Variant report

Variant	nsv948158
Chromosome Location	chr10:99189320-99193095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:180)
CpG islands
(count:61)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:180 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr10:99193051-99194644	A549	lung:	n/a	n/a
2	CTCF	chr10:99191060-99191210	GM12872	blood:	n/a	n/a
3	CTCF	chr10:99192620-99192688	LNCaP	prostate:	n/a	n/a
4	CTCF	chr10:99193077-99193097	Kidney_OC	kidney:	n/a	n/a
5	CTCF	chr10:99193053-99193069	Kidney_OC	kidney:	n/a	n/a
6	EBF1	chr10:99191832-99191917	GM12878	blood:	n/a	n/a
7	FOSL2	chr10:99192216-99192796	HepG2	liver:	n/a	n/a
8	FOSL2	chr10:99192836-99194456	HepG2	liver:	n/a	chr10:99193843-99193853 chr10:99193843-99193853
9	FOXA1	chr10:99192359-99192692	HepG2	liver:	n/a	n/a
10	FOXA2	chr10:99189851-99190128	HepG2	liver:	n/a	n/a
11	GABPA	chr10:99190215-99190352	Hela-S3	cervix:	n/a	n/a
12	HEY1	chr10:99191590-99191942	HepG2	liver:	n/a	n/a
13	HEY1	chr10:99189969-99190480	HepG2	liver:	n/a	n/a
14	HEY1	chr10:99192036-99192589	K562	blood:	n/a	n/a
15	HEY1	chr10:99192210-99194447	HepG2	liver:	n/a	n/a
16	HEY1	chr10:99190634-99190972	K562	blood:	n/a	n/a
17	JUND	chr10:99192540-99192809	HepG2	liver:	n/a	n/a
18	JUND	chr10:99192869-99193127	HepG2	liver:	n/a	n/a
19	MBD4	chr10:99193093-99194359	HepG2	liver:	n/a	n/a
20	MTA3	chr10:99193068-99195204	GM12878	blood:	n/a	n/a
21	NFATC1	chr10:99193079-99194542	GM12878	blood:	n/a	n/a
22	PAX5	chr10:99192253-99192443	GM12878	blood:	n/a	n/a
23	PML	chr10:99193071-99194803	GM12878	blood:	n/a	n/a
24	POLR2A	chr10:99192906-99193764	H1-hESC	embryonic stem cell:	n/a	n/a
25	POLR2A	chr10:99193090-99194487	K562	blood:	n/a	n/a
26	POLR2A	chr10:99191675-99191890	K562	blood:	n/a	n/a
27	POLR2A	chr10:99189759-99190161	U87	brain:	n/a	n/a
28	POLR2A	chr10:99191750-99191919	ProgFib	skin:	n/a	n/a
29	POLR2A	chr10:99191818-99191858	HUVEC	blood vessel:	n/a	n/a
30	POLR2A	chr10:99192031-99192884	GM12892	blood:	n/a	n/a
31	POLR2A	chr10:99190811-99191153	K562	blood:	n/a	n/a
32	POLR2A	chr10:99189935-99190541	GM12878	blood:	n/a	n/a
33	POLR2A	chr10:99189567-99190022	HepG2	liver:	n/a	n/a
34	POLR2A	chr10:99191681-99191960	HepG2	liver:	n/a	n/a
35	POLR2A	chr10:99191538-99192515	PANC-1	pancreas:	n/a	n/a
36	POLR2A	chr10:99189754-99190161	U87	brain:	n/a	n/a
37	POLR2A	chr10:99191736-99191807	HUVEC	blood vessel:	n/a	n/a
38	POLR2A	chr10:99189804-99190333	GM12878	blood:	n/a	n/a
39	POLR2A	chr10:99190865-99191575	HepG2	liver:	n/a	n/a
40	POLR2A	chr10:99189065-99189555	HepG2	liver:	n/a	n/a
41	POLR2A	chr10:99192572-99192779	HepG2	liver:	n/a	n/a
42	POLR2A	chr10:99189678-99195364	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr10:99192196-99192298	MCF-7	breast:	n/a	n/a
44	POLR2A	chr10:99192574-99192794	A549	lung:	n/a	n/a
45	POLR2A	chr10:99191896-99191898	HUVEC	blood vessel:	n/a	n/a
46	POLR2A	chr10:99191185-99191422	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr10:99189784-99190179	HepG2	liver:	n/a	n/a
48	POLR2A	chr10:99190926-99192436	PANC-1	pancreas:	n/a	n/a
49	POLR2A	chr10:99191215-99191593	ECC-1	luminal epithelium:	n/a	n/a
50	POLR2A	chr10:99191069-99195440	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:99192404-99192454	ovcar-3	ovarian:	n/a
2	chr10:99192404-99192454	SKMC	muscle:	n/a
3	chr10:99192404-99192454	AG09319	gingival:	n/a
4	chr10:99192404-99192454	NB4	blood:	n/a
5	chr10:99192404-99192454	HIPEpiC	eye:	n/a
6	chr10:99192404-99192454	HEK293	kidney:	embryo
7	chr10:99192404-99192454	AoSMC	blood vessel:	n/a
8	chr10:99192404-99192454	NHBE	bronchial:	n/a
9	chr10:99192404-99192454	ProgFib	skin:	n/a
10	chr10:99192404-99192454	HepG2	liver:	n/a
11	chr10:99192404-99192454	HRPEpiC	eye:	n/a
12	chr10:99192404-99192454	HPAEpiC	pulmonary alveolar:	n/a
13	chr10:99192404-99192454	PrEC	prostate:	n/a
14	chr10:99192404-99192454	LNCaP	prostate:	n/a
15	chr10:99192404-99192454	SK-N-SH	brain:	n/a
16	chr10:99192404-99192454	AG04449	skin:	fetal
17	chr10:99192404-99192454	PFSK-1	brain:	n/a
18	chr10:99192404-99192454	SK-N-SH_RA	brain:	n/a
19	chr10:99192404-99192454	HL-60	blood:	n/a
20	chr10:99192404-99192454	PANC-1	pancreas:	n/a
21	chr10:99192404-99192454	Hela-S3	cervix:	n/a
22	chr10:99192404-99192454	AG10803	skin:	n/a
23	chr10:99192404-99192454	HAEpiC	amniotic membrane:	n/a
24	chr10:99192404-99192454	U87	brain:	n/a
25	chr10:99192404-99192454	HCPEpiC	choroid plexus:	n/a
26	chr10:99192404-99192454	A549	lung:	n/a
27	chr10:99192404-99192454	GM19239	blood:	n/a
28	chr10:99192404-99192454	HCF	heart:	n/a
29	chr10:99192404-99192454	K562	blood:	n/a
30	chr10:99192404-99192454	MCF-7	breast:	n/a
31	chr10:99192404-99192454	ECC-1	luminal epithelium:	n/a
32	chr10:99192404-99192454	Hepatocyte	liver:	n/a
33	chr10:99192404-99192454	HNPCEpiC	eye:	n/a
34	chr10:99192404-99192454	CMK	blood:	n/a
35	chr10:99192404-99192454	AG09309	skin:	n/a
36	chr10:99192404-99192454	NHDF-neo	bronchial:	n/a
37	chr10:99192404-99192454	HEEpiC	esophagus:	n/a
38	chr10:99192404-99192454	HRCEpiC	kidney:	n/a
39	chr10:99192404-99192454	BE2_C	brain:	n/a
40	chr10:99192404-99192454	T-47D	breast:	n/a
41	chr10:99192404-99192454	HCM	heart:	n/a
42	chr10:99192404-99192454	HMEC	breast:	n/a
43	chr10:99192404-99192454	HRE	kidney:	n/a
44	chr10:99192404-99192454	Caco-2	colon:	n/a
45	chr10:99192404-99192454	NT2-D1	testis:	n/a
46	chr10:99192404-99192454	GM06990	blood:	n/a
47	chr10:99192404-99192454	SK-N-MC	brain:	n/a
48	chr10:99192404-99192454	RPTEC	kidney:	n/a
49	chr10:99192404-99192454	GM12892	blood:	n/a
50	chr10:99192404-99192454	NH-A	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:99190230..99197642-chr10:99200865..99207415,15	MCF-7	breast:
2	chr10:99183836..99188749-chr10:99192584..99200160,10	MCF-7	breast:
3	chr10:99191825..99193525-chr10:99195250..99196824,2	K562	blood:
4	chr10:99176991..99182775-chr10:99183273..99189892,9	MCF-7	breast:
5	chr10:99159614..99162570-chr10:99184923..99189339,4	K562	blood:
6	chr10:99191980..99193948-chr10:99205365..99208348,2	MCF-7	breast:
7	chr10:99158229..99164055-chr10:99184399..99190088,9	MCF-7	breast:
8	chr10:99178965..99181268-chr10:99192516..99194954,2	MCF-7	breast:
9	chr10:99189135..99191052-chr10:99205351..99206988,2	K562	blood:
10	chr10:99188867..99192186-chr10:99193906..99196769,3	MCF-7	breast:
11	chr10:99190546..99193434-chr10:99194147..99197999,4	K562	blood:
12	chr10:99165495..99167483-chr10:99187813..99189704,2	K562	blood:
13	chr10:99183719..99185811-chr10:99191759..99194746,2	K562	blood:
14	chr10:99148085..99150519-chr10:99189341..99192060,3	K562	blood:
15	chr10:99187101..99190236-chr10:99202891..99208015,7	MCF-7	breast:
16	chr10:99185211..99187426-chr10:99187705..99189889,2	MCF-7	breast:
17	chr10:99186982..99190152-chr10:99256815..99259689,3	K562	blood:
18	chr10:99160927..99162886-chr10:99190238..99192558,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000224474	TF binding region
ENSG00000224474	CpG island
ENSG00000200737	chromatin interactions
ENSG00000171311	chromatin interactions
ENSG00000165886	chromatin interactions
ENSG00000231970	chromatin interactions
ENSG00000052749	chromatin interactions
ENSG00000155229	chromatin interactions
ENSG00000171307	chromatin interactions
ENSG00000224474	chromatin interactions
ENSG00000171314	chromatin interactions

Extended variants
information (count: 160 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:160 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559122277	chr10:99189373-99189374	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs183632903	chr10:99189379-99189380	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs563184040	chr10:99189381-99189382	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs12573086	chr10:99189389-99189390	Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs549700571	chr10:99189424-99189425	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs575506069	chr10:99189435-99189436	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs188518371	chr10:99189535-99189536	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs528991468	chr10:99189538-99189539	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs368684240	chr10:99189582-99189583	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs12570015	chr10:99189583-99189584	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs566743534	chr10:99189589-99189590	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs190159977	chr10:99189593-99189594	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs547325049	chr10:99189601-99189602	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs565563130	chr10:99189610-99189611	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs571037421	chr10:99189619-99189620	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs538625217	chr10:99189648-99189649	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs9702168	chr10:99189655-99189656	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs556722813	chr10:99189672-99189673	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs567982370	chr10:99189709-99189710	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs575456738	chr10:99189727-99189728	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs536159769	chr10:99189763-99189764	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs370117811	chr10:99189793-99189794	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs573092512	chr10:99189795-99189796	Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs539329930	chr10:99189801-99189802	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs117603972	chr10:99189814-99189815	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs200784458	chr10:99189820-99189821	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs372461077	chr10:99189825-99189826	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs140578861	chr10:99189842-99189843	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs374881900	chr10:99189862-99189863	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs577304675	chr10:99189894-99189895	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs150405032	chr10:99189907-99189908	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs562740491	chr10:99189916-99189917	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs565225276	chr10:99189949-99189950	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs533230209	chr10:99189962-99189963	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs548486101	chr10:99189990-99189991	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs76098305	chr10:99189992-99189993	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs113668589	chr10:99190010-99190011	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs527857779	chr10:99190014-99190015	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs112283346	chr10:99190023-99190024	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs138140388	chr10:99190031-99190032	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs374798118	chr10:99190034-99190035	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs532118917	chr10:99190038-99190039	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs559274445	chr10:99190097-99190098	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs551677267	chr10:99190105-99190106	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs200094503	chr10:99190133-99190134	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs2861949	chr10:99190162-99190163	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs559703869	chr10:99190184-99190185	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs149177007	chr10:99190189-99190190	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs568783858	chr10:99190190-99190191	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs536514405	chr10:99190194-99190195	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Autosomal dominant partial epilepsy	18472482	CNVD
Breast cancer	16397240	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:99186000-99190200	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
2	chr10:99186200-99189600	Transcr. at gene 5' and 3'	Primary T helper cells PMA-I stimulated	--
3	chr10:99187000-99190600	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
4	chr10:99187400-99189400	Genic enhancers	Thymus	Thymus
5	chr10:99187600-99189800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr10:99187800-99191000	Weak transcription	Ovary	ovary
7	chr10:99187800-99191200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr10:99188200-99189400	Genic enhancers	Brain Angular Gyrus	brain
9	chr10:99188200-99190400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr10:99188400-99189400	Genic enhancers	Primary T cells from cord blood	blood
11	chr10:99188400-99189400	Weak transcription	Fetal Brain Female	brain
12	chr10:99188400-99189800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr10:99188400-99190200	Genic enhancers	Fetal Heart	heart
14	chr10:99188400-99190400	Weak transcription	Brain Cingulate Gyrus	brain
15	chr10:99188400-99190800	Weak transcription	Pancreas	Pancrea
16	chr10:99188600-99189400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr10:99188600-99189400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr10:99188600-99189400	Transcr. at gene 5' and 3'	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr10:99188600-99189400	Weak transcription	Colonic Mucosa	Colon
20	chr10:99188600-99189800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr10:99188600-99190000	Weak transcription	Brain Germinal Matrix	brain
22	chr10:99188600-99190000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr10:99188600-99190200	Weak transcription	Adipose Nuclei	Adipose
24	chr10:99188600-99190200	Weak transcription	Lung	lung
25	chr10:99188600-99190200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr10:99188600-99190200	Genic enhancers	HepG2	liver
27	chr10:99188600-99190400	Weak transcription	Brain Substantia Nigra	brain
28	chr10:99188600-99190600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr10:99188600-99190600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr10:99188600-99190800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr10:99188600-99190800	Weak transcription	Gastric	stomach
32	chr10:99188600-99190800	Weak transcription	Right Ventricle	heart
33	chr10:99188600-99190800	Weak transcription	Spleen	Spleen
34	chr10:99188600-99191000	Weak transcription	Aorta	Aorta
35	chr10:99188600-99191000	Weak transcription	Esophagus	oesophagus
36	chr10:99188600-99191000	Weak transcription	Psoas Muscle	Psoas
37	chr10:99188600-99191000	Weak transcription	Small Intestine	intestine
38	chr10:99188600-99191200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr10:99188600-99192200	Strong transcription	H9 Cell Line	embryonic stem cell
40	chr10:99188600-99192200	Strong transcription	Brain Anterior Caudate	brain
41	chr10:99188600-99192200	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr10:99188600-99195000	Weak transcription	Fetal Brain Male	brain
43	chr10:99188600-99197200	Strong transcription	HSMM	muscle
44	chr10:99188600-99200600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr10:99188600-99201400	Strong transcription	Left Ventricle	heart
46	chr10:99188600-99203200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr10:99188600-99203200	Strong transcription	Primary B cells from peripheral blood	blood
48	chr10:99188600-99203200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr10:99188600-99203200	Strong transcription	Fetal Muscle Leg	muscle
50	chr10:99188600-99203600	Strong transcription	Primary hematopoietic stem cells short term culture	blood

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