Variant report

Variant	nsv600994
Chromosome Location	chr6:13426539-13519434
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2277)
CpG islands
(count:2384)
Chromatin interactive
region (count:135)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2277 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:13484142-13484766	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:13474635-13474878	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:13517443-13517812	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:13485120-13485440	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:13487615-13487775	HepG2	liver:	n/a	n/a
6	ATF1	chr6:13437938-13438131	K562	blood:	n/a	n/a
7	ATF1	chr6:13454918-13455453	K562	blood:	n/a	n/a
8	ATF1	chr6:13466703-13466890	K562	blood:	n/a	n/a
9	ATF1	chr6:13429410-13429956	K562	blood:	n/a	n/a
10	ATF1	chr6:13432236-13432275	K562	blood:	n/a	n/a
11	ATF1	chr6:13484426-13484881	K562	blood:	n/a	n/a
12	ATF2	chr6:13454807-13455498	GM12878	blood:	n/a	n/a
13	ATF2	chr6:13454541-13455562	GM12878	blood:	n/a	n/a
14	ATF2	chr6:13427718-13429909	GM12878	blood:	n/a	n/a
15	ATF2	chr6:13453964-13454484	GM12878	blood:	n/a	n/a
16	ATF2	chr6:13453887-13454369	GM12878	blood:	n/a	n/a
17	ATF2	chr6:13431279-13432384	GM12878	blood:	n/a	n/a
18	ATF2	chr6:13427591-13429942	GM12878	blood:	n/a	n/a
19	ATF2	chr6:13426300-13426842	GM12878	blood:	n/a	n/a
20	ATF3	chr6:13429643-13429898	K562	blood:	n/a	chr6:13429774-13429784 chr6:13429777-13429785 chr6:13429777-13429784 chr6:13429773-13429788 chr6:13429775-13429786
21	BACH1	chr6:13487322-13487860	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:13486112-13486307	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:13486528-13486759	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr6:13427950-13428723	GM12878	blood:	n/a	n/a
25	BATF	chr6:13466547-13466871	GM12878	blood:	n/a	n/a
26	BATF	chr6:13484332-13484753	GM12878	blood:	n/a	chr6:13484343-13484351 chr6:13484524-13484535
27	BATF	chr6:13464225-13464440	GM12878	blood:	n/a	chr6:13464355-13464366 chr6:13464356-13464366
28	BATF	chr6:13428757-13429143	GM12878	blood:	n/a	n/a
29	BATF	chr6:13426424-13426768	GM12878	blood:	n/a	n/a
30	BATF	chr6:13484323-13484710	GM12878	blood:	n/a	chr6:13484343-13484351 chr6:13484524-13484535
31	BATF	chr6:13453955-13454302	GM12878	blood:	n/a	n/a
32	BATF	chr6:13427973-13429104	GM12878	blood:	n/a	n/a
33	BATF	chr6:13432127-13432401	GM12878	blood:	n/a	chr6:13432274-13432284 chr6:13432273-13432284
34	BATF	chr6:13454765-13455167	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:13426462-13426755	GM12878	blood:	n/a	n/a
36	BCL11A	chr6:13427957-13429097	GM12878	blood:	n/a	chr6:13428613-13428622 chr6:13428759-13428768
37	BCL11A	chr6:13484332-13484676	GM12878	blood:	n/a	chr6:13484618-13484627
38	BCL11A	chr6:13427929-13428828	GM12878	blood:	n/a	chr6:13428613-13428622 chr6:13428759-13428768
39	BCL11A	chr6:13434391-13434880	GM12878	blood:	n/a	n/a
40	BCL11A	chr6:13484440-13484701	GM12878	blood:	n/a	chr6:13484618-13484627
41	BCL11A	chr6:13454785-13455108	GM12878	blood:	n/a	n/a
42	BCL3	chr6:13466487-13466827	GM12878	blood:	n/a	n/a
43	BCL3	chr6:13427898-13429132	GM12878	blood:	n/a	chr6:13428613-13428622 chr6:13428759-13428768
44	BCL3	chr6:13428011-13428813	GM12878	blood:	n/a	chr6:13428613-13428622 chr6:13428759-13428768
45	BCL3	chr6:13518956-13519406	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:13427740-13429744	GM12878	blood:	n/a	chr6:13428613-13428622 chr6:13428759-13428768
47	BCLAF1	chr6:13487425-13487979	GM12878	blood:	n/a	chr6:13487731-13487744 chr6:13487728-13487741
48	BCLAF1	chr6:13484293-13484912	GM12878	blood:	n/a	chr6:13484618-13484627
49	BCLAF1	chr6:13427625-13428816	GM12878	blood:	n/a	chr6:13428613-13428622 chr6:13428759-13428768
50	BCLAF1	chr6:13454739-13455491	GM12878	blood:	n/a	n/a

(count:2384 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13487018-13487068	SAEC	small airway:	n/a
2	chr6:13489248-13489298	NB4	blood:	n/a
3	chr6:13511614-13511664	AoSMC	blood vessel:	n/a
4	chr6:13455261-13455311	AoSMC	blood vessel:	n/a
5	chr6:13487879-13487929	HRCEpiC	kidney:	n/a
6	chr6:13487018-13487068	SAEC	small airway:	n/a
7	chr6:13489248-13489298	NB4	blood:	n/a
8	chr6:13511614-13511664	AoSMC	blood vessel:	n/a
9	chr6:13455261-13455311	AoSMC	blood vessel:	n/a
10	chr6:13487879-13487929	HRCEpiC	kidney:	n/a
11	chr6:13486249-13486299	NHBE	bronchial:	n/a
12	chr6:13431216-13431266	GM12878	blood:	n/a
13	chr6:13470414-13470464	ECC-1	luminal epithelium:	n/a
14	chr6:13431216-13431266	HRE	kidney:	n/a
15	chr6:13431216-13431266	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:13487668-13487718	PrEC	prostate:	n/a
17	chr6:13486599-13486649	HCT-116	colon:	n/a
18	chr6:13486608-13486658	AG04450	lung:	fetal
19	chr6:13486608-13486658	SK-N-SH_RA	brain:	n/a
20	chr6:13486599-13486649	AG09309	skin:	n/a
21	chr6:13483832-13483882	ProgFib	skin:	n/a
22	chr6:13495838-13495888	AG04449	skin:	fetal
23	chr6:13495838-13495888	HRPEpiC	eye:	n/a
24	chr6:13486933-13486983	HNPCEpiC	eye:	n/a
25	chr6:13511629-13511679	SK-N-MC	brain:	n/a
26	chr6:13486608-13486658	NT2-D1	testis:	n/a
27	chr6:13428588-13428638	NT2-D1	testis:	n/a
28	chr6:13463084-13463134	HCPEpiC	choroid plexus:	n/a
29	chr6:13466329-13466379	SK-N-SH_RA	brain:	n/a
30	chr6:13489246-13489296	HRE	kidney:	n/a
31	chr6:13483832-13483882	ovcar-3	ovarian:	n/a
32	chr6:13455261-13455311	RPTEC	kidney:	n/a
33	chr6:13428588-13428638	HCM	heart:	n/a
34	chr6:13488404-13488454	PANC-1	pancreas:	n/a
35	chr6:13487883-13487933	PANC-1	pancreas:	n/a
36	chr6:13486249-13486299	K562	blood:	n/a
37	chr6:13486415-13486465	HL-60	blood:	n/a
38	chr6:13487879-13487929	HCF	heart:	n/a
39	chr6:13486425-13486475	Jurkat	blood:	n/a
40	chr6:13492509-13492559	HPAEpiC	pulmonary alveolar:	n/a
41	chr6:13486545-13486595	HPAEpiC	pulmonary alveolar:	n/a
42	chr6:13486545-13486595	AoSMC	blood vessel:	n/a
43	chr6:13486415-13486465	ovcar-3	ovarian:	n/a
44	chr6:13487668-13487718	NHDF-neo	bronchial:	n/a
45	chr6:13469700-13469750	AG04449	skin:	fetal
46	chr6:13486608-13486658	HEK293	kidney:	embryo
47	chr6:13431216-13431266	NHDF-neo	bronchial:	n/a
48	chr6:13487863-13487913	HL-60	blood:	n/a
49	chr6:13487018-13487068	RPTEC	kidney:	n/a
50	chr6:13487879-13487929	HRE	kidney:	n/a

(count:135 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:13423766..13425699-chr6:13428540..13431249,2	K562	blood:
2	chr6:13460797..13463308-chr6:13464460..13467196,3	K562	blood:
3	chr6:13495505..13498857-chr6:13499271..13502154,4	K562	blood:
4	chr6:13486350..13490681-chr6:13504668..13507736,4	K562	blood:
5	chr6:13471064..13474808-chr6:13475712..13480057,5	K562	blood:
6	chr6:13491132..13493545-chr6:13494855..13497448,2	K562	blood:
7	chr6:13485388..13489511-chr6:13572660..13577514,13	MCF-7	breast:
8	chr6:13461316..13464526-chr6:13474276..13478535,4	MCF-7	breast:
9	chr6:13487471..13489124-chr6:13489749..13491815,3	MCF-7	breast:
10	chr6:13516073..13517719-chr6:13525004..13527132,2	MCF-7	breast:
11	chr6:13488196..13489716-chr6:13537164..13538771,2	MCF-7	breast:
12	chr6:13426718..13428428-chr6:13429369..13431705,2	K562	blood:
13	chr6:13463240..13466213-chr6:13468578..13470561,2	MCF-7	breast:
14	chr6:13465251..13472690-chr6:13481619..13489131,10	K562	blood:
15	chr6:13451248..13453948-chr6:13613649..13615932,2	MCF-7	breast:
16	chr6:13508787..13510378-chr6:13511004..13513571,2	K562	blood:
17	chr6:13466729..13469720-chr6:13485556..13487664,2	MCF-7	breast:
18	chr6:13486736..13489619-chr6:13614070..13616875,2	MCF-7	breast:
19	chr6:13406145..13408180-chr6:13453724..13455818,2	MCF-7	breast:
20	chr6:13328740..13330326-chr6:13487032..13488615,2	K562	blood:
21	chr6:13481880..13484650-chr6:13615357..13616960,2	K562	blood:
22	chr6:13446993..13448620-chr6:13450498..13451999,2	K562	blood:
23	chr6:13509314..13512710-chr6:13515099..13518078,3	MCF-7	breast:
24	chr6:13463059..13465217-chr6:13614576..13616808,2	MCF-7	breast:
25	chr6:13459869..13463008-chr6:13572189..13575188,3	MCF-7	breast:
26	chr6:13426005..13428428-chr6:13430205..13432759,2	K562	blood:
27	chr6:13458780..13460333-chr6:13460354..13463119,2	MCF-7	breast:
28	chr6:13452284..13455212-chr6:13484298..13488054,4	K562	blood:
29	chr6:13476011..13478760-chr6:13574075..13576220,2	MCF-7	breast:
30	chr6:13474713..13477366-chr6:13526684..13528787,2	MCF-7	breast:
31	chr6:13463587..13466564-chr6:13486037..13488504,4	MCF-7	breast:
32	chr6:13408139..13410381-chr6:13486541..13489029,3	MCF-7	breast:
33	chr6:13486149..13488629-chr6:13509157..13510950,2	MCF-7	breast:
34	chr6:13466304..13467866-chr6:13471367..13474038,2	K562	blood:
35	chr6:13515710..13517282-chr6:13519419..13521735,2	K562	blood:
36	chr6:13464385..13467011-chr6:13494544..13496840,2	MCF-7	breast:
37	chr6:13483604..13490047-chr6:13490051..13499001,13	K562	blood:
38	chr6:13489026..13490564-chr6:13494155..13495687,2	K562	blood:
39	chr6:13493859..13496685-chr6:13512133..13514978,2	K562	blood:
40	chr6:13458896..13460538-chr6:13462649..13464736,2	K562	blood:
41	chr6:13489525..13492132-chr6:13508702..13511366,2	MCF-7	breast:
42	chr6:13471702..13473623-chr6:13477516..13479025,2	K562	blood:
43	chr6:13483604..13488920-chr6:13494786..13499283,6	K562	blood:
44	chr6:13469372..13471111-chr6:13483426..13485334,2	MCF-7	breast:
45	chr6:13454561..13455464-chr6:13538054..13539004,3	MCF-7	breast:
46	chr6:13450822..13452338-chr6:13457314..13458935,2	K562	blood:
47	chr6:13477336..13479814-chr6:13494111..13495894,2	MCF-7	breast:
48	chr6:13500313..13501819-chr6:13573924..13575697,2	K562	blood:
49	chr6:13426718..13428428-chr6:13429369..13431705,2	K562	blood:
50	chr6:13461316..13464526-chr6:13474276..13478535,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL583828.1-1	chr6:13472213-13472295	NONHSAT107806
2	lnc-SIRT5-3	chr6:13437936-13438069	l_3117_chr6:13436803-13438069_testes
3	lnc-SIRT5-3	chr6:13436804-13437109	l_3117_chr6:13436803-13438069_testes
4	lnc-AL583828.1-1	chr6:13469502-13470862	NONHSAT107806

No data

Variant related genes	Relation type
GFOD1-AS1	TF binding region
ENSG00000187461	TF binding region
RPS4XP7	TF binding region
GFOD1	TF binding region
GFOD1-AS1	CpG island
ENSG00000187461	CpG island
RPS4XP7	CpG island
GFOD1	CpG island
ENSG00000237786	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000187461	chromatin interactions
ENSG00000145990	chromatin interactions
ENSG00000215022	chromatin interactions
ENSG00000124523	chromatin interactions
ENSG00000218265	chromatin interactions

Extended variants
information (count: 3764 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3764 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7739234	chr6:13426539-13426540	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573159407	chr6:13426544-13426545	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs9395768	chr6:13426567-13426568	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs139136823	chr6:13426569-13426570	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs575667159	chr6:13426645-13426646	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs143987895	chr6:13426666-13426667	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7752876	chr6:13426668-13426669	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs180999674	chr6:13426690-13426691	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs541472236	chr6:13426715-13426716	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs113574831	chr6:13426751-13426752	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs545735853	chr6:13426768-13426769	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs559549125	chr6:13426778-13426779	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs7758003	chr6:13426784-13426785	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541772042	chr6:13426785-13426786	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs576812309	chr6:13426789-13426790	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs80046049	chr6:13426791-13426792	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs76235113	chr6:13426793-13426794	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs78998131	chr6:13426796-13426797	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs561649463	chr6:13426826-13426827	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs542415610	chr6:13426852-13426853	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs530649455	chr6:13426880-13426881	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs35383924	chr6:13426947-13426948	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs550680934	chr6:13426987-13426988	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs16874149	chr6:13427041-13427042	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs76477305	chr6:13427062-13427063	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs146409031	chr6:13427064-13427065	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs148640804	chr6:13427073-13427074	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs142095892	chr6:13427074-13427075	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs373116486	chr6:13427181-13427182	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs185831601	chr6:13427236-13427237	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs569144419	chr6:13427245-13427246	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs114072466	chr6:13427253-13427254	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs151200974	chr6:13427263-13427264	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs935061	chr6:13427287-13427288	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs545549868	chr6:13427296-13427297	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs140273892	chr6:13427299-13427300	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs7740220	chr6:13427302-13427303	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs188747829	chr6:13427319-13427320	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs541735876	chr6:13427322-13427323	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs181126422	chr6:13427412-13427413	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs533401627	chr6:13427439-13427440	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs530508886	chr6:13427590-13427591	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs186112570	chr6:13427600-13427601	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs34982994	chr6:13427646-13427647	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs564129701	chr6:13427723-13427724	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs533583571	chr6:13427751-13427752	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs190831060	chr6:13427798-13427799	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs549913754	chr6:13427799-13427800	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs1550521	chr6:13427800-13427801	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs114678991	chr6:13427807-13427808	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Myelodysplastic syndrome	21251322	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
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
small cell lung cancer	20016488	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
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Cancer	21183584	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
abnormal development	18461090	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	16790693	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD

Chromatin state (count:3488 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13417800-13427000	Enhancers	Psoas Muscle	Psoas
2	chr6:13419200-13428200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr6:13419400-13429800	Enhancers	Fetal Lung	lung
4	chr6:13420200-13427600	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr6:13420200-13430000	Enhancers	Fetal Stomach	stomach
6	chr6:13420400-13427400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr6:13420600-13428000	Weak transcription	Thymus	Thymus
8	chr6:13421000-13427200	Weak transcription	Primary B cells from cord blood	blood
9	chr6:13421400-13426600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr6:13421400-13427800	Weak transcription	Primary T cells from cord blood	blood
11	chr6:13422000-13427800	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:13422000-13428600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr6:13422200-13432800	Weak transcription	NHDF-Ad	bronchial
14	chr6:13423200-13427600	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr6:13423400-13427400	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr6:13423400-13427800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:13423400-13428000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:13423400-13428200	Weak transcription	K562	blood
19	chr6:13423400-13428800	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr6:13423400-13428800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:13423400-13432200	Weak transcription	A549	lung
22	chr6:13423800-13426600	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr6:13423800-13428000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:13423800-13428000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:13423800-13428800	Weak transcription	Fetal Brain Female	brain
26	chr6:13423800-13431400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr6:13423800-13431400	Weak transcription	Brain Germinal Matrix	brain
28	chr6:13423800-13433000	Weak transcription	Pancreas	Pancrea
29	chr6:13424000-13427600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr6:13424000-13427800	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr6:13424000-13428000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr6:13424000-13428000	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr6:13424000-13428000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr6:13424000-13428200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:13424000-13428400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr6:13424000-13428800	Enhancers	Stomach Smooth Muscle	stomach
37	chr6:13424000-13429000	Weak transcription	Aorta	Aorta
38	chr6:13424000-13429200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr6:13424200-13427600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr6:13424200-13427600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr6:13424200-13427600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr6:13424200-13428000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr6:13424200-13428200	Weak transcription	HUVEC	blood vessel
44	chr6:13425200-13426800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr6:13425200-13429600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr6:13425200-13430000	Enhancers	Lung	lung
47	chr6:13425200-13430200	Enhancers	Primary B cells from peripheral blood	blood
48	chr6:13425200-13431200	Enhancers	Left Ventricle	heart
49	chr6:13425200-13432200	Enhancers	Right Ventricle	heart
50	chr6:13425400-13426600	Enhancers	Rectal Smooth Muscle	rectum

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