Variant report

Variant	esv2830162
Chromosome Location	chr6:32450121-32556530
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:953)
CpG islands
(count:6900)
Chromatin interactive
region (count:58)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:32522777-32523015	HepG2	liver:	n/a	n/a
2	ATF2	chr6:32543602-32544865	GM12878	blood:	n/a	n/a
3	ATF2	chr6:32548141-32548546	GM12878	blood:	n/a	n/a
4	ATF2	chr6:32544973-32546270	GM12878	blood:	n/a	n/a
5	ATF2	chr6:32543611-32546362	GM12878	blood:	n/a	n/a
6	BATF	chr6:32498191-32498485	GM12878	blood:	n/a	n/a
7	BATF	chr6:32497788-32498190	GM12878	blood:	n/a	n/a
8	BATF	chr6:32537608-32537865	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:32497757-32498420	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:32543926-32544477	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:32545004-32545617	GM12878	blood:	n/a	n/a
12	BCL3	chr6:32545035-32545822	GM12878	blood:	n/a	n/a
13	BCL3	chr6:32543687-32544523	GM12878	blood:	n/a	n/a
14	BCL3	chr6:32544981-32545603	GM12878	blood:	n/a	n/a
15	BCL3	chr6:32543622-32544530	GM12878	blood:	n/a	n/a
16	BCL3	chr6:32542606-32543106	GM12878	blood:	n/a	n/a
17	BCLAF1	chr6:32548062-32548585	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:32548065-32548461	GM12878	blood:	n/a	n/a
19	BCLAF1	chr6:32543511-32546294	GM12878	blood:	n/a	n/a
20	BCLAF1	chr6:32553630-32554178	GM12878	blood:	n/a	n/a
21	BCLAF1	chr6:32543625-32544575	GM12878	blood:	n/a	n/a
22	BCLAF1	chr6:32497559-32498097	GM12878	blood:	n/a	n/a
23	BCLAF1	chr6:32497233-32498192	GM12878	blood:	n/a	n/a
24	BCLAF1	chr6:32555287-32555782	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:32549427-32549909	GM12878	blood:	n/a	chr6:32549640-32549649
26	BCLAF1	chr6:32544982-32546331	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:32555981-32557926	GM12878	blood:	n/a	n/a
28	BCLAF1	chr6:32554014-32554513	GM12878	blood:	n/a	n/a
29	BCLAF1	chr6:32542671-32543499	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:32517788-32517836	K562	blood:	n/a	n/a
31	BHLHE40	chr6:32498065-32498253	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:32493926-32494025	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:32551503-32551512	GM12878	blood:	n/a	n/a
34	CEBPB	chr6:32519351-32519645	HepG2	liver:	n/a	chr6:32519504-32519515
35	CEBPB	chr6:32519464-32519577	K562	blood:	n/a	chr6:32519504-32519515
36	CEBPB	chr6:32498060-32498200	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr6:32534489-32534689	HepG2	liver:	n/a	n/a
38	CEBPB	chr6:32504062-32504262	A549	lung:	n/a	n/a
39	CEBPB	chr6:32498063-32498112	K562	blood:	n/a	n/a
40	CHD1	chr6:32553697-32554853	GM12878	blood:	n/a	n/a
41	CHD1	chr6:32553084-32553137	GM12878	blood:	n/a	n/a
42	CHD1	chr6:32555302-32557664	GM12878	blood:	n/a	n/a
43	CHD1	chr6:32549622-32549754	GM12878	blood:	n/a	n/a
44	CHD1	chr6:32497360-32498091	GM12878	blood:	n/a	n/a
45	CHD2	chr6:32545419-32545704	GM12878	blood:	n/a	n/a
46	CHD2	chr6:32497862-32498076	GM12878	blood:	n/a	n/a
47	CREB1	chr6:32497839-32498347	GM12878	blood:	n/a	n/a
48	CTCF	chr6:32489506-32489582	MCF-7	breast:	n/a	n/a
49	CTCF	chr6:32526589-32526718	Lung_OC	lung:	n/a	n/a
50	CTCF	chr6:32525555-32525603	MCF-7	breast:	n/a	n/a

(count:6900 , 50 per page) page: 1 2 3 4 5 6 7 ... 138

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:32526669-32526719	SK-N-SH	brain:	n/a
2	chr6:32525813-32525863	RPTEC	kidney:	n/a
3	chr6:32551888-32551938	SK-N-SH	brain:	n/a
4	chr6:32549849-32549899	SK-N-SH_RA	brain:	n/a
5	chr6:32498677-32498727	HNPCEpiC	eye:	n/a
6	chr6:32515069-32515119	GM12892	blood:	n/a
7	chr6:32490444-32490494	SK-N-SH_RA	brain:	n/a
8	chr6:32526669-32526719	SK-N-SH	brain:	n/a
9	chr6:32525813-32525863	RPTEC	kidney:	n/a
10	chr6:32551888-32551938	SK-N-SH	brain:	n/a
11	chr6:32549849-32549899	SK-N-SH_RA	brain:	n/a
12	chr6:32498677-32498727	HNPCEpiC	eye:	n/a
13	chr6:32515069-32515119	GM12892	blood:	n/a
14	chr6:32490444-32490494	SK-N-SH_RA	brain:	n/a
15	chr6:32551954-32552004	CMK	blood:	n/a
16	chr6:32556093-32556143	GM12891	blood:	n/a
17	chr6:32499860-32499910	SK-N-MC	brain:	n/a
18	chr6:32526027-32526077	Caco-2	colon:	n/a
19	chr6:32499368-32499418	MCF10A-Er-Src	breast:	n/a
20	chr6:32486399-32486449	PANC-1	pancreas:	n/a
21	chr6:32489750-32489800	K562	blood:	n/a
22	chr6:32553920-32553970	CMK	blood:	n/a
23	chr6:32551891-32551941	HepG2	liver:	n/a
24	chr6:32549849-32549899	HCF	heart:	n/a
25	chr6:32515815-32515865	ECC-1	luminal epithelium:	n/a
26	chr6:32526260-32526310	Hela-S3	cervix:	n/a
27	chr6:32526021-32526071	AG04450	lung:	fetal
28	chr6:32496326-32496376	MCF10A-Er-Src	breast:	n/a
29	chr6:32489801-32489851	SK-N-SH	brain:	n/a
30	chr6:32523136-32523186	NH-A	brain:	n/a
31	chr6:32499860-32499910	HNPCEpiC	eye:	n/a
32	chr6:32525805-32525855	HEK293	kidney:	embryo
33	chr6:32546743-32546793	AoSMC	blood vessel:	n/a
34	chr6:32556093-32556143	HCT-116	colon:	n/a
35	chr6:32499860-32499910	SK-N-SH_RA	brain:	n/a
36	chr6:32466447-32466497	HUVEC	blood vessel:	n/a
37	chr6:32552106-32552156	IMR90	lung:	fetal
38	chr6:32485396-32485446	IMR90	lung:	fetal
39	chr6:32526702-32526752	GM12892	blood:	n/a
40	chr6:32452388-32452438	RPTEC	kidney:	n/a
41	chr6:32490421-32490471	Jurkat	blood:	n/a
42	chr6:32552246-32552296	K562	blood:	n/a
43	chr6:32554385-32554435	HUVEC	blood vessel:	n/a
44	chr6:32546743-32546793	SK-N-SH	brain:	n/a
45	chr6:32493917-32493967	U87	brain:	n/a
46	chr6:32556475-32556525	H1-hESC	embryonic stem cell:	embryo
47	chr6:32526021-32526071	HUVEC	blood vessel:	n/a
48	chr6:32490421-32490471	Hepatocyte	liver:	n/a
49	chr6:32546614-32546664	Hela-S3	cervix:	n/a
50	chr6:32549935-32549985	IMR90	lung:	fetal

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:32526932..32529683-chr6:32550345..32552618,2	MCF-7	breast:
2	chr6:32541380..32543244-chr6:32544659..32546648,2	MCF-7	breast:
3	chr6:32521669..32522700-chr6:32534356..32535262,5	MCF-7	breast:
4	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:
5	chr6:32542997..32546229-chr6:32547055..32549461,4	MCF-7	breast:
6	chr6:32521673..32522686-chr6:32534361..32535349,9	MCF-7	breast:
7	chr6:32521739..32522615-chr6:32530472..32531387,2	MCF-7	breast:
8	chr6:32541266..32542954-chr6:32547776..32551278,3	MCF-7	breast:
9	chr6:32446571..32447329-chr6:32534338..32534901,2	MCF-7	breast:
10	chr6:32536592..32539147-chr6:32551420..32553637,3	MCF-7	breast:
11	chr6:32516326..32519059-chr6:32543039..32547182,3	K562	blood:
12	chr6:32496441..32498666-chr6:32501268..32503290,2	MCF-7	breast:
13	chr6:32519836..32522790-chr6:32547584..32550109,2	MCF-7	breast:
14	chr6:32483984..32486232-chr6:32528948..32530708,2	MCF-7	breast:
15	chr6:32478863..32481240-chr6:32540968..32542884,2	K562	blood:
16	chr6:32543691..32546736-chr6:32549742..32552725,4	MCF-7	breast:
17	chr6:32521739..32522687-chr6:32530472..32531394,3	MCF-7	breast:
18	chr6:32526956..32529024-chr6:32939826..32941640,2	MCF-7	breast:
19	chr6:32521673..32522686-chr6:32534361..32535388,13	MCF-7	breast:
20	chr6:32521739..32522687-chr6:32530472..32531394,3	MCF-7	breast:
21	chr6:32537173..32539635-chr6:32541454..32544282,2	MCF-7	breast:
22	chr6:32526081..32528703-chr6:32550750..32554481,3	MCF-7	breast:
23	chr6:32521669..32522700-chr6:32534356..32535262,5	MCF-7	breast:
24	chr6:32536592..32539147-chr6:32551420..32553637,3	MCF-7	breast:
25	chr6:32548567..32551051-chr6:32674017..32675826,2	K562	blood:
26	chr6:32531056..32533444-chr6:32548227..32552178,3	MCF-7	breast:
27	chr6:32521673..32522686-chr6:32534361..32535388,13	MCF-7	breast:
28	chr6:32543931..32545888-chr6:32553009..32554780,2	MCF-7	breast:
29	chr6:32526115..32530219-chr6:32533457..32537358,4	MCF-7	breast:
30	chr6:32542997..32546229-chr6:32547055..32549461,4	MCF-7	breast:
31	chr6:32541380..32543244-chr6:32544659..32546648,2	MCF-7	breast:
32	chr6:32497873..32498399-chr6:32557101..32557832,2	HCT-116	colon:
33	chr6:32540752..32543456-chr6:32544418..32546730,2	MCF-7	breast:
34	chr6:32533882..32536611-chr6:32536867..32538539,2	MCF-7	breast:
35	chr6:32521739..32522615-chr6:32530472..32531387,2	MCF-7	breast:
36	chr6:32489338..32491320-chr6:32492335..32495194,2	MCF-7	breast:
37	chr6:32546755..32548791-chr6:32550343..32552231,2	MCF-7	breast:
38	chr6:32483984..32486232-chr6:32528948..32530708,2	MCF-7	breast:
39	chr6:32537173..32539635-chr6:32541454..32544282,2	MCF-7	breast:
40	chr6:32478863..32481240-chr6:32540968..32542884,2	K562	blood:
41	chr6:32533882..32536611-chr6:32536867..32538539,2	MCF-7	breast:
42	chr6:32540752..32543456-chr6:32544418..32546730,2	MCF-7	breast:
43	chr6:32428191..32430542-chr6:32458841..32460810,2	MCF-7	breast:
44	chr6:32531056..32533444-chr6:32548227..32552178,3	MCF-7	breast:
45	chr6:32547452..32553622-chr6:32554180..32560378,10	MCF-7	breast:
46	chr6:32525928..32528506-chr6:32628820..32630854,2	MCF-7	breast:
47	chr6:32519836..32522790-chr6:32547584..32550109,2	MCF-7	breast:
48	chr6:32521673..32522686-chr6:32534361..32535349,9	MCF-7	breast:
49	chr6:32543931..32545888-chr6:32553009..32554780,2	MCF-7	breast:
50	chr6:32546755..32548791-chr6:32550343..32552231,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HLA-DRA-5	chr6:32475256-32475512	NONHSAT108909
2	lnc-HLA-DQA1-7	chr6:32549461-32549608	NONHSAT108916
3	lnc-HLA-DQA1-7	chr6:32549438-32549606	NONHSAT108910
4	lnc-HLA-DQA1-7	chr6:32522471-32522593	NONHSAT108916
5	lnc-HLA-DQA1-7	chr6:32487174-32487196	NONHSAT108910
6	lnc-HLA-DRA-4	chr6:32474307-32474692	NONHSAT108908
7	lnc-HLA-DQA1-7	chr6:32522517-32522570	NONHSAT108910
8	lnc-HLA-DRB1-4	chr6:32546123-32546497	NONHSAT108917

No data

Variant related genes	Relation type
RNU1-61P	TF binding region
HLA-DRB6	TF binding region
HLA-DRB5	TF binding region
RNU1-61P	CpG island
HLA-DRB6	CpG island
HLA-DRB5	CpG island
ENSG00000235040	chromatin interactions
ENSG00000229391	chromatin interactions
ENSG00000263756	chromatin interactions
ENSG00000251916	chromatin interactions
ENSG00000196126	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000241287	chromatin interactions
ENSG00000198502	chromatin interactions

Extended variants
information (count: 10742 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:10742 , 50 per page) page: 1 2 3 4 5 6 7 ... 215

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144181804	chr6:32450121-32450122	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs202102492	chr6:32450127-32450128	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs67384805	chr6:32450128-32450129	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs5020945	chr6:32450134-32450135	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
5	rs5020944	chr6:32450140-32450141	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs111918110	chr6:32450149-32450150	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs569302716	chr6:32450151-32450152	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs2395196	chr6:32450154-32450155	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
9	rs112906696	chr6:32450174-32450175	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs113498629	chr6:32450189-32450190	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs77871181	chr6:32450193-32450194	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs113653545	chr6:32450203-32450204	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs534555076	chr6:32450211-32450212	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs552840808	chr6:32450230-32450231	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs9269212	chr6:32450249-32450250	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs9269213	chr6:32450250-32450251	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs373688012	chr6:32450257-32450258	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs551392838	chr6:32450271-32450272	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs9269214	chr6:32450272-32450273	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
20	rs556704361	chr6:32450273-32450274	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs575264978	chr6:32450276-32450277	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs377693490	chr6:32450278-32450279	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs576817083	chr6:32450286-32450287	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs9269216	chr6:32450291-32450292	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs115154852	chr6:32450297-32450298	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs113788503	chr6:32450304-32450305	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs9269217	chr6:32450308-32450309	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs9269218	chr6:32450314-32450315	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs9501641	chr6:32450319-32450320	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs9269219	chr6:32450333-32450334	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs9501642	chr6:32450343-32450344	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs200152662	chr6:32450354-32450355	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs3998189	chr6:32450357-32450358	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs9269222	chr6:32450378-32450379	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs536448285	chr6:32450379-32450380	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs386699381	chr6:32450385-32450386	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs73729300	chr6:32450391-32450392	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs115529904	chr6:32450404-32450405	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs369981736	chr6:32450405-32450406	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs184679616	chr6:32450445-32450446	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs34074553	chr6:32450452-32450453	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	mRNA abundance
42	rs373340133	chr6:32450453-32450454	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs112442055	chr6:32450461-32450462	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs113993648	chr6:32450462-32450463	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs571719935	chr6:32450465-32450466	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs9269223	chr6:32450475-32450476	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs9269224	chr6:32450478-32450479	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs9269225	chr6:32450489-32450490	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs9269226	chr6:32450497-32450498	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs9269227	chr6:32450515-32450516	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Lung cancer	18438408	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	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
Ovarian cancer	21781307	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	22522925	CNVD
Rheumatoid arthritis	22536334	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Oral cancer	21386901	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD

Chromatin state (count:691 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:32447200-32452000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:32449800-32450200	Enhancers	GM12878-XiMat	blood
3	chr6:32449800-32451000	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr6:32450000-32450200	Flanking Active TSS	Primary B cells from peripheral blood	blood
5	chr6:32450000-32450400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr6:32450000-32450600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr6:32450200-32450600	Active TSS	Primary B cells from peripheral blood	blood
8	chr6:32450600-32450800	Flanking Active TSS	Primary B cells from peripheral blood	blood
9	chr6:32450800-32451200	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:32451200-32452200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr6:32452000-32452200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr6:32452000-32452600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr6:32452000-32452600	Enhancers	Spleen	Spleen
14	chr6:32452200-32452600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr6:32452400-32452600	Enhancers	Primary B cells from peripheral blood	blood
16	chr6:32452400-32452600	Bivalent Enhancer	Esophagus	oesophagus
17	chr6:32452600-32452800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr6:32452600-32453000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr6:32453200-32453400	Enhancers	NHEK	skin
20	chr6:32453400-32453600	Enhancers	Esophagus	oesophagus
21	chr6:32455800-32456200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr6:32457400-32457600	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr6:32458200-32458400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr6:32468800-32469200	Enhancers	Brain Anterior Caudate	brain
25	chr6:32468800-32469200	Enhancers	Fetal Stomach	stomach
26	chr6:32468800-32469400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr6:32479600-32479800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:32479800-32486000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:32480600-32485200	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr6:32480600-32487200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:32483800-32486600	Weak transcription	Adipose Nuclei	Adipose
32	chr6:32484000-32496600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
33	chr6:32484200-32485600	Weak transcription	Primary B cells from peripheral blood	blood
34	chr6:32484200-32485800	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr6:32484400-32486800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr6:32484600-32486800	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr6:32485000-32486600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr6:32485200-32485800	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr6:32485400-32485800	Enhancers	Fetal Kidney	kidney
40	chr6:32485400-32489200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr6:32485400-32490600	Weak transcription	Primary B cells from cord blood	blood
42	chr6:32485400-32496600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:32485600-32486000	Strong transcription	Primary B cells from peripheral blood	blood
44	chr6:32485600-32486400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr6:32485600-32491200	Weak transcription	GM12878-XiMat	blood
46	chr6:32485800-32488600	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr6:32485800-32490800	Strong transcription	Monocytes-CD14+_RO01746	blood
48	chr6:32486000-32488200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr6:32486000-32489600	Genic enhancers	Primary B cells from peripheral blood	blood
50	chr6:32486400-32489400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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