Variant report

Variant	nsv1025068
Chromosome Location	chr8:49953397-50370208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2150)
CpG islands
(count:796)
Chromatin interactive
region (count:153)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2150 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:50189742-50189896	K562	blood:	n/a	n/a
2	ARID3A	chr8:50142326-50142343	K562	blood:	n/a	n/a
3	ARID3A	chr8:50033978-50034353	K562	blood:	n/a	n/a
4	ARID3A	chr8:50139129-50140149	K562	blood:	n/a	n/a
5	ARID3A	chr8:50037822-50038312	K562	blood:	n/a	n/a
6	ARID3A	chr8:50142928-50143249	K562	blood:	n/a	n/a
7	ARID3A	chr8:50022835-50023624	K562	blood:	n/a	n/a
8	ARID3A	chr8:50038776-50039400	K562	blood:	n/a	n/a
9	ARID3A	chr8:50042305-50042634	K562	blood:	n/a	n/a
10	ARID3A	chr8:50045458-50045469	K562	blood:	n/a	n/a
11	ARID3A	chr8:50176389-50176820	K562	blood:	n/a	n/a
12	ARID3A	chr8:50137796-50138000	K562	blood:	n/a	n/a
13	ARID3A	chr8:50163861-50164727	K562	blood:	n/a	n/a
14	ATF1	chr8:50213509-50213949	K562	blood:	n/a	n/a
15	ATF1	chr8:50005517-50005735	K562	blood:	n/a	n/a
16	ATF1	chr8:50212341-50212528	K562	blood:	n/a	n/a
17	ATF1	chr8:50146602-50146783	K562	blood:	n/a	n/a
18	ATF1	chr8:50043141-50043408	K562	blood:	n/a	n/a
19	ATF1	chr8:50042268-50042716	K562	blood:	n/a	n/a
20	ATF1	chr8:50022908-50023300	K562	blood:	n/a	n/a
21	ATF1	chr8:50129384-50129937	K562	blood:	n/a	n/a
22	ATF1	chr8:50164658-50164824	K562	blood:	n/a	n/a
23	ATF1	chr8:50119038-50119092	K562	blood:	n/a	n/a
24	ATF1	chr8:50204080-50204452	K562	blood:	n/a	n/a
25	ATF1	chr8:50141709-50141977	K562	blood:	n/a	n/a
26	ATF1	chr8:50176434-50176846	K562	blood:	n/a	n/a
27	ATF1	chr8:50139582-50140080	K562	blood:	n/a	n/a
28	ATF2	chr8:50135514-50136034	GM12878	blood:	n/a	n/a
29	ATF2	chr8:50164032-50164513	GM12878	blood:	n/a	n/a
30	ATF2	chr8:50064675-50065110	GM12878	blood:	n/a	n/a
31	ATF2	chr8:50211599-50211898	GM12878	blood:	n/a	n/a
32	ATF2	chr8:50164138-50164888	GM12878	blood:	n/a	n/a
33	ATF2	chr8:50063467-50063855	GM12878	blood:	n/a	n/a
34	ATF2	chr8:50064665-50065098	GM12878	blood:	n/a	n/a
35	ATF2	chr8:50063437-50063916	GM12878	blood:	n/a	n/a
36	ATF2	chr8:50135529-50136160	GM12878	blood:	n/a	n/a
37	ATF3	chr8:50022637-50023275	K562	blood:	n/a	n/a
38	ATF3	chr8:50042276-50042621	K562	blood:	n/a	chr8:50042553-50042561 chr8:50042553-50042563 chr8:50042549-50042564 chr8:50042551-50042564
39	BACH1	chr8:50021996-50022013	K562	blood:	n/a	n/a
40	BACH1	chr8:50033867-50033912	K562	blood:	n/a	n/a
41	BACH1	chr8:50039590-50039608	K562	blood:	n/a	n/a
42	BATF	chr8:50164094-50164475	GM12878	blood:	n/a	n/a
43	BATF	chr8:50279332-50279551	GM12878	blood:	n/a	n/a
44	BATF	chr8:50135514-50135715	GM12878	blood:	n/a	n/a
45	BATF	chr8:50064660-50065058	GM12878	blood:	n/a	n/a
46	BATF	chr8:50084554-50084785	GM12878	blood:	n/a	n/a
47	BATF	chr8:50064654-50065062	GM12878	blood:	n/a	n/a
48	BATF	chr8:49977482-49977864	GM12878	blood:	n/a	n/a
49	BATF	chr8:50284873-50285140	GM12878	blood:	n/a	n/a
50	BATF	chr8:50135732-50136065	GM12878	blood:	n/a	n/a

(count:796 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:49954840-49954890	Hela-S3	cervix:	n/a
2	chr8:50220067-50220117	IMR90	lung:	fetal
3	chr8:50020154-50020204	MCF10A-Er-Src	breast:	n/a
4	chr8:49954840-49954890	Hela-S3	cervix:	n/a
5	chr8:50220067-50220117	IMR90	lung:	fetal
6	chr8:50020154-50020204	MCF10A-Er-Src	breast:	n/a
7	chr8:50220067-50220117	HNPCEpiC	eye:	n/a
8	chr8:49984776-49984826	HCPEpiC	choroid plexus:	n/a
9	chr8:50020154-50020204	HCF	heart:	n/a
10	chr8:49984830-49984880	MCF-7	breast:	n/a
11	chr8:50220067-50220117	NHDF-neo	bronchial:	n/a
12	chr8:49987774-49987824	NT2-D1	testis:	n/a
13	chr8:50020154-50020204	ProgFib	skin:	n/a
14	chr8:49959180-49959230	AG10803	skin:	n/a
15	chr8:49985379-49985429	AG10803	skin:	n/a
16	chr8:49985021-49985071	PrEC	prostate:	n/a
17	chr8:50213812-50213862	BE2_C	brain:	n/a
18	chr8:49984776-49984826	Caco-2	colon:	n/a
19	chr8:49954840-49954890	PrEC	prostate:	n/a
20	chr8:50020154-50020204	H1-hESC	embryonic stem cell:	embryo
21	chr8:50314174-50314224	HRE	kidney:	n/a
22	chr8:49987774-49987824	GM06990	blood:	n/a
23	chr8:49984776-49984826	LNCaP	prostate:	n/a
24	chr8:49954840-49954890	SK-N-MC	brain:	n/a
25	chr8:49984564-49984614	HMEC	breast:	n/a
26	chr8:49987774-49987824	HCT-116	colon:	n/a
27	chr8:49983488-49983538	Caco-2	colon:	n/a
28	chr8:50314174-50314224	HIPEpiC	eye:	n/a
29	chr8:49987774-49987824	HRPEpiC	eye:	n/a
30	chr8:49954840-49954890	A549	lung:	n/a
31	chr8:49984564-49984614	SKMC	muscle:	n/a
32	chr8:50220067-50220117	HCM	heart:	n/a
33	chr8:49959180-49959230	AoSMC	blood vessel:	n/a
34	chr8:50020154-50020204	SKMC	muscle:	n/a
35	chr8:49984830-49984880	SK-N-SH_RA	brain:	n/a
36	chr8:50220067-50220117	MCF10A-Er-Src	breast:	n/a
37	chr8:50220067-50220117	AG09319	gingival:	n/a
38	chr8:49983488-49983538	NHBE	bronchial:	n/a
39	chr8:49984776-49984826	U87	brain:	n/a
40	chr8:49985021-49985071	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:49987774-49987824	HEEpiC	esophagus:	n/a
42	chr8:50213812-50213862	AG04449	skin:	fetal
43	chr8:50220067-50220117	SAEC	small airway:	n/a
44	chr8:50314174-50314224	HCPEpiC	choroid plexus:	n/a
45	chr8:49985021-49985071	HEK293	kidney:	embryo
46	chr8:49984776-49984826	MCF10A-Er-Src	breast:	n/a
47	chr8:49985379-49985429	PFSK-1	brain:	n/a
48	chr8:49954840-49954890	ovcar-3	ovarian:	n/a
49	chr8:49984776-49984826	HIPEpiC	eye:	n/a
50	chr8:49954840-49954890	NHBE	bronchial:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr8:50084279..50086501-chr8:50089833..50092255,3	K562	blood:
2	chr8:49959412..49962230-chr8:50108460..50111062,2	K562	blood:
3	chr8:50223069..50226256-chr8:50227030..50231187,6	K562	blood:
4	chr8:49957324..49959280-chr8:49961057..49962998,2	K562	blood:
5	chr8:49958445..49960562-chr8:49978608..49980368,2	K562	blood:
6	chr8:50220433..50222102-chr8:50312150..50314977,2	K562	blood:
7	chr8:50224322..50226256-chr8:50228266..50231187,2	K562	blood:
8	chr8:50174406..50177036-chr8:50205443..50207064,2	K562	blood:
9	chr8:50158291..50160893-chr8:50161385..50163707,3	K562	blood:
10	chr8:49955516..49959345-chr8:49967725..49970729,4	K562	blood:
11	chr8:50256870..50259516-chr8:50263115..50264722,2	K562	blood:
12	chr8:49991750..49994604-chr8:49995400..49997837,2	K562	blood:
13	chr8:50083760..50086501-chr8:50089833..50092673,4	K562	blood:
14	chr8:49984428..49986126-chr8:49991060..49993581,2	K562	blood:
15	chr8:49959355..49961119-chr8:50034461..50036687,2	K562	blood:
16	chr8:50142308..50144662-chr8:50148420..50150993,2	K562	blood:
17	chr8:49955334..49957010-chr8:49957761..49960286,2	K562	blood:
18	chr8:50032130..50034951-chr8:50036647..50039869,3	K562	blood:
19	chr8:50220131..50222425-chr8:50223280..50225514,2	K562	blood:
20	chr8:50306965..50309491-chr8:50313061..50314583,2	K562	blood:
21	chr8:49990025..49992623-chr8:49996686..49998822,3	K562	blood:
22	chr8:49990906..49993749-chr8:49994694..49997206,2	MCF-7	breast:
23	chr8:50219874..50222720-chr8:50223488..50225514,3	K562	blood:
24	chr8:50158291..50160893-chr8:50161385..50163707,3	K562	blood:
25	chr8:50019288..50021191-chr8:50037884..50039646,2	K562	blood:
26	chr8:49972978..49975777-chr8:49977348..49979719,2	K562	blood:
27	chr8:49960045..49962235-chr8:49963261..49965628,2	K562	blood:
28	chr8:50198141..50200837-chr8:50202344..50203937,2	K562	blood:
29	chr8:50003812..50005388-chr8:50034210..50037111,2	K562	blood:
30	chr8:49954242..49956834-chr8:49957466..49960286,2	K562	blood:
31	chr8:50307157..50309606-chr8:50310313..50312486,2	K562	blood:
32	chr8:50052529..50054341-chr8:50060024..50062622,2	K562	blood:
33	chr8:50114787..50117721-chr8:50120524..50123676,3	K562	blood:
34	chr8:50122009..50123670-chr8:50128301..50129864,2	K562	blood:
35	chr8:50286271..50288690-chr8:50292901..50294552,2	K562	blood:
36	chr8:49968146..49970039-chr8:49971741..49973749,3	K562	blood:
37	chr8:50032130..50034951-chr8:50036647..50039869,3	K562	blood:
38	chr8:49977011..49978877-chr8:49988078..49990673,2	K562	blood:
39	chr8:50130806..50133714-chr8:50138525..50141483,2	K562	blood:
40	chr8:50152755..50154447-chr8:50156418..50158497,2	K562	blood:
41	chr8:50201423..50204477-chr8:50211622..50215340,4	K562	blood:
42	chr8:50157489..50159096-chr8:50164088..50165590,2	K562	blood:
43	chr8:49955334..49957010-chr8:49957761..49960286,2	K562	blood:
44	chr8:50152755..50154447-chr8:50156418..50158497,2	K562	blood:
45	chr8:50224322..50226256-chr8:50228266..50231187,2	K562	blood:
46	chr8:50220433..50222102-chr8:50312150..50314977,2	K562	blood:
47	chr8:50288741..50291361-chr8:50315909..50318142,2	K562	blood:
48	chr8:50142308..50144662-chr8:50148420..50150993,2	K562	blood:
49	chr8:50207112..50210089-chr8:50216692..50218806,2	K562	blood:
50	chr8:49991750..49994604-chr8:49995400..49997837,2	K562	blood:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf22-10	chr8:50242769-50243106	NONHSAT126514
2	lnc-C8orf22-1	chr8:50013387-50013639	XLOC_006792
3	lnc-C8orf22-2	chr8:50141117-50141484	ENSG00000253474
4	lnc-C8orf22-12	chr8:50243331-50243643	l_3592_chr8:50243194-50268365_ovary
5	lnc-C8orf22-2	chr8:50080641-50081407	NONHSAT126506
6	lnc-C8orf22-2	chr8:50140699-50140779	XLOC_006794
7	lnc-C8orf22-12	chr8:50243195-50243330	l_3592_chr8:50243194-50268365_ovary
8	lnc-C8orf22-12	chr8:50243796-50243921	l_3592_chr8:50243194-50268365_ovary
9	lnc-C8orf22-2	chr8:50105666-50105812	XLOC_006793
10	lnc-C8orf22-2	chr8:50118940-50119026	NONHSAT126506
11	lnc-C8orf22-2	chr8:50140699-50140779	ENSG00000253474
12	lnc-C8orf22-2	chr8:50140698-50140779	NONHSAT126506
13	lnc-C8orf22-2	chr8:50137497-50137609	ENSG00000253474
14	lnc-C8orf22-2	chr8:50081098-50081368	ENSG00000253474
15	lnc-C8orf22-2	chr8:50080642-50081090	XLOC_006793
16	lnc-C8orf22-2	chr8:50103993-50107149	NONHSAT126506
17	lnc-RP11-738G5.2.1-4	chr8:50312748-50312854	NONHSAT126516
18	lnc-C8orf22-2	chr8:50141117-50142346	XLOC_006794
19	lnc-C8orf22-2	chr8:50081241-50081368	ENSG00000253474
20	lnc-C8orf22-2	chr8:50081243-50081368	XLOC_006793
21	lnc-C8orf22-2	chr8:50105666-50105812	XLOC_006793
22	lnc-RP11-738G5.2.1-6	chr8:50209735-50210341	ucscGeneNc_uc003xqr_2
23	lnc-C8orf22-2	chr8:50137497-50137609	XLOC_006794
24	lnc-C8orf22-2	chr8:50140699-50140944	XLOC_006794
25	lnc-C8orf22-2	chr8:50105666-50105754	ENSG00000253474
26	lnc-RP11-738G5.2.1-5	chr8:50265189-50265403	NONHSAT126515
27	lnc-C8orf22-2	chr8:50137496-50137609	NONHSAT126506
28	lnc-C8orf22-2	chr8:50081243-50081368	XLOC_006793
29	lnc-C8orf22-12	chr8:50268219-50268365	l_3592_chr8:50243194-50268365_ovary
30	lnc-SNAI2-1	chr8:50047181-50047788	NONHSAT126505
31	lnc-C8orf22-2	chr8:50141116-50142388	NONHSAT126506
32	lnc-C8orf22-1	chr8:49998879-49999091	XLOC_006792
33	lnc-C8orf22-2	chr8:50137497-50137609	XLOC_006794
34	lnc-C8orf22-2	chr8:50137500-50137588	ENSG00000253474
35	lnc-RP11-738G5.2.1-4	chr8:50307783-50308267	NONHSAT126516
36	lnc-C8orf22-2	chr8:50080642-50080861	XLOC_006793
37	lnc-RP11-738G5.2.1-4	chr8:50313617-50313650	NONHSAT126516

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C8orf22	hsa-miR-124-3p	chr8:49988031-49988050
2	C8orf22	hsa-miR-124-3p	chr8:49988178-49988197

Variant related genes	Relation type
RFPL4AP7	TF binding region
RN7SKP294	TF binding region
C8orf22	TF binding region
ENSG00000253474	TF binding region
RFPL4AP7	CpG island
RN7SKP294	CpG island
C8orf22	CpG island
ENSG00000253474	CpG island
ENSG00000168333	chromatin interactions
ENSG00000253474	chromatin interactions
C7orf60	miRNA target sites

Extended variants
information (count: 9245 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:9245 , 50 per page) page: 1 2 3 4 5 6 7 ... 185

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555648176	chr8:49953407-49953408	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574298491	chr8:49953413-49953414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541321605	chr8:49953414-49953415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374566596	chr8:49953420-49953421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190879878	chr8:49953437-49953438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577754491	chr8:49953446-49953447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs112142405	chr8:49953447-49953448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs368757255	chr8:49953488-49953489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146959151	chr8:49953502-49953503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183518017	chr8:49953508-49953509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575437518	chr8:49953543-49953544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138076934	chr8:49953596-49953597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186863806	chr8:49953606-49953607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142200732	chr8:49953607-49953608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs191298924	chr8:49953653-49953654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529200095	chr8:49953660-49953661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369643041	chr8:49953678-49953679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547367784	chr8:49953683-49953684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538429547	chr8:49953760-49953761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565729247	chr8:49953813-49953814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539420923	chr8:49953923-49953924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551536465	chr8:49953926-49953927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183206884	chr8:49953927-49953928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs236494	chr8:49953928-49953929	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs555931720	chr8:49953946-49953947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574142509	chr8:49953980-49953981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs527413918	chr8:49953988-49953989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373862741	chr8:49954004-49954005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553229514	chr8:49954029-49954030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187746706	chr8:49954069-49954070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545014673	chr8:49954074-49954075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546678622	chr8:49954087-49954088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563311591	chr8:49954121-49954122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs575336283	chr8:49954138-49954139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542712250	chr8:49954143-49954144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575035647	chr8:49954157-49954158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372139351	chr8:49954161-49954162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529077687	chr8:49954193-49954194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547700543	chr8:49954194-49954195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540710889	chr8:49954220-49954221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559670337	chr8:49954226-49954227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375119180	chr8:49954260-49954261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533229810	chr8:49954283-49954284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551420349	chr8:49954306-49954307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569624532	chr8:49954310-49954311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191272623	chr8:49954323-49954324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540573417	chr8:49954339-49954340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148284138	chr8:49954340-49954341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534890546	chr8:49954349-49954350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553114847	chr8:49954354-49954355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
low-grade B-cell lymphoma tumor	18367492	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	22286061	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:619 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49952000-49956800	Weak transcription	Psoas Muscle	Psoas
2	chr8:49952600-49955400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr8:49952800-49955600	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr8:49955200-49955600	Enhancers	GM12878-XiMat	blood
5	chr8:49955400-49958600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr8:49955600-49958000	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr8:49956800-49957200	Enhancers	Psoas Muscle	Psoas
8	chr8:49957200-49958400	Weak transcription	Psoas Muscle	Psoas
9	chr8:49958400-49959000	Enhancers	K562	blood
10	chr8:49958600-49958800	Enhancers	Psoas Muscle	Psoas
11	chr8:49958600-49959800	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr8:49959000-49961200	Active TSS	K562	blood
13	chr8:49959800-49960400	Enhancers	Fetal Muscle Leg	muscle
14	chr8:49960000-49960200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr8:49964600-49965200	Enhancers	Hela-S3	cervix
16	chr8:49965200-49966600	Weak transcription	Hela-S3	cervix
17	chr8:49966600-49966800	Enhancers	Hela-S3	cervix
18	chr8:49971400-49972000	Enhancers	Psoas Muscle	Psoas
19	chr8:49971800-49972000	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr8:49972000-49977800	Weak transcription	Psoas Muscle	Psoas
21	chr8:49972200-49974600	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr8:49974600-49974800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr8:49974600-49979600	Enhancers	Adipose Nuclei	Adipose
24	chr8:49974800-49975600	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr8:49975200-49978400	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr8:49975200-49978600	Enhancers	Hela-S3	cervix
27	chr8:49975600-49978200	Enhancers	Skeletal Muscle Male	skeletal muscle
28	chr8:49976400-49977000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr8:49976400-49978000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr8:49976600-49977000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr8:49976600-49977000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:49976600-49979400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr8:49976800-49977200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr8:49976800-49978000	Enhancers	H9 Cell Line	embryonic stem cell
35	chr8:49977000-49978000	Enhancers	NHDF-Ad	bronchial
36	chr8:49977000-49978200	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr8:49977000-49978200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:49977000-49978400	Enhancers	GM12878-XiMat	blood
39	chr8:49977000-49978800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr8:49977000-49979000	Enhancers	Primary hematopoietic stem cells	blood
41	chr8:49977200-49978000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr8:49977200-49978200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr8:49977200-49978600	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr8:49977200-49978600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr8:49977200-49979200	Enhancers	K562	blood
46	chr8:49977400-49977800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr8:49977400-49978000	Enhancers	HSMMtube	muscle
48	chr8:49977400-49978400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr8:49977400-49978600	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr8:49977400-49978800	Enhancers	HUVEC	blood vessel

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