Variant report

Variant	nsv497853
Chromosome Location	chr4:69276372-69592846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1513)
CpG islands
(count:979)
Chromatin interactive
region (count:24)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1513 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
8	ATF1	chr4:69559343-69559671	K562	blood:	n/a	n/a
9	ATF2	chr4:69275508-69277104	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
11	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
13	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
14	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
15	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
16	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
17	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
18	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
21	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
22	BHLHE40	chr4:69559209-69559522	K562	blood:	n/a	n/a
23	BHLHE40	chr4:69583763-69584005	GM12878	blood:	n/a	n/a
24	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
25	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
26	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:69305163-69305286	GM12878	blood:	n/a	n/a
28	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
29	CEBPB	chr4:69279112-69279415	K562	blood:	n/a	n/a
30	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
31	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
32	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
33	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
34	CEBPB	chr4:69574454-69574539	H1-hESC	embryonic stem cell:	n/a	chr4:69574511-69574522
35	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
36	CEBPB	chr4:69279178-69279415	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
38	CEBPB	chr4:69578074-69578242	A549	lung:	n/a	n/a
39	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
40	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
41	CEBPB	chr4:69300033-69300365	HepG2	liver:	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
42	CEBPB	chr4:69279166-69279328	K562	blood:	n/a	n/a
43	CEBPB	chr4:69279172-69279414	K562	blood:	n/a	n/a
44	CEBPB	chr4:69277211-69277380	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
46	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
47	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
48	CEBPB	chr4:69310875-69311174	IMR90	lung:	n/a	chr4:69310996-69311009 chr4:69310996-69311009 chr4:69310996-69311007
49	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
50	CEBPB	chr4:69300021-69300356	K562	blood:	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

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69340916-69340966	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:69340916-69340966	AG04450	lung:	fetal
3	chr4:69340916-69340966	HEK293	kidney:	embryo
4	chr4:69340916-69340966	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:69340916-69340966	AG04450	lung:	fetal
6	chr4:69340916-69340966	HEK293	kidney:	embryo
7	chr4:69355121-69355171	LNCaP	prostate:	n/a
8	chr4:69435250-69435300	ovcar-3	ovarian:	n/a
9	chr4:69434475-69434525	PrEC	prostate:	n/a
10	chr4:69313197-69313247	NB4	blood:	n/a
11	chr4:69537589-69537639	HRE	kidney:	n/a
12	chr4:69537826-69537876	ECC-1	luminal epithelium:	n/a
13	chr4:69313197-69313247	ovcar-3	ovarian:	n/a
14	chr4:69381368-69381418	AoSMC	blood vessel:	n/a
15	chr4:69536319-69536369	GM12892	blood:	n/a
16	chr4:69434475-69434525	HCT-116	colon:	n/a
17	chr4:69434475-69434525	AoSMC	blood vessel:	n/a
18	chr4:69435601-69435651	AG04450	lung:	fetal
19	chr4:69435250-69435300	T-47D	breast:	n/a
20	chr4:69514031-69514081	MCF10A-Er-Src	breast:	n/a
21	chr4:69312514-69312564	RPTEC	kidney:	n/a
22	chr4:69537589-69537639	HepG2	liver:	n/a
23	chr4:69340916-69340966	Caco-2	colon:	n/a
24	chr4:69536319-69536369	HEEpiC	esophagus:	n/a
25	chr4:69381368-69381418	GM12891	blood:	n/a
26	chr4:69537589-69537639	HRPEpiC	eye:	n/a
27	chr4:69537589-69537639	SAEC	small airway:	n/a
28	chr4:69435593-69435643	ProgFib	skin:	n/a
29	chr4:69537826-69537876	RPTEC	kidney:	n/a
30	chr4:69435593-69435643	AoSMC	blood vessel:	n/a
31	chr4:69355121-69355171	ovcar-3	ovarian:	n/a
32	chr4:69434475-69434525	HMEC	breast:	n/a
33	chr4:69434475-69434525	A549	lung:	n/a
34	chr4:69514031-69514081	IMR90	lung:	fetal
35	chr4:69537826-69537876	LNCaP	prostate:	n/a
36	chr4:69434475-69434525	BJ	skin:	n/a
37	chr4:69435593-69435643	HRPEpiC	eye:	n/a
38	chr4:69536319-69536369	A549	lung:	n/a
39	chr4:69313197-69313247	AoSMC	blood vessel:	n/a
40	chr4:69313197-69313247	SK-N-SH_RA	brain:	n/a
41	chr4:69435601-69435651	HCF	heart:	n/a
42	chr4:69313197-69313247	HCPEpiC	choroid plexus:	n/a
43	chr4:69522639-69522689	HRCEpiC	kidney:	n/a
44	chr4:69514031-69514081	SAEC	small airway:	n/a
45	chr4:69536319-69536369	CMK	blood:	n/a
46	chr4:69312104-69312154	CMK	blood:	n/a
47	chr4:69313197-69313247	GM19239	blood:	n/a
48	chr4:69435250-69435300	SK-N-SH	brain:	n/a
49	chr4:69313197-69313247	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:69435250-69435300	PANC-1	pancreas:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
2	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
3	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
4	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
5	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
6	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
7	chr4:69590462..69592610-chr4:69729563..69731579,3	MCF-7	breast:
8	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
9	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
10	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
11	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
12	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
13	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
14	chr4:68794213..68794935-chr4:69590279..69590859,2	MCF-7	breast:
15	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
16	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
17	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
18	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
19	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
20	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
21	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
22	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
23	chr3:73105975..73106777-chr4:69561197..69562068,2	MCF-7	breast:
24	chr4:68794694..68797024-chr4:69366841..69368465,2	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-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
3	lnc-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
4	lnc-UGT2B15-2	chr4:69492565-69492700	NONHSAT096737
5	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
6	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737

No data

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

Extended variants
information (count: 9108 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:9108 , 50 per page) page: 1 2 3 4 5 6 7 ... 183

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140224313	chr4:69276389-69276390	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs150382732	chr4:69276402-69276403	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs145058339	chr4:69276418-69276419	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs149088461	chr4:69276461-69276462	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs143107541	chr4:69276492-69276493	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs375299518	chr4:69276497-69276498	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs138826337	chr4:69276552-69276553	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs554258250	chr4:69276556-69276557	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
9	rs143152160	chr4:69276572-69276573	Genic enhancers Enhancers Weak transcription Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs542849554	chr4:69276634-69276635	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs113862453	chr4:69276644-69276645	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
12	rs541958901	chr4:69276676-69276677	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs553104814	chr4:69276691-69276692	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs577862967	chr4:69276692-69276693	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs147058019	chr4:69276729-69276730	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs138322149	chr4:69276741-69276742	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs386675574	chr4:69276768-69276769	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs141824722	chr4:69276769-69276770	Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs150696452	chr4:69276820-69276821	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547147527	chr4:69276834-69276835	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561040942	chr4:69276899-69276900	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542971424	chr4:69276962-69276963	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112629580	chr4:69277021-69277022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34703110	chr4:69277036-69277037	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549156658	chr4:69277093-69277094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369188782	chr4:69277095-69277096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182198776	chr4:69277118-69277119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185938428	chr4:69277156-69277157	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs35581194	chr4:69277171-69277172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372955012	chr4:69277174-69277175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34105933	chr4:69277228-69277229	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs3903591	chr4:69277234-69277235	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534221444	chr4:69277278-69277279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553931514	chr4:69277312-69277313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146377698	chr4:69277328-69277329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs190712146	chr4:69277337-69277338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs79340726	chr4:69277490-69277491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs112273780	chr4:69277493-69277494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370226977	chr4:69277510-69277511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs371454514	chr4:69277512-69277513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556391334	chr4:69277527-69277528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs139680817	chr4:69277613-69277614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs568971512	chr4:69277615-69277616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs373655304	chr4:69277626-69277627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs377687895	chr4:69277694-69277695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545308658	chr4:69277735-69277736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143301520	chr4:69277775-69277776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182360156	chr4:69277790-69277791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185442975	chr4:69277791-69277792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146687438	chr4:69277809-69277810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

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
Non-syndromic sensorineural hearing loss	22297974	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69273200-69279600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:69273800-69276400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:69274200-69276800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:69274400-69276400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr4:69274600-69277000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:69275000-69276800	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr4:69275000-69276800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:69275600-69276800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:69276000-69276400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:69276000-69276600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:69276000-69276800	Enhancers	H9 Cell Line	embryonic stem cell
12	chr4:69276200-69276400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:69276200-69276600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr4:69276200-69276800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:69276200-69277000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:69276400-69276800	Genic enhancers	H1 Cell Line	embryonic stem cell
17	chr4:69276400-69276800	Genic enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr4:69276400-69283600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr4:69276600-69277600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr4:69276800-69278600	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr4:69276800-69279400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr4:69276800-69279600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr4:69276800-69279600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr4:69276800-69282200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr4:69276800-69283400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr4:69276800-69284600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:69277000-69278200	Enhancers	HMEC	breast
28	chr4:69277000-69278600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr4:69277000-69278600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:69277000-69279400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr4:69277200-69277800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr4:69277400-69278000	Enhancers	NHEK	skin
33	chr4:69277400-69278400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:69277600-69277800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr4:69277800-69278200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:69278200-69278400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:69278200-69278600	Weak transcription	HMEC	breast
38	chr4:69278400-69282200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:69278400-69282200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:69278600-69278800	Enhancers	H9 Cell Line	embryonic stem cell
41	chr4:69278600-69278800	Enhancers	Placenta	Placenta
42	chr4:69278600-69278800	Enhancers	HMEC	breast
43	chr4:69278600-69280000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:69278600-69282200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:69278800-69279000	Flanking Active TSS	Placenta	Placenta
46	chr4:69278800-69281600	Weak transcription	HMEC	breast
47	chr4:69278800-69283400	Weak transcription	H9 Cell Line	embryonic stem cell
48	chr4:69279000-69279200	Active TSS	Placenta	Placenta
49	chr4:69279200-69280000	Enhancers	Placenta	Placenta
50	chr4:69279400-69280000	Enhancers	HUES48 Cell Line	embryonic stem cell

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