Variant report

Variant	nsv1036645
Chromosome Location	chr10:52804961-53159076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1803)
CpG islands
(count:1893)
Chromatin interactive
region (count:56)
LncRNA
region (count:8)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1803 , 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	chr10:52823525-52823717	HepG2	liver:	n/a	n/a
2	ATF1	chr10:52852243-52852266	K562	blood:	n/a	n/a
3	BACH1	chr10:52846737-52846747	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:52833419-52834110	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr10:53141090-53141352	GM12878	blood:	n/a	n/a
6	BATF	chr10:52873506-52873775	GM12878	blood:	n/a	n/a
7	BATF	chr10:53141142-53141352	GM12878	blood:	n/a	n/a
8	BATF	chr10:52842750-52843001	GM12878	blood:	n/a	n/a
9	BCLAF1	chr10:53149066-53149376	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:53149192-53149350	K562	blood:	n/a	n/a
11	BHLHE40	chr10:53116577-53116594	A549	lung:	n/a	n/a
12	BRCA1	chr10:53141091-53141633	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr10:52835646-52835901	K562	blood:	n/a	n/a
14	CEBPB	chr10:52860110-52860230	IMR90	lung:	n/a	chr10:52860125-52860136
15	CEBPB	chr10:52903944-52904299	HepG2	liver:	n/a	chr10:52904113-52904124
16	CEBPB	chr10:53141070-53141763	Hela-S3	cervix:	n/a	chr10:53141351-53141359
17	CEBPB	chr10:52903939-52904300	IMR90	lung:	n/a	chr10:52904113-52904124
18	CEBPB	chr10:52918031-52918256	IMR90	lung:	n/a	chr10:52918075-52918086
19	CEBPB	chr10:52840363-52840576	Hela-S3	cervix:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
20	CEBPB	chr10:53010289-53010617	IMR90	lung:	n/a	chr10:53010468-53010479 chr10:53010467-53010478 chr10:53010467-53010480 chr10:53010467-53010480
21	CEBPB	chr10:52891288-52891607	A549	lung:	n/a	chr10:52891436-52891447
22	CEBPB	chr10:53081605-53082063	IMR90	lung:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
23	CEBPB	chr10:52835578-52835941	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr10:53104142-53104419	IMR90	lung:	n/a	n/a
25	CEBPB	chr10:52917983-52918173	HepG2	liver:	n/a	chr10:52918075-52918086
26	CEBPB	chr10:53057215-53057551	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:53004743-53004973	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr10:52964585-52964785	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:53020902-53020958	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr10:52903985-52904252	H1-hESC	embryonic stem cell:	n/a	chr10:52904113-52904124
31	CEBPB	chr10:52840318-52840628	H1-hESC	embryonic stem cell:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
32	CEBPB	chr10:52984449-52984925	Hela-S3	cervix:	n/a	chr10:52984830-52984841
33	CEBPB	chr10:53081693-53081969	MCF-7	breast:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
34	CEBPB	chr10:53081676-53082033	A549	lung:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
35	CEBPB	chr10:52902042-52902176	A549	lung:	n/a	chr10:52902108-52902121
36	CEBPB	chr10:53081709-53081988	K562	blood:	n/a	chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081860-53081869 chr10:53081859-53081870
37	CEBPB	chr10:53041673-53042000	HepG2	liver:	n/a	chr10:53041816-53041827
38	CEBPB	chr10:52965168-52965306	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr10:52835586-52835897	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr10:52967991-52968093	HepG2	liver:	n/a	chr10:52968050-52968061 chr10:52968060-52968072
41	CEBPB	chr10:52931819-52932091	HepG2	liver:	n/a	chr10:52931956-52931967 chr10:52931937-52931950 chr10:52931958-52931969 chr10:52931937-52931948
42	CEBPB	chr10:52835575-52835945	A549	lung:	n/a	n/a
43	CEBPB	chr10:52977840-52978269	IMR90	lung:	n/a	chr10:52977864-52977875 chr10:52978136-52978149
44	CEBPB	chr10:52907708-52907998	IMR90	lung:	n/a	chr10:52907853-52907864
45	CEBPB	chr10:52891379-52891579	H1-hESC	embryonic stem cell:	n/a	chr10:52891436-52891447
46	CEBPB	chr10:52824024-52824139	A549	lung:	n/a	chr10:52824068-52824079
47	CEBPB	chr10:52871231-52871495	IMR90	lung:	n/a	n/a
48	CEBPB	chr10:52984424-52984952	HepG2	liver:	n/a	chr10:52984830-52984841
49	CEBPB	chr10:52840279-52840625	IMR90	lung:	n/a	chr10:52840440-52840451 chr10:52840439-52840452 chr10:52840439-52840450
50	CEBPB	chr10:52954533-52954712	HepG2	liver:	n/a	chr10:52954559-52954570

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:52984440-52984490	NB4	blood:	n/a
2	chr10:52834093-52834143	GM06990	blood:	n/a
3	chr10:52984440-52984490	NB4	blood:	n/a
4	chr10:52834093-52834143	GM06990	blood:	n/a
5	chr10:52833444-52833494	Hepatocyte	liver:	n/a
6	chr10:52835078-52835128	IMR90	lung:	fetal
7	chr10:52833444-52833494	HL-60	blood:	n/a
8	chr10:53004308-53004358	K562	blood:	n/a
9	chr10:52974426-52974476	H1-hESC	embryonic stem cell:	embryo
10	chr10:52984440-52984490	HCT-116	colon:	n/a
11	chr10:53143287-53143337	GM12891	blood:	n/a
12	chr10:52976168-52976218	PFSK-1	brain:	n/a
13	chr10:53004308-53004358	HEK293	kidney:	embryo
14	chr10:52974426-52974476	HEK293	kidney:	embryo
15	chr10:53137547-53137597	HL-60	blood:	n/a
16	chr10:53149243-53149293	AG09309	skin:	n/a
17	chr10:52840377-52840427	HCPEpiC	choroid plexus:	n/a
18	chr10:52984440-52984490	GM12891	blood:	n/a
19	chr10:53143287-53143337	H1-hESC	embryonic stem cell:	embryo
20	chr10:52843235-52843285	SK-N-MC	brain:	n/a
21	chr10:52834676-52834726	AG04450	lung:	fetal
22	chr10:52843235-52843285	NB4	blood:	n/a
23	chr10:53071348-53071398	NB4	blood:	n/a
24	chr10:52829575-52829625	BE2_C	brain:	n/a
25	chr10:52834189-52834239	NT2-D1	testis:	n/a
26	chr10:53058473-53058523	PrEC	prostate:	n/a
27	chr10:52984440-52984490	HepG2	liver:	n/a
28	chr10:52963388-52963438	GM19239	blood:	n/a
29	chr10:52976168-52976218	LNCaP	prostate:	n/a
30	chr10:52834498-52834548	BE2_C	brain:	n/a
31	chr10:52834676-52834726	GM12891	blood:	n/a
32	chr10:52834498-52834548	GM12878	blood:	n/a
33	chr10:52833902-52833952	PANC-1	pancreas:	n/a
34	chr10:53149243-53149293	SK-N-SH	brain:	n/a
35	chr10:53004308-53004358	AG04450	lung:	fetal
36	chr10:52829575-52829625	NB4	blood:	n/a
37	chr10:52833902-52833952	NH-A	brain:	n/a
38	chr10:53071348-53071398	AG10803	skin:	n/a
39	chr10:53058473-53058523	HIPEpiC	eye:	n/a
40	chr10:52834121-52834171	AG04450	lung:	fetal
41	chr10:52840377-52840427	NH-A	brain:	n/a
42	chr10:53149243-53149293	HPAEpiC	pulmonary alveolar:	n/a
43	chr10:53137547-53137597	HRCEpiC	kidney:	n/a
44	chr10:52833610-52833660	ProgFib	skin:	n/a
45	chr10:52898733-52898783	GM19239	blood:	n/a
46	chr10:52834189-52834239	GM06990	blood:	n/a
47	chr10:52840377-52840427	AG09319	gingival:	n/a
48	chr10:52840377-52840427	HPAEpiC	pulmonary alveolar:	n/a
49	chr10:53071348-53071398	Hepatocyte	liver:	n/a
50	chr10:52834676-52834726	ProgFib	skin:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:53134398..53136579-chr10:53137759..53139607,2	K562	blood:
2	chr10:52855387..52858289-chr10:52859088..52861078,2	K562	blood:
3	chr10:52860891..52863860-chr11:62621758..62623546,2	K562	blood:
4	chr10:53148869..53149613-chr10:53763797..53764717,2	MCF-7	breast:
5	chr10:52928917..52931370-chr10:52940832..52942855,2	K562	blood:
6	chr10:53098772..53100977-chr10:53116314..53119071,2	K562	blood:
7	chr10:53008618..53010801-chr10:53013381..53015189,3	K562	blood:
8	chr10:52900464..52903171-chr10:52913931..52915447,2	MCF-7	breast:
9	chr10:53134398..53136579-chr10:53137759..53139607,2	K562	blood:
10	chr10:52845255..52847999-chr10:52848856..52851821,2	K562	blood:
11	chr10:52855387..52858289-chr10:52859088..52861078,2	K562	blood:
12	chr10:53149203..53149747-chr10:53635097..53636033,2	MCF-7	breast:
13	chr10:52823077..52823678-chr10:53719716..53720617,2	MCF-7	breast:
14	chr10:52945796..52948103-chr10:52948624..52950543,2	K562	blood:
15	chr10:52770367..52771306-chr10:52807728..52808411,3	MCF-7	breast:
16	chr10:52912333..52914102-chr10:52919856..52922632,2	MCF-7	breast:
17	chr10:53000277..53002226-chr10:53004321..53006404,2	K562	blood:
18	chr10:52942150..52943804-chr10:52944403..52946743,2	K562	blood:
19	chr10:53091191..53095808-chr10:53099838..53103049,4	K562	blood:
20	chr10:53145130..53146653-chr10:54068648..54071560,2	K562	blood:
21	chr10:53008618..53010801-chr10:53013381..53015189,3	K562	blood:
22	chr10:52832484..52833988-chr10:52835992..52837513,2	K562	blood:
23	chr10:52928917..52931370-chr10:52940832..52942855,2	K562	blood:
24	chr10:52839499..52841510-chr10:52846608..52849576,2	K562	blood:
25	chr10:52945796..52948103-chr10:52948624..52950543,2	K562	blood:
26	chr10:52942150..52943804-chr10:52944403..52946743,2	K562	blood:
27	chr10:52805414..52807391-chr10:52810252..52811808,2	MCF-7	breast:
28	chr10:52953285..52955453-chr10:52955956..52958454,2	MCF-7	breast:
29	chr10:52839499..52841510-chr10:52846608..52849576,2	K562	blood:
30	chr10:52973848..52976452-chr10:52979650..52982235,2	MCF-7	breast:
31	chr10:53146560..53148101-chr10:53149083..53151252,2	MCF-7	breast:
32	chr10:53150184..53151965-chr10:53152581..53154476,2	K562	blood:
33	chr10:53148841..53149455-chr10:53652709..53653694,2	MCF-7	breast:
34	chr10:52823455..52824113-chr10:53182409..53182910,2	MCF-7	breast:
35	chr10:53150184..53151965-chr10:53152581..53154476,2	K562	blood:
36	chr10:52805414..52807391-chr10:52810252..52811808,2	MCF-7	breast:
37	chr10:53008618..53010640-chr10:53013381..53015189,2	K562	blood:
38	chr10:52900464..52903171-chr10:52913931..52915447,2	MCF-7	breast:
39	chr10:53098772..53100977-chr10:53116314..53119071,2	K562	blood:
40	chr10:53149205..53149730-chr10:53720127..53720824,2	MCF-7	breast:
41	chr10:52824508..52825384-chr17:56387619..56388193,2	MCF-7	breast:
42	chr10:52823519..52824020-chr10:53763789..53764326,2	MCF-7	breast:
43	chr10:52973848..52976452-chr10:52979650..52982235,2	MCF-7	breast:
44	chr10:53146560..53148101-chr10:53149083..53151252,2	MCF-7	breast:
45	chr10:52770484..52771339-chr10:52807377..52808118,3	MCF-7	breast:
46	chr10:52984696..52986392-chr10:53018336..53020821,2	K562	blood:
47	chr10:52852996..52855697-chr10:52862209..52864368,2	MCF-7	breast:
48	chr10:52761120..52762328-chr10:52807357..52808643,3	MCF-7	breast:
49	chr10:53008618..53010640-chr10:53013381..53015189,2	K562	blood:
50	chr10:52984696..52986392-chr10:53018336..53020821,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASAH2B-4	chr10:53066329-53066469	ENSG00000235279.1
2	lnc-ASAH2B-6	chr10:53079586-53080420	NONHSAT013412
3	lnc-A1CF-1	chr10:52822339-52822690	ENSG00000223502.1
4	lnc-A1CF-3	chr10:53005249-53005366	ENSG00000231132.1
5	lnc-A1CF-3	chr10:53004654-53004895	ENSG00000231132.1
6	lnc-ASAH2B-4	chr10:53062326-53062584	ENSG00000235279.1
7	lnc-A1CF-3	chr10:53005481-53005566	ENSG00000231132.1
8	lnc-A1CF-1	chr10:52828245-52828313	ENSG00000223502.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-605-5p	chr10:53059348-53059370	MIMAT0003273
hsa-miR-605-3p	chr10:53059383-53059404	MIMAT0026621

No data

Variant related genes	Relation type
ENSG00000235279	TF binding region
ENSG00000223502	TF binding region
ENSG00000266591	TF binding region
PRKG1	TF binding region
ENSG00000231132	TF binding region
MIR605	TF binding region
RSU1P3	TF binding region
ENSG00000235279	CpG island
ENSG00000223502	CpG island
ENSG00000266591	CpG island
PRKG1	CpG island
ENSG00000231132	CpG island
MIR605	CpG island
RSU1P3	CpG island
ENSG00000168003	chromatin interactions
ENSG00000124006	chromatin interactions
ENSG00000005379	chromatin interactions
ENSG00000255717	chromatin interactions
ENSG00000185532	chromatin interactions
ENSG00000123999	chromatin interactions
ENSG00000231132	chromatin interactions
BCL9	Mature miRNA region
TCEAL1	Mature miRNA region
TP53	Mature miRNA region
DRG1	Mature miRNA region
TMEM64	Mature miRNA region
TRAF4	Mature miRNA region
MDM2	Mature miRNA region
YBX1	Mature miRNA region
KDM5C	Mature miRNA region
SEC24D	Mature miRNA region

Extended variants
information (count: 13001 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:13001 , 50 per page) page: 1 2 3 4 5 6 7 ... 261

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547101306	chr10:52805067-52805068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113146187	chr10:52805068-52805069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs143630857	chr10:52805088-52805089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201453377	chr10:52805096-52805097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373964549	chr10:52805121-52805122	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs536945190	chr10:52805131-52805132	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs550606298	chr10:52805139-52805140	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs187877852	chr10:52805144-52805145	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs192441128	chr10:52805156-52805157	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs553406706	chr10:52805182-52805183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs559628696	chr10:52805191-52805192	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs148092477	chr10:52805214-52805215	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371859032	chr10:52805234-52805235	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs558986462	chr10:52805236-52805237	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183033921	chr10:52805239-52805240	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs544877242	chr10:52805246-52805247	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs187360483	chr10:52805286-52805287	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs529855381	chr10:52805287-52805288	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs574947824	chr10:52805328-52805329	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs370037557	chr10:52805337-52805338	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs377070072	chr10:52805370-52805371	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs540447975	chr10:52805372-52805373	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs560771462	chr10:52805375-52805376	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs528164034	chr10:52805443-52805444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs551108798	chr10:52805467-52805468	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs191697629	chr10:52805509-52805510	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs530435749	chr10:52805514-52805515	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs550819637	chr10:52805524-52805525	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs567473146	chr10:52805567-52805568	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs530034055	chr10:52805617-52805618	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs184587789	chr10:52805642-52805643	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs546465018	chr10:52805657-52805658	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141874013	chr10:52805697-52805698	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs539086829	chr10:52805721-52805722	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs150215553	chr10:52805804-52805805	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs569240079	chr10:52805814-52805815	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs537873439	chr10:52805860-52805861	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs369583932	chr10:52805873-52805874	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs554976409	chr10:52805877-52805878	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs138892442	chr10:52805918-52805919	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs141743319	chr10:52805927-52805928	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs146255158	chr10:52805947-52805948	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549798358	chr10:52805956-52805957	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs139371751	chr10:52806038-52806039	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs551660574	chr10:52806056-52806057	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs142669448	chr10:52806116-52806117	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530399541	chr10:52806175-52806176	Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563299000	chr10:52806272-52806273	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543843783	chr10:52806301-52806302	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs143858810	chr10:52806320-52806321	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Thoracic aortic aneurysm	21092924	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
Autism	22495311	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Chronic lymphocytic leukemia	21546498	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21785460	CNVD
Intellectual disability	21948486	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Cancer	20164920	CNVD
Ollier disease	21235737	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:2799 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:52796600-52806800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr10:52796600-52806800	Weak transcription	Fetal Stomach	stomach
3	chr10:52804200-52805800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr10:52804200-52807800	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr10:52805800-52806000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:52805800-52807000	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr10:52806000-52806400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr10:52806200-52806600	Active TSS	Right Atrium	heart
9	chr10:52806200-52806800	Active TSS	Aorta	Aorta
10	chr10:52806200-52808400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:52806400-52806600	Enhancers	HSMMtube	muscle
12	chr10:52806400-52808200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr10:52806600-52810400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr10:52806800-52807000	Flanking Active TSS	Aorta	Aorta
15	chr10:52806800-52807000	Enhancers	Fetal Stomach	stomach
16	chr10:52806800-52809000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr10:52807000-52807600	Enhancers	Aorta	Aorta
18	chr10:52807000-52808400	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr10:52807000-52812400	Weak transcription	Fetal Stomach	stomach
20	chr10:52807400-52807600	Enhancers	Right Atrium	heart
21	chr10:52807600-52808200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr10:52807600-52821000	Weak transcription	Aorta	Aorta
23	chr10:52807800-52809000	Enhancers	Skeletal Muscle Female	skeletal muscle
24	chr10:52808400-52810400	Enhancers	Skeletal Muscle Male	skeletal muscle
25	chr10:52808400-52814000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr10:52809000-52810000	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr10:52810000-52810200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:52810000-52811000	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr10:52810200-52811000	Enhancers	Fetal Lung	lung
30	chr10:52810400-52811200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr10:52811000-52812200	Weak transcription	Fetal Lung	lung
32	chr10:52811000-52812200	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr10:52812200-52812600	Enhancers	Fetal Lung	lung
34	chr10:52812400-52812600	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr10:52812400-52812800	Enhancers	Fetal Stomach	stomach
36	chr10:52813200-52814400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr10:52814000-52814200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr10:52821000-52821200	Enhancers	Aorta	Aorta
39	chr10:52821200-52821600	Weak transcription	Aorta	Aorta
40	chr10:52821600-52821800	Active TSS	Aorta	Aorta
41	chr10:52823200-52824000	Enhancers	Rectal Smooth Muscle	rectum
42	chr10:52823400-52823600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr10:52823600-52824200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr10:52823600-52825000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr10:52823800-52824200	Enhancers	NHLF	lung
46	chr10:52824000-52825200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr10:52824600-52825200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr10:52825000-52825200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:52825200-52826000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr10:52825200-52832600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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