Variant report

Variant	nsv518636
Chromosome Location	chr8:95196794-95233336
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:738)
CpG islands
(count:610)
Chromatin interactive
region (count:30)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:95218407-95218446	K562	blood:	n/a	n/a
2	ATF1	chr8:95231164-95231381	K562	blood:	n/a	n/a
3	ATF2	chr8:95232569-95233051	GM12878	blood:	n/a	n/a
4	ATF2	chr8:95229597-95230197	GM12878	blood:	n/a	n/a
5	ATF2	chr8:95230930-95231587	GM12878	blood:	n/a	n/a
6	ATF2	chr8:95230950-95231630	GM12878	blood:	n/a	n/a
7	ATF2	chr8:95232611-95233091	GM12878	blood:	n/a	n/a
8	BACH1	chr8:95231967-95232122	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:95231134-95231401	GM12878	blood:	n/a	n/a
10	BATF	chr8:95229668-95229959	GM12878	blood:	n/a	n/a
11	BATF	chr8:95230966-95231514	GM12878	blood:	n/a	n/a
12	BATF	chr8:95232624-95232998	GM12878	blood:	n/a	n/a
13	BATF	chr8:95232596-95233020	GM12878	blood:	n/a	n/a
14	BCL11A	chr8:95232740-95232973	GM12878	blood:	n/a	n/a
15	BCL11A	chr8:95221856-95222050	GM12878	blood:	n/a	chr8:95222039-95222048
16	BCL11A	chr8:95231167-95231430	GM12878	blood:	n/a	n/a
17	BCL11A	chr8:95232697-95233050	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:95231060-95231542	GM12878	blood:	n/a	n/a
19	BCL3	chr8:95231078-95231513	GM12878	blood:	n/a	n/a
20	BCLAF1	chr8:95229554-95230109	GM12878	blood:	n/a	n/a
21	BCLAF1	chr8:95231000-95231623	GM12878	blood:	n/a	n/a
22	BCLAF1	chr8:95232585-95232979	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:95231021-95231589	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:95221813-95222111	GM12878	blood:	n/a	n/a
25	BRCA1	chr8:95231883-95232347	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr8:95231641-95232411	HCT-116	colon:	n/a	n/a
27	CBX3	chr8:95231655-95232418	HCT-116	colon:	n/a	n/a
28	CBX3	chr8:95210615-95211285	HCT-116	colon:	n/a	n/a
29	CEBPB	chr8:95215723-95215969	Hela-S3	cervix:	n/a	chr8:95215842-95215853
30	CEBPB	chr8:95210794-95211093	A549	lung:	n/a	n/a
31	CEBPB	chr8:95211452-95211703	IMR90	lung:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
32	CEBPB	chr8:95215809-95216001	HepG2	liver:	n/a	chr8:95215842-95215853
33	CEBPB	chr8:95211432-95211741	HepG2	liver:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
34	CEBPB	chr8:95231751-95232213	A549	lung:	n/a	n/a
35	CEBPB	chr8:95217366-95217645	HepG2	liver:	n/a	chr8:95217525-95217536 chr8:95217522-95217539
36	CEBPB	chr8:95218787-95219031	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr8:95219338-95219696	IMR90	lung:	n/a	n/a
38	CEBPB	chr8:95230947-95231600	GM12878	blood:	n/a	n/a
39	CEBPB	chr8:95232576-95233079	IMR90	lung:	n/a	chr8:95232884-95232895
40	CEBPB	chr8:95209598-95209888	HepG2	liver:	n/a	chr8:95209752-95209763 chr8:95209750-95209761
41	CEBPB	chr8:95218272-95218526	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:95219343-95219704	A549	lung:	n/a	n/a
43	CEBPB	chr8:95231664-95232216	A549	lung:	n/a	n/a
44	CEBPB	chr8:95218254-95218537	A549	lung:	n/a	n/a
45	CEBPB	chr8:95231749-95232216	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:95231651-95232357	HCT-116	colon:	n/a	n/a
47	CEBPB	chr8:95211554-95211626	K562	blood:	n/a	chr8:95211568-95211579 chr8:95211567-95211578 chr8:95211569-95211578
48	CEBPB	chr8:95232739-95232968	Hela-S3	cervix:	n/a	chr8:95232884-95232895
49	CEBPB	chr8:95210377-95211262	A549	lung:	n/a	n/a
50	CEBPB	chr8:95209585-95209785	IMR90	lung:	n/a	chr8:95209752-95209763 chr8:95209750-95209761

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95229525-95229575	MCF10A-Er-Src	breast:	n/a
2	chr8:95229664-95229714	BE2_C	brain:	n/a
3	chr8:95220779-95220829	HCPEpiC	choroid plexus:	n/a
4	chr8:95229664-95229714	ProgFib	skin:	n/a
5	chr8:95222020-95222070	AG04450	lung:	fetal
6	chr8:95221197-95221247	PANC-1	pancreas:	n/a
7	chr8:95221342-95221392	A549	lung:	n/a
8	chr8:95229525-95229575	GM06990	blood:	n/a
9	chr8:95229872-95229922	HL-60	blood:	n/a
10	chr8:95221342-95221392	NH-A	brain:	n/a
11	chr8:95229525-95229575	HAEpiC	amniotic membrane:	n/a
12	chr8:95229664-95229714	H1-hESC	embryonic stem cell:	embryo
13	chr8:95229872-95229922	RPTEC	kidney:	n/a
14	chr8:95221197-95221247	H1-hESC	embryonic stem cell:	embryo
15	chr8:95229754-95229804	SK-N-SH_RA	brain:	n/a
16	chr8:95222020-95222070	HAEpiC	amniotic membrane:	n/a
17	chr8:95222020-95222070	AG09319	gingival:	n/a
18	chr8:95229525-95229575	K562	blood:	n/a
19	chr8:95221342-95221392	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:95229754-95229804	SAEC	small airway:	n/a
21	chr8:95220779-95220829	H1-hESC	embryonic stem cell:	embryo
22	chr8:95230984-95231034	BJ	skin:	n/a
23	chr8:95222020-95222070	HRCEpiC	kidney:	n/a
24	chr8:95229664-95229714	Caco-2	colon:	n/a
25	chr8:95230984-95231034	HCF	heart:	n/a
26	chr8:95221342-95221392	HIPEpiC	eye:	n/a
27	chr8:95229525-95229575	HEEpiC	esophagus:	n/a
28	chr8:95229872-95229922	SK-N-SH	brain:	n/a
29	chr8:95221197-95221247	Hepatocyte	liver:	n/a
30	chr8:95230984-95231034	AG04450	lung:	fetal
31	chr8:95229872-95229922	HCPEpiC	choroid plexus:	n/a
32	chr8:95230984-95231034	AG04449	skin:	fetal
33	chr8:95222020-95222070	BJ	skin:	n/a
34	chr8:95221197-95221247	HNPCEpiC	eye:	n/a
35	chr8:95220779-95220829	HEEpiC	esophagus:	n/a
36	chr8:95229872-95229922	HRE	kidney:	n/a
37	chr8:95229664-95229714	A549	lung:	n/a
38	chr8:95221197-95221247	PFSK-1	brain:	n/a
39	chr8:95220779-95220829	HCT-116	colon:	n/a
40	chr8:95229754-95229804	SKMC	muscle:	n/a
41	chr8:95229664-95229714	SK-N-SH_RA	brain:	n/a
42	chr8:95222020-95222070	HCPEpiC	choroid plexus:	n/a
43	chr8:95220779-95220829	SK-N-SH	brain:	n/a
44	chr8:95221197-95221247	ovcar-3	ovarian:	n/a
45	chr8:95222020-95222070	GM12891	blood:	n/a
46	chr8:95222020-95222070	U87	brain:	n/a
47	chr8:95229664-95229714	HCM	heart:	n/a
48	chr8:95220583-95220633	GM12878	blood:	n/a
49	chr8:95229525-95229575	HepG2	liver:	n/a
50	chr8:95220583-95220633	IMR90	lung:	fetal

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95176962..95177482-chr8:95225796..95226601,2	MCF-7	breast:
2	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:
3	chr8:95217922..95218880-chr8:95369574..95370256,2	MCF-7	breast:
4	chr8:95224589..95225412-chr8:95369113..95370095,2	MCF-7	breast:
5	chr8:95199696..95200396-chr8:95284281..95284998,2	MCF-7	breast:
6	chr21:41711010..41712741-chr8:95200062..95201579,2	MCF-7	breast:
7	chr8:95181437..95183595-chr8:95195671..95197695,2	MCF-7	breast:
8	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
9	chr8:95201827..95203670-chr8:95208153..95211021,2	MCF-7	breast:
10	chr8:95206766..95209394-chr8:95210564..95212309,3	MCF-7	breast:
11	chr8:95216472..95218639-chr8:95229347..95231439,2	MCF-7	breast:
12	chr8:95218436..95218963-chr8:95284617..95285220,2	MCF-7	breast:
13	chr8:95091661..95092727-chr8:95199725..95200487,4	MCF-7	breast:
14	chr8:95200777..95202734-chr8:95202948..95204607,2	K562	blood:
15	chr8:95091864..95092388-chr8:95200565..95201228,2	MCF-7	breast:
16	chr8:95219101..95220726-chr8:95272538..95274563,2	MCF-7	breast:
17	chr8:95223330..95225554-chr8:95230383..95232655,2	MCF-7	breast:
18	chr8:95200777..95202734-chr8:95202948..95204607,2	K562	blood:
19	chr8:95104717..95105462-chr8:95199836..95200440,2	MCF-7	breast:
20	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
21	chr8:94751681..94753437-chr8:95200264..95202250,2	MCF-7	breast:
22	chr8:95200401..95202545-chr8:95205826..95207380,2	K562	blood:
23	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
24	chr8:95201827..95203670-chr8:95208153..95211021,2	MCF-7	breast:
25	chr8:95215544..95217656-chr8:95220305..95222366,3	MCF-7	breast:
26	chr8:95221810..95224176-chr8:95226339..95228964,2	MCF-7	breast:
27	chr8:95092028..95092964-chr8:95199448..95200050,4	MCF-7	breast:
28	chr8:95217720..95220608-chr8:95221827..95224129,2	MCF-7	breast:
29	chr8:95006687..95007623-chr8:95199581..95200583,4	MCF-7	breast:
30	chr8:95200401..95202545-chr8:95205826..95207380,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GEM-1	chr8:95214701-95215280	NONHSAT127766
2	lnc-GEM-1	chr8:95214141-95214393	NONHSAT127766

No data

Variant related genes	Relation type
CDH17	TF binding region
ENSG00000249510	TF binding region
CDH17	CpG island
ENSG00000249510	CpG island
ENSG00000183808	chromatin interactions
ENSG00000164949	chromatin interactions
ENSG00000079112	chromatin interactions
ENSG00000253848	chromatin interactions
ENSG00000212998	chromatin interactions

Extended variants
information (count: 1424 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10098632	chr8:95196794-95196795	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150832761	chr8:95196801-95196802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139246669	chr8:95196805-95196806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572429246	chr8:95196831-95196832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573100917	chr8:95196893-95196894	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183091880	chr8:95196894-95196895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561316017	chr8:95196907-95196908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532436102	chr8:95196918-95196919	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542128241	chr8:95196920-95196921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74671749	chr8:95196975-95196976	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376804523	chr8:95196976-95196977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561928974	chr8:95196990-95196991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs187691649	chr8:95197030-95197031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs543710514	chr8:95197061-95197062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs75759452	chr8:95197068-95197069	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs62526263	chr8:95197126-95197127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531227456	chr8:95197156-95197157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs551067452	chr8:95197177-95197178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530844859	chr8:95197189-95197190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs369290448	chr8:95197229-95197230	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35670873	chr8:95197246-95197247	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547615486	chr8:95197253-95197254	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs34429581	chr8:95197263-95197264	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2514819	chr8:95197291-95197292	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs191467431	chr8:95197323-95197324	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183339985	chr8:95197372-95197373	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564330943	chr8:95197469-95197470	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145701627	chr8:95197472-95197473	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199680821	chr8:95197502-95197503	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556516192	chr8:95197505-95197506	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs71277462	chr8:95197539-95197540	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533455693	chr8:95197543-95197544	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188082857	chr8:95197586-95197587	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546828494	chr8:95197613-95197614	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2623170	chr8:95197655-95197656	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs149599646	chr8:95197686-95197687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs192077993	chr8:95197690-95197691	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs549185215	chr8:95197705-95197706	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs534805555	chr8:95197707-95197708	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184675492	chr8:95197750-95197751	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73695143	chr8:95197760-95197761	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs543581420	chr8:95197800-95197801	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375469432	chr8:95197822-95197823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs138513390	chr8:95197927-95197928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs190060201	chr8:95197954-95197955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577104995	chr8:95197996-95197997	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545027850	chr8:95198007-95198008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564722223	chr8:95198015-95198016	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527236385	chr8:95198025-95198026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547182361	chr8:95198041-95198042	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:112)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	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
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:420 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95189600-95200600	Weak transcription	Colonic Mucosa	Colon
2	chr8:95189800-95205800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr8:95192000-95198600	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr8:95193200-95197200	Weak transcription	Fetal Intestine Small	intestine
5	chr8:95194400-95196800	Weak transcription	Fetal Intestine Large	intestine
6	chr8:95196200-95196800	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr8:95196400-95197200	Weak transcription	Duodenum Mucosa	Duodenum
8	chr8:95196600-95197000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr8:95196600-95202600	Weak transcription	Small Intestine	intestine
10	chr8:95196800-95197600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr8:95196800-95200600	Strong transcription	Fetal Intestine Large	intestine
12	chr8:95197000-95200200	Strong transcription	Rectal Mucosa Donor 31	rectum
13	chr8:95197200-95197400	Strong transcription	Fetal Intestine Small	intestine
14	chr8:95197200-95197600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr8:95197200-95197800	Enhancers	NHDF-Ad	bronchial
16	chr8:95197200-95200000	Strong transcription	Duodenum Mucosa	Duodenum
17	chr8:95197400-95197800	Enhancers	Osteobl	bone
18	chr8:95197400-95198600	Weak transcription	Fetal Intestine Small	intestine
19	chr8:95197600-95198000	Strong transcription	Rectal Mucosa Donor 29	rectum
20	chr8:95198000-95198200	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr8:95198200-95200000	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr8:95198600-95199000	Strong transcription	Sigmoid Colon	Sigmoid Colon
23	chr8:95198600-95200000	Strong transcription	Fetal Intestine Small	intestine
24	chr8:95199000-95199200	Genic enhancers	Sigmoid Colon	Sigmoid Colon
25	chr8:95199200-95200000	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr8:95199800-95200800	Enhancers	Stomach Mucosa	stomach
27	chr8:95200000-95201400	Genic enhancers	Rectal Mucosa Donor 29	rectum
28	chr8:95200000-95201600	Genic enhancers	Sigmoid Colon	Sigmoid Colon
29	chr8:95200000-95202800	Genic enhancers	Duodenum Mucosa	Duodenum
30	chr8:95200000-95210200	Genic enhancers	Fetal Intestine Small	intestine
31	chr8:95200200-95201400	Genic enhancers	Rectal Mucosa Donor 31	rectum
32	chr8:95200600-95201600	Enhancers	Colonic Mucosa	Colon
33	chr8:95200600-95207400	Genic enhancers	Fetal Intestine Large	intestine
34	chr8:95200800-95201200	Flanking Active TSS	Stomach Mucosa	stomach
35	chr8:95201000-95201200	Enhancers	Pancreas	Pancrea
36	chr8:95201200-95201600	Enhancers	Stomach Mucosa	stomach
37	chr8:95201200-95210800	Weak transcription	Pancreas	Pancrea
38	chr8:95201400-95201800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
39	chr8:95201400-95202400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr8:95201600-95202000	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr8:95201600-95202600	Weak transcription	Colonic Mucosa	Colon
42	chr8:95201600-95203000	Weak transcription	Stomach Mucosa	stomach
43	chr8:95201800-95202200	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr8:95202000-95203400	Genic enhancers	Sigmoid Colon	Sigmoid Colon
45	chr8:95202200-95202800	Genic enhancers	Rectal Mucosa Donor 31	rectum
46	chr8:95202400-95204600	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr8:95202600-95203400	Genic enhancers	Colonic Mucosa	Colon
48	chr8:95202600-95203600	Enhancers	Small Intestine	intestine
49	chr8:95202800-95204800	Enhancers	Duodenum Mucosa	Duodenum
50	chr8:95202800-95204800	Enhancers	Rectal Mucosa Donor 31	rectum

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