Variant report

Variant	nsv1048801
Chromosome Location	chr12:121695522-121761800
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1334)
CpG islands
(count:1771)
Chromatin interactive
region (count:79)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1334 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr12:121704105-121704314	K562	blood:	n/a	n/a
2	ATF2	chr12:121695443-121695867	GM12878	blood:	n/a	n/a
3	ATF2	chr12:121695530-121695816	GM12878	blood:	n/a	n/a
4	ATF2	chr12:121714720-121715269	GM12878	blood:	n/a	n/a
5	BACH1	chr12:121754034-121754383	K562	blood:	n/a	n/a
6	BACH1	chr12:121734250-121734410	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr12:121734864-121735087	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr12:121754001-121754387	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr12:121714886-121715159	GM12878	blood:	n/a	n/a
10	BATF	chr12:121714789-121715143	GM12878	blood:	n/a	n/a
11	BCL11A	chr12:121714810-121715205	GM12878	blood:	n/a	chr12:121714977-121714986 chr12:121714951-121714960
12	BCL11A	chr12:121697017-121697244	GM12878	blood:	n/a	n/a
13	BCL11A	chr12:121714869-121715070	GM12878	blood:	n/a	chr12:121714977-121714986 chr12:121714951-121714960
14	BCL3	chr12:121714797-121715068	GM12878	blood:	n/a	chr12:121714977-121714986 chr12:121714951-121714960
15	BCL3	chr12:121734660-121735055	A549	lung:	n/a	chr12:121734899-121734912
16	BCLAF1	chr12:121695445-121695888	GM12878	blood:	n/a	n/a
17	BCLAF1	chr12:121734655-121734991	GM12878	blood:	n/a	chr12:121734899-121734912
18	BHLHE40	chr12:121720761-121720923	K562	blood:	n/a	n/a
19	BHLHE40	chr12:121733894-121733896	GM12878	blood:	n/a	n/a
20	BHLHE40	chr12:121734233-121734261	K562	blood:	n/a	n/a
21	BHLHE40	chr12:121733157-121733267	GM12878	blood:	n/a	n/a
22	BHLHE40	chr12:121734675-121735006	GM12878	blood:	n/a	n/a
23	BHLHE40	chr12:121695489-121696026	GM12878	blood:	n/a	n/a
24	BHLHE40	chr12:121734705-121735503	K562	blood:	n/a	chr12:121735073-121735089
25	BHLHE40	chr12:121714798-121715132	A549	lung:	n/a	n/a
26	BHLHE40	chr12:121761784-121762038	GM12878	blood:	n/a	n/a
27	BHLHE40	chr12:121696926-121697304	GM12878	blood:	n/a	n/a
28	BHLHE40	chr12:121714752-121715341	GM12878	blood:	n/a	n/a
29	BHLHE40	chr12:121734236-121734429	GM12878	blood:	n/a	n/a
30	BRCA1	chr12:121734756-121735065	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr12:121734856-121734938	HepG2	liver:	n/a	n/a
32	CBX3	chr12:121733529-121734074	K562	blood:	n/a	n/a
33	CBX3	chr12:121735240-121735717	K562	blood:	n/a	n/a
34	CBX3	chr12:121734599-121735069	K562	blood:	n/a	n/a
35	CCNT2	chr12:121734016-121735180	K562	blood:	n/a	chr12:121734720-121734729
36	CCNT2	chr12:121720822-121721111	K562	blood:	n/a	n/a
37	CCNT2	chr12:121704193-121704397	K562	blood:	n/a	n/a
38	CEBPB	chr12:121754813-121755135	K562	blood:	n/a	chr12:121754972-121754983
39	CEBPB	chr12:121720429-121720641	K562	blood:	n/a	n/a
40	CEBPB	chr12:121754844-121755101	Hela-S3	cervix:	n/a	chr12:121754972-121754983
41	CEBPB	chr12:121714745-121715214	IMR90	lung:	n/a	n/a
42	CEBPB	chr12:121734660-121734916	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr12:121714736-121715150	A549	lung:	n/a	n/a
44	CEBPB	chr12:121714704-121715269	A549	lung:	n/a	n/a
45	CEBPB	chr12:121704926-121705401	K562	blood:	n/a	chr12:121705264-121705275
46	CEBPB	chr12:121752355-121752502	A549	lung:	n/a	chr12:121752455-121752466
47	CEBPB	chr12:121742997-121743132	K562	blood:	n/a	n/a
48	CEBPB	chr12:121703709-121704315	K562	blood:	n/a	n/a
49	CEBPB	chr12:121714778-121715205	A549	lung:	n/a	n/a
50	CEBPB	chr12:121752389-121752541	K562	blood:	n/a	chr12:121752455-121752466

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:121735363-121735413	H1-hESC	embryonic stem cell:	embryo
2	chr12:121717886-121717936	PFSK-1	brain:	n/a
3	chr12:121735363-121735413	H1-hESC	embryonic stem cell:	embryo
4	chr12:121717886-121717936	PFSK-1	brain:	n/a
5	chr12:121738449-121738499	HNPCEpiC	eye:	n/a
6	chr12:121735583-121735633	K562	blood:	n/a
7	chr12:121714889-121714939	MCF-7	breast:	n/a
8	chr12:121719066-121719116	HL-60	blood:	n/a
9	chr12:121712161-121712211	GM12892	blood:	n/a
10	chr12:121717737-121717787	Hepatocyte	liver:	n/a
11	chr12:121717737-121717787	NHDF-neo	bronchial:	n/a
12	chr12:121735396-121735446	AG09309	skin:	n/a
13	chr12:121718499-121718549	BE2_C	brain:	n/a
14	chr12:121711996-121712046	Hepatocyte	liver:	n/a
15	chr12:121712101-121712151	AG09319	gingival:	n/a
16	chr12:121710771-121710821	AG09309	skin:	n/a
17	chr12:121718499-121718549	ECC-1	luminal epithelium:	n/a
18	chr12:121735583-121735633	MCF-7	breast:	n/a
19	chr12:121735002-121735052	AG09309	skin:	n/a
20	chr12:121708654-121708704	NH-A	brain:	n/a
21	chr12:121712161-121712211	HCT-116	colon:	n/a
22	chr12:121735631-121735681	AG09319	gingival:	n/a
23	chr12:121708654-121708704	HEK293	kidney:	embryo
24	chr12:121734046-121734096	HCT-116	colon:	n/a
25	chr12:121734283-121734333	GM12892	blood:	n/a
26	chr12:121738449-121738499	SK-N-SH_RA	brain:	n/a
27	chr12:121736579-121736629	AoSMC	blood vessel:	n/a
28	chr12:121708654-121708704	ProgFib	skin:	n/a
29	chr12:121711847-121711897	HRCEpiC	kidney:	n/a
30	chr12:121733425-121733475	GM12891	blood:	n/a
31	chr12:121710771-121710821	HAEpiC	amniotic membrane:	n/a
32	chr12:121731226-121731276	SK-N-SH_RA	brain:	n/a
33	chr12:121718499-121718549	GM12891	blood:	n/a
34	chr12:121712245-121712295	AoSMC	blood vessel:	n/a
35	chr12:121738449-121738499	BJ	skin:	n/a
36	chr12:121734283-121734333	SKMC	muscle:	n/a
37	chr12:121712101-121712151	HEK293	kidney:	embryo
38	chr12:121719066-121719116	SK-N-SH	brain:	n/a
39	chr12:121714889-121714939	PANC-1	pancreas:	n/a
40	chr12:121711996-121712046	SK-N-SH_RA	brain:	n/a
41	chr12:121726240-121726290	T-47D	breast:	n/a
42	chr12:121719066-121719116	SAEC	small airway:	n/a
43	chr12:121735111-121735161	HCM	heart:	n/a
44	chr12:121708654-121708704	U87	brain:	n/a
45	chr12:121717886-121717936	ECC-1	luminal epithelium:	n/a
46	chr12:121718556-121718606	Caco-2	colon:	n/a
47	chr12:121735002-121735052	U87	brain:	n/a
48	chr12:121717737-121717787	GM12878	blood:	n/a
49	chr12:121726240-121726290	NH-A	brain:	n/a
50	chr12:121736579-121736629	PrEC	prostate:	n/a

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:121706801..121708995-chr12:121713234..121716382,3	MCF-7	breast:
2	chr12:121719593..121722706-chr12:121731899..121734872,4	K562	blood:
3	chr12:121736650..121739500-chr12:121740653..121743814,3	K562	blood:
4	chr12:121730096..121733083-chr12:121733229..121736419,3	K562	blood:
5	chr12:121713150..121717520-chr12:121730584..121734759,5	MCF-7	breast:
6	chr12:121716004..121718724-chr12:121719656..121721765,2	MCF-7	breast:
7	chr12:121733917..121734896-chr3:73159620..73160572,2	Hela-S3	cervix:
8	chr12:121746148..121747954-chr12:121790384..121792128,2	MCF-7	breast:
9	chr12:121755349..121757773-chr12:121759474..121762443,2	K562	blood:
10	chr12:121733327..121735828-chr12:121789056..121791412,2	MCF-7	breast:
11	chr12:121734916..121736998-chr12:121837533..121840449,2	MCF-7	breast:
12	chr12:121734016..121734526-chr5:176853560..176854122,2	Hela-S3	cervix:
13	chr12:121701879..121704227-chr12:121836701..121839231,2	MCF-7	breast:
14	chr12:121701635..121704379-chr12:121730216..121732499,2	MCF-7	breast:
15	chr12:121730283..121732631-chr12:121741118..121743378,2	MCF-7	breast:
16	chr12:121737101..121740224-chr12:121740653..121743951,4	K562	blood:
17	chr12:121708573..121710146-chr12:121731716..121734639,2	MCF-7	breast:
18	chr12:121731746..121734589-chr12:121836434..121839785,3	K562	blood:
19	chr12:121702788..121704693-chr12:121708345..121710619,2	MCF-7	breast:
20	chr12:121732992..121736295-chr12:121738254..121741705,3	MCF-7	breast:
21	chr12:121713637..121715499-chr12:121719759..121721908,2	MCF-7	breast:
22	chr12:121740867..121743563-chr12:121749932..121751434,2	K562	blood:
23	chr12:121742230..121744210-chr12:121746039..121747596,2	K562	blood:
24	chr12:121733110..121736069-chr3:81809721..81812341,2	MCF-7	breast:
25	chr12:121696462..121699185-chr12:121732816..121735056,2	MCF-7	breast:
26	chr12:121734467..121737087-chr12:121737229..121740129,2	MCF-7	breast:
27	chr12:121731746..121735132-chr12:121837281..121839785,4	K562	blood:
28	chr12:121731476..121733834-chr12:121779944..121781697,2	MCF-7	breast:
29	chr12:121733351..121735289-chr12:121789720..121791843,2	MCF-7	breast:
30	chr12:121734311..121735951-chr12:121758693..121760511,2	MCF-7	breast:
31	chr12:121737101..121740224-chr12:121740653..121743951,4	K562	blood:
32	chr12:121735315..121736924-chr12:121836977..121839840,2	K562	blood:
33	chr12:121742230..121744210-chr12:121746039..121747596,2	K562	blood:
34	chr12:121711495..121713766-chr12:121715448..121718429,2	MCF-7	breast:
35	chr12:121698437..121700965-chr12:121702669..121704736,2	K562	blood:
36	chr12:121721312..121723711-chr12:121725911..121728567,2	K562	blood:
37	chr12:121734311..121735951-chr12:121758693..121760511,2	MCF-7	breast:
38	chr12:121732846..121736440-chr12:121741046..121746496,5	MCF-7	breast:
39	chr12:121684993..121686828-chr12:121732453..121734188,2	K562	blood:
40	chr12:121734919..121737060-chr12:121743764..121745994,2	K562	blood:
41	chr12:121711232..121712807-chr12:121712826..121714423,2	MCF-7	breast:
42	chr12:121706801..121708995-chr12:121713234..121716382,3	MCF-7	breast:
43	chr12:121647374..121649276-chr12:121733272..121735230,2	K562	blood:
44	chr12:121723906..121727301-chr12:121738225..121741362,3	K562	blood:
45	chr12:121745234..121747818-chr12:121905283..121907102,2	MCF-7	breast:
46	chr12:121752880..121755223-chr12:121756738..121758316,2	K562	blood:
47	chr12:121745242..121747818-chr12:121788534..121790623,2	MCF-7	breast:
48	chr12:121739937..121742219-chr12:121783011..121784714,2	K562	blood:
49	chr12:121732234..121734700-chr12:121788857..121790730,2	K562	blood:
50	chr12:121721312..121723711-chr12:121725911..121728567,2	K562	blood:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	ANAPC5	hsa-miR-93-5p	chr12:121755888-121755913

Variant related genes	Relation type
CAMKK2	TF binding region
ANAPC5	TF binding region
CAMKK2	CpG island
ANAPC5	CpG island
ENSG00000100519	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000170633	chromatin interactions
ENSG00000167740	chromatin interactions
ENSG00000135124	chromatin interactions
ENSG00000114480	chromatin interactions
ENSG00000110931	chromatin interactions
ENSG00000089053	chromatin interactions
ENSG00000198055	chromatin interactions

Extended variants
information (count: 2669 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:2669 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2686346	chr12:121695522-121695523	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs202087371	chr12:121695526-121695527	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546538216	chr12:121695578-121695579	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545290316	chr12:121695595-121695596	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192675729	chr12:121695620-121695621	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374961325	chr12:121695662-121695663	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs184808500	chr12:121695670-121695671	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187739581	chr12:121695721-121695722	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147401446	chr12:121695746-121695747	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529835818	chr12:121695781-121695782	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs5801429	chr12:121695826-121695827	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139631648	chr12:121695891-121695892	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145144278	chr12:121695897-121695898	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527549020	chr12:121695911-121695912	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192249553	chr12:121695987-121695988	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs570708958	chr12:121696047-121696048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs533343821	chr12:121696071-121696072	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531777706	chr12:121696112-121696113	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs59139671	chr12:121696150-121696151	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs568574124	chr12:121696174-121696175	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150524987	chr12:121696177-121696178	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554377110	chr12:121696179-121696180	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs568173011	chr12:121696245-121696246	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566289369	chr12:121696293-121696294	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs540094471	chr12:121696339-121696340	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563766187	chr12:121696363-121696364	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558478524	chr12:121696427-121696428	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs139463893	chr12:121696428-121696429	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368758412	chr12:121696460-121696461	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184363270	chr12:121696462-121696463	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs190047445	chr12:121696475-121696476	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs574448138	chr12:121696478-121696479	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs181349252	chr12:121696514-121696515	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs541541864	chr12:121696538-121696539	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184737115	chr12:121696596-121696597	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs529350150	chr12:121696607-121696608	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs189309221	chr12:121696614-121696615	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537080430	chr12:121696644-121696645	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572824324	chr12:121696646-121696647	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs63519464	chr12:121696665-121696666	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs113592759	chr12:121696677-121696678	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs11065512	chr12:121696686-121696687	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs180783615	chr12:121696694-121696695	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1808636	chr12:121696707-121696708	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs531591638	chr12:121696711-121696712	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs527534597	chr12:121696731-121696732	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566237563	chr12:121696771-121696772	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149214034	chr12:121696777-121696778	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs186566114	chr12:121696781-121696782	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs547917755	chr12:121696802-121696803	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	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
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Beckwith-Wiedemann syndrome	20648245	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2742 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121653200-121698800	Weak transcription	Fetal Heart	heart
2	chr12:121674600-121704200	Strong transcription	Brain Germinal Matrix	brain
3	chr12:121677400-121695600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr12:121677400-121717000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr12:121677400-121717200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr12:121679000-121713000	Strong transcription	Fetal Intestine Large	intestine
7	chr12:121679200-121709200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr12:121679200-121714400	Weak transcription	Right Atrium	heart
9	chr12:121679400-121699000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr12:121679400-121713800	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr12:121679600-121708800	Strong transcription	Fetal Muscle Leg	muscle
12	chr12:121679600-121709200	Strong transcription	Stomach Smooth Muscle	stomach
13	chr12:121679600-121713000	Strong transcription	Liver	Liver
14	chr12:121679600-121732600	Strong transcription	Fetal Intestine Small	intestine
15	chr12:121679800-121703200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr12:121679800-121709000	Strong transcription	Fetal Muscle Trunk	muscle
17	chr12:121679800-121713000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
18	chr12:121679800-121713600	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr12:121680000-121709800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr12:121680800-121713800	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr12:121681000-121709000	Strong transcription	Adipose Nuclei	Adipose
22	chr12:121681000-121712600	Strong transcription	Duodenum Mucosa	Duodenum
23	chr12:121681200-121706400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr12:121681200-121708800	Strong transcription	HUES6 Cell Line	embryonic stem cell
25	chr12:121681200-121708800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr12:121681200-121708800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr12:121681200-121713600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr12:121681200-121717800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr12:121681400-121708800	Strong transcription	Sigmoid Colon	Sigmoid Colon
30	chr12:121684600-121696000	Strong transcription	Duodenum Smooth Muscle	Duodenum
31	chr12:121684800-121699800	Strong transcription	Ovary	ovary
32	chr12:121684800-121704200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr12:121684800-121711800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:121685000-121696000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:121685000-121699800	Strong transcription	Primary T cells from cord blood	blood
36	chr12:121685000-121701600	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr12:121685200-121712400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr12:121686200-121707400	Strong transcription	Rectal Mucosa Donor 31	rectum
39	chr12:121687400-121696600	Weak transcription	Small Intestine	intestine
40	chr12:121688400-121733000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr12:121688600-121697600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:121689000-121713000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr12:121689200-121717000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr12:121689400-121696000	Weak transcription	Hela-S3	cervix
45	chr12:121690200-121700200	Strong transcription	Fetal Brain Female	brain
46	chr12:121690400-121703000	Strong transcription	Brain Angular Gyrus	brain
47	chr12:121690400-121704400	Strong transcription	Placenta	Placenta
48	chr12:121690800-121714200	Strong transcription	Fetal Stomach	stomach
49	chr12:121691000-121706400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr12:121691200-121699200	Weak transcription	Stomach Mucosa	stomach

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