Variant report

Variant	nsv10424
Chromosome Location	chr4:3437534-3468325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1186)
CpG islands
(count:2627)
Chromatin interactive
region (count:68)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1186 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3445241-3445522	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:3443453-3443675	HepG2	liver:	n/a	n/a
3	ATF3	chr4:3445269-3445466	K562	blood:	n/a	n/a
4	BHLHE40	chr4:3445224-3445543	K562	blood:	n/a	chr4:3445365-3445381
5	BHLHE40	chr4:3445170-3445557	HepG2	liver:	n/a	chr4:3445365-3445381
6	BHLHE40	chr4:3454350-3454405	K562	blood:	n/a	n/a
7	BHLHE40	chr4:3445191-3445500	GM12878	blood:	n/a	chr4:3445365-3445381
8	BRCA1	chr4:3445279-3445522	HepG2	liver:	n/a	n/a
9	CBX3	chr4:3454169-3454489	K562	blood:	n/a	n/a
10	CBX3	chr4:3454139-3454516	K562	blood:	n/a	n/a
11	CCNT2	chr4:3445350-3445426	K562	blood:	n/a	n/a
12	CCNT2	chr4:3465851-3465998	K562	blood:	n/a	n/a
13	CCNT2	chr4:3454608-3454769	K562	blood:	n/a	n/a
14	CEBPB	chr4:3445210-3445549	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:3438739-3439132	Hela-S3	cervix:	n/a	n/a
16	CEBPD	chr4:3445106-3445439	HepG2	liver:	n/a	n/a
17	CEBPD	chr4:3456647-3457074	K562	blood:	n/a	n/a
18	CEBPD	chr4:3443344-3444000	HepG2	liver:	n/a	n/a
19	CHD2	chr4:3438403-3438499	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr4:3438705-3439109	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr4:3444625-3444775	HepG2	liver:	n/a	n/a
22	CHD2	chr4:3444229-3444230	HepG2	liver:	n/a	n/a
23	CHD2	chr4:3443379-3443859	HepG2	liver:	n/a	chr4:3443687-3443697
24	CHD2	chr4:3445219-3445398	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr4:3463166-3463490	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr4:3442759-3442777	HepG2	liver:	n/a	n/a
27	CHD2	chr4:3445341-3445531	HepG2	liver:	n/a	n/a
28	CHD2	chr4:3464168-3464354	HepG2	liver:	n/a	n/a
29	CREB1	chr4:3464885-3465183	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr4:3445232-3445485	A549	lung:	n/a	n/a
31	CTBP2	chr4:3467895-3468531	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr4:3468220-3468370	HPF	lung:	n/a	n/a
33	CTCF	chr4:3442660-3442810	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr4:3446835-3447208	K562	blood:	n/a	n/a
35	CTCF	chr4:3454247-3454547	GM12878	blood:	n/a	n/a
36	CTCF	chr4:3454340-3454490	AG09319	gingival:	n/a	n/a
37	CTCF	chr4:3454472-3454477	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:3454360-3454510	GM12872	blood:	n/a	n/a
39	CTCF	chr4:3454340-3454490	GM12878	blood:	n/a	n/a
40	CTCF	chr4:3445066-3445135	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr4:3445245-3445539	Pancreas_OC	pancreas:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
42	CTCF	chr4:3445113-3445165	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr4:3445300-3445450	GM12865	blood:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
44	CTCF	chr4:3454260-3454410	GM12873	blood:	n/a	n/a
45	CTCF	chr4:3454320-3454470	BE2_C	brain:	n/a	n/a
46	CTCF	chr4:3445280-3445430	HRPEpiC	eye:	n/a	chr4:3445365-3445381 chr4:3445364-3445382 chr4:3445367-3445377 chr4:3445370-3445379 chr4:3445366-3445379 chr4:3445366-3445379
47	CTCF	chr4:3454320-3454470	GM12871	blood:	n/a	n/a
48	CTCF	chr4:3467920-3468070	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr4:3468120-3468270	HCT-116	colon:	n/a	chr4:3468204-3468217 chr4:3468208-3468217 chr4:3468202-3468220
50	CTCF	chr4:3454260-3454410	GM12872	blood:	n/a	n/a

(count:2627 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3449663-3449713	HUVEC	blood vessel:	n/a
2	chr4:3465367-3465417	Caco-2	colon:	n/a
3	chr4:3448150-3448200	NH-A	brain:	n/a
4	chr4:3447665-3447715	BE2_C	brain:	n/a
5	chr4:3449663-3449713	HUVEC	blood vessel:	n/a
6	chr4:3465367-3465417	Caco-2	colon:	n/a
7	chr4:3448150-3448200	NH-A	brain:	n/a
8	chr4:3447665-3447715	BE2_C	brain:	n/a
9	chr4:3464702-3464752	AoSMC	blood vessel:	n/a
10	chr4:3449904-3449954	NB4	blood:	n/a
11	chr4:3449663-3449713	BE2_C	brain:	n/a
12	chr4:3465064-3465114	HPAEpiC	pulmonary alveolar:	n/a
13	chr4:3443694-3443744	AG04449	skin:	fetal
14	chr4:3462498-3462548	HNPCEpiC	eye:	n/a
15	chr4:3464653-3464703	NHBE	bronchial:	n/a
16	chr4:3449904-3449954	AG09319	gingival:	n/a
17	chr4:3443683-3443733	AG04449	skin:	fetal
18	chr4:3466246-3466296	HAEpiC	amniotic membrane:	n/a
19	chr4:3443735-3443785	Caco-2	colon:	n/a
20	chr4:3450770-3450820	NB4	blood:	n/a
21	chr4:3451216-3451266	SK-N-MC	brain:	n/a
22	chr4:3443025-3443075	U87	brain:	n/a
23	chr4:3443608-3443658	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:3449300-3449350	HEK293	kidney:	embryo
25	chr4:3447796-3447846	AG09309	skin:	n/a
26	chr4:3446682-3446732	GM06990	blood:	n/a
27	chr4:3465367-3465417	SKMC	muscle:	n/a
28	chr4:3442962-3443012	NHDF-neo	bronchial:	n/a
29	chr4:3464996-3465046	HL-60	blood:	n/a
30	chr4:3451126-3451176	IMR90	lung:	fetal
31	chr4:3464870-3464920	Jurkat	blood:	n/a
32	chr4:3449300-3449350	SK-N-MC	brain:	n/a
33	chr4:3449904-3449954	U87	brain:	n/a
34	chr4:3450770-3450820	HCF	heart:	n/a
35	chr4:3466246-3466296	T-47D	breast:	n/a
36	chr4:3442962-3443012	HepG2	liver:	n/a
37	chr4:3442962-3443012	AG09309	skin:	n/a
38	chr4:3444147-3444197	HRPEpiC	eye:	n/a
39	chr4:3448150-3448200	NHDF-neo	bronchial:	n/a
40	chr4:3443025-3443075	NB4	blood:	n/a
41	chr4:3447796-3447846	AG04450	lung:	fetal
42	chr4:3446405-3446455	HCT-116	colon:	n/a
43	chr4:3449904-3449954	HRPEpiC	eye:	n/a
44	chr4:3451104-3451154	LNCaP	prostate:	n/a
45	chr4:3448150-3448200	MCF10A-Er-Src	breast:	n/a
46	chr4:3453754-3453804	HUVEC	blood vessel:	n/a
47	chr4:3439095-3439145	CMK	blood:	n/a
48	chr4:3443683-3443733	Jurkat	blood:	n/a
49	chr4:3464754-3464804	GM12892	blood:	n/a
50	chr4:3447796-3447846	NT2-D1	testis:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3464939..3465859-chr4:3486070..3487026,3	MCF-7	breast:
2	chr4:3346041..3348825-chr4:3461682..3464499,2	MCF-7	breast:
3	chr4:3439707..3441284-chr4:3443467..3445284,2	K562	blood:
4	chr4:3448773..3453068-chr4:3461459..3466470,7	MCF-7	breast:
5	chr4:3113077..3115750-chr4:3467353..3469747,2	MCF-7	breast:
6	chr4:3430343..3432771-chr4:3437903..3441095,3	K562	blood:
7	chr4:3076153..3077682-chr4:3463023..3464527,2	MCF-7	breast:
8	chr12:52607035..52609334-chr4:3440706..3442862,2	MCF-7	breast:
9	chr4:3437849..3440325-chr4:3440402..3441941,2	MCF-7	breast:
10	chr4:3464468..3466347-chr4:3532849..3534407,2	MCF-7	breast:
11	chr4:3464629..3465770-chr4:3486550..3487347,4	MCF-7	breast:
12	chr4:3110927..3117533-chr4:3461507..3465762,15	MCF-7	breast:
13	chr4:3453523..3456433-chr4:3460868..3465050,6	MCF-7	breast:
14	chr4:3464667..3465179-chr4:3486678..3487324,2	MCF-7	breast:
15	chr4:3457896..3459627-chr4:3532667..3535472,2	K562	blood:
16	chr4:3462844..3463532-chr4:3486166..3487066,3	MCF-7	breast:
17	chr4:3417191..3419894-chr4:3434904..3438347,3	MCF-7	breast:
18	chr4:3464614..3465179-chr4:3486100..3486697,2	MCF-7	breast:
19	chr4:3438186..3441523-chr4:3461903..3464658,4	MCF-7	breast:
20	chr4:3443905..3446475-chr4:3452886..3454519,2	MCF-7	breast:
21	chr4:3351060..3353090-chr4:3436592..3439411,2	MCF-7	breast:
22	chr4:3442877..3445560-chr4:3447912..3450981,3	MCF-7	breast:
23	chr4:3401369..3402190-chr4:3444884..3445429,2	K562	blood:
24	chr4:3365688..3366496-chr4:3463170..3464043,2	MCF-7	breast:
25	chr4:3444953..3445626-chr4:3481708..3482572,4	MCF-7	breast:
26	chr4:3444972..3445545-chr7:150654913..150655661,2	MCF-7	breast:
27	chr4:3447342..3448896-chr4:3452237..3453877,2	MCF-7	breast:
28	chr4:3438758..3441335-chr4:3441966..3444505,4	MCF-7	breast:
29	chr4:3288141..3289800-chr4:3461769..3463366,2	MCF-7	breast:
30	chr4:3347496..3348411-chr4:3444927..3445862,6	K562	blood:
31	chr4:3401278..3402259-chr4:3444676..3445847,3	MCF-7	breast:
32	chr11:61737950..61740369-chr4:3461504..3464468,2	MCF-7	breast:
33	chr4:3438642..3440686-chr4:3450024..3452220,2	MCF-7	breast:
34	chr4:3438145..3440558-chr4:3486054..3488354,2	MCF-7	breast:
35	chr4:3465519..3467686-chr4:3526203..3530625,4	MCF-7	breast:
36	chr4:3448881..3451468-chr4:3454721..3457029,2	K562	blood:
37	chr4:3433662..3435560-chr4:3437260..3439057,2	MCF-7	breast:
38	chr4:3292102..3294475-chr4:3451973..3453863,2	MCF-7	breast:
39	chr11:3078361..3079999-chr4:3467036..3469656,2	MCF-7	breast:
40	chr4:3321370..3323027-chr4:3448401..3450005,2	MCF-7	breast:
41	chr4:3347550..3348452-chr4:3441019..3441869,2	K562	blood:
42	chr4:3432863..3436671-chr4:3438111..3441622,5	K562	blood:
43	chr4:3355212..3358066-chr4:3437874..3440532,4	MCF-7	breast:
44	chr4:3437523..3439091-chr4:3448156..3450987,2	MCF-7	breast:
45	chr4:3195267..3196266-chr4:3444903..3445887,5	MCF-7	breast:
46	chr4:3448881..3451468-chr4:3454721..3457029,2	K562	blood:
47	chr4:3428890..3430804-chr4:3441748..3443973,2	MCF-7	breast:
48	chr4:3293054..3295146-chr4:3436472..3438232,3	MCF-7	breast:
49	chr4:3297878..3299647-chr4:3439847..3442316,2	MCF-7	breast:
50	chr4:3462755..3463804-chr4:3486304..3487219,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS12-1	chr4:3441182-3441640	NONHSAT094871

No data

Variant related genes	Relation type
DOK7	TF binding region
HGFAC	TF binding region
DOK7	CpG island
HGFAC	CpG island
ENSG00000109758	chromatin interactions
ENSG00000110619	chromatin interactions
ENSG00000251075	chromatin interactions
ENSG00000197386	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000159788	chromatin interactions

Extended variants
information (count: 1621 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1621 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563962530	chr4:3437554-3437555	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577584367	chr4:3437566-3437567	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147115079	chr4:3437608-3437609	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs4613510	chr4:3437624-3437625	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs529497883	chr4:3437653-3437654	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs151056008	chr4:3437679-3437680	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs60135556	chr4:3437695-3437696	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs375935175	chr4:3437717-3437718	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570678579	chr4:3437739-3437740	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560064354	chr4:3437752-3437753	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528816772	chr4:3437755-3437756	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs552065629	chr4:3437760-3437761	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191004252	chr4:3437795-3437796	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs114803703	chr4:3437848-3437849	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548433103	chr4:3437855-3437856	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73079035	chr4:3437861-3437862	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs567462097	chr4:3437869-3437870	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs535268452	chr4:3437911-3437912	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117217837	chr4:3437925-3437926	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370911090	chr4:3437947-3437948	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571996272	chr4:3437953-3437954	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs368805733	chr4:3437984-3437985	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs558057385	chr4:3438016-3438017	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs373915963	chr4:3438042-3438043	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs111604443	chr4:3438103-3438104	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs368646625	chr4:3438104-3438105	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs35190604	chr4:3438111-3438112	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs543443365	chr4:3438149-3438150	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs74425283	chr4:3438220-3438221	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs573806519	chr4:3438221-3438222	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543226676	chr4:3438236-3438237	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs559950859	chr4:3438240-3438241	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184090894	chr4:3438262-3438263	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551740522	chr4:3438268-3438269	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565581934	chr4:3438269-3438270	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs143402639	chr4:3438287-3438288	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs574622280	chr4:3438301-3438302	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs188975924	chr4:3438316-3438317	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374204621	chr4:3438348-3438349	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs535156759	chr4:3438359-3438360	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs192238946	chr4:3438372-3438373	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs147147167	chr4:3438377-3438378	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536383850	chr4:3438384-3438385	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs546707122	chr4:3438385-3438386	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs116089088	chr4:3438396-3438397	Enhancers Weak transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534822441	chr4:3438414-3438415	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs563153720	chr4:3438454-3438455	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs138448960	chr4:3438482-3438483	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577913718	chr4:3438499-3438500	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs184394857	chr4:3438512-3438513	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:698 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3416600-3437800	Weak transcription	Stomach Mucosa	stomach
2	chr4:3416800-3438400	Weak transcription	NHDF-Ad	bronchial
3	chr4:3417200-3444800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr4:3418200-3438000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:3418200-3438000	Weak transcription	A549	lung
6	chr4:3419200-3444600	Weak transcription	Primary monocytes fromperipheralblood	blood
7	chr4:3419400-3438400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr4:3419600-3438400	Weak transcription	NH-A	brain
9	chr4:3419800-3438800	Weak transcription	NHLF	lung
10	chr4:3420200-3438400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr4:3420400-3438200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr4:3420400-3438600	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr4:3425600-3438400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr4:3425800-3438600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:3427000-3437800	Weak transcription	HMEC	breast
16	chr4:3427000-3442000	Weak transcription	Colon Smooth Muscle	Colon
17	chr4:3427000-3443200	Weak transcription	Brain Substantia Nigra	brain
18	chr4:3427200-3437800	Weak transcription	Brain Angular Gyrus	brain
19	chr4:3427200-3438400	Weak transcription	HUVEC	blood vessel
20	chr4:3430800-3445200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr4:3431400-3437800	Weak transcription	HSMMtube	muscle
22	chr4:3431400-3441400	Weak transcription	Fetal Lung	lung
23	chr4:3431600-3438000	Weak transcription	NHEK	skin
24	chr4:3431600-3442600	Weak transcription	Colonic Mucosa	Colon
25	chr4:3431800-3444600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:3432200-3438400	Weak transcription	HepG2	liver
27	chr4:3432400-3438600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr4:3432800-3438200	Weak transcription	Fetal Thymus	thymus
29	chr4:3433000-3438000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr4:3433000-3445200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr4:3433200-3444800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr4:3433600-3438400	Weak transcription	Brain Cingulate Gyrus	brain
33	chr4:3433600-3438400	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr4:3433600-3440200	Weak transcription	Ovary	ovary
35	chr4:3433600-3444600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:3433800-3438200	Weak transcription	Brain Anterior Caudate	brain
37	chr4:3433800-3441000	Weak transcription	Duodenum Mucosa	Duodenum
38	chr4:3434000-3438000	Weak transcription	HSMM	muscle
39	chr4:3434200-3438400	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr4:3434200-3439600	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr4:3434200-3442600	Weak transcription	Liver	Liver
42	chr4:3434800-3441400	Weak transcription	Brain Hippocampus Middle	brain
43	chr4:3435200-3437800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:3435200-3438000	Weak transcription	Gastric	stomach
45	chr4:3435200-3438200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:3435200-3439600	Weak transcription	Adipose Nuclei	Adipose
47	chr4:3435600-3437800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr4:3435600-3438400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr4:3435600-3441400	Weak transcription	Fetal Intestine Large	intestine
50	chr4:3436000-3437600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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