Variant report

Variant	esv35161
Chromosome Location	chr4:3624375-3722559
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:685)
CpG islands
(count:4517)
Chromatin interactive
region (count:74)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:685 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

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	ATF2	chr4:3677008-3677424	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:3677029-3677356	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr4:3647120-3647372	K562	blood:	n/a	n/a
5	BACH1	chr4:3677224-3677270	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:3705425-3705710	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:3642457-3642549	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr4:3714099-3714481	GM12878	blood:	n/a	n/a
9	BCL3	chr4:3715793-3716328	GM12878	blood:	n/a	chr4:3715840-3715849
10	BCL3	chr4:3714152-3714450	GM12878	blood:	n/a	n/a
11	BCL3	chr4:3715787-3716400	GM12878	blood:	n/a	chr4:3715840-3715849
12	BCL3	chr4:3654399-3654631	GM12878	blood:	n/a	n/a
13	BCL3	chr4:3687530-3687808	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:3642423-3642629	K562	blood:	n/a	n/a
15	BHLHE40	chr4:3677196-3677396	K562	blood:	n/a	n/a
16	BHLHE40	chr4:3656859-3656898	K562	blood:	n/a	n/a
17	BRCA1	chr4:3625592-3625788	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr4:3627837-3627845	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:3632378-3632408	HepG2	liver:	n/a	n/a
20	CEBPB	chr4:3653964-3654026	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:3665614-3665906	HepG2	liver:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
22	CEBPB	chr4:3710716-3710755	K562	blood:	n/a	n/a
23	CEBPB	chr4:3637726-3638137	HepG2	liver:	n/a	chr4:3637935-3637946
24	CEBPB	chr4:3637704-3638130	IMR90	lung:	n/a	chr4:3637935-3637946
25	CEBPB	chr4:3637695-3637923	K562	blood:	n/a	n/a
26	CEBPB	chr4:3698740-3698986	A549	lung:	n/a	chr4:3698828-3698839
27	CEBPB	chr4:3698714-3699007	K562	blood:	n/a	chr4:3698828-3698839
28	CEBPB	chr4:3659621-3660022	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:3679639-3679806	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:3637757-3638142	A549	lung:	n/a	chr4:3637935-3637946
31	CEBPB	chr4:3698747-3698974	IMR90	lung:	n/a	chr4:3698828-3698839
32	CEBPB	chr4:3637762-3638130	K562	blood:	n/a	chr4:3637935-3637946
33	CEBPB	chr4:3698703-3698973	HepG2	liver:	n/a	chr4:3698828-3698839
34	CEBPB	chr4:3637732-3638101	Hela-S3	cervix:	n/a	chr4:3637935-3637946
35	CEBPB	chr4:3658061-3658729	ECC-1	luminal epithelium:	n/a	chr4:3658694-3658707
36	CEBPB	chr4:3637797-3637997	H1-hESC	embryonic stem cell:	n/a	chr4:3637935-3637946
37	CEBPB	chr4:3665644-3665840	K562	blood:	n/a	chr4:3665736-3665749 chr4:3665736-3665747
38	CHD2	chr4:3677157-3677385	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr4:3642375-3642459	HepG2	liver:	n/a	n/a
40	CHD2	chr4:3631479-3631483	K562	blood:	n/a	n/a
41	CHD2	chr4:3657873-3658157	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr4:3676953-3677446	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr4:3677024-3677462	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:3717356-3717395	NHEK	skin:	n/a	n/a
45	CTCF	chr4:3703240-3703390	SK-N-SH_RA	brain:	n/a	chr4:3703375-3703384
46	CTCF	chr4:3677100-3677250	WERI-Rb-1	eye:	n/a	chr4:3677196-3677209 chr4:3677194-3677212
47	CTCF	chr4:3703257-3703425	HepG2	liver:	n/a	chr4:3703375-3703384
48	CTCF	chr4:3716502-3716563	GM12891	blood:	n/a	n/a
49	CTCF	chr4:3647171-3647273	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:3703280-3703430	NB4	blood:	n/a	chr4:3703375-3703384

(count:4517 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3651354-3651404	HL-60	blood:	n/a
2	chr4:3652433-3652483	MCF-7	breast:	n/a
3	chr4:3669900-3669950	HUVEC	blood vessel:	n/a
4	chr4:3651354-3651404	HL-60	blood:	n/a
5	chr4:3652433-3652483	MCF-7	breast:	n/a
6	chr4:3669900-3669950	HUVEC	blood vessel:	n/a
7	chr4:3713287-3713337	ovcar-3	ovarian:	n/a
8	chr4:3685695-3685745	SK-N-SH	brain:	n/a
9	chr4:3663974-3664024	HRCEpiC	kidney:	n/a
10	chr4:3652433-3652483	AG09309	skin:	n/a
11	chr4:3705147-3705197	PrEC	prostate:	n/a
12	chr4:3675363-3675413	RPTEC	kidney:	n/a
13	chr4:3680970-3681020	HCT-116	colon:	n/a
14	chr4:3671067-3671117	Hepatocyte	liver:	n/a
15	chr4:3643404-3643454	NB4	blood:	n/a
16	chr4:3677497-3677547	HepG2	liver:	n/a
17	chr4:3691297-3691347	HEK293	kidney:	embryo
18	chr4:3680721-3680771	LNCaP	prostate:	n/a
19	chr4:3663974-3664024	BE2_C	brain:	n/a
20	chr4:3681759-3681809	HAEpiC	amniotic membrane:	n/a
21	chr4:3664117-3664167	K562	blood:	n/a
22	chr4:3681759-3681809	Hela-S3	cervix:	n/a
23	chr4:3685695-3685745	NHBE	bronchial:	n/a
24	chr4:3681759-3681809	NB4	blood:	n/a
25	chr4:3683268-3683318	Hepatocyte	liver:	n/a
26	chr4:3650777-3650827	U87	brain:	n/a
27	chr4:3673098-3673148	PrEC	prostate:	n/a
28	chr4:3692712-3692762	GM19239	blood:	n/a
29	chr4:3667715-3667765	SK-N-SH_RA	brain:	n/a
30	chr4:3660005-3660055	HL-60	blood:	n/a
31	chr4:3692142-3692192	RPTEC	kidney:	n/a
32	chr4:3660005-3660055	GM12891	blood:	n/a
33	chr4:3664401-3664451	NHBE	bronchial:	n/a
34	chr4:3643770-3643820	AG04449	skin:	fetal
35	chr4:3705147-3705197	Jurkat	blood:	n/a
36	chr4:3692142-3692192	SK-N-SH_RA	brain:	n/a
37	chr4:3664240-3664290	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:3677497-3677547	HRE	kidney:	n/a
39	chr4:3677497-3677547	SAEC	small airway:	n/a
40	chr4:3643404-3643454	Jurkat	blood:	n/a
41	chr4:3671067-3671117	GM12891	blood:	n/a
42	chr4:3680721-3680771	HNPCEpiC	eye:	n/a
43	chr4:3690828-3690878	PrEC	prostate:	n/a
44	chr4:3692712-3692762	AG10803	skin:	n/a
45	chr4:3671380-3671430	ovcar-3	ovarian:	n/a
46	chr4:3657880-3657930	HCM	heart:	n/a
47	chr4:3669900-3669950	IMR90	lung:	fetal
48	chr4:3685357-3685407	HRPEpiC	eye:	n/a
49	chr4:3705147-3705197	RPTEC	kidney:	n/a
50	chr4:3681759-3681809	SKMC	muscle:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
2	chr4:3532356..3534055-chr4:3658252..3659865,2	K562	blood:
3	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
4	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
5	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
6	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
7	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
8	chr4:3629740..3632595-chr4:3633115..3635534,2	K562	blood:
9	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
10	chr4:3687613..3689939-chr4:3692634..3695319,3	K562	blood:
11	chr4:3646061..3648261-chr4:3650589..3653385,2	K562	blood:
12	chr4:3717857..3720056-chr4:3723644..3725873,2	MCF-7	breast:
13	chr4:3666324..3668294-chr4:3766330..3768153,2	MCF-7	breast:
14	chr4:3642324..3644160-chr4:3658134..3661040,2	K562	blood:
15	chr4:3717339..3719373-chr4:3721279..3722918,2	MCF-7	breast:
16	chr4:3687166..3689653-chr4:3692993..3695673,2	MCF-7	breast:
17	chr4:3688266..3689130-chr4:3828986..3829489,2	MCF-7	breast:
18	chr4:3623095..3627093-chr4:3627798..3631774,5	K562	blood:
19	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
20	chr4:3637539..3639374-chr4:3644306..3646390,2	MCF-7	breast:
21	chr4:3665678..3668678-chr4:3669594..3672149,4	MCF-7	breast:
22	chr4:3662225..3664999-chr4:3667626..3669601,2	MCF-7	breast:
23	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
24	chr4:3717339..3719373-chr4:3721279..3722918,2	MCF-7	breast:
25	chr4:3696636..3698190-chr4:3703877..3705848,2	K562	blood:
26	chr4:3685214..3686952-chr4:3688635..3690383,2	K562	blood:
27	chr4:3621204..3623586-chr4:3624430..3626099,2	MCF-7	breast:
28	chr4:3719651..3722174-chr4:3722524..3724517,2	K562	blood:
29	chr4:3672629..3675074-chr4:3688483..3690772,2	MCF-7	breast:
30	chr4:3671273..3672822-chr4:3674829..3676545,2	K562	blood:
31	chr4:3636950..3638485-chr4:3644033..3646093,2	K562	blood:
32	chr4:3630276..3631981-chr4:3635694..3637377,2	MCF-7	breast:
33	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
34	chr4:3658292..3659804-chr4:3662299..3664956,2	K562	blood:
35	chr4:3715270..3718190-chr4:3721526..3723393,2	K562	blood:
36	chr4:3715270..3718190-chr4:3721526..3723393,2	K562	blood:
37	chr4:3654292..3658387-chr4:3660533..3665112,5	MCF-7	breast:
38	chr4:3702976..3705970-chr4:3735549..3737209,2	K562	blood:
39	chr4:3631211..3633906-chr4:3645708..3648279,2	K562	blood:
40	chr4:3632753..3634488-chr4:3637791..3640162,2	MCF-7	breast:
41	chr4:3640864..3643694-chr4:3644152..3647066,2	MCF-7	breast:
42	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
43	chr4:3668100..3670779-chr4:3672162..3674939,3	MCF-7	breast:
44	chr4:3720840..3724300-chr4:3724381..3726602,3	MCF-7	breast:
45	chr4:3692469..3695326-chr4:3700612..3702603,2	MCF-7	breast:
46	chr4:3638839..3640408-chr4:3642278..3643885,2	K562	blood:
47	chr4:3485102..3487339-chr4:3632605..3634535,2	MCF-7	breast:
48	chr4:3719651..3722174-chr4:3722524..3724517,2	K562	blood:
49	chr4:3681658..3684055-chr4:3685027..3686555,2	MCF-7	breast:
50	chr4:3720745..3724824-chr4:3727644..3730429,3	K562	blood:

(count:13 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 5569 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:5569 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527850115	chr4:3624803-3624804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs547795086	chr4:3624844-3624845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs67244044	chr4:3624858-3624859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs5855794	chr4:3624867-3624868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5006422	chr4:3624895-3624896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571149099	chr4:3624900-3624901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs386670747	chr4:3624918-3624919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs5006424	chr4:3624919-3624920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372966955	chr4:3624965-3624966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs549802900	chr4:3624971-3624972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs5006425	chr4:3624992-3624993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569711766	chr4:3625002-3625003	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs35962454	chr4:3625012-3625013	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs535555199	chr4:3625018-3625019	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs5006426	chr4:3625027-3625028	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs55893469	chr4:3625030-3625031	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs568185372	chr4:3625033-3625034	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs5006427	chr4:3625034-3625035	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs534021965	chr4:3625050-3625051	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs5006428	chr4:3625067-3625068	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs553670760	chr4:3625070-3625071	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs5006429	chr4:3625081-3625082	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs577251085	chr4:3625082-3625083	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs187990666	chr4:3625099-3625100	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs556200613	chr4:3625100-3625101	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs5006430	chr4:3625101-3625102	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs576068632	chr4:3625118-3625119	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs541577343	chr4:3625119-3625120	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs561791921	chr4:3625128-3625129	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs150354791	chr4:3625137-3625138	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs541642210	chr4:3625171-3625172	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs5006431	chr4:3625183-3625184	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs564512810	chr4:3625190-3625191	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs143038723	chr4:3625222-3625223	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs550012948	chr4:3625223-3625224	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs73204983	chr4:3625226-3625227	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs56071701	chr4:3625228-3625229	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs58255189	chr4:3625230-3625231	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs566199232	chr4:3625233-3625234	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs145147729	chr4:3625236-3625237	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs534799779	chr4:3625237-3625238	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs145930485	chr4:3625238-3625239	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs547619738	chr4:3625239-3625240	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs73204985	chr4:3625251-3625252	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs77511497	chr4:3625252-3625253	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs539755888	chr4:3625257-3625258	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs556465143	chr4:3625284-3625285	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs576126121	chr4:3625285-3625286	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs113742971	chr4:3625301-3625302	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs57952977	chr4:3625305-3625306	Enhancers ZNF genes & repeats	n/a	n/a	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
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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:757 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3624800-3625400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:3625000-3625400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:3625000-3628000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
4	chr4:3625200-3629400	ZNF genes & repeats	Fetal Brain Female	brain
5	chr4:3625400-3625600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:3625400-3625600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:3625400-3625600	Bivalent Enhancer	Placenta	Placenta
8	chr4:3625400-3626000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:3625400-3626000	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr4:3625400-3626000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
11	chr4:3625400-3626000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr4:3625400-3626000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:3625400-3626000	Bivalent Enhancer	Brain Germinal Matrix	brain
14	chr4:3625400-3626000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr4:3625400-3626200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:3625400-3626200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
17	chr4:3625400-3626200	ZNF genes & repeats	Fetal Intestine Small	intestine
18	chr4:3625400-3626200	Bivalent Enhancer	Fetal Stomach	stomach
19	chr4:3625400-3626200	ZNF genes & repeats	Spleen	Spleen
20	chr4:3625400-3626400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr4:3625400-3626400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
22	chr4:3625400-3626400	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr4:3625400-3626800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:3625400-3626800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:3625400-3627000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:3625400-3627800	Enhancers	Fetal Brain Male	brain
27	chr4:3625600-3625800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:3625600-3625800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:3625600-3625800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:3625600-3626000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr4:3625600-3626000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr4:3625600-3626000	Enhancers	HSMM	muscle
33	chr4:3625600-3626000	Enhancers	Osteobl	bone
34	chr4:3625600-3626200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr4:3625600-3626600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
36	chr4:3625600-3626600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:3625800-3626000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:3625800-3626000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:3626000-3627400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr4:3626000-3628000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:3626800-3627000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr4:3626800-3627000	Bivalent Enhancer	Fetal Stomach	stomach
43	chr4:3626800-3627000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
44	chr4:3627000-3632000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:3627400-3627600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
46	chr4:3627400-3627800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:3627600-3627800	Weak transcription	Spleen	Spleen
48	chr4:3627600-3628000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr4:3627800-3628400	Weak transcription	Fetal Brain Male	brain
50	chr4:3627800-3629600	ZNF genes & repeats	Spleen	Spleen

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