Variant report

Variant	nsv872829
Chromosome Location	chr1:192230089-192370110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:536)
CpG islands
(count:122)
Chromatin interactive
region (count:47)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:192280293-192280660	K562	blood:	n/a	n/a
2	ARID3A	chr1:192233639-192233677	K562	blood:	n/a	n/a
3	ARID3A	chr1:192235810-192236187	K562	blood:	n/a	n/a
4	ARID3A	chr1:192246884-192247112	K562	blood:	n/a	n/a
5	ARID3A	chr1:192242011-192242235	K562	blood:	n/a	n/a
6	ATF1	chr1:192275036-192275081	K562	blood:	n/a	n/a
7	ATF1	chr1:192344749-192344769	K562	blood:	n/a	n/a
8	ATF1	chr1:192272985-192273118	K562	blood:	n/a	n/a
9	ATF1	chr1:192368786-192368852	K562	blood:	n/a	n/a
10	ATF1	chr1:192356272-192356274	K562	blood:	n/a	n/a
11	ATF1	chr1:192355441-192355519	K562	blood:	n/a	n/a
12	BACH1	chr1:192285827-192285912	K562	blood:	n/a	n/a
13	BCL11A	chr1:192348057-192348306	GM12878	blood:	n/a	chr1:192348127-192348136
14	BHLHE40	chr1:192232654-192232940	K562	blood:	n/a	n/a
15	BRCA1	chr1:192254302-192254344	H1-hESC	embryonic stem cell:	n/a	n/a
16	CBX3	chr1:192355006-192355437	K562	blood:	n/a	n/a
17	CBX3	chr1:192277415-192277815	K562	blood:	n/a	n/a
18	CBX3	chr1:192250251-192250667	K562	blood:	n/a	n/a
19	CBX3	chr1:192277478-192277742	K562	blood:	n/a	n/a
20	CCNT2	chr1:192344697-192344799	K562	blood:	n/a	n/a
21	CEBPB	chr1:192365717-192365902	IMR90	lung:	n/a	chr1:192365799-192365812
22	CEBPB	chr1:192351987-192352013	HepG2	liver:	n/a	n/a
23	CEBPB	chr1:192305030-192305200	HepG2	liver:	n/a	n/a
24	CEBPB	chr1:192345552-192345934	A549	lung:	n/a	chr1:192345768-192345779 chr1:192345767-192345780 chr1:192345767-192345780
25	CEBPB	chr1:192345488-192346019	A549	lung:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
26	CEBPB	chr1:192341494-192341588	K562	blood:	n/a	chr1:192341560-192341571
27	CEBPB	chr1:192355953-192356040	K562	blood:	n/a	n/a
28	CEBPB	chr1:192345612-192345905	Hela-S3	cervix:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
29	CEBPB	chr1:192341423-192341669	A549	lung:	n/a	chr1:192341560-192341571
30	CEBPB	chr1:192295571-192295831	HepG2	liver:	n/a	chr1:192295668-192295679 chr1:192295668-192295681
31	CEBPB	chr1:192281351-192281484	A549	lung:	n/a	n/a
32	CEBPB	chr1:192236875-192237056	K562	blood:	n/a	n/a
33	CEBPB	chr1:192345624-192345821	K562	blood:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
34	CEBPB	chr1:192238067-192238197	HepG2	liver:	n/a	chr1:192238142-192238153 chr1:192238141-192238154
35	CEBPB	chr1:192266856-192267080	HepG2	liver:	n/a	chr1:192266996-192267007
36	CEBPB	chr1:192345585-192345944	A549	lung:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
37	CEBPB	chr1:192345571-192346001	K562	blood:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
38	CEBPB	chr1:192278595-192278597	HepG2	liver:	n/a	n/a
39	CEBPB	chr1:192295560-192295826	K562	blood:	n/a	chr1:192295668-192295679 chr1:192295668-192295681
40	CEBPB	chr1:192345557-192345966	MCF-7	breast:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
41	CEBPB	chr1:192345590-192345942	HepG2	liver:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
42	CEBPB	chr1:192294118-192294318	HepG2	liver:	n/a	chr1:192294239-192294250
43	CEBPB	chr1:192345396-192345926	H1-hESC	embryonic stem cell:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
44	CEBPB	chr1:192365693-192365863	K562	blood:	n/a	chr1:192365799-192365812
45	CEBPB	chr1:192345590-192345945	IMR90	lung:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
46	CEBPB	chr1:192266819-192267127	K562	blood:	n/a	chr1:192266996-192267007
47	CEBPB	chr1:192341441-192341671	HepG2	liver:	n/a	chr1:192341560-192341571
48	CEBPB	chr1:192299264-192299313	HepG2	liver:	n/a	n/a
49	CEBPB	chr1:192345553-192345968	K562	blood:	n/a	chr1:192345767-192345780 chr1:192345767-192345780 chr1:192345768-192345779
50	CEBPB	chr1:192289480-192289498	HepG2	liver:	n/a	chr1:192289481-192289492

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:192304785-192304835	HRCEpiC	kidney:	n/a
2	chr1:192285333-192285383	PrEC	prostate:	n/a
3	chr1:192285333-192285383	HCF	heart:	n/a
4	chr1:192304785-192304835	MCF10A-Er-Src	breast:	n/a
5	chr1:192304785-192304835	Jurkat	blood:	n/a
6	chr1:192285333-192285383	HCPEpiC	choroid plexus:	n/a
7	chr1:192304785-192304835	HL-60	blood:	n/a
8	chr1:192304785-192304835	HAEpiC	amniotic membrane:	n/a
9	chr1:192304785-192304835	CMK	blood:	n/a
10	chr1:192285333-192285383	GM12891	blood:	n/a
11	chr1:192285333-192285383	IMR90	lung:	fetal
12	chr1:192285333-192285383	NB4	blood:	n/a
13	chr1:192285333-192285383	BE2_C	brain:	n/a
14	chr1:192304785-192304835	HepG2	liver:	n/a
15	chr1:192304785-192304835	PANC-1	pancreas:	n/a
16	chr1:192285333-192285383	PANC-1	pancreas:	n/a
17	chr1:192304785-192304835	NB4	blood:	n/a
18	chr1:192304785-192304835	ProgFib	skin:	n/a
19	chr1:192304785-192304835	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:192304785-192304835	NHDF-neo	bronchial:	n/a
21	chr1:192285333-192285383	HNPCEpiC	eye:	n/a
22	chr1:192285333-192285383	HRPEpiC	eye:	n/a
23	chr1:192285333-192285383	HRCEpiC	kidney:	n/a
24	chr1:192285333-192285383	AG04450	lung:	fetal
25	chr1:192285333-192285383	SK-N-SH_RA	brain:	n/a
26	chr1:192304785-192304835	GM06990	blood:	n/a
27	chr1:192304785-192304835	AG10803	skin:	n/a
28	chr1:192304785-192304835	HCM	heart:	n/a
29	chr1:192285333-192285383	NHDF-neo	bronchial:	n/a
30	chr1:192304785-192304835	ECC-1	luminal epithelium:	n/a
31	chr1:192285333-192285383	K562	blood:	n/a
32	chr1:192285333-192285383	Hepatocyte	liver:	n/a
33	chr1:192285333-192285383	A549	lung:	n/a
34	chr1:192304785-192304835	BJ	skin:	n/a
35	chr1:192304785-192304835	NHBE	bronchial:	n/a
36	chr1:192304785-192304835	Caco-2	colon:	n/a
37	chr1:192304785-192304835	SK-N-MC	brain:	n/a
38	chr1:192304785-192304835	GM12892	blood:	n/a
39	chr1:192285333-192285383	HUVEC	blood vessel:	n/a
40	chr1:192285333-192285383	HCM	heart:	n/a
41	chr1:192285333-192285383	SK-N-MC	brain:	n/a
42	chr1:192304785-192304835	HNPCEpiC	eye:	n/a
43	chr1:192304785-192304835	U87	brain:	n/a
44	chr1:192285333-192285383	HIPEpiC	eye:	n/a
45	chr1:192304785-192304835	HRE	kidney:	n/a
46	chr1:192304785-192304835	T-47D	breast:	n/a
47	chr1:192304785-192304835	A549	lung:	n/a
48	chr1:192285333-192285383	HPAEpiC	pulmonary alveolar:	n/a
49	chr1:192285333-192285383	Jurkat	blood:	n/a
50	chr1:192304785-192304835	Hepatocyte	liver:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:192249186..192250692-chr1:192255900..192258274,2	K562	blood:
2	chr1:192235673..192237400-chr1:192241842..192243346,2	K562	blood:
3	chr1:192364251..192366273-chr1:192371276..192373537,2	K562	blood:
4	chr1:192234066..192236164-chr1:192244600..192247164,2	K562	blood:
5	chr1:192296149..192298127-chr1:192303474..192305809,2	K562	blood:
6	chr1:192296149..192298127-chr1:192303474..192305809,2	K562	blood:
7	chr1:192315023..192317400-chr1:192318904..192321629,2	K562	blood:
8	chr1:192312588..192314663-chr1:192330429..192332047,2	K562	blood:
9	chr1:192344743..192346250-chr1:192353971..192356636,2	K562	blood:
10	chr1:192309320..192313053-chr1:192320479..192324101,4	K562	blood:
11	chr1:192295956..192298127-chr1:192303697..192305809,2	K562	blood:
12	chr1:192356695..192359398-chr1:192364454..192366779,3	K562	blood:
13	chr1:192086724..192088990-chr1:192228820..192231211,2	K562	blood:
14	chr1:192295956..192298127-chr1:192303697..192305809,2	K562	blood:
15	chr1:192234066..192236164-chr1:192244600..192247164,2	K562	blood:
16	chr1:192315023..192317400-chr1:192318904..192321629,2	K562	blood:
17	chr1:192344743..192346250-chr1:192353971..192356636,2	K562	blood:
18	chr1:192312588..192314663-chr1:192330429..192332047,2	K562	blood:
19	chr1:192307961..192309733-chr1:192310054..192313025,2	K562	blood:
20	chr1:192230860..192232760-chr1:192239586..192242389,2	K562	blood:
21	chr1:192356695..192359398-chr1:192364454..192366779,3	K562	blood:
22	chr1:192320095..192323308-chr1:192323829..192327005,3	K562	blood:
23	chr1:192344215..192347684-chr1:192348226..192352405,4	K562	blood:
24	chr1:192353018..192355468-chr1:192363241..192364892,2	K562	blood:
25	chr1:192320095..192323308-chr1:192323829..192327005,3	K562	blood:
26	chr1:192249186..192250692-chr1:192255900..192258274,2	K562	blood:
27	chr1:192368188..192369973-chr1:192371853..192374450,2	K562	blood:
28	chr1:192362224..192364335-chr1:192367712..192370018,2	K562	blood:
29	chr1:192235673..192237400-chr1:192241842..192243346,2	K562	blood:
30	chr1:192242181..192244363-chr1:192263112..192265270,2	K562	blood:
31	chr1:192344215..192347684-chr1:192348226..192352405,4	K562	blood:
32	chr1:192336641..192337331-chr11:76756837..76757401,2	MCF-7	breast:
33	chr1:191962409..191963306-chr1:192269925..192270965,3	MCF-7	breast:
34	chr1:192362224..192364335-chr1:192367712..192370018,2	K562	blood:
35	chr1:192309320..192313053-chr1:192320479..192324101,4	K562	blood:
36	chr1:192242181..192244363-chr1:192263112..192265270,2	K562	blood:
37	chr1:192238542..192241818-chr1:192250028..192252934,3	K562	blood:
38	chr1:192338308..192341245-chr1:192344798..192346639,2	K562	blood:
39	chr1:192353018..192355468-chr1:192363241..192364892,2	K562	blood:
40	chr1:192307961..192309733-chr1:192310054..192313025,2	K562	blood:
41	chr1:191962436..191963394-chr1:192279940..192280907,5	MCF-7	breast:
42	chr1:192314027..192317570-chr1:192318637..192321629,4	K562	blood:
43	chr1:192238542..192241818-chr1:192250028..192252934,3	K562	blood:
44	chr1:192314027..192317570-chr1:192318637..192321629,4	K562	blood:
45	chr1:192338308..192341245-chr1:192344798..192346639,2	K562	blood:
46	chr1:192230860..192232760-chr1:192239586..192242389,2	K562	blood:
47	chr1:191858532..191860860-chr1:192337438..192339553,2	K562	blood:

No data

Variant related genes	Relation type
RGS21	TF binding region
RGS21	CpG island
ENSG00000223344	chromatin interactions

Extended variants
information (count: 2537 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2537 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1175154	chr1:192230089-192230090	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs540230225	chr1:192230169-192230170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560153518	chr1:192230211-192230212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs75281419	chr1:192230283-192230284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138525764	chr1:192230286-192230287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs562706168	chr1:192230385-192230386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs531523975	chr1:192230423-192230424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116076492	chr1:192230452-192230453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561444811	chr1:192230470-192230471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs535401425	chr1:192230500-192230501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113003111	chr1:192230521-192230522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537270980	chr1:192230522-192230523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs554628998	chr1:192230566-192230567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146382531	chr1:192230609-192230610	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538984682	chr1:192230725-192230726	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552444832	chr1:192230769-192230770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368612090	chr1:192230883-192230884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs116028941	chr1:192230884-192230885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570037926	chr1:192230898-192230899	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs537123534	chr1:192230900-192230901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370932654	chr1:192230925-192230926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375355546	chr1:192230939-192230940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs74364551	chr1:192230941-192230942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs533621424	chr1:192230982-192230983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553828022	chr1:192231012-192231013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576891530	chr1:192231040-192231041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142909232	chr1:192231048-192231049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188498982	chr1:192231092-192231093	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77021829	chr1:192231113-192231114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542025166	chr1:192231131-192231132	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561705049	chr1:192231132-192231133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530240778	chr1:192231241-192231242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs114159103	chr1:192231242-192231243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs577448527	chr1:192231260-192231261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560157926	chr1:192231314-192231315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532370972	chr1:192231322-192231323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185148846	chr1:192231408-192231409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190525573	chr1:192231418-192231419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531875164	chr1:192231445-192231446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541618323	chr1:192231601-192231602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182297837	chr1:192231671-192231672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575145544	chr1:192231672-192231673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114901308	chr1:192231691-192231692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533921528	chr1:192231712-192231713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs117479693	chr1:192231766-192231767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369190047	chr1:192231789-192231790	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570508058	chr1:192231791-192231792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs150662223	chr1:192231804-192231805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556163428	chr1:192231865-192231866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs576308429	chr1:192231904-192231905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	19010865	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Urothelial carcinoma	21177765	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Mental retardation	21062444	CNVD
Liver carcinoma	19366792	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:192226000-192235800	Weak transcription	K562	blood
2	chr1:192228800-192230800	Enhancers	HUVEC	blood vessel
3	chr1:192229600-192232600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:192229600-192232800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr1:192230200-192235000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:192230800-192231000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:192230800-192232400	Weak transcription	HUVEC	blood vessel
8	chr1:192231000-192235200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:192231200-192232400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr1:192231200-192232400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr1:192232000-192233400	Enhancers	HSMM	muscle
12	chr1:192232200-192233600	Enhancers	Osteobl	bone
13	chr1:192232400-192233000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:192232400-192233200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr1:192232400-192233600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
16	chr1:192232400-192233600	Enhancers	HUVEC	blood vessel
17	chr1:192232400-192233600	Enhancers	NH-A	brain
18	chr1:192232400-192233800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr1:192232600-192233200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr1:192232600-192233600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr1:192232600-192233600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr1:192232800-192234200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr1:192233000-192233600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr1:192233600-192234400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr1:192233600-192234800	Enhancers	Muscle Satellite Cultured Cells	--
26	chr1:192233800-192239200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr1:192235200-192235600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:192235600-192236400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr1:192235800-192236000	Enhancers	K562	blood
30	chr1:192236000-192236600	Flanking Active TSS	K562	blood
31	chr1:192236400-192239200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr1:192236600-192241800	Weak transcription	K562	blood
33	chr1:192239200-192239400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:192239200-192239800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:192239200-192240400	Enhancers	HUVEC	blood vessel
36	chr1:192239400-192239800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:192239800-192240200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr1:192241200-192241400	Enhancers	Small Intestine	intestine
39	chr1:192241800-192242400	Enhancers	K562	blood
40	chr1:192242400-192242800	Weak transcription	K562	blood
41	chr1:192242800-192243400	Enhancers	K562	blood
42	chr1:192243400-192246200	Weak transcription	K562	blood
43	chr1:192246200-192246400	Enhancers	K562	blood
44	chr1:192246400-192247000	Weak transcription	K562	blood
45	chr1:192247000-192248000	Enhancers	K562	blood
46	chr1:192260400-192260800	Enhancers	HUVEC	blood vessel
47	chr1:192272200-192273000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:192273000-192276400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr1:192276400-192276800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr1:192280200-192280800	Enhancers	Dnd41	blood

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