Variant report

Variant	nsv526061
Chromosome Location	chr6:25708714-25725481
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:25718417-25718765	K562	blood:	n/a	n/a
2	ATF1	chr6:25720694-25720999	K562	blood:	n/a	n/a
3	BHLHE40	chr6:25719678-25719709	HepG2	liver:	n/a	n/a
4	CBX3	chr6:25720531-25721127	HCT-116	colon:	n/a	n/a
5	CEBPB	chr6:25716510-25716628	H1-hESC	embryonic stem cell:	n/a	chr6:25716558-25716567 chr6:25716556-25716569 chr6:25716556-25716567
6	CEBPB	chr6:25708984-25709189	K562	blood:	n/a	n/a
7	CEBPB	chr6:25720595-25720988	K562	blood:	n/a	n/a
8	CEBPB	chr6:25710534-25710966	A549	lung:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
9	CEBPB	chr6:25720635-25720963	A549	lung:	n/a	n/a
10	CEBPB	chr6:25710567-25710983	MCF-7	breast:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
11	CEBPB	chr6:25710602-25710871	A549	lung:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
12	CEBPB	chr6:25710601-25710982	HepG2	liver:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
13	CEBPB	chr6:25710619-25710968	A549	lung:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
14	CEBPB	chr6:25710356-25710995	K562	blood:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
15	CEBPB	chr6:25720608-25720962	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr6:25710591-25710982	H1-hESC	embryonic stem cell:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
17	CEBPB	chr6:25720628-25720974	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:25716416-25716736	K562	blood:	n/a	chr6:25716558-25716567 chr6:25716556-25716569 chr6:25716556-25716567
19	CEBPB	chr6:25710655-25710844	K562	blood:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
20	CEBPB	chr6:25716118-25716714	HepG2	liver:	n/a	chr6:25716558-25716567 chr6:25716556-25716569 chr6:25716556-25716567
21	CEBPB	chr6:25716378-25716691	IMR90	lung:	n/a	chr6:25716558-25716567 chr6:25716556-25716569 chr6:25716556-25716567
22	CEBPB	chr6:25710616-25710957	K562	blood:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
23	CEBPB	chr6:25710609-25710979	IMR90	lung:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
24	CEBPB	chr6:25710610-25710920	ECC-1	luminal epithelium:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
25	CEBPB	chr6:25720654-25720952	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr6:25720573-25721058	MCF-7	breast:	n/a	n/a
27	CEBPB	chr6:25710611-25710929	Hela-S3	cervix:	n/a	chr6:25710792-25710801 chr6:25710790-25710803 chr6:25710792-25710801 chr6:25710792-25710801
28	CTCF	chr6:25718414-25718677	A549	lung:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
29	CTCF	chr6:25720780-25720930	HFF-Myc	foreskin:	n/a	n/a
30	CTCF	chr6:25718140-25718290	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr6:25718448-25718707	SK-N-SH_RA	brain:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
32	CTCF	chr6:25720800-25720950	NB4	blood:	n/a	n/a
33	CTCF	chr6:25718540-25718690	GM12872	blood:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
34	CTCF	chr6:25720780-25720930	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr6:25718440-25718590	GM12872	blood:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
36	CTCF	chr6:25711762-25711817	K562	blood:	n/a	chr6:25711785-25711803 chr6:25711790-25711798 chr6:25711780-25711801
37	CTCF	chr6:25718520-25718670	MCF-7	breast:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
38	CTCF	chr6:25718500-25718650	HCM	heart:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
39	CTCF	chr6:25720760-25720910	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr6:25718540-25718690	AG04450	lung:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
41	CTCF	chr6:25720760-25720910	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr6:25720780-25720930	K562	blood:	n/a	n/a
43	CTCF	chr6:25720760-25720910	HCM	heart:	n/a	n/a
44	CTCF	chr6:25718540-25718690	HVMF	connective:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
45	CTCF	chr6:25714220-25714370	SK-N-SH_RA	brain:	n/a	chr6:25714335-25714348 chr6:25714337-25714347
46	CTCF	chr6:25718461-25718677	Hela-S3	cervix:	n/a	chr6:25718560-25718578 chr6:25718561-25718577 chr6:25718563-25718573
47	CTCF	chr6:25710100-25710250	K562	blood:	n/a	n/a
48	CTCF	chr6:25719360-25719510	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr6:25720715-25720993	Fibrobl	skin:	n/a	n/a
50	CTCF	chr6:25720720-25720870	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:25710535-25710585	PFSK-1	brain:	n/a
2	chr6:25710487-25710537	GM06990	blood:	n/a
3	chr6:25723861-25723911	HMEC	breast:	n/a
4	chr6:25723861-25723911	IMR90	lung:	fetal
5	chr6:25710487-25710537	Hela-S3	cervix:	n/a
6	chr6:25710694-25710744	ovcar-3	ovarian:	n/a
7	chr6:25723861-25723911	NB4	blood:	n/a
8	chr6:25710487-25710537	AG10803	skin:	n/a
9	chr6:25710487-25710537	IMR90	lung:	fetal
10	chr6:25710487-25710537	H1-hESC	embryonic stem cell:	embryo
11	chr6:25723861-25723911	ECC-1	luminal epithelium:	n/a
12	chr6:25723861-25723911	SKMC	muscle:	n/a
13	chr6:25710694-25710744	A549	lung:	n/a
14	chr6:25710487-25710537	NHBE	bronchial:	n/a
15	chr6:25710535-25710585	GM12891	blood:	n/a
16	chr6:25710487-25710537	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:25710535-25710585	HNPCEpiC	eye:	n/a
18	chr6:25710694-25710744	Hepatocyte	liver:	n/a
19	chr6:25710694-25710744	HPAEpiC	pulmonary alveolar:	n/a
20	chr6:25710535-25710585	NHDF-neo	bronchial:	n/a
21	chr6:25710535-25710585	GM12878	blood:	n/a
22	chr6:25710694-25710744	ProgFib	skin:	n/a
23	chr6:25710535-25710585	LNCaP	prostate:	n/a
24	chr6:25710694-25710744	SK-N-MC	brain:	n/a
25	chr6:25710694-25710744	HAEpiC	amniotic membrane:	n/a
26	chr6:25710535-25710585	GM12892	blood:	n/a
27	chr6:25710535-25710585	AG10803	skin:	n/a
28	chr6:25710535-25710585	HEK293	kidney:	embryo
29	chr6:25710694-25710744	HEK293	kidney:	embryo
30	chr6:25710535-25710585	Hela-S3	cervix:	n/a
31	chr6:25710535-25710585	A549	lung:	n/a
32	chr6:25710487-25710537	ovcar-3	ovarian:	n/a
33	chr6:25710694-25710744	Jurkat	blood:	n/a
34	chr6:25710535-25710585	K562	blood:	n/a
35	chr6:25710535-25710585	HAEpiC	amniotic membrane:	n/a
36	chr6:25710535-25710585	T-47D	breast:	n/a
37	chr6:25710487-25710537	GM12892	blood:	n/a
38	chr6:25710487-25710537	Hepatocyte	liver:	n/a
39	chr6:25710694-25710744	GM12892	blood:	n/a
40	chr6:25723861-25723911	HIPEpiC	eye:	n/a
41	chr6:25710694-25710744	HCPEpiC	choroid plexus:	n/a
42	chr6:25710694-25710744	NH-A	brain:	n/a
43	chr6:25710535-25710585	AoSMC	blood vessel:	n/a
44	chr6:25723861-25723911	SAEC	small airway:	n/a
45	chr6:25710535-25710585	HCPEpiC	choroid plexus:	n/a
46	chr6:25710694-25710744	AG09309	skin:	n/a
47	chr6:25723861-25723911	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:25710487-25710537	GM12878	blood:	n/a
49	chr6:25723861-25723911	AG10803	skin:	n/a
50	chr6:25710487-25710537	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:25720748..25721343-chr6:26003022..26004000,3	K562	blood:
2	chr6:25717832..25722141-chr6:25722443..25725099,3	K562	blood:
3	chr6:25714065..25716059-chr6:25718396..25720053,2	MCF-7	breast:
4	chr6:25721772..25722321-chr6:25942888..25943611,2	MCF-7	breast:
5	chr6:25717832..25722141-chr6:25722443..25725099,3	K562	blood:
6	chr6:25717672..25720763-chr6:26020986..26022680,3	K562	blood:
7	chr6:25720423..25721266-chr6:25942492..25943015,2	K562	blood:
8	chr6:25719318..25721096-chr6:26029005..26031442,2	K562	blood:
9	chr6:25711420..25713335-chr6:26022573..26024303,2	K562	blood:
10	chr6:25725442..25728537-chr6:25991436..25993393,3	K562	blood:
11	chr6:25724700..25728805-chr6:26024464..26033486,16	K562	blood:
12	chr6:25712922..25715328-chr6:25716054..25718089,2	K562	blood:
13	chr6:25721163..25723233-chr6:25730118..25732339,2	K562	blood:
14	chr6:25720425..25720937-chr6:25942489..25943337,2	MCF-7	breast:
15	chr6:25709867..25711418-chr6:25725337..25726991,2	K562	blood:
16	chr6:25714065..25716059-chr6:25718396..25720053,2	MCF-7	breast:
17	chr6:25703063..25705075-chr6:25709483..25712996,3	K562	blood:
18	chr6:25709624..25713572-chr6:25719236..25722296,3	K562	blood:
19	chr6:25712922..25715328-chr6:25716054..25718089,2	K562	blood:
20	chr6:25721531..25723347-chr6:25999446..26002287,2	K562	blood:
21	chr6:25721163..25723350-chr6:25730212..25732339,2	K562	blood:
22	chr6:25710507..25713000-chr6:25726986..25729102,2	K562	blood:
23	chr6:25671372..25671922-chr6:25716866..25717391,2	MCF-7	breast:
24	chr6:25719009..25724659-chr6:26022891..26031442,10	K562	blood:
25	chr6:25720399..25720975-chr6:25890640..25891324,2	K562	blood:
26	chr6:25709624..25713572-chr6:25719236..25722296,3	K562	blood:
27	chr6:25715103..25717600-chr6:26025342..26027006,2	K562	blood:

Variant related genes	Relation type
HIST1H2BA	TF binding region
HIST1H2BA	CpG island
ENSG00000164508	chromatin interactions
ENSG00000124529	chromatin interactions
ENSG00000146047	chromatin interactions
ENSG00000272462	chromatin interactions
ENSG00000124693	chromatin interactions
ENSG00000196176	chromatin interactions
ENSG00000178762	chromatin interactions

Extended variants
information (count: 725 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:725 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4395714	chr6:25708714-25708715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs566511356	chr6:25708716-25708717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577813297	chr6:25708735-25708736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115131355	chr6:25708801-25708802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs188092844	chr6:25708824-25708825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192888317	chr6:25708889-25708890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6456688	chr6:25708960-25708961	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs11441045	chr6:25709010-25709011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs70977221	chr6:25709021-25709022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs143531620	chr6:25709022-25709023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs6901027	chr6:25709042-25709043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs572913023	chr6:25709048-25709049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs6900721	chr6:25709066-25709067	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs144884581	chr6:25709084-25709085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531059153	chr6:25709100-25709101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551287575	chr6:25709142-25709143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561603805	chr6:25709159-25709160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs185340478	chr6:25709161-25709162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6456689	chr6:25709168-25709169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11343918	chr6:25709178-25709179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6456690	chr6:25709203-25709204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs7739653	chr6:25709214-25709215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs539126257	chr6:25709217-25709218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6456691	chr6:25709223-25709224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571409111	chr6:25709239-25709240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536878821	chr6:25709361-25709362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562325334	chr6:25709364-25709365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187512054	chr6:25709365-25709366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191975804	chr6:25709382-25709383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535813558	chr6:25709396-25709397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375633063	chr6:25709457-25709458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs145107975	chr6:25709541-25709542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529482317	chr6:25709552-25709553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184945119	chr6:25709568-25709569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112057259	chr6:25709589-25709590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs138905762	chr6:25709599-25709600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562921466	chr6:25709658-25709659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544848776	chr6:25709670-25709671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561530123	chr6:25709710-25709711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4712956	chr6:25709714-25709715	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs540585046	chr6:25709733-25709734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs560536162	chr6:25709763-25709764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532438977	chr6:25709765-25709766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150410882	chr6:25709793-25709794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569279285	chr6:25709821-25709822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530588825	chr6:25709829-25709830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550378623	chr6:25709839-25709840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565344353	chr6:25709840-25709841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536146421	chr6:25709858-25709859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs553042065	chr6:25709880-25709881	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25701800-25715400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr6:25707400-25713000	Weak transcription	Brain Germinal Matrix	brain
3	chr6:25707800-25710200	Weak transcription	HepG2	liver
4	chr6:25710200-25710600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:25710200-25710800	Enhancers	HepG2	liver
6	chr6:25710400-25710800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:25710400-25710800	Enhancers	Gastric	stomach
8	chr6:25710800-25714200	Weak transcription	HepG2	liver
9	chr6:25713000-25718200	Enhancers	Brain Germinal Matrix	brain
10	chr6:25713200-25715000	Enhancers	Fetal Brain Male	brain
11	chr6:25713400-25715000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:25713400-25715000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr6:25713600-25714800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr6:25713600-25715400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:25713800-25714400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr6:25713800-25714600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr6:25713800-25714600	Enhancers	Fetal Brain Female	brain
18	chr6:25713800-25715600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:25714000-25714400	Enhancers	Brain Hippocampus Middle	brain
20	chr6:25714000-25716400	Enhancers	HUVEC	blood vessel
21	chr6:25714200-25714400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr6:25714200-25714600	Enhancers	HSMMtube	muscle
23	chr6:25714200-25715800	Enhancers	HepG2	liver
24	chr6:25714400-25716000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:25714800-25715400	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr6:25714800-25715600	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr6:25714800-25715800	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr6:25714800-25715800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:25714800-25715800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:25714800-25716200	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr6:25715000-25715400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:25715000-25715400	Weak transcription	Fetal Brain Male	brain
33	chr6:25715000-25715600	Enhancers	Primary hematopoietic stem cells	blood
34	chr6:25715000-25715600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:25715000-25716000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr6:25715400-25715600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr6:25715400-25715600	Enhancers	Fetal Brain Male	brain
38	chr6:25715400-25716000	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr6:25715600-25715800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:25715600-25718200	Weak transcription	Fetal Brain Male	brain
41	chr6:25715800-25716600	Flanking Active TSS	HepG2	liver
42	chr6:25716000-25716200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
43	chr6:25716000-25717400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr6:25716200-25716400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr6:25716200-25716600	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr6:25716200-25717200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr6:25716600-25717400	Enhancers	HepG2	liver
48	chr6:25717400-25717600	Enhancers	Primary hematopoietic stem cells short term culture	blood
49	chr6:25717400-25717800	Weak transcription	HepG2	liver
50	chr6:25717400-25726600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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