Variant report

Variant	nsv830706
Chromosome Location	chr6:79825910-79994878
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1842)
CpG islands
(count:1282)
Chromatin interactive
region (count:71)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1842 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:79862059-79862259	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:79943174-79943762	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:79867574-79867985	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:79943282-79943482	K562	blood:	n/a	n/a
5	ATF1	chr6:79856225-79856366	K562	blood:	n/a	n/a
6	ATF1	chr6:79979486-79979888	K562	blood:	n/a	n/a
7	ATF1	chr6:79967096-79967382	K562	blood:	n/a	n/a
8	ATF1	chr6:79861920-79862372	K562	blood:	n/a	n/a
9	ATF2	chr6:79949227-79949937	GM12878	blood:	n/a	n/a
10	ATF2	chr6:79943230-79943820	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:79944153-79944741	GM12878	blood:	n/a	n/a
12	ATF2	chr6:79944032-79944773	GM12878	blood:	n/a	n/a
13	ATF2	chr6:79943457-79944066	GM12878	blood:	n/a	n/a
14	ATF2	chr6:79959732-79960373	GM12878	blood:	n/a	n/a
15	ATF2	chr6:79959689-79960296	GM12878	blood:	n/a	n/a
16	ATF2	chr6:79861793-79862593	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:79949452-79949911	GM12878	blood:	n/a	n/a
18	ATF2	chr6:79943088-79943904	GM12878	blood:	n/a	n/a
19	ATF2	chr6:79944046-79944619	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:79958394-79958469	K562	blood:	n/a	n/a
21	BACH1	chr6:79943855-79944753	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:79944456-79944610	K562	blood:	n/a	n/a
23	BATF	chr6:79959843-79960174	GM12878	blood:	n/a	n/a
24	BATF	chr6:79950322-79950573	GM12878	blood:	n/a	n/a
25	BATF	chr6:79950264-79950603	GM12878	blood:	n/a	n/a
26	BATF	chr6:79949414-79949898	GM12878	blood:	n/a	n/a
27	BATF	chr6:79949411-79949835	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:79949547-79949808	GM12878	blood:	n/a	chr6:79949665-79949674 chr6:79949650-79949659 chr6:79949664-79949673
29	BCL11A	chr6:79949438-79949883	GM12878	blood:	n/a	chr6:79949665-79949674 chr6:79949650-79949659 chr6:79949664-79949673
30	BCL11A	chr6:79928601-79928753	H1-hESC	embryonic stem cell:	n/a	n/a
31	BCL11A	chr6:79949149-79949471	GM12878	blood:	n/a	n/a
32	BCLAF1	chr6:79943409-79943909	GM12878	blood:	n/a	chr6:79943719-79943728
33	BCLAF1	chr6:79959706-79960264	GM12878	blood:	n/a	n/a
34	BCLAF1	chr6:79943930-79944752	GM12878	blood:	n/a	n/a
35	BCLAF1	chr6:79943356-79944665	GM12878	blood:	n/a	chr6:79943719-79943728
36	BHLHE40	chr6:79943289-79944584	K562	blood:	n/a	n/a
37	BHLHE40	chr6:79943948-79944593	HepG2	liver:	n/a	n/a
38	BHLHE40	chr6:79949201-79949986	GM12878	blood:	n/a	n/a
39	BHLHE40	chr6:79979437-79979922	K562	blood:	n/a	n/a
40	BHLHE40	chr6:79959749-79960272	GM12878	blood:	n/a	n/a
41	BHLHE40	chr6:79943332-79944686	GM12878	blood:	n/a	n/a
42	BRCA1	chr6:79944136-79944752	Hela-S3	cervix:	n/a	n/a
43	CBX3	chr6:79979454-79979856	K562	blood:	n/a	n/a
44	CBX3	chr6:79944264-79944592	K562	blood:	n/a	n/a
45	CBX3	chr6:79943207-79943905	K562	blood:	n/a	n/a
46	CBX3	chr6:79944169-79944755	K562	blood:	n/a	n/a
47	CBX3	chr6:79944243-79944820	HCT-116	colon:	n/a	n/a
48	CCNT2	chr6:79979561-79979907	K562	blood:	n/a	chr6:79979744-79979764
49	CCNT2	chr6:79944208-79944639	K562	blood:	n/a	n/a
50	CCNT2	chr6:79943405-79943909	K562	blood:	n/a	chr6:79943678-79943687

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:79898777-79898827	HUVEC	blood vessel:	n/a
2	chr6:79898777-79898827	HUVEC	blood vessel:	n/a
3	chr6:79944526-79944576	HCPEpiC	choroid plexus:	n/a
4	chr6:79881191-79881241	IMR90	lung:	fetal
5	chr6:79926242-79926292	HEK293	kidney:	embryo
6	chr6:79944547-79944597	Jurkat	blood:	n/a
7	chr6:79943342-79943392	NHDF-neo	bronchial:	n/a
8	chr6:79944186-79944236	U87	brain:	n/a
9	chr6:79926242-79926292	AoSMC	blood vessel:	n/a
10	chr6:79944414-79944464	SAEC	small airway:	n/a
11	chr6:79944526-79944576	SK-N-SH	brain:	n/a
12	chr6:79944542-79944592	T-47D	breast:	n/a
13	chr6:79944526-79944576	ECC-1	luminal epithelium:	n/a
14	chr6:79940953-79941003	IMR90	lung:	fetal
15	chr6:79940953-79941003	HRPEpiC	eye:	n/a
16	chr6:79862196-79862246	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:79943342-79943392	HIPEpiC	eye:	n/a
18	chr6:79943498-79943548	HNPCEpiC	eye:	n/a
19	chr6:79948298-79948348	HNPCEpiC	eye:	n/a
20	chr6:79881191-79881241	U87	brain:	n/a
21	chr6:79944830-79944880	SK-N-MC	brain:	n/a
22	chr6:79948298-79948348	NH-A	brain:	n/a
23	chr6:79944547-79944597	AoSMC	blood vessel:	n/a
24	chr6:79943796-79943846	SK-N-SH_RA	brain:	n/a
25	chr6:79943592-79943642	LNCaP	prostate:	n/a
26	chr6:79944526-79944576	BJ	skin:	n/a
27	chr6:79943796-79943846	AG09309	skin:	n/a
28	chr6:79943498-79943548	HAEpiC	amniotic membrane:	n/a
29	chr6:79944547-79944597	NH-A	brain:	n/a
30	chr6:79862196-79862246	T-47D	breast:	n/a
31	chr6:79944414-79944464	HMEC	breast:	n/a
32	chr6:79944399-79944449	HEK293	kidney:	embryo
33	chr6:79943592-79943642	Jurkat	blood:	n/a
34	chr6:79944547-79944597	ProgFib	skin:	n/a
35	chr6:79898777-79898827	AG04449	skin:	fetal
36	chr6:79881191-79881241	K562	blood:	n/a
37	chr6:79944526-79944576	Hela-S3	cervix:	n/a
38	chr6:79943796-79943846	NB4	blood:	n/a
39	chr6:79948298-79948348	MCF10A-Er-Src	breast:	n/a
40	chr6:79944399-79944449	PFSK-1	brain:	n/a
41	chr6:79911416-79911466	T-47D	breast:	n/a
42	chr6:79943796-79943846	AG10803	skin:	n/a
43	chr6:79943498-79943548	LNCaP	prostate:	n/a
44	chr6:79943592-79943642	AG10803	skin:	n/a
45	chr6:79944186-79944236	NHDF-neo	bronchial:	n/a
46	chr6:79926242-79926292	Jurkat	blood:	n/a
47	chr6:79898777-79898827	GM12891	blood:	n/a
48	chr6:79944414-79944464	HCF	heart:	n/a
49	chr6:79944186-79944236	HCT-116	colon:	n/a
50	chr6:79943498-79943548	HIPEpiC	eye:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:79953679..79955836-chr6:79957498..79959042,2	K562	blood:
2	chr6:79852069..79854687-chr6:79872579..79874335,2	K562	blood:
3	chr6:79973733..79976265-chr6:79977192..79978930,2	K562	blood:
4	chr6:79973733..79976265-chr6:79977192..79978930,2	K562	blood:
5	chr6:79922096..79924489-chr6:79928328..79930333,2	K562	blood:
6	chr6:79852069..79854687-chr6:79872579..79874335,2	K562	blood:
7	chr6:79901753..79904243-chr6:79911000..79912740,2	MCF-7	breast:
8	chr6:79953679..79955836-chr6:79957498..79959042,2	K562	blood:
9	chr6:79944377..79946215-chr6:79950972..79952889,2	K562	blood:
10	chr6:79910255..79912410-chr6:79943496..79945323,2	MCF-7	breast:
11	chr6:79861129..79863468-chr6:79865472..79868083,2	MCF-7	breast:
12	chr6:79782683..79789958-chr6:79939846..79945776,22	MCF-7	breast:
13	chr6:79755918..79758564-chr6:79949007..79951329,2	K562	blood:
14	chr6:79934991..79937963-chr6:79941108..79944156,4	K562	blood:
15	chr6:79927796..79930108-chr6:79949418..79951893,2	K562	blood:
16	chr6:79907861..79910027-chr6:79941828..79944247,2	K562	blood:
17	chr6:79786645..79789143-chr6:79938512..79942027,3	MCF-7	breast:
18	chr1:6844739..6845346-chr6:79943133..79943886,2	Hela-S3	cervix:
19	chr6:79934006..79937126-chr6:79938281..79940748,3	K562	blood:
20	chr6:79927796..79930108-chr6:79949418..79951893,2	K562	blood:
21	chr6:79813577..79816233-chr6:79868594..79870801,2	K562	blood:
22	chr6:79786884..79788713-chr6:79939941..79941491,2	K562	blood:
23	chr6:79938105..79940918-chr6:79942151..79944715,2	K562	blood:
24	chr6:79936163..79939514-chr6:79941809..79945122,5	MCF-7	breast:
25	chr6:79786930..79789086-chr6:79883415..79885349,2	MCF-7	breast:
26	chr6:79861129..79863468-chr6:79865472..79868083,2	MCF-7	breast:
27	chr6:79934006..79937126-chr6:79938281..79940748,3	K562	blood:
28	chr6:79917961..79920649-chr6:79922906..79925816,3	K562	blood:
29	chr6:79922512..79924677-chr6:79941315..79943922,2	MCF-7	breast:
30	chr6:79927857..79931747-chr6:79940094..79945264,7	K562	blood:
31	chr6:79943131..79946336-chr6:79950146..79952771,3	MCF-7	breast:
32	chr6:79815142..79817932-chr6:79824976..79828157,3	MCF-7	breast:
33	chr6:79786954..79788591-chr6:79935695..79937215,2	K562	blood:
34	chr6:79786929..79788709-chr6:79859954..79862909,2	MCF-7	breast:
35	chr6:79903183..79905835-chr6:79909088..79912448,3	K562	blood:
36	chr6:79910795..79911579-chr6:80175671..80176696,3	MCF-7	breast:
37	chr6:79786696..79788317-chr6:79910357..79912297,2	MCF-7	breast:
38	chr6:79786599..79788294-chr6:79949135..79951411,2	K562	blood:
39	chr6:79913005..79914594-chr6:79916746..79918687,2	K562	blood:
40	chr4:6695602..6696103-chr6:79949045..79949545,2	NB4	blood:
41	chr6:79903183..79905835-chr6:79909088..79912448,3	K562	blood:
42	chr6:79943689..79947670-chr6:79956197..79959605,3	K562	blood:
43	chr6:79950572..79952331-chr6:79953663..79956541,2	K562	blood:
44	chr6:79913005..79914594-chr6:79916746..79918687,2	K562	blood:
45	chr6:79786538..79788311-chr6:79866801..79868498,2	MCF-7	breast:
46	chr1:115300319..115300982-chr6:79943552..79944486,2	HCT-116	colon:
47	chr6:79922096..79924489-chr6:79928328..79930333,2	K562	blood:
48	chr6:79787878..79790499-chr6:79943656..79946271,3	K562	blood:
49	chr6:79786321..79788665-chr6:79827363..79828888,2	MCF-7	breast:
50	chr6:79813406..79815631-chr6:79824618..79827244,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IRAK1BP1-1	chr6:79944457-79946310	NONHSAT113680
2	lnc-IRAK1BP1-1	chr6:79943391-79943644	NONHSAT113679
3	lnc-IRAK1BP1-1	chr6:79943435-79943644	ENSG00000247783
4	lnc-IRAK1BP1-1	chr6:79943435-79943644	ENSG00000270362.1
5	lnc-IRAK1BP1-1	chr6:79943779-79946510	ENSG00000247783
6	lnc-HMGN3-3	chr6:79983892-79984689	NONHSAT113682
7	lnc-SH3BGRL2-3	chr6:79980095-79980310	XLOC_005359
8	lnc-HMGN3-1	chr6:79904123-79904440	NONHSAT113678
9	lnc-IRAK1BP1-1	chr6:79943779-79946517	NONHSAT113679
10	lnc-SH3BGRL2-3	chr6:79980626-79980669	XLOC_005359
11	lnc-IRAK1BP1-1	chr6:79943779-79946514	ENSG00000270362.1
12	lnc-HMGN3-2	chr6:79987822-79988144	NONHSAT113683

No data

Variant related genes	Relation type
ENSG00000220154	TF binding region
HMGN3	TF binding region
HMGN3-AS1	TF binding region
ENSG00000220154	CpG island
HMGN3	CpG island
HMGN3-AS1	CpG island
ENSG00000237436	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000118418	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000270362	chromatin interactions
ENSG00000183586	chromatin interactions
ENSG00000146247	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000163993	chromatin interactions
ZYG11B	miRNA target sites
ZSWIM6	miRNA target sites
ASCC3	miRNA target sites

Extended variants
information (count: 5435 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5435 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540719799	chr6:79825922-79825923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114024253	chr6:79825926-79825927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116604944	chr6:79826006-79826007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543628940	chr6:79826008-79826009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185212291	chr6:79826012-79826013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139688611	chr6:79826126-79826127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs9361491	chr6:79826148-79826149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs559781208	chr6:79826150-79826151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs528529085	chr6:79826174-79826175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs551882616	chr6:79826175-79826176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189678806	chr6:79826199-79826200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547680698	chr6:79826213-79826214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs9352696	chr6:79826230-79826231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs149359344	chr6:79826309-79826310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs73466246	chr6:79826334-79826335	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs527329738	chr6:79826482-79826483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144720044	chr6:79826483-79826484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183215801	chr6:79826517-79826518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565323342	chr6:79826523-79826524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75032319	chr6:79826563-79826564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186593457	chr6:79826577-79826578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373519627	chr6:79826625-79826626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551350373	chr6:79826668-79826669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs56998714	chr6:79826740-79826741	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs139589112	chr6:79826741-79826742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34096134	chr6:79826820-79826821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557227247	chr6:79826839-79826840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs574331958	chr6:79826855-79826856	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370651036	chr6:79826873-79826874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs560115838	chr6:79826903-79826904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114713334	chr6:79826921-79826922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs545386742	chr6:79826943-79826944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565287307	chr6:79826944-79826945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551448028	chr6:79826945-79826946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs191042438	chr6:79826956-79826957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375267742	chr6:79826980-79826981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138623312	chr6:79827009-79827010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs115884327	chr6:79827032-79827033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529088502	chr6:79827035-79827036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs183754485	chr6:79827066-79827067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534448865	chr6:79827082-79827083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs73466248	chr6:79827123-79827124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555409315	chr6:79827126-79827127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574061928	chr6:79827146-79827147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs13437410	chr6:79827148-79827149	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs557431365	chr6:79827169-79827170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144308566	chr6:79827171-79827172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs187443909	chr6:79827300-79827301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs114553263	chr6:79827309-79827310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183331516	chr6:79827314-79827315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

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
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1733 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:79825800-79826800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:79825800-79827000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr6:79825800-79827200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr6:79826800-79827000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr6:79827000-79827400	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr6:79827400-79827600	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr6:79827400-79827800	Enhancers	H1 Cell Line	embryonic stem cell
8	chr6:79827400-79827800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:79827600-79827800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr6:79827600-79827800	Enhancers	Psoas Muscle	Psoas
11	chr6:79827600-79828000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:79837200-79837400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr6:79837600-79837800	Enhancers	H9 Cell Line	embryonic stem cell
14	chr6:79837600-79838000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr6:79837800-79838200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr6:79838000-79838200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr6:79841400-79843000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:79843000-79844400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:79844400-79845200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr6:79844400-79845200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:79844400-79845200	Enhancers	HMEC	breast
22	chr6:79844600-79845000	Enhancers	NHEK	skin
23	chr6:79844600-79845200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
24	chr6:79844600-79845200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:79844600-79845600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:79845200-79845400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:79845400-79846200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:79846200-79856400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr6:79847200-79847600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:79852600-79853600	Enhancers	HepG2	liver
31	chr6:79852800-79853400	Enhancers	Liver	Liver
32	chr6:79853000-79853400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:79853000-79853400	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr6:79853000-79853400	Enhancers	Stomach Smooth Muscle	stomach
35	chr6:79853000-79853600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr6:79853200-79853400	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr6:79853400-79858600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr6:79853400-79859600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr6:79854800-79855000	Enhancers	Primary T cells from cord blood	blood
40	chr6:79855800-79856200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:79855800-79856200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr6:79856200-79858600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr6:79856200-79859400	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr6:79858400-79859000	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr6:79858600-79858800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr6:79858600-79858800	Enhancers	H1 Cell Line	embryonic stem cell
47	chr6:79858600-79858800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr6:79858600-79858800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr6:79858600-79862400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr6:79858800-79859200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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