Variant report

Variant	nsv560491
Chromosome Location	chr12:123425575-123444422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:931)
CpG islands
(count:367)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:931 , 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	chr12:123427273-123427515	HepG2	liver:	n/a	n/a
2	ATF2	chr12:123431295-123431816	GM12878	blood:	n/a	n/a
3	ATF2	chr12:123431351-123431654	GM12878	blood:	n/a	n/a
4	BACH1	chr12:123431100-123431159	K562	blood:	n/a	n/a
5	BACH1	chr12:123427461-123427485	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr12:123436523-123437162	GM12878	blood:	n/a	n/a
7	BATF	chr12:123435931-123436247	GM12878	blood:	n/a	n/a
8	BATF	chr12:123431397-123431751	GM12878	blood:	n/a	n/a
9	BCL3	chr12:123436632-123437430	A549	lung:	n/a	n/a
10	BCL3	chr12:123431388-123431819	GM12878	blood:	n/a	n/a
11	BCLAF1	chr12:123436733-123437270	GM12878	blood:	n/a	n/a
12	BCLAF1	chr12:123431231-123431826	GM12878	blood:	n/a	n/a
13	BHLHE40	chr12:123431325-123431713	K562	blood:	n/a	n/a
14	BHLHE40	chr12:123436905-123437190	K562	blood:	n/a	n/a
15	BHLHE40	chr12:123431353-123431611	A549	lung:	n/a	n/a
16	BHLHE40	chr12:123427179-123427377	HepG2	liver:	n/a	n/a
17	BHLHE40	chr12:123431252-123431717	GM12878	blood:	n/a	n/a
18	BHLHE40	chr12:123431326-123431710	HepG2	liver:	n/a	n/a
19	BRCA1	chr12:123436907-123437226	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr12:123431258-123431672	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr12:123431287-123431691	K562	blood:	n/a	n/a
22	CBX3	chr12:123431076-123431795	HCT-116	colon:	n/a	n/a
23	CBX3	chr12:123427159-123427581	K562	blood:	n/a	n/a
24	CBX3	chr12:123436753-123437299	K562	blood:	n/a	n/a
25	CCNT2	chr12:123431351-123431892	K562	blood:	n/a	chr12:123431779-123431788
26	CEBPB	chr12:123431149-123431921	IMR90	lung:	n/a	chr12:123431294-123431307 chr12:123431295-123431306
27	CEBPB	chr12:123431731-123431806	HepG2	liver:	n/a	n/a
28	CEBPB	chr12:123425846-123426202	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr12:123436044-123436144	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr12:123431077-123431546	MCF-7	breast:	n/a	chr12:123431294-123431307 chr12:123431295-123431306
31	CEBPB	chr12:123436082-123436137	A549	lung:	n/a	n/a
32	CEBPB	chr12:123431202-123431397	K562	blood:	n/a	chr12:123431294-123431307 chr12:123431295-123431306
33	CEBPB	chr12:123431158-123431492	HepG2	liver:	n/a	chr12:123431294-123431307 chr12:123431295-123431306
34	CEBPB	chr12:123427062-123427411	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr12:123431230-123431816	GM12878	blood:	n/a	chr12:123431294-123431307 chr12:123431295-123431306
36	CEBPB	chr12:123431024-123431740	Hela-S3	cervix:	n/a	chr12:123431294-123431307 chr12:123431295-123431306
37	CEBPB	chr12:123436877-123437197	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr12:123436912-123437197	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr12:123431300-123431730	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr12:123436926-123437143	A549	lung:	n/a	n/a
41	CREB1	chr12:123431277-123431719	A549	lung:	n/a	n/a
42	CTCF	chr12:123432220-123432370	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr12:123431320-123431470	AG04450	lung:	n/a	n/a
44	CTCF	chr12:123431320-123431470	HBMEC	blood vessel:	n/a	n/a
45	CTCF	chr12:123436960-123437110	HMF	breast:	n/a	chr12:123437050-123437071 chr12:123437033-123437051 chr12:123437035-123437048 chr12:123437028-123437049
46	CTCF	chr12:123431343-123431488	MCF-7	breast:	n/a	n/a
47	CTCF	chr12:123432201-123432280	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr12:123431340-123431490	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr12:123436980-123437130	HFF	foreskin:	n/a	chr12:123437050-123437071 chr12:123437033-123437051 chr12:123437035-123437048 chr12:123437028-123437049
50	CTCF	chr12:123436906-123437175	LNCaP	prostate:	n/a	chr12:123437050-123437071 chr12:123437033-123437051 chr12:123437035-123437048 chr12:123437028-123437049

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:123444284-123444334	MCF-7	breast:	n/a
2	chr12:123444284-123444334	MCF-7	breast:	n/a
3	chr12:123433185-123433235	Jurkat	blood:	n/a
4	chr12:123431865-123431915	SK-N-SH_RA	brain:	n/a
5	chr12:123444414-123444464	HCF	heart:	n/a
6	chr12:123430862-123430912	GM12892	blood:	n/a
7	chr12:123444414-123444464	HMEC	breast:	n/a
8	chr12:123431865-123431915	NB4	blood:	n/a
9	chr12:123444414-123444464	HEEpiC	esophagus:	n/a
10	chr12:123444414-123444464	NT2-D1	testis:	n/a
11	chr12:123444094-123444144	MCF10A-Er-Src	breast:	n/a
12	chr12:123433185-123433235	HCT-116	colon:	n/a
13	chr12:123430862-123430912	PrEC	prostate:	n/a
14	chr12:123444284-123444334	HCT-116	colon:	n/a
15	chr12:123444284-123444334	NHDF-neo	bronchial:	n/a
16	chr12:123433185-123433235	A549	lung:	n/a
17	chr12:123444094-123444144	HEEpiC	esophagus:	n/a
18	chr12:123431865-123431915	SK-N-MC	brain:	n/a
19	chr12:123431865-123431915	CMK	blood:	n/a
20	chr12:123444284-123444334	HEK293	kidney:	embryo
21	chr12:123431865-123431915	ProgFib	skin:	n/a
22	chr12:123431865-123431915	AG04449	skin:	fetal
23	chr12:123444414-123444464	HNPCEpiC	eye:	n/a
24	chr12:123444094-123444144	NB4	blood:	n/a
25	chr12:123431865-123431915	HRPEpiC	eye:	n/a
26	chr12:123430862-123430912	HEK293	kidney:	embryo
27	chr12:123431865-123431915	HAEpiC	amniotic membrane:	n/a
28	chr12:123444284-123444334	GM12878	blood:	n/a
29	chr12:123433185-123433235	ECC-1	luminal epithelium:	n/a
30	chr12:123444414-123444464	AG04450	lung:	fetal
31	chr12:123433185-123433235	CMK	blood:	n/a
32	chr12:123444094-123444144	HepG2	liver:	n/a
33	chr12:123444284-123444334	HMEC	breast:	n/a
34	chr12:123444284-123444334	GM12891	blood:	n/a
35	chr12:123431865-123431915	A549	lung:	n/a
36	chr12:123433185-123433235	Hela-S3	cervix:	n/a
37	chr12:123444094-123444144	HNPCEpiC	eye:	n/a
38	chr12:123430862-123430912	BJ	skin:	n/a
39	chr12:123430862-123430912	PFSK-1	brain:	n/a
40	chr12:123444284-123444334	IMR90	lung:	fetal
41	chr12:123444414-123444464	BE2_C	brain:	n/a
42	chr12:123430862-123430912	NT2-D1	testis:	n/a
43	chr12:123431865-123431915	IMR90	lung:	fetal
44	chr12:123444094-123444144	LNCaP	prostate:	n/a
45	chr12:123433185-123433235	ProgFib	skin:	n/a
46	chr12:123430862-123430912	HRE	kidney:	n/a
47	chr12:123444284-123444334	RPTEC	kidney:	n/a
48	chr12:123444284-123444334	HEEpiC	esophagus:	n/a
49	chr12:123433185-123433235	HPAEpiC	pulmonary alveolar:	n/a
50	chr12:123433185-123433235	NT2-D1	testis:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:123424761..123427438-chr12:123430033..123431700,2	K562	blood:
2	chr12:123366502..123367195-chr12:123436795..123437335,2	MCF-7	breast:
3	chr12:123277944..123278843-chr12:123436966..123437523,2	K562	blood:
4	chr12:123277865..123278865-chr12:123436617..123437472,2	MCF-7	breast:
5	chr12:123428831..123431560-chr12:123448558..123451555,2	K562	blood:
6	chr12:123318920..123320804-chr12:123431971..123434703,2	MCF-7	breast:
7	chr12:123349951..123350563-chr12:123436556..123437356,2	MCF-7	breast:
8	chr12:123348847..123350779-chr12:123438689..123440697,2	K562	blood:
9	chr12:123426745..123429433-chr12:123432536..123436941,4	K562	blood:
10	chr12:123344900..123345435-chr12:123431652..123432233,2	K562	blood:
11	chr12:123415535..123420026-chr12:123422545..123426280,4	K562	blood:
12	chr12:123430132..123431757-chr12:123435986..123437614,2	MCF-7	breast:
13	chr12:123235580..123237478-chr12:123432464..123434294,2	MCF-7	breast:
14	chr12:123344033..123345790-chr12:123436594..123437583,6	K562	blood:
15	chr12:123436582..123437364-chr12:123722407..123722993,2	MCF-7	breast:
16	chr12:123379526..123381919-chr12:123430934..123433003,2	MCF-7	breast:
17	chr12:123426745..123429433-chr12:123432536..123436941,4	K562	blood:
18	chr12:123343330..123344224-chr12:123436558..123437338,2	MCF-7	breast:
19	chr12:123443368..123448710-chr12:123448756..123452152,6	MCF-7	breast:
20	chr12:123351930..123352762-chr12:123436973..123437518,2	MCF-7	breast:
21	chr12:123442313..123444976-chr12:123717456..123719233,2	K562	blood:
22	chr12:123344434..123345913-chr12:123436269..123437707,10	MCF-7	breast:
23	chr12:123433587..123436454-chr12:123458977..123461529,2	K562	blood:
24	chr12:123341218..123343418-chr12:123435392..123437282,2	MCF-7	breast:
25	chr12:123344910..123345440-chr12:123436821..123437509,2	HCT-116	colon:
26	chr12:123365086..123366070-chr12:123436544..123437474,3	MCF-7	breast:
27	chr12:98896342..98897176-chr12:123436322..123436849,2	Hela-S3	cervix:
28	chr12:123427499..123429140-chr12:123435163..123436941,2	K562	blood:
29	chr12:123345450..123347445-chr12:123435441..123437142,2	K562	blood:
30	chr12:123344516..123345436-chr12:123436080..123437135,3	MCF-7	breast:
31	chr12:123434699..123436305-chr12:123439447..123441545,2	K562	blood:
32	chr12:123418526..123420273-chr12:123424780..123426394,2	K562	blood:
33	chr12:123354937..123357622-chr12:123439392..123442120,2	MCF-7	breast:
34	chr12:123436728..123438817-chr12:123451024..123452828,2	MCF-7	breast:
35	chr12:123352169..123352839-chr12:123436532..123437356,4	MCF-7	breast:
36	chr12:123424712..123426973-chr12:123428403..123431628,3	K562	blood:
37	chr12:123428831..123432471-chr12:123448558..123452277,3	K562	blood:
38	chr12:123342536..123343202-chr12:123436624..123437128,3	MCF-7	breast:

No data

Variant related genes	Relation type
ABCB9	TF binding region
ABCB9	CpG island
ENSG00000130921	chromatin interactions
ENSG00000150967	chromatin interactions
ENSG00000256152	chromatin interactions
ENSG00000111325	chromatin interactions
ENSG00000139726	chromatin interactions
ENSG00000130787	chromatin interactions
ENSG00000051825	chromatin interactions
ENSG00000139722	chromatin interactions
ENSG00000256028	chromatin interactions

Extended variants
information (count: 668 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4148866	chr12:123425575-123425576	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs376463598	chr12:123425580-123425581	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs555886541	chr12:123425583-123425584	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574157164	chr12:123425695-123425696	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs541325323	chr12:123425765-123425766	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs548307361	chr12:123425799-123425800	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577601605	chr12:123425852-123425853	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs77745126	chr12:123425857-123425858	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs386378025	chr12:123425858-123425859	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs77481491	chr12:123425859-123425860	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs386378026	chr12:123425874-123425875	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568215085	chr12:123425895-123425896	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs372883867	chr12:123425899-123425900	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545030295	chr12:123425913-123425914	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs369732200	chr12:123425918-123425919	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs143087795	chr12:123425942-123425943	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs144758767	chr12:123425957-123425958	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs190927685	chr12:123425959-123425960	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs202203025	chr12:123425979-123425980	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527926495	chr12:123426005-123426006	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561916952	chr12:123426018-123426019	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs7956760	chr12:123426038-123426039	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs547697501	chr12:123426252-123426253	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs530522529	chr12:123426311-123426312	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35176773	chr12:123426320-123426321	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539764139	chr12:123426324-123426325	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs551321318	chr12:123426326-123426327	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78441825	chr12:123426363-123426364	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs183297229	chr12:123426364-123426365	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142928729	chr12:123426365-123426366	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75031048	chr12:123426369-123426370	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555221191	chr12:123426415-123426416	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574171636	chr12:123426436-123426437	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534923903	chr12:123426496-123426497	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369661516	chr12:123426539-123426540	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553231661	chr12:123426568-123426569	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs577889866	chr12:123426577-123426578	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545311779	chr12:123426585-123426586	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557282734	chr12:123426601-123426602	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs575596359	chr12:123426607-123426608	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12231264	chr12:123426663-123426664	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs543097927	chr12:123426799-123426800	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs570979060	chr12:123426825-123426826	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7298563	chr12:123426873-123426874	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs541196637	chr12:123426885-123426886	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs559602038	chr12:123426909-123426910	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533218769	chr12:123426933-123426934	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs140194429	chr12:123426954-123426955	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs143971667	chr12:123426957-123426958	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532642160	chr12:123426959-123426960	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
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
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
Ependymoma	20639864	CNVD
Pancreatic cancer	17952125	CNVD
head and neck squamous cell carcinoma	24351288	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:806 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:123401400-123426000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr12:123402600-123429200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr12:123402800-123426600	Weak transcription	NHLF	lung
4	chr12:123402800-123429200	Weak transcription	Gastric	stomach
5	chr12:123402800-123430800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr12:123403000-123426400	Weak transcription	Left Ventricle	heart
7	chr12:123403000-123428800	Weak transcription	Lung	lung
8	chr12:123403000-123444200	Weak transcription	Aorta	Aorta
9	chr12:123403400-123427000	Weak transcription	A549	lung
10	chr12:123405200-123428600	Weak transcription	NHEK	skin
11	chr12:123406800-123426600	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr12:123409400-123427600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr12:123411800-123428800	Weak transcription	Fetal Brain Male	brain
14	chr12:123412400-123427200	Weak transcription	Adipose Nuclei	Adipose
15	chr12:123412800-123427400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr12:123412800-123431800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr12:123412800-123449200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:123413400-123427200	Weak transcription	Small Intestine	intestine
19	chr12:123413400-123427400	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr12:123413400-123427600	Weak transcription	Primary hematopoietic stem cells	blood
21	chr12:123413400-123427600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:123413400-123449600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr12:123413600-123431400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr12:123413600-123450000	Weak transcription	Primary T cells from cord blood	blood
25	chr12:123414000-123432400	Weak transcription	Fetal Kidney	kidney
26	chr12:123414800-123427400	Weak transcription	Spleen	Spleen
27	chr12:123414800-123427800	Weak transcription	Right Ventricle	heart
28	chr12:123415600-123429000	Weak transcription	Pancreas	Pancrea
29	chr12:123415800-123431600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr12:123417400-123427200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr12:123417400-123441800	Weak transcription	Ovary	ovary
32	chr12:123417600-123446200	Weak transcription	Fetal Lung	lung
33	chr12:123417800-123426600	Weak transcription	HepG2	liver
34	chr12:123417800-123427400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr12:123418000-123427400	Weak transcription	Brain Hippocampus Middle	brain
36	chr12:123418400-123427200	Weak transcription	HUVEC	blood vessel
37	chr12:123419600-123425800	Strong transcription	Brain Angular Gyrus	brain
38	chr12:123420200-123427400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:123420400-123425600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr12:123420400-123425600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr12:123420400-123425600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:123420400-123427200	Weak transcription	Fetal Muscle Trunk	muscle
43	chr12:123420600-123427200	Weak transcription	Fetal Muscle Leg	muscle
44	chr12:123420600-123428000	Weak transcription	K562	blood
45	chr12:123420800-123427200	Weak transcription	NHDF-Ad	bronchial
46	chr12:123421200-123426600	Weak transcription	Right Atrium	heart
47	chr12:123422000-123425600	Strong transcription	Brain Germinal Matrix	brain
48	chr12:123422000-123429200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr12:123422200-123425600	Strong transcription	Brain Substantia Nigra	brain
50	chr12:123422400-123427400	Weak transcription	NH-A	brain

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