Variant report

Variant	esv2752578
Chromosome Location	chr8:90990091-90995971
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:90995791-90997104	K562	blood:	n/a	n/a
2	ATF1	chr8:90995970-90997121	K562	blood:	n/a	n/a
3	ATF2	chr8:90993691-90994238	GM12878	blood:	n/a	n/a
4	ATF2	chr8:90995909-90997242	GM12878	blood:	n/a	n/a
5	BACH1	chr8:90995776-90996607	K562	blood:	n/a	n/a
6	BCLAF1	chr8:90995963-90997155	GM12878	blood:	n/a	chr8:90996578-90996591 chr8:90996508-90996517
7	BHLHE40	chr8:90993731-90994146	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:90995749-90997182	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:90995683-90997405	K562	blood:	n/a	n/a
10	BRCA1	chr8:90995836-90997130	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr8:90995899-90997282	HCT-116	colon:	n/a	n/a
12	CCNT2	chr8:90995936-90997077	K562	blood:	n/a	chr8:90996500-90996509
13	CEBPB	chr8:90995828-90997208	A549	lung:	n/a	n/a
14	CEBPB	chr8:90995806-90997086	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr8:90995608-90997140	GM12878	blood:	n/a	n/a
16	CEBPD	chr8:90995664-90996895	K562	blood:	n/a	n/a
17	CHD1	chr8:90993030-90995111	GM12878	blood:	n/a	n/a
18	CHD1	chr8:90995329-90997044	GM12878	blood:	n/a	chr8:90996506-90996516
19	CHD1	chr8:90995806-90995958	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr8:90992645-90992723	GM12878	blood:	n/a	n/a
21	CHD2	chr8:90993702-90994033	GM12878	blood:	n/a	n/a
22	CREB1	chr8:90995927-90997080	GM12878	blood:	n/a	n/a
23	CTCF	chr8:90995670-90997383	SK-N-SH	brain:	n/a	chr8:90996955-90996968 chr8:90996956-90996966 chr8:90996519-90996537 chr8:90996521-90996542 chr8:90996524-90996534 chr8:90996522-90996531 chr8:90996954-90996970 chr8:90996418-90996431 chr8:90996522-90996535 chr8:90996519-90996532 chr8:90996522-90996535 chr8:90996520-90996536 chr8:90996959-90996968 chr8:90996948-90996969 chr8:90996953-90996971 chr8:90996955-90996968
24	CTCF	chr8:90995855-90997305	MCF-7	breast:	n/a	chr8:90996955-90996968 chr8:90996956-90996966 chr8:90996519-90996537 chr8:90996521-90996542 chr8:90996524-90996534 chr8:90996522-90996531 chr8:90996954-90996970 chr8:90996418-90996431 chr8:90996522-90996535 chr8:90996519-90996532 chr8:90996522-90996535 chr8:90996520-90996536 chr8:90996959-90996968 chr8:90996948-90996969 chr8:90996953-90996971 chr8:90996955-90996968
25	CTCF	chr8:90995896-90997407	HCT-116	colon:	n/a	chr8:90996955-90996968 chr8:90996956-90996966 chr8:90996519-90996537 chr8:90996521-90996542 chr8:90996524-90996534 chr8:90996522-90996531 chr8:90996954-90996970 chr8:90996418-90996431 chr8:90996522-90996535 chr8:90996519-90996532 chr8:90996522-90996535 chr8:90996520-90996536 chr8:90996959-90996968 chr8:90996948-90996969 chr8:90996953-90996971 chr8:90996955-90996968
26	CTCF	chr8:90995940-90996090	HCT-116	colon:	n/a	n/a
27	CTCF	chr8:90995940-90996090	AG09309	skin:	n/a	n/a
28	CTCF	chr8:90995075-90997592	A549	lung:	n/a	chr8:90996955-90996968 chr8:90996956-90996966 chr8:90996519-90996537 chr8:90996521-90996542 chr8:90996524-90996534 chr8:90996522-90996531 chr8:90996954-90996970 chr8:90996418-90996431 chr8:90996522-90996535 chr8:90996519-90996532 chr8:90996522-90996535 chr8:90996520-90996536 chr8:90996959-90996968 chr8:90996948-90996969 chr8:90996953-90996971 chr8:90996955-90996968
29	CTCF	chr8:90995940-90996090	NHLF	lung:	n/a	n/a
30	CUX1	chr8:90993312-90994211	GM12878	blood:	n/a	n/a
31	CUX1	chr8:90995855-90997170	K562	blood:	n/a	n/a
32	CUX1	chr8:90994899-90995089	K562	blood:	n/a	n/a
33	CUX1	chr8:90995866-90997123	GM12878	blood:	n/a	n/a
34	E2F4	chr8:90995930-90997071	MCF10A-Er-Src	breast:	n/a	chr8:90996079-90996089 chr8:90996079-90996090 chr8:90996080-90996087
35	EBF1	chr8:90995555-90997101	GM12878	blood:	n/a	chr8:90996029-90996038 chr8:90996027-90996038
36	EBF1	chr8:90993028-90995036	GM12878	blood:	n/a	chr8:90994136-90994149
37	EBF1	chr8:90993243-90993558	GM12878	blood:	n/a	n/a
38	EBF1	chr8:90995875-90996365	GM12878	blood:	n/a	chr8:90996029-90996038 chr8:90996027-90996038
39	EBF1	chr8:90993769-90994260	GM12878	blood:	n/a	chr8:90994136-90994149
40	ELF1	chr8:90995952-90997169	MCF-7	breast:	n/a	n/a
41	ELF1	chr8:90995860-90997250	MCF-7	breast:	n/a	n/a
42	ELK1	chr8:90993928-90994054	GM12878	blood:	n/a	n/a
43	ELK1	chr8:90995886-90996976	K562	blood:	n/a	n/a
44	ELK1	chr8:90995837-90997039	GM12878	blood:	n/a	n/a
45	ELK1	chr8:90994628-90994629	GM12878	blood:	n/a	n/a
46	EP300	chr8:90993784-90994094	GM12878	blood:	n/a	n/a
47	EP300	chr8:90995874-90997292	SK-N-SH	brain:	n/a	chr8:90996290-90996304 chr8:90996528-90996537 chr8:90996458-90996474
48	EP300	chr8:90995717-90997110	K562	blood:	n/a	chr8:90995873-90995887 chr8:90996290-90996304 chr8:90996528-90996537 chr8:90996458-90996474
49	EP300	chr8:90993892-90994329	GM12878	blood:	n/a	n/a
50	EP300	chr8:90993802-90994108	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:90992387-90992437	AoSMC	blood vessel:	n/a
2	chr8:90992387-90992437	HepG2	liver:	n/a
3	chr8:90992387-90992437	A549	lung:	n/a
4	chr8:90992387-90992437	ECC-1	luminal epithelium:	n/a
5	chr8:90992387-90992437	SKMC	muscle:	n/a
6	chr8:90992387-90992437	HEK293	kidney:	embryo
7	chr8:90992387-90992437	CMK	blood:	n/a
8	chr8:90992387-90992437	Caco-2	colon:	n/a
9	chr8:90992387-90992437	NT2-D1	testis:	n/a
10	chr8:90992387-90992437	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:90992387-90992437	NHDF-neo	bronchial:	n/a
12	chr8:90992387-90992437	GM19239	blood:	n/a
13	chr8:90992387-90992437	ProgFib	skin:	n/a
14	chr8:90992387-90992437	PrEC	prostate:	n/a
15	chr8:90992387-90992437	SK-N-MC	brain:	n/a
16	chr8:90992387-90992437	SK-N-SH_RA	brain:	n/a
17	chr8:90992387-90992437	AG04450	lung:	fetal
18	chr8:90992387-90992437	HCT-116	colon:	n/a
19	chr8:90992387-90992437	GM12892	blood:	n/a
20	chr8:90992387-90992437	ovcar-3	ovarian:	n/a
21	chr8:90992387-90992437	HRE	kidney:	n/a
22	chr8:90992387-90992437	MCF10A-Er-Src	breast:	n/a
23	chr8:90992387-90992437	HEEpiC	esophagus:	n/a
24	chr8:90992387-90992437	PFSK-1	brain:	n/a
25	chr8:90992387-90992437	H1-hESC	embryonic stem cell:	embryo
26	chr8:90992387-90992437	HL-60	blood:	n/a
27	chr8:90992387-90992437	Hela-S3	cervix:	n/a
28	chr8:90992387-90992437	IMR90	lung:	fetal
29	chr8:90992387-90992437	T-47D	breast:	n/a
30	chr8:90992387-90992437	HMEC	breast:	n/a
31	chr8:90992387-90992437	MCF-7	breast:	n/a
32	chr8:90992387-90992437	GM12891	blood:	n/a
33	chr8:90992387-90992437	LNCaP	prostate:	n/a
34	chr8:90992387-90992437	HNPCEpiC	eye:	n/a
35	chr8:90992387-90992437	PANC-1	pancreas:	n/a
36	chr8:90992387-90992437	HRCEpiC	kidney:	n/a
37	chr8:90992387-90992437	HCM	heart:	n/a
38	chr8:90992387-90992437	U87	brain:	n/a
39	chr8:90992387-90992437	NH-A	brain:	n/a
40	chr8:90992387-90992437	Jurkat	blood:	n/a
41	chr8:90992387-90992437	SK-N-SH	brain:	n/a
42	chr8:90992387-90992437	AG09319	gingival:	n/a
43	chr8:90992387-90992437	K562	blood:	n/a
44	chr8:90992387-90992437	HIPEpiC	eye:	n/a
45	chr8:90992387-90992437	SAEC	small airway:	n/a
46	chr8:90992387-90992437	BJ	skin:	n/a
47	chr8:90992387-90992437	AG04449	skin:	fetal
48	chr8:90992387-90992437	AG10803	skin:	n/a
49	chr8:90992387-90992437	HCPEpiC	choroid plexus:	n/a
50	chr8:90992387-90992437	HUVEC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:90914584..90915234-chr8:90995916..90996860,2	MCF-7	breast:
2	chr8:90994579..90998162-chr8:91656500..91661270,5	K562	blood:
3	chr8:90912595..90916756-chr8:90994852..90998205,9	K562	blood:
4	chr8:90911185..90916499-chr8:90992960..90998209,20	MCF-7	breast:
5	chr8:90991149..90993502-chr8:91207366..91210281,2	K562	blood:
6	chr8:90859372..90863594-chr8:90985537..90991967,6	MCF-7	breast:
7	chr8:90913353..90915903-chr8:90994626..90998419,6	K562	blood:
8	chr8:90889480..90891758-chr8:90994219..90995933,2	MCF-7	breast:
9	chr8:90770081..90772255-chr8:90988919..90991592,2	MCF-7	breast:
10	chr8:90766719..90773256-chr8:90991979..90999179,19	MCF-7	breast:
11	chr8:90995516..90998828-chr8:91010778..91014105,5	K562	blood:
12	chr8:90735826..90740064-chr8:90995306..90998250,3	MCF-7	breast:
13	chr8:90913007..90918207-chr8:90995257..90997906,9	MCF-7	breast:
14	chr8:90995523..90999017-chr8:91656346..91659175,4	K562	blood:
15	chr8:90735002..90740593-chr8:90994599..90998168,11	MCF-7	breast:
16	chr8:90995093..90997814-chr8:91010770..91014611,5	MCF-7	breast:
17	chr8:90984484..90993091-chr8:90993260..90998893,16	MCF-7	breast:
18	chr8:90737113..90738638-chr8:90994961..90997124,2	K562	blood:
19	chr8:90790967..90797055-chr8:90994383..90998113,5	MCF-7	breast:
20	chr8:90769588..90771314-chr8:90995090..90996692,2	K562	blood:
21	chr8:90766360..90773428-chr8:90991217..91000142,22	MCF-7	breast:
22	chr8:90993651..90998172-chr8:91012740..91014695,4	MCF-7	breast:
23	chr8:90953083..90955250-chr8:90994003..90995794,2	K562	blood:
24	chr8:90984874..90987349-chr8:90988956..90993202,5	MCF-7	breast:

Variant related genes	Relation type
NBN	TF binding region
NBN	CpG island
ENSG00000104320	chromatin interactions
ENSG00000207359	chromatin interactions
ENSG00000246792	chromatin interactions
ENSG00000180694	chromatin interactions
ENSG00000164823	chromatin interactions
ENSG00000251136	chromatin interactions
ENSG00000104325	chromatin interactions
ENSG00000104312	chromatin interactions

Extended variants
information (count: 233 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:233 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1805793	chr8:90990091-90990092	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544630250	chr8:90990097-90990098	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574883990	chr8:90990099-90990100	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs114391718	chr8:90990118-90990119	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs1805834	chr8:90990121-90990122	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs570296417	chr8:90990159-90990160	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs537037358	chr8:90990198-90990199	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs558298089	chr8:90990243-90990244	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576795517	chr8:90990259-90990260	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187999418	chr8:90990341-90990342	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552661078	chr8:90990386-90990387	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs192240705	chr8:90990416-90990417	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs541669441	chr8:90990422-90990423	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs1805794	chr8:90990479-90990480	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs151070415	chr8:90990485-90990486	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs61754966	chr8:90990521-90990522	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182756889	chr8:90990527-90990528	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373764513	chr8:90990581-90990582	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs367769892	chr8:90990585-90990586	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs200034959	chr8:90990590-90990591	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs13312873	chr8:90990607-90990608	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs397843982	chr8:90990610-90990611	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs187046429	chr8:90990710-90990711	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532564035	chr8:90990713-90990714	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541494069	chr8:90990718-90990719	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs104895037	chr8:90990719-90990720	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs530311443	chr8:90990848-90990849	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150163091	chr8:90990853-90990854	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs570309272	chr8:90990861-90990862	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566645734	chr8:90990874-90990875	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531083909	chr8:90990880-90990881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13312872	chr8:90990881-90990882	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570073638	chr8:90990909-90990910	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs534322017	chr8:90990934-90990935	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs192193474	chr8:90990948-90990949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs13312871	chr8:90990960-90990961	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs371257582	chr8:90991030-90991031	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs77171980	chr8:90991042-90991043	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs527532266	chr8:90991066-90991067	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs58089706	chr8:90991075-90991076	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs527406607	chr8:90991106-90991107	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs143665775	chr8:90991121-90991122	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1805835	chr8:90991144-90991145	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs138357157	chr8:90991230-90991231	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs143916395	chr8:90991234-90991235	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs577261168	chr8:90991237-90991238	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs541481419	chr8:90991245-90991246	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs559873207	chr8:90991247-90991248	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs530247805	chr8:90991252-90991253	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs7832009	chr8:90991268-90991269	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:108)

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
Autism	22495311	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
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	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
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
Breast cancer	20409316	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:515 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:90915800-90995000	Weak transcription	Fetal Brain Male	brain
2	chr8:90927800-90996000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr8:90962000-90994400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr8:90962000-90995000	Weak transcription	Aorta	Aorta
5	chr8:90970800-90993200	Weak transcription	Psoas Muscle	Psoas
6	chr8:90971000-90994000	Weak transcription	Brain Substantia Nigra	brain
7	chr8:90971200-90994400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr8:90971400-90993800	Weak transcription	Small Intestine	intestine
9	chr8:90971800-90995600	Weak transcription	Right Ventricle	heart
10	chr8:90973800-90993800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr8:90974200-90993800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr8:90975600-90993800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr8:90975600-90993800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr8:90975600-90994000	Weak transcription	Brain Angular Gyrus	brain
15	chr8:90975600-90995800	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr8:90975800-90993200	Weak transcription	NHDF-Ad	bronchial
17	chr8:90976000-90993800	Weak transcription	Fetal Heart	heart
18	chr8:90976200-90993600	Weak transcription	Brain Hippocampus Middle	brain
19	chr8:90976200-90993800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
20	chr8:90976200-90993800	Weak transcription	Brain Germinal Matrix	brain
21	chr8:90976200-90995800	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:90976400-90993600	Weak transcription	NHEK	skin
23	chr8:90976400-90993800	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr8:90976400-90994400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr8:90976400-90995400	Weak transcription	Thymus	Thymus
26	chr8:90976400-90995600	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr8:90976400-90995800	Weak transcription	Esophagus	oesophagus
28	chr8:90976600-90994400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr8:90976800-90993400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr8:90977000-90993400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr8:90977200-90993600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr8:90979600-90993000	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr8:90980600-90993600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr8:90980800-90995600	Weak transcription	Ovary	ovary
35	chr8:90981000-90993000	Weak transcription	Brain Anterior Caudate	brain
36	chr8:90981600-90994800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:90982000-90994200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr8:90983200-90991400	Weak transcription	Placenta	Placenta
39	chr8:90983200-90993600	Weak transcription	HepG2	liver
40	chr8:90983200-90993800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr8:90983200-90993800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr8:90983600-90994000	Weak transcription	NH-A	brain
43	chr8:90983800-90994800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr8:90983800-90995600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr8:90985400-90993200	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr8:90986000-90993800	Weak transcription	HSMMtube	muscle
47	chr8:90986600-90990200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr8:90986800-90993200	Strong transcription	HSMM	muscle
49	chr8:90987000-90994200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr8:90987000-90996000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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