Variant report

Variant	nsv1043242
Chromosome Location	chr10:116655057-116883386
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1587)
CpG islands
(count:1955)
Chromatin interactive
region (count:54)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1587 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:116789382-116789792	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:116697487-116698196	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:116665348-116665349	HepG2	liver:	n/a	n/a
4	ATF1	chr10:116676782-116676906	K562	blood:	n/a	n/a
5	ATF1	chr10:116775074-116775335	K562	blood:	n/a	n/a
6	ATF1	chr10:116697725-116698158	K562	blood:	n/a	n/a
7	ATF2	chr10:116670736-116671263	GM12878	blood:	n/a	n/a
8	ATF2	chr10:116712761-116713172	GM12878	blood:	n/a	n/a
9	ATF2	chr10:116697696-116698258	GM12878	blood:	n/a	n/a
10	ATF2	chr10:116716225-116716691	GM12878	blood:	n/a	n/a
11	ATF2	chr10:116712725-116713282	GM12878	blood:	n/a	n/a
12	ATF2	chr10:116697682-116698205	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr10:116697582-116698196	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr10:116697755-116698198	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr10:116697681-116698175	HepG2	liver:	n/a	n/a
16	ATF3	chr10:116697747-116698104	K562	blood:	n/a	n/a
17	ATF3	chr10:116697730-116698169	K562	blood:	n/a	n/a
18	ATF3	chr10:116697789-116698079	HepG2	liver:	n/a	n/a
19	ATF3	chr10:116697671-116698196	A549	lung:	n/a	n/a
20	ATF3	chr10:116665174-116665584	HCT-116	colon:	n/a	n/a
21	ATF3	chr10:116697687-116698181	GM12878	blood:	n/a	n/a
22	ATF3	chr10:116697778-116698092	GM12878	blood:	n/a	n/a
23	ATF3	chr10:116697701-116698199	A549	lung:	n/a	n/a
24	ATF3	chr10:116697726-116698181	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr10:116852386-116853318	H1-hESC	embryonic stem cell:	n/a	n/a
26	BACH1	chr10:116853916-116854116	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr10:116678165-116678365	H1-hESC	embryonic stem cell:	n/a	n/a
28	BATF	chr10:116685626-116686056	GM12878	blood:	n/a	chr10:116685856-116685867
29	BATF	chr10:116670818-116671149	GM12878	blood:	n/a	chr10:116671008-116671019
30	BATF	chr10:116712890-116713128	GM12878	blood:	n/a	chr10:116713021-116713030
31	BATF	chr10:116878147-116878431	GM12878	blood:	n/a	chr10:116878279-116878290
32	BATF	chr10:116697782-116698110	GM12878	blood:	n/a	n/a
33	BATF	chr10:116685727-116685999	GM12878	blood:	n/a	chr10:116685856-116685867
34	BCL11A	chr10:116694869-116695397	GM12878	blood:	n/a	n/a
35	BCL3	chr10:116697620-116698304	A549	lung:	n/a	n/a
36	BCL3	chr10:116751581-116751840	GM12878	blood:	n/a	n/a
37	BCLAF1	chr10:116712754-116713184	GM12878	blood:	n/a	n/a
38	BCLAF1	chr10:116697659-116698172	GM12878	blood:	n/a	n/a
39	BHLHE40	chr10:116761761-116762162	GM12878	blood:	n/a	n/a
40	BHLHE40	chr10:116712856-116713181	GM12878	blood:	n/a	n/a
41	BHLHE40	chr10:116852842-116853079	HepG2	liver:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
42	BHLHE40	chr10:116697615-116698384	GM12878	blood:	n/a	n/a
43	BHLHE40	chr10:116789264-116789703	HepG2	liver:	n/a	n/a
44	BHLHE40	chr10:116852859-116853122	GM12878	blood:	n/a	chr10:116852939-116852955 chr10:116852927-116852943
45	BHLHE40	chr10:116697775-116698294	K562	blood:	n/a	n/a
46	BRCA1	chr10:116697800-116698265	GM12878	blood:	n/a	n/a
47	BRCA1	chr10:116697801-116698104	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr10:116699028-116699121	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr10:116697736-116698156	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr10:116697849-116698119	HepG2	liver:	n/a	n/a

(count:1955 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116852470-116852520	ProgFib	skin:	n/a
2	chr10:116755155-116755205	SK-N-SH_RA	brain:	n/a
3	chr10:116853118-116853168	T-47D	breast:	n/a
4	chr10:116852470-116852520	ProgFib	skin:	n/a
5	chr10:116755155-116755205	SK-N-SH_RA	brain:	n/a
6	chr10:116853118-116853168	T-47D	breast:	n/a
7	chr10:116849473-116849523	NB4	blood:	n/a
8	chr10:116697924-116697974	HIPEpiC	eye:	n/a
9	chr10:116852186-116852236	HPAEpiC	pulmonary alveolar:	n/a
10	chr10:116697898-116697948	IMR90	lung:	fetal
11	chr10:116697907-116697957	NT2-D1	testis:	n/a
12	chr10:116853468-116853518	Hela-S3	cervix:	n/a
13	chr10:116697070-116697120	HNPCEpiC	eye:	n/a
14	chr10:116852687-116852737	SAEC	small airway:	n/a
15	chr10:116853814-116853864	ovcar-3	ovarian:	n/a
16	chr10:116698451-116698501	HEK293	kidney:	embryo
17	chr10:116852811-116852861	Hepatocyte	liver:	n/a
18	chr10:116853118-116853168	NHBE	bronchial:	n/a
19	chr10:116698451-116698501	HCT-116	colon:	n/a
20	chr10:116809201-116809251	ECC-1	luminal epithelium:	n/a
21	chr10:116854028-116854078	HIPEpiC	eye:	n/a
22	chr10:116852811-116852861	ECC-1	luminal epithelium:	n/a
23	chr10:116678438-116678488	HRE	kidney:	n/a
24	chr10:116697985-116698035	SK-N-MC	brain:	n/a
25	chr10:116849473-116849523	SK-N-SH	brain:	n/a
26	chr10:116853664-116853714	HRE	kidney:	n/a
27	chr10:116852687-116852737	AoSMC	blood vessel:	n/a
28	chr10:116697070-116697120	IMR90	lung:	fetal
29	chr10:116698168-116698218	ProgFib	skin:	n/a
30	chr10:116697973-116698023	HNPCEpiC	eye:	n/a
31	chr10:116854028-116854078	Hela-S3	cervix:	n/a
32	chr10:116852470-116852520	HCPEpiC	choroid plexus:	n/a
33	chr10:116854028-116854078	SK-N-MC	brain:	n/a
34	chr10:116852186-116852236	NHBE	bronchial:	n/a
35	chr10:116852687-116852737	MCF10A-Er-Src	breast:	n/a
36	chr10:116853814-116853864	A549	lung:	n/a
37	chr10:116678438-116678488	NHBE	bronchial:	n/a
38	chr10:116697924-116697974	HEEpiC	esophagus:	n/a
39	chr10:116856408-116856458	MCF10A-Er-Src	breast:	n/a
40	chr10:116849473-116849523	Caco-2	colon:	n/a
41	chr10:116755155-116755205	HCT-116	colon:	n/a
42	chr10:116854028-116854078	AoSMC	blood vessel:	n/a
43	chr10:116697924-116697974	U87	brain:	n/a
44	chr10:116856408-116856458	GM12878	blood:	n/a
45	chr10:116852811-116852861	PrEC	prostate:	n/a
46	chr10:116697894-116697944	SK-N-SH	brain:	n/a
47	chr10:116698451-116698501	T-47D	breast:	n/a
48	chr10:116849473-116849523	AG04449	skin:	fetal
49	chr10:116856408-116856458	U87	brain:	n/a
50	chr10:116853664-116853714	AG09319	gingival:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:116691563..116693571-chr10:116695644..116697264,2	MCF-7	breast:
2	chr10:116682984..116685830-chr10:116689938..116692838,2	K562	blood:
3	chr10:116739587..116740088-chr8:43092410..43093248,2	MCF-7	breast:
4	chr10:116747111..116749787-chr10:116750033..116752654,2	MCF-7	breast:
5	chr10:116777335..116780032-chr10:116781033..116782789,3	MCF-7	breast:
6	chr10:116721231..116723812-chr10:116727155..116729844,2	K562	blood:
7	chr10:116782925..116784506-chr10:116795352..116797997,2	MCF-7	breast:
8	chr10:116751496..116754432-chr10:116766030..116768303,2	MCF-7	breast:
9	chr10:116702780..116705298-chr10:116717545..116719063,2	MCF-7	breast:
10	chr10:116696953..116700606-chr10:116852065..116855116,4	MCF-7	breast:
11	chr10:116698018..116699998-chr10:116702576..116705255,2	K562	blood:
12	chr10:116777335..116780032-chr10:116781033..116782789,3	MCF-7	breast:
13	chr10:116691563..116693571-chr10:116695644..116697264,2	MCF-7	breast:
14	chr10:116731834..116734462-chr10:116737301..116739152,2	K562	blood:
15	chr10:116668856..116672009-chr10:116672893..116675260,3	K562	blood:
16	chr10:116718109..116720528-chr10:116722759..116724977,2	K562	blood:
17	chr10:116704116..116706945-chr10:116736952..116739415,3	K562	blood:
18	chr10:116697085..116699595-chr10:116722929..116725734,2	MCF-7	breast:
19	chr10:116734818..116737513-chr10:116740129..116742144,2	MCF-7	breast:
20	chr10:116747111..116749787-chr10:116750033..116752654,2	MCF-7	breast:
21	chr10:116722299..116723812-chr10:116727808..116729844,2	K562	blood:
22	chr10:116697582..116698356-chr11:94964692..94965293,2	NB4	blood:
23	chr10:116697261..116699951-chr10:116709059..116711441,4	MCF-7	breast:
24	chr10:116697944..116699780-chr10:116701947..116704062,3	MCF-7	breast:
25	chr10:116704116..116706945-chr10:116736952..116739415,3	K562	blood:
26	chr10:116681770..116684136-chr10:116685910..116687423,2	MCF-7	breast:
27	chr10:116697590..116699653-chr10:116710525..116713221,2	MCF-7	breast:
28	chr10:116668856..116672009-chr10:116672893..116675260,3	K562	blood:
29	chr10:116697881..116698507-chr9:34619924..34620603,2	NB4	blood:
30	chr10:116702780..116705298-chr10:116717545..116719063,2	MCF-7	breast:
31	chr10:116666525..116669510-chr10:116698929..116700670,2	MCF-7	breast:
32	chr10:116869478..116872129-chr10:116874892..116876661,2	MCF-7	breast:
33	chr10:116696953..116700606-chr10:116852065..116855116,4	MCF-7	breast:
34	chr10:116681770..116684136-chr10:116685910..116687423,2	MCF-7	breast:
35	chr10:116731834..116734462-chr10:116737301..116739152,2	K562	blood:
36	chr10:116708122..116710473-chr10:116713973..116715764,2	MCF-7	breast:
37	chr10:116675458..116677157-chr10:116697462..116699320,2	MCF-7	breast:
38	chr10:116818326..116821419-chr10:116821811..116825642,4	K562	blood:
39	chr10:116696802..116699955-chr10:116713362..116716908,4	MCF-7	breast:
40	chr10:116698116..116699981-chr10:116719436..116721924,2	K562	blood:
41	chr10:116718109..116720528-chr10:116722759..116724977,2	K562	blood:
42	chr10:116734818..116737513-chr10:116740129..116742144,2	MCF-7	breast:
43	chr10:116682984..116685830-chr10:116689938..116692838,2	K562	blood:
44	chr10:116696911..116699473-chr10:116702208..116704843,4	MCF-7	breast:
45	chr10:116260065..116262593-chr10:116698525..116701420,2	MCF-7	breast:
46	chr10:116702154..116704292-chr10:116706734..116708655,2	K562	blood:
47	chr10:116666525..116669510-chr10:116698929..116700670,2	MCF-7	breast:
48	chr10:116782925..116784506-chr10:116795352..116797997,2	MCF-7	breast:
49	chr10:116818326..116821419-chr10:116821811..116825642,4	K562	blood:
50	chr10:116697901..116698524-chr14:74485364..74486290,2	NB4	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRUB1-1	chr10:116754301-116754688	NONHSAT016471
2	lnc-TRUB1-1	chr10:116755201-116755297	NONHSAT016471
3	lnc-TRUB1-3	chr10:116751175-116751631	NONHSAT016470
4	lnc-TRUB1-2	chr10:116746224-116746342	NONHSAT016469
5	lnc-TRUB1-1	chr10:116756233-116756352	NONHSAT016471
6	lnc-TRUB1-3	chr10:116751678-116751759	NONHSAT016470
7	lnc-TRUB1-2	chr10:116744406-116744534	NONHSAT016469
8	lnc-TRUB1-3	chr10:116751805-116751835	NONHSAT016470
9	lnc-TRUB1-1	chr10:116756234-116756352	XLOC_008629
10	lnc-TRUB1-2	chr10:116745192-116745287	NONHSAT016469
11	lnc-ABLIM1-4	chr10:116786294-116786531	NONHSAT016473
12	lnc-ABLIM1-4	chr10:116787612-116787799	NONHSAT016473
13	lnc-TRUB1-1	chr10:116755202-116755297	XLOC_008629
14	lnc-TRUB1-1	chr10:116754416-116754544	XLOC_008629

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TRUB1	hsa-miR-17-5p	chr10:116735871-116735894

Variant related genes	Relation type
ATRNL1	TF binding region
TRUB1	TF binding region
ENSG00000226428	TF binding region
RNU6-1121P	TF binding region
ENSG00000236799	TF binding region
ATRNL1	CpG island
TRUB1	CpG island
ENSG00000226428	CpG island
RNU6-1121P	CpG island
ENSG00000236799	CpG island
ENSG00000187097	chromatin interactions
ENSG00000107518	chromatin interactions
ENSG00000137100	chromatin interactions
ENSG00000236799	chromatin interactions
ENSG00000229668	chromatin interactions
ENSG00000119636	chromatin interactions
ENSG00000252611	chromatin interactions
ENSG00000245552	chromatin interactions
ENSG00000165832	chromatin interactions

Extended variants
information (count: 8023 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:8023 , 50 per page) page: 1 2 3 4 5 6 7 ... 161

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs567235077	chr10:116655060-116655061	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74158089	chr10:116655062-116655063	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs371845674	chr10:116655128-116655129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549830974	chr10:116655143-116655144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs571362788	chr10:116655193-116655194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186746402	chr10:116655195-116655196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558294293	chr10:116655278-116655279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149222113	chr10:116655285-116655286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190201154	chr10:116655290-116655291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139458843	chr10:116655316-116655317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555802992	chr10:116655320-116655321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs181701355	chr10:116655321-116655322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544195090	chr10:116655365-116655366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550904961	chr10:116655395-116655396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185997811	chr10:116655410-116655411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545174297	chr10:116655465-116655466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191108466	chr10:116655520-116655521	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554183899	chr10:116655528-116655529	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115257499	chr10:116655597-116655598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561146310	chr10:116655610-116655611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs531684428	chr10:116655612-116655613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549793956	chr10:116655622-116655623	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs537505967	chr10:116655648-116655649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532189382	chr10:116655659-116655660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10885628	chr10:116655660-116655661	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs183256164	chr10:116655674-116655675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534108454	chr10:116655707-116655708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs143215113	chr10:116655755-116655756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114996108	chr10:116655796-116655797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538156305	chr10:116655825-116655826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556091220	chr10:116655833-116655834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs187611805	chr10:116655935-116655936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75210259	chr10:116655950-116655951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553958213	chr10:116655952-116655953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs572532468	chr10:116655969-116655970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191223311	chr10:116655974-116655975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542455939	chr10:116655992-116655993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376424235	chr10:116656007-116656008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138813275	chr10:116656063-116656064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572778460	chr10:116656064-116656065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs543746757	chr10:116656080-116656081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs60727007	chr10:116656099-116656100	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs532028370	chr10:116656141-116656142	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs547406032	chr10:116656159-116656160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs559179397	chr10:116656212-116656213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529835461	chr10:116656259-116656260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549123903	chr10:116656282-116656283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs577381666	chr10:116656359-116656360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567520639	chr10:116656364-116656365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs74345821	chr10:116656399-116656400	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:3055 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116642200-116655800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:116655400-116655800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr10:116655600-116656800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr10:116655800-116656200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr10:116655800-116657200	Enhancers	H1 Cell Line	embryonic stem cell
6	chr10:116655800-116657200	Enhancers	HMEC	breast
7	chr10:116656000-116656600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr10:116656000-116656600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr10:116656000-116656800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr10:116656000-116657200	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr10:116656000-116657200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr10:116656200-116657200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr10:116656200-116657200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr10:116656400-116656600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr10:116656400-116657200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr10:116656400-116657200	Enhancers	NHEK	skin
17	chr10:116656600-116660400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:116657800-116658000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr10:116658200-116661400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr10:116660400-116660800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr10:116660600-116660800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr10:116660800-116666200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr10:116660800-116666400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:116660800-116676400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:116661400-116661800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr10:116661400-116662000	Enhancers	A549	lung
27	chr10:116661400-116662400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr10:116661400-116662400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr10:116661600-116662400	Enhancers	HSMMtube	muscle
30	chr10:116661600-116662400	Enhancers	Osteobl	bone
31	chr10:116661600-116662600	Enhancers	Muscle Satellite Cultured Cells	--
32	chr10:116661800-116662000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr10:116661800-116662200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr10:116661800-116662400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr10:116661800-116662400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr10:116661800-116662400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:116661800-116662400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr10:116661800-116662400	Enhancers	HSMM	muscle
39	chr10:116661800-116662400	Enhancers	NH-A	brain
40	chr10:116662000-116662200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr10:116662000-116664200	Weak transcription	A549	lung
42	chr10:116662200-116662400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr10:116662200-116666200	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr10:116662400-116662600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr10:116662400-116664600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr10:116662400-116664600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr10:116662400-116664800	Weak transcription	Osteobl	bone
48	chr10:116662400-116665000	Weak transcription	HSMMtube	muscle
49	chr10:116662400-116671000	Weak transcription	NH-A	brain
50	chr10:116662600-116664600	Weak transcription	Muscle Satellite Cultured Cells	--

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