Variant report

Variant	nsv878487
Chromosome Location	chr4:3477299-3504562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:929)
CpG islands
(count:1833)
Chromatin interactive
region (count:59)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:929 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:3482260-3482611	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:3482298-3482759	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:3496152-3496215	K562	blood:	n/a	n/a
4	BACH1	chr4:3482323-3482523	K562	blood:	n/a	n/a
5	BACH1	chr4:3482512-3482601	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr4:3491237-3491472	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:3479316-3479464	K562	blood:	n/a	chr4:3479409-3479418 chr4:3479409-3479418 chr4:3479408-3479417 chr4:3479403-3479424
8	BHLHE40	chr4:3501057-3501246	K562	blood:	n/a	n/a
9	BHLHE40	chr4:3496279-3496546	HepG2	liver:	n/a	chr4:3496388-3496404
10	BHLHE40	chr4:3482294-3482545	K562	blood:	n/a	n/a
11	BHLHE40	chr4:3486975-3487201	GM12878	blood:	n/a	n/a
12	BHLHE40	chr4:3479250-3479561	HepG2	liver:	n/a	chr4:3479409-3479418 chr4:3479409-3479418 chr4:3479408-3479417 chr4:3479403-3479424
13	BHLHE40	chr4:3478312-3478492	HepG2	liver:	n/a	n/a
14	BHLHE40	chr4:3486390-3486566	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:3482383-3482568	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:3480551-3480684	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3482321-3482582	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:3491263-3491395	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:3482384-3482586	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr4:3482275-3482539	H1-hESC	embryonic stem cell:	n/a	n/a
21	CBX3	chr4:3482279-3482637	K562	blood:	n/a	n/a
22	CCNT2	chr4:3482381-3482557	K562	blood:	n/a	n/a
23	CCNT2	chr4:3499800-3499935	K562	blood:	n/a	n/a
24	CCNT2	chr4:3503956-3504114	K562	blood:	n/a	chr4:3504025-3504034
25	CCNT2	chr4:3499440-3499519	K562	blood:	n/a	n/a
26	CCNT2	chr4:3480418-3480529	K562	blood:	n/a	n/a
27	CEBPB	chr4:3482205-3482557	K562	blood:	n/a	n/a
28	CEBPB	chr4:3482224-3482577	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:3482226-3482506	MCF-7	breast:	n/a	n/a
30	CEBPB	chr4:3482236-3482560	K562	blood:	n/a	n/a
31	CEBPB	chr4:3482279-3482561	A549	lung:	n/a	n/a
32	CEBPB	chr4:3482210-3482696	ECC-1	luminal epithelium:	n/a	n/a
33	CEBPB	chr4:3482295-3482572	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:3485772-3486821	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr4:3493665-3493953	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:3482254-3482576	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:3482293-3482579	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPD	chr4:3498169-3498383	HepG2	liver:	n/a	n/a
39	CHD1	chr4:3482157-3482731	IMR90	lung:	n/a	n/a
40	CHD2	chr4:3482373-3482576	K562	blood:	n/a	n/a
41	CHD2	chr4:3482842-3483195	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr4:3498169-3498177	HepG2	liver:	n/a	n/a
43	CHD2	chr4:3486927-3487016	Hela-S3	cervix:	n/a	n/a
44	CHD2	chr4:3482486-3482565	HepG2	liver:	n/a	n/a
45	CHD2	chr4:3486506-3486633	GM12878	blood:	n/a	n/a
46	CHD2	chr4:3486913-3487328	GM12878	blood:	n/a	n/a
47	CHD2	chr4:3482312-3482602	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr4:3486077-3486391	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr4:3496377-3496397	K562	blood:	n/a	n/a
50	CREB1	chr4:3485934-3486768	ECC-1	luminal epithelium:	n/a	n/a

(count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3485326-3485376	HCT-116	colon:	n/a
2	chr4:3480318-3480368	BJ	skin:	n/a
3	chr4:3480656-3480706	Caco-2	colon:	n/a
4	chr4:3485326-3485376	HCT-116	colon:	n/a
5	chr4:3480318-3480368	BJ	skin:	n/a
6	chr4:3480656-3480706	Caco-2	colon:	n/a
7	chr4:3496300-3496350	HUVEC	blood vessel:	n/a
8	chr4:3495341-3495391	Jurkat	blood:	n/a
9	chr4:3478348-3478398	HRPEpiC	eye:	n/a
10	chr4:3495341-3495391	HRE	kidney:	n/a
11	chr4:3478348-3478398	BE2_C	brain:	n/a
12	chr4:3486204-3486254	HCF	heart:	n/a
13	chr4:3502518-3502568	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:3502381-3502431	HCF	heart:	n/a
15	chr4:3486116-3486166	HCF	heart:	n/a
16	chr4:3502575-3502625	GM19239	blood:	n/a
17	chr4:3484049-3484099	HCF	heart:	n/a
18	chr4:3494582-3494632	MCF10A-Er-Src	breast:	n/a
19	chr4:3485263-3485313	Caco-2	colon:	n/a
20	chr4:3485393-3485443	K562	blood:	n/a
21	chr4:3495242-3495292	BE2_C	brain:	n/a
22	chr4:3500688-3500738	HEEpiC	esophagus:	n/a
23	chr4:3496300-3496350	GM12878	blood:	n/a
24	chr4:3482507-3482557	HRPEpiC	eye:	n/a
25	chr4:3486204-3486254	AG10803	skin:	n/a
26	chr4:3478209-3478259	BE2_C	brain:	n/a
27	chr4:3486380-3486430	NHDF-neo	bronchial:	n/a
28	chr4:3480590-3480640	HRPEpiC	eye:	n/a
29	chr4:3489931-3489981	SK-N-MC	brain:	n/a
30	chr4:3502575-3502625	PANC-1	pancreas:	n/a
31	chr4:3487334-3487384	U87	brain:	n/a
32	chr4:3489931-3489981	SAEC	small airway:	n/a
33	chr4:3482507-3482557	A549	lung:	n/a
34	chr4:3486204-3486254	NH-A	brain:	n/a
35	chr4:3486116-3486166	HRCEpiC	kidney:	n/a
36	chr4:3494582-3494632	SK-N-MC	brain:	n/a
37	chr4:3499546-3499596	ProgFib	skin:	n/a
38	chr4:3485326-3485376	HMEC	breast:	n/a
39	chr4:3486380-3486430	SK-N-MC	brain:	n/a
40	chr4:3486204-3486254	GM19239	blood:	n/a
41	chr4:3502381-3502431	Hela-S3	cervix:	n/a
42	chr4:3487164-3487214	Caco-2	colon:	n/a
43	chr4:3500688-3500738	HL-60	blood:	n/a
44	chr4:3480590-3480640	NT2-D1	testis:	n/a
45	chr4:3482507-3482557	AG04450	lung:	fetal
46	chr4:3485263-3485313	HepG2	liver:	n/a
47	chr4:3478348-3478398	H1-hESC	embryonic stem cell:	embryo
48	chr4:3482507-3482557	HEEpiC	esophagus:	n/a
49	chr4:3485263-3485313	RPTEC	kidney:	n/a
50	chr4:3495242-3495292	NB4	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3500184..3501840-chr4:3502540..3504182,2	MCF-7	breast:
2	chr4:3484714..3487220-chr4:3532599..3535251,4	MCF-7	breast:
3	chr4:3497012..3499150-chr4:3532552..3535474,2	K562	blood:
4	chr4:3488541..3491242-chr4:3495615..3498535,2	K562	blood:
5	chr4:3481020..3484183-chr4:3488790..3491004,5	K562	blood:
6	chr4:3500336..3503326-chr4:3533188..3535879,5	MCF-7	breast:
7	chr4:3496124..3499190-chr4:3513529..3517461,3	MCF-7	breast:
8	chr4:3354072..3356995-chr4:3479067..3480969,2	MCF-7	breast:
9	chr4:3496237..3498612-chr4:3527624..3529896,2	K562	blood:
10	chr4:3082342..3084920-chr4:3490322..3492500,2	K562	blood:
11	chr4:3500639..3503471-chr4:3531403..3534143,3	K562	blood:
12	chr4:3489490..3491516-chr4:3532625..3534130,2	K562	blood:
13	chr4:3464614..3465179-chr4:3486100..3486697,2	MCF-7	breast:
14	chr4:3502958..3505472-chr4:3506122..3508605,2	K562	blood:
15	chr4:3481517..3483185-chr4:3946552..3949445,2	MCF-7	breast:
16	chr4:3497012..3500128-chr4:3532348..3534141,3	K562	blood:
17	chr4:3445342..3446316-chr4:3482040..3482882,2	K562	blood:
18	chr4:3488541..3491242-chr4:3495615..3498535,2	K562	blood:
19	chr4:3491033..3494897-chr4:3496204..3500010,5	K562	blood:
20	chr4:3495965..3498998-chr4:3502013..3504996,4	K562	blood:
21	chr4:3464939..3465859-chr4:3486070..3487026,3	MCF-7	breast:
22	chr4:3464629..3465770-chr4:3486550..3487347,4	MCF-7	breast:
23	chr4:3344785..3347772-chr4:3481036..3482952,2	MCF-7	breast:
24	chr4:3346980..3350932-chr4:3475951..3478417,3	MCF-7	breast:
25	chr4:3478548..3481215-chr4:3487290..3489311,2	K562	blood:
26	chr4:3495267..3497538-chr4:3499931..3501588,2	K562	blood:
27	chr4:3471602..3475518-chr4:3476351..3479966,4	K562	blood:
28	chr4:3386285..3389665-chr4:3485168..3487566,3	MCF-7	breast:
29	chr4:3485927..3488368-chr4:3533732..3536345,3	MCF-7	breast:
30	chr4:3464667..3465179-chr4:3486678..3487324,2	MCF-7	breast:
31	chr4:3490007..3491895-chr4:3517979..3519812,2	K562	blood:
32	chr4:3293993..3296488-chr4:3491954..3495229,3	MCF-7	breast:
33	chr4:3501592..3503192-chr4:3503261..3504809,2	MCF-7	breast:
34	chr4:3444953..3445626-chr4:3481708..3482572,4	MCF-7	breast:
35	chr4:3483725..3485778-chr4:3827881..3829780,2	MCF-7	breast:
36	chr4:3292637..3295776-chr4:3483843..3488274,4	MCF-7	breast:
37	chr4:3487684..3490277-chr4:3491908..3495748,6	K562	blood:
38	chr4:3500184..3501840-chr4:3502540..3504182,2	MCF-7	breast:
39	chr4:3495965..3498998-chr4:3502013..3504996,4	K562	blood:
40	chr4:3215167..3215891-chr4:3479590..3480357,2	K562	blood:
41	chr4:3499355..3501891-chr4:3505956..3508239,2	K562	blood:
42	chr4:3439130..3442230-chr4:3483136..3486025,3	MCF-7	breast:
43	chr4:3484197..3487656-chr4:3491883..3496058,4	K562	blood:
44	chr4:3418569..3420412-chr4:3484561..3487471,2	MCF-7	breast:
45	chr4:3481101..3483332-chr4:3533329..3535150,2	MCF-7	breast:
46	chr4:3495267..3497538-chr4:3499931..3501588,2	K562	blood:
47	chr4:3499074..3501837-chr4:3515567..3517558,2	K562	blood:
48	chr4:3502316..3505177-chr4:3506173..3509072,3	MCF-7	breast:
49	chr4:3108064..3109057-chr4:3481789..3482473,3	K562	blood:
50	chr4:3292635..3294292-chr4:3500969..3502505,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-4	chr4:3480710-3483420	ucscGeneNc_uc003ghh_2

No data

Variant related genes	Relation type
DOK7	TF binding region
DOK7	CpG island
ENSG00000163956	chromatin interactions
ENSG00000109758	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000261643	chromatin interactions

Extended variants
information (count: 2095 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2095 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6842419	chr4:3477299-3477300	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574125283	chr4:3477359-3477360	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562301510	chr4:3477360-3477361	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs527843173	chr4:3477379-3477380	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547988635	chr4:3477398-3477399	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370098496	chr4:3477425-3477426	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs535760045	chr4:3477426-3477427	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533475740	chr4:3477445-3477446	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549749336	chr4:3477456-3477457	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111415330	chr4:3477481-3477482	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569756852	chr4:3477518-3477519	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535942245	chr4:3477557-3477558	Bivalent Enhancer Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192587342	chr4:3477600-3477601	Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531022827	chr4:3477633-3477634	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs566172873	chr4:3477713-3477714	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs73080926	chr4:3477715-3477716	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs553953170	chr4:3477718-3477719	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374386901	chr4:3477729-3477730	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112795540	chr4:3477848-3477849	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs116737061	chr4:3477870-3477871	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556184219	chr4:3477878-3477879	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576150526	chr4:3477879-3477880	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs146928945	chr4:3477880-3477881	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116334007	chr4:3477883-3477884	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61597318	chr4:3477896-3477897	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs76913605	chr4:3477900-3477901	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564376382	chr4:3477908-3477909	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184482471	chr4:3477911-3477912	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs189006416	chr4:3477925-3477926	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192654648	chr4:3477930-3477931	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145980128	chr4:3477943-3477944	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548157926	chr4:3477948-3477949	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563602472	chr4:3477953-3477954	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530579837	chr4:3477956-3477957	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34427903	chr4:3477957-3477958	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184901863	chr4:3477961-3477962	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566011453	chr4:3477967-3477968	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528612818	chr4:3477968-3477969	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138352103	chr4:3477969-3477970	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547597121	chr4:3477971-3477972	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570698581	chr4:3477973-3477974	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539738234	chr4:3477974-3477975	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113470082	chr4:3477977-3477978	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534393569	chr4:3477979-3477980	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370393198	chr4:3477982-3477983	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113204233	chr4:3477986-3477987	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs113261250	chr4:3477987-3477988	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs2857985	chr4:3478000-3478001	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs115797134	chr4:3478003-3478004	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2699424	chr4:3478013-3478014	Enhancers Weak transcription Bivalent Enhancer Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:59)

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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3466400-3482400	Weak transcription	Right Atrium	heart
2	chr4:3467000-3493600	Weak transcription	Aorta	Aorta
3	chr4:3468600-3478400	Weak transcription	HSMMtube	muscle
4	chr4:3468800-3486400	Weak transcription	Psoas Muscle	Psoas
5	chr4:3470800-3478800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:3473000-3478800	Weak transcription	Gastric	stomach
7	chr4:3473800-3481200	Weak transcription	HSMM	muscle
8	chr4:3475400-3478600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:3475400-3481200	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr4:3475400-3485200	Weak transcription	Pancreas	Pancrea
11	chr4:3476000-3477600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
12	chr4:3476200-3478400	Weak transcription	Fetal Muscle Leg	muscle
13	chr4:3476200-3481200	Weak transcription	Left Ventricle	heart
14	chr4:3476800-3490800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr4:3477000-3477600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:3477000-3482200	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr4:3477200-3478000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:3477200-3478200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr4:3477200-3478400	Weak transcription	Right Ventricle	heart
20	chr4:3477200-3479200	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr4:3477200-3481000	Weak transcription	Fetal Heart	heart
22	chr4:3477600-3478200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr4:3477600-3479000	Strong transcription	Skeletal Muscle Male	skeletal muscle
24	chr4:3478000-3479000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:3478200-3478800	Bivalent Enhancer	HepG2	liver
26	chr4:3478200-3479200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr4:3478200-3479200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:3478400-3478600	Enhancers	Fetal Muscle Leg	muscle
29	chr4:3478400-3478600	Genic enhancers	Right Ventricle	heart
30	chr4:3478400-3479000	Genic enhancers	HSMMtube	muscle
31	chr4:3478400-3479400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr4:3478600-3479000	Genic enhancers	Fetal Muscle Leg	muscle
33	chr4:3478600-3479400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:3478600-3480200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:3478600-3480800	Strong transcription	Right Ventricle	heart
36	chr4:3478600-3481400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:3478800-3480600	Strong transcription	Gastric	stomach
38	chr4:3478800-3480800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr4:3479000-3479200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
40	chr4:3479000-3479400	Enhancers	Liver	Liver
41	chr4:3479000-3480000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:3479000-3480400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:3479000-3481400	Genic enhancers	Skeletal Muscle Male	skeletal muscle
44	chr4:3479000-3481800	Weak transcription	HSMMtube	muscle
45	chr4:3479000-3482400	Enhancers	Fetal Muscle Leg	muscle
46	chr4:3479200-3479400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr4:3479200-3479400	Active TSS	Spleen	Spleen
48	chr4:3479200-3479600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:3479200-3479600	Enhancers	Brain Cingulate Gyrus	brain
50	chr4:3479200-3480000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell

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