Variant report

Variant	nsv878549
Chromosome Location	chr4:7295154-7376694
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr4:7325347-7326029	A549	lung:	n/a	n/a
2	ATF3	chr4:7325569-7325906	A549	lung:	n/a	n/a
3	BACH1	chr4:7351001-7351177	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCL3	chr4:7309477-7309799	GM12878	blood:	n/a	n/a
5	BCL3	chr4:7309436-7309751	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:7342329-7342469	K562	blood:	n/a	chr4:7342363-7342376
7	BHLHE40	chr4:7337542-7337783	K562	blood:	n/a	n/a
8	BHLHE40	chr4:7371415-7371470	K562	blood:	n/a	n/a
9	BHLHE40	chr4:7332888-7333034	K562	blood:	n/a	chr4:7332974-7332983 chr4:7332968-7332989 chr4:7332975-7332984 chr4:7332974-7332983 chr4:7332972-7332985
10	BHLHE40	chr4:7297755-7297955	GM12878	blood:	n/a	chr4:7297811-7297827
11	BHLHE40	chr4:7326359-7326668	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:7297759-7297998	K562	blood:	n/a	chr4:7297811-7297827
13	BRCA1	chr4:7297835-7297868	GM12878	blood:	n/a	n/a
14	BRCA1	chr4:7337624-7337876	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr4:7297940-7298009	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr4:7360137-7360214	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:7314977-7315349	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
18	CEBPB	chr4:7314983-7315346	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
19	CEBPB	chr4:7314974-7315334	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
20	CEBPB	chr4:7314946-7315363	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
21	CEBPB	chr4:7360125-7360418	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:7315082-7315202	HepG2	liver:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
23	CEBPB	chr4:7314937-7315345	MCF-7	breast:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
24	CEBPB	chr4:7350677-7351048	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
25	CEBPB	chr4:7350688-7351037	K562	blood:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
26	CEBPB	chr4:7349851-7350214	A549	lung:	n/a	n/a
27	CEBPB	chr4:7324731-7324857	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:7314977-7315363	H1-hESC	embryonic stem cell:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
29	CEBPB	chr4:7314975-7315351	IMR90	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
30	CEBPB	chr4:7315008-7315270	K562	blood:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
31	CEBPB	chr4:7350682-7351059	HepG2	liver:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
32	CEBPB	chr4:7314956-7315381	ECC-1	luminal epithelium:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
33	CEBPB	chr4:7315029-7315275	ECC-1	luminal epithelium:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
34	CEBPB	chr4:7350739-7350998	Hela-S3	cervix:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
35	CEBPB	chr4:7350554-7351087	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
36	CEBPB	chr4:7314975-7315352	K562	blood:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
37	CEBPB	chr4:7360151-7360464	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:7315017-7315331	Hela-S3	cervix:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
39	CEBPB	chr4:7350773-7351029	MCF-7	breast:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
40	CEBPB	chr4:7314905-7315396	A549	lung:	n/a	chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315161-7315170 chr4:7315160-7315171 chr4:7315161-7315170
41	CEBPB	chr4:7350683-7351098	A549	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
42	CEBPB	chr4:7350681-7351058	IMR90	lung:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
43	CEBPB	chr4:7324654-7324913	IMR90	lung:	n/a	chr4:7324854-7324865
44	CEBPB	chr4:7350726-7351008	H1-hESC	embryonic stem cell:	n/a	chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872 chr4:7350863-7350872
45	CHD2	chr4:7337159-7337242	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr4:7337620-7337770	GM12868	blood:	n/a	chr4:7337675-7337696 chr4:7337680-7337698 chr4:7337682-7337695
47	CTCF	chr4:7337380-7337981	K562	blood:	n/a	chr4:7337675-7337696 chr4:7337680-7337698 chr4:7337682-7337695
48	CTCF	chr4:7337459-7337820	A549	lung:	n/a	chr4:7337675-7337696 chr4:7337680-7337698 chr4:7337682-7337695
49	CTCF	chr4:7337600-7337750	HPF	lung:	n/a	chr4:7337675-7337696 chr4:7337680-7337698 chr4:7337682-7337695
50	CTCF	chr4:7357360-7357510	AG04449	skin:	n/a	chr4:7357478-7357494

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7368808-7368858	HepG2	liver:	n/a
2	chr4:7368808-7368858	HepG2	liver:	n/a
3	chr4:7326576-7326626	HPAEpiC	pulmonary alveolar:	n/a
4	chr4:7338837-7338887	ECC-1	luminal epithelium:	n/a
5	chr4:7373088-7373138	HCT-116	colon:	n/a
6	chr4:7374622-7374672	Hela-S3	cervix:	n/a
7	chr4:7301176-7301226	HMEC	breast:	n/a
8	chr4:7373065-7373115	GM12878	blood:	n/a
9	chr4:7373375-7373425	PFSK-1	brain:	n/a
10	chr4:7338792-7338842	HMEC	breast:	n/a
11	chr4:7301176-7301226	GM12892	blood:	n/a
12	chr4:7333381-7333431	GM06990	blood:	n/a
13	chr4:7301854-7301904	HepG2	liver:	n/a
14	chr4:7373451-7373501	BJ	skin:	n/a
15	chr4:7368808-7368858	SAEC	small airway:	n/a
16	chr4:7330616-7330666	AG09309	skin:	n/a
17	chr4:7338792-7338842	HRE	kidney:	n/a
18	chr4:7337225-7337275	NT2-D1	testis:	n/a
19	chr4:7338837-7338887	BJ	skin:	n/a
20	chr4:7368808-7368858	GM12891	blood:	n/a
21	chr4:7301491-7301541	HAEpiC	amniotic membrane:	n/a
22	chr4:7373088-7373138	HAEpiC	amniotic membrane:	n/a
23	chr4:7337225-7337275	U87	brain:	n/a
24	chr4:7338730-7338780	Hela-S3	cervix:	n/a
25	chr4:7301854-7301904	HPAEpiC	pulmonary alveolar:	n/a
26	chr4:7301176-7301226	AG09319	gingival:	n/a
27	chr4:7301176-7301226	SKMC	muscle:	n/a
28	chr4:7301823-7301873	Jurkat	blood:	n/a
29	chr4:7373375-7373425	SK-N-MC	brain:	n/a
30	chr4:7373375-7373425	AoSMC	blood vessel:	n/a
31	chr4:7326576-7326626	NT2-D1	testis:	n/a
32	chr4:7301854-7301904	GM12878	blood:	n/a
33	chr4:7338792-7338842	HEK293	kidney:	embryo
34	chr4:7338792-7338842	CMK	blood:	n/a
35	chr4:7337225-7337275	HCM	heart:	n/a
36	chr4:7301594-7301644	AG04449	skin:	fetal
37	chr4:7374582-7374632	HCPEpiC	choroid plexus:	n/a
38	chr4:7301529-7301579	SK-N-SH	brain:	n/a
39	chr4:7304739-7304789	SK-N-SH	brain:	n/a
40	chr4:7301823-7301873	AG09319	gingival:	n/a
41	chr4:7304777-7304827	HNPCEpiC	eye:	n/a
42	chr4:7373065-7373115	HRE	kidney:	n/a
43	chr4:7374622-7374672	Caco-2	colon:	n/a
44	chr4:7373022-7373072	HCPEpiC	choroid plexus:	n/a
45	chr4:7301854-7301904	NB4	blood:	n/a
46	chr4:7301594-7301644	H1-hESC	embryonic stem cell:	embryo
47	chr4:7301823-7301873	HRCEpiC	kidney:	n/a
48	chr4:7301176-7301226	Jurkat	blood:	n/a
49	chr4:7374582-7374632	HCF	heart:	n/a
50	chr4:7337225-7337275	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:7190742..7191404-chr4:7337213..7337934,2	MCF-7	breast:
2	chr4:7335965..7337731-chr4:7346043..7348434,2	MCF-7	breast:
3	chr4:7331028..7333099-chr4:7336513..7338486,2	K562	blood:
4	chr4:7335965..7337731-chr4:7346043..7348434,2	MCF-7	breast:
5	chr4:7368817..7370379-chr4:7371392..7373136,2	MCF-7	breast:
6	chr4:7343522..7345728-chr4:7361522..7364374,3	MCF-7	breast:
7	chr4:7308048..7310472-chr4:7320955..7323841,2	MCF-7	breast:
8	chr4:7320638..7322307-chr4:7344162..7346358,2	K562	blood:
9	chr4:7328869..7330375-chr4:7332248..7333752,2	MCF-7	breast:
10	chr4:7355383..7357989-chr4:7359924..7361691,2	MCF-7	breast:
11	chr4:7192934..7196110-chr4:7296657..7299976,3	MCF-7	breast:
12	chr4:7195671..7196829-chr4:7297061..7298292,4	MCF-7	breast:
13	chr4:7343522..7345728-chr4:7361522..7364374,3	MCF-7	breast:
14	chr4:7344494..7346063-chr4:7349701..7352195,2	MCF-7	breast:
15	chr4:7375155..7379159-chr4:7380747..7383834,3	K562	blood:
16	chr4:7193444..7195418-chr4:7373102..7374832,2	MCF-7	breast:
17	chr4:7337216..7338143-chr4:7463851..7464757,3	MCF-7	breast:
18	chr4:7195636..7196730-chr4:7297372..7298445,9	MCF-7	breast:
19	chr4:7288760..7290651-chr4:7292846..7295423,2	MCF-7	breast:
20	chr4:7368817..7370379-chr4:7371392..7373136,2	MCF-7	breast:
21	chr4:7368964..7371820-chr4:7419661..7422236,2	K562	blood:
22	chr4:7331028..7333099-chr4:7336513..7338486,2	K562	blood:
23	chr4:7308048..7310472-chr4:7320955..7323841,2	MCF-7	breast:
24	chr4:7193590..7194707-chr4:7297338..7298352,5	MCF-7	breast:
25	chr4:7207636..7209824-chr4:7302272..7304285,2	MCF-7	breast:
26	chr4:7193870..7194671-chr4:7337290..7338117,4	MCF-7	breast:
27	chr4:7355383..7357989-chr4:7359924..7361691,2	MCF-7	breast:
28	chr4:7196173..7199298-chr4:7297617..7300967,3	MCF-7	breast:
29	chr4:7193728..7194793-chr4:7297053..7298951,15	MCF-7	breast:
30	chr4:7344494..7346063-chr4:7349701..7352195,2	MCF-7	breast:
31	chr4:7328869..7330375-chr4:7332248..7333752,2	MCF-7	breast:
32	chr4:7320638..7322307-chr4:7344162..7346358,2	K562	blood:
33	chr4:7193764..7194622-chr4:7297791..7298316,3	K562	blood:
34	chr4:7193774..7194640-chr4:7337221..7338106,5	K562	blood:
35	chr4:7196017..7196563-chr4:7337188..7337952,2	MCF-7	breast:
36	chr4:7153324..7154166-chr4:7297397..7298037,2	MCF-7	breast:
37	chr4:7200738..7202710-chr4:7296032..7298626,2	MCF-7	breast:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4798-3p	chr4:7312223-7312244	MIMAT0019975
hsa-miR-4798-5p	chr4:7312186-7312207	MIMAT0019974

Variant related genes	Relation type
MIR4798	TF binding region
MIR4798	CpG island
ENSG00000184985	chromatin interactions

Extended variants
information (count: 4451 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4451 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7656453	chr4:7295154-7295155	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs146937871	chr4:7295198-7295199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545228067	chr4:7295209-7295210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560301547	chr4:7295213-7295214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138200008	chr4:7295305-7295306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527993823	chr4:7295408-7295409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547605052	chr4:7295425-7295426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549238480	chr4:7295432-7295433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs370021119	chr4:7295434-7295435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115545491	chr4:7295439-7295440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs529927207	chr4:7295440-7295441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550301975	chr4:7295447-7295448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568960335	chr4:7295468-7295469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143771156	chr4:7295561-7295562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376613596	chr4:7295588-7295589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs577415592	chr4:7295616-7295617	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534081688	chr4:7295617-7295618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555593499	chr4:7295622-7295623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548439110	chr4:7295623-7295624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573842361	chr4:7295637-7295638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538286773	chr4:7295638-7295639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567570150	chr4:7295714-7295715	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs556264385	chr4:7295731-7295732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577752068	chr4:7295739-7295740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs150551160	chr4:7295769-7295770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79241102	chr4:7295772-7295773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs112616411	chr4:7295783-7295784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60147274	chr4:7295792-7295793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs181570365	chr4:7295793-7295794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561671125	chr4:7295821-7295822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs531888927	chr4:7295852-7295853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149581028	chr4:7295878-7295879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144294506	chr4:7295879-7295880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185674929	chr4:7295891-7295892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79781879	chr4:7295895-7295896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192507206	chr4:7295898-7295899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527521939	chr4:7295929-7295930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10937800	chr4:7295943-7295944	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs183836500	chr4:7295944-7295945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572727057	chr4:7295949-7295950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140095507	chr4:7295993-7295994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs542973504	chr4:7296030-7296031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78673260	chr4:7296065-7296066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs571279998	chr4:7296075-7296076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538752145	chr4:7296106-7296107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553810425	chr4:7296126-7296127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79178630	chr4:7296134-7296135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188013727	chr4:7296143-7296144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554847251	chr4:7296146-7296147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111355840	chr4:7296148-7296149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1239 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7283400-7297000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:7289200-7296800	Weak transcription	Fetal Brain Male	brain
3	chr4:7290400-7296400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr4:7291600-7297000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr4:7291800-7297200	Weak transcription	Liver	Liver
6	chr4:7293600-7300200	Weak transcription	Fetal Lung	lung
7	chr4:7293800-7296400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:7293800-7297000	Weak transcription	Colon Smooth Muscle	Colon
9	chr4:7293800-7297000	Weak transcription	Right Atrium	heart
10	chr4:7293800-7297000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr4:7293800-7297200	Weak transcription	Brain Angular Gyrus	brain
12	chr4:7293800-7297200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr4:7293800-7304400	Weak transcription	Gastric	stomach
14	chr4:7294000-7295200	Weak transcription	Brain Anterior Caudate	brain
15	chr4:7294000-7297000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:7294000-7297000	Weak transcription	Left Ventricle	heart
17	chr4:7294000-7297000	Weak transcription	Ovary	ovary
18	chr4:7294000-7297200	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr4:7294000-7297200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr4:7294200-7295800	Weak transcription	Brain Substantia Nigra	brain
21	chr4:7294200-7296800	Weak transcription	Right Ventricle	heart
22	chr4:7294200-7297000	Weak transcription	Brain Germinal Matrix	brain
23	chr4:7294200-7297200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr4:7294400-7295400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr4:7294800-7295400	Weak transcription	Brain Hippocampus Middle	brain
26	chr4:7295200-7295600	Enhancers	Brain Anterior Caudate	brain
27	chr4:7295400-7295600	Enhancers	Brain Hippocampus Middle	brain
28	chr4:7295400-7297000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:7295600-7296000	Enhancers	Fetal Brain Female	brain
30	chr4:7295600-7297000	Weak transcription	Brain Hippocampus Middle	brain
31	chr4:7295600-7297200	Weak transcription	Brain Anterior Caudate	brain
32	chr4:7295800-7296200	Enhancers	Brain Substantia Nigra	brain
33	chr4:7296200-7296400	Bivalent Enhancer	Fetal Stomach	stomach
34	chr4:7296200-7297200	Weak transcription	Brain Substantia Nigra	brain
35	chr4:7296400-7296800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
36	chr4:7296400-7297000	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr4:7296400-7297000	Flanking Active TSS	HSMM	muscle
38	chr4:7296800-7297000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr4:7296800-7297400	Enhancers	Fetal Brain Male	brain
40	chr4:7296800-7297800	Enhancers	Fetal Stomach	stomach
41	chr4:7296800-7298000	Enhancers	Right Ventricle	heart
42	chr4:7296800-7301800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:7297000-7297200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr4:7297000-7297200	Enhancers	Brain Germinal Matrix	brain
45	chr4:7297000-7297200	Active TSS	Brain Hippocampus Middle	brain
46	chr4:7297000-7297200	Enhancers	Colonic Mucosa	Colon
47	chr4:7297000-7297200	Enhancers	Skeletal Muscle Female	skeletal muscle
48	chr4:7297000-7297400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:7297000-7297400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
50	chr4:7297000-7297400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin

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