Variant report

Variant	esv1793983
Chromosome Location	chr1:150804748-150825924
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:123)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr1:150824771-150825000	K562	blood:	n/a	n/a
2	BHLHE40	chr1:150824796-150824961	HepG2	liver:	n/a	n/a
3	BHLHE40	chr1:150814292-150814492	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:150808687-150809131	GM12878	blood:	n/a	n/a
5	CEBPB	chr1:150819392-150819708	MCF-7	breast:	n/a	n/a
6	CEBPB	chr1:150805468-150805622	A549	lung:	n/a	chr1:150805558-150805569
7	CEBPB	chr1:150819095-150819594	A549	lung:	n/a	chr1:150819172-150819183
8	CEBPB	chr1:150805495-150805504	K562	blood:	n/a	n/a
9	CEBPB	chr1:150805491-150805645	IMR90	lung:	n/a	chr1:150805558-150805569
10	CEBPB	chr1:150819104-150819651	IMR90	lung:	n/a	chr1:150819172-150819183
11	CEBPB	chr1:150824956-150824974	IMR90	lung:	n/a	chr1:150824963-150824974
12	CEBPB	chr1:150820989-150821125	HepG2	liver:	n/a	n/a
13	CEBPB	chr1:150805513-150805693	HepG2	liver:	n/a	chr1:150805558-150805569
14	CEBPB	chr1:150824792-150825035	HepG2	liver:	n/a	chr1:150824963-150824974
15	CEBPB	chr1:150821035-150821169	K562	blood:	n/a	n/a
16	CEBPB	chr1:150819012-150819719	K562	blood:	n/a	chr1:150819172-150819183
17	CEBPB	chr1:150819048-150819702	K562	blood:	n/a	chr1:150819172-150819183
18	CEBPB	chr1:150819096-150819600	HepG2	liver:	n/a	chr1:150819172-150819183
19	CHD2	chr1:150808782-150808993	GM12878	blood:	n/a	n/a
20	CTCF	chr1:150813621-150813703	Fibrobl	skin:	n/a	n/a
21	CTCF	chr1:150824780-150824930	AG04449	skin:	n/a	n/a
22	CTCF	chr1:150817466-150817514	Spleen_OC	spleen:	n/a	n/a
23	CUX1	chr1:150808990-150809187	GM12878	blood:	n/a	n/a
24	EBF1	chr1:150808743-150808959	GM12878	blood:	n/a	n/a
25	EBF1	chr1:150813983-150814362	GM12878	blood:	n/a	chr1:150814167-150814178 chr1:150814167-150814180
26	EBF1	chr1:150813984-150814439	GM12878	blood:	n/a	chr1:150814167-150814178 chr1:150814167-150814180
27	EP300	chr1:150824825-150825047	K562	blood:	n/a	n/a
28	EP300	chr1:150824665-150825102	HepG2	liver:	n/a	n/a
29	EP300	chr1:150819433-150819633	K562	blood:	n/a	n/a
30	EP300	chr1:150808759-150809148	GM12878	blood:	n/a	n/a
31	EP300	chr1:150814229-150814418	GM12878	blood:	n/a	n/a
32	EP300	chr1:150808771-150809191	GM12878	blood:	n/a	n/a
33	EP300	chr1:150814159-150814445	GM12878	blood:	n/a	n/a
34	EP300	chr1:150808794-150808992	GM12878	blood:	n/a	n/a
35	ESR1	chr1:150819313-150819636	T-47D	breast:	n/a	n/a
36	FOXA1	chr1:150824653-150825073	HepG2	liver:	n/a	n/a
37	FOXA1	chr1:150824716-150825133	HepG2	liver:	n/a	n/a
38	FOXA1	chr1:150824715-150825118	HepG2	liver:	n/a	n/a
39	FOXA1	chr1:150824802-150825102	HepG2	liver:	n/a	n/a
40	FOXA1	chr1:150824766-150825008	T-47D	breast:	n/a	n/a
41	FOXA2	chr1:150824758-150825085	HepG2	liver:	n/a	n/a
42	FOXM1	chr1:150814073-150814585	GM12878	blood:	n/a	n/a
43	GATA1	chr1:150813193-150813663	PBDE	blood:	n/a	chr1:150813405-150813414 chr1:150813404-150813414 chr1:150813405-150813412 chr1:150813402-150813412
44	GATA2	chr1:150824705-150824947	K562	blood:	n/a	n/a
45	GATA3	chr1:150807992-150808109	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr1:150808219-150809074	MCF-7	breast:	n/a	chr1:150808496-150808504
47	HDAC2	chr1:150824766-150825073	HepG2	liver:	n/a	n/a
48	IKZF1	chr1:150814269-150814380	GM12878	blood:	n/a	n/a
49	MAX	chr1:150808810-150809093	GM12878	blood:	n/a	n/a
50	MAX	chr1:150824748-150825025	NB4	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:150808973-150809023	GM06990	blood:	n/a
2	chr1:150808973-150809023	GM06990	blood:	n/a
3	chr1:150808973-150809023	CMK	blood:	n/a
4	chr1:150808973-150809023	NH-A	brain:	n/a
5	chr1:150825365-150825415	AG10803	skin:	n/a
6	chr1:150808973-150809023	HIPEpiC	eye:	n/a
7	chr1:150808973-150809023	GM19239	blood:	n/a
8	chr1:150808973-150809023	Hepatocyte	liver:	n/a
9	chr1:150808973-150809023	SK-N-MC	brain:	n/a
10	chr1:150825365-150825415	HCF	heart:	n/a
11	chr1:150808973-150809023	Hela-S3	cervix:	n/a
12	chr1:150825365-150825415	IMR90	lung:	fetal
13	chr1:150808973-150809023	HCT-116	colon:	n/a
14	chr1:150825365-150825415	HMEC	breast:	n/a
15	chr1:150825365-150825415	HRPEpiC	eye:	n/a
16	chr1:150825365-150825415	HCT-116	colon:	n/a
17	chr1:150825365-150825415	NHBE	bronchial:	n/a
18	chr1:150825365-150825415	A549	lung:	n/a
19	chr1:150808973-150809023	HAEpiC	amniotic membrane:	n/a
20	chr1:150808973-150809023	NB4	blood:	n/a
21	chr1:150825365-150825415	HUVEC	blood vessel:	n/a
22	chr1:150825365-150825415	CMK	blood:	n/a
23	chr1:150808973-150809023	GM12892	blood:	n/a
24	chr1:150825365-150825415	PFSK-1	brain:	n/a
25	chr1:150825365-150825415	ovcar-3	ovarian:	n/a
26	chr1:150825365-150825415	GM06990	blood:	n/a
27	chr1:150825365-150825415	AG09319	gingival:	n/a
28	chr1:150808973-150809023	U87	brain:	n/a
29	chr1:150808973-150809023	ECC-1	luminal epithelium:	n/a
30	chr1:150808973-150809023	HRE	kidney:	n/a
31	chr1:150825365-150825415	HRCEpiC	kidney:	n/a
32	chr1:150825365-150825415	AG04450	lung:	fetal
33	chr1:150825365-150825415	SK-N-SH_RA	brain:	n/a
34	chr1:150825365-150825415	PANC-1	pancreas:	n/a
35	chr1:150808973-150809023	PANC-1	pancreas:	n/a
36	chr1:150808973-150809023	HCF	heart:	n/a
37	chr1:150825365-150825415	SKMC	muscle:	n/a
38	chr1:150808973-150809023	Jurkat	blood:	n/a
39	chr1:150808973-150809023	PrEC	prostate:	n/a
40	chr1:150808973-150809023	SK-N-SH_RA	brain:	n/a
41	chr1:150825365-150825415	MCF-7	breast:	n/a
42	chr1:150808973-150809023	RPTEC	kidney:	n/a
43	chr1:150808973-150809023	HL-60	blood:	n/a
44	chr1:150825365-150825415	GM19239	blood:	n/a
45	chr1:150825365-150825415	SK-N-SH	brain:	n/a
46	chr1:150825365-150825415	HPAEpiC	pulmonary alveolar:	n/a
47	chr1:150825365-150825415	HL-60	blood:	n/a
48	chr1:150808973-150809023	Caco-2	colon:	n/a
49	chr1:150825365-150825415	SK-N-MC	brain:	n/a
50	chr1:150808973-150809023	MCF10A-Er-Src	breast:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:150598853..150601139-chr1:150818426..150820155,2	K562	blood:
2	chr1:150825805..150828519-chr1:150980841..150983000,2	K562	blood:
3	chr1:150808768..150811697-chr1:150895772..150898745,2	MCF-7	breast:
4	chr1:150809240..150812046-chr1:150847558..150849215,2	MCF-7	breast:
5	chr1:150805087..150807211-chr1:150850902..150853301,2	MCF-7	breast:
6	chr1:150818877..150820546-chr1:151019775..151022165,2	MCF-7	breast:
7	chr1:150788780..150790984-chr1:150810777..150813008,2	MCF-7	breast:
8	chr1:150803170..150805446-chr1:150810913..150813203,2	K562	blood:
9	chr1:150816940..150818547-chr1:150824662..150826760,2	MCF-7	breast:
10	chr1:150824595..150826389-chr1:150944188..150947184,2	K562	blood:
11	chr1:150800531..150803502-chr1:150811550..150815655,4	MCF-7	breast:
12	chr1:150824355..150826588-chr1:150896874..150898598,2	MCF-7	breast:
13	chr1:150824402..150827386-chr1:150847961..150849827,2	MCF-7	breast:
14	chr1:150807087..150808986-chr1:150811625..150814317,2	MCF-7	breast:
15	chr1:150818986..150820930-chr1:150847610..150849442,2	MCF-7	breast:
16	chr1:150803316..150805877-chr1:150806523..150810039,3	MCF-7	breast:
17	chr1:150803501..150805260-chr1:150810074..150811870,2	K562	blood:
18	chr1:150803170..150805446-chr1:150810913..150813203,2	K562	blood:
19	chr1:150802438..150804523-chr1:150806061..150808496,2	MCF-7	breast:
20	chr1:150825294..150827430-chr1:150885825..150887706,2	MCF-7	breast:
21	chr1:150803501..150805260-chr1:150810074..150811870,2	K562	blood:
22	chr1:150545938..150547543-chr1:150804208..150806124,2	K562	blood:
23	chr1:150799945..150802460-chr1:150803944..150806773,2	K562	blood:
24	chr1:150818101..150820451-chr1:150845957..150847581,2	K562	blood:
25	chr1:150808474..150808974-chr8:117000058..117000576,2	MCF-7	breast:
26	chr1:150816940..150818547-chr1:150824662..150826760,2	MCF-7	breast:
27	chr1:150813417..150816056-chr1:150946516..150948387,2	K562	blood:

No data

Variant related genes	Relation type
ARNT	TF binding region
ARNT	CpG island
ENSG00000143409	chromatin interactions
ENSG00000143379	chromatin interactions
ENSG00000231073	chromatin interactions
ENSG00000143437	chromatin interactions
ENSG00000143418	chromatin interactions
ENSG00000143443	chromatin interactions
ENSG00000143363	chromatin interactions

Extended variants
information (count: 652 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:652 , 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	rs369510385	chr1:150804768-150804769	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs149172717	chr1:150804777-150804778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143275383	chr1:150804813-150804814	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs150467759	chr1:150804829-150804830	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587676009	chr1:150804861-150804862	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs9325979	chr1:150804903-150804904	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs373894722	chr1:150804914-150804915	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371357044	chr1:150804935-150804936	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs370080791	chr1:150805004-150805005	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs587632224	chr1:150805047-150805048	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191746556	chr1:150805062-150805063	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs587748918	chr1:150805077-150805078	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs368653632	chr1:150805118-150805119	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs375834336	chr1:150805140-150805141	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587624229	chr1:150805155-150805156	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs148301196	chr1:150805213-150805214	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs587751589	chr1:150805358-150805359	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587626361	chr1:150805488-150805489	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs587682192	chr1:150805541-150805542	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs114641696	chr1:150805584-150805585	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587714975	chr1:150805615-150805616	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs587640008	chr1:150805730-150805731	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587713878	chr1:150805732-150805733	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587771863	chr1:150805748-150805749	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs587673069	chr1:150805777-150805778	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs183876904	chr1:150805796-150805797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs190345163	chr1:150805825-150805826	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587671679	chr1:150805864-150805865	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs141388962	chr1:150806054-150806055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587601947	chr1:150806096-150806097	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs181672761	chr1:150806190-150806191	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs58859566	chr1:150806201-150806202	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs587739029	chr1:150806222-150806223	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs75271330	chr1:150806235-150806236	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs138780302	chr1:150806247-150806248	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs587736923	chr1:150806295-150806296	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs112503429	chr1:150806346-150806347	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs12403459	chr1:150806395-150806396	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587633933	chr1:150806410-150806411	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587683334	chr1:150806447-150806448	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs587767154	chr1:150806516-150806517	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs587613147	chr1:150806563-150806564	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587698301	chr1:150806571-150806572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs587774854	chr1:150806587-150806588	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs587660223	chr1:150806626-150806627	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs141831352	chr1:150806733-150806734	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs10305702	chr1:150806734-150806735	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs587648669	chr1:150806831-150806832	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587699643	chr1:150806837-150806838	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs10305701	chr1:150806970-150806971	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Incontinentia Pigmenti	22033527	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	chr1:150782200-150809600	Strong transcription	Fetal Muscle Leg	muscle
2	chr1:150782200-150809800	Strong transcription	Stomach Smooth Muscle	stomach
3	chr1:150782200-150813000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr1:150782400-150812200	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr1:150783200-150809800	Strong transcription	Fetal Thymus	thymus
6	chr1:150783200-150816600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr1:150783200-150816800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:150785800-150806400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr1:150785800-150812400	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr1:150786000-150808600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:150788400-150808000	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr1:150788400-150809800	Strong transcription	Fetal Muscle Trunk	muscle
13	chr1:150788400-150812200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr1:150790800-150811400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:150791200-150806600	Weak transcription	Small Intestine	intestine
16	chr1:150791800-150809000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
17	chr1:150792200-150814800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr1:150792600-150815400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:150792800-150812400	Strong transcription	Primary B cells from peripheral blood	blood
20	chr1:150793000-150816400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:150793200-150823200	Strong transcription	Placenta	Placenta
22	chr1:150793600-150815800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:150793800-150813800	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr1:150794000-150805800	Strong transcription	Osteobl	bone
25	chr1:150794000-150809600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr1:150794000-150813600	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr1:150794200-150807800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr1:150794600-150812800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr1:150795600-150808200	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr1:150797000-150814400	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chr1:150797400-150809200	Strong transcription	Brain Inferior Temporal Lobe	brain
32	chr1:150797400-150809600	Strong transcription	Left Ventricle	heart
33	chr1:150797400-150810200	Strong transcription	NHLF	lung
34	chr1:150797400-150812400	Strong transcription	HUES64 Cell Line	embryonic stem cell
35	chr1:150797400-150813000	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr1:150797400-150813400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:150797600-150809200	Strong transcription	Dnd41	blood
38	chr1:150797600-150809400	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr1:150797600-150810200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr1:150797600-150810400	Strong transcription	HUES48 Cell Line	embryonic stem cell
41	chr1:150797600-150810800	Strong transcription	Cortex derived primary cultured neurospheres	brain
42	chr1:150797600-150812400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:150797600-150812400	Strong transcription	Duodenum Mucosa	Duodenum
44	chr1:150797600-150812400	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr1:150797600-150812600	Strong transcription	Adipose Nuclei	Adipose
46	chr1:150797600-150813400	Strong transcription	Muscle Satellite Cultured Cells	--
47	chr1:150797600-150815600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr1:150797800-150809400	Strong transcription	NHDF-Ad	bronchial
49	chr1:150797800-150811800	Strong transcription	Primary T cells from cord blood	blood
50	chr1:150797800-150812600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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