Variant report

Variant	esv3333601
Chromosome Location	chr3:145940702-146068210
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1052)
CpG islands
(count:857)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1052 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:145939594-145940831	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:146044949-146045258	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:145941119-145941527	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:145995769-145995872	HepG2	liver:	n/a	n/a
5	ATF1	chr3:145959778-145959950	K562	blood:	n/a	n/a
6	BACH1	chr3:145968459-145969085	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr3:145939979-145940826	A549	lung:	n/a	n/a
8	BHLHE40	chr3:145968815-145968925	K562	blood:	n/a	n/a
9	BHLHE40	chr3:145940155-145940799	HepG2	liver:	n/a	n/a
10	BRCA1	chr3:146031031-146032435	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr3:146028606-146029007	HCT-116	colon:	n/a	n/a
12	CBX3	chr3:146028686-146029049	HCT-116	colon:	n/a	n/a
13	CCNT2	chr3:145968563-145969088	K562	blood:	n/a	n/a
14	CEBPB	chr3:145967604-145968179	Hela-S3	cervix:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
15	CEBPB	chr3:145995666-145996074	IMR90	lung:	n/a	chr3:145995856-145995867
16	CEBPB	chr3:145943941-145944226	HepG2	liver:	n/a	chr3:145944070-145944081
17	CEBPB	chr3:145995622-145996180	A549	lung:	n/a	chr3:145995856-145995867
18	CEBPB	chr3:145995685-145996059	Hela-S3	cervix:	n/a	chr3:145995856-145995867
19	CEBPB	chr3:145943966-145944149	Hela-S3	cervix:	n/a	chr3:145944070-145944081
20	CEBPB	chr3:145967646-145968183	A549	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
21	CEBPB	chr3:145941324-145941541	A549	lung:	n/a	n/a
22	CEBPB	chr3:145982753-145983062	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr3:146044962-146045293	IMR90	lung:	n/a	n/a
24	CEBPB	chr3:145943995-145944194	K562	blood:	n/a	chr3:145944070-145944081
25	CEBPB	chr3:145967627-145968119	IMR90	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
26	CEBPB	chr3:145943940-145944249	IMR90	lung:	n/a	chr3:145944070-145944081
27	CEBPB	chr3:146050265-146050341	K562	blood:	n/a	n/a
28	CEBPB	chr3:145995668-145996055	A549	lung:	n/a	chr3:145995856-145995867
29	CEBPB	chr3:146043001-146043313	IMR90	lung:	n/a	chr3:146043140-146043151
30	CEBPB	chr3:145995697-145996043	HepG2	liver:	n/a	chr3:145995856-145995867
31	CEBPB	chr3:146025863-146026853	Hela-S3	cervix:	n/a	chr3:146026620-146026633
32	CEBPB	chr3:146043015-146043294	HepG2	liver:	n/a	chr3:146043140-146043151
33	CEBPB	chr3:146000445-146000740	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr3:146032282-146032340	A549	lung:	n/a	n/a
35	CEBPB	chr3:145989088-145989213	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr3:145965734-145966053	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:145992582-145992988	IMR90	lung:	n/a	n/a
38	CEBPB	chr3:146031135-146032514	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:146012250-146012313	A549	lung:	n/a	n/a
40	CEBPB	chr3:145946751-145947057	IMR90	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
41	CEBPB	chr3:145967647-145967801	K562	blood:	n/a	n/a
42	CEBPB	chr3:145975222-145975278	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr3:146067053-146067336	HepG2	liver:	n/a	chr3:146067178-146067189
44	CEBPB	chr3:145946749-145947065	HepG2	liver:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
45	CEBPB	chr3:146025941-146026793	IMR90	lung:	n/a	chr3:146026620-146026633
46	CEBPB	chr3:145946758-145947067	A549	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
47	CEBPB	chr3:145995660-145996069	ECC-1	luminal epithelium:	n/a	chr3:145995856-145995867
48	CEBPB	chr3:145995594-145996124	ECC-1	luminal epithelium:	n/a	chr3:145995856-145995867
49	CEBPB	chr3:146060963-146061244	IMR90	lung:	n/a	chr3:146061156-146061169
50	CEBPB	chr3:145989091-145989307	A549	lung:	n/a	n/a

(count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145969579-145969629	NT2-D1	testis:	n/a
2	chr3:145969007-145969057	HepG2	liver:	n/a
3	chr3:145970385-145970435	HCF	heart:	n/a
4	chr3:145969579-145969629	NT2-D1	testis:	n/a
5	chr3:145969007-145969057	HepG2	liver:	n/a
6	chr3:145970385-145970435	HCF	heart:	n/a
7	chr3:145968620-145968670	HAEpiC	amniotic membrane:	n/a
8	chr3:145968389-145968439	AG10803	skin:	n/a
9	chr3:145968722-145968772	Hela-S3	cervix:	n/a
10	chr3:145968389-145968439	AG09309	skin:	n/a
11	chr3:145968389-145968439	LNCaP	prostate:	n/a
12	chr3:145968696-145968746	ovcar-3	ovarian:	n/a
13	chr3:145969625-145969675	PrEC	prostate:	n/a
14	chr3:145969718-145969768	HCPEpiC	choroid plexus:	n/a
15	chr3:145969007-145969057	HNPCEpiC	eye:	n/a
16	chr3:145969579-145969629	U87	brain:	n/a
17	chr3:145970385-145970435	HCM	heart:	n/a
18	chr3:145969718-145969768	BE2_C	brain:	n/a
19	chr3:145969625-145969675	AG09309	skin:	n/a
20	chr3:146026497-146026547	HIPEpiC	eye:	n/a
21	chr3:145969625-145969675	HNPCEpiC	eye:	n/a
22	chr3:145969718-145969768	U87	brain:	n/a
23	chr3:145968726-145968776	PrEC	prostate:	n/a
24	chr3:145968692-145968742	AG09309	skin:	n/a
25	chr3:145968242-145968292	NHDF-neo	bronchial:	n/a
26	chr3:145968722-145968772	RPTEC	kidney:	n/a
27	chr3:145968696-145968746	H1-hESC	embryonic stem cell:	embryo
28	chr3:145968620-145968670	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:145968722-145968772	AG04449	skin:	fetal
30	chr3:145968696-145968746	AG10803	skin:	n/a
31	chr3:145968389-145968439	HUVEC	blood vessel:	n/a
32	chr3:145968726-145968776	SK-N-SH	brain:	n/a
33	chr3:145968722-145968772	BE2_C	brain:	n/a
34	chr3:145968722-145968772	ECC-1	luminal epithelium:	n/a
35	chr3:145968620-145968670	IMR90	lung:	fetal
36	chr3:145968692-145968742	CMK	blood:	n/a
37	chr3:145969718-145969768	H1-hESC	embryonic stem cell:	embryo
38	chr3:145968692-145968742	GM19239	blood:	n/a
39	chr3:145969718-145969768	ovcar-3	ovarian:	n/a
40	chr3:145968700-145968750	HUVEC	blood vessel:	n/a
41	chr3:145968620-145968670	NHDF-neo	bronchial:	n/a
42	chr3:145968722-145968772	LNCaP	prostate:	n/a
43	chr3:145969579-145969629	HRCEpiC	kidney:	n/a
44	chr3:145969625-145969675	SAEC	small airway:	n/a
45	chr3:145968620-145968670	GM06990	blood:	n/a
46	chr3:145968726-145968776	Hepatocyte	liver:	n/a
47	chr3:145968700-145968750	AG10803	skin:	n/a
48	chr3:145968389-145968439	HEEpiC	esophagus:	n/a
49	chr3:145968620-145968670	NT2-D1	testis:	n/a
50	chr3:145969625-145969675	GM06990	blood:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:145937350..145938198-chr3:146044684..146045576,2	K562	blood:
2	chr3:146048795..146051583-chr3:146054776..146056566,2	MCF-7	breast:
3	chr3:145961600..145965107-chr3:145968575..145970473,3	K562	blood:
4	chr3:145944002..145945741-chr3:145946348..145947988,2	K562	blood:
5	chr3:145783038..145783586-chr3:146044661..146045578,2	MCF-7	breast:
6	chr3:145979759..145981408-chr3:145991775..145993643,2	K562	blood:
7	chr3:145986622..145989134-chr3:145993598..145995580,2	MCF-7	breast:
8	chr3:146051675..146052565-chr3:146295209..146295722,2	MCF-7	breast:
9	chr3:145986622..145989134-chr3:145993598..145995580,2	MCF-7	breast:
10	chr3:145992454..145994295-chr3:145994384..145997157,2	K562	blood:
11	chr3:145979759..145981408-chr3:145991775..145993643,2	K562	blood:
12	chr3:145938654..145939295-chr3:146044870..146045659,2	MCF-7	breast:
13	chr3:146048795..146051583-chr3:146054776..146056566,2	MCF-7	breast:
14	chr3:145944002..145945741-chr3:145946348..145947988,2	K562	blood:
15	chr3:145878599..145881384-chr3:145968449..145970595,2	MCF-7	breast:
16	chr20:56268200..56270406-chr3:146031191..146033715,2	MCF-7	breast:
17	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:
18	chr3:145936384..145937370-chr3:146044670..146045567,4	MCF-7	breast:
19	chr3:145956753..145960171-chr3:145962648..145965540,3	K562	blood:
20	chr3:146017468..146019765-chr3:146026465..146028948,2	MCF-7	breast:
21	chr3:146051931..146052494-chr3:146139879..146140654,2	MCF-7	breast:
22	chr3:145940299..145941372-chr3:146044662..146045624,8	MCF-7	breast:
23	chr3:145938109..145938869-chr3:146044708..146045495,2	MCF-7	breast:
24	chr3:146044568..146045746-chr3:146099870..146100750,3	MCF-7	breast:
25	chr3:146017468..146019765-chr3:146026465..146028948,2	MCF-7	breast:
26	chr3:145936462..145937370-chr3:146044619..146045821,9	MCF-7	breast:
27	chr3:146053792..146056507-chr3:146270955..146273271,2	K562	blood:
28	chr3:145940254..145941134-chr3:146295120..146295978,3	MCF-7	breast:
29	chr3:146044616..146045587-chr3:146295200..146296047,4	MCF-7	breast:
30	chr3:146051922..146052597-chr3:146295303..146296107,2	MCF-7	breast:
31	chr3:145907332..145908011-chr3:146044703..146045227,2	K562	blood:
32	chr3:145940299..145941372-chr3:146044662..146045624,8	MCF-7	breast:
33	chr3:145992454..145994295-chr3:145994384..145997157,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000243596	TF binding region
PLSCR4	TF binding region
ENSG00000243596	CpG island
PLSCR4	CpG island
ENSG00000114698	chromatin interactions
ENSG00000152952	chromatin interactions

Extended variants
information (count: 4501 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4501 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147432632	chr3:145940725-145940726	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs112154741	chr3:145940741-145940742	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs370953714	chr3:145940764-145940765	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs550254078	chr3:145940831-145940832	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs114446601	chr3:145940864-145940865	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs181441587	chr3:145940875-145940876	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs548129975	chr3:145940882-145940883	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs371469067	chr3:145940886-145940887	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs373337934	chr3:145940887-145940888	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs566360340	chr3:145940889-145940890	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs397806353	chr3:145940891-145940892	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs75586954	chr3:145940892-145940893	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs13079270	chr3:145940962-145940963	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs547346070	chr3:145940969-145940970	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs138243886	chr3:145940978-145940979	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs73150841	chr3:145940985-145940986	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs367660896	chr3:145941001-145941002	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs9809574	chr3:145941020-145941021	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs369996676	chr3:145941038-145941039	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs143620400	chr3:145941060-145941061	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536357069	chr3:145941077-145941078	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs554913532	chr3:145941100-145941101	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs377361569	chr3:145941108-145941109	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs572920490	chr3:145941128-145941129	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374755837	chr3:145941182-145941183	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs1512888	chr3:145941189-145941190	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs372228794	chr3:145941204-145941205	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs377069931	chr3:145941206-145941207	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs564868062	chr3:145941243-145941244	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs200929922	chr3:145941261-145941262	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs576626751	chr3:145941264-145941265	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs147201156	chr3:145941289-145941290	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs186080826	chr3:145941296-145941297	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs529761872	chr3:145941315-145941316	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs548002457	chr3:145941328-145941329	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs560073805	chr3:145941345-145941346	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs200818830	chr3:145941390-145941391	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs527320541	chr3:145941397-145941398	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs547303510	chr3:145941435-145941436	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs572016403	chr3:145941452-145941453	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs188105583	chr3:145941474-145941475	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs551112155	chr3:145941484-145941485	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs569364337	chr3:145941555-145941556	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs536720085	chr3:145941561-145941562	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs180915024	chr3:145941577-145941578	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs567272737	chr3:145941580-145941581	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs7633252	chr3:145941608-145941609	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs10553978	chr3:145941635-145941636	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs66981902	chr3:145941658-145941659	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs7611293	chr3:145941712-145941713	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:57)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autism	21956041	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Breast cancer	16608533	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1189 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:145924400-145944000	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:145924400-145945200	Weak transcription	HSMMtube	muscle
3	chr3:145925000-145945600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:145925400-145952800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr3:145925600-145950800	Weak transcription	Fetal Kidney	kidney
6	chr3:145932600-145943800	Weak transcription	Brain Hippocampus Middle	brain
7	chr3:145932800-145941000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:145934600-145952200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr3:145936000-145945200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr3:145938600-145941200	Active TSS	HepG2	liver
11	chr3:145938600-145941400	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr3:145938800-145940800	Enhancers	Fetal Lung	lung
13	chr3:145939200-145940800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:145939200-145940800	Enhancers	Stomach Smooth Muscle	stomach
15	chr3:145939200-145940800	Enhancers	Hela-S3	cervix
16	chr3:145939800-145940800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr3:145939800-145941400	Flanking Active TSS	Liver	Liver
18	chr3:145939800-145941400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
19	chr3:145939800-145941400	Flanking Active TSS	A549	lung
20	chr3:145940000-145940800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
21	chr3:145940000-145941000	Enhancers	Ovary	ovary
22	chr3:145940000-145941000	Flanking Active TSS	HUVEC	blood vessel
23	chr3:145940000-145941400	Enhancers	NHLF	lung
24	chr3:145940200-145940800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr3:145940200-145940800	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr3:145940200-145940800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr3:145940200-145940800	Enhancers	Aorta	Aorta
28	chr3:145940200-145940800	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr3:145940200-145940800	Enhancers	Fetal Stomach	stomach
30	chr3:145940200-145940800	Enhancers	Psoas Muscle	Psoas
31	chr3:145940200-145941200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:145940200-145941200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr3:145940200-145941400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr3:145940200-145941400	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr3:145940200-145941400	Enhancers	Stomach Mucosa	stomach
36	chr3:145940200-145941400	Enhancers	NH-A	brain
37	chr3:145940400-145940800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr3:145940400-145940800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr3:145940400-145940800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr3:145940400-145940800	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr3:145940400-145940800	Flanking Active TSS	Colonic Mucosa	Colon
42	chr3:145940400-145940800	Flanking Active TSS	Duodenum Mucosa	Duodenum
43	chr3:145940400-145940800	Flanking Active TSS	Fetal Intestine Small	intestine
44	chr3:145940400-145940800	Enhancers	Sigmoid Colon	Sigmoid Colon
45	chr3:145940400-145940800	Enhancers	Skeletal Muscle Male	skeletal muscle
46	chr3:145940400-145940800	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr3:145940400-145940800	Enhancers	Small Intestine	intestine
48	chr3:145940400-145940800	Enhancers	Spleen	Spleen
49	chr3:145940400-145941000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr3:145940400-145941000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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