Variant report

Variant	nsv1029934
Chromosome Location	chr8:11747133-11858466
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2546)
CpG islands
(count:3240)
Chromatin interactive
region (count:64)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2546 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:11746984-11747236	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:11799803-11800003	K562	blood:	n/a	n/a
3	ARID3A	chr8:11758928-11760170	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:11767366-11767469	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:11769447-11769628	K562	blood:	n/a	n/a
6	ARID3A	chr8:11801213-11801488	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:11754879-11755097	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:11813783-11814113	HepG2	liver:	n/a	n/a
9	ATF1	chr8:11799573-11800081	K562	blood:	n/a	n/a
10	ATF1	chr8:11793688-11793744	K562	blood:	n/a	n/a
11	ATF1	chr8:11807083-11807365	K562	blood:	n/a	n/a
12	ATF2	chr8:11754279-11755628	GM12878	blood:	n/a	n/a
13	ATF2	chr8:11759720-11760180	GM12878	blood:	n/a	n/a
14	ATF2	chr8:11754354-11755726	GM12878	blood:	n/a	n/a
15	ATF3	chr8:11801205-11801436	K562	blood:	n/a	n/a
16	ATF3	chr8:11801205-11801445	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF3	chr8:11759787-11760027	K562	blood:	n/a	n/a
18	BACH1	chr8:11816433-11816692	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:11791553-11791787	K562	blood:	n/a	n/a
20	BACH1	chr8:11766653-11766839	K562	blood:	n/a	n/a
21	BACH1	chr8:11759765-11760312	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:11815300-11815374	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr8:11754598-11755318	GM12878	blood:	n/a	n/a
24	BATF	chr8:11764476-11764781	GM12878	blood:	n/a	n/a
25	BATF	chr8:11754746-11755153	GM12878	blood:	n/a	n/a
26	BATF	chr8:11768607-11768792	GM12878	blood:	n/a	n/a
27	BCL11A	chr8:11754571-11755235	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
28	BCL11A	chr8:11754614-11755041	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
29	BCL11A	chr8:11783650-11783829	GM12878	blood:	n/a	n/a
30	BCL3	chr8:11754724-11755297	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
31	BCL3	chr8:11822405-11822652	GM12878	blood:	n/a	n/a
32	BCLAF1	chr8:11754337-11755211	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
33	BCLAF1	chr8:11754389-11755233	GM12878	blood:	n/a	chr8:11754779-11754792 chr8:11754784-11754793 chr8:11754786-11754799
34	BHLHE40	chr8:11759743-11760084	GM12878	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
35	BHLHE40	chr8:11801183-11801540	HepG2	liver:	n/a	chr8:11801359-11801372
36	BHLHE40	chr8:11815192-11815513	HepG2	liver:	n/a	n/a
37	BHLHE40	chr8:11754544-11755330	K562	blood:	n/a	chr8:11754786-11754802
38	BHLHE40	chr8:11769211-11769482	K562	blood:	n/a	n/a
39	BHLHE40	chr8:11793297-11793881	K562	blood:	n/a	n/a
40	BHLHE40	chr8:11748511-11748817	K562	blood:	n/a	n/a
41	BHLHE40	chr8:11812950-11813081	K562	blood:	n/a	n/a
42	BHLHE40	chr8:11806929-11807352	K562	blood:	n/a	n/a
43	BHLHE40	chr8:11754703-11755212	HepG2	liver:	n/a	chr8:11754786-11754802
44	BHLHE40	chr8:11815181-11815494	K562	blood:	n/a	n/a
45	BHLHE40	chr8:11801158-11801425	A549	lung:	n/a	chr8:11801359-11801372
46	BHLHE40	chr8:11801130-11801571	K562	blood:	n/a	chr8:11801359-11801372
47	BHLHE40	chr8:11759739-11760276	K562	blood:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
48	BHLHE40	chr8:11816398-11816683	K562	blood:	n/a	n/a
49	BHLHE40	chr8:11759086-11760250	HepG2	liver:	n/a	chr8:11759889-11759905 chr8:11759886-11759902
50	BHLHE40	chr8:11801171-11801545	GM12878	blood:	n/a	chr8:11801359-11801372

(count:3240 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:11843807-11843857	HRPEpiC	eye:	n/a
2	chr8:11759930-11759980	NB4	blood:	n/a
3	chr8:11813211-11813261	SK-N-MC	brain:	n/a
4	chr8:11832039-11832089	K562	blood:	n/a
5	chr8:11841980-11842030	Hela-S3	cervix:	n/a
6	chr8:11833191-11833241	ovcar-3	ovarian:	n/a
7	chr8:11795273-11795323	LNCaP	prostate:	n/a
8	chr8:11843807-11843857	HRPEpiC	eye:	n/a
9	chr8:11759930-11759980	NB4	blood:	n/a
10	chr8:11813211-11813261	SK-N-MC	brain:	n/a
11	chr8:11832039-11832089	K562	blood:	n/a
12	chr8:11841980-11842030	Hela-S3	cervix:	n/a
13	chr8:11833191-11833241	ovcar-3	ovarian:	n/a
14	chr8:11795273-11795323	LNCaP	prostate:	n/a
15	chr8:11773969-11774019	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:11759665-11759715	HMEC	breast:	n/a
17	chr8:11843807-11843857	NB4	blood:	n/a
18	chr8:11772568-11772618	HRCEpiC	kidney:	n/a
19	chr8:11763828-11763878	LNCaP	prostate:	n/a
20	chr8:11771244-11771294	HCM	heart:	n/a
21	chr8:11772734-11772784	SAEC	small airway:	n/a
22	chr8:11833191-11833241	NHBE	bronchial:	n/a
23	chr8:11839764-11839814	GM19239	blood:	n/a
24	chr8:11772119-11772169	HRE	kidney:	n/a
25	chr8:11832565-11832615	Hepatocyte	liver:	n/a
26	chr8:11790639-11790689	RPTEC	kidney:	n/a
27	chr8:11801320-11801370	ProgFib	skin:	n/a
28	chr8:11853121-11853171	GM12892	blood:	n/a
29	chr8:11839764-11839814	BE2_C	brain:	n/a
30	chr8:11772734-11772784	NH-A	brain:	n/a
31	chr8:11832565-11832615	SK-N-MC	brain:	n/a
32	chr8:11853878-11853928	H1-hESC	embryonic stem cell:	embryo
33	chr8:11795273-11795323	PANC-1	pancreas:	n/a
34	chr8:11813211-11813261	HEK293	kidney:	embryo
35	chr8:11832565-11832615	AG04450	lung:	fetal
36	chr8:11756069-11756119	HNPCEpiC	eye:	n/a
37	chr8:11770970-11771020	HEK293	kidney:	embryo
38	chr8:11843816-11843866	HL-60	blood:	n/a
39	chr8:11759930-11759980	Caco-2	colon:	n/a
40	chr8:11763828-11763878	SAEC	small airway:	n/a
41	chr8:11759663-11759713	HUVEC	blood vessel:	n/a
42	chr8:11772734-11772784	AG04450	lung:	fetal
43	chr8:11771345-11771395	NHDF-neo	bronchial:	n/a
44	chr8:11831823-11831873	Hela-S3	cervix:	n/a
45	chr8:11839844-11839894	SK-N-MC	brain:	n/a
46	chr8:11773969-11774019	GM12891	blood:	n/a
47	chr8:11832762-11832812	SKMC	muscle:	n/a
48	chr8:11772568-11772618	HUVEC	blood vessel:	n/a
49	chr8:11832039-11832089	HMEC	breast:	n/a
50	chr8:11835607-11835657	HAEpiC	amniotic membrane:	n/a

(count:64 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:11622902..11623629-chr8:11759456..11760412,3	MCF-7	breast:
2	chr8:11724948..11727474-chr8:11747087..11750082,2	MCF-7	breast:
3	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
4	chr8:11612285..11613206-chr8:11801217..11801735,2	MCF-7	breast:
5	chr8:11702751..11703651-chr8:11759392..11760311,3	MCF-7	breast:
6	chr8:11718467..11721222-chr8:11754378..11756104,3	K562	blood:
7	chr8:11622652..11623752-chr8:11800899..11801806,5	MCF-7	breast:
8	chr8:11724101..11727184-chr8:11750037..11752895,4	K562	blood:
9	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
10	chr8:11699877..11702780-chr8:11758303..11760780,3	K562	blood:
11	chr8:11421685..11422256-chr8:11800840..11801381,2	K562	blood:
12	chr8:11838617..11840884-chr8:11844089..11846019,2	K562	blood:
13	chr8:11724650..11727565-chr8:11758155..11761309,4	MCF-7	breast:
14	chr8:11424139..11425217-chr8:11815416..11817027,6	K562	blood:
15	chr8:11851923..11853652-chr8:11853797..11856578,2	K562	blood:
16	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
17	chr8:11603020..11605526-chr8:11757590..11759777,2	K562	blood:
18	chr8:11836841..11840054-chr8:11842955..11845395,3	MCF-7	breast:
19	chr8:11819737..11820672-chr8:11872272..11872975,3	MCF-7	breast:
20	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
21	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
22	chr8:11711030..11711819-chr8:11759482..11760312,2	MCF-7	breast:
23	chr8:11835676..11837241-chr8:11840654..11843342,2	K562	blood:
24	chr8:11622669..11623564-chr8:11800869..11801753,3	K562	blood:
25	chr8:11720357..11728660-chr8:11741310..11749437,9	K562	blood:
26	chr8:11835676..11838476-chr8:11840654..11843385,2	K562	blood:
27	chr8:11746436..11748896-chr8:11754900..11757322,2	K562	blood:
28	chr8:11724192..11726313-chr8:11753136..11754724,2	MCF-7	breast:
29	chr8:11622750..11623420-chr8:11815244..11815854,2	MCF-7	breast:
30	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
31	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
32	chr8:11801089..11802817-chr8:11804319..11806900,3	K562	blood:
33	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
34	chr8:11752267..11756149-chr8:11756562..11759200,3	MCF-7	breast:
35	chr8:11798435..11800299-chr8:11803537..11805187,2	K562	blood:
36	chr8:11421707..11422824-chr8:11816126..11817083,9	K562	blood:
37	chr8:11622903..11623629-chr8:11815893..11817036,5	K562	blood:
38	chr8:11724862..11726557-chr8:11758521..11760693,2	MCF-7	breast:
39	chr8:11702698..11703665-chr8:11759456..11760160,2	MCF-7	breast:
40	chr8:11833455..11835537-chr8:11843531..11845955,2	K562	blood:
41	chr8:11820183..11822422-chr8:11827376..11829261,2	K562	blood:
42	chr8:11662199..11664746-chr8:11796348..11798802,2	K562	blood:
43	chr8:11759679..11760322-chr8:11800851..11801844,2	K562	blood:
44	chr8:11827300..11830194-chr8:11832454..11834607,2	K562	blood:
45	chr8:11424253..11424822-chr8:11800849..11801372,2	K562	blood:
46	chr8:11742257..11745256-chr8:11747591..11749952,2	K562	blood:
47	chr8:11759912..11760480-chr8:11816112..11816711,2	K562	blood:
48	chr8:11768991..11769997-chr8:11800815..11801744,4	MCF-7	breast:
49	chr8:11816131..11817071-chr8:11827985..11828641,3	K562	blood:
50	chr8:11658805..11661004-chr8:11802756..11805427,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB135-1	chr8:11856596-11856977	NONHSAT125105
2	lnc-CTSB-1	chr8:11753359-11753626	NONHSAT125100
3	lnc-CTSB-1	chr8:11754271-11754379	NONHSAT125100
4	lnc-CTSB-2	chr8:11777409-11778318	NONHSAT125102

No data

Variant related genes	Relation type
DEFB136	TF binding region
OR7E161P	TF binding region
ENSG00000255174	TF binding region
DEFB134	TF binding region
DEFB135	TF binding region
OR7E158P	TF binding region
ENSG00000255144	TF binding region
DEFB136	CpG island
OR7E161P	CpG island
ENSG00000255174	CpG island
DEFB134	CpG island
DEFB135	CpG island
OR7E158P	CpG island
ENSG00000255144	CpG island
ENSG00000255046	chromatin interactions
ENSG00000255144	chromatin interactions
ENSG00000205884	chromatin interactions
ENSG00000205883	chromatin interactions
ENSG00000164733	chromatin interactions
ENSG00000205882	chromatin interactions
ENSG00000079459	chromatin interactions

Extended variants
information (count: 6363 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:6363 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182441715	chr8:11747147-11747148	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs576095865	chr8:11747155-11747156	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145995513	chr8:11747158-11747159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs118105989	chr8:11747171-11747172	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185483862	chr8:11747172-11747173	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540593248	chr8:11747194-11747195	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs7839524	chr8:11747212-11747213	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7818169	chr8:11747232-11747233	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs543694524	chr8:11747233-11747234	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7818321	chr8:11747331-11747332	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs114934512	chr8:11747341-11747342	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs563490285	chr8:11747383-11747384	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs535339822	chr8:11747392-11747393	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs530942956	chr8:11747406-11747407	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs7836316	chr8:11747423-11747424	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs552619655	chr8:11747438-11747439	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139987881	chr8:11747452-11747453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs528503620	chr8:11747482-11747483	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1692795	chr8:11747540-11747541	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs1736128	chr8:11747554-11747555	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs1692794	chr8:11747557-11747558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557304512	chr8:11747563-11747564	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190362532	chr8:11747578-11747579	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs367900733	chr8:11747602-11747603	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs75754060	chr8:11747625-11747626	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs558633170	chr8:11747632-11747633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1692792	chr8:11747653-11747654	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs571097556	chr8:11747705-11747706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs554462195	chr8:11747733-11747734	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs540630897	chr8:11747734-11747735	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs367784726	chr8:11747771-11747772	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371237193	chr8:11747774-11747775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs145731164	chr8:11747778-11747779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs181598688	chr8:11747781-11747782	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542092820	chr8:11747794-11747795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563367246	chr8:11747805-11747806	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530754953	chr8:11747815-11747816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545645497	chr8:11747821-11747822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148497494	chr8:11747823-11747824	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs28735487	chr8:11747841-11747842	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs76620842	chr8:11747853-11747854	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs114757414	chr8:11747855-11747856	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2645405	chr8:11747858-11747859	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs2645404	chr8:11747868-11747869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs569413696	chr8:11747898-11747899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2645403	chr8:11747919-11747920	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs558024424	chr8:11747921-11747922	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570261431	chr8:11747965-11747966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs113775508	chr8:11747972-11747973	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs534405462	chr8:11748004-11748005	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	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
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11736400-11748600	Weak transcription	HSMMtube	muscle
2	chr8:11736400-11749000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr8:11738000-11755800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:11740400-11754200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr8:11742000-11747800	Weak transcription	NHLF	lung
6	chr8:11742200-11747600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:11742800-11748800	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr8:11743800-11752200	Weak transcription	K562	blood
9	chr8:11744600-11747400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr8:11745200-11747200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:11745200-11747600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr8:11745200-11748400	Enhancers	NHDF-Ad	bronchial
13	chr8:11745400-11747600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:11745400-11747600	Enhancers	Osteobl	bone
15	chr8:11745400-11748800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr8:11745400-11750000	Enhancers	HMEC	breast
17	chr8:11745600-11750000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr8:11745800-11747400	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr8:11745800-11749800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:11745800-11759600	Weak transcription	Right Atrium	heart
21	chr8:11746000-11748600	Weak transcription	Fetal Brain Male	brain
22	chr8:11746200-11749800	Enhancers	NHEK	skin
23	chr8:11746400-11749000	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr8:11746400-11750600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:11746600-11747800	Weak transcription	Lung	lung
26	chr8:11746600-11754400	Weak transcription	Esophagus	oesophagus
27	chr8:11746800-11747600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr8:11746800-11747800	Weak transcription	Spleen	Spleen
29	chr8:11746800-11754600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
30	chr8:11746800-11754600	Weak transcription	Placenta	Placenta
31	chr8:11747000-11747200	Enhancers	A549	lung
32	chr8:11747000-11748400	Weak transcription	Colon Smooth Muscle	Colon
33	chr8:11747000-11748400	Weak transcription	Hela-S3	cervix
34	chr8:11747000-11750200	Enhancers	HepG2	liver
35	chr8:11747200-11747400	Flanking Active TSS	A549	lung
36	chr8:11747200-11747600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:11747400-11748400	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr8:11747400-11749000	Enhancers	A549	lung
39	chr8:11747600-11748000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr8:11747600-11748000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr8:11747600-11748000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr8:11747600-11748000	Weak transcription	Osteobl	bone
43	chr8:11747600-11749800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:11747600-11750000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr8:11747800-11748000	Enhancers	Lung	lung
46	chr8:11747800-11748000	Enhancers	Spleen	Spleen
47	chr8:11747800-11749200	Enhancers	NHLF	lung
48	chr8:11748000-11748400	Enhancers	Osteobl	bone
49	chr8:11748000-11748800	Weak transcription	Lung	lung
50	chr8:11748000-11749800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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