Variant report

Variant	nsv593441
Chromosome Location	chr4:3283422-3342137
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1213)
CpG islands
(count:3486)
Chromatin interactive
region (count:92)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3293525-3293690	HepG2	liver:	n/a	n/a
2	ATF1	chr4:3307432-3307768	K562	blood:	n/a	n/a
3	ATF2	chr4:3287771-3288267	GM12878	blood:	n/a	n/a
4	ATF2	chr4:3287878-3288195	GM12878	blood:	n/a	n/a
5	ATF2	chr4:3320239-3320654	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:3320244-3320681	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr4:3307402-3307727	K562	blood:	n/a	n/a
8	BACH1	chr4:3293851-3294599	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:3320428-3320702	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:3336099-3336319	GM12878	blood:	n/a	n/a
11	BATF	chr4:3287890-3288189	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:3287860-3288159	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:3287908-3288214	GM12878	blood:	n/a	n/a
14	BCL3	chr4:3301718-3302065	GM12878	blood:	n/a	chr4:3301978-3301991
15	BCL3	chr4:3299125-3299446	GM12878	blood:	n/a	n/a
16	BCL3	chr4:3298257-3298480	GM12878	blood:	n/a	n/a
17	BCL3	chr4:3299110-3299479	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:3325831-3326196	K562	blood:	n/a	n/a
19	BHLHE40	chr4:3295622-3295699	K562	blood:	n/a	n/a
20	BHLHE40	chr4:3320378-3320586	K562	blood:	n/a	n/a
21	BHLHE40	chr4:3294320-3294520	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:3286433-3286738	K562	blood:	n/a	n/a
23	BHLHE40	chr4:3293912-3294112	GM12878	blood:	n/a	chr4:3294055-3294071 chr4:3293992-3294008
24	BHLHE40	chr4:3287854-3288237	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:3315413-3315724	K562	blood:	n/a	n/a
26	BHLHE40	chr4:3286429-3286762	HepG2	liver:	n/a	n/a
27	BHLHE40	chr4:3304008-3304550	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:3306416-3306948	K562	blood:	n/a	n/a
29	BHLHE40	chr4:3325977-3326132	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:3326437-3326489	K562	blood:	n/a	n/a
31	BHLHE40	chr4:3293893-3294609	K562	blood:	n/a	chr4:3294055-3294071 chr4:3293992-3294008
32	BHLHE40	chr4:3293310-3294186	HepG2	liver:	n/a	chr4:3294055-3294071 chr4:3293992-3294008
33	BHLHE40	chr4:3294399-3294612	HepG2	liver:	n/a	n/a
34	BHLHE40	chr4:3307360-3307718	K562	blood:	n/a	n/a
35	BRCA1	chr4:3295798-3295907	GM12878	blood:	n/a	n/a
36	BRCA1	chr4:3294288-3294477	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr4:3294300-3294363	HepG2	liver:	n/a	n/a
38	BRCA1	chr4:3320417-3320671	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr4:3294295-3294586	K562	blood:	n/a	n/a
40	CCNT2	chr4:3307394-3307657	K562	blood:	n/a	n/a
41	CCNT2	chr4:3294235-3295326	K562	blood:	n/a	n/a
42	CEBPB	chr4:3287881-3288189	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:3324937-3325156	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:3337143-3337506	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr4:3320432-3320672	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:3297260-3297479	K562	blood:	n/a	n/a
47	CEBPB	chr4:3287826-3288147	HepG2	liver:	n/a	n/a
48	CEBPD	chr4:3294628-3295006	HepG2	liver:	n/a	n/a
49	CEBPD	chr4:3294159-3294517	HepG2	liver:	n/a	n/a
50	CHD1	chr4:3304151-3304621	GM12878	blood:	n/a	chr4:3304554-3304564

(count:3486 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3310100-3310150	HAEpiC	amniotic membrane:	n/a
2	chr4:3288876-3288926	HRE	kidney:	n/a
3	chr4:3318625-3318675	K562	blood:	n/a
4	chr4:3319541-3319591	HL-60	blood:	n/a
5	chr4:3310191-3310241	HEK293	kidney:	embryo
6	chr4:3318625-3318675	HCPEpiC	choroid plexus:	n/a
7	chr4:3315925-3315975	HRPEpiC	eye:	n/a
8	chr4:3287777-3287827	ECC-1	luminal epithelium:	n/a
9	chr4:3324940-3324990	SKMC	muscle:	n/a
10	chr4:3310100-3310150	HAEpiC	amniotic membrane:	n/a
11	chr4:3288876-3288926	HRE	kidney:	n/a
12	chr4:3318625-3318675	K562	blood:	n/a
13	chr4:3319541-3319591	HL-60	blood:	n/a
14	chr4:3310191-3310241	HEK293	kidney:	embryo
15	chr4:3318625-3318675	HCPEpiC	choroid plexus:	n/a
16	chr4:3315925-3315975	HRPEpiC	eye:	n/a
17	chr4:3287777-3287827	ECC-1	luminal epithelium:	n/a
18	chr4:3324940-3324990	SKMC	muscle:	n/a
19	chr4:3319127-3319177	AG04450	lung:	fetal
20	chr4:3342111-3342161	AG09319	gingival:	n/a
21	chr4:3308933-3308983	U87	brain:	n/a
22	chr4:3312007-3312057	HEEpiC	esophagus:	n/a
23	chr4:3315107-3315157	BE2_C	brain:	n/a
24	chr4:3309966-3310016	HPAEpiC	pulmonary alveolar:	n/a
25	chr4:3312788-3312838	HIPEpiC	eye:	n/a
26	chr4:3306705-3306755	HPAEpiC	pulmonary alveolar:	n/a
27	chr4:3315107-3315157	GM12878	blood:	n/a
28	chr4:3288648-3288698	RPTEC	kidney:	n/a
29	chr4:3318072-3318122	MCF-7	breast:	n/a
30	chr4:3309417-3309467	HRE	kidney:	n/a
31	chr4:3298514-3298564	K562	blood:	n/a
32	chr4:3309404-3309454	AG10803	skin:	n/a
33	chr4:3341937-3341987	HCM	heart:	n/a
34	chr4:3293715-3293765	HRPEpiC	eye:	n/a
35	chr4:3319541-3319591	LNCaP	prostate:	n/a
36	chr4:3308884-3308934	AG09319	gingival:	n/a
37	chr4:3341937-3341987	AG09319	gingival:	n/a
38	chr4:3292386-3292436	ProgFib	skin:	n/a
39	chr4:3338141-3338191	SK-N-SH_RA	brain:	n/a
40	chr4:3312007-3312057	NHBE	bronchial:	n/a
41	chr4:3312788-3312838	BJ	skin:	n/a
42	chr4:3322833-3322883	H1-hESC	embryonic stem cell:	embryo
43	chr4:3319669-3319719	MCF10A-Er-Src	breast:	n/a
44	chr4:3306705-3306755	GM12891	blood:	n/a
45	chr4:3315430-3315480	Hela-S3	cervix:	n/a
46	chr4:3317976-3318026	AG10803	skin:	n/a
47	chr4:3319127-3319177	HCM	heart:	n/a
48	chr4:3319127-3319177	HEEpiC	esophagus:	n/a
49	chr4:3325029-3325079	AoSMC	blood vessel:	n/a
50	chr4:3315040-3315090	SK-N-SH	brain:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3293485..3295010-chr4:3317459..3319780,2	K562	blood:
2	chr4:3297687..3301019-chr4:3306995..3308843,3	K562	blood:
3	chr4:3284056..3285844-chr4:3292232..3294141,2	MCF-7	breast:
4	chr4:3312683..3315321-chr4:3322350..3324047,2	MCF-7	breast:
5	chr4:3299078..3301560-chr4:3303600..3305932,2	MCF-7	breast:
6	chr4:3330077..3332907-chr4:3336771..3339582,2	K562	blood:
7	chr4:3297687..3301019-chr4:3306995..3308843,3	K562	blood:
8	chr4:3339354..3341969-chr4:3342389..3344050,2	MCF-7	breast:
9	chr4:3292637..3295776-chr4:3483843..3488274,4	MCF-7	breast:
10	chr4:3299302..3301321-chr4:3301598..3303131,2	MCF-7	breast:
11	chr4:3292471..3295854-chr4:3462941..3467927,8	MCF-7	breast:
12	chr4:3321816..3324737-chr4:3338680..3341161,2	MCF-7	breast:
13	chr4:3277870..3279701-chr4:3282246..3285205,2	MCF-7	breast:
14	chr4:3293263..3296251-chr4:3298199..3300477,2	K562	blood:
15	chr4:3292225..3296816-chr4:3337883..3341063,5	MCF-7	breast:
16	chr4:3313691..3315638-chr4:3318418..3320461,2	K562	blood:
17	chr4:3327302..3329528-chr4:3337997..3340171,2	MCF-7	breast:
18	chr4:3331295..3334505-chr4:3335850..3338005,3	MCF-7	breast:
19	chr4:3313691..3315638-chr4:3318418..3320461,2	K562	blood:
20	chr4:3297413..3300399-chr4:3305342..3309576,4	MCF-7	breast:
21	chr4:3272762..3274789-chr4:3288374..3291256,2	MCF-7	breast:
22	chr4:3325394..3328085-chr4:3328571..3331432,2	MCF-7	breast:
23	chr4:2798786..2800390-chr4:3294087..3295620,2	MCF-7	breast:
24	chr4:3294728..3297667-chr4:3300609..3302495,3	K562	blood:
25	chr4:3297413..3300399-chr4:3305342..3309576,4	MCF-7	breast:
26	chr4:3283519..3286259-chr4:3292639..3294370,2	K562	blood:
27	chr4:3299967..3302345-chr4:3306185..3308779,2	MCF-7	breast:
28	chr4:3320217..3323147-chr4:3474744..3477107,2	MCF-7	breast:
29	chr4:3293993..3296488-chr4:3491954..3495229,3	MCF-7	breast:
30	chr4:3281505..3284592-chr4:3285630..3289153,4	MCF-7	breast:
31	chr4:3330743..3332280-chr4:3339908..3342252,2	MCF-7	breast:
32	chr4:3316773..3319078-chr4:3532523..3535417,2	K562	blood:
33	chr4:3316605..3318231-chr4:3318399..3321148,2	K562	blood:
34	chr4:3298898..3300688-chr4:3301683..3304655,2	K562	blood:
35	chr4:3321816..3324737-chr4:3338680..3341161,2	MCF-7	breast:
36	chr4:3331295..3334505-chr4:3335850..3338005,3	MCF-7	breast:
37	chr4:3330743..3332280-chr4:3339908..3342252,2	MCF-7	breast:
38	chr4:3285178..3287998-chr4:3288416..3291256,2	K562	blood:
39	chr4:3220220..3221940-chr4:3299861..3302041,2	MCF-7	breast:
40	chr4:3281505..3284592-chr4:3285630..3289153,4	MCF-7	breast:
41	chr4:3287264..3290154-chr4:3470213..3472155,2	MCF-7	breast:
42	chr4:3338818..3342772-chr4:3461368..3467187,7	MCF-7	breast:
43	chr4:3287370..3290195-chr4:3296120..3298356,2	K562	blood:
44	chr4:3245063..3247633-chr4:3289230..3291965,2	MCF-7	breast:
45	chr4:3312095..3315185-chr4:3316131..3319628,4	MCF-7	breast:
46	chr4:3312095..3315185-chr4:3316131..3319628,4	MCF-7	breast:
47	chr4:3307561..3309945-chr4:3316347..3319248,2	MCF-7	breast:
48	chr4:3299078..3301560-chr4:3303600..3305932,2	MCF-7	breast:
49	chr4:3299099..3300843-chr4:3320328..3323004,2	MCF-7	breast:
50	chr4:3320336..3322310-chr4:3333644..3335356,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf44-3	chr4:3311226-3311715	NONHSAT094858
2	lnc-C4orf44-4	chr4:3314239-3314562	NONHSAT094860
3	lnc-C4orf44-4	chr4:3314545-3314789	NONHSAT094861
4	lnc-C4orf44-3	chr4:3311824-3312170	NONHSAT094859
5	lnc-C4orf44-3	chr4:3311264-3311294	NONHSAT094859
6	lnc-C4orf44-3	chr4:3311824-3312124	NONHSAT094858

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RGS12	hsa-miR-138-5p	chr4:3319133-3319155
2	RGS12	hsa-miR-138-5p	chr4:3319531-3319554

Variant related genes	Relation type
ENSG00000248843	TF binding region
RGS12	TF binding region
ENSG00000248840	TF binding region
ENSG00000248843	CpG island
RGS12	CpG island
ENSG00000248840	CpG island
ENSG00000109758	chromatin interactions
ENSG00000248840	chromatin interactions
ENSG00000251075	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000188981	chromatin interactions
ENSG00000197386	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000248843	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000087266	chromatin interactions

Extended variants
information (count: 2561 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2561 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7658462	chr4:3283422-3283423	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565898407	chr4:3283427-3283428	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534700352	chr4:3283440-3283441	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs553367842	chr4:3283517-3283518	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs577909548	chr4:3283518-3283519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185727028	chr4:3283524-3283525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189285268	chr4:3283572-3283573	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs181709485	chr4:3283648-3283649	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs75689104	chr4:3283685-3283686	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs575594349	chr4:3283783-3283784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559054387	chr4:3283791-3283792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7687619	chr4:3283828-3283829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1119291	chr4:3283856-3283857	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs57119019	chr4:3283857-3283858	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs531248227	chr4:3283879-3283880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550655768	chr4:3283917-3283918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs567675388	chr4:3283943-3283944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs545741980	chr4:3283944-3283945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs1119290	chr4:3283960-3283961	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs547101549	chr4:3283988-3283989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs57010886	chr4:3283996-3283997	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs184255141	chr4:3284024-3284025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534808575	chr4:3284032-3284033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs557993819	chr4:3284033-3284034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571403950	chr4:3284040-3284041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs1988007	chr4:3284095-3284096	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188677629	chr4:3284167-3284168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12504986	chr4:3284186-3284187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs573564328	chr4:3284242-3284243	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs542242266	chr4:3284300-3284301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12505018	chr4:3284305-3284306	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs12500459	chr4:3284340-3284341	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs181426407	chr4:3284359-3284360	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565480261	chr4:3284362-3284363	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs531085638	chr4:3284373-3284374	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs544905996	chr4:3284394-3284395	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs561460243	chr4:3284459-3284460	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs186233204	chr4:3284506-3284507	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547063362	chr4:3284520-3284521	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs12506821	chr4:3284560-3284561	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs532655546	chr4:3284567-3284568	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs878004	chr4:3284588-3284589	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs571433477	chr4:3284607-3284608	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs540646414	chr4:3284638-3284639	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs76075539	chr4:3284639-3284640	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550827882	chr4:3284657-3284658	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150873430	chr4:3284674-3284675	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530380487	chr4:3284678-3284679	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535832877	chr4:3284694-3284695	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs6446731	chr4:3284751-3284752	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:55)

Disease	PMID	Source
Retinitis pigmentosa	18421352	CNVD
Wolf-Hirschhorn syndrome	19259404	CNVD
Bladder cancer	19242612	CNVD
Breast cancer	19242612	CNVD
Congenital anomalies of the kidney and urinary tract	19242612	CNVD
abnormal development	18461090	CNVD
Olfactory neuroblastoma	18408657	CNVD
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
Developmental delay	21147756	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2362 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3114600-3292400	Weak transcription	Right Atrium	heart
2	chr4:3272400-3287600	Weak transcription	Pancreas	Pancrea
3	chr4:3282600-3285600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:3283800-3285000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr4:3284000-3285000	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr4:3284200-3285400	Enhancers	HSMMtube	muscle
7	chr4:3284400-3284600	Flanking Active TSS	NHDF-Ad	bronchial
8	chr4:3284400-3284800	Bivalent Enhancer	HepG2	liver
9	chr4:3284400-3284800	Enhancers	HSMM	muscle
10	chr4:3284600-3284800	Enhancers	NHDF-Ad	bronchial
11	chr4:3284800-3286600	Enhancers	HepG2	liver
12	chr4:3284800-3287600	Weak transcription	NHDF-Ad	bronchial
13	chr4:3285000-3286800	Weak transcription	Primary monocytes fromperipheralblood	blood
14	chr4:3285400-3286200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr4:3285600-3285800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:3285600-3285800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
17	chr4:3285600-3285800	Enhancers	Fetal Brain Female	brain
18	chr4:3285600-3285800	Enhancers	Ovary	ovary
19	chr4:3285600-3285800	Bivalent Enhancer	NHEK	skin
20	chr4:3285600-3286000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:3285600-3286200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:3285800-3286000	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr4:3285800-3286000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:3285800-3286000	Enhancers	HMEC	breast
25	chr4:3285800-3287800	Weak transcription	Fetal Brain Female	brain
26	chr4:3286000-3287000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr4:3286000-3287200	Weak transcription	HMEC	breast
28	chr4:3286000-3287600	Weak transcription	Ovary	ovary
29	chr4:3286200-3292200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:3286400-3286600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr4:3286600-3287000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
32	chr4:3286600-3287400	Flanking Active TSS	HepG2	liver
33	chr4:3286800-3287600	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr4:3286800-3287600	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
35	chr4:3286800-3290600	Enhancers	Fetal Brain Male	brain
36	chr4:3287000-3287600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
37	chr4:3287000-3287800	Bivalent Enhancer	Placenta	Placenta
38	chr4:3287000-3288600	Enhancers	Spleen	Spleen
39	chr4:3287000-3288600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
40	chr4:3287000-3290200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr4:3287000-3290800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr4:3287200-3287400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr4:3287200-3287400	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:3287200-3287600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr4:3287200-3287600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
46	chr4:3287200-3287600	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr4:3287200-3288400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr4:3287200-3288600	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr4:3287200-3288800	Enhancers	HMEC	breast
50	chr4:3287200-3289000	Enhancers	Primary hematopoietic stem cells	blood

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