Variant report

Variant	nsv1030400
Chromosome Location	chr6:119320153-119433830
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1224)
CpG islands
(count:1345)
Chromatin interactive
region (count:77)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:119357028-119357048	K562	blood:	n/a	n/a
2	ARID3A	chr6:119388308-119388636	K562	blood:	n/a	n/a
3	ARID3A	chr6:119359048-119359828	K562	blood:	n/a	n/a
4	ARID3A	chr6:119387925-119388005	K562	blood:	n/a	n/a
5	ARID3A	chr6:119400031-119400291	HepG2	liver:	n/a	n/a
6	ATF1	chr6:119388315-119388618	K562	blood:	n/a	n/a
7	ATF2	chr6:119399940-119400338	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:119399956-119400272	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:119356360-119356476	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr6:119400120-119400243	K562	blood:	n/a	n/a
11	BACH1	chr6:119399880-119400359	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:119396652-119396663	K562	blood:	n/a	n/a
13	BHLHE40	chr6:119399974-119400226	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:119398954-119399368	K562	blood:	n/a	n/a
15	BHLHE40	chr6:119399761-119400663	K562	blood:	n/a	chr6:119399848-119399864
16	BHLHE40	chr6:119399756-119400362	HepG2	liver:	n/a	chr6:119399848-119399864
17	BHLHE40	chr6:119388304-119388720	K562	blood:	n/a	n/a
18	BRCA1	chr6:119348308-119348435	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr6:119399910-119400178	HepG2	liver:	n/a	n/a
20	BRCA1	chr6:119399903-119400182	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr6:119399226-119399307	HepG2	liver:	n/a	n/a
22	CBX3	chr6:119398742-119399449	K562	blood:	n/a	n/a
23	CBX3	chr6:119330399-119330788	K562	blood:	n/a	n/a
24	CBX3	chr6:119404083-119404625	K562	blood:	n/a	n/a
25	CBX3	chr6:119359069-119359643	K562	blood:	n/a	n/a
26	CBX3	chr6:119399746-119400689	K562	blood:	n/a	n/a
27	CBX3	chr6:119404137-119404598	K562	blood:	n/a	n/a
28	CBX3	chr6:119399952-119400340	K562	blood:	n/a	n/a
29	CCNT2	chr6:119399120-119400331	K562	blood:	n/a	n/a
30	CCNT2	chr6:119359129-119359534	K562	blood:	n/a	n/a
31	CCNT2	chr6:119387842-119387939	K562	blood:	n/a	n/a
32	CCNT2	chr6:119356705-119356965	K562	blood:	n/a	n/a
33	CCNT2	chr6:119388430-119388532	K562	blood:	n/a	n/a
34	CEBPB	chr6:119430769-119431173	K562	blood:	n/a	chr6:119431009-119431018 chr6:119431007-119431018 chr6:119431009-119431018 chr6:119431007-119431020 chr6:119431009-119431018
35	CEBPB	chr6:119398865-119399362	H1-hESC	embryonic stem cell:	n/a	chr6:119399011-119399024 chr6:119399012-119399023
36	CEBPB	chr6:119392777-119393105	HepG2	liver:	n/a	chr6:119392926-119392939
37	CEBPB	chr6:119430832-119431172	ECC-1	luminal epithelium:	n/a	chr6:119431009-119431018 chr6:119431007-119431018 chr6:119431009-119431018 chr6:119431007-119431020 chr6:119431009-119431018
38	CEBPB	chr6:119382408-119382730	K562	blood:	n/a	chr6:119382576-119382587
39	CEBPB	chr6:119418739-119418991	IMR90	lung:	n/a	chr6:119418875-119418886
40	CEBPB	chr6:119430911-119431234	ECC-1	luminal epithelium:	n/a	chr6:119431009-119431018 chr6:119431007-119431018 chr6:119431009-119431018 chr6:119431007-119431020 chr6:119431009-119431018
41	CEBPB	chr6:119382420-119382741	HepG2	liver:	n/a	chr6:119382576-119382587
42	CEBPB	chr6:119398827-119399193	A549	lung:	n/a	chr6:119399011-119399024 chr6:119399012-119399023
43	CEBPB	chr6:119430831-119431195	A549	lung:	n/a	chr6:119431009-119431018 chr6:119431007-119431018 chr6:119431009-119431018 chr6:119431007-119431020 chr6:119431009-119431018
44	CEBPB	chr6:119430798-119431217	MCF-7	breast:	n/a	chr6:119431009-119431018 chr6:119431007-119431018 chr6:119431009-119431018 chr6:119431007-119431020 chr6:119431009-119431018
45	CEBPB	chr6:119382501-119382724	IMR90	lung:	n/a	chr6:119382576-119382587
46	CEBPB	chr6:119392760-119393082	HepG2	liver:	n/a	chr6:119392926-119392939
47	CEBPB	chr6:119382478-119382648	K562	blood:	n/a	chr6:119382576-119382587
48	CEBPB	chr6:119398552-119399213	K562	blood:	n/a	chr6:119399011-119399024 chr6:119399012-119399023
49	CEBPB	chr6:119418824-119418989	K562	blood:	n/a	chr6:119418875-119418886
50	CEBPB	chr6:119398845-119399213	MCF-7	breast:	n/a	chr6:119399011-119399024 chr6:119399012-119399023

(count:1345 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:119399550-119399600	CMK	blood:	n/a
2	chr6:119358124-119358174	LNCaP	prostate:	n/a
3	chr6:119390712-119390762	HL-60	blood:	n/a
4	chr6:119399550-119399600	CMK	blood:	n/a
5	chr6:119358124-119358174	LNCaP	prostate:	n/a
6	chr6:119390712-119390762	HL-60	blood:	n/a
7	chr6:119401102-119401152	NB4	blood:	n/a
8	chr6:119399550-119399600	Hela-S3	cervix:	n/a
9	chr6:119400380-119400430	ProgFib	skin:	n/a
10	chr6:119400462-119400512	GM19239	blood:	n/a
11	chr6:119358124-119358174	U87	brain:	n/a
12	chr6:119400041-119400091	LNCaP	prostate:	n/a
13	chr6:119399550-119399600	HCPEpiC	choroid plexus:	n/a
14	chr6:119395189-119395239	AG04449	skin:	fetal
15	chr6:119400114-119400164	HCF	heart:	n/a
16	chr6:119390418-119390468	LNCaP	prostate:	n/a
17	chr6:119401102-119401152	NH-A	brain:	n/a
18	chr6:119362940-119362990	HNPCEpiC	eye:	n/a
19	chr6:119358124-119358174	HepG2	liver:	n/a
20	chr6:119390712-119390762	GM12891	blood:	n/a
21	chr6:119390286-119390336	AG04450	lung:	fetal
22	chr6:119390712-119390762	NH-A	brain:	n/a
23	chr6:119400380-119400430	AG09319	gingival:	n/a
24	chr6:119399925-119399975	HMEC	breast:	n/a
25	chr6:119390646-119390696	Jurkat	blood:	n/a
26	chr6:119346816-119346866	SKMC	muscle:	n/a
27	chr6:119399550-119399600	ovcar-3	ovarian:	n/a
28	chr6:119399550-119399600	AG09309	skin:	n/a
29	chr6:119399928-119399978	RPTEC	kidney:	n/a
30	chr6:119400380-119400430	HUVEC	blood vessel:	n/a
31	chr6:119400114-119400164	Jurkat	blood:	n/a
32	chr6:119395189-119395239	HEK293	kidney:	embryo
33	chr6:119400462-119400512	HNPCEpiC	eye:	n/a
34	chr6:119399550-119399600	AG04450	lung:	fetal
35	chr6:119395189-119395239	SAEC	small airway:	n/a
36	chr6:119399320-119399370	T-47D	breast:	n/a
37	chr6:119400462-119400512	NHDF-neo	bronchial:	n/a
38	chr6:119402498-119402548	Caco-2	colon:	n/a
39	chr6:119390418-119390468	ECC-1	luminal epithelium:	n/a
40	chr6:119399320-119399370	GM19239	blood:	n/a
41	chr6:119401102-119401152	HEEpiC	esophagus:	n/a
42	chr6:119362849-119362899	Hela-S3	cervix:	n/a
43	chr6:119400380-119400430	SAEC	small airway:	n/a
44	chr6:119362940-119362990	PANC-1	pancreas:	n/a
45	chr6:119358124-119358174	AG10803	skin:	n/a
46	chr6:119346816-119346866	MCF10A-Er-Src	breast:	n/a
47	chr6:119346816-119346866	HUVEC	blood vessel:	n/a
48	chr6:119399550-119399600	NT2-D1	testis:	n/a
49	chr6:119400462-119400512	AG04449	skin:	fetal
50	chr6:119390418-119390468	HepG2	liver:	n/a

(count:77 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:119314602..119316807-chr6:119322501..119324038,2	K562	blood:
2	chr6:119254679..119257709-chr6:119345314..119348815,3	K562	blood:
3	chr6:119284118..119284702-chr6:119431708..119432445,2	MCF-7	breast:
4	chr6:119255727..119258203-chr6:119400226..119402388,2	K562	blood:
5	chr6:119381731..119385519-chr6:119386330..119388707,4	K562	blood:
6	chr6:119282607..119285041-chr6:119393256..119395593,2	K562	blood:
7	chr6:119289690..119290275-chr6:119431681..119432394,3	MCF-7	breast:
8	chr6:119398174..119401168-chr6:119668507..119671059,2	K562	blood:
9	chr6:119327639..119329995-chr6:119375600..119378343,2	K562	blood:
10	chr6:119366419..119369327-chr6:119386975..119389213,2	K562	blood:
11	chr6:119384404..119387073-chr6:119389709..119391211,2	K562	blood:
12	chr6:119214813..119215523-chr6:119431599..119432507,3	K562	blood:
13	chr6:119346161..119349573-chr6:119350909..119353024,3	K562	blood:
14	chr6:119398753..119400290-chr6:119419686..119422327,2	K562	blood:
15	chr6:119417250..119418843-chr6:119419120..119421662,2	K562	blood:
16	chr6:119340150..119341982-chr6:119399183..119401577,2	K562	blood:
17	chr6:119345576..119347207-chr6:119354495..119357299,2	K562	blood:
18	chr6:119422648..119424264-chr6:119429871..119432417,2	K562	blood:
19	chr6:119417250..119418843-chr6:119419120..119421662,2	K562	blood:
20	chr6:119340150..119341982-chr6:119399183..119401577,2	K562	blood:
21	chr6:119345576..119347207-chr6:119354495..119357299,2	K562	blood:
22	chr6:119418662..119420877-chr6:119421736..119424263,2	K562	blood:
23	chr6:119376891..119378894-chr6:119397399..119400605,3	K562	blood:
24	chr6:119383826..119386462-chr6:119386776..119389889,4	K562	blood:
25	chr6:119406648..119410008-chr6:119412778..119415979,5	K562	blood:
26	chr6:119348800..119350573-chr6:119357761..119359797,2	K562	blood:
27	chr6:119406648..119410008-chr6:119412778..119415979,5	K562	blood:
28	chr6:119344453..119347404-chr6:119349767..119351941,2	K562	blood:
29	chr6:119255593..119258017-chr6:119358336..119360410,2	K562	blood:
30	chr6:119318804..119321015-chr6:119323273..119326120,2	K562	blood:
31	chr6:119422648..119424264-chr6:119429871..119432417,2	K562	blood:
32	chr6:119344453..119347404-chr6:119349767..119351941,2	K562	blood:
33	chr6:119398081..119399812-chr6:119406583..119408212,2	K562	blood:
34	chr6:119253156..119256806-chr6:119394976..119399977,7	K562	blood:
35	chr6:119384109..119386949-chr6:119396336..119398560,2	K562	blood:
36	chr6:119363262..119365656-chr6:119366667..119368458,2	MCF-7	breast:
37	chr6:119346161..119349573-chr6:119350909..119353024,3	K562	blood:
38	chr6:119213805..119216904-chr6:119398441..119401842,5	K562	blood:
39	chr6:119253238..119258280-chr6:119398045..119402661,8	K562	blood:
40	chr6:119381731..119385519-chr6:119386330..119388707,4	K562	blood:
41	chr6:119383826..119386462-chr6:119386776..119389889,4	K562	blood:
42	chr6:119289303..119290241-chr6:119431643..119432582,8	K562	blood:
43	chr6:119418662..119420877-chr6:119421736..119424263,2	K562	blood:
44	chr6:119254512..119256806-chr6:119396471..119398017,2	K562	blood:
45	chr6:119284022..119285422-chr6:119431250..119432445,6	K562	blood:
46	chr6:119253532..119256038-chr6:119418154..119419905,2	K562	blood:
47	chr6:119330295..119333330-chr6:119397453..119401134,3	K562	blood:
48	chr6:119319940..119322469-chr6:119324553..119327875,4	K562	blood:
49	chr6:119357800..119360745-chr6:119397203..119399369,2	K562	blood:
50	chr6:119348800..119350573-chr6:119357761..119359797,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548b-5p	chr6:119390263-119390284	MIMAT0004798
hsa-miR-548b-3p	chr6:119390227-119390248	MIMAT0003254

No data

Variant related genes	Relation type
MIR548B	TF binding region
FAM184A	TF binding region
ENSG00000222649	TF binding region
MIR548B	CpG island
FAM184A	CpG island
ENSG00000222649	CpG island
ENSG00000253194	chromatin interactions
ENSG00000111877	chromatin interactions
ENSG00000111875	chromatin interactions
ENSG00000207982	chromatin interactions
ENSG00000111879	chromatin interactions
ENSG00000111885	chromatin interactions
ZBTB39	Mature miRNA region
NBEA	Mature miRNA region
ZBTB18	Mature miRNA region
SATB1	Mature miRNA region
SPRTN	Mature miRNA region
FAT2	Mature miRNA region
SNRNP200	Mature miRNA region
CD46	Mature miRNA region
CLCN3	Mature miRNA region
RER1	Mature miRNA region
INADL	Mature miRNA region
ZBTB21	Mature miRNA region
SLC25A44	Mature miRNA region
AREL1	Mature miRNA region
TET3	Mature miRNA region
AKAP11	Mature miRNA region
PRC1	Mature miRNA region
TMEM167A	Mature miRNA region
KCTD20	Mature miRNA region
TLE4	Mature miRNA region
COX7A2	Mature miRNA region
TST	Mature miRNA region
FRS2	Mature miRNA region

Extended variants
information (count: 3672 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:3672 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530651943	chr6:119320182-119320183	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550765741	chr6:119320187-119320188	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540789596	chr6:119320258-119320259	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570523731	chr6:119320274-119320275	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189386514	chr6:119320311-119320312	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs794266	chr6:119320313-119320314	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs140759983	chr6:119320323-119320324	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs369389794	chr6:119320324-119320325	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181792006	chr6:119320374-119320375	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552851562	chr6:119320443-119320444	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150094925	chr6:119320481-119320482	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575351718	chr6:119320484-119320485	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs544352684	chr6:119320542-119320543	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569486347	chr6:119320569-119320570	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs370152720	chr6:119320576-119320577	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs145451925	chr6:119320617-119320618	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs578081998	chr6:119320624-119320625	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs77213958	chr6:119320743-119320744	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs12529321	chr6:119320782-119320783	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs528119963	chr6:119320786-119320787	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs541831407	chr6:119320787-119320788	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561632500	chr6:119320803-119320804	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs794265	chr6:119320834-119320835	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs185100945	chr6:119320840-119320841	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs550355116	chr6:119320870-119320871	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs190631186	chr6:119320972-119320973	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs182821494	chr6:119320980-119320981	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs148913391	chr6:119320985-119320986	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566415024	chr6:119320989-119320990	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147008568	chr6:119320991-119320992	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555366357	chr6:119321059-119321060	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs374009222	chr6:119321108-119321109	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138159682	chr6:119321205-119321206	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538346171	chr6:119321211-119321212	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551129033	chr6:119321374-119321375	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs74608413	chr6:119321470-119321471	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs578157130	chr6:119321478-119321479	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34455711	chr6:119321479-119321480	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs10499090	chr6:119321551-119321552	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs574401575	chr6:119321639-119321640	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186531235	chr6:119321661-119321662	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143636734	chr6:119321671-119321672	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs145915082	chr6:119321694-119321695	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544332585	chr6:119321728-119321729	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564005700	chr6:119321735-119321736	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549044840	chr6:119321739-119321740	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs148331152	chr6:119321740-119321741	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141457792	chr6:119321782-119321783	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs150834552	chr6:119321890-119321891	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138142817	chr6:119321927-119321928	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1275 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119285800-119340000	Weak transcription	Fetal Brain Male	brain
2	chr6:119287200-119326600	Weak transcription	Fetal Brain Female	brain
3	chr6:119287400-119330000	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:119292400-119344000	Weak transcription	Brain Germinal Matrix	brain
5	chr6:119293200-119345400	Weak transcription	Lung	lung
6	chr6:119294200-119330800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr6:119300600-119344000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr6:119300800-119342600	Weak transcription	Brain Anterior Caudate	brain
9	chr6:119301000-119321800	Weak transcription	Placenta	Placenta
10	chr6:119313000-119329800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr6:119314400-119364400	Weak transcription	Fetal Muscle Trunk	muscle
12	chr6:119315200-119325200	Weak transcription	Pancreas	Pancrea
13	chr6:119315400-119320800	Weak transcription	HepG2	liver
14	chr6:119315400-119329800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr6:119315400-119330800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr6:119316600-119328800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:119318600-119321400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr6:119318600-119344200	Weak transcription	Fetal Lung	lung
19	chr6:119318800-119320400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr6:119319400-119321000	Enhancers	Fetal Intestine Small	intestine
21	chr6:119319400-119321200	Enhancers	Duodenum Mucosa	Duodenum
22	chr6:119319400-119330200	Weak transcription	Ovary	ovary
23	chr6:119319600-119320200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:119319600-119320200	Weak transcription	Brain Cingulate Gyrus	brain
25	chr6:119319600-119321800	Enhancers	Fetal Intestine Large	intestine
26	chr6:119319600-119333600	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr6:119319800-119342600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr6:119320000-119327000	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr6:119320200-119321800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:119320400-119329200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr6:119320800-119321200	Enhancers	HepG2	liver
32	chr6:119320800-119321400	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr6:119321000-119323000	Weak transcription	Fetal Intestine Small	intestine
34	chr6:119321400-119323000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:119321400-119325600	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr6:119321800-119322600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr6:119321800-119322600	Strong transcription	Placenta	Placenta
38	chr6:119321800-119329800	Weak transcription	Fetal Intestine Large	intestine
39	chr6:119322600-119323800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:119322600-119337800	Weak transcription	Placenta	Placenta
41	chr6:119323000-119324400	Enhancers	Fetal Intestine Small	intestine
42	chr6:119323000-119325800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
43	chr6:119323600-119327200	Weak transcription	Aorta	Aorta
44	chr6:119323800-119324400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:119324400-119331000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr6:119324400-119331000	Weak transcription	K562	blood
47	chr6:119324400-119333000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr6:119324800-119326600	Weak transcription	Adipose Nuclei	Adipose
49	chr6:119325200-119325400	Enhancers	Pancreas	Pancrea
50	chr6:119325200-119339800	Weak transcription	Primary T cells from cord blood	blood

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