Variant report

Variant	nsv890354
Chromosome Location	chr8:11176147-11266131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:864)
CpG islands
(count:2746)
Chromatin interactive
region (count:63)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:864 , 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	chr8:11194074-11194871	K562	blood:	n/a	n/a
2	ARID3A	chr8:11207682-11208854	K562	blood:	n/a	n/a
3	ARID3A	chr8:11204513-11204770	K562	blood:	n/a	n/a
4	ARID3A	chr8:11213076-11213342	K562	blood:	n/a	n/a
5	ATF1	chr8:11194325-11194713	K562	blood:	n/a	n/a
6	ATF1	chr8:11207768-11208156	K562	blood:	n/a	n/a
7	ATF2	chr8:11181267-11181696	GM12878	blood:	n/a	n/a
8	ATF3	chr8:11219063-11219574	A549	lung:	n/a	n/a
9	ATF3	chr8:11207702-11208193	K562	blood:	n/a	n/a
10	ATF3	chr8:11204829-11205126	K562	blood:	n/a	chr8:11204842-11204862
11	ATF3	chr8:11204348-11204805	K562	blood:	n/a	n/a
12	ATF3	chr8:11194299-11194719	K562	blood:	n/a	n/a
13	ATF3	chr8:11206179-11206608	K562	blood:	n/a	chr8:11206194-11206208
14	ATF3	chr8:11204406-11204786	K562	blood:	n/a	n/a
15	ATF3	chr8:11207755-11208037	K562	blood:	n/a	n/a
16	BACH1	chr8:11194334-11194619	K562	blood:	n/a	n/a
17	BACH1	chr8:11207790-11208696	K562	blood:	n/a	chr8:11207913-11207927
18	BACH1	chr8:11204167-11204990	K562	blood:	n/a	n/a
19	BACH1	chr8:11204201-11206211	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr8:11235937-11236160	GM12878	blood:	n/a	n/a
21	BCL3	chr8:11217596-11217998	GM12878	blood:	n/a	n/a
22	BCL3	chr8:11217527-11217956	GM12878	blood:	n/a	chr8:11217549-11217558
23	BCL3	chr8:11254759-11255021	GM12878	blood:	n/a	n/a
24	BCL3	chr8:11204491-11204917	A549	lung:	n/a	n/a
25	BHLHE40	chr8:11204744-11205031	GM12878	blood:	n/a	n/a
26	BHLHE40	chr8:11213031-11213375	K562	blood:	n/a	n/a
27	BHLHE40	chr8:11204251-11205108	K562	blood:	n/a	n/a
28	BHLHE40	chr8:11201913-11202107	K562	blood:	n/a	n/a
29	BHLHE40	chr8:11181454-11181536	GM12878	blood:	n/a	n/a
30	BHLHE40	chr8:11205469-11205676	K562	blood:	n/a	n/a
31	BHLHE40	chr8:11207644-11208566	K562	blood:	n/a	n/a
32	BRCA1	chr8:11204539-11204641	H1-hESC	embryonic stem cell:	n/a	n/a
33	CBX3	chr8:11207602-11208626	K562	blood:	n/a	n/a
34	CBX3	chr8:11194072-11194768	K562	blood:	n/a	n/a
35	CBX3	chr8:11190415-11191021	K562	blood:	n/a	n/a
36	CBX3	chr8:11190482-11190876	K562	blood:	n/a	n/a
37	CBX3	chr8:11207603-11208161	K562	blood:	n/a	n/a
38	CBX3	chr8:11204397-11205076	K562	blood:	n/a	n/a
39	CCNT2	chr8:11204446-11205552	K562	blood:	n/a	n/a
40	CCNT2	chr8:11213058-11213305	K562	blood:	n/a	n/a
41	CCNT2	chr8:11207754-11208632	K562	blood:	n/a	n/a
42	CCNT2	chr8:11194254-11194791	K562	blood:	n/a	n/a
43	CEBPB	chr8:11244101-11244368	HepG2	liver:	n/a	chr8:11244236-11244249 chr8:11244237-11244248 chr8:11244236-11244247 chr8:11244236-11244249
44	CEBPB	chr8:11244124-11244287	K562	blood:	n/a	chr8:11244236-11244249 chr8:11244237-11244248 chr8:11244236-11244247 chr8:11244236-11244249
45	CEBPB	chr8:11204475-11204481	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr8:11207735-11208581	K562	blood:	n/a	n/a
47	CEBPB	chr8:11218497-11218734	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:11218125-11218321	A549	lung:	n/a	n/a
49	CEBPB	chr8:11219169-11219602	A549	lung:	n/a	n/a
50	CEBPB	chr8:11244061-11244296	A549	lung:	n/a	chr8:11244236-11244249 chr8:11244237-11244248 chr8:11244236-11244247 chr8:11244236-11244249

(count:2746 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11225793-11225843	K562	blood:	n/a
2	chr8:11225793-11225843	K562	blood:	n/a
3	chr8:11213517-11213567	HAEpiC	amniotic membrane:	n/a
4	chr8:11204017-11204067	T-47D	breast:	n/a
5	chr8:11251609-11251659	HCT-116	colon:	n/a
6	chr8:11225385-11225435	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:11184217-11184267	NHBE	bronchial:	n/a
8	chr8:11225793-11225843	SK-N-SH	brain:	n/a
9	chr8:11188490-11188540	A549	lung:	n/a
10	chr8:11213424-11213474	ovcar-3	ovarian:	n/a
11	chr8:11189650-11189700	T-47D	breast:	n/a
12	chr8:11212812-11212862	RPTEC	kidney:	n/a
13	chr8:11250222-11250272	PFSK-1	brain:	n/a
14	chr8:11188490-11188540	SKMC	muscle:	n/a
15	chr8:11195810-11195860	HIPEpiC	eye:	n/a
16	chr8:11204541-11204591	IMR90	lung:	fetal
17	chr8:11205166-11205216	ECC-1	luminal epithelium:	n/a
18	chr8:11213517-11213567	BJ	skin:	n/a
19	chr8:11213517-11213567	U87	brain:	n/a
20	chr8:11197070-11197120	SK-N-SH	brain:	n/a
21	chr8:11251471-11251521	HUVEC	blood vessel:	n/a
22	chr8:11251471-11251521	MCF-7	breast:	n/a
23	chr8:11204132-11204182	AG09319	gingival:	n/a
24	chr8:11203882-11203932	AG04450	lung:	fetal
25	chr8:11197026-11197076	NB4	blood:	n/a
26	chr8:11205972-11206022	HEK293	kidney:	embryo
27	chr8:11184217-11184267	MCF-7	breast:	n/a
28	chr8:11205166-11205216	MCF10A-Er-Src	breast:	n/a
29	chr8:11212668-11212718	HEEpiC	esophagus:	n/a
30	chr8:11197070-11197120	AG04449	skin:	fetal
31	chr8:11224510-11224560	NH-A	brain:	n/a
32	chr8:11225385-11225435	MCF10A-Er-Src	breast:	n/a
33	chr8:11183844-11183894	Hela-S3	cervix:	n/a
34	chr8:11197070-11197120	GM12878	blood:	n/a
35	chr8:11251609-11251659	NB4	blood:	n/a
36	chr8:11205754-11205804	HMEC	breast:	n/a
37	chr8:11204132-11204182	HCPEpiC	choroid plexus:	n/a
38	chr8:11182979-11183029	NT2-D1	testis:	n/a
39	chr8:11206009-11206059	MCF-7	breast:	n/a
40	chr8:11206009-11206059	PrEC	prostate:	n/a
41	chr8:11205166-11205216	Caco-2	colon:	n/a
42	chr8:11225793-11225843	HRCEpiC	kidney:	n/a
43	chr8:11205619-11205669	HCF	heart:	n/a
44	chr8:11251609-11251659	HPAEpiC	pulmonary alveolar:	n/a
45	chr8:11188675-11188725	GM12891	blood:	n/a
46	chr8:11205619-11205669	ovcar-3	ovarian:	n/a
47	chr8:11205619-11205669	GM12891	blood:	n/a
48	chr8:11212812-11212862	HNPCEpiC	eye:	n/a
49	chr8:11205247-11205297	H1-hESC	embryonic stem cell:	embryo
50	chr8:11225385-11225435	AG04449	skin:	fetal

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11194174..11194960-chr8:11325192..11325823,2	K562	blood:
2	chr8:11141452..11143588-chr8:11203845..11206287,2	MCF-7	breast:
3	chr8:11220966..11222998-chr8:11244334..11246099,2	MCF-7	breast:
4	chr8:11200722..11203684-chr8:11734586..11737466,2	K562	blood:
5	chr8:11210953..11213367-chr8:11221125..11223002,2	K562	blood:
6	chr8:11205483..11207435-chr8:11216914..11218469,2	MCF-7	breast:
7	chr8:11190703..11193064-chr8:11198301..11200688,2	K562	blood:
8	chr8:11202546..11204675-chr8:11207385..11211000,3	MCF-7	breast:
9	chr8:11235300..11237155-chr8:11240662..11242925,2	K562	blood:
10	chr8:11160652..11163561-chr8:11179931..11182609,2	K562	blood:
11	chr8:11197853..11202085-chr8:11202628..11206812,8	K562	blood:
12	chr8:11195675..11197986-chr8:11203854..11205997,2	MCF-7	breast:
13	chr8:11192721..11196103-chr8:11203012..11206655,6	MCF-7	breast:
14	chr8:11193886..11197724-chr8:11199871..11205497,8	K562	blood:
15	chr8:11212238..11213947-chr8:11218852..11221758,2	MCF-7	breast:
16	chr8:11202670..11208385-chr8:11211112..11215163,10	K562	blood:
17	chr8:11202546..11204675-chr8:11207385..11211000,3	MCF-7	breast:
18	chr8:11174783..11177164-chr8:11178437..11180713,3	K562	blood:
19	chr8:11219674..11222977-chr8:11226282..11228003,4	MCF-7	breast:
20	chr8:11204525..11206554-chr8:11212652..11215291,3	MCF-7	breast:
21	chr8:11241230..11243986-chr8:11247872..11250169,2	K562	blood:
22	chr8:11218476..11220050-chr8:11220905..11223351,2	K562	blood:
23	chr8:11214329..11216300-chr8:11221586..11223456,2	K562	blood:
24	chr8:11202670..11208385-chr8:11211112..11215163,10	K562	blood:
25	chr8:11205933..11210781-chr8:11211287..11215199,6	K562	blood:
26	chr8:11202880..11204738-chr8:11213241..11216075,2	K562	blood:
27	chr8:11221017..11222981-chr8:11226248..11228543,2	K562	blood:
28	chr8:11193886..11197724-chr8:11199871..11205497,8	K562	blood:
29	chr8:11214329..11216300-chr8:11221586..11223456,2	K562	blood:
30	chr8:11182223..11183959-chr8:11192800..11194689,2	K562	blood:
31	chr8:11204525..11206554-chr8:11212652..11215291,3	MCF-7	breast:
32	chr8:11190703..11193064-chr8:11198301..11200688,2	K562	blood:
33	chr8:11220966..11222998-chr8:11244334..11246099,2	MCF-7	breast:
34	chr8:11210953..11213367-chr8:11221125..11223002,2	K562	blood:
35	chr8:11200246..11202306-chr8:11227732..11229716,2	K562	blood:
36	chr8:11177843..11179564-chr8:11181108..11182895,2	K562	blood:
37	chr8:11202674..11205995-chr8:11206285..11210798,7	K562	blood:
38	chr8:11140705..11143665-chr8:11184811..11187065,2	K562	blood:
39	chr8:11174783..11177164-chr8:11178437..11180713,3	K562	blood:
40	chr8:11142292..11144724-chr8:11241964..11244169,2	K562	blood:
41	chr8:11203206..11204716-chr8:11251549..11254468,2	K562	blood:
42	chr8:11213506..11215349-chr8:11216834..11218432,2	K562	blood:
43	chr8:11177843..11179564-chr8:11181108..11182895,2	K562	blood:
44	chr8:11141950..11143471-chr8:11205387..11207796,2	K562	blood:
45	chr8:11200246..11202306-chr8:11227732..11229716,2	K562	blood:
46	chr8:11224632..11226461-chr8:11227534..11229190,2	K562	blood:
47	chr8:11242265..11244818-chr8:11252582..11254482,2	MCF-7	breast:
48	chr8:11208459..11213186-chr8:11213672..11216072,5	K562	blood:
49	chr8:11208459..11213186-chr8:11213672..11216072,5	K562	blood:
50	chr8:11141824..11143509-chr8:11265608..11267420,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf12-1	chr8:11262050-11262211	NONHSAT125056
2	lnc-C8orf12-1	chr8:11251633-11251844	NONHSAT125056
3	lnc-C8orf12-1	chr8:11258575-11258674	NONHSAT125056
4	lnc-AF131216.5.1-1	chr8:11204806-11205011	ENSG00000255020.1
5	lnc-AF131216.6.1-2	chr8:11181416-11182018	NONHSAT125048
6	lnc-C8orf12-1	chr8:11247933-11248244	NONHSAT125054
7	lnc-C8orf12-1	chr8:11241322-11241510	NR_026814
8	lnc-AF131216.5.1-1	chr8:11203257-11204149	ENSG00000255020.1
9	lnc-C8orf12-1	chr8:11225911-11225961	NR_026814
10	lnc-SLC35G5-1	chr8:11236904-11237200	NONHSAT125053
11	lnc-C8orf12-1	chr8:11258575-11258674	NONHSAT125054
12	lnc-C8orf12-1	chr8:11263321-11263371	ucscGeneNc_uc003wtu_2
13	lnc-C8orf12-1	chr8:11258575-11258674	NR_026814

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MTMR9	hsa-miR-34a-5p	chr8:11181173-11181179
2	MTMR9	hsa-miR-148a-3p	chr8:11181171-11181177
3	MTMR9	hsa-miR-148a-3p	chr8:11185218-11185239
4	MTMR9	hsa-miR-148a-3p	chr8:11185232-11185238
5	MTMR9	hsa-miR-148a-3p	chr8:11181185-11181205
6	MTMR9	hsa-miR-34a-5p	chr8:11184946-11184952
7	MTMR9	hsa-miR-148a-3p	chr8:11181198-11181204
8	MTMR9	hsa-miR-130b-3p	chr8:11185214-11185238
9	MTMR9	hsa-miR-130b-3p	chr8:11185200-11185206
10	MTMR9	hsa-miR-130b-3p	chr8:11181184-11181204
11	MTMR9	hsa-miR-130b-3p	chr8:11185231-11185237

Variant related genes	Relation type
SLC35G5	TF binding region
ENSG00000255020	TF binding region
C8orf12	TF binding region
RNU6-1084P	TF binding region
TDH	TF binding region
RN7SL293P	TF binding region
ENSG00000246477	TF binding region
SLC35G5	CpG island
ENSG00000255020	CpG island
C8orf12	CpG island
RNU6-1084P	CpG island
TDH	CpG island
RN7SL293P	CpG island
ENSG00000246477	CpG island
ENSG00000199368	chromatin interactions
ENSG00000154316	chromatin interactions
ENSG00000242483	chromatin interactions
ENSG00000104643	chromatin interactions
ENSG00000184608	chromatin interactions
ENSG00000255020	chromatin interactions
ENSG00000246477	chromatin interactions

Extended variants
information (count: 4267 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:4267 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17153128	chr8:11176147-11176148	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552373841	chr8:11176149-11176150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6991606	chr8:11176159-11176160	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs80060889	chr8:11176163-11176164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547004434	chr8:11176164-11176165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568732775	chr8:11176173-11176174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536292791	chr8:11176203-11176204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs377513671	chr8:11176212-11176213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554565037	chr8:11176240-11176241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576207364	chr8:11176246-11176247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537116097	chr8:11176265-11176266	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188617214	chr8:11176348-11176349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181032068	chr8:11176388-11176389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2572397	chr8:11176403-11176404	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs559437579	chr8:11176443-11176444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs574669902	chr8:11176452-11176453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs74410499	chr8:11176469-11176470	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374644600	chr8:11176500-11176501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs530925191	chr8:11176557-11176558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552286043	chr8:11176614-11176615	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs368968476	chr8:11176625-11176626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550000274	chr8:11176641-11176642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs118123141	chr8:11176649-11176650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547160524	chr8:11176672-11176673	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140295761	chr8:11176685-11176686	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535940931	chr8:11176707-11176708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115130628	chr8:11176719-11176720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548230051	chr8:11176726-11176727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569636522	chr8:11176732-11176733	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185945548	chr8:11176745-11176746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75862247	chr8:11176957-11176958	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143534465	chr8:11176980-11176981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148041475	chr8:11176987-11176988	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs553094286	chr8:11176997-11176998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555870731	chr8:11177001-11177002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575817417	chr8:11177054-11177055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374058360	chr8:11177060-11177061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532237414	chr8:11177065-11177066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140874657	chr8:11177067-11177068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76179315	chr8:11177095-11177096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192310824	chr8:11177111-11177112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs2251473	chr8:11177126-11177127	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs369696571	chr8:11177127-11177128	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200016572	chr8:11177152-11177153	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181951547	chr8:11177159-11177160	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373234708	chr8:11177175-11177176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564461929	chr8:11177183-11177184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs140628884	chr8:11177200-11177201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs199649764	chr8:11177229-11177230	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370937399	chr8:11177232-11177233	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1059 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11154200-11181400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr8:11154200-11183800	Strong transcription	Liver	Liver
3	chr8:11154600-11183000	Strong transcription	Fetal Muscle Trunk	muscle
4	chr8:11155000-11184000	Strong transcription	Dnd41	blood
5	chr8:11155600-11183200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr8:11157200-11180800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr8:11157400-11182600	Strong transcription	Skeletal Muscle Female	skeletal muscle
8	chr8:11157600-11183000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr8:11160000-11176200	Strong transcription	Fetal Thymus	thymus
10	chr8:11160600-11176200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr8:11160600-11176200	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr8:11160600-11178800	Strong transcription	Fetal Intestine Large	intestine
13	chr8:11161600-11183200	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr8:11161800-11182600	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr8:11162000-11180200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr8:11162000-11181200	Strong transcription	HSMM	muscle
17	chr8:11162000-11182600	Strong transcription	Duodenum Mucosa	Duodenum
18	chr8:11162000-11183400	Strong transcription	Primary T cells from cord blood	blood
19	chr8:11162200-11176200	Strong transcription	Primary B cells from cord blood	blood
20	chr8:11162200-11180600	Strong transcription	Sigmoid Colon	Sigmoid Colon
21	chr8:11162200-11181000	Strong transcription	Placenta	Placenta
22	chr8:11162200-11181600	Strong transcription	Primary B cells from peripheral blood	blood
23	chr8:11162200-11183200	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr8:11162400-11176200	Strong transcription	Stomach Smooth Muscle	stomach
25	chr8:11162400-11179200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
26	chr8:11162400-11179600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr8:11162400-11180600	Strong transcription	Left Ventricle	heart
28	chr8:11162400-11180800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
29	chr8:11162400-11182600	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr8:11162400-11183000	Strong transcription	Primary monocytes fromperipheralblood	blood
31	chr8:11162400-11183000	Strong transcription	Adipose Nuclei	Adipose
32	chr8:11162400-11183200	Strong transcription	Duodenum Smooth Muscle	Duodenum
33	chr8:11162400-11183600	Strong transcription	Primary T helper cells fromperipheralblood	blood
34	chr8:11162400-11183800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
35	chr8:11162400-11184000	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr8:11162400-11184000	Strong transcription	Monocytes-CD14+_RO01746	blood
37	chr8:11162400-11184200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr8:11162600-11182800	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr8:11162600-11184000	Strong transcription	HUES48 Cell Line	embryonic stem cell
40	chr8:11164600-11178800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr8:11165400-11176200	Strong transcription	Brain Hippocampus Middle	brain
42	chr8:11165400-11181200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr8:11166200-11176200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr8:11166800-11177200	Weak transcription	NHEK	skin
45	chr8:11167400-11185200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr8:11167800-11184600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr8:11168400-11177200	Weak transcription	HepG2	liver
48	chr8:11170000-11179200	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr8:11170400-11177000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr8:11170600-11179200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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