Variant report

Variant	nsv5370
Chromosome Location	chr6:80715351-80751740
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:194)
CpG islands
(count:122)
Chromatin interactive
region (count:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:194 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr6:80739154-80739511	GM12878	blood:	n/a	n/a
2	BCLAF1	chr6:80739065-80739571	GM12878	blood:	n/a	n/a
3	CEBPB	chr6:80732540-80732829	IMR90	lung:	n/a	n/a
4	CEBPB	chr6:80748846-80749099	K562	blood:	n/a	chr6:80749021-80749032 chr6:80749019-80749032
5	CEBPB	chr6:80719286-80719553	IMR90	lung:	n/a	n/a
6	CTCF	chr6:80720120-80720270	SK-N-SH_RA	brain:	n/a	chr6:80720204-80720222
7	CTCF	chr6:80720140-80720290	HMEC	breast:	n/a	chr6:80720204-80720222
8	CTCF	chr6:80720155-80720268	HepG2	liver:	n/a	chr6:80720204-80720222
9	CTCF	chr6:80720120-80720270	GM12872	blood:	n/a	chr6:80720204-80720222
10	CTCF	chr6:80720120-80720270	HFF	foreskin:	n/a	chr6:80720204-80720222
11	CTCF	chr6:80720120-80720270	RPTEC	kidney:	n/a	chr6:80720204-80720222
12	CTCF	chr6:80720060-80720210	HRE	kidney:	n/a	n/a
13	CTCF	chr6:80720160-80720310	HepG2	liver:	n/a	chr6:80720204-80720222
14	CTCF	chr6:80720100-80720250	HEK293	kidney:	n/a	chr6:80720204-80720222
15	CTCF	chr6:80720193-80720253	GM12878	blood:	n/a	chr6:80720204-80720222
16	CTCF	chr6:80720100-80720250	HRPEpiC	eye:	n/a	chr6:80720204-80720222
17	CTCF	chr6:80720200-80720350	BE2_C	brain:	n/a	chr6:80720204-80720222
18	CTCF	chr6:80720140-80720290	GM12875	blood:	n/a	chr6:80720204-80720222
19	CTCF	chr6:80720037-80720386	GM12878	blood:	n/a	chr6:80720204-80720222
20	CTCF	chr6:80720122-80720381	MCF-7	breast:	n/a	chr6:80720204-80720222
21	CTCF	chr6:80720120-80720270	HPAF	blood vessel:	n/a	chr6:80720204-80720222
22	CTCF	chr6:80720160-80720310	HMEC	breast:	n/a	chr6:80720204-80720222
23	CTCF	chr6:80720180-80720330	BE2_C	brain:	n/a	chr6:80720204-80720222
24	CTCF	chr6:80720120-80720270	HBMEC	blood vessel:	n/a	chr6:80720204-80720222
25	CTCF	chr6:80720100-80720250	HCPEpiC	choroid plexus:	n/a	chr6:80720204-80720222
26	CTCF	chr6:80720120-80720270	WERI-Rb-1	eye:	n/a	chr6:80720204-80720222
27	CTCF	chr6:80720140-80720290	RPTEC	kidney:	n/a	chr6:80720204-80720222
28	CTCF	chr6:80720180-80720330	HepG2	liver:	n/a	chr6:80720204-80720222
29	CTCF	chr6:80720000-80720150	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr6:80720149-80720299	MCF-7	breast:	n/a	chr6:80720204-80720222
31	CTCF	chr6:80720121-80720307	MCF-7	breast:	n/a	chr6:80720204-80720222
32	CTCF	chr6:80720140-80720290	GM12878	blood:	n/a	chr6:80720204-80720222
33	CTCF	chr6:80720120-80720270	HMF	breast:	n/a	chr6:80720204-80720222
34	CTCF	chr6:80720200-80720350	HPF	lung:	n/a	chr6:80720204-80720222
35	CTCF	chr6:80720060-80720210	AG04450	lung:	n/a	n/a
36	CTCF	chr6:80720100-80720250	MCF-7	breast:	n/a	chr6:80720204-80720222
37	CTCF	chr6:80720040-80720190	HAc	cerebellar:	n/a	n/a
38	CTCF	chr6:80720160-80720310	HEEpiC	esophagus:	n/a	chr6:80720204-80720222
39	CTCF	chr6:80719960-80720110	GM12872	blood:	n/a	n/a
40	CTCF	chr6:80720120-80720270	A549	lung:	n/a	chr6:80720204-80720222
41	CTCF	chr6:80720136-80720238	K562	blood:	n/a	chr6:80720204-80720222
42	CTCF	chr6:80720120-80720270	NHDF-neo	bronchial:	n/a	chr6:80720204-80720222
43	CTCF	chr6:80720180-80720330	HFF-Myc	foreskin:	n/a	chr6:80720204-80720222
44	CTCF	chr6:80720160-80720310	Caco-2	colon:	n/a	chr6:80720204-80720222
45	CTCF	chr6:80720060-80720210	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr6:80720132-80720283	HepG2	liver:	n/a	chr6:80720204-80720222
47	CTCF	chr6:80720167-80720290	Hela-S3	cervix:	n/a	chr6:80720204-80720222
48	CTCF	chr6:80720120-80720270	HEEpiC	esophagus:	n/a	chr6:80720204-80720222
49	CTCF	chr6:80720080-80720230	HBMEC	blood vessel:	n/a	chr6:80720204-80720222
50	CUX1	chr6:80715963-80716042	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:80716898-80716948	HAEpiC	amniotic membrane:	n/a
2	chr6:80731107-80731157	HRCEpiC	kidney:	n/a
3	chr6:80716898-80716948	LNCaP	prostate:	n/a
4	chr6:80716898-80716948	A549	lung:	n/a
5	chr6:80731107-80731157	NT2-D1	testis:	n/a
6	chr6:80716898-80716948	H1-hESC	embryonic stem cell:	embryo
7	chr6:80716898-80716948	Hepatocyte	liver:	n/a
8	chr6:80731107-80731157	ProgFib	skin:	n/a
9	chr6:80731107-80731157	K562	blood:	n/a
10	chr6:80731107-80731157	SKMC	muscle:	n/a
11	chr6:80716898-80716948	Caco-2	colon:	n/a
12	chr6:80731107-80731157	HCF	heart:	n/a
13	chr6:80716898-80716948	GM12892	blood:	n/a
14	chr6:80731107-80731157	GM12891	blood:	n/a
15	chr6:80731107-80731157	PrEC	prostate:	n/a
16	chr6:80731107-80731157	AG04449	skin:	fetal
17	chr6:80716898-80716948	ECC-1	luminal epithelium:	n/a
18	chr6:80731107-80731157	LNCaP	prostate:	n/a
19	chr6:80731107-80731157	PFSK-1	brain:	n/a
20	chr6:80731107-80731157	Jurkat	blood:	n/a
21	chr6:80716898-80716948	HRPEpiC	eye:	n/a
22	chr6:80731107-80731157	GM12878	blood:	n/a
23	chr6:80716898-80716948	AG10803	skin:	n/a
24	chr6:80731107-80731157	HepG2	liver:	n/a
25	chr6:80731107-80731157	AG09319	gingival:	n/a
26	chr6:80731107-80731157	AoSMC	blood vessel:	n/a
27	chr6:80731107-80731157	SK-N-SH_RA	brain:	n/a
28	chr6:80731107-80731157	AG04450	lung:	fetal
29	chr6:80731107-80731157	H1-hESC	embryonic stem cell:	embryo
30	chr6:80716898-80716948	AG09309	skin:	n/a
31	chr6:80731107-80731157	SK-N-SH	brain:	n/a
32	chr6:80731107-80731157	HCT-116	colon:	n/a
33	chr6:80716898-80716948	HRE	kidney:	n/a
34	chr6:80716898-80716948	NB4	blood:	n/a
35	chr6:80716898-80716948	GM06990	blood:	n/a
36	chr6:80731107-80731157	NHBE	bronchial:	n/a
37	chr6:80731107-80731157	HRE	kidney:	n/a
38	chr6:80731107-80731157	GM12892	blood:	n/a
39	chr6:80716898-80716948	MCF10A-Er-Src	breast:	n/a
40	chr6:80716898-80716948	NT2-D1	testis:	n/a
41	chr6:80731107-80731157	NHDF-neo	bronchial:	n/a
42	chr6:80731107-80731157	MCF-7	breast:	n/a
43	chr6:80731107-80731157	MCF10A-Er-Src	breast:	n/a
44	chr6:80731107-80731157	HCM	heart:	n/a
45	chr6:80731107-80731157	BJ	skin:	n/a
46	chr6:80731107-80731157	HCPEpiC	choroid plexus:	n/a
47	chr6:80731107-80731157	BE2_C	brain:	n/a
48	chr6:80731107-80731157	HNPCEpiC	eye:	n/a
49	chr6:80716898-80716948	SAEC	small airway:	n/a
50	chr6:80716898-80716948	HCF	heart:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:80714432..80716349-chr6:80717842..80720279,2	MCF-7	breast:
2	chr6:80725547..80727630-chr6:80735210..80737325,2	K562	blood:
3	chr6:80725148..80727689-chr6:80727866..80729792,3	K562	blood:
4	chr6:80730895..80732973-chr6:80736170..80739701,4	K562	blood:
5	chr6:80649918..80652477-chr6:80718505..80720470,2	K562	blood:
6	chr6:80717535..80719093-chr6:80734932..80736458,2	K562	blood:
7	chr6:80726819..80729149-chr6:80732452..80734018,2	K562	blood:
8	chr6:80725547..80727630-chr6:80735210..80737325,2	K562	blood:
9	chr6:80729038..80731808-chr6:80734179..80735842,2	K562	blood:
10	chr6:80719003..80721359-chr6:80737643..80739358,2	K562	blood:
11	chr6:80731473..80734540-chr6:80736888..80739701,3	K562	blood:
12	chr6:80725148..80727689-chr6:80727866..80729792,3	K562	blood:
13	chr6:80729038..80731808-chr6:80734179..80735842,2	K562	blood:
14	chr6:80733040..80735460-chr6:80736846..80739439,3	K562	blood:
15	chr6:80722394..80725312-chr6:80736793..80739743,2	MCF-7	breast:
16	chr6:80731473..80734540-chr6:80736888..80739701,3	K562	blood:
17	chr6:80717535..80719093-chr6:80734932..80736458,2	K562	blood:
18	chr6:80712691..80715749-chr6:80750056..80753128,3	K562	blood:
19	chr6:80717752..80719460-chr6:80749306..80750878,2	K562	blood:
20	chr6:80720575..80723438-chr6:80727124..80728822,2	MCF-7	breast:
21	chr6:80717310..80719454-chr6:80764068..80766246,2	K562	blood:
22	chr6:80657745..80660049-chr6:80716512..80719051,2	MCF-7	breast:
23	chr6:80718444..80720486-chr6:80838754..80840605,2	K562	blood:
24	chr6:80730895..80732973-chr6:80736170..80739701,4	K562	blood:
25	chr6:80724231..80726532-chr6:80730064..80732881,2	K562	blood:
26	chr6:80743018..80745261-chr6:80747268..80749028,2	MCF-7	breast:
27	chr6:80713136..80715748-chr6:80737826..80739442,2	K562	blood:
28	chr6:80715006..80717903-chr6:80744998..80747221,3	K562	blood:
29	chr6:80745121..80747021-chr6:80747136..80749141,2	MCF-7	breast:
30	chr6:80742236..80743849-chr6:80785962..80787542,2	K562	blood:
31	chr6:80744876..80746467-chr6:80815463..80817793,2	K562	blood:
32	chr6:80726819..80729149-chr6:80732452..80734018,2	K562	blood:
33	chr6:80733040..80735460-chr6:80736846..80739439,3	K562	blood:
34	chr6:80719003..80721359-chr6:80737643..80739358,2	K562	blood:
35	chr6:80724231..80726532-chr6:80730064..80732881,2	K562	blood:
36	chr6:80717752..80719460-chr6:80749306..80750878,2	K562	blood:

No data

Variant related genes	Relation type
TTK	TF binding region
TTK	CpG island
ENSG00000112742	chromatin interactions
ENSG00000083123	chromatin interactions

Extended variants
information (count: 1434 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1434 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530655588	chr6:80715364-80715365	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs550711132	chr6:80715389-80715390	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs190885521	chr6:80715402-80715403	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs529660756	chr6:80715406-80715407	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs183311038	chr6:80715504-80715505	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs3757178	chr6:80715506-80715507	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs376651027	chr6:80715526-80715527	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs371037825	chr6:80715538-80715539	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs567093928	chr6:80715624-80715625	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs376037219	chr6:80715659-80715660	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368624175	chr6:80715696-80715697	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs377265033	chr6:80715732-80715733	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs539220898	chr6:80715750-80715751	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs240227	chr6:80715755-80715756	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568996341	chr6:80715756-80715757	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs537917681	chr6:80715759-80715760	Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs240226	chr6:80715838-80715839	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs377275832	chr6:80715865-80715866	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550408911	chr6:80715876-80715877	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188002721	chr6:80715897-80715898	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553226968	chr6:80715929-80715930	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373256552	chr6:80715959-80715960	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192145105	chr6:80715962-80715963	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs568656227	chr6:80715997-80715998	Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575530788	chr6:80716067-80716068	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs142821884	chr6:80716091-80716092	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs568837204	chr6:80716124-80716125	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs544278132	chr6:80716180-80716181	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs560975185	chr6:80716203-80716204	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs13195312	chr6:80716232-80716233	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs147427443	chr6:80716277-80716278	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs560818428	chr6:80716321-80716322	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs111819273	chr6:80716329-80716330	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs552470495	chr6:80716356-80716357	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs547370744	chr6:80716390-80716391	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs187817986	chr6:80716435-80716436	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs77602623	chr6:80716470-80716471	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs192958738	chr6:80716496-80716497	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs568505943	chr6:80716498-80716499	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs5877688	chr6:80716547-80716548	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs374964918	chr6:80716550-80716551	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs184172698	chr6:80716620-80716621	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs553911279	chr6:80716707-80716708	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs9448874	chr6:80716803-80716804	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs577182756	chr6:80716831-80716832	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs565862947	chr6:80716848-80716849	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs539517769	chr6:80716853-80716854	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs558894036	chr6:80716888-80716889	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs73747961	chr6:80716895-80716896	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs240225	chr6:80716936-80716937	Weak transcription Strong transcription Active TSS Enhancers Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:105)

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
Endometrioid adenocarcinoma	16974079	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Ductal carcinoma	22052326	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:80713200-80715400	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr6:80713200-80715400	Active TSS	NHDF-Ad	bronchial
3	chr6:80713200-80715600	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr6:80713400-80715400	Active TSS	Fetal Intestine Large	intestine
5	chr6:80713400-80715600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr6:80713400-80715800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:80713400-80715800	Active TSS	A549	lung
8	chr6:80713400-80717200	Active TSS	Thymus	Thymus
9	chr6:80713600-80715400	Active TSS	H9 Cell Line	embryonic stem cell
10	chr6:80713600-80715400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:80713600-80715400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:80713600-80715600	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr6:80713600-80715600	Active TSS	H1 Cell Line	embryonic stem cell
14	chr6:80713600-80715600	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr6:80713600-80715600	Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr6:80713600-80716000	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr6:80713600-80716000	Active TSS	NHLF	lung
18	chr6:80713800-80715800	Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr6:80713800-80716600	Active TSS	Fetal Thymus	thymus
20	chr6:80714000-80715600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr6:80714000-80715800	Active TSS	HMEC	breast
22	chr6:80714000-80716000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr6:80714000-80716000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr6:80714000-80716800	Active TSS	GM12878-XiMat	blood
25	chr6:80714600-80715400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:80714600-80715400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr6:80714600-80715400	Flanking Active TSS	Fetal Lung	lung
28	chr6:80714600-80715400	Flanking Active TSS	Fetal Stomach	stomach
29	chr6:80714600-80715600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr6:80714600-80715600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
31	chr6:80714600-80715600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:80714600-80715600	Flanking Active TSS	HUVEC	blood vessel
33	chr6:80714800-80715400	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:80714800-80715400	Flanking Active TSS	Fetal Heart	heart
35	chr6:80714800-80715400	Flanking Active TSS	Dnd41	blood
36	chr6:80714800-80715400	Flanking Active TSS	Osteobl	bone
37	chr6:80714800-80715600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
38	chr6:80714800-80715600	Flanking Active TSS	Hela-S3	cervix
39	chr6:80714800-80715600	Flanking Active TSS	HSMM	muscle
40	chr6:80714800-80738800	Weak transcription	Small Intestine	intestine
41	chr6:80715000-80715400	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:80715000-80715400	Active TSS	Brain Germinal Matrix	brain
43	chr6:80715000-80715400	Flanking Active TSS	Fetal Kidney	kidney
44	chr6:80715000-80715400	Active TSS	Fetal Muscle Leg	muscle
45	chr6:80715000-80715400	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr6:80715000-80715600	Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr6:80715000-80715600	Enhancers	Placenta Amnion	Placenta Amnion
48	chr6:80715000-80715600	Flanking Active TSS	HepG2	liver
49	chr6:80715000-80715600	Flanking Active TSS	NHEK	skin
50	chr6:80715000-80717400	Weak transcription	Primary monocytes fromperipheralblood	blood

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