Variant report

Variant	nsv822445
Chromosome Location	chr4:3765726-3770807
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:417)
CpG islands
(count:1039)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:3768564-3769140	H1-hESC	embryonic stem cell:	n/a	chr4:3768787-3768801
2	BACH1	chr4:3768715-3769081	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:3769358-3769598	H1-hESC	embryonic stem cell:	n/a	n/a
4	CCNT2	chr4:3767173-3768168	K562	blood:	n/a	chr4:3768060-3768069
5	CEBPD	chr4:3768042-3768292	HepG2	liver:	n/a	n/a
6	CEBPD	chr4:3767448-3767956	HepG2	liver:	n/a	n/a
7	CHD2	chr4:3768617-3769097	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr4:3769391-3769621	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr4:3767139-3767236	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr4:3768574-3769520	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr4:3768837-3769046	Medullo	brain:	n/a	n/a
12	CTCF	chr4:3768915-3769051	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr4:3767263-3767870	K562	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
14	CTCF	chr4:3767260-3767570	HepG2	liver:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
15	CTCF	chr4:3768102-3768135	NHEK	skin:	n/a	n/a
16	CTCF	chr4:3767686-3767777	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:3769360-3769510	HRPEpiC	eye:	n/a	n/a
18	CTCF	chr4:3768899-3768978	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr4:3767327-3767538	MCF-7	breast:	n/a	n/a
20	CTCF	chr4:3769340-3769490	AG04449	skin:	n/a	n/a
21	CTCF	chr4:3769300-3769450	GM12875	blood:	n/a	n/a
22	CTCF	chr4:3767380-3767530	RPTEC	kidney:	n/a	n/a
23	CTCF	chr4:3767340-3767490	HepG2	liver:	n/a	n/a
24	CTCF	chr4:3767309-3767561	A549	lung:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
25	CTCF	chr4:3767140-3767290	BE2_C	brain:	n/a	n/a
26	CTCF	chr4:3769401-3769523	Spleen_OC	spleen:	n/a	n/a
27	CTCF	chr4:3767360-3767510	GM12866	blood:	n/a	n/a
28	CTCF	chr4:3768616-3768716	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr4:3767096-3767885	A549	lung:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
30	CTCF	chr4:3768105-3768157	HepG2	liver:	n/a	n/a
31	CTCF	chr4:3768780-3768930	Caco-2	colon:	n/a	n/a
32	CTCF	chr4:3768058-3768216	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:3768880-3769030	HCM	heart:	n/a	n/a
34	CTCF	chr4:3769380-3769530	GM12866	blood:	n/a	n/a
35	CTCF	chr4:3767360-3767523	Medullo	brain:	n/a	n/a
36	CTCF	chr4:3769360-3769510	BE2_C	brain:	n/a	n/a
37	CTCF	chr4:3767327-3767553	LNCaP	prostate:	n/a	n/a
38	CTCF	chr4:3768820-3768970	BE2_C	brain:	n/a	n/a
39	CTCF	chr4:3768020-3768170	HepG2	liver:	n/a	n/a
40	CTCF	chr4:3767342-3767543	A549	lung:	n/a	n/a
41	CTCF	chr4:3767321-3767554	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr4:3767652-3767785	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:3768880-3769030	HEK293	kidney:	n/a	n/a
44	CTCF	chr4:3767300-3767450	AG04449	skin:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
45	CTCF	chr4:3767637-3767799	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr4:3767155-3767878	K562	blood:	n/a	chr4:3767314-3767327 chr4:3767312-3767325
47	CTCF	chr4:3769400-3769550	A549	lung:	n/a	n/a
48	CTCF	chr4:3767615-3767818	LNCaP	prostate:	n/a	n/a
49	CTCF	chr4:3769360-3769510	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr4:3768085-3768178	MCF-7	breast:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:3768078-3768128	Jurkat	blood:	n/a
2	chr4:3769754-3769804	MCF10A-Er-Src	breast:	n/a
3	chr4:3768078-3768128	Jurkat	blood:	n/a
4	chr4:3769754-3769804	MCF10A-Er-Src	breast:	n/a
5	chr4:3766875-3766925	RPTEC	kidney:	n/a
6	chr4:3766151-3766201	K562	blood:	n/a
7	chr4:3770608-3770658	GM12891	blood:	n/a
8	chr4:3768638-3768688	HEEpiC	esophagus:	n/a
9	chr4:3769810-3769860	MCF10A-Er-Src	breast:	n/a
10	chr4:3769754-3769804	HEEpiC	esophagus:	n/a
11	chr4:3769468-3769518	HAEpiC	amniotic membrane:	n/a
12	chr4:3768078-3768128	HL-60	blood:	n/a
13	chr4:3769810-3769860	GM06990	blood:	n/a
14	chr4:3768638-3768688	NHDF-neo	bronchial:	n/a
15	chr4:3767402-3767452	BJ	skin:	n/a
16	chr4:3768081-3768131	HEEpiC	esophagus:	n/a
17	chr4:3769558-3769608	AG04450	lung:	fetal
18	chr4:3768638-3768688	HRPEpiC	eye:	n/a
19	chr4:3767169-3767219	SK-N-MC	brain:	n/a
20	chr4:3768638-3768688	HEK293	kidney:	embryo
21	chr4:3768078-3768128	MCF-7	breast:	n/a
22	chr4:3769558-3769608	HRCEpiC	kidney:	n/a
23	chr4:3769468-3769518	ProgFib	skin:	n/a
24	chr4:3769754-3769804	NB4	blood:	n/a
25	chr4:3767073-3767123	HRE	kidney:	n/a
26	chr4:3770608-3770658	HMEC	breast:	n/a
27	chr4:3769810-3769860	GM12892	blood:	n/a
28	chr4:3769810-3769860	GM12878	blood:	n/a
29	chr4:3768081-3768131	AG09309	skin:	n/a
30	chr4:3769754-3769804	GM12892	blood:	n/a
31	chr4:3769754-3769804	ovcar-3	ovarian:	n/a
32	chr4:3768097-3768147	PANC-1	pancreas:	n/a
33	chr4:3769810-3769860	IMR90	lung:	fetal
34	chr4:3769810-3769860	HepG2	liver:	n/a
35	chr4:3766656-3766706	HMEC	breast:	n/a
36	chr4:3768458-3768508	HAEpiC	amniotic membrane:	n/a
37	chr4:3768097-3768147	GM19239	blood:	n/a
38	chr4:3768078-3768128	AG09319	gingival:	n/a
39	chr4:3769558-3769608	CMK	blood:	n/a
40	chr4:3769558-3769608	IMR90	lung:	fetal
41	chr4:3769558-3769608	HCF	heart:	n/a
42	chr4:3767402-3767452	HRE	kidney:	n/a
43	chr4:3766151-3766201	PFSK-1	brain:	n/a
44	chr4:3769810-3769860	HEEpiC	esophagus:	n/a
45	chr4:3766875-3766925	GM12892	blood:	n/a
46	chr4:3769558-3769608	GM06990	blood:	n/a
47	chr4:3766151-3766201	ovcar-3	ovarian:	n/a
48	chr4:3768078-3768128	GM12892	blood:	n/a
49	chr4:3766151-3766201	NHBE	bronchial:	n/a
50	chr4:3768638-3768688	NT2-D1	testis:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:3767101..3767926-chr4:3787451..3788371,3	MCF-7	breast:
2	chr4:3767078..3767943-chr4:3882124..3882913,2	MCF-7	breast:
3	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
4	chr4:3532933..3534970-chr4:3765784..3768236,2	MCF-7	breast:
5	chr4:3769693..3772648-chr4:3773478..3776740,3	MCF-7	breast:
6	chr4:3767671..3769192-chr4:3769796..3772388,2	MCF-7	breast:
7	chr4:3770762..3772814-chr4:3782317..3785191,2	K562	blood:
8	chr4:3766468..3768028-chr4:3774128..3775785,2	MCF-7	breast:
9	chr4:3769000..3769555-chr4:3785283..3786137,2	MCF-7	breast:
10	chr4:3577022..3579696-chr4:3767335..3769205,3	MCF-7	breast:
11	chr4:3767262..3767834-chr4:3882421..3882953,2	K562	blood:
12	chr4:3764325..3766691-chr4:3767145..3769852,3	MCF-7	breast:
13	chr4:3741522..3743412-chr4:3768536..3771001,2	MCF-7	breast:
14	chr4:3710796..3712372-chr4:3766142..3767754,2	MCF-7	breast:
15	chr19:54974695..54977436-chr4:3766258..3768919,2	MCF-7	breast:
16	chr4:3754576..3757273-chr4:3765729..3767791,3	MCF-7	breast:
17	chr4:3750111..3752894-chr4:3765280..3767505,2	MCF-7	breast:
18	chr4:3768745..3771580-chr4:3802446..3805073,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000250986	TF binding region
ADRA2C	TF binding region
ENSG00000250986	CpG island
ADRA2C	CpG island
ENSG00000250986	chromatin interactions
ENSG00000216560	chromatin interactions
ENSG00000163956	chromatin interactions
ENSG00000184160	chromatin interactions
ENSG00000182909	chromatin interactions

Extended variants
information (count: 194 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:194 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555271408	chr4:3765728-3765729	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574912380	chr4:3765747-3765748	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs13118771	chr4:3765755-3765756	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs565137143	chr4:3765771-3765772	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs560421687	chr4:3765792-3765793	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs577264778	chr4:3765843-3765844	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs545931230	chr4:3765893-3765894	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76020435	chr4:3765918-3765919	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs180770225	chr4:3765938-3765939	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185752032	chr4:3765943-3765944	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76323688	chr4:3765977-3765978	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560832975	chr4:3765986-3765987	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs529695362	chr4:3765994-3765995	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547612755	chr4:3766049-3766050	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs28576409	chr4:3766054-3766055	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs566294481	chr4:3766068-3766069	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs370251216	chr4:3766071-3766072	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs551954609	chr4:3766126-3766127	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs569497512	chr4:3766138-3766139	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538422121	chr4:3766176-3766177	Bivalent Enhancer Weak transcription Enhancers	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs555338703	chr4:3766209-3766210	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs559870379	chr4:3766212-3766213	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111271749	chr4:3766235-3766236	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs575202431	chr4:3766236-3766237	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs6846820	chr4:3766265-3766266	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs143633304	chr4:3766267-3766268	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs190324456	chr4:3766270-3766271	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs116893661	chr4:3766329-3766330	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs148087727	chr4:3766388-3766389	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs61754810	chr4:3766408-3766409	Bivalent Enhancer Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs543992455	chr4:3766433-3766434	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs560894307	chr4:3766475-3766476	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs530002938	chr4:3766485-3766486	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs540111344	chr4:3766509-3766510	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs560106139	chr4:3766555-3766556	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs531986442	chr4:3766575-3766576	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs75576268	chr4:3766642-3766643	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs568959270	chr4:3766689-3766690	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs531984980	chr4:3766797-3766798	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs74832750	chr4:3766821-3766822	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs140988404	chr4:3766828-3766829	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs534516855	chr4:3766845-3766846	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs554142498	chr4:3766861-3766862	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs570852768	chr4:3766868-3766869	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs531849472	chr4:3766938-3766939	Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs144791572	chr4:3767064-3767065	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs80277987	chr4:3767072-3767073	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs576123005	chr4:3767100-3767101	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs577147100	chr4:3767133-3767134	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs77962119	chr4:3767136-3767137	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	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
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
Lung cancer	18438408	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:399 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:3761800-3766600	Weak transcription	HSMM	muscle
2	chr4:3762000-3765800	Weak transcription	Aorta	Aorta
3	chr4:3762400-3766800	Weak transcription	Right Atrium	heart
4	chr4:3763000-3766800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr4:3764000-3766000	Weak transcription	Pancreas	Pancrea
6	chr4:3764400-3767400	Weak transcription	Fetal Kidney	kidney
7	chr4:3764600-3766000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr4:3764800-3765800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:3765200-3766000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr4:3765400-3765800	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr4:3765400-3766000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:3765400-3766000	Enhancers	Spleen	Spleen
13	chr4:3765400-3766800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
14	chr4:3765800-3766000	Enhancers	Aorta	Aorta
15	chr4:3765800-3766000	Enhancers	Brain Anterior Caudate	brain
16	chr4:3765800-3766200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
17	chr4:3765800-3766200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr4:3766000-3766600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:3766000-3766600	Weak transcription	Aorta	Aorta
20	chr4:3766000-3766800	Weak transcription	Brain Anterior Caudate	brain
21	chr4:3766000-3767000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:3766000-3767000	Enhancers	Pancreas	Pancrea
23	chr4:3766000-3767000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
24	chr4:3766000-3767400	Bivalent Enhancer	Spleen	Spleen
25	chr4:3766400-3766600	Enhancers	HepG2	liver
26	chr4:3766400-3766800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr4:3766400-3766800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
28	chr4:3766400-3766800	Bivalent Enhancer	Liver	Liver
29	chr4:3766400-3767000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
30	chr4:3766400-3767000	Bivalent Enhancer	Fetal Stomach	stomach
31	chr4:3766600-3766800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
32	chr4:3766600-3766800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr4:3766600-3766800	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:3766600-3766800	Enhancers	Aorta	Aorta
35	chr4:3766600-3766800	Enhancers	HSMM	muscle
36	chr4:3766600-3767000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr4:3766600-3767000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
38	chr4:3766600-3767000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
39	chr4:3766600-3767000	Enhancers	Brain Angular Gyrus	brain
40	chr4:3766600-3767000	Enhancers	Brain Cingulate Gyrus	brain
41	chr4:3766600-3767000	Enhancers	Brain Inferior Temporal Lobe	brain
42	chr4:3766600-3767000	Bivalent/Poised TSS	Fetal Brain Female	brain
43	chr4:3766600-3767000	Enhancers	HSMMtube	muscle
44	chr4:3766600-3767200	Bivalent Enhancer	Placenta	Placenta
45	chr4:3766600-3767200	Flanking Active TSS	HepG2	liver
46	chr4:3766600-3767400	Bivalent Enhancer	Fetal Brain Male	brain
47	chr4:3766600-3767400	Enhancers	Gastric	stomach
48	chr4:3766600-3767400	Flanking Active TSS	Osteobl	bone
49	chr4:3766800-3767000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
50	chr4:3766800-3767000	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived

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