Variant report

Variant	nsv879230
Chromosome Location	chr4:69315236-69527406
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1047)
CpG islands
(count:550)
Chromatin interactive
region (count:20)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1047 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:69489457-69489609	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:69524230-69524826	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:69386831-69387059	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:69364158-69364549	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:69521827-69522720	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:69464978-69465269	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:69479543-69479775	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	chr4:69441350-69441539	GM12878	blood:	n/a	n/a
11	BATF	chr4:69522977-69523278	GM12878	blood:	n/a	n/a
12	BATF	chr4:69441348-69441590	GM12878	blood:	n/a	n/a
13	BATF	chr4:69419767-69419937	GM12878	blood:	n/a	n/a
14	BATF	chr4:69364212-69364472	GM12878	blood:	n/a	n/a
15	BATF	chr4:69523003-69523215	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:69419791-69419969	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:69523069-69523272	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:69435323-69435604	K562	blood:	n/a	n/a
19	BHLHE40	chr4:69364150-69364589	GM12878	blood:	n/a	n/a
20	BHLHE40	chr4:69522248-69522562	GM12878	blood:	n/a	n/a
21	CCNT2	chr4:69328625-69328750	K562	blood:	n/a	n/a
22	CEBPB	chr4:69321712-69322175	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:69447436-69447754	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr4:69419232-69419353	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:69463247-69463520	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:69431039-69431053	HepG2	liver:	n/a	chr4:69431039-69431050 chr4:69431041-69431050
27	CEBPB	chr4:69447453-69447718	K562	blood:	n/a	n/a
28	CEBPB	chr4:69462434-69462560	A549	lung:	n/a	chr4:69462483-69462500
29	CEBPB	chr4:69325378-69325503	K562	blood:	n/a	n/a
30	CEBPB	chr4:69447506-69447748	A549	lung:	n/a	n/a
31	CEBPB	chr4:69471903-69472154	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:69327525-69327817	MCF-7	breast:	n/a	n/a
33	CEBPB	chr4:69482880-69482916	A549	lung:	n/a	n/a
34	CEBPB	chr4:69321591-69322194	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:69364240-69364390	AG04449	skin:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
36	CTCF	chr4:69443360-69443510	GM12873	blood:	n/a	n/a
37	CTCF	chr4:69364126-69364538	K562	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
38	CTCF	chr4:69523079-69523241	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:69364181-69364466	Lung_OC	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
40	CTCF	chr4:69364220-69364370	HL-60	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
41	CTCF	chr4:69364033-69364752	A549	lung:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
42	CTCF	chr4:69364160-69364310	WI-38	lung:	n/a	n/a
43	CTCF	chr4:69364155-69364475	Spleen_OC	spleen:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
44	CTCF	chr4:69419763-69419979	GM13977	blood:	n/a	n/a
45	CTCF	chr4:69418660-69418810	HepG2	liver:	n/a	n/a
46	CTCF	chr4:69443461-69443509	A549	lung:	n/a	n/a
47	CTCF	chr4:69364238-69364417	GM19239	blood:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
48	CTCF	chr4:69419773-69419978	GM19240	blood:	n/a	n/a
49	CTCF	chr4:69364200-69364605	MCF-7	breast:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327
50	CTCF	chr4:69364300-69364450	BE2_C	brain:	n/a	chr4:69364312-69364333 chr4:69364310-69364328 chr4:69364311-69364327

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:69435250-69435300	SK-N-SH	brain:	n/a
2	chr4:69435250-69435300	SK-N-SH	brain:	n/a
3	chr4:69522639-69522689	AoSMC	blood vessel:	n/a
4	chr4:69355121-69355171	SK-N-SH_RA	brain:	n/a
5	chr4:69435593-69435643	AG10803	skin:	n/a
6	chr4:69340916-69340966	Jurkat	blood:	n/a
7	chr4:69435593-69435643	SK-N-SH	brain:	n/a
8	chr4:69434475-69434525	T-47D	breast:	n/a
9	chr4:69522639-69522689	HNPCEpiC	eye:	n/a
10	chr4:69355121-69355171	HL-60	blood:	n/a
11	chr4:69435593-69435643	NHDF-neo	bronchial:	n/a
12	chr4:69355121-69355171	NHDF-neo	bronchial:	n/a
13	chr4:69522639-69522689	HIPEpiC	eye:	n/a
14	chr4:69435593-69435643	ovcar-3	ovarian:	n/a
15	chr4:69435593-69435643	HUVEC	blood vessel:	n/a
16	chr4:69381368-69381418	HepG2	liver:	n/a
17	chr4:69435250-69435300	RPTEC	kidney:	n/a
18	chr4:69340916-69340966	HUVEC	blood vessel:	n/a
19	chr4:69435593-69435643	BJ	skin:	n/a
20	chr4:69340916-69340966	MCF10A-Er-Src	breast:	n/a
21	chr4:69340916-69340966	Hepatocyte	liver:	n/a
22	chr4:69381368-69381418	LNCaP	prostate:	n/a
23	chr4:69340916-69340966	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:69340916-69340966	CMK	blood:	n/a
25	chr4:69381368-69381418	HEEpiC	esophagus:	n/a
26	chr4:69522639-69522689	CMK	blood:	n/a
27	chr4:69381368-69381418	ECC-1	luminal epithelium:	n/a
28	chr4:69435250-69435300	NHBE	bronchial:	n/a
29	chr4:69435593-69435643	GM12892	blood:	n/a
30	chr4:69522639-69522689	HRPEpiC	eye:	n/a
31	chr4:69435250-69435300	HEEpiC	esophagus:	n/a
32	chr4:69355121-69355171	U87	brain:	n/a
33	chr4:69435593-69435643	SKMC	muscle:	n/a
34	chr4:69435601-69435651	K562	blood:	n/a
35	chr4:69522639-69522689	HepG2	liver:	n/a
36	chr4:69381368-69381418	T-47D	breast:	n/a
37	chr4:69340916-69340966	NB4	blood:	n/a
38	chr4:69355121-69355171	Jurkat	blood:	n/a
39	chr4:69435601-69435651	NHBE	bronchial:	n/a
40	chr4:69522639-69522689	HRE	kidney:	n/a
41	chr4:69435250-69435300	NH-A	brain:	n/a
42	chr4:69340916-69340966	BE2_C	brain:	n/a
43	chr4:69514031-69514081	HNPCEpiC	eye:	n/a
44	chr4:69435593-69435643	GM19239	blood:	n/a
45	chr4:69381368-69381418	PANC-1	pancreas:	n/a
46	chr4:69435250-69435300	U87	brain:	n/a
47	chr4:69355121-69355171	RPTEC	kidney:	n/a
48	chr4:69340916-69340966	SAEC	small airway:	n/a
49	chr4:69522639-69522689	GM12891	blood:	n/a
50	chr4:69434475-69434525	SK-N-SH_RA	brain:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:69326187..69328959-chr4:69331153..69333884,3	MCF-7	breast:
2	chr4:69235222..69236888-chr4:69330787..69333108,2	MCF-7	breast:
3	chr4:69308561..69313812-chr4:69314832..69320961,6	K562	blood:
4	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
5	chr4:69211043..69213753-chr4:69341284..69343236,2	K562	blood:
6	chr4:69319066..69321050-chr4:69325892..69327547,2	MCF-7	breast:
7	chr4:69375140..69375898-chr4:69492301..69492816,2	MCF-7	breast:
8	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
9	chr4:69215797..69217317-chr4:69361139..69363891,2	MCF-7	breast:
10	chr4:69293251..69295177-chr4:69318009..69319544,2	K562	blood:
11	chr4:69313083..69315969-chr4:69334821..69336429,2	MCF-7	breast:
12	chr4:69362843..69365661-chr4:69770776..69774163,4	MCF-7	breast:
13	chr4:68794694..68797024-chr4:69366841..69368465,2	MCF-7	breast:
14	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
15	chr4:69314066..69315762-chr4:69317720..69319307,2	K562	blood:
16	chr4:69363348..69364328-chr4:69890914..69891634,2	MCF-7	breast:
17	chr4:68794156..68795825-chr4:69317354..69319516,2	MCF-7	breast:
18	chr4:69330018..69331837-chr4:69335427..69337976,2	MCF-7	breast:
19	chr4:69317417..69319881-chr4:69327468..69329389,2	MCF-7	breast:
20	chr4:69311298..69314792-chr4:69316366..69319525,5	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-UGT2B15-3	chr4:69481111-69481855	NONHSAT096736
3	lnc-UGT2B15-2	chr4:69493903-69494617	NONHSAT096737
4	lnc-UGT2B17-1	chr4:69375159-69375392	NONHSAT096733
5	lnc-TMPRSS11E-2	chr4:69480137-69480731	NONHSAT096735
6	lnc-UGT2B15-2	chr4:69492565-69492700	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
UGT2B29P	TF binding region
TMPRSS11E	CpG island
ENSG00000249472	CpG island
ENSG00000251074	CpG island
ENSG00000251101	CpG island
UGT2B17	CpG island
UGT2B29P	CpG island
ENSG00000272626	chromatin interactions
ENSG00000249985	chromatin interactions
ENSG00000087128	chromatin interactions
ENSG00000083896	chromatin interactions

Extended variants
information (count: 6210 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:6210 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79034235	chr4:69315236-69315237	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs563234761	chr4:69315256-69315257	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs138348941	chr4:69315274-69315275	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369757736	chr4:69315342-69315343	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551957890	chr4:69315458-69315459	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs36030967	chr4:69315548-69315549	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs527954703	chr4:69315575-69315576	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs547755690	chr4:69315579-69315580	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs187816276	chr4:69315613-69315614	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs529039650	chr4:69315615-69315616	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371326883	chr4:69315616-69315617	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs35998156	chr4:69315671-69315672	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs10518053	chr4:69315711-69315712	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs192916203	chr4:69315715-69315716	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs183318065	chr4:69315761-69315762	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs141592151	chr4:69315777-69315778	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs558303881	chr4:69315787-69315788	Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs542823956	chr4:69315817-69315818	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs386675578	chr4:69315818-69315819	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs200454225	chr4:69315819-69315820	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531672980	chr4:69315820-69315821	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs150897608	chr4:69315835-69315836	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs188719605	chr4:69315880-69315881	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs138279549	chr4:69315889-69315890	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs34956644	chr4:69315905-69315906	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192216613	chr4:69315915-69315916	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563276110	chr4:69315925-69315926	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs200915901	chr4:69315989-69315990	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs576984629	chr4:69316001-69316002	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs146213241	chr4:69316032-69316033	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs139247084	chr4:69316085-69316086	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs142446790	chr4:69316100-69316101	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs548013382	chr4:69316104-69316105	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184695671	chr4:69316128-69316129	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs530434415	chr4:69316153-69316154	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs549862606	chr4:69316275-69316276	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs569738607	chr4:69316276-69316277	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs532437436	chr4:69316281-69316282	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs546733688	chr4:69316325-69316326	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552239143	chr4:69316334-69316335	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs565865136	chr4:69316340-69316341	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143893291	chr4:69316376-69316377	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148605752	chr4:69316394-69316395	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs532138372	chr4:69316422-69316423	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs568218042	chr4:69316456-69316457	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs537373569	chr4:69316482-69316483	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189488246	chr4:69316484-69316485	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs191127645	chr4:69316499-69316500	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs545840191	chr4:69316542-69316543	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs553099463	chr4:69316587-69316588	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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

Chromatin state (count:416 , 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	chr4:69314400-69316400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:69314400-69321400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr4:69314600-69316800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:69314800-69317400	Weak transcription	Primary T cells from cord blood	blood
14	chr4:69315200-69315400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
15	chr4:69315200-69315400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr4:69315200-69317200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr4:69315400-69315600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:69315400-69315600	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:69315600-69315800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr4:69315600-69315800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr4:69315600-69316000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr4:69315800-69319800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr4:69315800-69320000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:69316000-69316800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr4:69316400-69318400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:69316400-69319200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:69316600-69317400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr4:69316600-69318400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:69316600-69319600	Enhancers	HMEC	breast
30	chr4:69316800-69317000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr4:69316800-69317000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:69316800-69317200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr4:69316800-69317200	Active TSS	Esophagus	oesophagus
34	chr4:69316800-69319200	Enhancers	NHEK	skin
35	chr4:69317000-69317400	Enhancers	Placenta Amnion	Placenta Amnion
36	chr4:69317000-69317800	Enhancers	Colon Smooth Muscle	Colon
37	chr4:69317000-69318200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr4:69317200-69317800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr4:69317200-69318200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr4:69317200-69319800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr4:69317400-69317600	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr4:69317400-69317800	Enhancers	Primary T cells from cord blood	blood
43	chr4:69317400-69317800	Enhancers	NH-A	brain
44	chr4:69317600-69317800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:69317600-69318600	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr4:69317600-69319200	Enhancers	Primary B cells from peripheral blood	blood
47	chr4:69317800-69318000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
48	chr4:69318000-69318400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr4:69318200-69319000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr4:69318200-69319000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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