Variant report

Variant	esv3416330
Chromosome Location	chr3:145941029-146068457
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:922)
CpG islands
(count:854)
Chromatin interactive
region (count:33)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:922 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:146044949-146045258	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:145995769-145995872	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:145941119-145941527	HepG2	liver:	n/a	n/a
4	ATF1	chr3:145959778-145959950	K562	blood:	n/a	n/a
5	BACH1	chr3:145968459-145969085	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr3:145968815-145968925	K562	blood:	n/a	n/a
7	BRCA1	chr3:146031031-146032435	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr3:146028606-146029007	HCT-116	colon:	n/a	n/a
9	CBX3	chr3:146028686-146029049	HCT-116	colon:	n/a	n/a
10	CCNT2	chr3:145968563-145969088	K562	blood:	n/a	n/a
11	CEBPB	chr3:145967646-145968183	A549	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
12	CEBPB	chr3:145992582-145992988	IMR90	lung:	n/a	n/a
13	CEBPB	chr3:145946751-145947057	IMR90	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
14	CEBPB	chr3:146000445-146000740	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:145995660-145996069	ECC-1	luminal epithelium:	n/a	chr3:145995856-145995867
16	CEBPB	chr3:145995712-145996041	A549	lung:	n/a	chr3:145995856-145995867
17	CEBPB	chr3:145943940-145944249	IMR90	lung:	n/a	chr3:145944070-145944081
18	CEBPB	chr3:145941324-145941541	A549	lung:	n/a	n/a
19	CEBPB	chr3:145995666-145996074	IMR90	lung:	n/a	chr3:145995856-145995867
20	CEBPB	chr3:146060963-146061244	IMR90	lung:	n/a	chr3:146061156-146061169
21	CEBPB	chr3:145965734-145966053	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:146012250-146012313	A549	lung:	n/a	n/a
23	CEBPB	chr3:145989091-145989307	A549	lung:	n/a	n/a
24	CEBPB	chr3:145995697-145996043	HepG2	liver:	n/a	chr3:145995856-145995867
25	CEBPB	chr3:145967627-145968119	IMR90	lung:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
26	CEBPB	chr3:145943941-145944226	HepG2	liver:	n/a	chr3:145944070-145944081
27	CEBPB	chr3:145995668-145996055	A549	lung:	n/a	chr3:145995856-145995867
28	CEBPB	chr3:146025863-146026853	Hela-S3	cervix:	n/a	chr3:146026620-146026633
29	CEBPB	chr3:145967604-145968179	Hela-S3	cervix:	n/a	chr3:145968037-145968048 chr3:145968037-145968050 chr3:145968037-145968048
30	CEBPB	chr3:145968381-145969227	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:145975222-145975278	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr3:146032282-146032340	A549	lung:	n/a	n/a
33	CEBPB	chr3:145943995-145944194	K562	blood:	n/a	chr3:145944070-145944081
34	CEBPB	chr3:145946749-145947065	HepG2	liver:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
35	CEBPB	chr3:145946758-145947067	A549	lung:	n/a	chr3:145946887-145946900 chr3:145946887-145946900 chr3:145946887-145946898
36	CEBPB	chr3:146043015-146043294	HepG2	liver:	n/a	chr3:146043140-146043151
37	CEBPB	chr3:146043001-146043313	IMR90	lung:	n/a	chr3:146043140-146043151
38	CEBPB	chr3:146044962-146045293	IMR90	lung:	n/a	n/a
39	CEBPB	chr3:145943966-145944149	Hela-S3	cervix:	n/a	chr3:145944070-145944081
40	CEBPB	chr3:145982753-145983062	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:145967647-145967801	K562	blood:	n/a	n/a
42	CEBPB	chr3:146025941-146026793	IMR90	lung:	n/a	chr3:146026620-146026633
43	CEBPB	chr3:145995594-145996124	ECC-1	luminal epithelium:	n/a	chr3:145995856-145995867
44	CEBPB	chr3:146050265-146050341	K562	blood:	n/a	n/a
45	CEBPB	chr3:145995685-145996059	Hela-S3	cervix:	n/a	chr3:145995856-145995867
46	CEBPB	chr3:145968610-145968627	K562	blood:	n/a	n/a
47	CEBPB	chr3:146031135-146032514	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr3:145989088-145989213	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr3:145995622-145996180	A549	lung:	n/a	chr3:145995856-145995867
50	CEBPB	chr3:146067053-146067336	HepG2	liver:	n/a	chr3:146067178-146067189

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:145968692-145968742	HepG2	liver:	n/a
2	chr3:145970385-145970435	PANC-1	pancreas:	n/a
3	chr3:146026497-146026547	HEEpiC	esophagus:	n/a
4	chr3:145969718-145969768	AG04449	skin:	fetal
5	chr3:145968242-145968292	HUVEC	blood vessel:	n/a
6	chr3:145968700-145968750	NHDF-neo	bronchial:	n/a
7	chr3:145968722-145968772	NB4	blood:	n/a
8	chr3:145969625-145969675	K562	blood:	n/a
9	chr3:145968389-145968439	T-47D	breast:	n/a
10	chr3:145970385-145970435	PFSK-1	brain:	n/a
11	chr3:145968722-145968772	SKMC	muscle:	n/a
12	chr3:145968726-145968776	HL-60	blood:	n/a
13	chr3:145969007-145969057	GM12892	blood:	n/a
14	chr3:145968696-145968746	PANC-1	pancreas:	n/a
15	chr3:145970385-145970435	AG10803	skin:	n/a
16	chr3:145968722-145968772	U87	brain:	n/a
17	chr3:145968620-145968670	AoSMC	blood vessel:	n/a
18	chr3:145968692-145968742	MCF-7	breast:	n/a
19	chr3:145968696-145968746	PFSK-1	brain:	n/a
20	chr3:145969718-145969768	IMR90	lung:	fetal
21	chr3:145969579-145969629	HCPEpiC	choroid plexus:	n/a
22	chr3:145968242-145968292	CMK	blood:	n/a
23	chr3:145970385-145970435	SAEC	small airway:	n/a
24	chr3:145968722-145968772	ProgFib	skin:	n/a
25	chr3:145968696-145968746	BJ	skin:	n/a
26	chr3:146026497-146026547	MCF-7	breast:	n/a
27	chr3:145970385-145970435	HRPEpiC	eye:	n/a
28	chr3:145969579-145969629	GM06990	blood:	n/a
29	chr3:145968726-145968776	BE2_C	brain:	n/a
30	chr3:145969579-145969629	ECC-1	luminal epithelium:	n/a
31	chr3:145968722-145968772	Caco-2	colon:	n/a
32	chr3:145968696-145968746	GM12878	blood:	n/a
33	chr3:145968242-145968292	HIPEpiC	eye:	n/a
34	chr3:145968620-145968670	HepG2	liver:	n/a
35	chr3:145968242-145968292	Hela-S3	cervix:	n/a
36	chr3:145968726-145968776	PANC-1	pancreas:	n/a
37	chr3:145968389-145968439	HCF	heart:	n/a
38	chr3:145968722-145968772	AG10803	skin:	n/a
39	chr3:145968242-145968292	HAEpiC	amniotic membrane:	n/a
40	chr3:145968692-145968742	SK-N-SH_RA	brain:	n/a
41	chr3:145968700-145968750	SK-N-MC	brain:	n/a
42	chr3:145970385-145970435	BE2_C	brain:	n/a
43	chr3:145968722-145968772	NH-A	brain:	n/a
44	chr3:145969007-145969057	K562	blood:	n/a
45	chr3:145968620-145968670	HEEpiC	esophagus:	n/a
46	chr3:145968722-145968772	A549	lung:	n/a
47	chr3:146026497-146026547	NHDF-neo	bronchial:	n/a
48	chr3:145968692-145968742	HCM	heart:	n/a
49	chr3:145968726-145968776	HIPEpiC	eye:	n/a
50	chr3:145969579-145969629	HL-60	blood:	n/a

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

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

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: 4495 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4495 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369996676	chr3:145941038-145941039	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs143620400	chr3:145941060-145941061	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536357069	chr3:145941077-145941078	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs554913532	chr3:145941100-145941101	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs377361569	chr3:145941108-145941109	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572920490	chr3:145941128-145941129	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs374755837	chr3:145941182-145941183	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	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
9	rs372228794	chr3:145941204-145941205	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs377069931	chr3:145941206-145941207	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs564868062	chr3:145941243-145941244	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs200929922	chr3:145941261-145941262	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs576626751	chr3:145941264-145941265	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs147201156	chr3:145941289-145941290	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs186080826	chr3:145941296-145941297	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs529761872	chr3:145941315-145941316	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs548002457	chr3:145941328-145941329	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs560073805	chr3:145941345-145941346	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs200818830	chr3:145941390-145941391	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs527320541	chr3:145941397-145941398	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs547303510	chr3:145941435-145941436	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs572016403	chr3:145941452-145941453	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs188105583	chr3:145941474-145941475	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs551112155	chr3:145941484-145941485	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs569364337	chr3:145941555-145941556	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs536720085	chr3:145941561-145941562	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs180915024	chr3:145941577-145941578	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs567272737	chr3:145941580-145941581	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs7633252	chr3:145941608-145941609	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs10553978	chr3:145941635-145941636	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs66981902	chr3:145941658-145941659	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs7611293	chr3:145941712-145941713	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs7611299	chr3:145941740-145941741	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs72179951	chr3:145941746-145941747	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs73865362	chr3:145941761-145941762	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs544197954	chr3:145941788-145941789	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556296485	chr3:145941816-145941817	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs191121797	chr3:145941825-145941826	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs149803597	chr3:145941848-145941849	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs557177419	chr3:145941858-145941859	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs181545820	chr3:145941882-145941883	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs77036446	chr3:145941886-145941887	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs7611459	chr3:145941891-145941892	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs564080519	chr3:145941910-145941911	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs7633567	chr3:145941931-145941932	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs115247422	chr3:145941958-145941959	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs569408390	chr3:145941975-145941976	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs7611582	chr3:145942015-145942016	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs548652023	chr3:145942024-145942025	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs373011304	chr3:145942028-145942029	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

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:1152 , 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	chr3:145934600-145952200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr3:145936000-145945200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr3:145938600-145941200	Active TSS	HepG2	liver
10	chr3:145938600-145941400	Enhancers	Pancreatic Islets	Pancreatic Islet
11	chr3:145939800-145941400	Flanking Active TSS	Liver	Liver
12	chr3:145939800-145941400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr3:145939800-145941400	Flanking Active TSS	A549	lung
14	chr3:145940000-145941400	Enhancers	NHLF	lung
15	chr3:145940200-145941200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr3:145940200-145941200	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr3:145940200-145941400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr3:145940200-145941400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr3:145940200-145941400	Enhancers	Stomach Mucosa	stomach
20	chr3:145940200-145941400	Enhancers	NH-A	brain
21	chr3:145940400-145941200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
22	chr3:145940400-145941600	Enhancers	Pancreas	Pancrea
23	chr3:145940400-145942000	Enhancers	Fetal Intestine Large	intestine
24	chr3:145940600-145941400	Enhancers	Brain Anterior Caudate	brain
25	chr3:145940600-145941400	Enhancers	Osteobl	bone
26	chr3:145940600-145941600	Enhancers	Gastric	stomach
27	chr3:145940600-145943600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr3:145940600-145944800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr3:145940600-145953000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr3:145940600-145953600	Weak transcription	NHDF-Ad	bronchial
31	chr3:145940800-145941400	Enhancers	Adipose Nuclei	Adipose
32	chr3:145940800-145941400	Enhancers	Duodenum Mucosa	Duodenum
33	chr3:145940800-145941600	Enhancers	Fetal Intestine Small	intestine
34	chr3:145940800-145941600	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr3:145940800-145941800	Weak transcription	Fetal Lung	lung
36	chr3:145940800-145943200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr3:145940800-145944000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr3:145940800-145944000	Weak transcription	Stomach Smooth Muscle	stomach
39	chr3:145940800-145944400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr3:145940800-145944400	Weak transcription	Fetal Stomach	stomach
41	chr3:145940800-145945000	Weak transcription	Aorta	Aorta
42	chr3:145940800-145945000	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr3:145940800-145945200	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr3:145940800-145945200	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr3:145941000-145941200	Weak transcription	Right Atrium	heart
46	chr3:145941000-145941400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr3:145941000-145941400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:145941000-145941400	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr3:145941000-145941400	Weak transcription	Left Ventricle	heart
50	chr3:145941000-145941400	Weak transcription	Lung	lung

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