Variant report

Variant	nsv524211
Chromosome Location	chr4:3215835-3270488
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:855)
CpG islands
(count:3665)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:3243690-3244135	K562	blood:	n/a	n/a
2	ATF1	chr4:3265569-3265894	K562	blood:	n/a	n/a
3	ATF2	chr4:3239383-3239970	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:3245851-3246200	GM12878	blood:	n/a	n/a
5	BACH1	chr4:3244171-3244268	K562	blood:	n/a	n/a
6	BACH1	chr4:3239388-3240090	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr4:3247680-3247998	GM12878	blood:	n/a	chr4:3247818-3247831 chr4:3247871-3247880
8	BCL3	chr4:3245776-3246316	GM12878	blood:	n/a	chr4:3245972-3245980 chr4:3245926-3245935
9	BCL3	chr4:3246538-3247516	GM12878	blood:	n/a	chr4:3247225-3247234
10	BHLHE40	chr4:3235484-3235883	K562	blood:	n/a	n/a
11	BHLHE40	chr4:3243555-3244450	K562	blood:	n/a	n/a
12	BHLHE40	chr4:3269888-3269923	K562	blood:	n/a	n/a
13	BHLHE40	chr4:3255694-3255733	K562	blood:	n/a	n/a
14	BHLHE40	chr4:3246475-3246584	K562	blood:	n/a	n/a
15	BHLHE40	chr4:3245002-3245230	K562	blood:	n/a	n/a
16	BRCA1	chr4:3252858-3253000	HepG2	liver:	n/a	n/a
17	CBX3	chr4:3243623-3244050	K562	blood:	n/a	n/a
18	CCNT2	chr4:3243632-3244031	K562	blood:	n/a	n/a
19	CCNT2	chr4:3249958-3250015	K562	blood:	n/a	n/a
20	CCNT2	chr4:3258507-3258654	K562	blood:	n/a	n/a
21	CEBPB	chr4:3269765-3270208	MCF-7	breast:	n/a	n/a
22	CEBPB	chr4:3269842-3270158	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:3269798-3270088	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr4:3269742-3270204	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:3269820-3270074	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:3233782-3233805	HepG2	liver:	n/a	n/a
27	CEBPB	chr4:3243776-3243897	K562	blood:	n/a	n/a
28	CEBPB	chr4:3269820-3270145	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:3269888-3270143	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:3269796-3270131	K562	blood:	n/a	n/a
31	CEBPB	chr4:3259805-3260172	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:3269915-3270022	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:3241757-3241760	HepG2	liver:	n/a	n/a
34	CREB1	chr4:3246926-3247149	A549	lung:	n/a	n/a
35	CREB1	chr4:3265506-3265967	K562	blood:	n/a	n/a
36	CREB1	chr4:3265525-3265907	K562	blood:	n/a	n/a
37	CTCF	chr4:3252313-3252378	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr4:3235660-3235810	AG04450	lung:	n/a	n/a
39	CTCF	chr4:3235600-3235750	SAEC	small airway:	n/a	n/a
40	CTCF	chr4:3246640-3246790	GM12864	blood:	n/a	chr4:3246741-3246759
41	CTCF	chr4:3221740-3221890	GM12866	blood:	n/a	n/a
42	CTCF	chr4:3235633-3235908	IMR90	lung:	n/a	n/a
43	CTCF	chr4:3248440-3248590	HMF	breast:	n/a	chr4:3248466-3248484 chr4:3248468-3248481
44	CTCF	chr4:3235707-3235776	GM12878	blood:	n/a	n/a
45	CTCF	chr4:3235900-3236050	AG04449	skin:	n/a	n/a
46	CTCF	chr4:3235680-3235830	HAc	cerebellar:	n/a	n/a
47	CTCF	chr4:3248380-3248530	SK-N-SH_RA	brain:	n/a	chr4:3248466-3248484 chr4:3248468-3248481 chr4:3248412-3248421
48	CTCF	chr4:3248340-3248490	GM12869	blood:	n/a	chr4:3248466-3248484 chr4:3248468-3248481 chr4:3248412-3248421
49	CTCF	chr4:3255900-3256050	HAc	cerebellar:	n/a	n/a
50	CTCF	chr4:3248360-3248510	HUVEC	blood vessel:	n/a	chr4:3248466-3248484 chr4:3248468-3248481 chr4:3248412-3248421

(count:3665 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3244239-3244289	AG04450	lung:	fetal
2	chr4:3253559-3253609	SKMC	muscle:	n/a
3	chr4:3257477-3257527	Jurkat	blood:	n/a
4	chr4:3240754-3240804	LNCaP	prostate:	n/a
5	chr4:3250090-3250140	HUVEC	blood vessel:	n/a
6	chr4:3244239-3244289	AG04450	lung:	fetal
7	chr4:3253559-3253609	SKMC	muscle:	n/a
8	chr4:3257477-3257527	Jurkat	blood:	n/a
9	chr4:3240754-3240804	LNCaP	prostate:	n/a
10	chr4:3250090-3250140	HUVEC	blood vessel:	n/a
11	chr4:3257791-3257841	ovcar-3	ovarian:	n/a
12	chr4:3234814-3234864	U87	brain:	n/a
13	chr4:3263249-3263299	HCM	heart:	n/a
14	chr4:3251225-3251275	H1-hESC	embryonic stem cell:	embryo
15	chr4:3255174-3255224	AG04450	lung:	fetal
16	chr4:3251386-3251436	SAEC	small airway:	n/a
17	chr4:3263229-3263279	HL-60	blood:	n/a
18	chr4:3233865-3233915	T-47D	breast:	n/a
19	chr4:3234417-3234467	RPTEC	kidney:	n/a
20	chr4:3235000-3235050	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:3233786-3233836	T-47D	breast:	n/a
22	chr4:3250921-3250971	HCM	heart:	n/a
23	chr4:3235319-3235369	SK-N-SH_RA	brain:	n/a
24	chr4:3265280-3265330	Hela-S3	cervix:	n/a
25	chr4:3233774-3233824	NHDF-neo	bronchial:	n/a
26	chr4:3233774-3233824	AG04450	lung:	fetal
27	chr4:3231709-3231759	AG04450	lung:	fetal
28	chr4:3247372-3247422	SK-N-MC	brain:	n/a
29	chr4:3244206-3244256	AG04450	lung:	fetal
30	chr4:3235000-3235050	AG10803	skin:	n/a
31	chr4:3252413-3252463	PANC-1	pancreas:	n/a
32	chr4:3263456-3263506	GM12891	blood:	n/a
33	chr4:3250295-3250345	GM12878	blood:	n/a
34	chr4:3234519-3234569	AG09309	skin:	n/a
35	chr4:3235000-3235050	H1-hESC	embryonic stem cell:	embryo
36	chr4:3255128-3255178	SK-N-SH	brain:	n/a
37	chr4:3250845-3250895	HepG2	liver:	n/a
38	chr4:3249975-3250025	HAEpiC	amniotic membrane:	n/a
39	chr4:3257477-3257527	HIPEpiC	eye:	n/a
40	chr4:3250090-3250140	HAEpiC	amniotic membrane:	n/a
41	chr4:3239323-3239373	NHDF-neo	bronchial:	n/a
42	chr4:3234417-3234467	T-47D	breast:	n/a
43	chr4:3265114-3265164	AoSMC	blood vessel:	n/a
44	chr4:3263229-3263279	ProgFib	skin:	n/a
45	chr4:3234462-3234512	SAEC	small airway:	n/a
46	chr4:3254969-3255019	ProgFib	skin:	n/a
47	chr4:3239323-3239373	GM06990	blood:	n/a
48	chr4:3235000-3235050	ovcar-3	ovarian:	n/a
49	chr4:3244206-3244256	Caco-2	colon:	n/a
50	chr4:3265114-3265164	HAEpiC	amniotic membrane:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:3243269..3245646-chr4:3270348..3272217,2	MCF-7	breast:
2	chr4:3237753..3241593-chr4:3242889..3245748,3	K562	blood:
3	chr4:3265031..3267765-chr4:3268616..3271432,2	K562	blood:
4	chr4:3210706..3212458-chr4:3214564..3216514,2	MCF-7	breast:
5	chr4:3243269..3245646-chr4:3270348..3272217,2	MCF-7	breast:
6	chr4:3232769..3236525-chr4:3484558..3488114,4	MCF-7	breast:
7	chr4:3241533..3243545-chr4:3294017..3295653,2	K562	blood:
8	chr4:3213997..3215990-chr4:3485524..3487678,2	MCF-7	breast:
9	chr4:3236424..3238868-chr4:3242147..3244588,4	MCF-7	breast:
10	chr4:3220220..3221940-chr4:3299861..3302041,2	MCF-7	breast:
11	chr4:3231863..3234034-chr4:3238136..3239944,2	MCF-7	breast:
12	chr4:3215167..3215891-chr4:3479590..3480357,2	K562	blood:
13	chr4:3251210..3252923-chr4:3261294..3264079,2	K562	blood:
14	chr4:3230862..3233203-chr4:3234391..3237131,2	K562	blood:
15	chr4:3251580..3254728-chr4:3256046..3259468,3	MCF-7	breast:
16	chr4:3243567..3245468-chr4:3259325..3261175,2	MCF-7	breast:
17	chr4:3217030..3219170-chr4:3223005..3224879,2	K562	blood:
18	chr4:3195952..3197606-chr4:3265003..3267231,2	K562	blood:
19	chr4:3177702..3180138-chr4:3219195..3221114,2	K562	blood:
20	chr4:3243758..3245995-chr4:3246893..3248968,3	K562	blood:
21	chr4:3265031..3267765-chr4:3268616..3271432,2	K562	blood:
22	chr4:3231863..3234034-chr4:3238136..3239944,2	MCF-7	breast:
23	chr4:3233193..3236137-chr4:3292325..3293850,2	MCF-7	breast:
24	chr4:3233021..3235441-chr4:3240275..3242127,2	K562	blood:
25	chr4:3236106..3239124-chr4:3240475..3243482,3	K562	blood:
26	chr4:3231157..3234122-chr4:3467560..3470032,2	MCF-7	breast:
27	chr4:3075638..3077191-chr4:3246487..3249347,2	MCF-7	breast:
28	chr4:3252719..3255661-chr4:3256230..3259529,3	K562	blood:
29	chr4:3242999..3245101-chr4:3255147..3256649,2	MCF-7	breast:
30	chr4:3251892..3254308-chr4:3255097..3257902,2	MCF-7	breast:
31	chr4:3186114..3188312-chr4:3216098..3217780,2	MCF-7	breast:
32	chr4:3251580..3254728-chr4:3256046..3259468,3	MCF-7	breast:
33	chr4:3251892..3254308-chr4:3255097..3257902,2	MCF-7	breast:
34	chr4:3239414..3242186-chr4:3248483..3251148,2	MCF-7	breast:
35	chr4:3225798..3228316-chr4:3230639..3233767,3	K562	blood:
36	chr4:3225798..3227751-chr4:3230639..3233084,3	K562	blood:
37	chr4:3268743..3271551-chr4:3273568..3275857,3	MCF-7	breast:
38	chr4:3249484..3252398-chr4:3294414..3296079,2	K562	blood:
39	chr4:3218350..3221030-chr4:3221970..3224465,2	MCF-7	breast:
40	chr4:3242200..3244508-chr4:3250830..3252457,2	MCF-7	breast:
41	chr4:3243758..3245995-chr4:3246893..3248968,3	K562	blood:
42	chr4:3218350..3221030-chr4:3221970..3224465,2	MCF-7	breast:
43	chr4:3242999..3245101-chr4:3255147..3256649,2	MCF-7	breast:
44	chr4:3214912..3216884-chr4:3292944..3295719,2	MCF-7	breast:
45	chr4:3251210..3252923-chr4:3261294..3264079,2	K562	blood:
46	chr4:3243567..3245468-chr4:3259325..3261175,2	MCF-7	breast:
47	chr4:3269730..3272201-chr4:3294200..3296416,2	MCF-7	breast:
48	chr4:3225798..3228316-chr4:3230639..3233767,3	K562	blood:
49	chr4:3230862..3233203-chr4:3234391..3237131,2	K562	blood:
50	chr4:3241569..3245545-chr4:3246325..3249295,4	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C4orf44	hsa-miR-185-5p	chr4:3258181-3258202

Variant related genes	Relation type
HTT	TF binding region
MSANTD1	TF binding region
HTT	CpG island
MSANTD1	CpG island
ENSG00000197386	chromatin interactions
ENSG00000188981	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000251075	chromatin interactions

Extended variants
information (count: 2678 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2678 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs362331	chr4:3215835-3215836	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200129223	chr4:3215836-3215837	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376635317	chr4:3215861-3215862	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs201280285	chr4:3215873-3215874	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs371221527	chr4:3215879-3215880	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs368710938	chr4:3215882-3215883	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs374327813	chr4:3215883-3215884	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs367731348	chr4:3215888-3215889	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs373379676	chr4:3215897-3215898	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs182137830	chr4:3215903-3215904	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs552240071	chr4:3215925-3215926	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs185797886	chr4:3215983-3215984	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs568954849	chr4:3215986-3215987	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs537953425	chr4:3216009-3216010	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs555157126	chr4:3216028-3216029	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568641085	chr4:3216031-3216032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs534171944	chr4:3216094-3216095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs190212557	chr4:3216112-3216113	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs141061243	chr4:3216125-3216126	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs539425945	chr4:3216253-3216254	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs362330	chr4:3216270-3216271	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs576094376	chr4:3216281-3216282	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs200738607	chr4:3216297-3216298	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541930548	chr4:3216329-3216330	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs3025823	chr4:3216332-3216333	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs362329	chr4:3216356-3216357	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs59535611	chr4:3216433-3216434	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10000252	chr4:3216484-3216485	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs540097687	chr4:3216492-3216493	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144862572	chr4:3216494-3216495	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs362328	chr4:3216520-3216521	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs202218497	chr4:3216541-3216542	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs112624856	chr4:3216542-3216543	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs58813224	chr4:3216543-3216544	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs3025822	chr4:3216544-3216545	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs182603737	chr4:3216548-3216549	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140919237	chr4:3216552-3216553	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs531386191	chr4:3216553-3216554	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553648083	chr4:3216608-3216609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs76164594	chr4:3216640-3216641	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138762073	chr4:3216649-3216650	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs568101802	chr4:3216705-3216706	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs534387370	chr4:3216741-3216742	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs362327	chr4:3216750-3216751	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs916171	chr4:3216815-3216816	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs200857448	chr4:3216846-3216847	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368077431	chr4:3216860-3216861	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570781020	chr4:3216863-3216864	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186882443	chr4:3216894-3216895	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373205907	chr4:3216905-3216906	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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 cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1169 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3114600-3292400	Weak transcription	Right Atrium	heart
2	chr4:3145800-3239200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:3172400-3238800	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:3193800-3233000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:3194000-3237600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:3196000-3242600	Strong transcription	Fetal Intestine Small	intestine
7	chr4:3201400-3238400	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:3204800-3246000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:3205400-3224800	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr4:3205600-3216600	Weak transcription	Hela-S3	cervix
11	chr4:3205800-3228000	Strong transcription	Left Ventricle	heart
12	chr4:3206000-3220400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr4:3206000-3234800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:3206000-3244600	Strong transcription	Primary neutrophils fromperipheralblood	blood
15	chr4:3206000-3246400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr4:3206400-3229600	Strong transcription	Fetal Stomach	stomach
17	chr4:3206800-3221600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr4:3207200-3229000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr4:3207600-3221000	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr4:3207600-3238600	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr4:3207600-3243600	Strong transcription	Primary B cells from peripheral blood	blood
22	chr4:3207600-3244000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:3207600-3244600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr4:3207600-3245400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr4:3207600-3246400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr4:3207800-3219400	Strong transcription	HSMM	muscle
27	chr4:3207800-3221400	Strong transcription	Skeletal Muscle Male	skeletal muscle
28	chr4:3207800-3221600	Strong transcription	Fetal Muscle Trunk	muscle
29	chr4:3207800-3221600	Strong transcription	Fetal Muscle Leg	muscle
30	chr4:3207800-3226400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr4:3207800-3226600	Strong transcription	Primary B cells from cord blood	blood
32	chr4:3207800-3228200	Strong transcription	Rectal Mucosa Donor 31	rectum
33	chr4:3207800-3228400	Strong transcription	H1 Cell Line	embryonic stem cell
34	chr4:3207800-3229000	Strong transcription	Aorta	Aorta
35	chr4:3207800-3229800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:3207800-3243200	Strong transcription	Sigmoid Colon	Sigmoid Colon
37	chr4:3207800-3243800	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr4:3207800-3244400	Strong transcription	Duodenum Mucosa	Duodenum
39	chr4:3207800-3245400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr4:3208000-3219000	Strong transcription	Pancreas	Pancrea
41	chr4:3208000-3221800	Strong transcription	Brain Inferior Temporal Lobe	brain
42	chr4:3208000-3227000	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr4:3208000-3235800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chr4:3208000-3243600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr4:3208200-3221200	Strong transcription	Right Ventricle	heart
46	chr4:3208200-3227200	Strong transcription	NH-A	brain
47	chr4:3208200-3228400	Strong transcription	Stomach Smooth Muscle	stomach
48	chr4:3208200-3237400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chr4:3208200-3239200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:3208200-3246400	Strong transcription	Fetal Thymus	thymus

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