Variant report

Variant	nsv1013420
Chromosome Location	chr4:69316439-69540013
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1264)
CpG islands
(count:795)
Chromatin interactive
region (count:19)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69479543-69479775	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
8	BACH1	chr4:69318318-69318341	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:69316907-69317183	H1-hESC	embryonic stem cell:	n/a	chr4:69317106-69317120
10	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
11	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
12	BATF	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
13	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
14	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
15	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
16	BATF	chr4:69538989-69539205	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
19	BCL3	chr4:69536262-69536632	A549	lung:	n/a	n/a
20	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
21	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
22	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
23	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
24	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
25	CEBPB	chr4:69530299-69530470	HepG2	liver:	n/a	chr4:69530340-69530351
26	CEBPB	chr4:69536198-69536502	MCF-7	breast:	n/a	chr4:69536341-69536354
27	CEBPB	chr4:69536204-69536567	A549	lung:	n/a	chr4:69536341-69536354
28	CEBPB	chr4:69536277-69536474	HepG2	liver:	n/a	chr4:69536341-69536354
29	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
30	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
31	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
32	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
35	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
36	CEBPB	chr4:69530297-69530431	A549	lung:	n/a	chr4:69530340-69530351
37	CEBPB	chr4:69536174-69536504	A549	lung:	n/a	chr4:69536341-69536354
38	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
40	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
41	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
42	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
43	CTCF	chr4:69443360-69443510	GM12867	blood:	n/a	n/a
44	CTCF	chr4:69531989-69532010	Lung_OC	lung:	n/a	n/a
45	CTCF	chr4:69539025-69539079	GM12891	blood:	n/a	n/a
46	CTCF	chr4:69364220-69364370	HUVEC	blood vessel:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
47	CTCF	chr4:69364300-69364450	SAEC	small airway:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
48	CTCF	chr4:69539680-69539830	GM12873	blood:	n/a	n/a
49	CTCF	chr4:69539740-69539890	GM12874	blood:	n/a	n/a
50	CTCF	chr4:69538988-69539100	GM12892	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69522639-69522689	SK-N-SH	brain:	n/a
2	chr4:69522639-69522689	ovcar-3	ovarian:	n/a
3	chr4:69522639-69522689	SK-N-SH	brain:	n/a
4	chr4:69522639-69522689	ovcar-3	ovarian:	n/a
5	chr4:69537826-69537876	NT2-D1	testis:	n/a
6	chr4:69381368-69381418	GM12891	blood:	n/a
7	chr4:69435601-69435651	AG04449	skin:	fetal
8	chr4:69435593-69435643	HNPCEpiC	eye:	n/a
9	chr4:69355121-69355171	RPTEC	kidney:	n/a
10	chr4:69435250-69435300	MCF10A-Er-Src	breast:	n/a
11	chr4:69537826-69537876	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:69435601-69435651	ovcar-3	ovarian:	n/a
13	chr4:69537589-69537639	HCM	heart:	n/a
14	chr4:69435593-69435643	GM19239	blood:	n/a
15	chr4:69340916-69340966	HCPEpiC	choroid plexus:	n/a
16	chr4:69435593-69435643	H1-hESC	embryonic stem cell:	embryo
17	chr4:69381368-69381418	NHDF-neo	bronchial:	n/a
18	chr4:69435593-69435643	SK-N-MC	brain:	n/a
19	chr4:69435593-69435643	HUVEC	blood vessel:	n/a
20	chr4:69536319-69536369	NB4	blood:	n/a
21	chr4:69514031-69514081	U87	brain:	n/a
22	chr4:69435250-69435300	PFSK-1	brain:	n/a
23	chr4:69435601-69435651	T-47D	breast:	n/a
24	chr4:69537826-69537876	BJ	skin:	n/a
25	chr4:69514031-69514081	A549	lung:	n/a
26	chr4:69537589-69537639	RPTEC	kidney:	n/a
27	chr4:69522639-69522689	HCT-116	colon:	n/a
28	chr4:69537826-69537876	GM12891	blood:	n/a
29	chr4:69435250-69435300	BJ	skin:	n/a
30	chr4:69536319-69536369	PrEC	prostate:	n/a
31	chr4:69340916-69340966	IMR90	lung:	fetal
32	chr4:69434475-69434525	Jurkat	blood:	n/a
33	chr4:69537826-69537876	HepG2	liver:	n/a
34	chr4:69522639-69522689	NB4	blood:	n/a
35	chr4:69435250-69435300	LNCaP	prostate:	n/a
36	chr4:69435250-69435300	AG04449	skin:	fetal
37	chr4:69381368-69381418	SK-N-SH	brain:	n/a
38	chr4:69537826-69537876	HCF	heart:	n/a
39	chr4:69514031-69514081	HMEC	breast:	n/a
40	chr4:69340916-69340966	Jurkat	blood:	n/a
41	chr4:69340916-69340966	GM12891	blood:	n/a
42	chr4:69435593-69435643	AG09319	gingival:	n/a
43	chr4:69434475-69434525	AG04449	skin:	fetal
44	chr4:69537826-69537876	HRCEpiC	kidney:	n/a
45	chr4:69381368-69381418	MCF-7	breast:	n/a
46	chr4:69537589-69537639	HUVEC	blood vessel:	n/a
47	chr4:69434475-69434525	HNPCEpiC	eye:	n/a
48	chr4:69537826-69537876	HMEC	breast:	n/a
49	chr4:69537806-69537856	NH-A	brain:	n/a
50	chr4:69537589-69537639	GM06990	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
2	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
3	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
4	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
5	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
6	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
7	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
8	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
9	chr4:69311298..69314792-chr4:69316366..69319525,5	MCF-7	breast:
10	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
11	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
12	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
13	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
14	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
15	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
16	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
17	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
18	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
19	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:

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

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

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
TMPRSS11E	CpG island
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B15	CpG island
UGT2B29P	CpG island
ENSG00000272626	chromatin interactions
ENSG00000083896	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000087128	chromatin interactions

Extended variants
information (count: 6655 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:6655 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568218042	chr4:69316456-69316457	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs537373569	chr4:69316482-69316483	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189488246	chr4:69316484-69316485	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs191127645	chr4:69316499-69316500	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545840191	chr4:69316542-69316543	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553099463	chr4:69316587-69316588	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184496760	chr4:69316596-69316597	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs34931688	chr4:69316601-69316602	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142231064	chr4:69316622-69316623	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs541222220	chr4:69316639-69316640	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs368067986	chr4:69316655-69316656	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs151211685	chr4:69316668-69316669	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs112822279	chr4:69316718-69316719	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537783622	chr4:69316769-69316770	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs189465118	chr4:69316785-69316786	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs543723106	chr4:69316870-69316871	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs563674739	chr4:69316905-69316906	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139669497	chr4:69316911-69316912	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs181461823	chr4:69316912-69316913	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs145268837	chr4:69316953-69316954	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554421326	chr4:69316959-69316960	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371156010	chr4:69316962-69316963	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs147612485	chr4:69316969-69316970	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142474372	chr4:69316979-69316980	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs186501723	chr4:69317054-69317055	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs536881684	chr4:69317057-69317058	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs567935555	chr4:69317059-69317060	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs386675579	chr4:69317078-69317079	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs1554890	chr4:69317080-69317081	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs553011583	chr4:69317094-69317095	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs553855473	chr4:69317127-69317128	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs572807006	chr4:69317138-69317139	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577220192	chr4:69317163-69317164	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs188975590	chr4:69317180-69317181	Enhancers Weak transcription Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs148920556	chr4:69317243-69317244	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574504428	chr4:69317259-69317260	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs143822755	chr4:69317274-69317275	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181741659	chr4:69317284-69317285	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148153797	chr4:69317369-69317370	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545751985	chr4:69317459-69317460	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs559718741	chr4:69317472-69317473	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528542308	chr4:69317484-69317485	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs548647661	chr4:69317539-69317540	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs143054129	chr4:69317560-69317561	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs530719923	chr4:69317616-69317617	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550833364	chr4:69317630-69317631	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs145129239	chr4:69317692-69317693	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs539746017	chr4:69317712-69317713	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368007315	chr4:69317811-69317812	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs138950495	chr4:69317865-69317866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

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	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:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:69308400-69317800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr4:69311800-69321200	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:69312000-69320000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:69312000-69321400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:69312200-69318200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:69312800-69318200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr4:69313200-69318200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr4:69313600-69316600	Weak transcription	HMEC	breast
9	chr4:69313600-69316800	Weak transcription	NHEK	skin
10	chr4:69314400-69321400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr4:69314600-69316800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:69314800-69317400	Weak transcription	Primary T cells from cord blood	blood
13	chr4:69315200-69317200	Enhancers	H9 Cell Line	embryonic stem cell
14	chr4:69315800-69319800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr4:69315800-69320000	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr4:69316000-69316800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr4:69316400-69318400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:69316400-69319200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:69316600-69317400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:69316600-69318400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:69316600-69319600	Enhancers	HMEC	breast
22	chr4:69316800-69317000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr4:69316800-69317000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:69316800-69317200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
25	chr4:69316800-69317200	Active TSS	Esophagus	oesophagus
26	chr4:69316800-69319200	Enhancers	NHEK	skin
27	chr4:69317000-69317400	Enhancers	Placenta Amnion	Placenta Amnion
28	chr4:69317000-69317800	Enhancers	Colon Smooth Muscle	Colon
29	chr4:69317000-69318200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
30	chr4:69317200-69317800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:69317200-69318200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr4:69317200-69319800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr4:69317400-69317600	Enhancers	Primary T helper cells PMA-I stimulated	--
34	chr4:69317400-69317800	Enhancers	Primary T cells from cord blood	blood
35	chr4:69317400-69317800	Enhancers	NH-A	brain
36	chr4:69317600-69317800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr4:69317600-69318600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr4:69317600-69319200	Enhancers	Primary B cells from peripheral blood	blood
39	chr4:69317800-69318000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr4:69318000-69318400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr4:69318200-69319000	Enhancers	H1 Cell Line	embryonic stem cell
42	chr4:69318200-69319000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr4:69318200-69319600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
44	chr4:69318200-69319600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr4:69318200-69319600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:69318400-69318800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr4:69318600-69319200	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr4:69319000-69325600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:69319600-69335800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:69319800-69320800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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