Variant report

Variant	nsv1014854
Chromosome Location	chr3:46789175-46849577
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr3:46792308-46792631	K562	blood:	n/a	n/a
2	ATF3	chr3:46792267-46792609	K562	blood:	n/a	n/a
3	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
4	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
5	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
7	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
8	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
9	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
10	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
11	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
12	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
13	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
14	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
15	CTCF	chr3:46798136-46798509	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
16	CTCF	chr3:46797989-46798564	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
17	CTCF	chr3:46798300-46798450	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
18	CTCF	chr3:46819600-46819750	GM12873	blood:	n/a	n/a
19	CTCF	chr3:46798300-46798450	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
20	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
21	CTCF	chr3:46794560-46794710	HCT-116	colon:	n/a	n/a
22	CTCF	chr3:46798354-46798408	Gliobla	brain:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
23	CTCF	chr3:46792356-46792487	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
24	CTCF	chr3:46792209-46792538	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
25	CTCF	chr3:46794500-46794650	GM12873	blood:	n/a	n/a
26	CTCF	chr3:46798156-46798539	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
27	CTCF	chr3:46794616-46794658	GM19240	blood:	n/a	n/a
28	CTCF	chr3:46798280-46798430	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
29	CTCF	chr3:46794600-46794750	GM12875	blood:	n/a	n/a
30	CTCF	chr3:46794520-46794670	GM12864	blood:	n/a	n/a
31	CTCF	chr3:46846100-46846250	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr3:46792152-46792625	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792234-46792247 chr3:46792394-46792407
33	CTCF	chr3:46792360-46792510	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
34	CTCF	chr3:46798336-46798412	H1-hESC	embryonic stem cell:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
35	CTCF	chr3:46794460-46794610	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr3:46846140-46846290	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr3:46798134-46798571	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
38	CTCF	chr3:46798034-46798529	K562	blood:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
39	CTCF	chr3:46794460-46794610	GM06990	blood:	n/a	n/a
40	CTCF	chr3:46794360-46794510	GM12873	blood:	n/a	n/a
41	CTCF	chr3:46794180-46794330	GM12873	blood:	n/a	n/a
42	CTCF	chr3:46798359-46798450	LNCaP	prostate:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
43	CTCF	chr3:46794500-46794650	GM12866	blood:	n/a	n/a
44	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr3:46792287-46792555	K562	blood:	n/a	chr3:46792393-46792409 chr3:46792392-46792410 chr3:46792397-46792410 chr3:46792394-46792407
46	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
47	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
48	CTCF	chr3:46798400-46798550	HVMF	connective:	n/a	n/a
49	CTCF	chr3:46798280-46798435	HepG2	liver:	n/a	chr3:46798379-46798397 chr3:46798381-46798394 chr3:46798380-46798396
50	CTCF	chr3:46794500-46794650	GM12872	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46801208-46801258	ProgFib	skin:	n/a
2	chr3:46792357-46792407	NHBE	bronchial:	n/a
3	chr3:46790182-46790232	AG04450	lung:	fetal
4	chr3:46801208-46801258	ProgFib	skin:	n/a
5	chr3:46792357-46792407	NHBE	bronchial:	n/a
6	chr3:46790182-46790232	AG04450	lung:	fetal
7	chr3:46792192-46792242	NH-A	brain:	n/a
8	chr3:46790182-46790232	SK-N-SH_RA	brain:	n/a
9	chr3:46792357-46792407	HCM	heart:	n/a
10	chr3:46792462-46792512	PFSK-1	brain:	n/a
11	chr3:46796026-46796076	PANC-1	pancreas:	n/a
12	chr3:46789735-46789785	HRPEpiC	eye:	n/a
13	chr3:46790182-46790232	A549	lung:	n/a
14	chr3:46790182-46790232	SK-N-MC	brain:	n/a
15	chr3:46801208-46801258	GM12878	blood:	n/a
16	chr3:46792357-46792407	Caco-2	colon:	n/a
17	chr3:46792364-46792414	NHDF-neo	bronchial:	n/a
18	chr3:46792192-46792242	K562	blood:	n/a
19	chr3:46790182-46790232	H1-hESC	embryonic stem cell:	embryo
20	chr3:46801208-46801258	Hepatocyte	liver:	n/a
21	chr3:46798240-46798290	Caco-2	colon:	n/a
22	chr3:46796026-46796076	NB4	blood:	n/a
23	chr3:46791477-46791527	T-47D	breast:	n/a
24	chr3:46797928-46797978	CMK	blood:	n/a
25	chr3:46792023-46792073	SK-N-MC	brain:	n/a
26	chr3:46794154-46794204	HRE	kidney:	n/a
27	chr3:46792364-46792414	HL-60	blood:	n/a
28	chr3:46792192-46792242	ProgFib	skin:	n/a
29	chr3:46794154-46794204	HCF	heart:	n/a
30	chr3:46789735-46789785	Jurkat	blood:	n/a
31	chr3:46792462-46792512	GM12892	blood:	n/a
32	chr3:46792462-46792512	AG04450	lung:	fetal
33	chr3:46799010-46799060	NT2-D1	testis:	n/a
34	chr3:46798240-46798290	HEEpiC	esophagus:	n/a
35	chr3:46792023-46792073	NT2-D1	testis:	n/a
36	chr3:46797928-46797978	MCF10A-Er-Src	breast:	n/a
37	chr3:46797928-46797978	HRCEpiC	kidney:	n/a
38	chr3:46792357-46792407	NT2-D1	testis:	n/a
39	chr3:46792357-46792407	AG04450	lung:	fetal
40	chr3:46798240-46798290	ECC-1	luminal epithelium:	n/a
41	chr3:46792462-46792512	BJ	skin:	n/a
42	chr3:46801208-46801258	SKMC	muscle:	n/a
43	chr3:46798240-46798290	SK-N-SH	brain:	n/a
44	chr3:46801208-46801258	MCF10A-Er-Src	breast:	n/a
45	chr3:46801208-46801258	ovcar-3	ovarian:	n/a
46	chr3:46792364-46792414	SAEC	small airway:	n/a
47	chr3:46794154-46794204	K562	blood:	n/a
48	chr3:46789735-46789785	MCF-7	breast:	n/a
49	chr3:46790182-46790232	AoSMC	blood vessel:	n/a
50	chr3:46789735-46789785	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
2	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
3	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
4	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
5	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
6	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
7	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
8	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
9	chr3:46783977..46786592-chr3:46791856..46793997,2	MCF-7	breast:
10	chr3:46792775..46794351-chr3:46906387..46908133,2	K562	blood:
11	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
12	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
13	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
14	chr3:46785802..46787615-chr3:46790135..46792444,2	K562	blood:
15	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
16	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
17	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
18	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
19	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
20	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
21	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
22	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
23	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
24	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
25	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
26	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTH1R-2	chr3:46839613-46839880	NONHSAT089458
2	lnc-PRSS50-1	chr3:46795974-46796138	NONHSAT089457
3	lnc-PRSS50-1	chr3:46797532-46798119	NONHSAT089457

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS45	TF binding region
ENSG00000238013	CpG island
PRSS45	CpG island
ENSG00000188086	chromatin interactions

Extended variants
information (count: 818 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:818 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6777190	chr3:46789175-46789176	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs567039815	chr3:46789185-46789186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190545563	chr3:46789202-46789203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534955092	chr3:46789205-46789206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138637073	chr3:46789233-46789234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77996010	chr3:46789250-46789251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs386660754	chr3:46789262-46789263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs72899433	chr3:46789269-46789270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs556109414	chr3:46789275-46789276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374041198	chr3:46789299-46789300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34462434	chr3:46789370-46789371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149335064	chr3:46789470-46789471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539104138	chr3:46789483-46789484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554011387	chr3:46789494-46789495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375571570	chr3:46789531-46789532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182507906	chr3:46789538-46789539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186661937	chr3:46789566-46789567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190712088	chr3:46789570-46789571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557207455	chr3:46789593-46789594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573949100	chr3:46789643-46789644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368361688	chr3:46789677-46789678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs532024335	chr3:46789690-46789691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549915698	chr3:46789735-46789736	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs562449298	chr3:46789736-46789737	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs532823819	chr3:46789750-46789751	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs551447922	chr3:46789754-46789755	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs560038904	chr3:46789779-46789780	Enhancers Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs372126566	chr3:46789817-46789818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs55806728	chr3:46789835-46789836	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs542988239	chr3:46789848-46789849	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62246255	chr3:46789869-46789870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182663537	chr3:46789872-46789873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145451095	chr3:46790022-46790023	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs567541032	chr3:46790045-46790046	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs573956810	chr3:46790069-46790070	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs137973955	chr3:46790092-46790093	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs550094713	chr3:46790110-46790111	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs372616942	chr3:46790124-46790125	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs375165206	chr3:46790147-46790148	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs571603537	chr3:46790182-46790183	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs538701433	chr3:46790219-46790220	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs554137615	chr3:46790247-46790248	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs76132367	chr3:46790293-46790294	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs377273639	chr3:46790308-46790309	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555575430	chr3:46790367-46790368	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs573911441	chr3:46790390-46790391	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs187666723	chr3:46790392-46790393	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs7614762	chr3:46790397-46790398	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs577563851	chr3:46790432-46790433	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs573264709	chr3:46790450-46790451	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
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
small cell lung cancer	20016488	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
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	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
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46744000-46792200	Weak transcription	Right Atrium	heart
2	chr3:46769000-46792400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
4	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
5	chr3:46779800-46792800	Weak transcription	Thymus	Thymus
6	chr3:46785000-46789800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
8	chr3:46785600-46789800	Weak transcription	Placenta	Placenta
9	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr3:46787800-46789200	Enhancers	GM12878-XiMat	blood
11	chr3:46789200-46794200	Weak transcription	GM12878-XiMat	blood
12	chr3:46789600-46789800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr3:46789600-46790400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr3:46789600-46790400	Enhancers	Fetal Muscle Leg	muscle
15	chr3:46789800-46790000	Enhancers	Fetal Stomach	stomach
16	chr3:46789800-46790200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr3:46789800-46790400	Enhancers	Placenta	Placenta
18	chr3:46789800-46790600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr3:46790600-46791800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr3:46791800-46792400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr3:46792200-46792800	Flanking Bivalent TSS/Enh	K562	blood
22	chr3:46792400-46794200	Enhancers	Placenta Amnion	Placenta Amnion
23	chr3:46792400-46797800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr3:46792800-46795000	Enhancers	Thymus	Thymus
25	chr3:46793400-46795200	Enhancers	Fetal Thymus	thymus
26	chr3:46793400-46800000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:46793800-46794200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
28	chr3:46794200-46795000	Enhancers	GM12878-XiMat	blood
29	chr3:46795000-46796000	Weak transcription	Thymus	Thymus
30	chr3:46795200-46796200	Weak transcription	Fetal Thymus	thymus
31	chr3:46795600-46798000	Strong transcription	Skeletal Muscle Male	skeletal muscle
32	chr3:46796000-46796800	Enhancers	Thymus	Thymus
33	chr3:46796400-46796600	Enhancers	Fetal Thymus	thymus
34	chr3:46797600-46797800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
35	chr3:46797600-46797800	Bivalent Enhancer	K562	blood
36	chr3:46797600-46798400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr3:46797800-46798400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr3:46798000-46798600	Enhancers	Placenta	Placenta
39	chr3:46798000-46798600	Active TSS	K562	blood
40	chr3:46798000-46801400	Weak transcription	Skeletal Muscle Male	skeletal muscle
41	chr3:46798400-46801200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr3:46800600-46801400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr3:46801000-46801200	Enhancers	Fetal Stomach	stomach
44	chr3:46801000-46801400	Enhancers	Fetal Kidney	kidney
45	chr3:46801000-46801800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr3:46801000-46801800	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr3:46801000-46802000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr3:46801000-46802000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:46801000-46802000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr3:46801200-46801400	Enhancers	HUES6 Cell Line	embryonic stem cell

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