Variant report

Variant	esv3467169
Chromosome Location	chr4:69250079-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1686)
CpG islands
(count:978)
Chromatin interactive
region (count:29)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1686 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
8	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
9	ATF2	chr4:69269806-69270384	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr4:69271370-69272360	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:69272567-69273233	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:69275508-69277104	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:69273374-69273928	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr4:69269850-69270608	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:69271320-69273979	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr4:69274713-69275097	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr4:69274062-69274402	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
20	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
21	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
22	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
23	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
24	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
25	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
26	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:69273602-69273847	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr4:69275877-69276040	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
31	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
32	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
33	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
35	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
36	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
37	BHLHE40	chr4:69250331-69250703	K562	blood:	n/a	n/a
38	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
39	BRCA1	chr4:69272255-69272927	H1-hESC	embryonic stem cell:	n/a	n/a
40	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
41	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
42	CEBPB	chr4:69271962-69272301	K562	blood:	n/a	n/a
43	CEBPB	chr4:69300028-69300381	IMR90	lung:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
44	CEBPB	chr4:69273497-69273975	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:69277211-69277380	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
47	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
49	CEBPB	chr4:69300096-69300253	H1-hESC	embryonic stem cell:	n/a	chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300190-69300199 chr4:69300188-69300201 chr4:69300188-69300199 chr4:69300190-69300199 chr4:69300190-69300201 chr4:69300190-69300199 chr4:69300188-69300201
50	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69537826-69537876	HMEC	breast:	n/a
2	chr4:69537589-69537639	NHBE	bronchial:	n/a
3	chr4:69537826-69537876	HMEC	breast:	n/a
4	chr4:69537589-69537639	NHBE	bronchial:	n/a
5	chr4:69355121-69355171	PFSK-1	brain:	n/a
6	chr4:69312514-69312564	GM06990	blood:	n/a
7	chr4:69435250-69435300	PrEC	prostate:	n/a
8	chr4:69435593-69435643	MCF10A-Er-Src	breast:	n/a
9	chr4:69340916-69340966	MCF10A-Er-Src	breast:	n/a
10	chr4:69537806-69537856	BJ	skin:	n/a
11	chr4:69435250-69435300	HEK293	kidney:	embryo
12	chr4:69537806-69537856	NHDF-neo	bronchial:	n/a
13	chr4:69312104-69312154	LNCaP	prostate:	n/a
14	chr4:69312104-69312154	T-47D	breast:	n/a
15	chr4:69522639-69522689	A549	lung:	n/a
16	chr4:69435593-69435643	PANC-1	pancreas:	n/a
17	chr4:69522639-69522689	T-47D	breast:	n/a
18	chr4:69312514-69312564	Hepatocyte	liver:	n/a
19	chr4:69537589-69537639	CMK	blood:	n/a
20	chr4:69522639-69522689	SAEC	small airway:	n/a
21	chr4:69340916-69340966	PrEC	prostate:	n/a
22	chr4:69355121-69355171	AG04450	lung:	fetal
23	chr4:69435593-69435643	PFSK-1	brain:	n/a
24	chr4:69340916-69340966	HCM	heart:	n/a
25	chr4:69355121-69355171	NT2-D1	testis:	n/a
26	chr4:69355121-69355171	HNPCEpiC	eye:	n/a
27	chr4:69514031-69514081	HCF	heart:	n/a
28	chr4:69537589-69537639	GM19239	blood:	n/a
29	chr4:69537826-69537876	AG09309	skin:	n/a
30	chr4:69514031-69514081	NH-A	brain:	n/a
31	chr4:69537826-69537876	ECC-1	luminal epithelium:	n/a
32	chr4:69514031-69514081	CMK	blood:	n/a
33	chr4:69340916-69340966	SK-N-MC	brain:	n/a
34	chr4:69434475-69434525	U87	brain:	n/a
35	chr4:69537826-69537876	MCF10A-Er-Src	breast:	n/a
36	chr4:69537589-69537639	U87	brain:	n/a
37	chr4:69313197-69313247	BE2_C	brain:	n/a
38	chr4:69537806-69537856	HRPEpiC	eye:	n/a
39	chr4:69435601-69435651	H1-hESC	embryonic stem cell:	embryo
40	chr4:69313197-69313247	GM12878	blood:	n/a
41	chr4:69435593-69435643	ovcar-3	ovarian:	n/a
42	chr4:69312104-69312154	SAEC	small airway:	n/a
43	chr4:69381368-69381418	A549	lung:	n/a
44	chr4:69312514-69312564	Jurkat	blood:	n/a
45	chr4:69537826-69537876	HCPEpiC	choroid plexus:	n/a
46	chr4:69537806-69537856	SK-N-SH	brain:	n/a
47	chr4:69340916-69340966	BE2_C	brain:	n/a
48	chr4:69435593-69435643	NH-A	brain:	n/a
49	chr4:69313197-69313247	PANC-1	pancreas:	n/a
50	chr4:69522639-69522689	SKMC	muscle:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
2	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
3	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
4	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
5	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
6	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
7	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
8	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
9	chr4:69214168..69215842-chr4:69249504..69252039,2	MCF-7	breast:
10	chr4:69261479..69263949-chr4:69265088..69267687,3	K562	blood:
11	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
12	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
13	chr4:69243264..69245251-chr4:69248916..69251183,2	K562	blood:
14	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
15	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
16	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
17	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
18	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
19	chr4:69261479..69263949-chr4:69265088..69267687,3	K562	blood:
20	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
21	chr4:69177090..69179857-chr4:69251602..69253290,2	MCF-7	breast:
22	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
23	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
24	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
25	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
26	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
27	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
28	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
29	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UGT2B17-1	chr4:69382627-69383365	NONHSAT096733
2	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
3	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
4	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
5	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
6	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737

No data

Variant related genes	Relation type
TMPRSS11E	TF binding region
ENSG00000249472	TF binding region
ENSG00000251074	TF binding region
ENSG00000251101	TF binding region
UGT2B17	TF binding region
UGT2B15	TF binding region
UGT2B29P	TF binding region
ENSG00000248635	TF binding region
TMPRSS11E	CpG island
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000248635	CpG island
ENSG00000272626	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000083896	chromatin interactions
ENSG00000087128	chromatin interactions

Extended variants
information (count: 10113 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:10113 , 50 per page) page: 1 2 3 4 5 6 7 ... 203

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546975932	chr4:69250110-69250111	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs139311303	chr4:69250114-69250115	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs529254995	chr4:69250122-69250123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548980840	chr4:69250127-69250128	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144253924	chr4:69250130-69250131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs4860294	chr4:69250177-69250178	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs551117220	chr4:69250213-69250214	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs189171949	chr4:69250221-69250222	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs139680234	chr4:69250234-69250235	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs553758951	chr4:69250276-69250277	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs573897215	chr4:69250304-69250305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs62298444	chr4:69250321-69250322	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs4860936	chr4:69250347-69250348	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs576168737	chr4:69250375-69250376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs141905915	chr4:69250407-69250408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs545865015	chr4:69250469-69250470	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs565020703	chr4:69250502-69250503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs578094634	chr4:69250505-69250506	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs540857698	chr4:69250518-69250519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs374870272	chr4:69250566-69250567	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs560587127	chr4:69250586-69250587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181885104	chr4:69250596-69250597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs548917906	chr4:69250604-69250605	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562552096	chr4:69250607-69250608	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs183522052	chr4:69250632-69250633	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551456705	chr4:69250662-69250663	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571739860	chr4:69250665-69250666	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs533715158	chr4:69250666-69250667	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs547592883	chr4:69250674-69250675	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567404949	chr4:69250698-69250699	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs189234057	chr4:69250732-69250733	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371750249	chr4:69250815-69250816	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556538706	chr4:69250835-69250836	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534172888	chr4:69250879-69250880	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538667450	chr4:69250880-69250881	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2037886	chr4:69250882-69250883	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs368454695	chr4:69250890-69250891	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147708825	chr4:69250949-69250950	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs540443226	chr4:69250950-69250951	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181027593	chr4:69250958-69250959	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs574210956	chr4:69250965-69250966	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142553659	chr4:69250978-69250979	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs367711360	chr4:69250983-69250984	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs3867396	chr4:69251052-69251053	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs557833305	chr4:69251063-69251064	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs148015500	chr4:69251065-69251066	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565208767	chr4:69251067-69251068	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs527790563	chr4:69251070-69251071	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs34887788	chr4:69251086-69251087	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs34584198	chr4:69251103-69251104	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Alcoholism	21790672	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69232200-69255600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:69242200-69255400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr4:69245600-69250600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:69245600-69252800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:69245800-69254200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:69249400-69254600	Weak transcription	Fetal Intestine Large	intestine
7	chr4:69250600-69250800	Enhancers	Esophagus	oesophagus
8	chr4:69250600-69251400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:69251400-69252800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr4:69252800-69253000	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:69252800-69253000	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:69252800-69253800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:69253000-69253400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr4:69253000-69254400	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr4:69253200-69254800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr4:69253400-69255600	Enhancers	Fetal Intestine Small	intestine
17	chr4:69253400-69258000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:69253800-69254200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr4:69254000-69257400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr4:69254200-69254800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:69254200-69255000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:69254200-69256800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr4:69254200-69257400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr4:69254200-69257400	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:69254400-69255400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr4:69254600-69256400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr4:69254600-69256400	Enhancers	Fetal Intestine Large	intestine
28	chr4:69254600-69258600	Enhancers	Fetal Lung	lung
29	chr4:69254800-69255200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
30	chr4:69254800-69255200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr4:69254800-69255800	Enhancers	H9 Cell Line	embryonic stem cell
32	chr4:69255000-69256600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:69255200-69255600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:69255200-69258200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:69255400-69255800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr4:69255400-69256400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr4:69255400-69256400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:69255600-69256000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
39	chr4:69255600-69256200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr4:69255600-69256200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr4:69255600-69256600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:69255600-69260600	Weak transcription	Fetal Intestine Small	intestine
43	chr4:69255800-69257400	Enhancers	H1 Cell Line	embryonic stem cell
44	chr4:69255800-69270200	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr4:69256000-69256200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr4:69256000-69256400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:69256000-69256400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:69256000-69256600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr4:69256200-69256600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
50	chr4:69256200-69260200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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