Variant report

Variant	nsv6072
Chromosome Location	chr8:8414563-8440656
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:342)
CpG islands
(count:184)
Chromatin interactive
region (count:18)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:342 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr8:8426436-8427026	GM12878	blood:	n/a	n/a
2	ATF2	chr8:8426361-8427059	GM12878	blood:	n/a	n/a
3	BACH1	chr8:8422093-8422283	H1-hESC	embryonic stem cell:	n/a	chr8:8422188-8422202
4	BATF	chr8:8426529-8426975	GM12878	blood:	n/a	n/a
5	BATF	chr8:8426530-8427011	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:8426517-8426963	GM12878	blood:	n/a	chr8:8426749-8426758 chr8:8426641-8426650
7	BCL11A	chr8:8426505-8426978	GM12878	blood:	n/a	chr8:8426749-8426758 chr8:8426641-8426650
8	BCLAF1	chr8:8426415-8426984	GM12878	blood:	n/a	chr8:8426749-8426758 chr8:8426641-8426650
9	BCLAF1	chr8:8426415-8427052	GM12878	blood:	n/a	chr8:8426749-8426758 chr8:8426641-8426650
10	BHLHE40	chr8:8423112-8423388	HepG2	liver:	n/a	n/a
11	BHLHE40	chr8:8423087-8423380	K562	blood:	n/a	n/a
12	BHLHE40	chr8:8426372-8427065	GM12878	blood:	n/a	n/a
13	CBX3	chr8:8418135-8418451	HCT-116	colon:	n/a	n/a
14	CEBPB	chr8:8417756-8418091	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:8417758-8418114	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:8430206-8430619	A549	lung:	n/a	n/a
17	CEBPB	chr8:8433197-8433597	HepG2	liver:	n/a	chr8:8433379-8433390
18	CEBPB	chr8:8426566-8426952	GM12878	blood:	n/a	n/a
19	CEBPB	chr8:8435844-8436134	IMR90	lung:	n/a	n/a
20	CEBPB	chr8:8430233-8430733	ECC-1	luminal epithelium:	n/a	n/a
21	CEBPB	chr8:8417765-8418100	A549	lung:	n/a	n/a
22	CEBPB	chr8:8417817-8418096	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr8:8435910-8436076	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr8:8430292-8430647	A549	lung:	n/a	n/a
25	CEBPB	chr8:8417901-8417987	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:8434607-8434972	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr8:8433200-8433578	A549	lung:	n/a	chr8:8433379-8433390
28	CEBPB	chr8:8433280-8433612	MCF-7	breast:	n/a	chr8:8433379-8433390
29	CEBPB	chr8:8417795-8418159	A549	lung:	n/a	n/a
30	CEBPB	chr8:8430249-8430712	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:8422075-8422196	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr8:8430242-8430728	IMR90	lung:	n/a	n/a
33	CEBPB	chr8:8433199-8433618	Hela-S3	cervix:	n/a	chr8:8433379-8433390
34	CEBPB	chr8:8430186-8430736	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPZ	chr8:8426916-8427015	HepG2	liver:	n/a	n/a
36	CHD1	chr8:8426321-8426989	GM12878	blood:	n/a	n/a
37	CHD2	chr8:8426530-8426993	GM12878	blood:	n/a	n/a
38	CREB1	chr8:8426433-8426972	GM12878	blood:	n/a	n/a
39	CTCF	chr8:8436040-8436190	GM12870	blood:	n/a	n/a
40	CTCF	chr8:8436022-8436212	GM12878	blood:	n/a	n/a
41	CTCF	chr8:8436080-8436230	HCT-116	colon:	n/a	n/a
42	CTCF	chr8:8436055-8436174	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr8:8436040-8436190	GM12878	blood:	n/a	n/a
44	CTCF	chr8:8436140-8436290	A549	lung:	n/a	n/a
45	CTCF	chr8:8436029-8436214	K562	blood:	n/a	n/a
46	CTCF	chr8:8436120-8436270	GM12865	blood:	n/a	n/a
47	CTCF	chr8:8436040-8436190	HEK293	kidney:	n/a	n/a
48	CTCF	chr8:8436040-8436190	GM12866	blood:	n/a	n/a
49	CTCF	chr8:8436008-8436182	GM19238	blood:	n/a	n/a
50	CTCF	chr8:8436040-8436190	WERI-Rb-1	eye:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8439596-8439646	HUVEC	blood vessel:	n/a
2	chr8:8439596-8439646	HUVEC	blood vessel:	n/a
3	chr8:8419587-8419637	PANC-1	pancreas:	n/a
4	chr8:8419587-8419637	HEK293	kidney:	embryo
5	chr8:8420735-8420785	AG04449	skin:	fetal
6	chr8:8439596-8439646	AG04449	skin:	fetal
7	chr8:8420735-8420785	LNCaP	prostate:	n/a
8	chr8:8419587-8419637	GM12891	blood:	n/a
9	chr8:8420735-8420785	Hela-S3	cervix:	n/a
10	chr8:8420735-8420785	GM12891	blood:	n/a
11	chr8:8420735-8420785	HRCEpiC	kidney:	n/a
12	chr8:8439596-8439646	HRCEpiC	kidney:	n/a
13	chr8:8439596-8439646	NHBE	bronchial:	n/a
14	chr8:8439596-8439646	HL-60	blood:	n/a
15	chr8:8439596-8439646	HEEpiC	esophagus:	n/a
16	chr8:8420735-8420785	HRE	kidney:	n/a
17	chr8:8419587-8419637	RPTEC	kidney:	n/a
18	chr8:8439596-8439646	K562	blood:	n/a
19	chr8:8420735-8420785	AG04450	lung:	fetal
20	chr8:8439596-8439646	Caco-2	colon:	n/a
21	chr8:8439596-8439646	NB4	blood:	n/a
22	chr8:8419587-8419637	HL-60	blood:	n/a
23	chr8:8420735-8420785	GM06990	blood:	n/a
24	chr8:8439596-8439646	ProgFib	skin:	n/a
25	chr8:8419587-8419637	Hepatocyte	liver:	n/a
26	chr8:8420735-8420785	ovcar-3	ovarian:	n/a
27	chr8:8419587-8419637	NB4	blood:	n/a
28	chr8:8420735-8420785	AG09309	skin:	n/a
29	chr8:8420735-8420785	RPTEC	kidney:	n/a
30	chr8:8439596-8439646	ovcar-3	ovarian:	n/a
31	chr8:8419587-8419637	NHDF-neo	bronchial:	n/a
32	chr8:8439596-8439646	HNPCEpiC	eye:	n/a
33	chr8:8420735-8420785	H1-hESC	embryonic stem cell:	embryo
34	chr8:8420735-8420785	Hepatocyte	liver:	n/a
35	chr8:8420735-8420785	ECC-1	luminal epithelium:	n/a
36	chr8:8439596-8439646	GM12891	blood:	n/a
37	chr8:8419587-8419637	SK-N-SH_RA	brain:	n/a
38	chr8:8420735-8420785	NHDF-neo	bronchial:	n/a
39	chr8:8420735-8420785	HIPEpiC	eye:	n/a
40	chr8:8419587-8419637	AG04449	skin:	fetal
41	chr8:8419587-8419637	GM19239	blood:	n/a
42	chr8:8439596-8439646	HCT-116	colon:	n/a
43	chr8:8439596-8439646	PANC-1	pancreas:	n/a
44	chr8:8439596-8439646	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:8419587-8419637	PrEC	prostate:	n/a
46	chr8:8420735-8420785	K562	blood:	n/a
47	chr8:8419587-8419637	HPAEpiC	pulmonary alveolar:	n/a
48	chr8:8420735-8420785	NH-A	brain:	n/a
49	chr8:8439596-8439646	HCF	heart:	n/a
50	chr8:8419587-8419637	GM06990	blood:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8395182..8397914-chr8:8412349..8414858,2	MCF-7	breast:
2	chr8:8422238..8425021-chr8:8428768..8430499,2	MCF-7	breast:
3	chr8:8426650..8428995-chr8:8432055..8433956,2	MCF-7	breast:
4	chr8:8411447..8415576-chr8:8419918..8422813,4	MCF-7	breast:
5	chr8:8424041..8426477-chr8:8428202..8430360,2	K562	blood:
6	chr8:8411664..8414236-chr8:8423427..8425709,2	MCF-7	breast:
7	chr8:8412630..8415274-chr8:8423101..8424700,2	K562	blood:
8	chr8:8422023..8423577-chr8:8457115..8459478,2	MCF-7	breast:
9	chr8:8431429..8434026-chr8:8436657..8439955,3	MCF-7	breast:
10	chr8:8412630..8415274-chr8:8423101..8424700,2	K562	blood:
11	chr8:8411447..8415576-chr8:8419918..8422813,4	MCF-7	breast:
12	chr8:8424041..8426477-chr8:8428202..8430360,2	K562	blood:
13	chr8:8422238..8425021-chr8:8428768..8430499,2	MCF-7	breast:
14	chr8:8242353..8245621-chr8:8412264..8415410,4	MCF-7	breast:
15	chr8:8426650..8428995-chr8:8432055..8433956,2	MCF-7	breast:
16	chr8:8431429..8434026-chr8:8436657..8439955,3	MCF-7	breast:
17	chr8:8430219..8432230-chr8:8438202..8440679,2	K562	blood:
18	chr8:8241776..8244765-chr8:8431330..8433692,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLDN23-1	chr8:8426697-8427048	XLOC_006698
2	lnc-CLDN23-2	chr8:8418711-8418847	ENSG00000253774
3	lnc-CLDN23-1	chr8:8426474-8428227	NONHSAT124878
4	lnc-PRAGMIN.1-4	chr8:8418430-8418475	ENSG00000253343
5	lnc-PRAGMIN.1-9	chr8:8439864-8440165	NONHSAT124884
6	lnc-CLDN23-2	chr8:8419343-8419634	ENSG00000253774
7	lnc-CLDN23-1	chr8:8418904-8419044	ENSG00000253130
8	lnc-CLDN23-1	chr8:8418711-8418867	NONHSAT124878
9	lnc-CLDN23-1	chr8:8431228-8435105	NONHSAT124878
10	lnc-CLDN23-1	chr8:8422143-8422213	XLOC_006698
11	lnc-CLDN23-1	chr8:8426697-8427198	ENSG00000253130
12	lnc-CLDN23-1	chr8:8418901-8419044	NONHSAT124878
13	lnc-CLDN23-2	chr8:8417404-8417553	ENSG00000253774
14	lnc-CLDN23-1	chr8:8421617-8422045	ENSG00000253130
15	lnc-CLDN23-1	chr8:8418901-8419044	ENSG00000253130
16	lnc-CLDN23-1	chr8:8421329-8422570	NONHSAT124878
17	lnc-CLDN23-1	chr8:8419343-8419634	NONHSAT124878
18	lnc-CLDN23-1	chr8:8417404-8417553	NONHSAT124878

No data

Variant related genes	Relation type
ENSG00000253774	TF binding region
ENSG00000253343	TF binding region
RN7SL178P	TF binding region
ENSG00000253130	TF binding region
ENSG00000253774	CpG island
ENSG00000253343	CpG island
RN7SL178P	CpG island
ENSG00000253130	CpG island
ENSG00000263616	chromatin interactions
ENSG00000182319	chromatin interactions

Extended variants
information (count: 1344 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111231386	chr8:8414600-8414601	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs553547857	chr8:8414608-8414609	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs189790045	chr8:8414610-8414611	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs534262929	chr8:8414632-8414633	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs554006036	chr8:8414699-8414700	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs570717338	chr8:8414712-8414713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539619317	chr8:8414714-8414715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368276414	chr8:8414734-8414735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs556399014	chr8:8414775-8414776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs141152815	chr8:8414790-8414791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182121871	chr8:8414797-8414798	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555779806	chr8:8414825-8414826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73518861	chr8:8414838-8414839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs540535966	chr8:8414840-8414841	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs560458553	chr8:8414848-8414849	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs115539451	chr8:8414854-8414855	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528523598	chr8:8414859-8414860	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs369571136	chr8:8414880-8414881	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562520385	chr8:8414888-8414889	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375000129	chr8:8414951-8414952	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs373532388	chr8:8415048-8415049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs531479188	chr8:8415064-8415065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs187139521	chr8:8415122-8415123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547972603	chr8:8415153-8415154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs28713404	chr8:8415178-8415179	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs28611351	chr8:8415209-8415210	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547707894	chr8:8415214-8415215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190058317	chr8:8415280-8415281	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs11777722	chr8:8415295-8415296	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs201147285	chr8:8415305-8415306	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570727815	chr8:8415344-8415345	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs112099226	chr8:8415388-8415389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34421768	chr8:8415390-8415391	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs6986005	chr8:8415404-8415405	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs535953206	chr8:8415408-8415409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs28578218	chr8:8415424-8415425	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs552276483	chr8:8415430-8415431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140189606	chr8:8415442-8415443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565633593	chr8:8415462-8415463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs34715712	chr8:8415482-8415483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs66460042	chr8:8415483-8415484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10699722	chr8:8415484-8415485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541401937	chr8:8415496-8415497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113787432	chr8:8415551-8415552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547885897	chr8:8415563-8415564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558166051	chr8:8415613-8415614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs118170206	chr8:8415617-8415618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374289126	chr8:8415635-8415636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs143936459	chr8:8415641-8415642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531366824	chr8:8415655-8415656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16774939	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8403600-8421400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:8406400-8414800	Enhancers	NHDF-Ad	bronchial
3	chr8:8410800-8414600	Weak transcription	Fetal Lung	lung
4	chr8:8412000-8414800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr8:8412400-8414800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:8412600-8414800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr8:8412600-8414800	Enhancers	A549	lung
8	chr8:8413000-8414600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr8:8413400-8418800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr8:8413400-8419000	Weak transcription	Ovary	ovary
11	chr8:8413600-8414600	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:8413600-8419000	Weak transcription	HSMMtube	muscle
13	chr8:8413600-8419000	Weak transcription	NHLF	lung
14	chr8:8413800-8414600	Enhancers	HUVEC	blood vessel
15	chr8:8413800-8415000	Enhancers	Fetal Intestine Small	intestine
16	chr8:8413800-8415800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr8:8413800-8419000	Weak transcription	NH-A	brain
18	chr8:8414000-8414600	Enhancers	Left Ventricle	heart
19	chr8:8414200-8414600	Enhancers	Stomach Mucosa	stomach
20	chr8:8414200-8414800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:8414200-8414800	Enhancers	Spleen	Spleen
22	chr8:8414200-8415000	Enhancers	Fetal Intestine Large	intestine
23	chr8:8414400-8418600	Weak transcription	Osteobl	bone
24	chr8:8414400-8420200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr8:8414600-8414800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr8:8414600-8414800	Enhancers	Fetal Lung	lung
27	chr8:8414600-8420000	Weak transcription	Stomach Mucosa	stomach
28	chr8:8414800-8415000	Weak transcription	Fetal Lung	lung
29	chr8:8414800-8418800	Weak transcription	A549	lung
30	chr8:8414800-8421600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr8:8414800-8422000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:8415200-8416600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr8:8415800-8416200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:8416200-8419400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr8:8418600-8419600	Enhancers	Osteobl	bone
36	chr8:8418800-8419600	Enhancers	A549	lung
37	chr8:8418800-8419800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:8419000-8419400	Enhancers	NH-A	brain
39	chr8:8419000-8419600	Enhancers	Ovary	ovary
40	chr8:8419000-8419600	Enhancers	HSMMtube	muscle
41	chr8:8419000-8420800	Enhancers	NHLF	lung
42	chr8:8419000-8423600	Enhancers	Fetal Lung	lung
43	chr8:8419200-8419400	Enhancers	Duodenum Mucosa	Duodenum
44	chr8:8419200-8420400	Bivalent Enhancer	HepG2	liver
45	chr8:8419200-8420600	Enhancers	Fetal Brain Male	brain
46	chr8:8419400-8420200	Weak transcription	Duodenum Mucosa	Duodenum
47	chr8:8419400-8421600	Weak transcription	NH-A	brain
48	chr8:8419400-8423200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:8419600-8420000	Weak transcription	Ovary	ovary
50	chr8:8419600-8421800	Enhancers	Fetal Intestine Large	intestine

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