Variant report

Variant	esv2763553
Chromosome Location	chr6:54687979-54820487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1080)
CpG islands
(count:978)
Chromatin interactive
region (count:117)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1080 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:54743522-54743837	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:54796068-54796208	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:54793969-54795493	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:54715351-54715429	K562	blood:	n/a	n/a
5	ATF2	chr6:54742355-54742958	GM12878	blood:	n/a	n/a
6	ATF2	chr6:54764715-54765220	GM12878	blood:	n/a	n/a
7	ATF2	chr6:54742405-54742922	GM12878	blood:	n/a	n/a
8	ATF3	chr6:54794083-54794667	HepG2	liver:	n/a	n/a
9	ATF3	chr6:54800434-54801109	HCT-116	colon:	n/a	n/a
10	ATF3	chr6:54800395-54801067	HCT-116	colon:	n/a	n/a
11	BACH1	chr6:54711553-54712128	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:54786835-54786854	K562	blood:	n/a	n/a
13	BACH1	chr6:54773944-54774030	K562	blood:	n/a	n/a
14	BACH1	chr6:54792525-54792579	K562	blood:	n/a	n/a
15	BACH1	chr6:54800547-54800647	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr6:54781957-54782011	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr6:54783895-54783943	K562	blood:	n/a	n/a
18	BACH1	chr6:54710981-54711290	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:54757586-54757972	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr6:54764773-54765121	GM12878	blood:	n/a	n/a
21	BATF	chr6:54764838-54765022	GM12878	blood:	n/a	n/a
22	BATF	chr6:54742424-54742840	GM12878	blood:	n/a	chr6:54742728-54742738
23	BATF	chr6:54742421-54742897	GM12878	blood:	n/a	chr6:54742728-54742738
24	BCL11A	chr6:54742424-54742777	GM12878	blood:	n/a	chr6:54742730-54742739
25	BCL3	chr6:54742496-54742859	GM12878	blood:	n/a	chr6:54742730-54742739
26	BHLHE40	chr6:54794100-54794691	HepG2	liver:	n/a	n/a
27	BRCA1	chr6:54711810-54713462	Hela-S3	cervix:	n/a	n/a
28	CBX3	chr6:54739431-54740001	HCT-116	colon:	n/a	n/a
29	CBX3	chr6:54800389-54800993	HCT-116	colon:	n/a	n/a
30	CBX3	chr6:54725523-54725993	HCT-116	colon:	n/a	n/a
31	CBX3	chr6:54781616-54782128	HCT-116	colon:	n/a	n/a
32	CBX3	chr6:54797509-54797899	HCT-116	colon:	n/a	n/a
33	CBX3	chr6:54797338-54797844	HCT-116	colon:	n/a	n/a
34	CBX3	chr6:54725485-54725931	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:54757533-54758107	HCT-116	colon:	n/a	n/a
36	CBX3	chr6:54745871-54746574	HCT-116	colon:	n/a	n/a
37	CBX3	chr6:54748603-54749552	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:54800308-54801123	HCT-116	colon:	n/a	n/a
39	CBX3	chr6:54781548-54782165	HCT-116	colon:	n/a	n/a
40	CEBPB	chr6:54800576-54800843	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr6:54712407-54713894	Hela-S3	cervix:	n/a	chr6:54712847-54712864
42	CEBPB	chr6:54743863-54744415	MCF-7	breast:	n/a	chr6:54744236-54744245 chr6:54744236-54744245 chr6:54744234-54744245 chr6:54744236-54744245 chr6:54744234-54744247
43	CEBPB	chr6:54800581-54800851	A549	lung:	n/a	n/a
44	CEBPB	chr6:54739181-54739931	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr6:54800509-54800915	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr6:54736432-54736599	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr6:54715031-54715166	A549	lung:	n/a	n/a
48	CEBPB	chr6:54800516-54800896	A549	lung:	n/a	n/a
49	CEBPB	chr6:54744123-54744532	K562	blood:	n/a	chr6:54744236-54744245 chr6:54744236-54744245 chr6:54744234-54744245 chr6:54744236-54744245 chr6:54744234-54744247
50	CEBPB	chr6:54800532-54800903	ECC-1	luminal epithelium:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:54711471-54711521	SKMC	muscle:	n/a
2	chr6:54763001-54763051	K562	blood:	n/a
3	chr6:54711471-54711521	SKMC	muscle:	n/a
4	chr6:54763001-54763051	K562	blood:	n/a
5	chr6:54763001-54763051	NT2-D1	testis:	n/a
6	chr6:54711378-54711428	AG09319	gingival:	n/a
7	chr6:54711378-54711428	A549	lung:	n/a
8	chr6:54711417-54711467	NT2-D1	testis:	n/a
9	chr6:54710399-54710449	GM12891	blood:	n/a
10	chr6:54763001-54763051	SK-N-MC	brain:	n/a
11	chr6:54711417-54711467	NHDF-neo	bronchial:	n/a
12	chr6:54711276-54711326	AG09309	skin:	n/a
13	chr6:54710399-54710449	AG10803	skin:	n/a
14	chr6:54711388-54711438	HCPEpiC	choroid plexus:	n/a
15	chr6:54775185-54775235	HUVEC	blood vessel:	n/a
16	chr6:54711471-54711521	NB4	blood:	n/a
17	chr6:54711429-54711479	Caco-2	colon:	n/a
18	chr6:54711838-54711888	RPTEC	kidney:	n/a
19	chr6:54711429-54711479	HCF	heart:	n/a
20	chr6:54711378-54711428	K562	blood:	n/a
21	chr6:54711471-54711521	Jurkat	blood:	n/a
22	chr6:54722227-54722277	HUVEC	blood vessel:	n/a
23	chr6:54713309-54713359	HRE	kidney:	n/a
24	chr6:54711417-54711467	HRE	kidney:	n/a
25	chr6:54711388-54711438	AG04450	lung:	fetal
26	chr6:54711388-54711438	NHBE	bronchial:	n/a
27	chr6:54711429-54711479	HL-60	blood:	n/a
28	chr6:54725458-54725508	NB4	blood:	n/a
29	chr6:54711276-54711326	HIPEpiC	eye:	n/a
30	chr6:54711227-54711277	NB4	blood:	n/a
31	chr6:54722227-54722277	BJ	skin:	n/a
32	chr6:54711227-54711277	Caco-2	colon:	n/a
33	chr6:54711227-54711277	HCPEpiC	choroid plexus:	n/a
34	chr6:54722227-54722277	HMEC	breast:	n/a
35	chr6:54763001-54763051	HMEC	breast:	n/a
36	chr6:54711838-54711888	GM12891	blood:	n/a
37	chr6:54763001-54763051	GM06990	blood:	n/a
38	chr6:54711471-54711521	ProgFib	skin:	n/a
39	chr6:54725458-54725508	PrEC	prostate:	n/a
40	chr6:54711276-54711326	PFSK-1	brain:	n/a
41	chr6:54711429-54711479	Hepatocyte	liver:	n/a
42	chr6:54763001-54763051	PFSK-1	brain:	n/a
43	chr6:54722227-54722277	H1-hESC	embryonic stem cell:	embryo
44	chr6:54711429-54711479	HNPCEpiC	eye:	n/a
45	chr6:54775185-54775235	RPTEC	kidney:	n/a
46	chr6:54711476-54711526	RPTEC	kidney:	n/a
47	chr6:54711227-54711277	ProgFib	skin:	n/a
48	chr6:54711378-54711428	ECC-1	luminal epithelium:	n/a
49	chr6:54710399-54710449	AG09319	gingival:	n/a
50	chr6:54713309-54713359	RPTEC	kidney:	n/a

(count:117 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:54711527..54714203-chr6:54793086..54795700,2	MCF-7	breast:
2	chr6:54810051..54812419-chr6:54813190..54815495,2	MCF-7	breast:
3	chr6:54783940..54786131-chr6:54788426..54790892,2	MCF-7	breast:
4	chr6:54793235..54795806-chr6:54798273..54802120,4	MCF-7	breast:
5	chr6:54765548..54767184-chr6:54768955..54771943,2	MCF-7	breast:
6	chr6:54688351..54691007-chr6:54693141..54697889,4	MCF-7	breast:
7	chr6:54582003..54585202-chr6:54737626..54739872,3	MCF-7	breast:
8	chr6:54666819..54668967-chr6:54700012..54702691,2	MCF-7	breast:
9	chr6:54711853..54714484-chr8:48522444..48524308,2	MCF-7	breast:
10	chr6:54577953..54579734-chr6:54746271..54747974,2	MCF-7	breast:
11	chr6:54709728..54711702-chr6:54712389..54714158,2	K562	blood:
12	chr6:54699132..54700691-chr6:54704780..54706904,2	MCF-7	breast:
13	chr6:54768464..54771380-chr6:54772937..54774749,2	MCF-7	breast:
14	chr6:54788156..54789737-chr6:54792237..54794375,2	K562	blood:
15	chr6:54587916..54591176-chr6:54736715..54740306,4	MCF-7	breast:
16	chr6:54721521..54725055-chr6:54731692..54735464,4	MCF-7	breast:
17	chr6:54596752..54599206-chr6:54723703..54726514,2	MCF-7	breast:
18	chr6:54722087..54723804-chr6:54738855..54741615,2	MCF-7	breast:
19	chr6:54789461..54791108-chr6:54797681..54800253,2	MCF-7	breast:
20	chr6:54560857..54562671-chr6:54739251..54742148,2	MCF-7	breast:
21	chr6:54582146..54584053-chr6:54741073..54743084,2	MCF-7	breast:
22	chr6:54562300..54564099-chr6:54779694..54781853,2	MCF-7	breast:
23	chr6:54582865..54585119-chr6:54718425..54721186,2	MCF-7	breast:
24	chr6:54713425..54714965-chr6:54753003..54756000,2	MCF-7	breast:
25	chr6:54736804..54741584-chr6:54742863..54746409,5	MCF-7	breast:
26	chr6:54585158..54588149-chr6:54741239..54743201,2	MCF-7	breast:
27	chr6:54718981..54722041-chr6:54724023..54729682,8	MCF-7	breast:
28	chr6:54768464..54771380-chr6:54772937..54774749,2	MCF-7	breast:
29	chr6:54585487..54587893-chr6:54738565..54741108,3	MCF-7	breast:
30	chr6:54556132..54558033-chr6:54708676..54711461,2	MCF-7	breast:
31	chr6:54583465..54585924-chr6:54724133..54726618,2	MCF-7	breast:
32	chr6:54709202..54711186-chr6:54779955..54782595,2	MCF-7	breast:
33	chr6:54682109..54683920-chr6:54686335..54689206,2	MCF-7	breast:
34	chr6:54763489..54765995-chr6:54799336..54801622,2	MCF-7	breast:
35	chr6:54695865..54698667-chr6:54699652..54702495,2	MCF-7	breast:
36	chr6:54659157..54661825-chr6:54711858..54713372,2	MCF-7	breast:
37	chr6:54564170..54566593-chr6:54739128..54740974,2	MCF-7	breast:
38	chr6:54758702..54760512-chr6:54764567..54767361,2	MCF-7	breast:
39	chr6:54594451..54596147-chr6:54739921..54742591,2	MCF-7	breast:
40	chr6:54790477..54792574-chr6:54798805..54800751,2	MCF-7	breast:
41	chr6:54696307..54700316-chr6:54709756..54713142,5	MCF-7	breast:
42	chr6:54736804..54741584-chr6:54742863..54746409,5	MCF-7	breast:
43	chr6:54704497..54716767-chr6:54728797..54750947,71	MCF-7	breast:
44	chr6:54692819..54694720-chr6:54713504..54715357,2	MCF-7	breast:
45	chr6:54787385..54788945-chr6:54793642..54795973,2	MCF-7	breast:
46	chr15:31283483..31284320-chr6:54711525..54712159,2	Hela-S3	cervix:
47	chr6:54582065..54584949-chr6:54722187..54724387,3	MCF-7	breast:
48	chr6:54561752..54563922-chr6:54714449..54716896,3	MCF-7	breast:
49	chr6:54740124..54741737-chr6:55103503..55105754,2	MCF-7	breast:
50	chr6:54751952..54753804-chr6:54753869..54755428,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMGCLL1-1	chr6:54705439-54705653	XLOC_005749
2	lnc-HMGCLL1-2	chr6:54813398-54813612	NONHSAT113230
3	lnc-HMGCLL1-1	chr6:54704916-54705286	XLOC_005749
4	lnc-HMGCLL1-2	chr6:54812875-54813245	NONHSAT113230
5	lnc-FAM83B-1	chr6:54807965-54809897	ENSG00000261116.1

No data

Variant related genes	Relation type
FAM83B	TF binding region
ENSG00000224984	TF binding region
ENSG00000261116	TF binding region
FAM83B	CpG island
ENSG00000224984	CpG island
ENSG00000261116	CpG island
ENSG00000007944	chromatin interactions
ENSG00000138246	chromatin interactions
ENSG00000166912	chromatin interactions
ENSG00000131876	chromatin interactions
ENSG00000261116	chromatin interactions
ENSG00000168143	chromatin interactions
ENSG00000220635	chromatin interactions
ENSG00000033170	chromatin interactions
ENSG00000166888	chromatin interactions
ENSG00000197837	chromatin interactions
ENSG00000224984	chromatin interactions

Extended variants
information (count: 4755 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:4755 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9475023	chr6:54687979-54687980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542155638	chr6:54687995-54687996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562408606	chr6:54688059-54688060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189088887	chr6:54688069-54688070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs193226472	chr6:54688097-54688098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185616464	chr6:54688104-54688105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142095848	chr6:54688130-54688131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6922162	chr6:54688131-54688132	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs150724198	chr6:54688138-54688139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs13192463	chr6:54688177-54688178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138611255	chr6:54688200-54688201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs60621605	chr6:54688202-54688203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189369016	chr6:54688225-54688226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6901946	chr6:54688247-54688248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs565674315	chr6:54688260-54688261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6901963	chr6:54688269-54688270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs557344767	chr6:54688270-54688271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564895045	chr6:54688299-54688300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs201613487	chr6:54688300-54688301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs146529848	chr6:54688347-54688348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557062148	chr6:54688351-54688352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs6922543	chr6:54688358-54688359	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs377762893	chr6:54688368-54688369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181054788	chr6:54688375-54688376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547473553	chr6:54688452-54688453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567084770	chr6:54688459-54688460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs183947594	chr6:54688481-54688482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188383208	chr6:54688503-54688504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536029755	chr6:54688504-54688505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181205554	chr6:54688542-54688543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185748402	chr6:54688604-54688605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543549604	chr6:54688625-54688626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191635810	chr6:54688669-54688670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182309737	chr6:54688676-54688677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs187331391	chr6:54688705-54688706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191027356	chr6:54688744-54688745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs535488870	chr6:54688750-54688751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182463646	chr6:54688753-54688754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550912714	chr6:54688754-54688755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200961493	chr6:54688767-54688768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569482132	chr6:54688768-54688769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373776857	chr6:54688769-54688770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs571150565	chr6:54688771-54688772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs79664176	chr6:54688772-54688773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201250511	chr6:54688773-54688774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs12210433	chr6:54688853-54688854	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186830423	chr6:54688866-54688867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567381392	chr6:54688885-54688886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536029522	chr6:54688891-54688892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541182683	chr6:54688896-54688897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	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
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	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
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Neurocytoma	17123091	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Neuroblastoma	19686582	CNVD
Neuroblastoma	17289879	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	16912164	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	20164919	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:980 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54683400-54689600	Weak transcription	Pancreas	Pancrea
2	chr6:54689000-54689400	Enhancers	Esophagus	oesophagus
3	chr6:54689000-54689800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:54689600-54689800	Enhancers	Pancreas	Pancrea
5	chr6:54691000-54692600	Enhancers	Fetal Heart	heart
6	chr6:54699800-54700400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr6:54699800-54700400	Enhancers	HMEC	breast
8	chr6:54700400-54701600	Weak transcription	HMEC	breast
9	chr6:54705000-54707200	Weak transcription	HMEC	breast
10	chr6:54706600-54706800	Enhancers	Duodenum Mucosa	Duodenum
11	chr6:54706800-54707400	Enhancers	NHEK	skin
12	chr6:54707000-54707200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr6:54707000-54707400	Enhancers	Placenta	Placenta
14	chr6:54707000-54707800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr6:54707200-54707400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr6:54707200-54707400	Enhancers	HMEC	breast
17	chr6:54707200-54710800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:54707400-54709200	Weak transcription	HMEC	breast
19	chr6:54707400-54710200	Weak transcription	NHEK	skin
20	chr6:54707400-54710800	Weak transcription	Placenta	Placenta
21	chr6:54707800-54709000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr6:54708600-54708800	Enhancers	Duodenum Mucosa	Duodenum
23	chr6:54708600-54709000	Enhancers	Breast Myoepithelial Primary Cells	Breast
24	chr6:54708800-54709000	Flanking Active TSS	Duodenum Mucosa	Duodenum
25	chr6:54709000-54709200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:54709000-54709400	Enhancers	Fetal Intestine Small	intestine
27	chr6:54709000-54710000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr6:54709000-54710400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr6:54709000-54713400	Active TSS	Rectal Mucosa Donor 29	rectum
30	chr6:54709000-54714200	Active TSS	Duodenum Mucosa	Duodenum
31	chr6:54709200-54709800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr6:54709200-54710200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr6:54709200-54710200	Enhancers	HMEC	breast
34	chr6:54709400-54709800	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr6:54709400-54710800	Weak transcription	Fetal Intestine Small	intestine
36	chr6:54709600-54709800	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr6:54709800-54710400	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr6:54709800-54713400	Active TSS	Rectal Mucosa Donor 31	rectum
39	chr6:54710000-54710400	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
40	chr6:54710000-54710600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr6:54710200-54710400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:54710200-54710400	Enhancers	NHEK	skin
43	chr6:54710200-54710800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr6:54710200-54711200	Flanking Active TSS	HMEC	breast
45	chr6:54710200-54711600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:54710400-54710600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr6:54710400-54710600	Enhancers	Stomach Mucosa	stomach
48	chr6:54710400-54710800	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr6:54710400-54710800	Enhancers	Placenta Amnion	Placenta Amnion
50	chr6:54710400-54710800	Enhancers	Hela-S3	cervix

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