Variant report

Variant	nsv1003204
Chromosome Location	chr3:53820070-53877149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:840)
CpG islands
(count:1038)
Chromatin interactive
region (count:39)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:53875409-53875638	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:53876698-53878019	HepG2	liver:	n/a	chr3:53877014-53877030
3	BACH1	chr3:53876560-53877103	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr3:53850518-53850789	GM12878	blood:	n/a	n/a
5	BCL3	chr3:53832194-53832489	GM12878	blood:	n/a	n/a
6	BCL3	chr3:53832200-53832481	GM12878	blood:	n/a	n/a
7	BHLHE40	chr3:53876633-53877763	HepG2	liver:	n/a	n/a
8	BHLHE40	chr3:53840974-53841053	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:53832306-53832468	K562	blood:	n/a	n/a
10	BHLHE40	chr3:53827434-53827500	K562	blood:	n/a	chr3:53827438-53827447 chr3:53827438-53827447 chr3:53827439-53827448
11	BHLHE40	chr3:53839195-53839556	GM12878	blood:	n/a	chr3:53839342-53839363 chr3:53839346-53839359
12	BHLHE40	chr3:53876815-53877169	HepG2	liver:	n/a	n/a
13	BHLHE40	chr3:53876853-53877464	GM12878	blood:	n/a	n/a
14	BRCA1	chr3:53876900-53877389	HepG2	liver:	n/a	n/a
15	BRCA1	chr3:53836759-53836763	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr3:53852292-53852425	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:53828657-53828912	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:53822069-53822404	HepG2	liver:	n/a	chr3:53822251-53822262
19	CEBPB	chr3:53876851-53877764	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:53876034-53876183	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:53823016-53823597	A549	lung:	n/a	n/a
22	CEBPB	chr3:53876832-53877005	HepG2	liver:	n/a	n/a
23	CEBPD	chr3:53876698-53877268	HepG2	liver:	n/a	n/a
24	CEBPD	chr3:53876789-53877212	HepG2	liver:	n/a	n/a
25	CHD1	chr3:53876879-53876933	GM12878	blood:	n/a	n/a
26	CHD2	chr3:53876590-53877911	HepG2	liver:	n/a	n/a
27	CHD2	chr3:53845847-53845978	HepG2	liver:	n/a	n/a
28	CHD2	chr3:53875490-53875659	HepG2	liver:	n/a	n/a
29	CHD2	chr3:53876755-53877184	GM12878	blood:	n/a	n/a
30	CHD2	chr3:53851341-53851397	HepG2	liver:	n/a	n/a
31	CHD2	chr3:53849305-53849342	HepG2	liver:	n/a	n/a
32	CREB1	chr3:53828576-53829085	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr3:53840640-53840790	NHDF-neo	bronchial:	n/a	chr3:53840714-53840727
34	CTCF	chr3:53876860-53877010	HMF	breast:	n/a	chr3:53876929-53876938
35	CTCF	chr3:53876760-53876910	GM12866	blood:	n/a	n/a
36	CTCF	chr3:53846600-53846750	HFF	foreskin:	n/a	n/a
37	CTCF	chr3:53876780-53876930	HMEC	breast:	n/a	n/a
38	CTCF	chr3:53846575-53846675	Gliobla	brain:	n/a	n/a
39	CTCF	chr3:53875520-53875670	SAEC	small airway:	n/a	chr3:53875550-53875559
40	CTCF	chr3:53840660-53840810	RPTEC	kidney:	n/a	chr3:53840714-53840727
41	CTCF	chr3:53846600-53846750	GM12872	blood:	n/a	n/a
42	CTCF	chr3:53846520-53846670	GM12866	blood:	n/a	n/a
43	CTCF	chr3:53837648-53837920	H1-hESC	embryonic stem cell:	n/a	chr3:53837814-53837823 chr3:53837674-53837687
44	CTCF	chr3:53876840-53876990	AG04449	skin:	n/a	chr3:53876929-53876938
45	CTCF	chr3:53876820-53876970	Hela-S3	cervix:	n/a	chr3:53876929-53876938
46	CTCF	chr3:53875500-53875650	GM12864	blood:	n/a	chr3:53875550-53875559
47	CTCF	chr3:53876840-53876990	HRPEpiC	eye:	n/a	chr3:53876929-53876938
48	CTCF	chr3:53875500-53875650	HCT-116	colon:	n/a	chr3:53875550-53875559
49	CTCF	chr3:53846465-53846759	GM12878	blood:	n/a	n/a
50	CTCF	chr3:53840700-53840850	HRE	kidney:	n/a	chr3:53840714-53840727

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:53845930-53845980	NHBE	bronchial:	n/a
2	chr3:53845930-53845980	NHBE	bronchial:	n/a
3	chr3:53857939-53857989	HCM	heart:	n/a
4	chr3:53843939-53843989	HRCEpiC	kidney:	n/a
5	chr3:53839251-53839301	Hela-S3	cervix:	n/a
6	chr3:53857876-53857926	K562	blood:	n/a
7	chr3:53857939-53857989	NHBE	bronchial:	n/a
8	chr3:53857876-53857926	BE2_C	brain:	n/a
9	chr3:53857445-53857495	U87	brain:	n/a
10	chr3:53857876-53857926	GM12878	blood:	n/a
11	chr3:53857939-53857989	GM19239	blood:	n/a
12	chr3:53857953-53858003	HMEC	breast:	n/a
13	chr3:53855125-53855175	NH-A	brain:	n/a
14	chr3:53857876-53857926	MCF10A-Er-Src	breast:	n/a
15	chr3:53855125-53855175	HNPCEpiC	eye:	n/a
16	chr3:53857876-53857926	GM12892	blood:	n/a
17	chr3:53844068-53844118	HepG2	liver:	n/a
18	chr3:53845287-53845337	A549	lung:	n/a
19	chr3:53844068-53844118	AG04450	lung:	fetal
20	chr3:53845930-53845980	GM12891	blood:	n/a
21	chr3:53855929-53855979	Caco-2	colon:	n/a
22	chr3:53860720-53860770	BJ	skin:	n/a
23	chr3:53843939-53843989	HL-60	blood:	n/a
24	chr3:53839251-53839301	AoSMC	blood vessel:	n/a
25	chr3:53857698-53857748	GM06990	blood:	n/a
26	chr3:53855125-53855175	PFSK-1	brain:	n/a
27	chr3:53857989-53858039	HAEpiC	amniotic membrane:	n/a
28	chr3:53857989-53858039	HepG2	liver:	n/a
29	chr3:53857953-53858003	SK-N-MC	brain:	n/a
30	chr3:53857445-53857495	HRCEpiC	kidney:	n/a
31	chr3:53855125-53855175	A549	lung:	n/a
32	chr3:53843939-53843989	HRPEpiC	eye:	n/a
33	chr3:53844172-53844222	RPTEC	kidney:	n/a
34	chr3:53855125-53855175	BE2_C	brain:	n/a
35	chr3:53844068-53844118	SAEC	small airway:	n/a
36	chr3:53839251-53839301	K562	blood:	n/a
37	chr3:53857445-53857495	RPTEC	kidney:	n/a
38	chr3:53857989-53858039	PANC-1	pancreas:	n/a
39	chr3:53855929-53855979	SK-N-MC	brain:	n/a
40	chr3:53844172-53844222	SK-N-SH_RA	brain:	n/a
41	chr3:53857876-53857926	AG04449	skin:	fetal
42	chr3:53850724-53850774	ECC-1	luminal epithelium:	n/a
43	chr3:53845287-53845337	HMEC	breast:	n/a
44	chr3:53845287-53845337	RPTEC	kidney:	n/a
45	chr3:53850724-53850774	T-47D	breast:	n/a
46	chr3:53839251-53839301	HRCEpiC	kidney:	n/a
47	chr3:53855125-53855175	HCF	heart:	n/a
48	chr3:53857989-53858039	HCPEpiC	choroid plexus:	n/a
49	chr3:53857989-53858039	SAEC	small airway:	n/a
50	chr3:53850724-53850774	ovcar-3	ovarian:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:53866511..53869792-chr3:53878002..53881981,4	MCF-7	breast:
2	chr17:41464201..41466333-chr3:53844168..53847168,4	K562	blood:
3	chr17:41398908..41400636-chr3:53845668..53847188,2	K562	blood:
4	chr3:53841487..53843004-chr3:53876631..53879451,2	MCF-7	breast:
5	chr3:53849527..53851449-chr3:53878802..53881652,2	MCF-7	breast:
6	chr3:53844168..53847188-chr3:73158624..73161592,4	K562	blood:
7	chr3:53866125..53868465-chr3:53874787..53877078,2	K562	blood:
8	chr3:53874952..53876547-chr3:53878295..53881175,2	K562	blood:
9	chr3:53844168..53845668-chr3:73159088..73161601,2	K562	blood:
10	chr3:53815441..53817589-chr3:53822941..53824697,2	K562	blood:
11	chr3:53874777..53878635-chr3:53878874..53882397,7	MCF-7	breast:
12	chr3:53844590..53847374-chr3:53851329..53853049,2	K562	blood:
13	chr3:53846376..53848488-chr3:53854187..53856200,2	MCF-7	breast:
14	chr17:41465368..41466186-chr3:53845668..53846168,2	NB4	blood:
15	chr3:53871494..53874275-chr3:53875042..53877358,2	MCF-7	breast:
16	chr1:160082467..160082984-chr3:53845168..53845688,2	MCF-7	breast:
17	chr3:53859983..53863659-chr3:53876929..53880341,3	MCF-7	breast:
18	chr11:62609137..62610648-chr3:53844188..53845688,2	MCF-7	breast:
19	chr3:53841128..53843687-chr3:53845515..53847366,2	K562	blood:
20	chr10:103124630..103126130-chr3:53844188..53847168,2	K562	blood:
21	chr3:53865722..53867529-chr3:53870209..53872321,2	MCF-7	breast:
22	chr3:53871494..53874275-chr3:53875042..53877358,2	MCF-7	breast:
23	chr11:62609135..62609723-chr3:53845168..53845688,6	HCT-116	colon:
24	chr1:160082464..160083987-chr3:53844168..53845688,2	K562	blood:
25	chr3:53827199..53830305-chr3:53832365..53836212,3	MCF-7	breast:
26	chr3:53866125..53868465-chr3:53874787..53877078,2	K562	blood:
27	chr3:53841128..53843687-chr3:53845515..53847366,2	K562	blood:
28	chr3:53826568..53829356-chr3:53836868..53838582,2	K562	blood:
29	chr3:53846376..53848488-chr3:53854187..53856200,2	MCF-7	breast:
30	chr3:53827661..53829202-chr3:53830415..53833221,2	MCF-7	breast:
31	chr3:53865722..53867529-chr3:53870209..53872321,2	MCF-7	breast:
32	chr17:41399053..41400665-chr3:53844168..53845688,2	MCF-7	breast:
33	chr3:53825519..53828140-chr3:53828616..53831592,4	K562	blood:
34	chr11:62607628..62610723-chr3:53844168..53845688,3	K562	blood:
35	chr3:53853872..53855809-chr3:53924023..53926528,2	K562	blood:
36	chr3:53844590..53847374-chr3:53851329..53853049,2	K562	blood:
37	chr3:53826568..53829356-chr3:53836868..53838582,2	K562	blood:
38	chr3:53857432..53859908-chr3:53878977..53881329,3	MCF-7	breast:
39	chr3:53826640..53828312-chr3:53828616..53830435,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACTR8-3	chr3:53868060-53870643	ncRnaDb_ncrna_FR081823_1
2	lnc-CHDH-1	chr3:53831791-53832046	ENSG00000271916.1

No data

Variant related genes	Relation type
CACNA1D	TF binding region
IL17RB	TF binding region
ENSG00000271916	TF binding region
CACNA1D	CpG island
IL17RB	CpG island
ENSG00000271916	CpG island
ENSG00000016391	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000056736	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000271916	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000157388	chromatin interactions
ENSG00000113811	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2348 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2348 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3774595	chr3:53820070-53820071	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs538376130	chr3:53820105-53820106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73843306	chr3:53820125-53820126	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs3774596	chr3:53820179-53820180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571717070	chr3:53820186-53820187	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534315779	chr3:53820203-53820204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554472122	chr3:53820216-53820217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574376145	chr3:53820257-53820258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140195539	chr3:53820301-53820302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563361287	chr3:53820308-53820309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143884778	chr3:53820314-53820315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545994524	chr3:53820376-53820377	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559874849	chr3:53820411-53820412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571063439	chr3:53820422-53820423	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs553264319	chr3:53820424-53820425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528539557	chr3:53820425-53820426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548578872	chr3:53820456-53820457	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562400067	chr3:53820483-53820484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531125436	chr3:53820490-53820491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183454976	chr3:53820497-53820498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115135403	chr3:53820543-53820544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs146791559	chr3:53820586-53820587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76105596	chr3:53820595-53820596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565415855	chr3:53820635-53820636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554949577	chr3:53820655-53820656	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534350860	chr3:53820711-53820712	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375612793	chr3:53820719-53820720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554161391	chr3:53820731-53820732	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568022057	chr3:53820735-53820736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536951652	chr3:53820743-53820744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557182598	chr3:53820745-53820746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577007771	chr3:53820748-53820749	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546013899	chr3:53820754-53820755	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200698990	chr3:53820794-53820795	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370085938	chr3:53820896-53820897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145414503	chr3:53820920-53820921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75832356	chr3:53820928-53820929	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201969994	chr3:53820954-53820955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373449217	chr3:53820964-53820965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375601296	chr3:53820967-53820968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542307394	chr3:53821008-53821009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370194983	chr3:53821013-53821014	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562085264	chr3:53821019-53821020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530886970	chr3:53821045-53821046	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148921587	chr3:53821050-53821051	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs573158101	chr3:53821110-53821111	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533390278	chr3:53821165-53821166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9654000	chr3:53821166-53821167	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs566691277	chr3:53821175-53821176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2289212	chr3:53821207-53821208	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Septo-optic dysplasia	21572526	CNVD
Biliary cancer	19435499	CNVD
Squamous cell cancer	20885788	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Ventriculomegaly	21325761	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Lung cancer	16618734	CNVD
Neuroblastoma	19686582	CNVD
Renal cell carcinoma	18765545	CNVD
Adrenocortical carcinoma	18281524	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:840 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:53807600-53829800	Weak transcription	Brain Angular Gyrus	brain
2	chr3:53808200-53827800	Strong transcription	Fetal Intestine Small	intestine
3	chr3:53808800-53830200	Weak transcription	Pancreas	Pancrea
4	chr3:53809400-53824400	Strong transcription	Fetal Intestine Large	intestine
5	chr3:53811400-53838600	Weak transcription	Spleen	Spleen
6	chr3:53811600-53843600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr3:53813400-53821400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr3:53815200-53829000	Weak transcription	Brain Anterior Caudate	brain
9	chr3:53815200-53829400	Weak transcription	Brain Hippocampus Middle	brain
10	chr3:53815400-53829800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr3:53816600-53822800	Strong transcription	Fetal Lung	lung
12	chr3:53818200-53821200	Weak transcription	Lung	lung
13	chr3:53818200-53826800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:53819600-53830000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr3:53821200-53821800	ZNF genes & repeats	Lung	lung
16	chr3:53821400-53821600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr3:53821600-53822800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr3:53822000-53822400	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr3:53822200-53822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr3:53822400-53822800	Enhancers	H1 Cell Line	embryonic stem cell
21	chr3:53822400-53823000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr3:53822600-53822800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr3:53822800-53823200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr3:53822800-53823400	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr3:53822800-53828200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr3:53822800-53828800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr3:53822800-53832000	Weak transcription	Fetal Lung	lung
28	chr3:53823000-53823600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:53823200-53823800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr3:53823400-53824000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr3:53823600-53823800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:53823800-53832200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr3:53824000-53828800	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr3:53824400-53827600	Enhancers	Fetal Thymus	thymus
35	chr3:53824400-53832000	Weak transcription	Fetal Intestine Large	intestine
36	chr3:53825600-53825800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr3:53825600-53826000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr3:53825800-53828400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr3:53826000-53828800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:53826800-53827200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:53827000-53827200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:53827000-53827200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr3:53827200-53828800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr3:53827200-53830200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr3:53827800-53832200	Weak transcription	Fetal Intestine Small	intestine
46	chr3:53828000-53830400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr3:53828200-53829800	Enhancers	NHDF-Ad	bronchial
48	chr3:53828200-53830200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:53828200-53830400	Enhancers	HMEC	breast
50	chr3:53828200-53830600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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