Variant report

Variant	nsv891218
Chromosome Location	chr8:99507313-99906221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3569)
CpG islands
(count:1040)
Chromatin interactive
region (count:246)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3569 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:99737967-99738396	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:99767855-99768102	K562	blood:	n/a	n/a
3	ARID3A	chr8:99717819-99718081	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:99901338-99901881	K562	blood:	n/a	n/a
5	ARID3A	chr8:99780710-99781281	K562	blood:	n/a	n/a
6	ARID3A	chr8:99877975-99877985	K562	blood:	n/a	n/a
7	ARID3A	chr8:99871493-99871678	K562	blood:	n/a	n/a
8	ARID3A	chr8:99838257-99838602	K562	blood:	n/a	n/a
9	ARID3A	chr8:99717786-99718244	K562	blood:	n/a	n/a
10	ARID3A	chr8:99819786-99820263	K562	blood:	n/a	n/a
11	ARID3A	chr8:99837828-99837841	K562	blood:	n/a	n/a
12	ARID3A	chr8:99787627-99788034	K562	blood:	n/a	n/a
13	ARID3A	chr8:99570483-99570523	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:99552839-99553223	K562	blood:	n/a	n/a
15	ARID3A	chr8:99538862-99539314	K562	blood:	n/a	n/a
16	ARID3A	chr8:99547792-99547835	K562	blood:	n/a	n/a
17	ARID3A	chr8:99625239-99625312	K562	blood:	n/a	n/a
18	ARID3A	chr8:99838272-99838703	HepG2	liver:	n/a	n/a
19	ARID3A	chr8:99617652-99618214	K562	blood:	n/a	n/a
20	ARID3A	chr8:99848855-99848891	K562	blood:	n/a	n/a
21	ARID3A	chr8:99853209-99853500	K562	blood:	n/a	n/a
22	ARID3A	chr8:99610167-99611383	HepG2	liver:	n/a	n/a
23	ARID3A	chr8:99803222-99803452	K562	blood:	n/a	n/a
24	ARID3A	chr8:99865515-99866269	K562	blood:	n/a	n/a
25	ARID3A	chr8:99837090-99837848	HepG2	liver:	n/a	n/a
26	ATF1	chr8:99774162-99774482	K562	blood:	n/a	n/a
27	ATF1	chr8:99767808-99768061	K562	blood:	n/a	n/a
28	ATF1	chr8:99787524-99787978	K562	blood:	n/a	n/a
29	ATF1	chr8:99717793-99718078	K562	blood:	n/a	n/a
30	ATF1	chr8:99865642-99866046	K562	blood:	n/a	n/a
31	ATF1	chr8:99780792-99781251	K562	blood:	n/a	n/a
32	ATF1	chr8:99793198-99793446	K562	blood:	n/a	n/a
33	ATF1	chr8:99617828-99618195	K562	blood:	n/a	n/a
34	ATF1	chr8:99853094-99853450	K562	blood:	n/a	n/a
35	ATF1	chr8:99552873-99553325	K562	blood:	n/a	n/a
36	ATF1	chr8:99692816-99692821	K562	blood:	n/a	n/a
37	ATF1	chr8:99901652-99901857	K562	blood:	n/a	n/a
38	ATF2	chr8:99823227-99823817	GM12878	blood:	n/a	n/a
39	ATF2	chr8:99740507-99741015	GM12878	blood:	n/a	n/a
40	ATF2	chr8:99746079-99746783	GM12878	blood:	n/a	n/a
41	ATF2	chr8:99740370-99741034	GM12878	blood:	n/a	n/a
42	ATF2	chr8:99613740-99614238	GM12878	blood:	n/a	n/a
43	ATF2	chr8:99757361-99757820	GM12878	blood:	n/a	n/a
44	ATF2	chr8:99700578-99700905	GM12878	blood:	n/a	n/a
45	ATF3	chr8:99780903-99781219	K562	blood:	n/a	n/a
46	ATF3	chr8:99865644-99866112	K562	blood:	n/a	n/a
47	BACH1	chr8:99613674-99614154	H1-hESC	embryonic stem cell:	n/a	n/a
48	BACH1	chr8:99837334-99837379	K562	blood:	n/a	n/a
49	BACH1	chr8:99838387-99838704	K562	blood:	n/a	n/a
50	BACH1	chr8:99901634-99901998	K562	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:99602540-99602590	NHBE	bronchial:	n/a
2	chr8:99602609-99602659	GM19239	blood:	n/a
3	chr8:99903985-99904035	NB4	blood:	n/a
4	chr8:99602540-99602590	NHBE	bronchial:	n/a
5	chr8:99602609-99602659	GM19239	blood:	n/a
6	chr8:99903985-99904035	NB4	blood:	n/a
7	chr8:99834971-99835021	HCPEpiC	choroid plexus:	n/a
8	chr8:99813010-99813060	GM12892	blood:	n/a
9	chr8:99836388-99836438	HCF	heart:	n/a
10	chr8:99838318-99838368	Caco-2	colon:	n/a
11	chr8:99813010-99813060	ovcar-3	ovarian:	n/a
12	chr8:99602609-99602659	HEK293	kidney:	embryo
13	chr8:99837846-99837896	K562	blood:	n/a
14	chr8:99836388-99836438	HEEpiC	esophagus:	n/a
15	chr8:99738789-99738839	MCF10A-Er-Src	breast:	n/a
16	chr8:99835768-99835818	NHBE	bronchial:	n/a
17	chr8:99838488-99838538	SK-N-SH	brain:	n/a
18	chr8:99602568-99602618	HL-60	blood:	n/a
19	chr8:99602609-99602659	HEEpiC	esophagus:	n/a
20	chr8:99602568-99602618	U87	brain:	n/a
21	chr8:99903985-99904035	HRCEpiC	kidney:	n/a
22	chr8:99835768-99835818	PrEC	prostate:	n/a
23	chr8:99602609-99602659	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:99837846-99837896	AoSMC	blood vessel:	n/a
25	chr8:99837480-99837530	AG09319	gingival:	n/a
26	chr8:99837480-99837530	HRCEpiC	kidney:	n/a
27	chr8:99841169-99841219	H1-hESC	embryonic stem cell:	embryo
28	chr8:99602568-99602618	BE2_C	brain:	n/a
29	chr8:99837491-99837541	HepG2	liver:	n/a
30	chr8:99835768-99835818	ProgFib	skin:	n/a
31	chr8:99834971-99835021	SK-N-SH_RA	brain:	n/a
32	chr8:99836388-99836438	AG09309	skin:	n/a
33	chr8:99838488-99838538	IMR90	lung:	fetal
34	chr8:99836388-99836438	PrEC	prostate:	n/a
35	chr8:99602568-99602618	Hela-S3	cervix:	n/a
36	chr8:99838318-99838368	SK-N-SH	brain:	n/a
37	chr8:99602609-99602659	GM12892	blood:	n/a
38	chr8:99903985-99904035	AG04450	lung:	fetal
39	chr8:99738789-99738839	RPTEC	kidney:	n/a
40	chr8:99837480-99837530	AoSMC	blood vessel:	n/a
41	chr8:99602609-99602659	GM12878	blood:	n/a
42	chr8:99834971-99835021	RPTEC	kidney:	n/a
43	chr8:99835768-99835818	Jurkat	blood:	n/a
44	chr8:99841169-99841219	ProgFib	skin:	n/a
45	chr8:99838318-99838368	PrEC	prostate:	n/a
46	chr8:99837846-99837896	HRCEpiC	kidney:	n/a
47	chr8:99837480-99837530	NHBE	bronchial:	n/a
48	chr8:99738789-99738839	SK-N-SH	brain:	n/a
49	chr8:99834971-99835021	Jurkat	blood:	n/a
50	chr8:99903985-99904035	AG04449	skin:	fetal

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:99896042..99898462-chr8:99956313..99958983,2	MCF-7	breast:
2	chr8:99536690..99539147-chr8:99552855..99554572,2	K562	blood:
3	chr8:99853190..99853725-chr8:99877624..99878163,2	MCF-7	breast:
4	chr8:99868075..99870379-chr8:99872051..99875214,3	K562	blood:
5	chr8:99757864..99758569-chrX:66831854..66832517,2	MCF-7	breast:
6	chr8:99568854..99571836-chr8:99577056..99579865,2	K562	blood:
7	chr8:99524025..99526128-chr8:99527392..99529757,2	MCF-7	breast:
8	chr8:99610760..99613076-chr8:99616322..99619231,2	K562	blood:
9	chr8:99522297..99524358-chr8:99525451..99528433,2	K562	blood:
10	chr8:99833993..99836005-chr8:99853206..99854890,2	MCF-7	breast:
11	chr8:99717734..99718483-chr8:100009688..100010929,4	MCF-7	breast:
12	chr8:99818410..99822032-chr8:99835031..99838163,3	K562	blood:
13	chr8:99854034..99856710-chr8:99857442..99860131,3	K562	blood:
14	chr8:99679404..99682234-chr8:99684167..99686390,2	K562	blood:
15	chr8:99848239..99850661-chr8:99854990..99857357,2	MCF-7	breast:
16	chr8:99738155..99743366-chr8:99746593..99750391,4	MCF-7	breast:
17	chr8:99570092..99570986-chr8:100009815..100010452,2	MCF-7	breast:
18	chr8:99805802..99807780-chr8:99809302..99811541,2	K562	blood:
19	chr8:99539907..99541519-chr8:99544944..99547169,2	K562	blood:
20	chr8:99570067..99570984-chr8:99843872..99844522,2	MCF-7	breast:
21	chr8:99542296..99548423-chr8:99550336..99556395,6	K562	blood:
22	chr8:99836010..99840004-chr8:99859824..99865808,6	K562	blood:
23	chr8:99887420..99890238-chr8:99891754..99894333,2	K562	blood:
24	chr8:99898466..99900537-chr8:99903987..99905809,2	MCF-7	breast:
25	chr8:99677331..99680175-chr8:100027131..100030033,2	K562	blood:
26	chr8:99852891..99853780-chr8:99878037..99878943,2	MCF-7	breast:
27	chr8:99836481..99839453-chr8:99955374..99958557,4	MCF-7	breast:
28	chr8:99730740..99733168-chr8:99733468..99735673,2	MCF-7	breast:
29	chr8:99739291..99741165-chr8:99741627..99744092,2	MCF-7	breast:
30	chr8:99537016..99539977-chr8:99549369..99551043,2	K562	blood:
31	chr8:99739323..99741904-chr8:99743613..99745750,2	K562	blood:
32	chr8:99713408..99715331-chr8:99956897..99958843,2	MCF-7	breast:
33	chr8:99739323..99741904-chr8:99743613..99745750,2	K562	blood:
34	chr8:99838808..99842623-chr8:99842733..99845711,4	MCF-7	breast:
35	chr8:99552951..99554839-chr8:99564123..99567093,2	K562	blood:
36	chr8:99766460..99769407-chr8:99772354..99774228,2	K562	blood:
37	chr8:99714532..99716117-chr8:99964323..99966058,2	MCF-7	breast:
38	chr8:99618677..99620459-chr8:99649251..99652743,3	K562	blood:
39	chr8:99540019..99542563-chr8:99545669..99547224,2	K562	blood:
40	chr8:99903292..99905323-chr8:99955326..99958042,2	K562	blood:
41	chr8:99531201..99534381-chr8:99534640..99537501,3	K562	blood:
42	chr8:99717210..99719465-chr8:99720134..99722023,2	K562	blood:
43	chr8:99542843..99544364-chr8:99551083..99552848,2	K562	blood:
44	chr8:99774390..99776428-chr8:99778183..99780400,2	K562	blood:
45	chr8:99852770..99853592-chr8:100009889..100010836,2	MCF-7	breast:
46	chr8:99735526..99738976-chr8:99742014..99743636,3	K562	blood:
47	chr8:99742630..99744951-chr8:99747576..99749535,2	MCF-7	breast:
48	chr8:99901039..99903111-chr8:100022856..100025470,2	MCF-7	breast:
49	chr8:99679404..99682234-chr8:99684167..99686390,2	K562	blood:
50	chr8:99606089..99608819-chr8:99618482..99621119,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NIPAL2-3	chr8:99607830-99607978	NONHSAT127930
2	lnc-NIPAL2-3	chr8:99614407-99614410	NONHSAT127929
3	lnc-NIPAL2-3	chr8:99591987-99592017	NONHSAT127928
4	lnc-KCNS2-1	chr8:99618382-99618568	ENSG00000253911.1
5	lnc-NIPAL2-3	chr8:99608260-99608397	NONHSAT127929
6	lnc-NIPAL2-3	chr8:99607105-99607978	NONHSAT127929
7	lnc-KCNS2-3	chr8:99645775-99646093	NONHSAT127932
8	lnc-NIPAL2-5	chr8:99887485-99887922	NONHSAT127934
9	lnc-NIPAL2-5	chr8:99902003-99902130	NONHSAT127935
10	lnc-NIPAL2-3	chr8:99607201-99607346	NONHSAT127930
11	lnc-NIPAL2-3	chr8:99614407-99614504	NONHSAT127930
12	lnc-NIPAL2-5	chr8:99895875-99896023	NONHSAT127934
13	lnc-NIPAL2-5	chr8:99891126-99896062	NONHSAT127935
14	lnc-NIPAL2-3	chr8:99608260-99608397	NONHSAT127930
15	lnc-NIPAL2-3	chr8:99607089-99607273	NONHSAT127928
16	lnc-NIPAL2-3	chr8:99608260-99608620	NONHSAT127928
17	lnc-KCNS2-1	chr8:99615481-99615594	ENSG00000253911.1

No data

Variant related genes	Relation type
STK3	TF binding region
ENSG00000253911	TF binding region
RPL19P14	TF binding region
ENSG00000254112	TF binding region
STK3	CpG island
ENSG00000253911	CpG island
RPL19P14	CpG island
ENSG00000254112	CpG island
ENSG00000253948	chromatin interactions
ENSG00000253415	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000240870	chromatin interactions
ENSG00000104375	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000271930	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000104361	chromatin interactions
ENSG00000254112	chromatin interactions
ENSG00000223281	chromatin interactions
ENSG00000253911	chromatin interactions

Extended variants
information (count: 13564 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:13564 , 50 per page) page: 1 2 3 4 5 6 7 ... 272

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4734407	chr8:99507313-99507314	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565042043	chr8:99507319-99507320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113723477	chr8:99507357-99507358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139543097	chr8:99507385-99507386	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143448440	chr8:99507437-99507438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs368356430	chr8:99507456-99507457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570548368	chr8:99507470-99507471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113290169	chr8:99507490-99507491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113438031	chr8:99507594-99507595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150502107	chr8:99507608-99507609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs552271851	chr8:99507649-99507650	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200471552	chr8:99507668-99507669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565809536	chr8:99507675-99507676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139636336	chr8:99507723-99507724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554529426	chr8:99507735-99507736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs575118415	chr8:99507758-99507759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537341677	chr8:99507766-99507767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557586612	chr8:99507773-99507774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577375298	chr8:99507794-99507795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs16897058	chr8:99507810-99507811	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs553124424	chr8:99507835-99507836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149735330	chr8:99507844-99507845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112518536	chr8:99507886-99507887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145567996	chr8:99507994-99507995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561656670	chr8:99508002-99508003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139355881	chr8:99508045-99508046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544191802	chr8:99508065-99508066	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144091686	chr8:99508077-99508078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533004636	chr8:99508167-99508168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546369739	chr8:99508168-99508169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs565871315	chr8:99508194-99508195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs528556830	chr8:99508211-99508212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs548225227	chr8:99508270-99508271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs146587155	chr8:99508274-99508275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs187314702	chr8:99508294-99508295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs565638805	chr8:99508356-99508357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141285187	chr8:99508410-99508411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs551333412	chr8:99508417-99508418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571096136	chr8:99508474-99508475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200681156	chr8:99508519-99508520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540065245	chr8:99508592-99508593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549696158	chr8:99508597-99508598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs76283650	chr8:99508612-99508613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs111891339	chr8:99508649-99508650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553585913	chr8:99508720-99508721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75274186	chr8:99508782-99508783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541939992	chr8:99508790-99508791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371509422	chr8:99508862-99508863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555391629	chr8:99508925-99508926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575150236	chr8:99508926-99508927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

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
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Gastric cancer	22014070	CNVD

Chromatin state (count:4295 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99461800-99525000	Weak transcription	Psoas Muscle	Psoas
2	chr8:99486600-99536000	Weak transcription	Placenta	Placenta
3	chr8:99490400-99547600	Weak transcription	Ovary	ovary
4	chr8:99500200-99517600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:99500400-99558800	Weak transcription	Aorta	Aorta
6	chr8:99503200-99530600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr8:99503200-99536200	Weak transcription	Liver	Liver
8	chr8:99504400-99508400	Enhancers	NHDF-Ad	bronchial
9	chr8:99504600-99536200	Weak transcription	Fetal Lung	lung
10	chr8:99506000-99519800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:99506200-99522400	Weak transcription	HSMMtube	muscle
12	chr8:99506400-99509400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:99506600-99510600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr8:99506800-99518400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:99507200-99507800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr8:99507800-99528200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr8:99509400-99525400	Weak transcription	Pancreas	Pancrea
18	chr8:99510600-99511600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr8:99511000-99518200	Weak transcription	Fetal Muscle Trunk	muscle
20	chr8:99511600-99517400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:99515000-99550800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr8:99515400-99517800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr8:99515600-99518600	Weak transcription	Fetal Intestine Large	intestine
24	chr8:99516000-99517600	Weak transcription	Duodenum Mucosa	Duodenum
25	chr8:99516000-99542800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr8:99516200-99517800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr8:99516200-99543000	Weak transcription	GM12878-XiMat	blood
28	chr8:99516600-99525400	Weak transcription	Lung	lung
29	chr8:99516800-99542800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr8:99517000-99518200	Weak transcription	Fetal Stomach	stomach
31	chr8:99517400-99517600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr8:99517400-99518000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr8:99517400-99519600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr8:99517600-99517800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr8:99517600-99518400	Strong transcription	Duodenum Mucosa	Duodenum
36	chr8:99517600-99518600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:99517600-99520200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr8:99517800-99518000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr8:99517800-99519000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr8:99517800-99519200	ZNF genes & repeats	Fetal Intestine Small	intestine
41	chr8:99517800-99519200	ZNF genes & repeats	Fetal Muscle Leg	muscle
42	chr8:99517800-99538200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:99518000-99518600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:99518000-99522200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr8:99518200-99518400	ZNF genes & repeats	Fetal Muscle Trunk	muscle
46	chr8:99518200-99518600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:99518200-99519000	ZNF genes & repeats	Fetal Stomach	stomach
48	chr8:99518400-99518800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr8:99518400-99519600	Strong transcription	Fetal Muscle Trunk	muscle
50	chr8:99518400-99542800	Weak transcription	Duodenum Mucosa	Duodenum

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