Variant report

Variant	nsv522875
Chromosome Location	chr6:149643709-149762537
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1251)
CpG islands
(count:1099)
Chromatin interactive
region (count:151)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:13)

(count:1251 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:149679111-149679474	K562	blood:	n/a	n/a
2	ARID3A	chr6:149680622-149681136	K562	blood:	n/a	n/a
3	ARID3A	chr6:149761833-149761881	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:149728695-149728717	K562	blood:	n/a	n/a
5	ARID3A	chr6:149678634-149678740	K562	blood:	n/a	n/a
6	ARID3A	chr6:149753093-149753436	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:149762478-149762931	HepG2	liver:	n/a	n/a
8	ATF1	chr6:149727101-149727335	K562	blood:	n/a	n/a
9	ATF1	chr6:149655360-149655560	K562	blood:	n/a	n/a
10	ATF2	chr6:149753021-149753565	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:149753036-149753475	GM12878	blood:	n/a	n/a
12	ATF3	chr6:149727009-149727485	K562	blood:	n/a	chr6:149727355-149727365
13	BACH1	chr6:149680602-149680872	K562	blood:	n/a	n/a
14	BACH1	chr6:149679031-149679341	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:149679017-149679418	K562	blood:	n/a	n/a
16	BATF	chr6:149657035-149657451	GM12878	blood:	n/a	chr6:149657194-149657205 chr6:149657252-149657263
17	BATF	chr6:149759878-149760455	GM12878	blood:	n/a	n/a
18	BATF	chr6:149701714-149702007	GM12878	blood:	n/a	chr6:149701818-149701829
19	BATF	chr6:149760096-149760455	GM12878	blood:	n/a	n/a
20	BCL11A	chr6:149713689-149714085	GM12878	blood:	n/a	n/a
21	BCL11A	chr6:149713704-149714053	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:149760019-149760454	GM12878	blood:	n/a	n/a
23	BCL3	chr6:149761942-149762469	GM12878	blood:	n/a	n/a
24	BCL3	chr6:149762178-149762410	GM12878	blood:	n/a	n/a
25	BCLAF1	chr6:149753042-149753521	GM12878	blood:	n/a	n/a
26	BCLAF1	chr6:149759965-149760388	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:149753100-149753494	K562	blood:	n/a	n/a
28	BHLHE40	chr6:149760223-149760371	GM12878	blood:	n/a	n/a
29	BHLHE40	chr6:149753137-149753431	GM12878	blood:	n/a	n/a
30	BHLHE40	chr6:149699806-149699846	K562	blood:	n/a	n/a
31	BRCA1	chr6:149753154-149753362	HepG2	liver:	n/a	n/a
32	BRCA1	chr6:149753165-149753443	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr6:149753303-149753611	GM12878	blood:	n/a	n/a
34	CBX3	chr6:149655297-149656426	HCT-116	colon:	n/a	n/a
35	CBX3	chr6:149656939-149658169	HCT-116	colon:	n/a	n/a
36	CBX3	chr6:149656929-149657609	HCT-116	colon:	n/a	n/a
37	CCNT2	chr6:149680640-149680887	K562	blood:	n/a	n/a
38	CCNT2	chr6:149685620-149685886	K562	blood:	n/a	n/a
39	CEBPB	chr6:149727106-149727506	A549	lung:	n/a	n/a
40	CEBPB	chr6:149680484-149680928	K562	blood:	n/a	n/a
41	CEBPB	chr6:149714443-149714679	IMR90	lung:	n/a	chr6:149714524-149714541 chr6:149714529-149714540 chr6:149714527-149714540
42	CEBPB	chr6:149657123-149657452	A549	lung:	n/a	n/a
43	CEBPB	chr6:149685681-149686037	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:149727046-149727522	K562	blood:	n/a	n/a
45	CEBPB	chr6:149671052-149671219	K562	blood:	n/a	n/a
46	CEBPB	chr6:149727838-149727862	K562	blood:	n/a	n/a
47	CEBPB	chr6:149657132-149657479	A549	lung:	n/a	n/a
48	CEBPB	chr6:149652557-149652869	IMR90	lung:	n/a	n/a
49	CEBPB	chr6:149727026-149727573	A549	lung:	n/a	n/a
50	CEBPB	chr6:149656962-149657586	HCT-116	colon:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:149721844-149721894	SK-N-MC	brain:	n/a
2	chr6:149721844-149721894	SK-N-MC	brain:	n/a
3	chr6:149744830-149744880	Hepatocyte	liver:	n/a
4	chr6:149721359-149721409	H1-hESC	embryonic stem cell:	embryo
5	chr6:149751225-149751275	HPAEpiC	pulmonary alveolar:	n/a
6	chr6:149658548-149658598	HCPEpiC	choroid plexus:	n/a
7	chr6:149658548-149658598	NH-A	brain:	n/a
8	chr6:149653214-149653264	HRE	kidney:	n/a
9	chr6:149721145-149721195	GM12891	blood:	n/a
10	chr6:149674055-149674105	HAEpiC	amniotic membrane:	n/a
11	chr6:149716235-149716285	K562	blood:	n/a
12	chr6:149674055-149674105	HUVEC	blood vessel:	n/a
13	chr6:149751415-149751465	BJ	skin:	n/a
14	chr6:149732642-149732692	CMK	blood:	n/a
15	chr6:149721844-149721894	HCT-116	colon:	n/a
16	chr6:149657288-149657338	Caco-2	colon:	n/a
17	chr6:149744830-149744880	T-47D	breast:	n/a
18	chr6:149721376-149721426	SKMC	muscle:	n/a
19	chr6:149653214-149653264	BJ	skin:	n/a
20	chr6:149674055-149674105	NH-A	brain:	n/a
21	chr6:149744830-149744880	NHDF-neo	bronchial:	n/a
22	chr6:149674055-149674105	HPAEpiC	pulmonary alveolar:	n/a
23	chr6:149657288-149657338	IMR90	lung:	fetal
24	chr6:149716235-149716285	SK-N-MC	brain:	n/a
25	chr6:149721376-149721426	IMR90	lung:	fetal
26	chr6:149721367-149721417	HCF	heart:	n/a
27	chr6:149721425-149721475	HCPEpiC	choroid plexus:	n/a
28	chr6:149674055-149674105	HNPCEpiC	eye:	n/a
29	chr6:149658548-149658598	HCM	heart:	n/a
30	chr6:149657288-149657338	HepG2	liver:	n/a
31	chr6:149721359-149721409	HIPEpiC	eye:	n/a
32	chr6:149721376-149721426	HCT-116	colon:	n/a
33	chr6:149716235-149716285	HMEC	breast:	n/a
34	chr6:149653214-149653264	ECC-1	luminal epithelium:	n/a
35	chr6:149657288-149657338	HRE	kidney:	n/a
36	chr6:149721844-149721894	ECC-1	luminal epithelium:	n/a
37	chr6:149657288-149657338	RPTEC	kidney:	n/a
38	chr6:149674055-149674105	GM12892	blood:	n/a
39	chr6:149732642-149732692	GM19239	blood:	n/a
40	chr6:149721367-149721417	SKMC	muscle:	n/a
41	chr6:149721376-149721426	AG09309	skin:	n/a
42	chr6:149721367-149721417	NH-A	brain:	n/a
43	chr6:149653214-149653264	SK-N-SH_RA	brain:	n/a
44	chr6:149721376-149721426	Jurkat	blood:	n/a
45	chr6:149721844-149721894	Jurkat	blood:	n/a
46	chr6:149721480-149721530	A549	lung:	n/a
47	chr6:149721367-149721417	MCF10A-Er-Src	breast:	n/a
48	chr6:149744830-149744880	IMR90	lung:	fetal
49	chr6:149674055-149674105	MCF-7	breast:	n/a
50	chr6:149721145-149721195	Hepatocyte	liver:	n/a

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:149742080..149743974-chr6:149748766..149751309,2	MCF-7	breast:
2	chr6:149762143..149764363-chr6:149765543..149768268,2	K562	blood:
3	chr6:149680069..149683623-chr6:149692115..149695638,3	MCF-7	breast:
4	chr6:149637077..149638837-chr6:149727129..149729209,2	K562	blood:
5	chr6:149681410..149684153-chr6:149703161..149705168,2	MCF-7	breast:
6	chr6:149681016..149683227-chr6:149684607..149686407,2	K562	blood:
7	chr6:149637223..149639527-chr6:149652423..149654557,3	K562	blood:
8	chr6:149637223..149641886-chr6:149650956..149658366,12	K562	blood:
9	chr6:149654628..149657508-chr6:149659280..149661788,2	MCF-7	breast:
10	chr6:149683181..149685215-chr6:149697904..149699618,2	MCF-7	breast:
11	chr6:149704358..149706531-chr6:149865675..149867741,2	K562	blood:
12	chr6:149669144..149671922-chr6:149672663..149676405,4	K562	blood:
13	chr6:149350092..149350652-chr6:149752991..149753790,4	MCF-7	breast:
14	chr6:149648554..149650974-chr6:149651371..149654134,3	K562	blood:
15	chr6:149687354..149691284-chr6:149691727..149695160,5	K562	blood:
16	chr6:149681016..149683227-chr6:149684607..149686407,2	K562	blood:
17	chr6:149656360..149658618-chr6:149662826..149665284,3	MCF-7	breast:
18	chr6:149740980..149743677-chr6:149744800..149747765,2	K562	blood:
19	chr6:149749032..149751401-chr6:149754918..149757804,2	K562	blood:
20	chr6:149517097..149517616-chr6:149753109..149753764,2	K562	blood:
21	chr6:149451723..149453741-chr6:149733693..149735273,2	MCF-7	breast:
22	chr6:149646598..149650161-chr6:149650268..149655691,6	MCF-7	breast:
23	chr6:149643394..149646422-chr6:149647403..149650011,4	K562	blood:
24	chr6:149665295..149667971-chr6:149694420..149696243,2	MCF-7	breast:
25	chr6:149673851..149675432-chr6:149684048..149686168,2	K562	blood:
26	chr6:149663709..149665488-chr6:149673072..149675210,2	K562	blood:
27	chr6:149379361..149382289-chr6:149745014..149748004,4	MCF-7	breast:
28	chr6:149695296..149697351-chr6:149699878..149702367,3	K562	blood:
29	chr6:149745176..149748304-chr6:149748732..149751749,4	MCF-7	breast:
30	chr6:149349695..149350816-chr6:149752428..149753382,4	K562	blood:
31	chr6:149637886..149640856-chr6:149672929..149675312,2	MCF-7	breast:
32	chr6:149658537..149661655-chr6:149675884..149678661,3	MCF-7	breast:
33	chr6:149717319..149720273-chr6:149729105..149731048,2	K562	blood:
34	chr6:149677655..149680872-chr6:149681238..149685381,4	K562	blood:
35	chr6:149729233..149730981-chr6:149733344..149735087,2	K562	blood:
36	chr6:149748430..149751387-chr6:149751741..149754089,3	MCF-7	breast:
37	chr6:149698800..149699364-chr8:109157847..109158643,2	MCF-7	breast:
38	chr6:149695296..149697351-chr6:149699878..149702367,3	K562	blood:
39	chr6:149401238..149401990-chr6:149748324..149749629,5	MCF-7	breast:
40	chr6:149403286..149404899-chr6:149752639..149753736,6	MCF-7	breast:
41	chr6:149404330..149406131-chr6:149751650..149753242,2	MCF-7	breast:
42	chr15:97940504..97941049-chr6:149697137..149698006,2	MCF-7	breast:
43	chr6:149708149..149710549-chr6:149711025..149713026,3	K562	blood:
44	chr6:149748841..149750725-chr6:149751621..149753759,2	K562	blood:
45	chr6:149407753..149410844-chr6:149747576..149751159,3	MCF-7	breast:
46	chr6:149641665..149643677-chr6:149697235..149699195,2	MCF-7	breast:
47	chr6:149757368..149759713-chr6:149765073..149766703,2	K562	blood:
48	chr6:149733372..149735281-chr6:149738078..149740684,2	K562	blood:
49	chr6:149379587..149381868-chr6:149752319..149755254,2	MCF-7	breast:
50	chr6:149349740..149350625-chr6:149750799..149751756,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUMO4-2	chr6:149704969-149707007	NONHSAT115498

No data

(count:13 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	TAB2	hsa-let-7b-5p	chr6:149730998-149731021
2	TAB2	hsa-let-7f-5p	chr6:149731000-149731021
3	TAB2	hsa-miR-155-5p	chr6:149731673-149731680
4	TAB2	hsa-miR-98-5p	chr6:149730998-149731021
5	TAB2	hsa-miR-181a-5p	chr6:149732429-149732451
6	TAB2	hsa-miR-181a-5p	chr6:149732230-149732252
7	TAB2	hsa-miR-23b-3p	chr6:149732729-149732748
8	TAB2	hsa-let-7f-5p	chr6:149731015-149731021
9	TAB2	hsa-let-7a-5p	chr6:149730998-149731021
10	TAB2	hsa-miR-155-5p	chr6:149731657-149731680
11	TAB2	hsa-let-7a-5p	chr6:149731015-149731021
12	TAB2	hsa-miR-98-5p	chr6:149731015-149731021
13	TAB2	hsa-let-7b-5p	chr6:149731015-149731021

Variant related genes	Relation type
TAB2	TF binding region
SUMO4	TF binding region
TAB2	CpG island
SUMO4	CpG island
ENSG00000055208	chromatin interactions
ENSG00000131013	chromatin interactions
ENSG00000177688	chromatin interactions
ENSG00000236591	chromatin interactions

Extended variants
information (count: 4458 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:4458 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9498321	chr6:149643709-149643710	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs562375640	chr6:149643719-149643720	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs377372866	chr6:149643740-149643741	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs531413130	chr6:149643745-149643746	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs34522908	chr6:149643751-149643752	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs571332673	chr6:149643764-149643765	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs376915761	chr6:149643776-149643777	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs553458889	chr6:149643803-149643804	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs567561689	chr6:149643848-149643849	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs474369	chr6:149643962-149643963	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs554602532	chr6:149643999-149644000	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs574653888	chr6:149644058-149644059	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs73611045	chr6:149644060-149644061	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs188054842	chr6:149644078-149644079	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs543278728	chr6:149644085-149644086	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs538260214	chr6:149644215-149644216	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs192708037	chr6:149644339-149644340	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs563151932	chr6:149644365-149644366	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs374503529	chr6:149644367-149644368	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs529362585	chr6:149644396-149644397	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs377758892	chr6:149644417-149644418	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs560363515	chr6:149644455-149644456	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs556772954	chr6:149644509-149644510	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs200272936	chr6:149644515-149644516	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs573987310	chr6:149644558-149644559	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs542940016	chr6:149644593-149644594	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs563216567	chr6:149644596-149644597	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs143444941	chr6:149644633-149644634	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs551364133	chr6:149644656-149644657	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs148385182	chr6:149644674-149644675	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs472620	chr6:149644698-149644699	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs75274681	chr6:149644704-149644705	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs115224198	chr6:149644761-149644762	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs11155640	chr6:149644784-149644785	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs569950210	chr6:149644804-149644805	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs559387675	chr6:149644810-149644811	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs141562725	chr6:149644812-149644813	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs150896542	chr6:149644815-149644816	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs571649839	chr6:149644863-149644864	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs138485454	chr6:149644878-149644879	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs553924239	chr6:149644921-149644922	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs572711748	chr6:149644989-149644990	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs11441324	chr6:149645054-149645055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs397721094	chr6:149645062-149645063	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs143949077	chr6:149645091-149645092	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs184468124	chr6:149645094-149645095	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs549120521	chr6:149645105-149645106	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs576676693	chr6:149645112-149645113	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs566031778	chr6:149645267-149645268	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs544674521	chr6:149645294-149645295	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Cancer	17160897	CNVD
Breast cancer	17417639	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3801 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149640000-149649400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:149640200-149645600	Weak transcription	Left Ventricle	heart
3	chr6:149640200-149655400	Weak transcription	Esophagus	oesophagus
4	chr6:149640200-149655600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:149640400-149645600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:149640400-149648600	Weak transcription	Right Ventricle	heart
7	chr6:149640600-149645800	Weak transcription	Fetal Muscle Leg	muscle
8	chr6:149640600-149648600	Weak transcription	Skeletal Muscle Male	skeletal muscle
9	chr6:149640800-149645400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:149640800-149645600	Weak transcription	Fetal Intestine Small	intestine
11	chr6:149640800-149649000	Weak transcription	Thymus	Thymus
12	chr6:149640800-149652800	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr6:149640800-149653200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:149641000-149648400	Weak transcription	Fetal Intestine Large	intestine
15	chr6:149641200-149644000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr6:149641200-149644200	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr6:149641200-149647400	Enhancers	Primary T killer memory cells from peripheral blood	blood
18	chr6:149641200-149648400	Weak transcription	Fetal Kidney	kidney
19	chr6:149641200-149649200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:149641200-149657400	Weak transcription	Aorta	Aorta
21	chr6:149641200-149681400	Weak transcription	Fetal Stomach	stomach
22	chr6:149641400-149645600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr6:149641400-149655600	Weak transcription	Placenta	Placenta
24	chr6:149641600-149643800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr6:149641600-149644000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr6:149641600-149644600	Enhancers	Brain Hippocampus Middle	brain
27	chr6:149641600-149644800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr6:149641600-149645200	Weak transcription	Stomach Smooth Muscle	stomach
29	chr6:149641600-149645600	Weak transcription	Brain Cingulate Gyrus	brain
30	chr6:149641600-149645600	Weak transcription	Stomach Mucosa	stomach
31	chr6:149641600-149646800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr6:149641600-149646800	Weak transcription	Pancreas	Pancrea
33	chr6:149641600-149647200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
34	chr6:149641600-149648400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr6:149641600-149649400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:149641600-149652600	Weak transcription	Brain Germinal Matrix	brain
37	chr6:149641600-149656000	Weak transcription	Lung	lung
38	chr6:149641600-149660200	Enhancers	Primary T helper naive cells from peripheral blood	blood
39	chr6:149641800-149644200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
40	chr6:149641800-149645200	Weak transcription	Adipose Nuclei	Adipose
41	chr6:149641800-149645400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr6:149641800-149646600	Enhancers	A549	lung
43	chr6:149641800-149647200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:149641800-149660200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr6:149642000-149648800	Enhancers	Primary T cells from cord blood	blood
46	chr6:149642200-149644000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr6:149642200-149644600	Weak transcription	Rectal Smooth Muscle	rectum
48	chr6:149642200-149645200	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr6:149642200-149645200	Weak transcription	HMEC	breast
50	chr6:149642200-149645600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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