Variant report

Variant	esv3381643
Chromosome Location	chr10:975752-979950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:744)
CpG islands
(count:366)
Chromatin interactive
region (count:21)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:975612-976178	K562	blood:	n/a	n/a
2	ARID3A	chr10:977654-977803	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:977720-977747	K562	blood:	n/a	n/a
4	ATF1	chr10:977597-977929	K562	blood:	n/a	n/a
5	ATF2	chr10:977473-977853	GM12878	blood:	n/a	n/a
6	BACH1	chr10:976057-976295	K562	blood:	n/a	n/a
7	BACH1	chr10:976720-976818	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr10:975826-976665	GM12878	blood:	n/a	n/a
9	BCLAF1	chr10:976320-976797	GM12878	blood:	n/a	n/a
10	BHLHE40	chr10:975896-976809	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:977554-978115	K562	blood:	n/a	n/a
12	BHLHE40	chr10:977582-978159	GM12878	blood:	n/a	n/a
13	BHLHE40	chr10:976476-976810	K562	blood:	n/a	n/a
14	BHLHE40	chr10:977609-978009	HepG2	liver:	n/a	n/a
15	BRCA1	chr10:977585-977787	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr10:977564-977827	GM12878	blood:	n/a	n/a
17	BRCA1	chr10:977555-977858	Hela-S3	cervix:	n/a	n/a
18	CCNT2	chr10:976675-978128	K562	blood:	n/a	n/a
19	CEBPB	chr10:977489-977746	HepG2	liver:	n/a	n/a
20	CEBPB	chr10:977648-977792	A549	lung:	n/a	n/a
21	CEBPB	chr10:976002-976201	K562	blood:	n/a	n/a
22	CEBPB	chr10:977550-977764	K562	blood:	n/a	n/a
23	CEBPB	chr10:977555-977810	Hela-S3	cervix:	n/a	n/a
24	CHD1	chr10:975847-976842	GM12878	blood:	n/a	n/a
25	CHD1	chr10:975406-978308	IMR90	lung:	n/a	chr10:977804-977814 chr10:977690-977700
26	CHD1	chr10:976545-976804	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr10:976708-976964	HepG2	liver:	n/a	n/a
28	CHD2	chr10:977450-977923	K562	blood:	n/a	chr10:977804-977814 chr10:977690-977700
29	CHD2	chr10:976657-976885	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr10:977494-977954	GM12878	blood:	n/a	chr10:977804-977814 chr10:977690-977700
31	CHD2	chr10:976657-976873	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr10:977544-977899	H1-hESC	embryonic stem cell:	n/a	chr10:977804-977814 chr10:977690-977700
33	CHD2	chr10:977519-977905	HepG2	liver:	n/a	chr10:977804-977814 chr10:977690-977700
34	CHD2	chr10:977439-978125	Hela-S3	cervix:	n/a	chr10:977804-977814 chr10:977690-977700
35	CREB1	chr10:977542-977906	A549	lung:	n/a	n/a
36	CREB1	chr10:977505-978018	ECC-1	luminal epithelium:	n/a	n/a
37	CREB1	chr10:977535-978186	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr10:977403-978344	HepG2	liver:	n/a	n/a
39	CREB1	chr10:976607-976960	A549	lung:	n/a	n/a
40	CREB1	chr10:977494-978233	HepG2	liver:	n/a	n/a
41	CREB1	chr10:977416-978202	GM12878	blood:	n/a	n/a
42	CREB1	chr10:977487-978028	K562	blood:	n/a	n/a
43	CREB1	chr10:977174-978193	A549	lung:	n/a	n/a
44	CREB1	chr10:977528-978077	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr10:977900-978050	AG04449	skin:	n/a	n/a
46	CTCF	chr10:976720-976870	Caco-2	colon:	n/a	n/a
47	CTCF	chr10:976729-976975	HepG2	liver:	n/a	chr10:976876-976889
48	CTCF	chr10:976811-976957	GM19239	blood:	n/a	chr10:976876-976889
49	CTCF	chr10:976780-976930	GM12873	blood:	n/a	chr10:976876-976889
50	CTCF	chr10:976720-976870	HMEC	breast:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:978019-978069	MCF10A-Er-Src	breast:	n/a
2	chr10:976594-976644	T-47D	breast:	n/a
3	chr10:976594-976644	CMK	blood:	n/a
4	chr10:977622-977672	Hepatocyte	liver:	n/a
5	chr10:978019-978069	BJ	skin:	n/a
6	chr10:976940-976990	SKMC	muscle:	n/a
7	chr10:977622-977672	AoSMC	blood vessel:	n/a
8	chr10:977622-977672	ovcar-3	ovarian:	n/a
9	chr10:976548-976598	A549	lung:	n/a
10	chr10:978077-978127	AG10803	skin:	n/a
11	chr10:976594-976644	BJ	skin:	n/a
12	chr10:978077-978127	PrEC	prostate:	n/a
13	chr10:977622-977672	MCF10A-Er-Src	breast:	n/a
14	chr10:978077-978127	HUVEC	blood vessel:	n/a
15	chr10:976594-976644	Caco-2	colon:	n/a
16	chr10:976594-976644	HNPCEpiC	eye:	n/a
17	chr10:978077-978127	SK-N-SH	brain:	n/a
18	chr10:976548-976598	Hela-S3	cervix:	n/a
19	chr10:976548-976598	ovcar-3	ovarian:	n/a
20	chr10:977622-977672	RPTEC	kidney:	n/a
21	chr10:976548-976598	HCT-116	colon:	n/a
22	chr10:976940-976990	PFSK-1	brain:	n/a
23	chr10:976594-976644	ECC-1	luminal epithelium:	n/a
24	chr10:977622-977672	GM12878	blood:	n/a
25	chr10:978019-978069	SK-N-SH_RA	brain:	n/a
26	chr10:976548-976598	AG10803	skin:	n/a
27	chr10:976940-976990	NHBE	bronchial:	n/a
28	chr10:976594-976644	MCF10A-Er-Src	breast:	n/a
29	chr10:976594-976644	A549	lung:	n/a
30	chr10:978019-978069	RPTEC	kidney:	n/a
31	chr10:976548-976598	GM06990	blood:	n/a
32	chr10:976594-976644	HL-60	blood:	n/a
33	chr10:976548-976598	NT2-D1	testis:	n/a
34	chr10:976940-976990	AG04450	lung:	fetal
35	chr10:976548-976598	CMK	blood:	n/a
36	chr10:977622-977672	SK-N-SH_RA	brain:	n/a
37	chr10:978077-978127	NT2-D1	testis:	n/a
38	chr10:978077-978127	Jurkat	blood:	n/a
39	chr10:978019-978069	IMR90	lung:	fetal
40	chr10:978019-978069	Hepatocyte	liver:	n/a
41	chr10:978019-978069	A549	lung:	n/a
42	chr10:976548-976598	GM12878	blood:	n/a
43	chr10:978019-978069	AG10803	skin:	n/a
44	chr10:978019-978069	AG09309	skin:	n/a
45	chr10:978077-978127	HMEC	breast:	n/a
46	chr10:978019-978069	HUVEC	blood vessel:	n/a
47	chr10:978019-978069	NT2-D1	testis:	n/a
48	chr10:976594-976644	NB4	blood:	n/a
49	chr10:977622-977672	GM12892	blood:	n/a
50	chr10:978077-978127	HRE	kidney:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:
2	chr10:975309..980832-chr10:1031626..1035973,12	K562	blood:
3	chr10:974636..980819-chr10:1029938..1037009,15	MCF-7	breast:
4	chr10:975330..979545-chr10:1093428..1097529,6	K562	blood:
5	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
6	chr10:979434..982350-chr10:995576..997645,2	MCF-7	breast:
7	chr10:974758..976966-chr10:1110782..1112393,2	MCF-7	breast:
8	chr10:977031..978658-chr10:1101205..1103073,2	K562	blood:
9	chr10:977686..978278-chr3:23958133..23959063,2	HCT-116	colon:
10	chr10:975582..978698-chr10:1119494..1122267,3	MCF-7	breast:
11	chr10:974758..977274-chr10:1018618..1021450,2	K562	blood:
12	chr10:976647..980794-chr10:1093154..1097319,8	MCF-7	breast:
13	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
14	chr10:976344..979673-chr10:1032747..1036349,14	K562	blood:
15	chr10:976566..978917-chr20:33411823..33413821,2	MCF-7	breast:
16	chr10:976553..979064-chr17:56707717..56709888,2	MCF-7	breast:
17	chr10:974451..976397-chr10:1027362..1028867,2	MCF-7	breast:
18	chr10:974670..978531-chr10:1101117..1104171,5	K562	blood:
19	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
20	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
21	chr10:974339..976019-chr10:1070236..1073056,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTPBP4-3	chr10:978127-978179	NONHSAT010879
2	lnc-GTPBP4-3	chr10:978420-978683	NONHSAT010879
3	lnc-GTPBP4-3	chr10:978966-979055	ENSG00000229869.1

No data

Variant related genes	Relation type
ENSG00000229869	TF binding region
LARP4B	TF binding region
ENSG00000229869	CpG island
LARP4B	CpG island
ENSG00000174748	chromatin interactions
ENSG00000148377	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000205740	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000198646	chromatin interactions
ENSG00000047056	chromatin interactions

Extended variants
information (count: 128 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:128 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563523502	chr10:975832-975833	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs529372171	chr10:975888-975889	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs549085201	chr10:975899-975900	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs74117000	chr10:975926-975927	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs554530540	chr10:975939-975940	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs528499010	chr10:975949-975950	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs551443308	chr10:975954-975955	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs11253520	chr10:975961-975962	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs140088627	chr10:975969-975970	Active TSS Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs192526081	chr10:976006-976007	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs540079755	chr10:976016-976017	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs536641517	chr10:976088-976089	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs7090569	chr10:976145-976146	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144791416	chr10:976247-976248	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs555516993	chr10:976256-976257	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs556609688	chr10:976266-976267	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs148574128	chr10:976273-976274	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs576561650	chr10:976311-976312	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs541068093	chr10:976312-976313	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs557458131	chr10:976317-976318	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs184660733	chr10:976326-976327	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs376708788	chr10:976368-976369	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs142973934	chr10:976390-976391	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs189109386	chr10:976398-976399	Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs11253521	chr10:976416-976417	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs542768538	chr10:976437-976438	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs559426907	chr10:976557-976558	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs151127982	chr10:976561-976562	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs374711491	chr10:976585-976586	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs551795217	chr10:976622-976623	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs370546653	chr10:976681-976682	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs562080657	chr10:976707-976708	Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs572142454	chr10:976813-976814	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs569931707	chr10:976826-976827	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs535655879	chr10:976897-976898	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs375133750	chr10:976924-976925	Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs565808559	chr10:977016-977017	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs534403452	chr10:977066-977067	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs557761886	chr10:977086-977087	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs577585865	chr10:977114-977115	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs111734794	chr10:977123-977124	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs557238299	chr10:977129-977130	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs573951281	chr10:977144-977145	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs539210260	chr10:977187-977188	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs372505958	chr10:977224-977225	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs542862487	chr10:977280-977281	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs545507889	chr10:977312-977313	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs7082265	chr10:977341-977342	Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs7095754	chr10:977437-977438	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs201543910	chr10:977552-977553	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:929400-975800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:929400-976400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr10:956800-976400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:965800-976200	Weak transcription	Aorta	Aorta
5	chr10:968000-975800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr10:968400-975800	Weak transcription	NH-A	brain
7	chr10:969000-975800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr10:969200-976000	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr10:971200-975800	Weak transcription	Brain Germinal Matrix	brain
10	chr10:971400-975800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr10:972000-976000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr10:972400-975800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr10:972400-975800	Enhancers	Liver	Liver
14	chr10:972800-975800	Enhancers	Adipose Nuclei	Adipose
15	chr10:972800-975800	Enhancers	Fetal Intestine Large	intestine
16	chr10:972800-975800	Weak transcription	NHLF	lung
17	chr10:973000-976000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr10:973000-976000	Enhancers	Fetal Heart	heart
19	chr10:973200-975800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr10:973400-975800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr10:973400-975800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr10:973400-976000	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr10:973600-975800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
24	chr10:973600-976000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr10:973600-976000	Enhancers	Left Ventricle	heart
26	chr10:973800-975800	Enhancers	Ovary	ovary
27	chr10:973800-976200	Enhancers	Primary T cells fromperipheralblood	blood
28	chr10:974000-975800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:974200-975800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr10:974200-976200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr10:974200-976200	Enhancers	Colon Smooth Muscle	Colon
32	chr10:974400-976000	Enhancers	Brain Angular Gyrus	brain
33	chr10:974400-976000	Enhancers	Brain Anterior Caudate	brain
34	chr10:974400-976000	Enhancers	Brain Hippocampus Middle	brain
35	chr10:974400-976000	Enhancers	Right Ventricle	heart
36	chr10:974400-976000	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr10:974400-976000	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr10:974400-976200	Enhancers	Primary B cells from peripheral blood	blood
39	chr10:974400-976200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
40	chr10:974400-976200	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr10:974400-976400	Enhancers	Pancreas	Pancrea
42	chr10:974600-975800	Enhancers	H1 Cell Line	embryonic stem cell
43	chr10:974600-975800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr10:974600-975800	Enhancers	Colonic Mucosa	Colon
45	chr10:974600-976200	Weak transcription	Fetal Muscle Trunk	muscle
46	chr10:974600-976600	Weak transcription	Spleen	Spleen
47	chr10:974600-976800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr10:974800-975800	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr10:974800-976000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr10:974800-976000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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