Variant report

Variant	esv2758218
Chromosome Location	chr10:48593396-49299273
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2126)
CpG islands
(count:1528)
Chromatin interactive
region (count:16)
LncRNA
region (count:54)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2126 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:48659844-48660072	K562	blood:	n/a	n/a
2	BACH1	chr10:48649027-48649045	K562	blood:	n/a	n/a
3	BATF	chr10:48989549-48989912	GM12878	blood:	n/a	n/a
4	BATF	chr10:48952428-48952658	GM12878	blood:	n/a	n/a
5	BATF	chr10:48714324-48714566	GM12878	blood:	n/a	n/a
6	BATF	chr10:48956676-48956928	GM12878	blood:	n/a	chr10:48956771-48956782
7	BATF	chr10:48951827-48952054	GM12878	blood:	n/a	chr10:48951972-48951982
8	BATF	chr10:48989552-48989844	GM12878	blood:	n/a	n/a
9	BATF	chr10:48956627-48956981	GM12878	blood:	n/a	chr10:48956771-48956782
10	BCL11A	chr10:48956689-48956877	GM12878	blood:	n/a	n/a
11	BCL11A	chr10:48989531-48989902	GM12878	blood:	n/a	chr10:48989690-48989699
12	BCL11A	chr10:48952136-48952344	GM12878	blood:	n/a	n/a
13	BCL11A	chr10:49005020-49005346	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:48989616-48989790	GM12878	blood:	n/a	chr10:48989690-48989699
15	BCL11A	chr10:49005038-49005190	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:48956608-48956947	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:49080042-49080383	HepG2	liver:	n/a	n/a
18	BHLHE40	chr10:49045988-49046173	HepG2	liver:	n/a	n/a
19	BRCA1	chr10:49199990-49200190	Hela-S3	cervix:	n/a	n/a
20	CBX3	chr10:48952273-48952700	K562	blood:	n/a	n/a
21	CBX3	chr10:49249785-49250052	K562	blood:	n/a	n/a
22	CEBPB	chr10:48813073-48813507	K562	blood:	n/a	n/a
23	CEBPB	chr10:48813184-48813461	K562	blood:	n/a	n/a
24	CEBPB	chr10:49068108-49068463	K562	blood:	n/a	n/a
25	CEBPB	chr10:48659832-48660070	HepG2	liver:	n/a	chr10:48660044-48660057 chr10:48659964-48659975
26	CEBPB	chr10:48597243-48597394	HepG2	liver:	n/a	chr10:48597246-48597257 chr10:48597247-48597258
27	CEBPB	chr10:48601398-48602420	IMR90	lung:	n/a	n/a
28	CEBPB	chr10:49068168-49068380	K562	blood:	n/a	n/a
29	CEBPB	chr10:49197254-49197290	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr10:49272320-49272583	K562	blood:	n/a	n/a
31	CEBPB	chr10:48658854-48659191	HepG2	liver:	n/a	chr10:48659013-48659024
32	CEBPB	chr10:49004870-49005359	GM12878	blood:	n/a	n/a
33	CEBPB	chr10:49199984-49200016	HepG2	liver:	n/a	chr10:49199988-49199999
34	CEBPB	chr10:48751748-48752065	K562	blood:	n/a	n/a
35	CEBPB	chr10:48622391-48622901	IMR90	lung:	n/a	n/a
36	CEBPB	chr10:49199814-49200190	A549	lung:	n/a	chr10:49199988-49199999
37	CEBPB	chr10:48658860-48659208	K562	blood:	n/a	chr10:48659013-48659024
38	CEBPB	chr10:49199799-49200207	Hela-S3	cervix:	n/a	chr10:49199988-49199999
39	CEBPB	chr10:48634732-48635593	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:49046671-49046868	IMR90	lung:	n/a	chr10:49046694-49046707 chr10:49046696-49046705 chr10:49046696-49046705 chr10:49046696-49046705
41	CEBPB	chr10:48661944-48662298	IMR90	lung:	n/a	n/a
42	CEBPB	chr10:48658877-48659172	IMR90	lung:	n/a	chr10:48659013-48659024
43	CEBPB	chr10:48659830-48660156	A549	lung:	n/a	chr10:48660044-48660057 chr10:48659964-48659975
44	CEBPB	chr10:48658947-48659068	H1-hESC	embryonic stem cell:	n/a	chr10:48659013-48659024
45	CEBPB	chr10:48601463-48601780	A549	lung:	n/a	n/a
46	CEBPB	chr10:48648049-48648537	ECC-1	luminal epithelium:	n/a	n/a
47	CEBPB	chr10:48659802-48660302	IMR90	lung:	n/a	chr10:48660044-48660057 chr10:48659964-48659975
48	CEBPB	chr10:48648077-48648459	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPD	chr10:48813141-48813550	K562	blood:	n/a	n/a
50	CEBPD	chr10:48954264-48954686	K562	blood:	n/a	n/a

(count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:48634114-48634164	HRE	kidney:	n/a
2	chr10:48950242-48950292	RPTEC	kidney:	n/a
3	chr10:48634114-48634164	AG04449	skin:	fetal
4	chr10:48634114-48634164	HRE	kidney:	n/a
5	chr10:48950242-48950292	RPTEC	kidney:	n/a
6	chr10:48634114-48634164	AG04449	skin:	fetal
7	chr10:48949616-48949666	ProgFib	skin:	n/a
8	chr10:48855211-48855261	HRCEpiC	kidney:	n/a
9	chr10:48902368-48902418	MCF-7	breast:	n/a
10	chr10:49218579-49218629	SK-N-SH	brain:	n/a
11	chr10:48855211-48855261	K562	blood:	n/a
12	chr10:48855211-48855261	HUVEC	blood vessel:	n/a
13	chr10:48902368-48902418	HepG2	liver:	n/a
14	chr10:48807252-48807302	LNCaP	prostate:	n/a
15	chr10:48623215-48623265	AG09319	gingival:	n/a
16	chr10:48899772-48899822	HCF	heart:	n/a
17	chr10:48899772-48899822	RPTEC	kidney:	n/a
18	chr10:48807252-48807302	AG04449	skin:	fetal
19	chr10:48623215-48623265	Jurkat	blood:	n/a
20	chr10:48949616-48949666	GM12878	blood:	n/a
21	chr10:48807341-48807391	AG04449	skin:	fetal
22	chr10:48660050-48660100	Caco-2	colon:	n/a
23	chr10:48899772-48899822	HPAEpiC	pulmonary alveolar:	n/a
24	chr10:49205543-49205593	BJ	skin:	n/a
25	chr10:48660050-48660100	HRE	kidney:	n/a
26	chr10:48807341-48807391	GM12892	blood:	n/a
27	chr10:48807252-48807302	HRPEpiC	eye:	n/a
28	chr10:48601822-48601872	HIPEpiC	eye:	n/a
29	chr10:48807252-48807302	MCF-7	breast:	n/a
30	chr10:48905601-48905651	K562	blood:	n/a
31	chr10:48965159-48965209	SKMC	muscle:	n/a
32	chr10:48898075-48898125	BJ	skin:	n/a
33	chr10:48623215-48623265	K562	blood:	n/a
34	chr10:48760449-48760499	T-47D	breast:	n/a
35	chr10:48828106-48828156	ovcar-3	ovarian:	n/a
36	chr10:48660050-48660100	ovcar-3	ovarian:	n/a
37	chr10:48634114-48634164	ovcar-3	ovarian:	n/a
38	chr10:49218579-49218629	SKMC	muscle:	n/a
39	chr10:48807252-48807302	IMR90	lung:	fetal
40	chr10:49218579-49218629	HCM	heart:	n/a
41	chr10:48855211-48855261	BE2_C	brain:	n/a
42	chr10:49205543-49205593	HIPEpiC	eye:	n/a
43	chr10:48660050-48660100	NHDF-neo	bronchial:	n/a
44	chr10:49218579-49218629	SK-N-SH_RA	brain:	n/a
45	chr10:48828109-48828159	NHDF-neo	bronchial:	n/a
46	chr10:48898075-48898125	HRE	kidney:	n/a
47	chr10:48899772-48899822	K562	blood:	n/a
48	chr10:48981581-48981631	HMEC	breast:	n/a
49	chr10:48601822-48601872	AG09319	gingival:	n/a
50	chr10:48623215-48623265	HMEC	breast:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:48631773..48635312-chr10:48638153..48641553,3	MCF-7	breast:
2	chr10:48574920..48577214-chr10:48596773..48599642,2	K562	blood:
3	chr10:48621142..48624293-chr10:48626876..48630799,3	K562	blood:
4	chr10:48631773..48635312-chr10:48638153..48641553,3	MCF-7	breast:
5	chr10:48595136..48596866-chr10:48604058..48606210,2	K562	blood:
6	chr10:48621884..48623411-chr10:48639407..48642353,2	MCF-7	breast:
7	chr10:48613560..48615529-chr10:48619856..48622729,2	K562	blood:
8	chr10:48595136..48596866-chr10:48604058..48606210,2	K562	blood:
9	chr10:48644628..48646786-chr10:48648332..48651407,3	K562	blood:
10	chr10:48621884..48623411-chr10:48639407..48642353,2	MCF-7	breast:
11	chr10:48585104..48587866-chr10:48597542..48600033,2	MCF-7	breast:
12	chr10:48635828..48638231-chr10:48639241..48640747,2	MCF-7	breast:
13	chr10:48635828..48638231-chr10:48639241..48640747,2	MCF-7	breast:
14	chr10:48621142..48624293-chr10:48626876..48630799,3	K562	blood:
15	chr10:48613560..48615529-chr10:48619856..48622729,2	K562	blood:
16	chr10:48644628..48646786-chr10:48648332..48651407,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPN20B-6	chr10:48608127-48608457	NONHSAT013226
2	lnc-MAPK8-2	chr10:48954322-48954975	NONHSAT013244
3	lnc-PTPN20B-6	chr10:48609115-48609274	NONHSAT013227
4	lnc-FAM25C-1	chr10:49205711-49205776	NONHSAT013257
5	lnc-PTPN20B-6	chr10:48608127-48608457	NONHSAT013227
6	lnc-PTPN20B-2	chr10:48987596-48988451	NONHSAT013248
7	lnc-GDF10-4	chr10:48738573-48738686	NONHSAT013233
8	lnc-PTPN20B-4	chr10:48652401-48652789	NONHSAT013230
9	lnc-FAM25C-3	chr10:49090136-49090419	NONHSAT013255
10	lnc-GDF10-4	chr10:48739388-48739450	NONHSAT013232
11	lnc-PTPN20B-2	chr10:48987596-48988451	NONHSAT013249
12	lnc-MAPK8-2	chr10:48966878-48966933	NONHSAT013243
13	lnc-GDF10-4	chr10:48739388-48739450	NONHSAT013233
14	lnc-MAPK8-2	chr10:48966878-48966933	NONHSAT013244
15	lnc-GDF10-4	chr10:48792687-48792799	NONHSAT013232
16	lnc-GDF10-4	chr10:48827520-48827581	NONHSAT013233
17	lnc-GDF10-4	chr10:48795347-48795444	NONHSAT013233
18	lnc-PTPN20B-1	chr10:49244690-49248867	NONHSAT013237
19	lnc-FAM25C-1	chr10:49199717-49199881	NONHSAT013256
20	lnc-MAPK8-2	chr10:48968560-48968623	NONHSAT013243
21	lnc-PTPN20B-2	chr10:48989082-48989262	XLOC_008814
22	lnc-PTPN20B-2	chr10:48987655-48988451	NONHSAT013251
23	lnc-PTPN20B-4	chr10:48655653-48655688	NONHSAT013230
24	lnc-GDF10-4	chr10:48795347-48795444	NONHSAT013232
25	lnc-PTPN20B-1	chr10:48927413-48927432	NONHSAT013237
26	lnc-GDF10-4	chr10:48792520-48792799	NONHSAT013234
27	lnc-MAPK8-2	chr10:48953761-48954799	NONHSAT013242
28	lnc-PTPN20B-2	chr10:48989140-48989262	XLOC_008814
29	lnc-PTPN20B-2	chr10:48987630-48988451	XLOC_008814
30	lnc-PTPN20B-2	chr10:48989082-48989267	NONHSAT013249
31	lnc-FAM25C-1	chr10:49199649-49199824	NONHSAT013257
32	lnc-FAM25C-1	chr10:49195626-49195779	NONHSAT013256
33	lnc-GDF10-4	chr10:48792687-48792799	NONHSAT013233
34	lnc-PTPN20B-2	chr10:48988121-48988451	XLOC_008814
35	lnc-PTPN20B-2	chr10:48989140-48989262	NONHSAT013251
36	lnc-PTPN20B-2	chr10:48989140-48989267	NONHSAT013248
37	lnc-PTPN20B-5	chr10:48643921-48644058	NONHSAT013228
38	lnc-PTPN20B-2	chr10:49018309-49018413	XLOC_008814
39	lnc-PTPN20B-2	chr10:48989109-48989268	XLOC_008814
40	lnc-PTPN20B-6	chr10:48618576-48618772	NONHSAT013226
41	lnc-MAPK8-2	chr10:48962529-48962620	NONHSAT013242
42	lnc-PTPN20B-5	chr10:48642776-48642962	NONHSAT013228
43	lnc-GDF10-4	chr10:48806829-48806896	NONHSAT013234
44	lnc-MAPK8-2	chr10:48954138-48954797	NONHSAT013243
45	lnc-PTPN20B-2	chr10:48998570-48998768	NONHSAT013251
46	lnc-PTPN20B-2	chr10:48988121-48988451	XLOC_008814
47	lnc-MAPK8-2	chr10:48980202-48980269	NONHSAT013243
48	lnc-GDF10-4	chr10:48827861-48827934	NONHSAT013232
49	lnc-MAPK8-2	chr10:48954405-48958083	NONHSAT013245
50	lnc-GDF10-4	chr10:48737040-48738686	NONHSAT013232

No data

Variant related genes	Relation type
FAM25C	TF binding region
BMS1P7	TF binding region
PTPN20B	TF binding region
DUSP8P1	TF binding region
RNA5SP315	TF binding region
BMS1P5	TF binding region
RN7SL527P	TF binding region
FAM35EP	TF binding region
FRMPD2P1	TF binding region
CTGLF12P	TF binding region
CTSLP3	TF binding region
ENSG00000232426	TF binding region
GLUD1P2	TF binding region
RNA5SP314	TF binding region
FAM25C	CpG island
BMS1P7	CpG island
PTPN20B	CpG island
DUSP8P1	CpG island
RNA5SP315	CpG island
BMS1P5	CpG island
RN7SL527P	CpG island
FAM35EP	CpG island
FRMPD2P1	CpG island
CTGLF12P	CpG island
CTSLP3	CpG island
ENSG00000232426	CpG island
GLUD1P2	CpG island
RNA5SP314	CpG island
MED28	miRNA target sites
MED8	miRNA target sites
MED6	miRNA target sites

Extended variants
information (count: 3572 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:3572 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559879016	chr10:48593405-48593406	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs896571	chr10:48593438-48593439	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs137897993	chr10:48593459-48593460	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552776159	chr10:48593507-48593508	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530951798	chr10:48593552-48593553	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs896570	chr10:48593635-48593636	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs190270181	chr10:48593644-48593645	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs142333677	chr10:48593707-48593708	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs146034871	chr10:48593721-48593722	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376052412	chr10:48593722-48593723	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs202001359	chr10:48593755-48593756	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9422325	chr10:48593767-48593768	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs71023192	chr10:48593771-48593772	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs370084529	chr10:48593774-48593775	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9422326	chr10:48593784-48593785	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs557026535	chr10:48593789-48593790	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575095008	chr10:48593801-48593802	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536272681	chr10:48593863-48593864	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112335920	chr10:48593922-48593923	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554880547	chr10:48594013-48594014	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182817104	chr10:48594020-48594021	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138619338	chr10:48594070-48594071	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564886132	chr10:48594090-48594091	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149300536	chr10:48594169-48594170	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144570136	chr10:48594223-48594224	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs530952491	chr10:48594224-48594225	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551062152	chr10:48594233-48594234	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542647786	chr10:48594238-48594239	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs58292802	chr10:48594270-48594271	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371327846	chr10:48594273-48594274	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374681931	chr10:48594274-48594275	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs148454760	chr10:48594286-48594287	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2790957	chr10:48594291-48594292	Genic enhancers Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs35211748	chr10:48594295-48594296	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547452253	chr10:48594302-48594303	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546892364	chr10:48594311-48594312	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs386508291	chr10:48594353-48594354	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs573156377	chr10:48594369-48594370	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs533916208	chr10:48594400-48594401	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546475237	chr10:48594434-48594435	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571708732	chr10:48594463-48594464	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs532753210	chr10:48594486-48594487	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186782045	chr10:48594503-48594504	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs568960003	chr10:48594552-48594553	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs142366919	chr10:48594561-48594562	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147480111	chr10:48594581-48594582	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554653738	chr10:48594594-48594595	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs372190822	chr10:48594613-48594614	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535316579	chr10:48594625-48594626	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566480637	chr10:48594630-48594631	Genic enhancers Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Schizophrenia	23813976	CNVD
Acute myeloid leukemia	19651601	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Rett syndrome	21593744	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Intellectual disability	22045946	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Autism	21948486	CNVD
cleft palate	21948486	CNVD
Encephalopathy	21948486	CNVD
Lung cancer	18438408	CNVD
T-cell primary immunodeficiency	21948486	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Autism	22543975	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
skeletal anomalies	21948486	CNVD
speech delay	21948486	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:449 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:48575600-48598200	Weak transcription	NH-A	brain
2	chr10:48591400-48594000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr10:48591800-48593400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:48592000-48593600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr10:48592400-48598200	Weak transcription	Osteobl	bone
6	chr10:48592400-48599000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr10:48593000-48595000	Enhancers	Thymus	Thymus
8	chr10:48593600-48595000	Enhancers	Fetal Thymus	thymus
9	chr10:48593600-48599800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr10:48595000-48604800	Weak transcription	Thymus	Thymus
11	chr10:48595800-48596400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr10:48595800-48603200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr10:48596000-48596200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:48596400-48598600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr10:48597400-48597600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:48597400-48597800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr10:48597600-48599800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:48598000-48598800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr10:48598200-48598800	Enhancers	Spleen	Spleen
20	chr10:48598200-48598800	Enhancers	NH-A	brain
21	chr10:48598200-48598800	Enhancers	Osteobl	bone
22	chr10:48598600-48598800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr10:48598800-48599800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:48598800-48599800	Weak transcription	NH-A	brain
25	chr10:48598800-48600000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr10:48598800-48600000	Weak transcription	Osteobl	bone
27	chr10:48598800-48603000	Weak transcription	Spleen	Spleen
28	chr10:48599000-48599400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr10:48599400-48599800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr10:48599800-48600000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr10:48599800-48600200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr10:48599800-48600200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr10:48599800-48600200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr10:48599800-48600200	Flanking Active TSS	NH-A	brain
35	chr10:48599800-48601200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr10:48599800-48602600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr10:48599800-48603400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr10:48600000-48600400	Enhancers	Osteobl	bone
39	chr10:48600200-48600400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr10:48600200-48600400	Active TSS	NH-A	brain
41	chr10:48600200-48600600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:48600200-48601200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr10:48600400-48600600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr10:48600400-48600600	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr10:48600400-48600600	Flanking Active TSS	NH-A	brain
46	chr10:48600400-48600800	Flanking Active TSS	Osteobl	bone
47	chr10:48600600-48600800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr10:48600600-48600800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr10:48600600-48600800	Active TSS	NH-A	brain
50	chr10:48600800-48601200	Active TSS	Osteobl	bone

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