Variant report

Variant	nsv830698
Chromosome Location	chr6:75968810-76115592
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2451)
CpG islands
(count:2503)
Chromatin interactive
region (count:127)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2451 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:75994224-75995352	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:76006923-76007258	HepG2	liver:	n/a	chr6:76006971-76006987
3	ARID3A	chr6:76077842-76078150	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:75976467-75976799	K562	blood:	n/a	n/a
5	ARID3A	chr6:76055127-76055487	K562	blood:	n/a	n/a
6	ATF1	chr6:76055151-76055664	K562	blood:	n/a	n/a
7	ATF1	chr6:75994470-75995206	K562	blood:	n/a	n/a
8	ATF1	chr6:76056520-76056587	K562	blood:	n/a	n/a
9	ATF2	chr6:75994307-75995618	GM12878	blood:	n/a	n/a
10	ATF2	chr6:76043668-76045032	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:75994260-75995501	GM12878	blood:	n/a	n/a
12	ATF2	chr6:76043502-76044884	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr6:76055107-76055457	K562	blood:	n/a	n/a
14	ATF3	chr6:76077768-76078490	A549	lung:	n/a	n/a
15	ATF3	chr6:76077729-76078468	A549	lung:	n/a	n/a
16	ATF3	chr6:76037568-76037846	K562	blood:	n/a	n/a
17	BACH1	chr6:75993397-75993848	K562	blood:	n/a	n/a
18	BACH1	chr6:75983709-75983780	K562	blood:	n/a	n/a
19	BACH1	chr6:76062077-76062250	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr6:76043656-76044226	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr6:76077818-76078169	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:75993810-75994247	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:76088303-76088325	K562	blood:	n/a	n/a
24	BACH1	chr6:75977860-75978616	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:76059300-76059652	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr6:75994960-75995137	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr6:75994338-75994903	GM12878	blood:	n/a	n/a
28	BCL11A	chr6:76036618-76036852	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr6:76044361-76044634	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr6:75994419-75994930	GM12878	blood:	n/a	n/a
31	BCL11A	chr6:75977824-75978126	H1-hESC	embryonic stem cell:	n/a	n/a
32	BCL3	chr6:76085853-76086426	A549	lung:	n/a	chr6:76086335-76086342
33	BCL3	chr6:76077606-76078934	A549	lung:	n/a	n/a
34	BCL3	chr6:76107396-76108096	A549	lung:	n/a	n/a
35	BCL3	chr6:76077713-76078534	A549	lung:	n/a	n/a
36	BCL3	chr6:75994445-75994982	A549	lung:	n/a	n/a
37	BCL3	chr6:75984792-75985379	A549	lung:	n/a	n/a
38	BCLAF1	chr6:75994359-75994916	K562	blood:	n/a	n/a
39	BCLAF1	chr6:75994225-75995381	GM12878	blood:	n/a	n/a
40	BCLAF1	chr6:75994298-75995124	GM12878	blood:	n/a	n/a
41	BCLAF1	chr6:75994293-75994927	K562	blood:	n/a	n/a
42	BHLHE40	chr6:75994237-75995170	HepG2	liver:	n/a	chr6:75995133-75995154
43	BHLHE40	chr6:76054211-76054411	K562	blood:	n/a	n/a
44	BHLHE40	chr6:75994743-75995213	A549	lung:	n/a	chr6:75995133-75995154
45	BHLHE40	chr6:75993846-75995819	K562	blood:	n/a	chr6:75995133-75995154
46	BHLHE40	chr6:76091834-76091895	K562	blood:	n/a	n/a
47	BHLHE40	chr6:76055135-76055616	K562	blood:	n/a	n/a
48	BHLHE40	chr6:75994230-75995556	GM12878	blood:	n/a	chr6:75995133-75995154
49	BRCA1	chr6:75994693-75995073	GM12878	blood:	n/a	n/a
50	BRCA1	chr6:76015493-76015500	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2503 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:75977411-75977461	HRPEpiC	eye:	n/a
2	chr6:76022250-76022300	HNPCEpiC	eye:	n/a
3	chr6:75977411-75977461	HRPEpiC	eye:	n/a
4	chr6:76022250-76022300	HNPCEpiC	eye:	n/a
5	chr6:76045920-76045970	K562	blood:	n/a
6	chr6:76059726-76059776	HAEpiC	amniotic membrane:	n/a
7	chr6:76078187-76078237	GM19239	blood:	n/a
8	chr6:75990769-75990819	ProgFib	skin:	n/a
9	chr6:75994709-75994759	HRPEpiC	eye:	n/a
10	chr6:76000847-76000897	HIPEpiC	eye:	n/a
11	chr6:76018362-76018412	BE2_C	brain:	n/a
12	chr6:75994713-75994763	SKMC	muscle:	n/a
13	chr6:76074059-76074109	HCM	heart:	n/a
14	chr6:76000847-76000897	ovcar-3	ovarian:	n/a
15	chr6:76022250-76022300	A549	lung:	n/a
16	chr6:75994713-75994763	HCF	heart:	n/a
17	chr6:76074059-76074109	AG04449	skin:	fetal
18	chr6:75994771-75994821	GM12892	blood:	n/a
19	chr6:76044678-76044728	A549	lung:	n/a
20	chr6:76037604-76037654	AG04450	lung:	fetal
21	chr6:75994833-75994883	PrEC	prostate:	n/a
22	chr6:75994873-75994923	GM06990	blood:	n/a
23	chr6:76092436-76092486	AG09309	skin:	n/a
24	chr6:76037604-76037654	MCF-7	breast:	n/a
25	chr6:76078187-76078237	NT2-D1	testis:	n/a
26	chr6:75994563-75994613	Caco-2	colon:	n/a
27	chr6:76059756-76059806	HRPEpiC	eye:	n/a
28	chr6:75990769-75990819	HEK293	kidney:	embryo
29	chr6:76059726-76059776	U87	brain:	n/a
30	chr6:76022219-76022269	AG09319	gingival:	n/a
31	chr6:76045920-76045970	HRCEpiC	kidney:	n/a
32	chr6:76000847-76000897	AG04450	lung:	fetal
33	chr6:76086013-76086063	SK-N-SH	brain:	n/a
34	chr6:75990769-75990819	NB4	blood:	n/a
35	chr6:76018362-76018412	H1-hESC	embryonic stem cell:	embryo
36	chr6:76073316-76073366	Caco-2	colon:	n/a
37	chr6:75984465-75984515	Jurkat	blood:	n/a
38	chr6:76059756-76059806	GM12891	blood:	n/a
39	chr6:76073316-76073366	NT2-D1	testis:	n/a
40	chr6:76074059-76074109	SK-N-MC	brain:	n/a
41	chr6:76074059-76074109	GM06990	blood:	n/a
42	chr6:75994470-75994520	NT2-D1	testis:	n/a
43	chr6:75994563-75994613	PFSK-1	brain:	n/a
44	chr6:76059726-76059776	AG09309	skin:	n/a
45	chr6:76073316-76073366	HCM	heart:	n/a
46	chr6:75994833-75994883	LNCaP	prostate:	n/a
47	chr6:75994833-75994883	PFSK-1	brain:	n/a
48	chr6:75995845-75995895	HIPEpiC	eye:	n/a
49	chr6:75994713-75994763	Hela-S3	cervix:	n/a
50	chr6:76022515-76022565	ProgFib	skin:	n/a

(count:127 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:75979010..75981926-chr6:75992579..75994330,2	MCF-7	breast:
2	chr6:75983517..75986641-chr6:75988092..75990242,3	MCF-7	breast:
3	chr6:75952062..75953597-chr6:75984103..75985781,2	MCF-7	breast:
4	chr6:75993069..75997866-chr6:75997918..76002426,9	MCF-7	breast:
5	chr6:76005916..76009397-chr6:76011180..76013740,3	K562	blood:
6	chr6:76086882..76088645-chr6:76090320..76093315,3	K562	blood:
7	chr6:76061198..76063210-chr6:76102541..76105002,2	K562	blood:
8	chr6:76086882..76089051-chr6:76090320..76093315,3	K562	blood:
9	chr6:76049155..76051886-chr6:76059205..76061282,2	MCF-7	breast:
10	chr6:75967149..75971293-chr6:75986356..75989401,5	K562	blood:
11	chr6:75949911..75955499-chr6:75993041..75995715,6	MCF-7	breast:
12	chr6:76015748..76017773-chr6:76019330..76020992,2	MCF-7	breast:
13	chr6:76099699..76101269-chr6:76104399..76106099,2	K562	blood:
14	chr6:76049155..76051886-chr6:76059205..76061282,2	MCF-7	breast:
15	chr6:76086882..76089051-chr6:76090320..76093315,3	K562	blood:
16	chr6:76008575..76011168-chr6:76015563..76017082,2	K562	blood:
17	chr6:75987095..75989976-chr6:75990032..75992457,3	MCF-7	breast:
18	chr6:75953197..75955267-chr6:75981448..75984407,2	K562	blood:
19	chr6:76006592..76007378-chr6:76077449..76078474,3	MCF-7	breast:
20	chr6:75949965..75952102-chr6:75989407..75991493,2	K562	blood:
21	chr6:75951942..75953572-chr6:75985751..75987713,2	K562	blood:
22	chr6:75976103..75976996-chr6:76006807..76007378,2	MCF-7	breast:
23	chr6:75994084..75996334-chr6:76010819..76013613,4	K562	blood:
24	chr6:75952125..75954686-chr6:76000719..76002598,2	K562	blood:
25	chr6:75976103..75976996-chr6:76006807..76007378,2	MCF-7	breast:
26	chr6:75964472..75966148-chr6:75966930..75969432,2	MCF-7	breast:
27	chr6:75951485..75954328-chr6:75992401..75995008,3	MCF-7	breast:
28	chr6:76064451..76067202-chr6:76069544..76071672,2	MCF-7	breast:
29	chr6:75994942..75996622-chr6:76062325..76064970,2	K562	blood:
30	chr6:75979468..75981742-chr6:75992719..75994647,2	MCF-7	breast:
31	chr6:76005916..76009397-chr6:76011180..76013740,3	K562	blood:
32	chr6:75993079..75996306-chr6:76012089..76014861,3	MCF-7	breast:
33	chr6:75981554..75983680-chr6:75993870..75995991,2	K562	blood:
34	chr6:76060441..76063386-chr6:76076678..76078572,2	K562	blood:
35	chr6:76058715..76060235-chr6:76071941..76074343,2	MCF-7	breast:
36	chr6:75959944..75962259-chr6:75992382..75994540,2	K562	blood:
37	chr19:55718165..55719128-chr6:75994850..75995681,2	Hela-S3	cervix:
38	chr4:76597747..76598353-chr6:75994277..75995225,2	Hela-S3	cervix:
39	chr6:75985223..75988429-chr6:75989694..75991807,3	MCF-7	breast:
40	chr6:76077364..76078435-chr6:76235905..76237284,7	MCF-7	breast:
41	chr6:75993518..75995468-chr6:75996205..75998181,2	K562	blood:
42	chr6:75951366..75953542-chr6:75992434..75995845,4	K562	blood:
43	chr6:76060441..76063386-chr6:76076678..76078572,2	K562	blood:
44	chr6:75975053..75977657-chr6:75987752..75989957,2	K562	blood:
45	chr6:75991061..75995848-chr6:76010819..76015075,6	K562	blood:
46	chr6:75972939..75974519-chr6:75996831..75999415,2	K562	blood:
47	chr6:76039197..76040840-chr6:76053935..76055529,2	K562	blood:
48	chr6:76015748..76017773-chr6:76019330..76020992,2	MCF-7	breast:
49	chr6:75983517..75986641-chr6:75988092..75990242,3	MCF-7	breast:
50	chr6:75981707..75983923-chr6:75986673..75988539,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SENP6-10	chr6:76108616-76108714	NONHSAT113613
2	lnc-SENP6-2	chr6:76070529-76070632	ENSG00000237174.3
3	lnc-SENP6-2	chr6:76072482-76072740	ENSG00000237174.3
4	lnc-SENP6-3	chr6:76006235-76007696	NONHSAT113605
5	lnc-SENP6-3	chr6:75999970-76000054	ENSG00000225793.2
6	lnc-SENP6-2	chr6:76070383-76070435	ENSG00000237174.3
7	lnc-FILIP1-1	chr6:76001574-76003213	NONHSAT113604
8	lnc-SENP6-2	chr6:76095374-76095400	ENSG00000237174.1
9	lnc-SENP6-3	chr6:76000665-76001217	ENSG00000225793.2
10	lnc-SENP6-3	chr6:76006237-76006283	ENSG00000225793
11	lnc-SENP6-11	chr6:76057403-76057457	l_3206_chr6:76057402-76060176_brain
12	lnc-SENP6-2	chr6:76068016-76068343	ENSG00000237174.3
13	lnc-SENP6-2	chr6:76066960-76067091	NONHSAT113608
14	lnc-SENP6-3	chr6:76000665-76001580	NONHSAT113602
15	lnc-SENP6-2	chr6:76072482-76072740	NONHSAT113608
16	lnc-SENP6-3	chr6:75999970-76000054	NONHSAT113602
17	lnc-SENP6-2	chr6:76094536-76094653	ENSG00000237174.1
18	lnc-SENP6-2	chr6:76070565-76070632	ENSG00000237174.1
19	lnc-SENP6-10	chr6:76107542-76107820	NONHSAT113613
20	lnc-SENP6-2	chr6:76071568-76071727	ENSG00000237174.1
21	lnc-SENP6-2	chr6:76070528-76070632	ENSG00000237174.1
22	lnc-SENP6-10	chr6:76108879-76109062	NONHSAT113613
23	lnc-SENP6-11	chr6:76059929-76060176	l_3206_chr6:76057402-76060176_brain
24	lnc-SENP6-2	chr6:76066930-76067091	ENSG00000237174.3
25	lnc-SENP6-2	chr6:76095856-76096096	ENSG00000237174.1
26	lnc-SENP6-3	chr6:76006237-76006719	ENSG00000225793.2
27	lnc-SENP6-3	chr6:76003209-76003310	ENSG00000225793
28	lnc-SENP6-3	chr6:75994762-75995025	ENSG00000225793.2
29	lnc-SENP6-2	chr6:76075753-76075804	ENSG00000237174.1
30	lnc-SENP6-3	chr6:75994749-75995025	ENSG00000225793.2
31	lnc-SENP6-2	chr6:76071568-76071610	ENSG00000237174.3
32	lnc-SENP6-3	chr6:75994730-75995025	NONHSAT113602
33	lnc-TMEM30A-2	chr6:76028817-76029696	NONHSAT113606
34	lnc-SENP6-3	chr6:75994749-75995107	NONHSAT113603
35	lnc-SENP6-3	chr6:75994730-75995025	ENSG00000225793
36	lnc-TMEM30A-3	chr6:76108577-76108783	NONHSAT113614

No data

Variant related genes	Relation type
ENSG00000221332	TF binding region
HMGB1P39	TF binding region
FILIP1	TF binding region
ENSG00000237174	TF binding region
ENSG00000225793	TF binding region
TMEM30A	TF binding region
ENSG00000221332	CpG island
HMGB1P39	CpG island
FILIP1	CpG island
ENSG00000237174	CpG island
ENSG00000225793	CpG island
TMEM30A	CpG island
ENSG00000112697	chromatin interactions
ENSG00000272273	chromatin interactions
ENSG00000237174	chromatin interactions
ENSG00000238156	chromatin interactions
ENSG00000118407	chromatin interactions
ENSG00000137312	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000080031	chromatin interactions
ENSG00000148057	chromatin interactions
ENSG00000225793	chromatin interactions
ENSG00000112695	chromatin interactions
ENSG00000138757	chromatin interactions
ENSG00000163689	chromatin interactions
RDH11	miRNA target sites
FASLG	miRNA target sites
EIF2S1	miRNA target sites

Extended variants
information (count: 5169 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:5169 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563727822	chr6:75968819-75968820	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2354390	chr6:75968875-75968876	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531249534	chr6:75968892-75968893	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575856836	chr6:75968917-75968918	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561803346	chr6:75968990-75968991	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs150796805	chr6:75968995-75968996	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547254615	chr6:75969008-75969009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188944117	chr6:75969022-75969023	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201602019	chr6:75969037-75969038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs368075032	chr6:75969069-75969070	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139174067	chr6:75969106-75969107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544711994	chr6:75969114-75969115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200587918	chr6:75969139-75969140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144159719	chr6:75969145-75969146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371897890	chr6:75969149-75969150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs538203329	chr6:75969162-75969163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs144512821	chr6:75969187-75969188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376577824	chr6:75969215-75969216	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs369832254	chr6:75969226-75969227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200462489	chr6:75969239-75969240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs183409691	chr6:75969241-75969242	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199925986	chr6:75969252-75969253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554056214	chr6:75969295-75969296	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572343433	chr6:75969328-75969329	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186587174	chr6:75969369-75969370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113123065	chr6:75969401-75969402	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs58046294	chr6:75969428-75969429	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs561277464	chr6:75969434-75969435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139935761	chr6:75969639-75969640	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557380707	chr6:75969640-75969641	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576598925	chr6:75969679-75969680	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373937681	chr6:75969680-75969681	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529160948	chr6:75969681-75969682	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78378243	chr6:75969762-75969763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs145783197	chr6:75969777-75969778	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs191474183	chr6:75969811-75969812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62415691	chr6:75969813-75969814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570924166	chr6:75969897-75969898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531864123	chr6:75969904-75969905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530070716	chr6:75969935-75969936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148928524	chr6:75969985-75969986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs555633558	chr6:75969990-75969991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79424517	chr6:75969995-75969996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375567115	chr6:75970030-75970031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554495145	chr6:75970055-75970056	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566033160	chr6:75970078-75970079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369195563	chr6:75970095-75970096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs240383	chr6:75970101-75970102	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs13209631	chr6:75970144-75970145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs240384	chr6:75970145-75970146	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:103)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioblastoma multiforme	21510904	CNVD

Chromatin state (count:3418 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:75953800-75978200	Weak transcription	Gastric	stomach
2	chr6:75953800-75982200	Weak transcription	Spleen	Spleen
3	chr6:75954000-75974000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:75954200-75969400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:75954200-75971600	Weak transcription	K562	blood
6	chr6:75954200-75973200	Weak transcription	Psoas Muscle	Psoas
7	chr6:75954200-75978000	Weak transcription	Pancreas	Pancrea
8	chr6:75954200-75978000	Weak transcription	Small Intestine	intestine
9	chr6:75954200-75978000	Weak transcription	Stomach Mucosa	stomach
10	chr6:75954200-75978200	Weak transcription	Esophagus	oesophagus
11	chr6:75954200-75978400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:75954400-75969000	Weak transcription	Colonic Mucosa	Colon
13	chr6:75954400-75972600	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr6:75954400-75976800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr6:75954400-75977200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr6:75954400-75977600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr6:75954400-75978000	Weak transcription	Right Ventricle	heart
18	chr6:75954400-75978000	Weak transcription	Hela-S3	cervix
19	chr6:75954400-75986000	Weak transcription	Brain Germinal Matrix	brain
20	chr6:75954600-75971800	Weak transcription	Fetal Stomach	stomach
21	chr6:75954600-75982400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr6:75954800-75969400	Weak transcription	HepG2	liver
23	chr6:75954800-75982200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:75954800-75988200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr6:75955000-75972600	Weak transcription	NHLF	lung
26	chr6:75955200-75969800	Weak transcription	Fetal Intestine Small	intestine
27	chr6:75955600-75969200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr6:75958600-75972400	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr6:75959600-75972800	Weak transcription	Thymus	Thymus
30	chr6:75959800-75971800	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr6:75959800-75977400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:75960600-75981400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr6:75961400-75974000	Strong transcription	HSMM	muscle
34	chr6:75961400-75975400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:75961600-75978200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr6:75962200-75972600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:75962400-75970200	Strong transcription	Fetal Intestine Large	intestine
38	chr6:75962400-75971400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:75962400-75975200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:75962400-75977600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr6:75962800-75969600	Strong transcription	NH-A	brain
42	chr6:75962800-75970000	Strong transcription	Left Ventricle	heart
43	chr6:75962800-75970800	Strong transcription	Liver	Liver
44	chr6:75962800-75974000	Strong transcription	Rectal Mucosa Donor 29	rectum
45	chr6:75962800-75974200	Strong transcription	Adipose Nuclei	Adipose
46	chr6:75962800-75974800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr6:75962800-75975000	Strong transcription	Primary monocytes fromperipheralblood	blood
48	chr6:75962800-75975600	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr6:75963000-75976800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr6:75963200-75971400	Strong transcription	HUES64 Cell Line	embryonic stem cell

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