Variant report

Variant	nsv891219
Chromosome Location	chr8:99526819-99643487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:862)
CpG islands
(count:183)
Chromatin interactive
region (count:90)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:862 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99625239-99625312	K562	blood:	n/a	n/a
2	ARID3A	chr8:99547792-99547835	K562	blood:	n/a	n/a
3	ARID3A	chr8:99538862-99539314	K562	blood:	n/a	n/a
4	ARID3A	chr8:99552839-99553223	K562	blood:	n/a	n/a
5	ARID3A	chr8:99610167-99611383	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:99570483-99570523	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:99617652-99618214	K562	blood:	n/a	n/a
8	ATF1	chr8:99552873-99553325	K562	blood:	n/a	n/a
9	ATF1	chr8:99617828-99618195	K562	blood:	n/a	n/a
10	ATF2	chr8:99613740-99614238	GM12878	blood:	n/a	n/a
11	BACH1	chr8:99533472-99533482	K562	blood:	n/a	n/a
12	BACH1	chr8:99613776-99614097	K562	blood:	n/a	n/a
13	BACH1	chr8:99625094-99625532	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr8:99625052-99625443	K562	blood:	n/a	n/a
15	BACH1	chr8:99613674-99614154	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr8:99613841-99614109	GM12878	blood:	n/a	chr8:99613940-99613951
17	BATF	chr8:99613825-99614144	GM12878	blood:	n/a	chr8:99613940-99613951
18	BHLHE40	chr8:99553115-99553231	K562	blood:	n/a	n/a
19	BRCA1	chr8:99612546-99612668	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr8:99613653-99614294	HCT-116	colon:	n/a	n/a
21	CBX3	chr8:99616582-99616969	K562	blood:	n/a	n/a
22	CBX3	chr8:99543429-99543836	HCT-116	colon:	n/a	n/a
23	CBX3	chr8:99617651-99618557	K562	blood:	n/a	n/a
24	CBX3	chr8:99613629-99614225	HCT-116	colon:	n/a	n/a
25	CBX3	chr8:99639639-99640036	K562	blood:	n/a	n/a
26	CBX3	chr8:99543471-99544159	K562	blood:	n/a	n/a
27	CBX3	chr8:99552776-99553837	K562	blood:	n/a	n/a
28	CCNT2	chr8:99538938-99539158	K562	blood:	n/a	n/a
29	CEBPB	chr8:99542244-99542487	A549	lung:	n/a	n/a
30	CEBPB	chr8:99561492-99561744	IMR90	lung:	n/a	chr8:99561589-99561600
31	CEBPB	chr8:99623280-99623515	MCF-7	breast:	n/a	chr8:99623394-99623405
32	CEBPB	chr8:99560789-99561031	K562	blood:	n/a	chr8:99560905-99560916
33	CEBPB	chr8:99561508-99561729	HepG2	liver:	n/a	chr8:99561589-99561600
34	CEBPB	chr8:99610884-99611378	IMR90	lung:	n/a	chr8:99611045-99611058
35	CEBPB	chr8:99592249-99592449	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:99623246-99623554	K562	blood:	n/a	chr8:99623394-99623405
37	CEBPB	chr8:99534918-99535293	A549	lung:	n/a	chr8:99535094-99535105
38	CEBPB	chr8:99610864-99611416	Hela-S3	cervix:	n/a	chr8:99611045-99611058
39	CEBPB	chr8:99534921-99535261	IMR90	lung:	n/a	chr8:99535094-99535105
40	CEBPB	chr8:99552821-99553181	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:99552777-99553194	K562	blood:	n/a	n/a
42	CEBPB	chr8:99584907-99585116	K562	blood:	n/a	chr8:99585037-99585050 chr8:99585037-99585050
43	CEBPB	chr8:99613594-99614736	HCT-116	colon:	n/a	n/a
44	CEBPB	chr8:99561461-99561666	K562	blood:	n/a	chr8:99561589-99561600
45	CEBPB	chr8:99561495-99561715	A549	lung:	n/a	chr8:99561589-99561600
46	CEBPB	chr8:99623228-99623560	IMR90	lung:	n/a	chr8:99623394-99623405
47	CEBPB	chr8:99560817-99561041	IMR90	lung:	n/a	chr8:99560905-99560916
48	CEBPB	chr8:99552887-99553258	MCF-7	breast:	n/a	n/a
49	CEBPB	chr8:99552828-99553181	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr8:99643424-99643784	IMR90	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99602568-99602618	PANC-1	pancreas:	n/a
2	chr8:99602540-99602590	GM12878	blood:	n/a
3	chr8:99602609-99602659	AG10803	skin:	n/a
4	chr8:99602540-99602590	HUVEC	blood vessel:	n/a
5	chr8:99602609-99602659	HCPEpiC	choroid plexus:	n/a
6	chr8:99602568-99602618	AG04449	skin:	fetal
7	chr8:99602568-99602618	H1-hESC	embryonic stem cell:	embryo
8	chr8:99602568-99602618	ProgFib	skin:	n/a
9	chr8:99602609-99602659	BE2_C	brain:	n/a
10	chr8:99602540-99602590	HL-60	blood:	n/a
11	chr8:99602540-99602590	SAEC	small airway:	n/a
12	chr8:99602609-99602659	PFSK-1	brain:	n/a
13	chr8:99602568-99602618	AG10803	skin:	n/a
14	chr8:99602540-99602590	AG09309	skin:	n/a
15	chr8:99602568-99602618	PrEC	prostate:	n/a
16	chr8:99602540-99602590	GM12891	blood:	n/a
17	chr8:99602568-99602618	GM06990	blood:	n/a
18	chr8:99602540-99602590	HIPEpiC	eye:	n/a
19	chr8:99602568-99602618	NH-A	brain:	n/a
20	chr8:99602568-99602618	MCF-7	breast:	n/a
21	chr8:99602568-99602618	CMK	blood:	n/a
22	chr8:99602540-99602590	PrEC	prostate:	n/a
23	chr8:99602540-99602590	NT2-D1	testis:	n/a
24	chr8:99602540-99602590	NB4	blood:	n/a
25	chr8:99602568-99602618	Jurkat	blood:	n/a
26	chr8:99602609-99602659	GM12891	blood:	n/a
27	chr8:99602609-99602659	AoSMC	blood vessel:	n/a
28	chr8:99602609-99602659	HRE	kidney:	n/a
29	chr8:99602540-99602590	HEK293	kidney:	embryo
30	chr8:99602568-99602618	HCF	heart:	n/a
31	chr8:99602540-99602590	HCT-116	colon:	n/a
32	chr8:99602540-99602590	MCF-7	breast:	n/a
33	chr8:99602568-99602618	SK-N-SH	brain:	n/a
34	chr8:99602540-99602590	ovcar-3	ovarian:	n/a
35	chr8:99602568-99602618	HRCEpiC	kidney:	n/a
36	chr8:99602609-99602659	NHBE	bronchial:	n/a
37	chr8:99602568-99602618	SK-N-MC	brain:	n/a
38	chr8:99602568-99602618	HL-60	blood:	n/a
39	chr8:99602568-99602618	NT2-D1	testis:	n/a
40	chr8:99602609-99602659	HEEpiC	esophagus:	n/a
41	chr8:99602568-99602618	HEEpiC	esophagus:	n/a
42	chr8:99602568-99602618	AG09319	gingival:	n/a
43	chr8:99602540-99602590	HNPCEpiC	eye:	n/a
44	chr8:99602609-99602659	HAEpiC	amniotic membrane:	n/a
45	chr8:99602568-99602618	PFSK-1	brain:	n/a
46	chr8:99602609-99602659	HRPEpiC	eye:	n/a
47	chr8:99602609-99602659	GM06990	blood:	n/a
48	chr8:99602609-99602659	HUVEC	blood vessel:	n/a
49	chr8:99602609-99602659	NT2-D1	testis:	n/a
50	chr8:99602540-99602590	MCF10A-Er-Src	breast:	n/a

(count:90 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:99581930..99583507-chr8:99587107..99589920,2	K562	blood:
2	chr8:99540019..99542563-chr8:99545669..99547224,2	K562	blood:
3	chr8:99561270..99563959-chr8:99566385..99568748,2	MCF-7	breast:
4	chr8:99609344..99611653-chr8:99621339..99623284,2	K562	blood:
5	chr8:99603037..99604820-chr8:99608384..99610236,2	MCF-7	breast:
6	chr8:99581930..99583507-chr8:99587107..99589920,2	K562	blood:
7	chr8:99618466..99620096-chr8:99645600..99647440,2	K562	blood:
8	chr8:99536690..99539147-chr8:99552855..99554572,2	K562	blood:
9	chr8:99642735..99645306-chr8:99645506..99647439,2	MCF-7	breast:
10	chr8:99542982..99544707-chr8:99547158..99548868,2	K562	blood:
11	chr8:99610760..99613076-chr8:99616322..99619231,2	K562	blood:
12	chr8:99527652..99530534-chr8:99540063..99542504,2	MCF-7	breast:
13	chr8:99552951..99554839-chr8:99564123..99567093,2	K562	blood:
14	chr8:99548500..99551679-chr8:99552322..99555998,3	K562	blood:
15	chr8:99527652..99530534-chr8:99540063..99542504,2	MCF-7	breast:
16	chr8:99486023..99488749-chr8:99617770..99619373,2	K562	blood:
17	chr8:99570092..99570986-chr8:100009815..100010452,2	MCF-7	breast:
18	chr8:99522297..99524358-chr8:99525451..99528433,2	K562	blood:
19	chr8:99586001..99587844-chr8:99593892..99596537,2	K562	blood:
20	chr8:99567325..99572845-chr8:99952617..99957549,5	MCF-7	breast:
21	chr8:99547855..99550787-chr8:99555161..99557416,2	MCF-7	breast:
22	chr8:99580951..99583147-chr8:99585319..99588307,2	MCF-7	breast:
23	chr8:99545068..99548423-chr8:99550336..99555475,4	K562	blood:
24	chr8:99568854..99571836-chr8:99577056..99579865,2	K562	blood:
25	chr8:99617084..99619037-chr8:99621813..99623940,2	K562	blood:
26	chr8:99522858..99524518-chr8:99525451..99527826,2	K562	blood:
27	chr8:99570440..99572311-chr8:99716067..99717678,2	MCF-7	breast:
28	chr8:99526234..99527955-chr8:99531276..99533264,2	MCF-7	breast:
29	chr8:99617084..99619037-chr8:99621813..99623940,2	K562	blood:
30	chr8:99568854..99571836-chr8:99577056..99579865,2	K562	blood:
31	chr8:99531201..99534381-chr8:99534640..99537501,3	K562	blood:
32	chr8:99591533..99593708-chr8:99612212..99613959,2	MCF-7	breast:
33	chr8:99608849..99611653-chr8:99620795..99623284,2	K562	blood:
34	chr7:100812765..100815379-chr8:99565140..99568111,2	MCF-7	breast:
35	chr8:99558108..99560568-chr8:99561487..99563992,2	MCF-7	breast:
36	chr8:99537550..99540460-chr8:99551301..99553310,2	MCF-7	breast:
37	chr8:99610770..99613655-chr8:99614678..99619231,4	K562	blood:
38	chr8:99532684..99535344-chr8:99632929..99635902,2	K562	blood:
39	chr8:99542296..99548423-chr8:99550336..99556395,6	K562	blood:
40	chr8:99586001..99587844-chr8:99593892..99596537,2	K562	blood:
41	chr8:99570015..99570973-chr8:100370433..100371359,3	K562	blood:
42	chr8:99524025..99526128-chr8:99527392..99529757,2	MCF-7	breast:
43	chr8:99537267..99539977-chr8:99549523..99551043,2	K562	blood:
44	chr8:99176565..99177464-chr8:99569990..99570552,2	MCF-7	breast:
45	chr8:99548557..99552364-chr8:99553180..99556021,3	MCF-7	breast:
46	chr8:99607382..99608915-chr8:99611725..99614614,2	K562	blood:
47	chr8:99580951..99583147-chr8:99585319..99588307,2	MCF-7	breast:
48	chr8:99610760..99613076-chr8:99616322..99619231,2	K562	blood:
49	chr8:99540019..99542563-chr8:99545669..99547224,2	K562	blood:
50	chr8:99522560..99525164-chr8:99531282..99533245,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPAL2-3	chr8:99591987-99592017	NONHSAT127928
2	lnc-KCNS2-1	chr8:99618382-99618568	ENSG00000253911.1
3	lnc-KCNS2-1	chr8:99615481-99615594	ENSG00000253911.1
4	lnc-NIPAL2-3	chr8:99614407-99614504	NONHSAT127930
5	lnc-NIPAL2-3	chr8:99607201-99607346	NONHSAT127930
6	lnc-NIPAL2-3	chr8:99608260-99608620	NONHSAT127928
7	lnc-NIPAL2-3	chr8:99608260-99608397	NONHSAT127930
8	lnc-NIPAL2-3	chr8:99614407-99614410	NONHSAT127929
9	lnc-NIPAL2-3	chr8:99607105-99607978	NONHSAT127929
10	lnc-NIPAL2-3	chr8:99607089-99607273	NONHSAT127928
11	lnc-NIPAL2-3	chr8:99608260-99608397	NONHSAT127929
12	lnc-NIPAL2-3	chr8:99607830-99607978	NONHSAT127930

No data

Variant related genes	Relation type
STK3	TF binding region
ENSG00000253911	TF binding region
ENSG00000254112	TF binding region
STK3	CpG island
ENSG00000253911	CpG island
ENSG00000254112	CpG island
ENSG00000164920	chromatin interactions
ENSG00000253948	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000254112	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000104361	chromatin interactions
ENSG00000253911	chromatin interactions
ENSG00000271930	chromatin interactions

Extended variants
information (count: 3694 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:3694 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17372001	chr8:99526819-99526820	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573987197	chr8:99526827-99526828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542862563	chr8:99526880-99526881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556344474	chr8:99526936-99526937	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143628538	chr8:99527014-99527015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185149739	chr8:99527040-99527041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs564963162	chr8:99527051-99527052	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs560254082	chr8:99527187-99527188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527315341	chr8:99527190-99527191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs541004820	chr8:99527220-99527221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs188298698	chr8:99527297-99527298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs371250154	chr8:99527329-99527330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs181177892	chr8:99527362-99527363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185619393	chr8:99527367-99527368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs16892238	chr8:99527394-99527395	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs569882754	chr8:99527436-99527437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73275828	chr8:99527477-99527478	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs551613545	chr8:99527481-99527482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs191660046	chr8:99527493-99527494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs533980329	chr8:99527514-99527515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs183433011	chr8:99527564-99527565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs567279207	chr8:99527567-99527568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34264189	chr8:99527619-99527620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536554806	chr8:99527661-99527662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34094945	chr8:99527662-99527663	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs200900683	chr8:99527663-99527664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545559112	chr8:99527682-99527683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs187259553	chr8:99527699-99527700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572095845	chr8:99527715-99527716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs540716328	chr8:99527774-99527775	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560869151	chr8:99527785-99527786	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372552852	chr8:99527899-99527900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560779265	chr8:99527916-99527917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs543760889	chr8:99527937-99527938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563554557	chr8:99527940-99527941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537628706	chr8:99527975-99527976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532242554	chr8:99528096-99528097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369768584	chr8:99528146-99528147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552342260	chr8:99528194-99528195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375120733	chr8:99528261-99528262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs192009080	chr8:99528271-99528272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs527792243	chr8:99528328-99528329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542613084	chr8:99528352-99528353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547448045	chr8:99528405-99528406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567335299	chr8:99528408-99528409	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs140801770	chr8:99528446-99528447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183520408	chr8:99528475-99528476	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs113701332	chr8:99528494-99528495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs570311322	chr8:99528507-99528508	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538901213	chr8:99528512-99528513	Weak transcription Enhancers	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
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
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	21611746	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:1307 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99486600-99536000	Weak transcription	Placenta	Placenta
2	chr8:99490400-99547600	Weak transcription	Ovary	ovary
3	chr8:99500400-99558800	Weak transcription	Aorta	Aorta
4	chr8:99503200-99530600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:99503200-99536200	Weak transcription	Liver	Liver
6	chr8:99504600-99536200	Weak transcription	Fetal Lung	lung
7	chr8:99507800-99528200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr8:99515000-99550800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr8:99516000-99542800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
10	chr8:99516200-99543000	Weak transcription	GM12878-XiMat	blood
11	chr8:99516800-99542800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr8:99517800-99538200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr8:99518400-99542800	Weak transcription	Duodenum Mucosa	Duodenum
14	chr8:99518800-99551000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr8:99519000-99543000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr8:99519000-99548400	Weak transcription	Fetal Stomach	stomach
17	chr8:99519200-99530800	Weak transcription	Fetal Muscle Leg	muscle
18	chr8:99519400-99530400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr8:99519600-99536200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr8:99520200-99535200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:99520600-99536400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr8:99523200-99529400	Weak transcription	HSMMtube	muscle
23	chr8:99523200-99530600	Weak transcription	HSMM	muscle
24	chr8:99523400-99536800	Weak transcription	NHEK	skin
25	chr8:99524000-99530000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:99525000-99527800	Enhancers	Dnd41	blood
27	chr8:99525600-99528000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr8:99525800-99527600	Weak transcription	Lung	lung
29	chr8:99525800-99530400	Weak transcription	Adipose Nuclei	Adipose
30	chr8:99525800-99576400	Weak transcription	Pancreas	Pancrea
31	chr8:99526000-99527200	Weak transcription	Small Intestine	intestine
32	chr8:99526000-99543200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr8:99526200-99549400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr8:99526400-99538800	Weak transcription	K562	blood
35	chr8:99526600-99536200	Weak transcription	Left Ventricle	heart
36	chr8:99527400-99536200	Weak transcription	Primary hematopoietic stem cells	blood
37	chr8:99527600-99527800	Enhancers	Lung	lung
38	chr8:99527800-99536600	Weak transcription	Dnd41	blood
39	chr8:99528200-99528800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr8:99528800-99530000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr8:99529000-99536800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr8:99529400-99530600	Enhancers	HSMMtube	muscle
43	chr8:99530000-99530800	Weak transcription	Psoas Muscle	Psoas
44	chr8:99530000-99531800	Enhancers	Fetal Brain Female	brain
45	chr8:99530000-99532200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:99530000-99533200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr8:99530200-99531400	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr8:99530200-99533400	Enhancers	Fetal Brain Male	brain
49	chr8:99530200-99536200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr8:99530400-99531800	Enhancers	Adipose Nuclei	Adipose

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