Variant report

Variant	nsv947889
Chromosome Location	chr10:43278237-43290003
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:730)
CpG islands
(count:366)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:730 , 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	chr10:43277794-43278837	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:43277876-43278461	K562	blood:	n/a	n/a
3	ATF1	chr10:43277837-43279020	K562	blood:	n/a	n/a
4	ATF2	chr10:43277891-43278637	GM12878	blood:	n/a	n/a
5	ATF2	chr10:43277906-43278566	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr10:43277895-43278451	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr10:43277935-43278664	GM12878	blood:	n/a	n/a
8	ATF3	chr10:43278350-43278642	K562	blood:	n/a	n/a
9	ATF3	chr10:43277853-43278406	A549	lung:	n/a	n/a
10	ATF3	chr10:43277721-43278499	A549	lung:	n/a	n/a
11	BACH1	chr10:43277990-43278352	K562	blood:	n/a	n/a
12	BACH1	chr10:43277956-43278287	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr10:43277973-43278382	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:43277864-43278662	GM12878	blood:	n/a	n/a
15	BCL3	chr10:43278010-43278387	GM12878	blood:	n/a	n/a
16	BCL3	chr10:43278061-43278405	GM12878	blood:	n/a	n/a
17	BCL3	chr10:43277795-43278523	A549	lung:	n/a	n/a
18	BCL3	chr10:43277861-43278491	A549	lung:	n/a	n/a
19	BCLAF1	chr10:43277795-43278504	K562	blood:	n/a	n/a
20	BCLAF1	chr10:43277746-43278546	GM12878	blood:	n/a	n/a
21	BCLAF1	chr10:43277681-43278535	GM12878	blood:	n/a	n/a
22	BCLAF1	chr10:43277828-43278426	K562	blood:	n/a	n/a
23	BHLHE40	chr10:43277879-43278655	GM12878	blood:	n/a	n/a
24	BHLHE40	chr10:43277898-43278552	HepG2	liver:	n/a	n/a
25	BHLHE40	chr10:43277825-43278574	K562	blood:	n/a	n/a
26	BRCA1	chr10:43277834-43278309	GM12878	blood:	n/a	n/a
27	BRCA1	chr10:43278004-43278357	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr10:43277924-43278356	HepG2	liver:	n/a	n/a
29	BRCA1	chr10:43277926-43278622	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr10:43277806-43278340	K562	blood:	n/a	n/a
31	CBX3	chr10:43277740-43278784	HCT-116	colon:	n/a	n/a
32	CBX3	chr10:43277280-43278684	K562	blood:	n/a	n/a
33	CCNT2	chr10:43277858-43278443	K562	blood:	n/a	n/a
34	CEBPB	chr10:43277970-43278374	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr10:43281214-43281532	A549	lung:	n/a	n/a
36	CEBPB	chr10:43281229-43281584	IMR90	lung:	n/a	chr10:43281559-43281570
37	CEBPB	chr10:43281233-43281592	A549	lung:	n/a	chr10:43281559-43281570
38	CEBPB	chr10:43277935-43278327	K562	blood:	n/a	n/a
39	CEBPB	chr10:43278023-43278330	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr10:43277950-43278513	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr10:43281221-43281646	MCF-7	breast:	n/a	chr10:43281559-43281570
42	CEBPB	chr10:43281255-43281592	Hela-S3	cervix:	n/a	chr10:43281559-43281570
43	CEBPB	chr10:43277863-43278498	GM12878	blood:	n/a	n/a
44	CEBPB	chr10:43281232-43281587	HepG2	liver:	n/a	chr10:43281559-43281570
45	CEBPB	chr10:43281233-43281600	A549	lung:	n/a	chr10:43281559-43281570
46	CEBPB	chr10:43277859-43278463	A549	lung:	n/a	n/a
47	CEBPB	chr10:43277850-43278446	MCF-7	breast:	n/a	n/a
48	CEBPB	chr10:43281233-43281587	K562	blood:	n/a	chr10:43281559-43281570
49	CEBPB	chr10:43277971-43278347	K562	blood:	n/a	n/a
50	CEBPB	chr10:43278010-43278329	GM12878	blood:	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	chr10:43278266-43278316	PFSK-1	brain:	n/a
2	chr10:43278230-43278280	HNPCEpiC	eye:	n/a
3	chr10:43280976-43281026	ovcar-3	ovarian:	n/a
4	chr10:43278700-43278750	HCF	heart:	n/a
5	chr10:43278349-43278399	HIPEpiC	eye:	n/a
6	chr10:43278230-43278280	Hela-S3	cervix:	n/a
7	chr10:43278230-43278280	K562	blood:	n/a
8	chr10:43278349-43278399	SKMC	muscle:	n/a
9	chr10:43278266-43278316	AG04449	skin:	fetal
10	chr10:43278214-43278264	AG09309	skin:	n/a
11	chr10:43278349-43278399	SK-N-SH	brain:	n/a
12	chr10:43278349-43278399	Jurkat	blood:	n/a
13	chr10:43278700-43278750	BE2_C	brain:	n/a
14	chr10:43278230-43278280	AG10803	skin:	n/a
15	chr10:43278700-43278750	Jurkat	blood:	n/a
16	chr10:43278266-43278316	HRPEpiC	eye:	n/a
17	chr10:43280976-43281026	H1-hESC	embryonic stem cell:	embryo
18	chr10:43278214-43278264	NHDF-neo	bronchial:	n/a
19	chr10:43278230-43278280	GM06990	blood:	n/a
20	chr10:43278349-43278399	GM12878	blood:	n/a
21	chr10:43278349-43278399	GM06990	blood:	n/a
22	chr10:43278214-43278264	HCM	heart:	n/a
23	chr10:43278214-43278264	AG04449	skin:	fetal
24	chr10:43280976-43281026	Hela-S3	cervix:	n/a
25	chr10:43278349-43278399	SK-N-SH_RA	brain:	n/a
26	chr10:43278266-43278316	GM12891	blood:	n/a
27	chr10:43278349-43278399	HAEpiC	amniotic membrane:	n/a
28	chr10:43278266-43278316	Hela-S3	cervix:	n/a
29	chr10:43278349-43278399	BE2_C	brain:	n/a
30	chr10:43278230-43278280	SK-N-SH_RA	brain:	n/a
31	chr10:43278349-43278399	AG09319	gingival:	n/a
32	chr10:43280976-43281026	NT2-D1	testis:	n/a
33	chr10:43280976-43281026	Jurkat	blood:	n/a
34	chr10:43278349-43278399	K562	blood:	n/a
35	chr10:43278214-43278264	U87	brain:	n/a
36	chr10:43278266-43278316	GM12878	blood:	n/a
37	chr10:43278214-43278264	AG10803	skin:	n/a
38	chr10:43280976-43281026	NH-A	brain:	n/a
39	chr10:43278230-43278280	IMR90	lung:	fetal
40	chr10:43278266-43278316	T-47D	breast:	n/a
41	chr10:43278349-43278399	PFSK-1	brain:	n/a
42	chr10:43280976-43281026	Caco-2	colon:	n/a
43	chr10:43280976-43281026	RPTEC	kidney:	n/a
44	chr10:43280976-43281026	NB4	blood:	n/a
45	chr10:43278214-43278264	CMK	blood:	n/a
46	chr10:43278230-43278280	PrEC	prostate:	n/a
47	chr10:43278230-43278280	AG09319	gingival:	n/a
48	chr10:43278230-43278280	HMEC	breast:	n/a
49	chr10:43278700-43278750	PFSK-1	brain:	n/a
50	chr10:43278266-43278316	H1-hESC	embryonic stem cell:	embryo

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:43276494..43279738-chr10:43283503..43286419,4	MCF-7	breast:
2	chr10:43285592..43290643-chr10:43292360..43294489,4	K562	blood:
3	chr10:43277931..43278431-chr11:62608637..62609557,2	Hela-S3	cervix:
4	chr10:43046301..43049301-chr10:43278095..43279962,3	K562	blood:
5	chr10:43133575..43134141-chr10:43278109..43279018,2	MCF-7	breast:
6	chr10:43287294..43289602-chr10:43294220..43295848,2	K562	blood:
7	chr10:43277379..43280402-chr10:43288985..43292909,5	MCF-7	breast:
8	chr10:43282048..43284162-chr10:43286079..43288954,3	K562	blood:
9	chr10:42969989..42972327-chr10:43278200..43280239,2	K562	blood:
10	chr10:43280780..43283548-chr10:43285550..43289909,6	K562	blood:
11	chr10:43132954..43135205-chr10:43277445..43279937,2	K562	blood:
12	chr10:43277103..43279687-chr10:43279795..43282779,2	MCF-7	breast:
13	chr10:43278228..43281116-chr10:43281806..43285386,3	K562	blood:
14	chr1:148241298..148242285-chr10:43278087..43278706,2	Hela-S3	cervix:
15	chr10:43278278..43279935-chr10:43297692..43300575,2	K562	blood:
16	chr10:43276752..43278431-chr10:43279781..43281532,2	K562	blood:
17	chr10:43280780..43283548-chr10:43285550..43289909,6	K562	blood:
18	chr10:43132020..43136600-chr10:43277441..43279853,5	MCF-7	breast:
19	chr10:43278046..43280773-chr10:43285758..43288568,2	MCF-7	breast:
20	chr10:43285411..43287004-chr10:43291005..43292621,2	K562	blood:
21	chr10:43283711..43286231-chr10:43299028..43301664,2	K562	blood:
22	chr10:43282048..43284162-chr10:43286079..43288954,3	K562	blood:
23	chr10:43277481..43279174-chr8:144910550..144912585,2	MCF-7	breast:
24	chr10:43132863..43135217-chr10:43276470..43279459,4	K562	blood:
25	chr10:43132257..43135644-chr10:43275563..43280155,11	MCF-7	breast:
26	chr10:43278401..43278901-chr12:52444991..52445906,2	Hela-S3	cervix:
27	chr10:43286994..43289477-chr10:43294510..43296751,2	MCF-7	breast:

No data

Variant related genes	Relation type
BMS1	TF binding region
BMS1	CpG island
ENSG00000179950	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000207501	chromatin interactions
ENSG00000185904	chromatin interactions
ENSG00000165733	chromatin interactions
ENSG00000234420	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 511 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577408784	chr10:43278255-43278256	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs544766643	chr10:43278273-43278274	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs113030441	chr10:43278282-43278283	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs575423644	chr10:43278301-43278302	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs542924230	chr10:43278321-43278322	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs368736678	chr10:43278332-43278333	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs561110297	chr10:43278373-43278374	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs528516547	chr10:43278374-43278375	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs547113840	chr10:43278384-43278385	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs565336799	chr10:43278447-43278448	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs532655376	chr10:43278459-43278460	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs183264809	chr10:43278467-43278468	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs569488050	chr10:43278485-43278486	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs3758514	chr10:43278534-43278535	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs3758515	chr10:43278568-43278569	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs187977308	chr10:43278587-43278588	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs150030602	chr10:43278617-43278618	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs7908539	chr10:43278659-43278660	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs577273327	chr10:43278670-43278671	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs538371455	chr10:43278714-43278715	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs113652473	chr10:43278758-43278759	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs556706737	chr10:43278796-43278797	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs575430405	chr10:43278829-43278830	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs145321909	chr10:43278836-43278837	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs550892023	chr10:43278884-43278885	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs561284383	chr10:43278932-43278933	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs191229623	chr10:43278956-43278957	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs540584940	chr10:43278984-43278985	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs74720648	chr10:43279009-43279010	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs565301680	chr10:43279081-43279082	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs183798102	chr10:43279187-43279188	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs551125959	chr10:43279188-43279189	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs374926874	chr10:43279189-43279190	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs562917305	chr10:43279195-43279196	Active TSS Flanking Active TSS Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs17158170	chr10:43279203-43279204	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs548589714	chr10:43279313-43279314	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs189525075	chr10:43279352-43279353	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs193000925	chr10:43279362-43279363	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs17429275	chr10:43279365-43279366	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs73252887	chr10:43279450-43279451	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs4949033	chr10:43279472-43279473	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs538330932	chr10:43279533-43279534	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs556666209	chr10:43279593-43279594	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs185115918	chr10:43279682-43279683	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs536489422	chr10:43279706-43279707	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs554469610	chr10:43279715-43279716	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs190113118	chr10:43279731-43279732	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs111741529	chr10:43279752-43279753	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs535216739	chr10:43279777-43279778	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs112856164	chr10:43279796-43279797	Weak transcription Enhancers Genic enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Lung cancer	18438408	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
Mental retardation	21062444	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	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
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:704 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:43277000-43279000	Active TSS	Stomach Mucosa	stomach
2	chr10:43277200-43278600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr10:43277200-43278600	Active TSS	Brain Anterior Caudate	brain
4	chr10:43277200-43278800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
5	chr10:43277200-43278800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
6	chr10:43277200-43278800	Active TSS	Primary T killer memory cells from peripheral blood	blood
7	chr10:43277200-43278800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr10:43277200-43278800	Active TSS	Brain Germinal Matrix	brain
9	chr10:43277200-43278800	Active TSS	Brain Substantia Nigra	brain
10	chr10:43277200-43278800	Active TSS	Colon Smooth Muscle	Colon
11	chr10:43277200-43278800	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr10:43277200-43278800	Active TSS	Fetal Kidney	kidney
13	chr10:43277200-43279000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr10:43277200-43279000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr10:43277200-43279000	Active TSS	Colonic Mucosa	Colon
16	chr10:43277200-43279000	Active TSS	Rectal Smooth Muscle	rectum
17	chr10:43277200-43279200	Active TSS	HSMM	muscle
18	chr10:43277200-43279400	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr10:43277200-43279400	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr10:43277200-43279400	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr10:43277200-43279400	Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr10:43277200-43279400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr10:43277200-43279800	Active TSS	GM12878-XiMat	blood
24	chr10:43277400-43278600	Active TSS	Primary hematopoietic stem cells short term culture	blood
25	chr10:43277400-43278600	Active TSS	Brain Angular Gyrus	brain
26	chr10:43277400-43278600	Active TSS	Rectal Mucosa Donor 31	rectum
27	chr10:43277400-43278800	Active TSS	Fetal Brain Female	brain
28	chr10:43277400-43279000	Active TSS	iPS-18 Cell Line	embryonic stem cell
29	chr10:43277400-43279000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr10:43277400-43279000	Active TSS	HSMMtube	muscle
31	chr10:43277400-43279000	Active TSS	NHEK	skin
32	chr10:43277400-43279000	Active TSS	NHLF	lung
33	chr10:43277400-43279200	Active TSS	H9 Cell Line	embryonic stem cell
34	chr10:43277400-43279200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:43277400-43279200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr10:43277400-43279200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr10:43277400-43279200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr10:43277400-43279200	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr10:43277400-43279200	Active TSS	Ovary	ovary
40	chr10:43277400-43279400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr10:43277400-43279400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr10:43277400-43279400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr10:43277400-43279400	Active TSS	HUES48 Cell Line	embryonic stem cell
44	chr10:43277400-43279400	Active TSS	iPS-15b Cell Line	embryonic stem cell
45	chr10:43277400-43279400	Active TSS	Fetal Intestine Large	intestine
46	chr10:43277400-43279400	Active TSS	Osteobl	bone
47	chr10:43277400-43279600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr10:43277400-43279800	Active TSS	A549	lung
49	chr10:43277600-43278400	Active TSS	Adipose Nuclei	Adipose
50	chr10:43277600-43278400	Active TSS	Duodenum Mucosa	Duodenum

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