Variant report

Variant	esv2759135
Chromosome Location	chr3:24652513-24942926
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1843)
CpG islands
(count:977)
Chromatin interactive
region (count:85)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1843 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:24724618-24725625	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:24725347-24725555	K562	blood:	n/a	n/a
3	ARID3A	chr3:24815309-24815518	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:24681816-24682096	HepG2	liver:	n/a	n/a
5	ATF1	chr3:24663608-24663866	K562	blood:	n/a	n/a
6	ATF2	chr3:24726039-24726569	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:24725933-24726511	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:24721976-24722378	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr3:24703026-24703115	K562	blood:	n/a	n/a
10	BACH1	chr3:24870529-24870833	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:24730303-24730480	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr3:24879181-24879377	GM12878	blood:	n/a	chr3:24879308-24879319
13	BATF	chr3:24844079-24844445	GM12878	blood:	n/a	n/a
14	BATF	chr3:24844083-24844506	GM12878	blood:	n/a	n/a
15	BCL11A	chr3:24844087-24844495	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:24844109-24844480	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:24719913-24720250	K562	blood:	n/a	n/a
18	BRCA1	chr3:24815336-24815559	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr3:24681701-24682222	HCT-116	colon:	n/a	n/a
20	CBX3	chr3:24722067-24722404	K562	blood:	n/a	n/a
21	CCNT2	chr3:24907314-24907622	K562	blood:	n/a	n/a
22	CEBPB	chr3:24719851-24720364	K562	blood:	n/a	n/a
23	CEBPB	chr3:24719971-24720398	HCT-116	colon:	n/a	n/a
24	CEBPB	chr3:24753856-24754117	HepG2	liver:	n/a	chr3:24753973-24753984
25	CEBPB	chr3:24898164-24898402	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:24715745-24716083	K562	blood:	n/a	chr3:24715902-24715911 chr3:24715900-24715913 chr3:24715902-24715911 chr3:24715902-24715911 chr3:24715902-24715911
27	CEBPB	chr3:24753868-24754042	A549	lung:	n/a	chr3:24753973-24753984
28	CEBPB	chr3:24746408-24746889	ECC-1	luminal epithelium:	n/a	chr3:24746624-24746637
29	CEBPB	chr3:24724716-24725086	HepG2	liver:	n/a	chr3:24724900-24724911 chr3:24724901-24724912 chr3:24724900-24724911 chr3:24724900-24724913
30	CEBPB	chr3:24941741-24941935	A549	lung:	n/a	n/a
31	CEBPB	chr3:24670107-24670397	K562	blood:	n/a	n/a
32	CEBPB	chr3:24745997-24746423	A549	lung:	n/a	n/a
33	CEBPB	chr3:24719952-24720325	K562	blood:	n/a	n/a
34	CEBPB	chr3:24715750-24716084	A549	lung:	n/a	chr3:24715902-24715911 chr3:24715900-24715913 chr3:24715902-24715911 chr3:24715902-24715911 chr3:24715902-24715911
35	CEBPB	chr3:24715798-24716144	MCF-7	breast:	n/a	chr3:24715902-24715911 chr3:24715900-24715913 chr3:24715902-24715911 chr3:24715902-24715911 chr3:24715902-24715911
36	CEBPB	chr3:24746576-24746706	A549	lung:	n/a	chr3:24746624-24746637
37	CEBPB	chr3:24895338-24895339	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:24804730-24805331	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:24681763-24682144	K562	blood:	n/a	n/a
40	CEBPB	chr3:24719817-24720405	IMR90	lung:	n/a	n/a
41	CEBPB	chr3:24681726-24682138	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:24681652-24682059	A549	lung:	n/a	n/a
43	CEBPB	chr3:24719877-24720306	A549	lung:	n/a	n/a
44	CEBPB	chr3:24670083-24670399	K562	blood:	n/a	n/a
45	CEBPB	chr3:24887291-24887586	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:24724779-24724952	HepG2	liver:	n/a	chr3:24724900-24724911 chr3:24724901-24724912 chr3:24724900-24724911 chr3:24724900-24724913
47	CEBPB	chr3:24681742-24682107	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr3:24670071-24670475	MCF-7	breast:	n/a	n/a
49	CEBPB	chr3:24940259-24940390	K562	blood:	n/a	chr3:24940297-24940308
50	CEBPB	chr3:24767129-24767346	Hela-S3	cervix:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:24869928-24869978	HRCEpiC	kidney:	n/a
2	chr3:24869928-24869978	HRCEpiC	kidney:	n/a
3	chr3:24729317-24729367	ProgFib	skin:	n/a
4	chr3:24867139-24867189	HCT-116	colon:	n/a
5	chr3:24782112-24782162	HepG2	liver:	n/a
6	chr3:24875040-24875090	CMK	blood:	n/a
7	chr3:24870785-24870835	NH-A	brain:	n/a
8	chr3:24729317-24729367	HRE	kidney:	n/a
9	chr3:24725365-24725415	AoSMC	blood vessel:	n/a
10	chr3:24871703-24871753	NHBE	bronchial:	n/a
11	chr3:24870666-24870716	GM06990	blood:	n/a
12	chr3:24867139-24867189	HepG2	liver:	n/a
13	chr3:24869928-24869978	HPAEpiC	pulmonary alveolar:	n/a
14	chr3:24870785-24870835	BE2_C	brain:	n/a
15	chr3:24869928-24869978	GM19239	blood:	n/a
16	chr3:24871948-24871998	PFSK-1	brain:	n/a
17	chr3:24870666-24870716	HepG2	liver:	n/a
18	chr3:24870666-24870716	NHDF-neo	bronchial:	n/a
19	chr3:24875040-24875090	HRE	kidney:	n/a
20	chr3:24782112-24782162	HRPEpiC	eye:	n/a
21	chr3:24725365-24725415	HPAEpiC	pulmonary alveolar:	n/a
22	chr3:24869928-24869978	HAEpiC	amniotic membrane:	n/a
23	chr3:24729317-24729367	SK-N-MC	brain:	n/a
24	chr3:24867139-24867189	SKMC	muscle:	n/a
25	chr3:24871948-24871998	GM19239	blood:	n/a
26	chr3:24872319-24872369	RPTEC	kidney:	n/a
27	chr3:24782112-24782162	SAEC	small airway:	n/a
28	chr3:24725365-24725415	ovcar-3	ovarian:	n/a
29	chr3:24782112-24782162	SK-N-SH	brain:	n/a
30	chr3:24887420-24887470	HIPEpiC	eye:	n/a
31	chr3:24870785-24870835	Caco-2	colon:	n/a
32	chr3:24867139-24867189	IMR90	lung:	fetal
33	chr3:24871017-24871067	Hepatocyte	liver:	n/a
34	chr3:24729317-24729367	GM12878	blood:	n/a
35	chr3:24872319-24872369	HIPEpiC	eye:	n/a
36	chr3:24870666-24870716	ECC-1	luminal epithelium:	n/a
37	chr3:24872319-24872369	Hela-S3	cervix:	n/a
38	chr3:24871703-24871753	HRE	kidney:	n/a
39	chr3:24870666-24870716	HEK293	kidney:	embryo
40	chr3:24869928-24869978	HEK293	kidney:	embryo
41	chr3:24870666-24870716	HIPEpiC	eye:	n/a
42	chr3:24871948-24871998	SKMC	muscle:	n/a
43	chr3:24872319-24872369	AG09319	gingival:	n/a
44	chr3:24871231-24871281	GM19239	blood:	n/a
45	chr3:24887420-24887470	PFSK-1	brain:	n/a
46	chr3:24875040-24875090	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:24870785-24870835	HepG2	liver:	n/a
48	chr3:24870785-24870835	HEK293	kidney:	embryo
49	chr3:24870666-24870716	GM12878	blood:	n/a
50	chr3:24870785-24870835	IMR90	lung:	fetal

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:24561121..24563271-chr3:24705181..24706740,2	MCF-7	breast:
2	chr3:24859239..24862090-chr3:24863979..24866552,3	K562	blood:
3	chr3:24535691..24537966-chr3:24685264..24688393,3	MCF-7	breast:
4	chr3:24681218..24682181-chr3:24725071..24725960,2	MCF-7	breast:
5	chr3:24755192..24756974-chr3:24759928..24761810,2	K562	blood:
6	chr3:24706572..24709640-chr3:24711345..24715027,3	K562	blood:
7	chr3:24647511..24649066-chr3:24682804..24685271,2	K562	blood:
8	chr3:24897875..24899735-chr3:24905907..24907899,2	K562	blood:
9	chr3:24847659..24849436-chr3:24851725..24853235,2	K562	blood:
10	chr3:24305875..24306747-chr3:24681516..24682374,2	K562	blood:
11	chr3:24040167..24041064-chr3:24724982..24725943,2	K562	blood:
12	chr3:24727648..24729843-chr3:24805310..24807941,2	K562	blood:
13	chr3:24693645..24696035-chr3:24699778..24702575,2	MCF-7	breast:
14	chr3:24885574..24888444-chr3:24888705..24892606,3	K562	blood:
15	chr3:24686579..24688285-chr3:24690404..24692715,2	K562	blood:
16	chr3:24720021..24724614-chr3:24726069..24732040,5	K562	blood:
17	chr3:24870259..24872185-chr3:24874165..24877170,4	MCF-7	breast:
18	chr3:24745399..24747659-chr3:24751181..24753513,2	K562	blood:
19	chr3:24719797..24722537-chr3:24723132..24725391,2	MCF-7	breast:
20	chr3:24843637..24846114-chr3:24850759..24853172,2	K562	blood:
21	chr3:24712205..24715427-chr3:24716569..24719125,3	K562	blood:
22	chr3:24535738..24537885-chr3:24721658..24723753,2	K562	blood:
23	chr3:24705103..24707129-chr3:24707585..24710989,3	K562	blood:
24	chr3:24870259..24872185-chr3:24874165..24877170,4	MCF-7	breast:
25	chr3:24720510..24723447-chr3:24727587..24729885,2	MCF-7	breast:
26	chr3:24535862..24537903-chr3:24720521..24722059,2	MCF-7	breast:
27	chr3:24715460..24717274-chr3:24717371..24719303,2	MCF-7	breast:
28	chr3:24129965..24130904-chr3:24724999..24725940,3	K562	blood:
29	chr3:24654929..24659787-chr3:24660015..24665677,5	K562	blood:
30	chr3:24654929..24659787-chr3:24660015..24665677,5	K562	blood:
31	chr3:24400847..24401899-chr3:24681498..24682394,3	MCF-7	breast:
32	chr3:24535338..24538241-chr3:24701326..24704002,2	MCF-7	breast:
33	chr3:24686579..24688285-chr3:24690404..24692715,2	K562	blood:
34	chr3:24227165..24227901-chr3:24724976..24725696,3	MCF-7	breast:
35	chr3:24766490..24768818-chr3:24773482..24775957,2	K562	blood:
36	chr3:24534671..24539332-chr3:24720695..24724748,4	K562	blood:
37	chr3:24712205..24715427-chr3:24716569..24719125,3	K562	blood:
38	chr3:24745399..24747659-chr3:24751181..24753513,2	K562	blood:
39	chr3:24535469..24538713-chr3:24703721..24706675,3	MCF-7	breast:
40	chr3:24697062..24699853-chr3:24700459..24702672,2	K562	blood:
41	chr3:24536470..24537232-chr3:24721929..24722671,2	K562	blood:
42	chr3:24653142..24655927-chr3:24664996..24667138,2	MCF-7	breast:
43	chr3:24279555..24280153-chr3:24725005..24725918,2	MCF-7	breast:
44	chr3:23957740..23960130-chr3:24717360..24719432,2	MCF-7	breast:
45	chr3:24890880..24892601-chr3:24892985..24895206,2	MCF-7	breast:
46	chr3:24890880..24892601-chr3:24892985..24895206,2	MCF-7	breast:
47	chr3:24802431..24804243-chr3:24805497..24807982,2	K562	blood:
48	chr3:24885574..24888444-chr3:24888705..24892606,3	K562	blood:
49	chr3:24623522..24626153-chr3:24655332..24658320,2	MCF-7	breast:
50	chr3:24697062..24699853-chr3:24700459..24702672,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RARB-1	chr3:24900165-24900243	ENSG00000237838
2	lnc-RARB-1	chr3:24803731-24803785	ENSG00000237838
3	lnc-RARB-1	chr3:24729410-24729486	ENSG00000237838
4	lnc-RARB-1	chr3:24874580-24874713	ENSG00000237838

No data

Variant related genes	Relation type
ENSG00000237838	TF binding region
ENSG00000237838	CpG island
ENSG00000265028	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000267637	chromatin interactions
ENSG00000228791	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000151090	chromatin interactions
ENSG00000237838	chromatin interactions

Extended variants
information (count: 6726 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6726 , 50 per page) page: 1 2 3 4 5 6 7 ... 135

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139872991	chr3:24652521-24652522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs116520216	chr3:24652535-24652536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567773133	chr3:24652569-24652570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537939094	chr3:24652636-24652637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548978786	chr3:24652656-24652657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs17014950	chr3:24652696-24652697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184106535	chr3:24652700-24652701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576386513	chr3:24652719-24652720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs145327485	chr3:24652721-24652722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528784990	chr3:24652757-24652758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs17014951	chr3:24652813-24652814	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs34422892	chr3:24652948-24652949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571710739	chr3:24652954-24652955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75288686	chr3:24652957-24652958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148714224	chr3:24652974-24652975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17014953	chr3:24653012-24653013	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs564899379	chr3:24653020-24653021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369486279	chr3:24653052-24653053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs559939435	chr3:24653080-24653081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199609334	chr3:24653081-24653082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528923757	chr3:24653102-24653103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547404563	chr3:24653117-24653118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142411310	chr3:24653123-24653124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs149322336	chr3:24653134-24653135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs72619930	chr3:24653144-24653145	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs187272386	chr3:24653178-24653179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371973672	chr3:24653179-24653180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567726504	chr3:24653221-24653222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142423174	chr3:24653244-24653245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35278683	chr3:24653253-24653254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35992196	chr3:24653262-24653263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376885393	chr3:24653265-24653266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191998869	chr3:24653274-24653275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184455541	chr3:24653283-24653284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539889219	chr3:24653286-24653287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186975319	chr3:24653301-24653302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562485356	chr3:24653312-24653313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531255148	chr3:24653336-24653337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs371609347	chr3:24653370-24653371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538688323	chr3:24653402-24653403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs193007999	chr3:24653411-24653412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184124310	chr3:24653444-24653445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553747400	chr3:24653460-24653461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12492959	chr3:24653488-24653489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs572037501	chr3:24653511-24653512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189501642	chr3:24653514-24653515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554769234	chr3:24653620-24653621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs111632584	chr3:24653664-24653665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151298721	chr3:24653669-24653670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564869363	chr3:24653693-24653694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
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
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
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Multiple myeloma	17550852	CNVD

Chromatin state (count:988 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:24648400-24654600	Weak transcription	Fetal Intestine Small	intestine
2	chr3:24651800-24655400	Weak transcription	NHDF-Ad	bronchial
3	chr3:24654200-24656400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr3:24654600-24654800	Enhancers	Fetal Intestine Small	intestine
5	chr3:24654800-24655200	Weak transcription	Fetal Intestine Small	intestine
6	chr3:24654800-24659400	Enhancers	Fetal Intestine Large	intestine
7	chr3:24655200-24659400	Enhancers	Fetal Intestine Small	intestine
8	chr3:24655400-24656400	Enhancers	NHDF-Ad	bronchial
9	chr3:24656000-24656400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:24656000-24656600	Enhancers	Stomach Mucosa	stomach
11	chr3:24656200-24658000	Enhancers	Duodenum Mucosa	Duodenum
12	chr3:24657800-24658000	Enhancers	Primary hematopoietic stem cells	blood
13	chr3:24658400-24658800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:24658800-24667000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:24659400-24660400	Weak transcription	Fetal Intestine Small	intestine
16	chr3:24660400-24660800	Enhancers	Fetal Intestine Small	intestine
17	chr3:24660800-24664400	Weak transcription	Fetal Intestine Small	intestine
18	chr3:24662800-24663600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr3:24662800-24664000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr3:24662800-24665400	Enhancers	Primary hematopoietic stem cells	blood
21	chr3:24662800-24666000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr3:24663600-24664800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr3:24663600-24665600	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr3:24663800-24666400	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr3:24664400-24664600	Enhancers	Fetal Intestine Small	intestine
26	chr3:24664600-24665000	Weak transcription	Fetal Intestine Small	intestine
27	chr3:24664800-24666000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr3:24664800-24666200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr3:24665000-24665400	Enhancers	Fetal Intestine Small	intestine
30	chr3:24665000-24665600	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr3:24665000-24665800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr3:24665600-24665800	Bivalent Enhancer	Fetal Kidney	kidney
33	chr3:24665600-24666200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr3:24666200-24667200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr3:24667200-24667400	Enhancers	H9 Cell Line	embryonic stem cell
36	chr3:24669400-24669600	Enhancers	Fetal Intestine Small	intestine
37	chr3:24669400-24672000	Enhancers	Fetal Intestine Large	intestine
38	chr3:24669600-24670400	Weak transcription	Fetal Intestine Small	intestine
39	chr3:24669600-24670400	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr3:24669800-24670000	Enhancers	Duodenum Mucosa	Duodenum
41	chr3:24669800-24670400	Enhancers	Hela-S3	cervix
42	chr3:24669800-24670600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:24669800-24670800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr3:24670200-24671200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr3:24670400-24672000	Enhancers	Fetal Intestine Small	intestine
46	chr3:24671200-24671800	Enhancers	Duodenum Mucosa	Duodenum
47	chr3:24671200-24672000	Enhancers	Stomach Mucosa	stomach
48	chr3:24671400-24671800	Enhancers	Liver	Liver
49	chr3:24672800-24673200	Enhancers	Fetal Brain Male	brain
50	chr3:24680000-24681800	Enhancers	Fetal Intestine Large	intestine

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