Variant report

Variant	nsv600992
Chromosome Location	chr6:12961922-13218549
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1432)
CpG islands
(count:1100)
Chromatin interactive
region (count:86)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1432 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:13181636-13181953	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:13195207-13195429	K562	blood:	n/a	n/a
3	ARID3A	chr6:13006839-13007149	K562	blood:	n/a	n/a
4	ATF1	chr6:13006843-13007212	K562	blood:	n/a	n/a
5	ATF1	chr6:13044676-13044918	K562	blood:	n/a	n/a
6	ATF1	chr6:13203376-13203876	K562	blood:	n/a	n/a
7	ATF1	chr6:13066996-13067033	K562	blood:	n/a	n/a
8	ATF1	chr6:13201680-13201880	K562	blood:	n/a	n/a
9	ATF2	chr6:13043046-13043436	GM12878	blood:	n/a	n/a
10	ATF2	chr6:13042991-13043420	GM12878	blood:	n/a	n/a
11	ATF3	chr6:13044511-13044870	K562	blood:	n/a	n/a
12	ATF3	chr6:13044617-13044912	K562	blood:	n/a	n/a
13	ATF3	chr6:13006833-13007215	K562	blood:	n/a	n/a
14	BACH1	chr6:13143882-13143889	K562	blood:	n/a	n/a
15	BACH1	chr6:13048406-13048684	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:13048450-13048632	K562	blood:	n/a	n/a
17	BACH1	chr6:13169246-13169333	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:13013595-13014006	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:13176056-13176256	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:12993127-12993142	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:13014970-13015157	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:12969163-12969325	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr6:13216512-13216782	GM12878	blood:	n/a	chr6:13216650-13216661
24	BATF	chr6:13216573-13216770	GM12878	blood:	n/a	chr6:13216650-13216661
25	BATF	chr6:13043180-13043430	GM12878	blood:	n/a	chr6:13043301-13043312
26	BATF	chr6:13099054-13099361	GM12878	blood:	n/a	n/a
27	BATF	chr6:12963323-12963572	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:13214221-13214389	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:13216473-13216790	GM12878	blood:	n/a	n/a
30	BCL3	chr6:13212865-13213054	GM12878	blood:	n/a	n/a
31	BCL3	chr6:13212783-13213120	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:13007081-13007084	K562	blood:	n/a	n/a
33	BHLHE40	chr6:13201614-13201891	K562	blood:	n/a	n/a
34	BHLHE40	chr6:13099199-13099444	GM12878	blood:	n/a	n/a
35	BHLHE40	chr6:13125004-13125032	K562	blood:	n/a	n/a
36	BHLHE40	chr6:12963415-12963493	GM12878	blood:	n/a	n/a
37	BHLHE40	chr6:13200524-13200748	K562	blood:	n/a	n/a
38	BHLHE40	chr6:13195193-13195429	K562	blood:	n/a	n/a
39	CBX3	chr6:13044539-13045093	HCT-116	colon:	n/a	n/a
40	CBX3	chr6:13195102-13195482	K562	blood:	n/a	n/a
41	CBX3	chr6:13214220-13214473	K562	blood:	n/a	n/a
42	CCNT2	chr6:13006967-13007217	K562	blood:	n/a	n/a
43	CCNT2	chr6:13127259-13127272	K562	blood:	n/a	n/a
44	CEBPB	chr6:13181755-13181943	HepG2	liver:	n/a	n/a
45	CEBPB	chr6:13161203-13161324	K562	blood:	n/a	n/a
46	CEBPB	chr6:12985864-12985958	K562	blood:	n/a	n/a
47	CEBPB	chr6:13203413-13203688	K562	blood:	n/a	n/a
48	CEBPB	chr6:13151092-13151223	K562	blood:	n/a	chr6:13151125-13151142 chr6:13151128-13151139
49	CEBPB	chr6:13215739-13215920	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:13173926-13174021	Hela-S3	cervix:	n/a	chr6:13173996-13174007

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13015221-13015271	AG04449	skin:	fetal
2	chr6:13015202-13015252	BE2_C	brain:	n/a
3	chr6:13015221-13015271	AG04449	skin:	fetal
4	chr6:13015202-13015252	BE2_C	brain:	n/a
5	chr6:13014491-13014541	AG04450	lung:	fetal
6	chr6:13015221-13015271	BJ	skin:	n/a
7	chr6:13120250-13120300	ovcar-3	ovarian:	n/a
8	chr6:13175441-13175491	HEK293	kidney:	embryo
9	chr6:13015005-13015055	SK-N-SH	brain:	n/a
10	chr6:13014871-13014921	ECC-1	luminal epithelium:	n/a
11	chr6:13014491-13014541	GM06990	blood:	n/a
12	chr6:12993135-12993185	HRPEpiC	eye:	n/a
13	chr6:13173168-13173218	Hepatocyte	liver:	n/a
14	chr6:13012998-13013048	Hela-S3	cervix:	n/a
15	chr6:13120250-13120300	Hepatocyte	liver:	n/a
16	chr6:13012998-13013048	PFSK-1	brain:	n/a
17	chr6:13012998-13013048	HCPEpiC	choroid plexus:	n/a
18	chr6:13015005-13015055	PANC-1	pancreas:	n/a
19	chr6:13120250-13120300	HRE	kidney:	n/a
20	chr6:13192742-13192792	LNCaP	prostate:	n/a
21	chr6:13120250-13120300	HIPEpiC	eye:	n/a
22	chr6:13120250-13120300	SK-N-SH_RA	brain:	n/a
23	chr6:12993135-12993185	ECC-1	luminal epithelium:	n/a
24	chr6:13014871-13014921	AG04450	lung:	fetal
25	chr6:13015005-13015055	NH-A	brain:	n/a
26	chr6:13120250-13120300	ProgFib	skin:	n/a
27	chr6:13134251-13134301	Jurkat	blood:	n/a
28	chr6:12993135-12993185	HUVEC	blood vessel:	n/a
29	chr6:13114660-13114710	NHDF-neo	bronchial:	n/a
30	chr6:13015202-13015252	K562	blood:	n/a
31	chr6:13012998-13013048	MCF10A-Er-Src	breast:	n/a
32	chr6:13114660-13114710	ECC-1	luminal epithelium:	n/a
33	chr6:13173168-13173218	HNPCEpiC	eye:	n/a
34	chr6:13013668-13013718	Caco-2	colon:	n/a
35	chr6:13014491-13014541	PFSK-1	brain:	n/a
36	chr6:13120250-13120300	GM12878	blood:	n/a
37	chr6:13134251-13134301	Caco-2	colon:	n/a
38	chr6:13114660-13114710	AG04450	lung:	fetal
39	chr6:13120250-13120300	HL-60	blood:	n/a
40	chr6:13134251-13134301	BJ	skin:	n/a
41	chr6:13192742-13192792	GM12891	blood:	n/a
42	chr6:13013668-13013718	ECC-1	luminal epithelium:	n/a
43	chr6:13013668-13013718	ovcar-3	ovarian:	n/a
44	chr6:13015202-13015252	AG09309	skin:	n/a
45	chr6:12993135-12993185	GM12892	blood:	n/a
46	chr6:13015106-13015156	HAEpiC	amniotic membrane:	n/a
47	chr6:13014491-13014541	HRPEpiC	eye:	n/a
48	chr6:13015202-13015252	ProgFib	skin:	n/a
49	chr6:13192742-13192792	A549	lung:	n/a
50	chr6:13192742-13192792	NHDF-neo	bronchial:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:13195285..13198115-chr6:13330626..13333611,2	K562	blood:
2	chr6:13026402..13029153-chr6:13041803..13044257,2	MCF-7	breast:
3	chr6:13035263..13037290-chr6:13041357..13044303,2	K562	blood:
4	chr17:64637600..64638236-chr6:13191039..13191624,2	MCF-7	breast:
5	chr6:13026402..13029153-chr6:13041803..13044257,2	MCF-7	breast:
6	chr6:13125100..13126853-chr6:13276005..13277621,2	K562	blood:
7	chr6:13049101..13052016-chr6:13052702..13054545,2	K562	blood:
8	chr6:13184097..13187942-chr6:13192836..13196557,4	K562	blood:
9	chr6:13116335..13118765-chr6:13119336..13122276,2	K562	blood:
10	chr6:12966482..12969474-chr6:12970571..12972855,2	MCF-7	breast:
11	chr6:12958071..12959752-chr6:12963422..12965473,2	K562	blood:
12	chr6:13097814..13100290-chr6:13115939..13117682,2	MCF-7	breast:
13	chr6:13073241..13075964-chr6:13078893..13081612,2	MCF-7	breast:
14	chr6:12980989..12983402-chr6:13027140..13029769,2	K562	blood:
15	chr6:13073241..13075964-chr6:13078893..13081612,2	MCF-7	breast:
16	chr6:12967955..12970126-chr6:12970232..12972155,2	K562	blood:
17	chr6:13101650..13103683-chr6:13109601..13111424,2	K562	blood:
18	chr6:13194824..13195828-chr6:13331712..13332687,6	K562	blood:
19	chr6:13019900..13022140-chr6:13027831..13030315,2	K562	blood:
20	chr6:13119238..13122024-chr6:13125784..13127890,2	K562	blood:
21	chr1:149223392..149224629-chr6:13213822..13214862,3	NB4	blood:
22	chr6:13100476..13102062-chr6:13103818..13105846,2	MCF-7	breast:
23	chr6:13000472..13003227-chr6:13006605..13008195,2	K562	blood:
24	chr6:13011536..13013286-chr6:13013661..13016505,2	MCF-7	breast:
25	chr6:13112250..13113799-chr6:13117217..13119459,2	K562	blood:
26	chr6:13088282..13090116-chr6:13091669..13093301,2	MCF-7	breast:
27	chr6:12927202..12927897-chr6:13148834..13149408,2	MCF-7	breast:
28	chr6:13019900..13022140-chr6:13027831..13030315,2	K562	blood:
29	chr6:13064599..13066218-chr6:13067982..13070062,2	K562	blood:
30	chr6:13086347..13087990-chr6:13089766..13092479,2	K562	blood:
31	chr6:13094526..13096309-chr6:13098089..13099829,2	K562	blood:
32	chr6:13113966..13116018-chr6:13116145..13117861,2	K562	blood:
33	chr17:64636119..64638158-chr6:13191283..13192914,2	MCF-7	breast:
34	chr6:13119238..13122024-chr6:13125784..13127890,2	K562	blood:
35	chr6:13197054..13199735-chr6:13296855..13299373,2	K562	blood:
36	chr6:13163839..13166326-chr6:13167451..13169624,2	K562	blood:
37	chr6:13011536..13013286-chr6:13013661..13016505,2	MCF-7	breast:
38	chr6:13116335..13118765-chr6:13119336..13122276,2	K562	blood:
39	chr6:13086347..13087990-chr6:13089766..13092479,2	K562	blood:
40	chr6:13184861..13186722-chr6:13190898..13192711,2	MCF-7	breast:
41	chr6:13011649..13013861-chr6:13014295..13015902,2	K562	blood:
42	chr6:13215378..13217758-chr6:13218972..13222173,4	K562	blood:
43	chr6:13004185..13006578-chr6:13012805..13015375,2	K562	blood:
44	chr6:13101650..13103683-chr6:13109601..13111424,2	K562	blood:
45	chr6:12966482..12969474-chr6:12970571..12972855,2	MCF-7	breast:
46	chr6:13192594..13195219-chr6:13328276..13330019,2	MCF-7	breast:
47	chr6:13088282..13090116-chr6:13091669..13093301,2	MCF-7	breast:
48	chr6:12967955..12970126-chr6:12970232..12972155,2	K562	blood:
49	chr6:13094526..13096309-chr6:13098089..13099829,2	K562	blood:
50	chr6:13194848..13195736-chr6:13331759..13332713,3	MCF-7	breast:

No data

Variant related genes	Relation type
RNU1-11P	TF binding region
PHACTR1	TF binding region
RNU1-11P	CpG island
PHACTR1	CpG island
ENSG00000112137	chromatin interactions
ENSG00000149809	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000215022	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 9425 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:9425 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6899754	chr6:12961922-12961923	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs62386823	chr6:12961929-12961930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548511165	chr6:12961947-12961948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187068931	chr6:12962017-12962018	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs145570267	chr6:12962056-12962057	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs551297136	chr6:12962091-12962092	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs570716852	chr6:12962100-12962101	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs561252279	chr6:12962126-12962127	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs539848253	chr6:12962153-12962154	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs547091139	chr6:12962158-12962159	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs77733229	chr6:12962185-12962186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs535990711	chr6:12962186-12962187	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs62386824	chr6:12962203-12962204	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs372190049	chr6:12962204-12962205	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs536935038	chr6:12962252-12962253	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs557231469	chr6:12962287-12962288	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs116749383	chr6:12962305-12962306	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs72820843	chr6:12962306-12962307	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs552614511	chr6:12962314-12962315	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs572582651	chr6:12962315-12962316	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs375548756	chr6:12962335-12962336	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs368937149	chr6:12962349-12962350	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs147017378	chr6:12962361-12962362	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs61691468	chr6:12962364-12962365	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs562134449	chr6:12962365-12962366	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs138191001	chr6:12962370-12962371	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs192412979	chr6:12962436-12962437	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs9473113	chr6:12962438-12962439	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs533332364	chr6:12962497-12962498	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs369499743	chr6:12962503-12962504	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs143696205	chr6:12962509-12962510	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs74996450	chr6:12962510-12962511	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs529401583	chr6:12962523-12962524	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs373064625	chr6:12962550-12962551	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs76851263	chr6:12962615-12962616	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs11755825	chr6:12962690-12962691	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs112311411	chr6:12962691-12962692	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs561474283	chr6:12962740-12962741	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs556947578	chr6:12962755-12962756	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs576649335	chr6:12962756-12962757	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs570427342	chr6:12962782-12962783	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs371070801	chr6:12962793-12962794	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs539381064	chr6:12962857-12962858	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138246102	chr6:12962938-12962939	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs375380774	chr6:12962955-12962956	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs552546537	chr6:12962970-12962971	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs572546802	chr6:12962986-12962987	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs13211739	chr6:12962995-12962996	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs73364167	chr6:12963054-12963055	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs182148985	chr6:12963139-12963140	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
small cell lung cancer	20016488	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Acute myeloid leukemia	18000384	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Metastatic melanoma	18483359	CNVD
Breast cancer	21990379	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2879 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12958200-12962200	Weak transcription	Spleen	Spleen
2	chr6:12958200-12963000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:12958400-12962800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr6:12958600-12963200	Weak transcription	Primary B cells from cord blood	blood
5	chr6:12958800-12962400	Weak transcription	Pancreas	Pancrea
6	chr6:12958800-12962800	Weak transcription	NHEK	skin
7	chr6:12958800-12963200	Weak transcription	NHLF	lung
8	chr6:12959000-12962000	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr6:12959000-12962800	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr6:12959000-12962800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:12959000-12963000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:12959000-12963000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:12959000-12963000	Weak transcription	Fetal Stomach	stomach
14	chr6:12959000-12963000	Weak transcription	HSMMtube	muscle
15	chr6:12959000-12963000	Weak transcription	NH-A	brain
16	chr6:12959000-12963000	Weak transcription	NHDF-Ad	bronchial
17	chr6:12959200-12962000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr6:12959200-12962000	Weak transcription	Right Ventricle	heart
19	chr6:12959200-12962200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr6:12959200-12962200	Weak transcription	Right Atrium	heart
21	chr6:12959200-12962400	Weak transcription	HSMM	muscle
22	chr6:12959200-12963000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:12959200-12963400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:12959200-12964000	Enhancers	Brain Cingulate Gyrus	brain
25	chr6:12959200-12968000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr6:12959400-12962000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr6:12959400-12962000	Weak transcription	Lung	lung
28	chr6:12960000-12962200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr6:12960200-12962400	Weak transcription	Brain Hippocampus Middle	brain
30	chr6:12960200-12962400	Enhancers	Fetal Heart	heart
31	chr6:12960200-12962800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr6:12960400-12962400	Enhancers	Stomach Smooth Muscle	stomach
33	chr6:12960600-12963800	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr6:12960800-12962600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:12960800-12962600	Weak transcription	Colon Smooth Muscle	Colon
36	chr6:12960800-12962600	Enhancers	HUVEC	blood vessel
37	chr6:12961000-12962200	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr6:12961000-12963400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr6:12961000-12968400	Weak transcription	Brain Substantia Nigra	brain
40	chr6:12961400-12962000	Weak transcription	Aorta	Aorta
41	chr6:12961600-12962400	Weak transcription	Brain Anterior Caudate	brain
42	chr6:12961800-12962800	Enhancers	Brain Angular Gyrus	brain
43	chr6:12961800-12963400	Enhancers	Left Ventricle	heart
44	chr6:12962000-12962200	Flanking Active TSS	Aorta	Aorta
45	chr6:12962000-12962400	Enhancers	Lung	lung
46	chr6:12962000-12962800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr6:12962000-12963200	Enhancers	Right Ventricle	heart
48	chr6:12962000-12963400	Weak transcription	Brain Germinal Matrix	brain
49	chr6:12962000-12964000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr6:12962000-12964400	Enhancers	Primary hematopoietic stem cells	blood

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