Variant report

Variant	nsv878458
Chromosome Location	chr4:3235518-3303976
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1347)
CpG islands
(count:3972)
Chromatin interactive
region (count:98)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1347 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

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	ARID3A	chr4:3243690-3244135	K562	blood:	n/a	n/a
3	ATF1	chr4:3265569-3265894	K562	blood:	n/a	n/a
4	ATF2	chr4:3239383-3239970	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:3287878-3288195	GM12878	blood:	n/a	n/a
6	ATF2	chr4:3287771-3288267	GM12878	blood:	n/a	n/a
7	ATF2	chr4:3245851-3246200	GM12878	blood:	n/a	n/a
8	BACH1	chr4:3293851-3294599	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:3239388-3240090	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:3244171-3244268	K562	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	chr4:3245776-3246316	GM12878	blood:	n/a	chr4:3245972-3245980 chr4:3245926-3245935
15	BCL3	chr4:3246538-3247516	GM12878	blood:	n/a	chr4:3247225-3247234
16	BCL3	chr4:3247680-3247998	GM12878	blood:	n/a	chr4:3247818-3247831 chr4:3247871-3247880
17	BCL3	chr4:3301718-3302065	GM12878	blood:	n/a	chr4:3301978-3301991
18	BCL3	chr4:3299125-3299446	GM12878	blood:	n/a	n/a
19	BCL3	chr4:3299110-3299479	GM12878	blood:	n/a	n/a
20	BCL3	chr4:3298257-3298480	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:3293893-3294609	K562	blood:	n/a	chr4:3294055-3294071 chr4:3293992-3294008
22	BHLHE40	chr4:3269888-3269923	K562	blood:	n/a	n/a
23	BHLHE40	chr4:3294320-3294520	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:3245002-3245230	K562	blood:	n/a	n/a
25	BHLHE40	chr4:3286429-3286762	HepG2	liver:	n/a	n/a
26	BHLHE40	chr4:3246475-3246584	K562	blood:	n/a	n/a
27	BHLHE40	chr4:3235484-3235883	K562	blood:	n/a	n/a
28	BHLHE40	chr4:3255694-3255733	K562	blood:	n/a	n/a
29	BHLHE40	chr4:3286433-3286738	K562	blood:	n/a	n/a
30	BHLHE40	chr4:3294399-3294612	HepG2	liver:	n/a	n/a
31	BHLHE40	chr4:3293310-3294186	HepG2	liver:	n/a	chr4:3294055-3294071 chr4:3293992-3294008
32	BHLHE40	chr4:3287854-3288237	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:3243555-3244450	K562	blood:	n/a	n/a
34	BHLHE40	chr4:3295622-3295699	K562	blood:	n/a	n/a
35	BHLHE40	chr4:3293912-3294112	GM12878	blood:	n/a	chr4:3294055-3294071 chr4:3293992-3294008
36	BRCA1	chr4:3294300-3294363	HepG2	liver:	n/a	n/a
37	BRCA1	chr4:3294288-3294477	H1-hESC	embryonic stem cell:	n/a	n/a
38	BRCA1	chr4:3295798-3295907	GM12878	blood:	n/a	n/a
39	BRCA1	chr4:3252858-3253000	HepG2	liver:	n/a	n/a
40	CBX3	chr4:3243623-3244050	K562	blood:	n/a	n/a
41	CBX3	chr4:3294295-3294586	K562	blood:	n/a	n/a
42	CCNT2	chr4:3294235-3295326	K562	blood:	n/a	n/a
43	CCNT2	chr4:3249958-3250015	K562	blood:	n/a	n/a
44	CCNT2	chr4:3258507-3258654	K562	blood:	n/a	n/a
45	CCNT2	chr4:3243632-3244031	K562	blood:	n/a	n/a
46	CEBPB	chr4:3269888-3270143	HepG2	liver:	n/a	n/a
47	CEBPB	chr4:3269842-3270158	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:3269915-3270022	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:3287826-3288147	HepG2	liver:	n/a	n/a
50	CEBPB	chr4:3243776-3243897	K562	blood:	n/a	n/a

(count:3972 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3251225-3251275	ovcar-3	ovarian:	n/a
2	chr4:3255689-3255739	HAEpiC	amniotic membrane:	n/a
3	chr4:3249975-3250025	GM12891	blood:	n/a
4	chr4:3257477-3257527	HRCEpiC	kidney:	n/a
5	chr4:3294241-3294291	HRPEpiC	eye:	n/a
6	chr4:3289826-3289876	NB4	blood:	n/a
7	chr4:3250726-3250776	Caco-2	colon:	n/a
8	chr4:3251225-3251275	ovcar-3	ovarian:	n/a
9	chr4:3255689-3255739	HAEpiC	amniotic membrane:	n/a
10	chr4:3249975-3250025	GM12891	blood:	n/a
11	chr4:3257477-3257527	HRCEpiC	kidney:	n/a
12	chr4:3294241-3294291	HRPEpiC	eye:	n/a
13	chr4:3289826-3289876	NB4	blood:	n/a
14	chr4:3250726-3250776	Caco-2	colon:	n/a
15	chr4:3261368-3261418	Hepatocyte	liver:	n/a
16	chr4:3250295-3250345	HIPEpiC	eye:	n/a
17	chr4:3252413-3252463	HEK293	kidney:	embryo
18	chr4:3263249-3263299	NHBE	bronchial:	n/a
19	chr4:3294400-3294450	SK-N-SH_RA	brain:	n/a
20	chr4:3294241-3294291	GM06990	blood:	n/a
21	chr4:3241813-3241863	NT2-D1	testis:	n/a
22	chr4:3240754-3240804	AoSMC	blood vessel:	n/a
23	chr4:3287376-3287426	LNCaP	prostate:	n/a
24	chr4:3265114-3265164	HRCEpiC	kidney:	n/a
25	chr4:3250090-3250140	HAEpiC	amniotic membrane:	n/a
26	chr4:3244239-3244289	HCT-116	colon:	n/a
27	chr4:3298514-3298564	PANC-1	pancreas:	n/a
28	chr4:3254969-3255019	AoSMC	blood vessel:	n/a
29	chr4:3244239-3244289	NHDF-neo	bronchial:	n/a
30	chr4:3257791-3257841	ovcar-3	ovarian:	n/a
31	chr4:3265114-3265164	Caco-2	colon:	n/a
32	chr4:3292386-3292436	HAEpiC	amniotic membrane:	n/a
33	chr4:3289826-3289876	SK-N-MC	brain:	n/a
34	chr4:3289776-3289826	HAEpiC	amniotic membrane:	n/a
35	chr4:3289776-3289826	HNPCEpiC	eye:	n/a
36	chr4:3254969-3255019	T-47D	breast:	n/a
37	chr4:3239323-3239373	NH-A	brain:	n/a
38	chr4:3257477-3257527	A549	lung:	n/a
39	chr4:3258018-3258068	NHBE	bronchial:	n/a
40	chr4:3263229-3263279	HRPEpiC	eye:	n/a
41	chr4:3244239-3244289	HRPEpiC	eye:	n/a
42	chr4:3240754-3240804	AG09309	skin:	n/a
43	chr4:3294241-3294291	HPAEpiC	pulmonary alveolar:	n/a
44	chr4:3250745-3250795	HAEpiC	amniotic membrane:	n/a
45	chr4:3294241-3294291	K562	blood:	n/a
46	chr4:3255689-3255739	HCPEpiC	choroid plexus:	n/a
47	chr4:3235589-3235639	ovcar-3	ovarian:	n/a
48	chr4:3278748-3278798	NH-A	brain:	n/a
49	chr4:3251105-3251155	AG09309	skin:	n/a
50	chr4:3292386-3292436	PrEC	prostate:	n/a

(count:98 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3297878..3299647-chr4:3439847..3442316,2	MCF-7	breast:
2	chr4:3287370..3290195-chr4:3296120..3298356,2	K562	blood:
3	chr4:3283519..3286259-chr4:3292639..3294370,2	K562	blood:
4	chr4:3283519..3286259-chr4:3292639..3294370,2	K562	blood:
5	chr4:3276746..3278804-chr4:3288196..3290777,2	K562	blood:
6	chr4:3251892..3254308-chr4:3255097..3257902,2	MCF-7	breast:
7	chr4:3299078..3301560-chr4:3303600..3305932,2	MCF-7	breast:
8	chr4:3276746..3278804-chr4:3288196..3290777,2	K562	blood:
9	chr4:3075638..3077191-chr4:3246487..3249347,2	MCF-7	breast:
10	chr4:3252719..3255661-chr4:3256230..3259529,3	K562	blood:
11	chr4:3241533..3243545-chr4:3294017..3295653,2	K562	blood:
12	chr4:3252719..3255661-chr4:3256230..3259529,3	K562	blood:
13	chr4:3299099..3300843-chr4:3320328..3323004,2	MCF-7	breast:
14	chr4:3302327..3305521-chr4:3308441..3313111,5	MCF-7	breast:
15	chr4:3269278..3270856-chr4:3292386..3294072,2	MCF-7	breast:
16	chr4:3233193..3236137-chr4:3292325..3293850,2	MCF-7	breast:
17	chr4:3301249..3303803-chr4:3305446..3308056,2	MCF-7	breast:
18	chr4:3279004..3281041-chr4:3293063..3295560,2	K562	blood:
19	chr4:3212742..3214641-chr4:3244184..3246248,2	K562	blood:
20	chr4:3276654..3280609-chr4:3292569..3295812,3	MCF-7	breast:
21	chr4:3292637..3295776-chr4:3483843..3488274,4	MCF-7	breast:
22	chr4:3289451..3291897-chr4:3292555..3295827,4	K562	blood:
23	chr4:3233193..3236137-chr4:3292325..3293850,2	MCF-7	breast:
24	chr4:3294026..3296810-chr4:3301953..3306532,4	MCF-7	breast:
25	chr4:3245063..3247633-chr4:3289230..3291965,2	MCF-7	breast:
26	chr4:3284172..3287055-chr4:3294600..3296499,2	K562	blood:
27	chr4:3272762..3274789-chr4:3288374..3291256,2	MCF-7	breast:
28	chr4:3287264..3290154-chr4:3470213..3472155,2	MCF-7	breast:
29	chr4:3231863..3234034-chr4:3238136..3239944,2	MCF-7	breast:
30	chr4:3288141..3289800-chr4:3461769..3463366,2	MCF-7	breast:
31	chr4:2798786..2800390-chr4:3294087..3295620,2	MCF-7	breast:
32	chr4:3251210..3252923-chr4:3261294..3264079,2	K562	blood:
33	chr4:3237753..3241593-chr4:3242889..3245748,3	K562	blood:
34	chr4:3236106..3239124-chr4:3240475..3243482,3	K562	blood:
35	chr4:3251892..3254308-chr4:3255097..3257902,2	MCF-7	breast:
36	chr4:3293993..3296488-chr4:3491954..3495229,3	MCF-7	breast:
37	chr4:3277870..3279701-chr4:3282246..3285205,2	MCF-7	breast:
38	chr4:3294728..3297667-chr4:3300609..3302495,3	K562	blood:
39	chr4:3242999..3245101-chr4:3255147..3256649,2	MCF-7	breast:
40	chr4:3243269..3245646-chr4:3270348..3272217,2	MCF-7	breast:
41	chr4:3242999..3245101-chr4:3255147..3256649,2	MCF-7	breast:
42	chr4:3269278..3270856-chr4:3292386..3294072,2	MCF-7	breast:
43	chr4:3299302..3301321-chr4:3301598..3303131,2	MCF-7	breast:
44	chr4:3243269..3245646-chr4:3270348..3272217,2	MCF-7	breast:
45	chr4:3293485..3295010-chr4:3317459..3319780,2	K562	blood:
46	chr4:3292635..3294292-chr4:3500969..3502505,2	MCF-7	breast:
47	chr4:3251580..3254728-chr4:3256046..3259468,3	MCF-7	breast:
48	chr4:3230862..3233203-chr4:3234391..3237131,2	K562	blood:
49	chr4:3277035..3279969-chr4:3294463..3296072,2	MCF-7	breast:
50	chr4:3220220..3221940-chr4:3299861..3302041,2	MCF-7	breast:

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
RGS12	TF binding region
HTT	TF binding region
MSANTD1	TF binding region
RGS12	CpG island
HTT	CpG island
MSANTD1	CpG island
ENSG00000251075	chromatin interactions
ENSG00000197386	chromatin interactions
ENSG00000159788	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000087266	chromatin interactions
ENSG00000188981	chromatin interactions

Extended variants
information (count: 3232 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:3232 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs362271	chr4:3235518-3235519	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559817231	chr4:3235525-3235526	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs527567345	chr4:3235544-3235545	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs362313	chr4:3235589-3235590	Strong transcription Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs142827283	chr4:3235606-3235607	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs549706343	chr4:3235634-3235635	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs147422679	chr4:3235635-3235636	Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs535106996	chr4:3235649-3235650	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs12649464	chr4:3235651-3235652	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs565651709	chr4:3235703-3235704	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs11940964	chr4:3235708-3235709	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs535188945	chr4:3235735-3235736	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs558071288	chr4:3235753-3235754	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs571694113	chr4:3235797-3235798	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs578239741	chr4:3235845-3235846	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs537729879	chr4:3235885-3235886	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs557732465	chr4:3235914-3235915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs190218897	chr4:3235944-3235945	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs368581733	chr4:3235945-3235946	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs138100826	chr4:3235951-3235952	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs559771147	chr4:3235989-3235990	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs573262273	chr4:3236007-3236008	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs541182661	chr4:3236053-3236054	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs564118502	chr4:3236055-3236056	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs149338875	chr4:3236083-3236084	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs533007339	chr4:3236103-3236104	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs362270	chr4:3236135-3236136	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs563275858	chr4:3236152-3236153	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs528823471	chr4:3236184-3236185	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs144671545	chr4:3236202-3236203	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs565721842	chr4:3236229-3236230	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs577577381	chr4:3236275-3236276	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs377179119	chr4:3236282-3236283	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs367707881	chr4:3236304-3236305	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs551495041	chr4:3236313-3236314	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs371797296	chr4:3236388-3236389	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs571865823	chr4:3236429-3236430	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs375354634	chr4:3236441-3236442	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs537676390	chr4:3236449-3236450	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs557652938	chr4:3236456-3236457	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs148519568	chr4:3236483-3236484	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs571008502	chr4:3236486-3236487	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs28507598	chr4:3236505-3236506	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs144268076	chr4:3236507-3236508	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs114035622	chr4:3236511-3236512	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs558657241	chr4:3236524-3236525	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs146101563	chr4:3236541-3236542	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs565358207	chr4:3236570-3236571	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs367895333	chr4:3236571-3236572	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs182610825	chr4:3236597-3236598	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:2072 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

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	chr4:3194000-3237600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:3196000-3242600	Strong transcription	Fetal Intestine Small	intestine
6	chr4:3201400-3238400	Strong transcription	HUES48 Cell Line	embryonic stem cell
7	chr4:3204800-3246000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr4:3206000-3244600	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr4:3206000-3246400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr4:3207600-3238600	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr4:3207600-3243600	Strong transcription	Primary B cells from peripheral blood	blood
12	chr4:3207600-3244000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr4:3207600-3244600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr4:3207600-3245400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
15	chr4:3207600-3246400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr4:3207800-3243200	Strong transcription	Sigmoid Colon	Sigmoid Colon
17	chr4:3207800-3243800	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr4:3207800-3244400	Strong transcription	Duodenum Mucosa	Duodenum
19	chr4:3207800-3245400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr4:3208000-3235800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
21	chr4:3208000-3243600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr4:3208200-3237400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
23	chr4:3208200-3239200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:3208200-3246400	Strong transcription	Fetal Thymus	thymus
25	chr4:3208400-3244800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:3210000-3244200	Strong transcription	Fetal Intestine Large	intestine
27	chr4:3210000-3245000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr4:3210000-3246600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr4:3210400-3247000	Strong transcription	Cortex derived primary cultured neurospheres	brain
30	chr4:3211600-3246400	Strong transcription	Thymus	Thymus
31	chr4:3213400-3242600	Strong transcription	Ovary	ovary
32	chr4:3213400-3243400	Strong transcription	Dnd41	blood
33	chr4:3213400-3245600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:3213600-3238800	Strong transcription	Primary T helper cells PMA-I stimulated	--
35	chr4:3213600-3245600	Strong transcription	Placenta Amnion	Placenta Amnion
36	chr4:3213800-3247600	Strong transcription	Primary T cells from cord blood	blood
37	chr4:3214000-3243400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr4:3221600-3238800	Weak transcription	Hela-S3	cervix
39	chr4:3222600-3241600	Strong transcription	Adipose Nuclei	Adipose
40	chr4:3223200-3243800	Strong transcription	Primary T cells fromperipheralblood	blood
41	chr4:3223400-3247600	Strong transcription	Fetal Brain Female	brain
42	chr4:3224000-3236200	Weak transcription	Psoas Muscle	Psoas
43	chr4:3225200-3240800	Strong transcription	Skeletal Muscle Male	skeletal muscle
44	chr4:3227000-3238200	Strong transcription	Primary B cells from cord blood	blood
45	chr4:3227200-3239200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr4:3228800-3237400	Strong transcription	HepG2	liver
47	chr4:3228800-3246600	Strong transcription	Liver	Liver
48	chr4:3229000-3243000	Strong transcription	Placenta	Placenta
49	chr4:3229000-3245400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr4:3229200-3243000	Strong transcription	Brain Angular Gyrus	brain

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