Variant report

Variant	nsv1013195
Chromosome Location	chr3:46771434-46847604
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:362)
CpG islands
(count:1403)
Chromatin interactive
region (count:36)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:362 , 50 per page) page: 1 2 3 4 5 6 7 8

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	chr3:46773261-46773680	GM12878	blood:	n/a	n/a
4	BATF	chr3:46834909-46835249	GM12878	blood:	n/a	n/a
5	BATF	chr3:46834950-46835224	GM12878	blood:	n/a	n/a
6	BATF	chr3:46773278-46773701	GM12878	blood:	n/a	n/a
7	BCL11A	chr3:46834834-46835220	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:46773339-46773653	GM12878	blood:	n/a	n/a
9	BHLHE40	chr3:46798309-46798511	K562	blood:	n/a	n/a
10	BHLHE40	chr3:46792161-46792741	K562	blood:	n/a	chr3:46792470-46792479 chr3:46792470-46792479
11	CBX3	chr3:46792069-46792673	K562	blood:	n/a	n/a
12	CBX3	chr3:46798157-46798548	K562	blood:	n/a	n/a
13	CBX3	chr3:46805384-46805615	K562	blood:	n/a	n/a
14	CCNT2	chr3:46792259-46792508	K562	blood:	n/a	n/a
15	CEBPB	chr3:46780720-46780724	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr3:46839064-46839245	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr3:46780721-46781004	HepG2	liver:	n/a	n/a
18	CHD2	chr3:46798208-46798651	K562	blood:	n/a	n/a
19	CHD2	chr3:46798433-46798503	HepG2	liver:	n/a	n/a
20	CTCF	chr3:46776298-46776448	GM12892	blood:	n/a	n/a
21	CTCF	chr3:46775220-46775370	AG09309	skin:	n/a	n/a
22	CTCF	chr3:46775162-46775259	GM20000	blood:	n/a	n/a
23	CTCF	chr3:46775200-46775350	BJ	skin:	n/a	n/a
24	CTCF	chr3:46775070-46775401	K562	blood:	n/a	n/a
25	CTCF	chr3:46846160-46846310	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr3:46775160-46775310	AG09309	skin:	n/a	n/a
27	CTCF	chr3:46775212-46775229	MCF-7	breast:	n/a	n/a
28	CTCF	chr3:46775080-46775230	GM12871	blood:	n/a	n/a
29	CTCF	chr3:46775260-46775410	HCM	heart:	n/a	n/a
30	CTCF	chr3:46775122-46775332	GM12892	blood:	n/a	n/a
31	CTCF	chr3:46775140-46775290	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr3:46775160-46775310	AG04449	skin:	n/a	n/a
33	CTCF	chr3:46775183-46775254	GM10266	blood:	n/a	n/a
34	CTCF	chr3:46775066-46775390	K562	blood:	n/a	n/a
35	CTCF	chr3:46776299-46776445	GM19240	blood:	n/a	n/a
36	CTCF	chr3:46775154-46775271	MCF-7	breast:	n/a	n/a
37	CTCF	chr3:46775160-46775310	GM12865	blood:	n/a	n/a
38	CTCF	chr3:46801730-46801825	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr3:46775140-46775290	AG04449	skin:	n/a	n/a
40	CTCF	chr3:46775084-46775395	GM12878	blood:	n/a	n/a
41	CTCF	chr3:46775160-46775310	HFF-Myc	foreskin:	n/a	n/a
42	CTCF	chr3:46776341-46776414	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:46775160-46775310	HPF	lung:	n/a	n/a
44	CTCF	chr3:46775140-46775290	AG10803	skin:	n/a	n/a
45	CTCF	chr3:46794460-46794610	GM06990	blood:	n/a	n/a
46	CTCF	chr3:46846080-46846230	NHEK	skin:	n/a	n/a
47	CTCF	chr3:46846120-46846270	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:46794600-46794750	GM12875	blood:	n/a	n/a
49	CTCF	chr3:46775120-46775270	NHLF	lung:	n/a	n/a
50	CTCF	chr3:46775204-46775243	Medullo	brain:	n/a	n/a

(count:1403 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46792364-46792414	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:46787073-46787123	AG04450	lung:	fetal
3	chr3:46787073-46787123	H1-hESC	embryonic stem cell:	embryo
4	chr3:46775544-46775594	ProgFib	skin:	n/a
5	chr3:46799010-46799060	HRCEpiC	kidney:	n/a
6	chr3:46792364-46792414	HAEpiC	amniotic membrane:	n/a
7	chr3:46796026-46796076	NHDF-neo	bronchial:	n/a
8	chr3:46791477-46791527	HNPCEpiC	eye:	n/a
9	chr3:46801208-46801258	PFSK-1	brain:	n/a
10	chr3:46776775-46776825	PFSK-1	brain:	n/a
11	chr3:46776775-46776825	SKMC	muscle:	n/a
12	chr3:46778871-46778921	CMK	blood:	n/a
13	chr3:46786387-46786437	AG09309	skin:	n/a
14	chr3:46775544-46775594	Hela-S3	cervix:	n/a
15	chr3:46798240-46798290	Jurkat	blood:	n/a
16	chr3:46778871-46778921	PFSK-1	brain:	n/a
17	chr3:46786238-46786288	HCPEpiC	choroid plexus:	n/a
18	chr3:46776775-46776825	Caco-2	colon:	n/a
19	chr3:46794154-46794204	HIPEpiC	eye:	n/a
20	chr3:46790182-46790232	ovcar-3	ovarian:	n/a
21	chr3:46786387-46786437	HMEC	breast:	n/a
22	chr3:46792192-46792242	HMEC	breast:	n/a
23	chr3:46775544-46775594	SKMC	muscle:	n/a
24	chr3:46775569-46775619	MCF10A-Er-Src	breast:	n/a
25	chr3:46792023-46792073	GM12878	blood:	n/a
26	chr3:46790182-46790232	NH-A	brain:	n/a
27	chr3:46797928-46797978	HepG2	liver:	n/a
28	chr3:46789735-46789785	SKMC	muscle:	n/a
29	chr3:46792357-46792407	AG10803	skin:	n/a
30	chr3:46786387-46786437	IMR90	lung:	fetal
31	chr3:46776775-46776825	A549	lung:	n/a
32	chr3:46790182-46790232	U87	brain:	n/a
33	chr3:46799010-46799060	A549	lung:	n/a
34	chr3:46789735-46789785	HMEC	breast:	n/a
35	chr3:46797928-46797978	HL-60	blood:	n/a
36	chr3:46786238-46786288	AG10803	skin:	n/a
37	chr3:46775544-46775594	AG09309	skin:	n/a
38	chr3:46789735-46789785	HepG2	liver:	n/a
39	chr3:46787073-46787123	Caco-2	colon:	n/a
40	chr3:46776775-46776825	AG09309	skin:	n/a
41	chr3:46786238-46786288	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:46792192-46792242	BE2_C	brain:	n/a
43	chr3:46794154-46794204	T-47D	breast:	n/a
44	chr3:46792192-46792242	T-47D	breast:	n/a
45	chr3:46787073-46787123	SKMC	muscle:	n/a
46	chr3:46787073-46787123	NHDF-neo	bronchial:	n/a
47	chr3:46792357-46792407	Hepatocyte	liver:	n/a
48	chr3:46792192-46792242	SK-N-SH_RA	brain:	n/a
49	chr3:46794154-46794204	HAEpiC	amniotic membrane:	n/a
50	chr3:46792023-46792073	IMR90	lung:	fetal

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
2	chr3:46792775..46794351-chr3:46906387..46908133,2	K562	blood:
3	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
4	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
5	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
6	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
7	chr3:46770529..46772210-chr3:46784902..46786498,2	K562	blood:
8	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
9	chr3:46776204..46778019-chr3:46778181..46780158,2	K562	blood:
10	chr3:46764632..46767218-chr3:46782393..46785331,2	K562	blood:
11	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
12	chr3:46780314..46782174-chr3:46791450..46793098,2	K562	blood:
13	chr3:46783977..46786592-chr3:46791856..46793997,2	MCF-7	breast:
14	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
15	chr3:46783774..46785518-chr3:46915413..46918248,2	MCF-7	breast:
16	chr3:46796598..46799185-chr3:46799676..46801957,2	MCF-7	breast:
17	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
18	chr3:46847486..46849953-chr3:46878692..46880394,2	K562	blood:
19	chr3:46803507..46806312-chr3:46807817..46810409,2	K562	blood:
20	chr3:46787160..46789838-chr3:46792836..46795181,2	K562	blood:
21	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
22	chr3:46780631..46782178-chr3:46786371..46787877,2	K562	blood:
23	chr3:46798748..46799515-chr3:46907913..46908649,2	K562	blood:
24	chr3:46789981..46792010-chr3:46794604..46797550,3	K562	blood:
25	chr3:46746227..46747136-chr3:46797879..46798830,2	K562	blood:
26	chr3:46789741..46793223-chr3:46794604..46798425,5	K562	blood:
27	chr3:46796974..46798578-chr3:46800470..46803376,2	K562	blood:
28	chr3:46720178..46722487-chr3:46787613..46789601,2	K562	blood:
29	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:
30	chr3:46774758..46775741-chr3:46797694..46798443,2	K562	blood:
31	chr3:46785802..46787615-chr3:46790135..46792444,2	K562	blood:
32	chr3:46819637..46822469-chr3:46912934..46914923,2	K562	blood:
33	chr3:46788120..46791042-chr3:46798895..46800766,2	K562	blood:
34	chr3:46774953..46775682-chr3:46936746..46937314,2	K562	blood:
35	chr3:46761792..46767256-chr3:46770894..46774909,6	K562	blood:
36	chr3:46796204..46798578-chr3:46800470..46803401,3	K562	blood:

(count:3 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000238013	TF binding region
PRSS45	TF binding region
PRSS46	TF binding region
ENSG00000238013	CpG island
PRSS45	CpG island
PRSS46	CpG island
ENSG00000261603	chromatin interactions
ENSG00000188086	chromatin interactions

Extended variants
information (count: 1497 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1497 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541510189	chr3:46771470-46771471	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs189728562	chr3:46771502-46771503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs553532582	chr3:46771524-46771525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs372132698	chr3:46771525-46771526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79292133	chr3:46771588-46771589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs76862326	chr3:46771590-46771591	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572256169	chr3:46771607-46771608	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575640155	chr3:46771612-46771613	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs7632771	chr3:46771619-46771620	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs12632563	chr3:46771651-46771652	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374434374	chr3:46771683-46771684	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561023424	chr3:46771709-46771710	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs531590473	chr3:46771732-46771733	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs543359951	chr3:46771735-46771736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs564862313	chr3:46771751-46771752	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs192941532	chr3:46771752-46771753	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs572181759	chr3:46771810-46771811	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs77538192	chr3:46771875-46771876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547065455	chr3:46771878-46771879	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs58376366	chr3:46771897-46771898	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530223057	chr3:46771900-46771901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs548809783	chr3:46771911-46771912	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369675341	chr3:46771915-46771916	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs60502774	chr3:46771916-46771917	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570156912	chr3:46771958-46771959	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs569446144	chr3:46771963-46771964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs35874021	chr3:46772007-46772008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs11437838	chr3:46772046-46772047	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs397817164	chr3:46772047-46772048	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs371137774	chr3:46772051-46772052	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs559010128	chr3:46772105-46772106	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs184194415	chr3:46772162-46772163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs369469264	chr3:46772236-46772237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535055741	chr3:46772266-46772267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553497727	chr3:46772302-46772303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575034615	chr3:46772309-46772310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs535958269	chr3:46772316-46772317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545868520	chr3:46772332-46772333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73833612	chr3:46772413-46772414	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs77548198	chr3:46772417-46772418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs188173287	chr3:46772427-46772428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs181757180	chr3:46772511-46772512	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186426709	chr3:46772521-46772522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7633456	chr3:46772526-46772527	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs188927468	chr3:46772527-46772528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs144564760	chr3:46772609-46772610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs529693720	chr3:46772649-46772650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs547996476	chr3:46772658-46772659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563879675	chr3:46772667-46772668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74443074	chr3:46772695-46772696	Weak transcription Enhancers	n/a	n/a	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:119 , 50 per page) page: 1 2 3

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	chr3:46770800-46776200	Weak transcription	Pancreas	Pancrea
4	chr3:46770800-46778000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:46772200-46773400	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr3:46772400-46773600	Enhancers	GM12878-XiMat	blood
7	chr3:46773000-46773200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr3:46775400-46775600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
9	chr3:46775600-46775800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr3:46776200-46776600	Enhancers	Pancreas	Pancrea
11	chr3:46776600-46778800	Weak transcription	Pancreas	Pancrea
12	chr3:46777000-46779800	Enhancers	Thymus	Thymus
13	chr3:46778000-46778200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:46778000-46778200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
15	chr3:46778000-46780000	Enhancers	Fetal Thymus	thymus
16	chr3:46778200-46778400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr3:46778200-46778800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:46778400-46779200	Enhancers	Fetal Muscle Trunk	muscle
19	chr3:46778600-46779200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr3:46778600-46779200	Enhancers	Fetal Muscle Leg	muscle
21	chr3:46778800-46779000	Bivalent Enhancer	HSMM	muscle
22	chr3:46778800-46779200	Enhancers	Left Ventricle	heart
23	chr3:46778800-46779400	Enhancers	Pancreas	Pancrea
24	chr3:46779000-46779200	Enhancers	Spleen	Spleen
25	chr3:46779000-46779400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
26	chr3:46779200-46782000	Weak transcription	Left Ventricle	heart
27	chr3:46779400-46795400	Weak transcription	Spleen	Spleen
28	chr3:46779400-46799600	Weak transcription	Pancreas	Pancrea
29	chr3:46779600-46780400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr3:46779800-46792800	Weak transcription	Thymus	Thymus
31	chr3:46780800-46785000	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr3:46784400-46785200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr3:46784400-46785200	Enhancers	Fetal Stomach	stomach
34	chr3:46784600-46785000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr3:46784600-46785000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr3:46784600-46785000	Enhancers	Placenta	Placenta
37	chr3:46784600-46785200	Enhancers	Fetal Lung	lung
38	chr3:46784600-46785200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr3:46784800-46785200	Enhancers	Fetal Intestine Small	intestine
40	chr3:46785000-46785200	Weak transcription	Placenta	Placenta
41	chr3:46785000-46785800	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr3:46785000-46786200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr3:46785000-46789800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr3:46785200-46785600	Enhancers	Placenta	Placenta
45	chr3:46785200-46799800	Weak transcription	Fetal Intestine Small	intestine
46	chr3:46785600-46789800	Weak transcription	Placenta	Placenta
47	chr3:46785800-46786200	Enhancers	GM12878-XiMat	blood
48	chr3:46785800-46795600	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr3:46786200-46787800	Weak transcription	GM12878-XiMat	blood
50	chr3:46786400-46786600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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