Variant report

Variant	nsv603763
Chromosome Location	chr6:75923605-76009426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2515)
CpG islands
(count:2137)
Chromatin interactive
region (count:150)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:2515 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:75930150-75930410	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:75994224-75995352	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:75976467-75976799	K562	blood:	n/a	n/a
4	ARID3A	chr6:75940210-75940490	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:75953300-75953850	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:75953154-75954148	K562	blood:	n/a	n/a
7	ARID3A	chr6:76006923-76007258	HepG2	liver:	n/a	chr6:76006971-76006987
8	ARID3A	chr6:75934106-75934434	HepG2	liver:	n/a	n/a
9	ATF1	chr6:75994470-75995206	K562	blood:	n/a	n/a
10	ATF1	chr6:75926896-75927190	K562	blood:	n/a	n/a
11	ATF1	chr6:75953113-75953797	K562	blood:	n/a	n/a
12	ATF2	chr6:75994307-75995618	GM12878	blood:	n/a	n/a
13	ATF2	chr6:75953222-75953822	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr6:75952767-75953962	GM12878	blood:	n/a	n/a
15	ATF2	chr6:75994260-75995501	GM12878	blood:	n/a	n/a
16	ATF2	chr6:75952828-75954042	GM12878	blood:	n/a	n/a
17	ATF2	chr6:75953126-75953917	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr6:75953227-75953811	A549	lung:	n/a	n/a
19	ATF3	chr6:75953245-75953755	A549	lung:	n/a	n/a
20	ATF3	chr6:75953304-75953796	K562	blood:	n/a	n/a
21	BACH1	chr6:75993397-75993848	K562	blood:	n/a	n/a
22	BACH1	chr6:75983709-75983780	K562	blood:	n/a	n/a
23	BACH1	chr6:75977860-75978616	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:75994960-75995137	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:75993810-75994247	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr6:75952918-75953345	GM12878	blood:	n/a	n/a
27	BATF	chr6:75994338-75994903	GM12878	blood:	n/a	n/a
28	BATF	chr6:75952863-75953819	GM12878	blood:	n/a	n/a
29	BCL11A	chr6:75977824-75978126	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr6:75952905-75953736	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:75952940-75953299	GM12878	blood:	n/a	n/a
32	BCL11A	chr6:75994419-75994930	GM12878	blood:	n/a	n/a
33	BCL3	chr6:75953243-75953990	A549	lung:	n/a	n/a
34	BCL3	chr6:75984792-75985379	A549	lung:	n/a	n/a
35	BCL3	chr6:75953024-75954258	A549	lung:	n/a	n/a
36	BCL3	chr6:75994445-75994982	A549	lung:	n/a	n/a
37	BCL3	chr6:75955997-75956763	A549	lung:	n/a	n/a
38	BCLAF1	chr6:75952782-75953876	GM12878	blood:	n/a	n/a
39	BCLAF1	chr6:75952850-75953907	GM12878	blood:	n/a	n/a
40	BCLAF1	chr6:75994225-75995381	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:75994298-75995124	GM12878	blood:	n/a	n/a
42	BCLAF1	chr6:75994293-75994927	K562	blood:	n/a	n/a
43	BCLAF1	chr6:75994359-75994916	K562	blood:	n/a	n/a
44	BHLHE40	chr6:75942333-75942370	GM12878	blood:	n/a	n/a
45	BHLHE40	chr6:75952926-75954074	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:75953017-75954063	K562	blood:	n/a	n/a
47	BHLHE40	chr6:75993846-75995819	K562	blood:	n/a	chr6:75995133-75995154
48	BHLHE40	chr6:75994237-75995170	HepG2	liver:	n/a	chr6:75995133-75995154
49	BHLHE40	chr6:75953253-75953975	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:75953431-75953849	A549	lung:	n/a	n/a

(count:2137 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:75953648-75953698	LNCaP	prostate:	n/a
2	chr6:75994825-75994875	T-47D	breast:	n/a
3	chr6:75953648-75953698	LNCaP	prostate:	n/a
4	chr6:75994825-75994875	T-47D	breast:	n/a
5	chr6:75994833-75994883	NHDF-neo	bronchial:	n/a
6	chr6:75990769-75990819	NHDF-neo	bronchial:	n/a
7	chr6:75994563-75994613	HRE	kidney:	n/a
8	chr6:75953667-75953717	AoSMC	blood vessel:	n/a
9	chr6:75977411-75977461	AG10803	skin:	n/a
10	chr6:75994713-75994763	SAEC	small airway:	n/a
11	chr6:75994771-75994821	GM12892	blood:	n/a
12	chr6:75988568-75988618	BJ	skin:	n/a
13	chr6:75954053-75954103	U87	brain:	n/a
14	chr6:75927964-75928014	HRCEpiC	kidney:	n/a
15	chr6:75953366-75953416	H1-hESC	embryonic stem cell:	embryo
16	chr6:75953935-75953985	HAEpiC	amniotic membrane:	n/a
17	chr6:75994833-75994883	AG04450	lung:	fetal
18	chr6:76000847-76000897	NHBE	bronchial:	n/a
19	chr6:75994262-75994312	PANC-1	pancreas:	n/a
20	chr6:75953566-75953616	HCF	heart:	n/a
21	chr6:75984465-75984515	SK-N-SH_RA	brain:	n/a
22	chr6:75994699-75994749	PFSK-1	brain:	n/a
23	chr6:75953675-75953725	HL-60	blood:	n/a
24	chr6:75994699-75994749	U87	brain:	n/a
25	chr6:75977411-75977461	HCF	heart:	n/a
26	chr6:75953366-75953416	HCT-116	colon:	n/a
27	chr6:75995845-75995895	CMK	blood:	n/a
28	chr6:75994873-75994923	SK-N-SH	brain:	n/a
29	chr6:75954053-75954103	ECC-1	luminal epithelium:	n/a
30	chr6:75953366-75953416	Hela-S3	cervix:	n/a
31	chr6:75933274-75933324	PrEC	prostate:	n/a
32	chr6:75965559-75965609	Hepatocyte	liver:	n/a
33	chr6:75953667-75953717	GM19239	blood:	n/a
34	chr6:75933274-75933324	Hela-S3	cervix:	n/a
35	chr6:75994262-75994312	HEK293	kidney:	embryo
36	chr6:75995845-75995895	RPTEC	kidney:	n/a
37	chr6:75990769-75990819	HPAEpiC	pulmonary alveolar:	n/a
38	chr6:75994713-75994763	MCF-7	breast:	n/a
39	chr6:75995845-75995895	Hela-S3	cervix:	n/a
40	chr6:75994709-75994759	SK-N-SH	brain:	n/a
41	chr6:75994699-75994749	HCF	heart:	n/a
42	chr6:75953667-75953717	MCF10A-Er-Src	breast:	n/a
43	chr6:75994470-75994520	AG09309	skin:	n/a
44	chr6:75953935-75953985	Caco-2	colon:	n/a
45	chr6:75988568-75988618	ovcar-3	ovarian:	n/a
46	chr6:75994262-75994312	NHBE	bronchial:	n/a
47	chr6:75994771-75994821	BE2_C	brain:	n/a
48	chr6:75953853-75953903	HCPEpiC	choroid plexus:	n/a
49	chr6:75934318-75934368	SAEC	small airway:	n/a
50	chr6:75945095-75945145	AG04450	lung:	fetal

(count:150 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:75949478..75951656-chr6:75961660..75963174,2	K562	blood:
2	chr6:75932967..75935533-chr6:75943736..75947301,4	K562	blood:
3	chr6:75972939..75974519-chr6:75996831..75999415,2	K562	blood:
4	chr6:75993518..75995468-chr6:75996205..75998181,2	K562	blood:
5	chr6:75976211..75977106-chr6:76235994..76236775,2	MCF-7	breast:
6	chr6:75942897..75944973-chr6:75945233..75947234,2	MCF-7	breast:
7	chr6:75940573..75942162-chr6:75964484..75966992,2	K562	blood:
8	chr6:75995037..75997566-chr6:76015682..76017767,2	K562	blood:
9	chr6:76006592..76007378-chr6:76077449..76078474,3	MCF-7	breast:
10	chr6:75985223..75988429-chr6:75989694..75991807,3	MCF-7	breast:
11	chr6:75965173..75970127-chr6:75970180..75976359,8	K562	blood:
12	chr6:75983517..75986641-chr6:75988092..75990242,3	MCF-7	breast:
13	chr6:75952128..75954360-chr6:75971473..75973567,2	K562	blood:
14	chr6:75932833..75934486-chr6:75934582..75937364,2	K562	blood:
15	chr6:75968627..75970817-chr6:75971024..75972906,2	K562	blood:
16	chr6:75979886..75981407-chr6:75985729..75987544,2	K562	blood:
17	chr6:75964472..75966148-chr6:75966930..75969432,2	MCF-7	breast:
18	chr6:75920298..75925190-chr6:75927139..75929991,4	K562	blood:
19	chr6:75952128..75954360-chr6:75971385..75973567,3	K562	blood:
20	chr6:75952178..75953795-chr6:76311805..76314377,2	K562	blood:
21	chr6:76006957..76007653-chr6:76235682..76236264,3	MCF-7	breast:
22	chr6:75979468..75981742-chr6:75992719..75994647,2	MCF-7	breast:
23	chr6:75993025..75996472-chr6:76005864..76009540,5	MCF-7	breast:
24	chr6:75951942..75953572-chr6:75985751..75987713,2	K562	blood:
25	chr6:75949965..75952102-chr6:75989407..75991493,2	K562	blood:
26	chr6:75921715..75924102-chr6:75924623..75927092,3	K562	blood:
27	chr6:75979010..75981926-chr6:75992579..75994330,2	MCF-7	breast:
28	chr6:75964680..75966328-chr6:75967865..75970436,2	K562	blood:
29	chr6:75981554..75983680-chr6:75993870..75995991,2	K562	blood:
30	chr6:74363322..74365404-chr6:75950708..75953547,2	MCF-7	breast:
31	chr6:75958503..75962615-chr6:75963016..75967089,5	K562	blood:
32	chr6:75992636..75994360-chr6:75994591..75996094,2	K562	blood:
33	chr6:75993232..75997783-chr6:75998816..76002122,5	MCF-7	breast:
34	chr6:75993176..75995308-chr6:76310710..76312367,2	MCF-7	breast:
35	chr6:75951699..75955124-chr6:75992599..75996025,9	K562	blood:
36	chr6:75982220..75984333-chr6:75991304..75993082,2	MCF-7	breast:
37	chr6:75976103..75976996-chr6:76006807..76007378,2	MCF-7	breast:
38	chr6:75963600..75966180-chr6:75967354..75969365,2	K562	blood:
39	chr6:75952974..75954563-chr6:75959436..75961084,2	MCF-7	breast:
40	chr6:75974447..75978306-chr6:75980001..75984136,4	MCF-7	breast:
41	chr6:76005916..76009397-chr6:76011180..76013740,3	K562	blood:
42	chr6:75937140..75939759-chr6:75945754..75948396,2	MCF-7	breast:
43	chr6:75968627..75970817-chr6:75971024..75972906,2	K562	blood:
44	chr6:75963600..75966180-chr6:75967354..75969365,2	K562	blood:
45	chr6:75993142..75995708-chr6:76310246..76313188,4	K562	blood:
46	chr6:75921545..75925190-chr6:75927734..75930385,3	K562	blood:
47	chr6:75953197..75955267-chr6:75981448..75984407,2	K562	blood:
48	chr6:75981554..75983680-chr6:75993870..75995991,2	K562	blood:
49	chr6:75981707..75983923-chr6:75986673..75988539,2	K562	blood:
50	chr6:75952131..75953877-chr6:75964575..75966530,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SENP6-3	chr6:76000665-76001217	ENSG00000225793.2
2	lnc-SENP6-3	chr6:75999970-76000054	ENSG00000225793.2
3	lnc-SENP6-3	chr6:75994749-75995025	ENSG00000225793.2
4	lnc-SENP6-3	chr6:76006237-76006283	ENSG00000225793
5	lnc-SENP6-3	chr6:76000665-76001580	NONHSAT113602
6	lnc-FILIP1-1	chr6:76001574-76003213	NONHSAT113604
7	lnc-SENP6-3	chr6:76006237-76006719	ENSG00000225793.2
8	lnc-SENP6-3	chr6:76003209-76003310	ENSG00000225793
9	lnc-SENP6-3	chr6:75999970-76000054	NONHSAT113602
10	lnc-SENP6-3	chr6:75994762-75995025	ENSG00000225793.2
11	lnc-SENP6-3	chr6:75994730-75995025	ENSG00000225793
12	lnc-SENP6-3	chr6:76006235-76007696	NONHSAT113605
13	lnc-SENP6-3	chr6:75994730-75995025	NONHSAT113602
14	lnc-SENP6-3	chr6:75994749-75995107	NONHSAT113603

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TMEM30A	hsa-miR-215-5p	chr6:75964787-75964806
2	TMEM30A	hsa-miR-26b-5p	chr6:75964470-75964491
3	TMEM30A	hsa-miR-128-3p	chr6:75963151-75963171
4	TMEM30A	hsa-miR-26b-5p	chr6:75964175-75964195
5	TMEM30A	hsa-miR-192-5p	chr6:75964787-75964806
6	TMEM30A	hsa-miR-27a-3p	chr6:75963150-75963170

Variant related genes	Relation type
COX7A2	TF binding region
ENSG00000225793	TF binding region
TMEM30A	TF binding region
COX7A2	CpG island
ENSG00000225793	CpG island
TMEM30A	CpG island
ENSG00000261423	chromatin interactions
ENSG00000223891	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000077147	chromatin interactions
ENSG00000132823	chromatin interactions
ENSG00000080031	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000166233	chromatin interactions
ENSG00000167182	chromatin interactions
ENSG00000092531	chromatin interactions
ENSG00000112695	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000070423	chromatin interactions
ENSG00000119899	chromatin interactions
ENSG00000148057	chromatin interactions
ENSG00000163689	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000103994	chromatin interactions
ENSG00000225793	chromatin interactions
ENSG00000264920	chromatin interactions
ENSG00000138757	chromatin interactions
ENSG00000112701	chromatin interactions
EIF2S1	miRNA target sites
RDH11	miRNA target sites
FASLG	miRNA target sites

Extended variants
information (count: 3066 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3066 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1323070	chr6:75923605-75923606	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs577119207	chr6:75923680-75923681	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373595767	chr6:75923693-75923694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76406486	chr6:75923721-75923722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs557446163	chr6:75923778-75923779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs73463842	chr6:75923837-75923838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545212298	chr6:75923838-75923839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543036579	chr6:75923847-75923848	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79685806	chr6:75923886-75923887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs181017788	chr6:75923904-75923905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371513609	chr6:75923922-75923923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565289060	chr6:75923998-75923999	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565092651	chr6:75924009-75924010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145067787	chr6:75924053-75924054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs117690191	chr6:75924103-75924104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562634945	chr6:75924104-75924105	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs73463845	chr6:75924109-75924110	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs183954867	chr6:75924137-75924138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs566762853	chr6:75924177-75924178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117171471	chr6:75924189-75924190	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138802242	chr6:75924203-75924204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs73463847	chr6:75924222-75924223	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs538079423	chr6:75924230-75924231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs113204995	chr6:75924268-75924269	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575740192	chr6:75924269-75924270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35495601	chr6:75924273-75924274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs536245729	chr6:75924285-75924286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543066814	chr6:75924297-75924298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200683333	chr6:75924317-75924318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530878059	chr6:75924352-75924353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111806292	chr6:75924356-75924357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs188585647	chr6:75924363-75924364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs181377885	chr6:75924364-75924365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148598104	chr6:75924368-75924369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs374561129	chr6:75924382-75924383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs367607360	chr6:75924387-75924388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187047710	chr6:75924393-75924394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs527934762	chr6:75924409-75924410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552502686	chr6:75924410-75924411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs529837439	chr6:75924424-75924425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs142011008	chr6:75924432-75924433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560141541	chr6:75924447-75924448	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191839878	chr6:75924488-75924489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370225506	chr6:75924495-75924496	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552485878	chr6:75924526-75924527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs240370	chr6:75924559-75924560	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs531900727	chr6:75924562-75924563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537642255	chr6:75924573-75924574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs549992306	chr6:75924574-75924575	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368141489	chr6:75924586-75924587	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Chronic lymphocytic leukemia	21546498	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
Myelodysplastic syndrome	18508791	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3304 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75917600-75946600	Weak transcription	Lung	lung
2	chr6:75918800-75924600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:75918800-75925000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:75918800-75925000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr6:75918800-75926400	Weak transcription	NHDF-Ad	bronchial
6	chr6:75918800-75926600	Weak transcription	Colon Smooth Muscle	Colon
7	chr6:75918800-75926600	Weak transcription	Ovary	ovary
8	chr6:75918800-75926800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr6:75918800-75926800	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr6:75919000-75924600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:75919200-75925000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr6:75919800-75926600	Weak transcription	Fetal Lung	lung
13	chr6:75920200-75923800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr6:75920800-75923800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr6:75921200-75923800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:75921400-75923800	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr6:75921600-75923800	Enhancers	H9 Cell Line	embryonic stem cell
18	chr6:75921600-75923800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:75921600-75923800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:75921600-75925800	Enhancers	Fetal Heart	heart
21	chr6:75921800-75925000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:75921800-75925000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr6:75921800-75926400	Weak transcription	NH-A	brain
24	chr6:75922000-75924600	Weak transcription	NHEK	skin
25	chr6:75922000-75926600	Weak transcription	Hela-S3	cervix
26	chr6:75922000-75926800	Weak transcription	NHLF	lung
27	chr6:75922200-75925000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr6:75922400-75924800	Weak transcription	Liver	Liver
29	chr6:75922600-75926400	Weak transcription	Left Ventricle	heart
30	chr6:75922600-75926600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:75922600-75926600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr6:75922600-75926600	Weak transcription	Fetal Muscle Leg	muscle
33	chr6:75922600-75926600	Weak transcription	HSMMtube	muscle
34	chr6:75922600-75947000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr6:75922800-75926600	Weak transcription	Adipose Nuclei	Adipose
36	chr6:75922800-75926600	Weak transcription	Osteobl	bone
37	chr6:75922800-75926800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr6:75922800-75927800	Weak transcription	Right Atrium	heart
39	chr6:75922800-75933200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr6:75923000-75926600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr6:75923200-75924200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:75923200-75926600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:75923200-75926600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr6:75923200-75932800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr6:75923400-75923800	Enhancers	Fetal Intestine Large	intestine
46	chr6:75923400-75924000	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr6:75923600-75923800	Enhancers	Fetal Intestine Small	intestine
48	chr6:75923600-75927600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr6:75923800-75924000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr6:75923800-75924800	Weak transcription	H9 Cell Line	embryonic stem cell

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