888400-58920000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr15:58889600-58919800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr15:58889800-58918800	Weak transcription	Osteobl	bone
9	chr15:58889800-58921000	Weak transcription	Ovary	ovary
10	chr15:58890000-58906200	Weak transcription	Small Intestine	intestine
11	chr15:58891000-58906800	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr15:58891400-58959600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr15:58893800-58906200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr15:58893800-58906200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:58894800-58906200	Strong transcription	Primary B cells from cord blood	blood
16	chr15:58894800-58906800	Weak transcription	Psoas Muscle	Psoas
17	chr15:58899200-58920200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr15:58899600-58906200	Strong transcription	Primary B cells from peripheral blood	blood
19	chr15:58900200-58908400	Weak transcription	Hela-S3	cervix
20	chr15:58900400-58906600	Strong transcription	Dnd41	blood
21	chr15:58901000-58906800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr15:58901400-58918800	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr15:58901600-58906200	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr15:58901600-58906800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr15:58901600-58906800	Weak transcription	Fetal Heart	heart
26	chr15:58901600-58913400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
27	chr15:58902600-58906600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr15:58902800-58911200	Weak transcription	HMEC	breast
29	chr15:58903000-58906200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:58903000-58906200	Weak transcription	NH-A	brain
31	chr15:58903200-58906600	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr15:58903200-58913400	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr15:58903400-58906200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr15:58903400-58906600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr15:58903400-58906800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
36	chr15:58903400-58906800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr15:58903400-58918600	Weak transcription	HUVEC	blood vessel
38	chr15:58903800-58914200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr15:58904200-58906600	Strong transcription	Primary T cells from cord blood	blood
40	chr15:58904200-58907800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr15:58904400-58906200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr15:58904400-58906400	Strong transcription	HSMMtube	muscle
43	chr15:58904600-58906200	Weak transcription	Liver	Liver
44	chr15:58904600-58906600	Strong transcription	Brain Hippocampus Middle	brain
45	chr15:58904600-58907000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr15:58904600-58907200	ZNF genes & repeats	HSMM	muscle
47	chr15:58904800-58913600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
48	chr15:58905000-58907200	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr15:58905000-58907800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr15:58905000-58907800	ZNF genes & repeats	Fetal Muscle Leg	muscle

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