Variant report

Variant	nsv822444
Chromosome Location	chr4:3597968-3714021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:895)
CpG islands
(count:4828)
Chromatin interactive
region (count:81)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:895 , 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	chr4:3673560-3674036	HepG2	liver:	n/a	n/a
2	ATF1	chr4:3622207-3622400	K562	blood:	n/a	n/a
3	ATF2	chr4:3677029-3677356	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:3677008-3677424	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr4:3647120-3647372	K562	blood:	n/a	n/a
6	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:3600326-3600440	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr4:3623754-3623964	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
12	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
14	BHLHE40	chr4:3608584-3609011	K562	blood:	n/a	n/a
15	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
16	BHLHE40	chr4:3600235-3600737	K562	blood:	n/a	n/a
17	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
18	BRCA1	chr4:3608320-3608528	HepG2	liver:	n/a	n/a
19	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
20	BRCA1	chr4:3605428-3605440	GM12878	blood:	n/a	n/a
21	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
22	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr4:3608319-3608550	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:3608695-3609153	A549	lung:	n/a	chr4:3608890-3608901
26	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
27	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
28	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
30	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
31	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946
32	CEBPB	chr4:3608690-3609116	K562	blood:	n/a	chr4:3608890-3608901
33	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
34	CEBPB	chr4:3608670-3609091	ECC-1	luminal epithelium:	n/a	chr4:3608890-3608901
35	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:3637695-3637923	K562	blood:	n/a	n/a
37	CEBPB	chr4:3608709-3609077	Hela-S3	cervix:	n/a	chr4:3608890-3608901
38	CEBPB	chr4:3608708-3609000	H1-hESC	embryonic stem cell:	n/a	chr4:3608890-3608901
39	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
40	CEBPB	chr4:3608779-3608986	K562	blood:	n/a	chr4:3608890-3608901
41	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
42	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
43	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
44	CEBPB	chr4:3608606-3609087	K562	blood:	n/a	chr4:3608890-3608901
45	CEBPB	chr4:3608006-3608007	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr4:3608726-3609033	IMR90	lung:	n/a	chr4:3608890-3608901
47	CEBPB	chr4:3621156-3621410	K562	blood:	n/a	n/a
48	CEBPB	chr4:3608752-3609056	A549	lung:	n/a	chr4:3608890-3608901
49	CEBPB	chr4:3608707-3609063	HepG2	liver:	n/a	chr4:3608890-3608901
50	CEBPB	chr4:3637704-3638130	IMR90	lung:	n/a	chr4:3637935-3637946

(count:4828 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3673098-3673148	ovcar-3	ovarian:	n/a
2	chr4:3692375-3692425	NHBE	bronchial:	n/a
3	chr4:3704880-3704930	GM12878	blood:	n/a
4	chr4:3685875-3685925	CMK	blood:	n/a
5	chr4:3685357-3685407	HNPCEpiC	eye:	n/a
6	chr4:3652326-3652376	PrEC	prostate:	n/a
7	chr4:3680970-3681020	AG09309	skin:	n/a
8	chr4:3671199-3671249	NH-A	brain:	n/a
9	chr4:3682627-3682677	AG04450	lung:	fetal
10	chr4:3673098-3673148	ovcar-3	ovarian:	n/a
11	chr4:3692375-3692425	NHBE	bronchial:	n/a
12	chr4:3704880-3704930	GM12878	blood:	n/a
13	chr4:3685875-3685925	CMK	blood:	n/a
14	chr4:3685357-3685407	HNPCEpiC	eye:	n/a
15	chr4:3652326-3652376	PrEC	prostate:	n/a
16	chr4:3680970-3681020	AG09309	skin:	n/a
17	chr4:3671199-3671249	NH-A	brain:	n/a
18	chr4:3682627-3682677	AG04450	lung:	fetal
19	chr4:3682525-3682575	ProgFib	skin:	n/a
20	chr4:3630603-3630653	Hepatocyte	liver:	n/a
21	chr4:3680970-3681020	NT2-D1	testis:	n/a
22	chr4:3644187-3644237	SK-N-SH	brain:	n/a
23	chr4:3691908-3691958	A549	lung:	n/a
24	chr4:3617256-3617306	T-47D	breast:	n/a
25	chr4:3692574-3692624	HRE	kidney:	n/a
26	chr4:3692375-3692425	AoSMC	blood vessel:	n/a
27	chr4:3640481-3640531	HEEpiC	esophagus:	n/a
28	chr4:3640481-3640531	AG04450	lung:	fetal
29	chr4:3660005-3660055	CMK	blood:	n/a
30	chr4:3664471-3664521	HepG2	liver:	n/a
31	chr4:3650777-3650827	HUVEC	blood vessel:	n/a
32	chr4:3675363-3675413	GM12878	blood:	n/a
33	chr4:3671199-3671249	HIPEpiC	eye:	n/a
34	chr4:3647047-3647097	H1-hESC	embryonic stem cell:	embryo
35	chr4:3692142-3692192	Caco-2	colon:	n/a
36	chr4:3682627-3682677	HCM	heart:	n/a
37	chr4:3685695-3685745	ProgFib	skin:	n/a
38	chr4:3681759-3681809	HPAEpiC	pulmonary alveolar:	n/a
39	chr4:3685309-3685359	U87	brain:	n/a
40	chr4:3682525-3682575	HAEpiC	amniotic membrane:	n/a
41	chr4:3691397-3691447	ECC-1	luminal epithelium:	n/a
42	chr4:3671503-3671553	T-47D	breast:	n/a
43	chr4:3647047-3647097	Caco-2	colon:	n/a
44	chr4:3664117-3664167	AG04449	skin:	fetal
45	chr4:3671199-3671249	GM12891	blood:	n/a
46	chr4:3691908-3691958	AG04449	skin:	fetal
47	chr4:3704852-3704902	HCF	heart:	n/a
48	chr4:3705147-3705197	PrEC	prostate:	n/a
49	chr4:3685357-3685407	SKMC	muscle:	n/a
50	chr4:3685695-3685745	LNCaP	prostate:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3702438..3704687-chr4:3706308..3708267,2	K562	blood:
2	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
3	chr14:52308290..52309229-chr4:3693785..3694520,2	MCF-7	breast:
4	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
5	chr4:3602447..3604350-chr4:3607841..3610609,2	K562	blood:
6	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
7	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
8	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
9	chr4:3532356..3534055-chr4:3658252..3659865,2	K562	blood:
10	chr4:3628819..3631240-chr4:3633976..3635534,2	K562	blood:
11	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
12	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
13	chr4:3597553..3600117-chr4:3602844..3606284,4	K562	blood:
14	chr4:3614687..3616600-chr4:3620839..3622694,2	MCF-7	breast:
15	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
16	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
17	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
18	chr4:3679034..3681438-chr4:3689559..3691418,2	K562	blood:
19	chr4:3603523..3606403-chr4:3623528..3625485,2	K562	blood:
20	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
21	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
22	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
23	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
24	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
25	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
26	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
27	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
28	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
29	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
30	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
31	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
32	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
33	chr4:3596211..3598668-chr4:3781245..3783965,2	K562	blood:
34	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
35	chr4:3602142..3603748-chr4:3605850..3607460,2	MCF-7	breast:
36	chr4:3614332..3616102-chr4:3632475..3634431,2	MCF-7	breast:
37	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
38	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
39	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
40	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
41	chr4:3608635..3609305-chr8:108914123..108914952,2	MCF-7	breast:
42	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
43	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
44	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
45	chr4:3649252..3651454-chr4:3653827..3655408,2	K562	blood:
46	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
47	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
48	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
49	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
50	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRPAP1-2	chr4:3678330-3678408	XLOC_003861
2	lnc-RP3-368B9.1.1-3	chr4:3635455-3635702	XLOC_003429
3	lnc-LRPAP1-6	chr4:3648128-3648206	ucscGeneNc_uc003ghl_2
4	lnc-LRPAP1-2	chr4:3675320-3675588	ENSG00000250632
5	lnc-LRPAP1-2	chr4:3675321-3675588	XLOC_003861
6	lnc-LRPAP1-2	chr4:3678898-3679582	ENSG00000250632
7	lnc-LRPAP1-6	chr4:3648696-3649380	ucscGeneNc_uc003ghl_2
8	lnc-RP3-368B9.1.1-5	chr4:3650783-3650922	XLOC_003431
9	lnc-LRPAP1-2	chr4:3678898-3679582	XLOC_003861
10	lnc-RP3-368B9.1.1-5	chr4:3650108-3650607	XLOC_003431
11	lnc-LRPAP1-5	chr4:3600844-3601755	NONHSAT094890
12	lnc-LRPAP1-2	chr4:3678330-3678408	ENSG00000250632
13	lnc-LRPAP1-6	chr4:3645119-3645386	ucscGeneNc_uc003ghl_2
14	lnc-RP3-368B9.1.1-3	chr4:3634756-3634973	XLOC_003429
15	lnc-LRPAP1-5	chr4:3600324-3600789	NONHSAT094890

No data

Variant related genes	Relation type
ENSG00000250681	TF binding region
ENSG00000250632	TF binding region
ENSG00000250681	CpG island
ENSG00000250632	CpG island
ENSG00000250681	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000175920	chromatin interactions
ENSG00000250632	chromatin interactions

Extended variants
information (count: 7011 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:7011 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35581309	chr4:3597988-3597989	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs2344229	chr4:3597989-3597990	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs529268322	chr4:3597994-3597995	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549261350	chr4:3598019-3598020	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1108643	chr4:3598032-3598033	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533749269	chr4:3598045-3598046	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2344230	chr4:3598046-3598047	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs2344231	chr4:3598055-3598056	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547144850	chr4:3598095-3598096	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2344232	chr4:3598106-3598107	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2344233	chr4:3598113-3598114	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2344234	chr4:3598144-3598145	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs16844935	chr4:3598145-3598146	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs1108644	chr4:3598161-3598162	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs556408771	chr4:3598165-3598166	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2344235	chr4:3598168-3598169	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs576001150	chr4:3598172-3598173	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2344236	chr4:3598261-3598262	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535421206	chr4:3598281-3598282	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372707909	chr4:3598293-3598294	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs62273025	chr4:3598294-3598295	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs2344237	chr4:3598308-3598309	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs113458583	chr4:3598312-3598313	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34513006	chr4:3598321-3598322	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2344238	chr4:3598341-3598342	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs2344239	chr4:3598367-3598368	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs578110215	chr4:3598400-3598401	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs529227461	chr4:3598402-3598403	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs147305099	chr4:3598409-3598410	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs72334416	chr4:3598417-3598418	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs76430824	chr4:3598424-3598425	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs5855804	chr4:3598428-3598429	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs111999194	chr4:3598434-3598435	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs543786006	chr4:3598437-3598438	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs564008051	chr4:3598447-3598448	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs78909968	chr4:3598448-3598449	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs529313392	chr4:3598450-3598451	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs386670730	chr4:3598480-3598481	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs73201111	chr4:3598481-3598482	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs2880812	chr4:3598527-3598528	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs2344241	chr4:3598536-3598537	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs2344242	chr4:3598548-3598549	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs199735115	chr4:3598567-3598568	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs2344243	chr4:3598593-3598594	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs73795608	chr4:3598602-3598603	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs2344244	chr4:3598667-3598668	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73795611	chr4:3598686-3598687	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528538426	chr4:3598687-3598688	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2344245	chr4:3598704-3598705	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547206397	chr4:3598706-3598707	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung cancer	18438408	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:912 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3595200-3598000	Weak transcription	Fetal Intestine Small	intestine
2	chr4:3595600-3600200	Weak transcription	Fetal Heart	heart
3	chr4:3595800-3599400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:3595800-3603400	Weak transcription	Right Atrium	heart
5	chr4:3597000-3598000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:3597000-3598000	Enhancers	Spleen	Spleen
7	chr4:3597000-3598200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:3597000-3598200	ZNF genes & repeats	Fetal Brain Female	brain
9	chr4:3597000-3604200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:3597000-3608000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:3597200-3599400	Enhancers	Fetal Brain Male	brain
12	chr4:3597400-3601200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
13	chr4:3598000-3598800	Weak transcription	Spleen	Spleen
14	chr4:3598400-3598600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr4:3598600-3599200	Enhancers	HepG2	liver
16	chr4:3598600-3607600	ZNF genes & repeats	Fetal Stomach	stomach
17	chr4:3598800-3601000	ZNF genes & repeats	Spleen	Spleen
18	chr4:3599200-3599600	Flanking Active TSS	HepG2	liver
19	chr4:3599400-3599800	Weak transcription	Fetal Brain Male	brain
20	chr4:3599400-3599800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr4:3599400-3601000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:3599600-3599800	Enhancers	HepG2	liver
23	chr4:3599600-3600400	Enhancers	Brain Anterior Caudate	brain
24	chr4:3599600-3601000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr4:3599800-3600600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr4:3599800-3600600	Enhancers	Fetal Brain Female	brain
27	chr4:3599800-3601800	ZNF genes & repeats	Fetal Brain Male	brain
28	chr4:3600000-3600400	Enhancers	Brain Cingulate Gyrus	brain
29	chr4:3600000-3600400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr4:3600000-3600800	ZNF genes & repeats	Duodenum Mucosa	Duodenum
31	chr4:3600000-3601600	ZNF genes & repeats	Fetal Lung	lung
32	chr4:3600000-3604200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:3600200-3600600	ZNF genes & repeats	Fetal Heart	heart
34	chr4:3600200-3600800	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr4:3600200-3601000	ZNF genes & repeats	Gastric	stomach
36	chr4:3600200-3601400	ZNF genes & repeats	Esophagus	oesophagus
37	chr4:3600200-3601600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:3600200-3601600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:3600200-3602200	ZNF genes & repeats	Pancreas	Pancrea
40	chr4:3600400-3601000	ZNF genes & repeats	Fetal Kidney	kidney
41	chr4:3600400-3601600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
42	chr4:3600600-3601400	Weak transcription	Fetal Brain Female	brain
43	chr4:3600800-3601000	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
44	chr4:3601000-3601200	Weak transcription	Spleen	Spleen
45	chr4:3601200-3601400	Enhancers	Spleen	Spleen
46	chr4:3601400-3601600	Enhancers	Fetal Brain Female	brain
47	chr4:3601400-3601600	Flanking Active TSS	Spleen	Spleen
48	chr4:3601600-3602000	Bivalent Enhancer	Placenta	Placenta
49	chr4:3601600-3602000	Active TSS	Spleen	Spleen
50	chr4:3601600-3611600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin

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