Variant report

Variant	esv1795965
Chromosome Location	chr12:118463329-118504859
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2279)
CpG islands
(count:1101)
Chromatin interactive
region (count:80)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2279 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:118490110-118490803	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:118496846-118497314	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:118492983-118493373	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:118501494-118502233	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:118493767-118493823	HepG2	liver:	n/a	n/a
6	ARID3A	chr12:118494032-118494531	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:118497384-118497704	K562	blood:	n/a	n/a
8	ARID3A	chr12:118491285-118491863	HepG2	liver:	n/a	n/a
9	ARID3A	chr12:118499313-118499469	HepG2	liver:	n/a	n/a
10	ATF1	chr12:118492928-118493172	K562	blood:	n/a	n/a
11	ATF2	chr12:118483431-118484035	GM12878	blood:	n/a	n/a
12	ATF2	chr12:118473006-118473890	GM12878	blood:	n/a	n/a
13	ATF2	chr12:118499805-118500513	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr12:118473125-118473832	GM12878	blood:	n/a	n/a
15	ATF2	chr12:118483364-118483982	GM12878	blood:	n/a	n/a
16	ATF3	chr12:118490108-118490760	A549	lung:	n/a	n/a
17	ATF3	chr12:118498894-118499036	GM12878	blood:	n/a	n/a
18	ATF3	chr12:118490144-118490714	A549	lung:	n/a	n/a
19	ATF3	chr12:118498827-118499044	HepG2	liver:	n/a	n/a
20	ATF3	chr12:118501434-118501751	K562	blood:	n/a	n/a
21	ATF3	chr12:118498855-118499094	K562	blood:	n/a	n/a
22	BACH1	chr12:118498020-118498596	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr12:118502351-118502604	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr12:118473076-118473306	K562	blood:	n/a	n/a
25	BACH1	chr12:118474123-118474283	K562	blood:	n/a	n/a
26	BATF	chr12:118473262-118473834	GM12878	blood:	n/a	n/a
27	BATF	chr12:118483507-118483791	GM12878	blood:	n/a	n/a
28	BATF	chr12:118473296-118473787	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:118473258-118473762	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:118473277-118473693	GM12878	blood:	n/a	n/a
31	BCL3	chr12:118467211-118467856	A549	lung:	n/a	n/a
32	BCL3	chr12:118489996-118490828	A549	lung:	n/a	n/a
33	BCL3	chr12:118471079-118473039	A549	lung:	n/a	n/a
34	BCL3	chr12:118473291-118473733	GM12878	blood:	n/a	n/a
35	BCL3	chr12:118489948-118491002	A549	lung:	n/a	n/a
36	BCL3	chr12:118499702-118500613	A549	lung:	n/a	n/a
37	BCLAF1	chr12:118492872-118493299	GM12878	blood:	n/a	n/a
38	BCLAF1	chr12:118473201-118473873	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:118492868-118493239	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:118473106-118473812	GM12878	blood:	n/a	n/a
41	BHLHE40	chr12:118498174-118498393	GM12878	blood:	n/a	n/a
42	BHLHE40	chr12:118500641-118500651	K562	blood:	n/a	n/a
43	BHLHE40	chr12:118489991-118490868	HepG2	liver:	n/a	n/a
44	BHLHE40	chr12:118493924-118493964	A549	lung:	n/a	n/a
45	BHLHE40	chr12:118498816-118499605	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:118498966-118499934	K562	blood:	n/a	n/a
47	BHLHE40	chr12:118473198-118473736	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:118500147-118500351	K562	blood:	n/a	n/a
49	BRCA1	chr12:118499462-118499467	GM12878	blood:	n/a	n/a
50	BRCA1	chr12:118472528-118472861	Hela-S3	cervix:	n/a	n/a

(count:1101 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:118500931-118500981	GM12892	blood:	n/a
2	chr12:118501232-118501282	Hepatocyte	liver:	n/a
3	chr12:118498668-118498718	GM19239	blood:	n/a
4	chr12:118500931-118500981	GM12892	blood:	n/a
5	chr12:118501232-118501282	Hepatocyte	liver:	n/a
6	chr12:118498668-118498718	GM19239	blood:	n/a
7	chr12:118500439-118500489	HL-60	blood:	n/a
8	chr12:118502338-118502388	GM19239	blood:	n/a
9	chr12:118499723-118499773	SK-N-MC	brain:	n/a
10	chr12:118480689-118480739	U87	brain:	n/a
11	chr12:118480739-118480789	HCT-116	colon:	n/a
12	chr12:118480739-118480789	NT2-D1	testis:	n/a
13	chr12:118500366-118500416	U87	brain:	n/a
14	chr12:118500439-118500489	HCF	heart:	n/a
15	chr12:118500366-118500416	LNCaP	prostate:	n/a
16	chr12:118499723-118499773	Hepatocyte	liver:	n/a
17	chr12:118480689-118480739	HAEpiC	amniotic membrane:	n/a
18	chr12:118501232-118501282	A549	lung:	n/a
19	chr12:118502338-118502388	HRE	kidney:	n/a
20	chr12:118500481-118500531	Hepatocyte	liver:	n/a
21	chr12:118480689-118480739	NHDF-neo	bronchial:	n/a
22	chr12:118499723-118499773	HRE	kidney:	n/a
23	chr12:118469768-118469818	HEEpiC	esophagus:	n/a
24	chr12:118500481-118500531	K562	blood:	n/a
25	chr12:118480689-118480739	NH-A	brain:	n/a
26	chr12:118477739-118477789	SAEC	small airway:	n/a
27	chr12:118499723-118499773	HCF	heart:	n/a
28	chr12:118500439-118500489	U87	brain:	n/a
29	chr12:118498675-118498725	MCF-7	breast:	n/a
30	chr12:118499723-118499773	NH-A	brain:	n/a
31	chr12:118499294-118499344	GM06990	blood:	n/a
32	chr12:118490276-118490326	NHBE	bronchial:	n/a
33	chr12:118499723-118499773	AoSMC	blood vessel:	n/a
34	chr12:118496434-118496484	HEEpiC	esophagus:	n/a
35	chr12:118498675-118498725	AG09309	skin:	n/a
36	chr12:118480739-118480789	U87	brain:	n/a
37	chr12:118500931-118500981	HepG2	liver:	n/a
38	chr12:118480689-118480739	ECC-1	luminal epithelium:	n/a
39	chr12:118480689-118480739	NHBE	bronchial:	n/a
40	chr12:118498668-118498718	GM06990	blood:	n/a
41	chr12:118469768-118469818	PrEC	prostate:	n/a
42	chr12:118490276-118490326	PANC-1	pancreas:	n/a
43	chr12:118500439-118500489	AoSMC	blood vessel:	n/a
44	chr12:118471960-118472010	HIPEpiC	eye:	n/a
45	chr12:118469768-118469818	GM12891	blood:	n/a
46	chr12:118499016-118499066	Caco-2	colon:	n/a
47	chr12:118480689-118480739	GM06990	blood:	n/a
48	chr12:118498668-118498718	AG09309	skin:	n/a
49	chr12:118501232-118501282	NB4	blood:	n/a
50	chr12:118490276-118490326	ovcar-3	ovarian:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:118498416..118504096-chr12:118537510..118543393,12	MCF-7	breast:
2	chr12:118499112..118499998-chr19:39902716..39903531,2	Hela-S3	cervix:
3	chr12:118312176..118313250-chr12:118492556..118493512,4	MCF-7	breast:
4	chr12:118491454..118494389-chr12:118600464..118603193,2	K562	blood:
5	chr12:118490377..118492216-chr12:118538475..118541095,2	MCF-7	breast:
6	chr12:118453400..118456332-chr12:118472162..118475770,4	K562	blood:
7	chr12:118478606..118480507-chr12:118486585..118488668,2	MCF-7	breast:
8	chr12:118472870..118474634-chr12:118475907..118478389,3	MCF-7	breast:
9	chr12:118467348..118470593-chr12:118472066..118473708,3	K562	blood:
10	chr12:118496436..118502396-chr12:118572063..118576805,10	MCF-7	breast:
11	chr12:118312320..118313517-chr12:118471942..118473668,17	MCF-7	breast:
12	chr12:118453440..118456018-chr12:118464200..118466334,2	MCF-7	breast:
13	chr12:118499217..118500774-chr12:118572851..118574591,2	MCF-7	breast:
14	chr12:118499092..118500000-chr6:30524301..30524884,2	Hela-S3	cervix:
15	chr12:118497611..118502023-chr12:118502151..118506801,7	MCF-7	breast:
16	chr12:118481150..118484033-chr12:118491704..118494262,2	K562	blood:
17	chr12:118481881..118483634-chr12:118588470..118590195,2	MCF-7	breast:
18	chr12:118503064..118505027-chr12:118506701..118508410,2	K562	blood:
19	chr12:118480642..118483852-chr12:118489666..118492317,3	K562	blood:
20	chr12:118500316..118502003-chr12:118542187..118545128,2	K562	blood:
21	chr12:118492599..118494701-chr12:118539022..118541742,2	MCF-7	breast:
22	chr12:118472870..118474634-chr12:118475907..118478389,3	MCF-7	breast:
23	chr12:118492994..118495394-chr12:118535946..118537983,2	MCF-7	breast:
24	chr12:118474167..118477019-chr12:118493239..118495940,2	MCF-7	breast:
25	chr12:118500895..118502503-chr12:118521704..118523739,2	K562	blood:
26	chr12:118469263..118471312-chr12:118478732..118480814,2	K562	blood:
27	chr11:65193091..65193924-chr12:118499181..118499883,2	Hela-S3	cervix:
28	chr12:118471552..118474946-chr12:118497683..118501709,5	MCF-7	breast:
29	chr12:118504697..118507371-chr12:118539472..118541470,2	MCF-7	breast:
30	chr12:118466683..118468213-chr12:118492761..118494413,2	K562	blood:
31	chr12:118496924..118498642-chr12:118498871..118500606,2	MCF-7	breast:
32	chr12:118453669..118455926-chr12:118502791..118505038,2	K562	blood:
33	chr12:118464460..118467329-chr12:118470748..118473473,2	MCF-7	breast:
34	chr12:118498692..118501195-chr12:118558625..118560440,2	MCF-7	breast:
35	chr12:118453221..118454913-chr12:118470349..118472863,2	MCF-7	breast:
36	chr12:118498119..118500024-chr12:118572981..118575568,2	K562	blood:
37	chr12:118405716..118409105-chr12:118489157..118492188,4	MCF-7	breast:
38	chr12:118492843..118495653-chr12:118505555..118507815,2	MCF-7	breast:
39	chr12:118475337..118478280-chr12:118499969..118502242,2	MCF-7	breast:
40	chr12:118503851..118505896-chr12:118506182..118508939,2	MCF-7	breast:
41	chr12:118499104..118499911-chr2:28614266..28615159,2	Hela-S3	cervix:
42	chr12:118456855..118459232-chr12:118466766..118469608,2	MCF-7	breast:
43	chr12:118476730..118480005-chr12:118496581..118498795,3	K562	blood:
44	chr12:118455151..118457113-chr12:118475615..118477971,2	MCF-7	breast:
45	chr12:118500782..118503248-chr12:118527475..118529536,2	K562	blood:
46	chr12:118470972..118472591-chr12:118485266..118487581,2	MCF-7	breast:
47	chr12:118321239..118322907-chr12:118502124..118504651,2	MCF-7	breast:
48	chr12:118466683..118468213-chr12:118492761..118494413,2	K562	blood:
49	chr12:118453491..118456024-chr12:118464128..118465788,2	MCF-7	breast:
50	chr12:118309128..118310740-chr12:118467939..118469710,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WSB2-3	chr12:118475736-118475833	ucscGeneNc_uc001txf_2

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RFC5	hsa-miR-339-5p	chr12:118469368-118469391
2	WSB2	hsa-miR-29c-3p	chr12:118472755-118472773

Variant related genes	Relation type
RFC5	TF binding region
WSB2	TF binding region
RFC5	CpG island
WSB2	CpG island
ENSG00000099250	chromatin interactions
ENSG00000176834	chromatin interactions
ENSG00000111445	chromatin interactions
ENSG00000090924	chromatin interactions
ENSG00000176871	chromatin interactions
ENSG00000089220	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000270066	chromatin interactions
ENSG00000204576	chromatin interactions
ENSG00000149257	chromatin interactions
ENSG00000171435	chromatin interactions

Extended variants
information (count: 1634 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1634 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5745861	chr12:118463329-118463330	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564319981	chr12:118463341-118463342	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs5745862	chr12:118463345-118463346	Strong transcription Weak transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs116657671	chr12:118463407-118463408	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs146434725	chr12:118463448-118463449	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs560582949	chr12:118463455-118463456	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529594799	chr12:118463483-118463484	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs368835750	chr12:118463509-118463510	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs548972381	chr12:118463511-118463512	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs562485601	chr12:118463573-118463574	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs531411039	chr12:118463585-118463586	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs372715527	chr12:118463591-118463592	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs374371013	chr12:118463608-118463609	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs368314339	chr12:118463624-118463625	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs76791598	chr12:118463652-118463653	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs75027009	chr12:118463656-118463657	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs75666760	chr12:118463657-118463658	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78224863	chr12:118463672-118463673	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs551546916	chr12:118463687-118463688	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571411174	chr12:118463706-118463707	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368137976	chr12:118463714-118463715	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547570083	chr12:118463757-118463758	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs374441931	chr12:118463761-118463762	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs567417611	chr12:118463796-118463797	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs563260998	chr12:118463804-118463805	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs536154617	chr12:118463835-118463836	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs555327717	chr12:118463845-118463846	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs575265376	chr12:118463908-118463909	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537948990	chr12:118464000-118464001	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs5745863	chr12:118464010-118464011	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs578056744	chr12:118464037-118464038	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs5745864	chr12:118464038-118464039	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs560761271	chr12:118464080-118464081	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs574218701	chr12:118464085-118464086	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs181021914	chr12:118464150-118464151	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs528926944	chr12:118464171-118464172	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs543343025	chr12:118464172-118464173	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs186155931	chr12:118464174-118464175	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs5745865	chr12:118464183-118464184	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs5745866	chr12:118464199-118464200	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs5745867	chr12:118464263-118464264	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs571833946	chr12:118464269-118464270	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530874480	chr12:118464270-118464271	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs191877250	chr12:118464281-118464282	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs140704217	chr12:118464322-118464323	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs567098218	chr12:118464348-118464349	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs184070236	chr12:118464404-118464405	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566377434	chr12:118464411-118464412	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550688929	chr12:118464426-118464427	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs111325163	chr12:118464459-118464460	Strong transcription Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2007 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118455200-118472800	Weak transcription	Right Atrium	heart
2	chr12:118455200-118497400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr12:118455600-118490200	Strong transcription	Fetal Muscle Trunk	muscle
4	chr12:118455800-118463800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr12:118455800-118469600	Weak transcription	Fetal Brain Male	brain
6	chr12:118455800-118471800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr12:118455800-118476000	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr12:118455800-118485000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr12:118455800-118490000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:118456000-118478000	Weak transcription	Fetal Heart	heart
11	chr12:118456000-118482800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
12	chr12:118456000-118484600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
13	chr12:118456000-118490200	Strong transcription	Fetal Stomach	stomach
14	chr12:118456200-118471000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr12:118456200-118472400	Strong transcription	A549	lung
16	chr12:118456200-118484000	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr12:118456200-118484200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr12:118456200-118484600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr12:118456200-118490000	Strong transcription	Fetal Muscle Leg	muscle
20	chr12:118456200-118490200	Strong transcription	HUES64 Cell Line	embryonic stem cell
21	chr12:118456200-118490400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr12:118456400-118472200	Weak transcription	Stomach Mucosa	stomach
23	chr12:118456400-118489800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr12:118456400-118491000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr12:118456600-118477400	Strong transcription	Fetal Thymus	thymus
26	chr12:118456600-118482800	Strong transcription	Primary T cells from cord blood	blood
27	chr12:118456600-118489800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr12:118456800-118471800	Strong transcription	Liver	Liver
29	chr12:118456800-118473000	Strong transcription	Primary B cells from peripheral blood	blood
30	chr12:118456800-118474400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr12:118456800-118482000	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr12:118456800-118484000	Strong transcription	Stomach Smooth Muscle	stomach
33	chr12:118456800-118489400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr12:118456800-118489800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr12:118457000-118465200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr12:118457000-118465600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr12:118457000-118466000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr12:118457000-118472800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr12:118457000-118482600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr12:118457000-118482800	Strong transcription	Primary neutrophils fromperipheralblood	blood
41	chr12:118457000-118482800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr12:118457000-118484600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr12:118457000-118488200	Strong transcription	Primary T cells fromperipheralblood	blood
44	chr12:118457000-118489600	Strong transcription	Duodenum Mucosa	Duodenum
45	chr12:118457200-118465200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr12:118457200-118465200	Strong transcription	Ovary	ovary
47	chr12:118457200-118483000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr12:118457200-118491400	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr12:118457400-118465200	Strong transcription	Fetal Intestine Small	intestine
50	chr12:118457400-118465200	Strong transcription	NHEK	skin

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