Variant report

Variant	nsv470802
Chromosome Location	chr6:13441424-13519371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1729)
CpG islands
(count:2080)
Chromatin interactive
region (count:125)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1729 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:13487615-13487775	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:13485120-13485440	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:13517443-13517812	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:13484142-13484766	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:13474635-13474878	HepG2	liver:	n/a	n/a
6	ATF1	chr6:13484426-13484881	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	ATF2	chr6:13454541-13455562	GM12878	blood:	n/a	n/a
10	ATF2	chr6:13453964-13454484	GM12878	blood:	n/a	n/a
11	ATF2	chr6:13453887-13454369	GM12878	blood:	n/a	n/a
12	ATF2	chr6:13454807-13455498	GM12878	blood:	n/a	n/a
13	BACH1	chr6:13486112-13486307	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr6:13486528-13486759	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr6:13487322-13487860	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr6:13464225-13464440	GM12878	blood:	n/a	chr6:13464355-13464366 chr6:13464356-13464366
17	BATF	chr6:13484332-13484753	GM12878	blood:	n/a	chr6:13484343-13484351 chr6:13484524-13484535
18	BATF	chr6:13453955-13454302	GM12878	blood:	n/a	n/a
19	BATF	chr6:13454765-13455167	GM12878	blood:	n/a	n/a
20	BATF	chr6:13484323-13484710	GM12878	blood:	n/a	chr6:13484343-13484351 chr6:13484524-13484535
21	BATF	chr6:13466547-13466871	GM12878	blood:	n/a	n/a
22	BCL11A	chr6:13484440-13484701	GM12878	blood:	n/a	chr6:13484618-13484627
23	BCL11A	chr6:13454785-13455108	GM12878	blood:	n/a	n/a
24	BCL11A	chr6:13484332-13484676	GM12878	blood:	n/a	chr6:13484618-13484627
25	BCL3	chr6:13518956-13519406	GM12878	blood:	n/a	n/a
26	BCL3	chr6:13466487-13466827	GM12878	blood:	n/a	n/a
27	BCLAF1	chr6:13487425-13487979	GM12878	blood:	n/a	chr6:13487731-13487744 chr6:13487728-13487741
28	BCLAF1	chr6:13454403-13455511	GM12878	blood:	n/a	n/a
29	BCLAF1	chr6:13454739-13455491	GM12878	blood:	n/a	n/a
30	BCLAF1	chr6:13484293-13484912	GM12878	blood:	n/a	chr6:13484618-13484627
31	BHLHE40	chr6:13466600-13466696	GM12878	blood:	n/a	n/a
32	BHLHE40	chr6:13454048-13454356	GM12878	blood:	n/a	n/a
33	BHLHE40	chr6:13486953-13487214	GM12878	blood:	n/a	n/a
34	BHLHE40	chr6:13488361-13488901	GM12878	blood:	n/a	chr6:13488677-13488693 chr6:13488523-13488539 chr6:13488692-13488701 chr6:13488692-13488701
35	BHLHE40	chr6:13486190-13486572	GM12878	blood:	n/a	chr6:13486336-13486352
36	BHLHE40	chr6:13485785-13487912	K562	blood:	n/a	chr6:13486336-13486352 chr6:13487437-13487453 chr6:13487232-13487248
37	BHLHE40	chr6:13488435-13488864	HepG2	liver:	n/a	chr6:13488677-13488693 chr6:13488523-13488539 chr6:13488692-13488701 chr6:13488692-13488701
38	BHLHE40	chr6:13446866-13446897	K562	blood:	n/a	n/a
39	BHLHE40	chr6:13454709-13455635	GM12878	blood:	n/a	n/a
40	BHLHE40	chr6:13474729-13474944	HepG2	liver:	n/a	n/a
41	BHLHE40	chr6:13454835-13455571	K562	blood:	n/a	n/a
42	BRCA1	chr6:13470061-13470110	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr6:13485959-13486471	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr6:13486781-13487276	K562	blood:	n/a	n/a
45	CBX3	chr6:13487452-13487949	K562	blood:	n/a	n/a
46	CBX3	chr6:13473073-13473599	K562	blood:	n/a	n/a
47	CBX3	chr6:13486083-13486758	K562	blood:	n/a	n/a
48	CCNT2	chr6:13486929-13488181	K562	blood:	n/a	n/a
49	CCNT2	chr6:13486483-13486682	K562	blood:	n/a	n/a
50	CCNT2	chr6:13488663-13488807	K562	blood:	n/a	n/a

(count:2080 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:13486415-13486465	GM12892	blood:	n/a
2	chr6:13487863-13487913	NHBE	bronchial:	n/a
3	chr6:13446618-13446668	HRCEpiC	kidney:	n/a
4	chr6:13455261-13455311	NHBE	bronchial:	n/a
5	chr6:13487903-13487953	IMR90	lung:	fetal
6	chr6:13488404-13488454	ovcar-3	ovarian:	n/a
7	chr6:13486415-13486465	GM12892	blood:	n/a
8	chr6:13487863-13487913	NHBE	bronchial:	n/a
9	chr6:13446618-13446668	HRCEpiC	kidney:	n/a
10	chr6:13455261-13455311	NHBE	bronchial:	n/a
11	chr6:13487903-13487953	IMR90	lung:	fetal
12	chr6:13488404-13488454	ovcar-3	ovarian:	n/a
13	chr6:13488257-13488307	Caco-2	colon:	n/a
14	chr6:13487662-13487712	PrEC	prostate:	n/a
15	chr6:13487018-13487068	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:13486608-13486658	IMR90	lung:	fetal
17	chr6:13486415-13486465	A549	lung:	n/a
18	chr6:13455261-13455311	NHDF-neo	bronchial:	n/a
19	chr6:13488257-13488307	CMK	blood:	n/a
20	chr6:13487883-13487933	HCM	heart:	n/a
21	chr6:13486933-13486983	NB4	blood:	n/a
22	chr6:13483832-13483882	HCM	heart:	n/a
23	chr6:13488404-13488454	AoSMC	blood vessel:	n/a
24	chr6:13487668-13487718	T-47D	breast:	n/a
25	chr6:13486425-13486475	HCF	heart:	n/a
26	chr6:13488167-13488217	PANC-1	pancreas:	n/a
27	chr6:13488167-13488217	HepG2	liver:	n/a
28	chr6:13487903-13487953	ProgFib	skin:	n/a
29	chr6:13446618-13446668	HRE	kidney:	n/a
30	chr6:13466329-13466379	LNCaP	prostate:	n/a
31	chr6:13446618-13446668	AG09319	gingival:	n/a
32	chr6:13488404-13488454	HNPCEpiC	eye:	n/a
33	chr6:13486599-13486649	AG09309	skin:	n/a
34	chr6:13470414-13470464	HepG2	liver:	n/a
35	chr6:13486249-13486299	HIPEpiC	eye:	n/a
36	chr6:13489248-13489298	HNPCEpiC	eye:	n/a
37	chr6:13486415-13486465	AG09309	skin:	n/a
38	chr6:13486249-13486299	GM12891	blood:	n/a
39	chr6:13486425-13486475	AoSMC	blood vessel:	n/a
40	chr6:13486415-13486465	Jurkat	blood:	n/a
41	chr6:13469700-13469750	HL-60	blood:	n/a
42	chr6:13511629-13511679	SAEC	small airway:	n/a
43	chr6:13483832-13483882	HNPCEpiC	eye:	n/a
44	chr6:13487879-13487929	GM06990	blood:	n/a
45	chr6:13470414-13470464	SK-N-SH	brain:	n/a
46	chr6:13483832-13483882	GM19239	blood:	n/a
47	chr6:13487903-13487953	BE2_C	brain:	n/a
48	chr6:13466329-13466379	IMR90	lung:	fetal
49	chr6:13471187-13471237	HNPCEpiC	eye:	n/a
50	chr6:13511629-13511679	AG04449	skin:	fetal

(count:125 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr6:13474713..13477366-chr6:13526684..13528787,2	MCF-7	breast:
2	chr6:13463587..13466564-chr6:13486037..13488504,4	MCF-7	breast:
3	chr6:13476011..13478760-chr6:13574075..13576220,2	MCF-7	breast:
4	chr6:13468490..13471439-chr6:13483203..13485930,2	K562	blood:
5	chr6:13493859..13496685-chr6:13512133..13514978,2	K562	blood:
6	chr6:13495546..13497355-chr6:13501574..13503680,2	MCF-7	breast:
7	chr6:13491461..13493545-chr6:13494855..13497740,2	K562	blood:
8	chr6:13453259..13455801-chr6:13460525..13463218,2	K562	blood:
9	chr6:13451477..13453744-chr6:13519512..13521827,2	MCF-7	breast:
10	chr6:13508787..13510378-chr6:13511004..13513571,2	K562	blood:
11	chr6:13487783..13489612-chr6:13498824..13500617,2	MCF-7	breast:
12	chr6:13460797..13463308-chr6:13464460..13467196,3	K562	blood:
13	chr6:13511916..13513600-chr6:13535489..13538424,2	K562	blood:
14	chr6:13486342..13488490-chr6:13504374..13507205,2	MCF-7	breast:
15	chr6:13491461..13493545-chr6:13494855..13497740,2	K562	blood:
16	chr6:13448651..13450456-chr6:13485569..13487578,2	MCF-7	breast:
17	chr6:13485719..13487951-chr6:13517533..13519891,2	MCF-7	breast:
18	chr6:13509314..13512710-chr6:13515099..13518078,3	MCF-7	breast:
19	chr6:13450822..13452338-chr6:13457314..13458935,2	K562	blood:
20	chr6:13484393..13490113-chr6:13572102..13578017,14	MCF-7	breast:
21	chr6:13447200..13448830-chr6:13453406..13456212,2	MCF-7	breast:
22	chr6:13494551..13497171-chr6:13614158..13616088,2	MCF-7	breast:
23	chr6:13509236..13512148-chr6:13513623..13517377,3	K562	blood:
24	chr6:13413198..13414739-chr6:13489299..13490913,2	MCF-7	breast:
25	chr6:13273285..13276286-chr6:13486162..13489029,4	K562	blood:
26	chr6:13408139..13410381-chr6:13486541..13489029,3	MCF-7	breast:
27	chr6:13476458..13478204-chr6:13481195..13483832,3	K562	blood:
28	chr6:13458896..13460538-chr6:13462649..13464736,2	K562	blood:
29	chr6:13327291..13329947-chr6:13444548..13447508,3	K562	blood:
30	chr6:13454821..13457095-chr6:13613822..13616173,2	MCF-7	breast:
31	chr6:13463240..13466213-chr6:13468578..13470561,2	MCF-7	breast:
32	chr6:13328740..13330326-chr6:13487032..13488615,2	K562	blood:
33	chr6:13483604..13488920-chr6:13494786..13499283,6	K562	blood:
34	chr6:13355838..13357537-chr6:13511461..13514141,2	K562	blood:
35	chr6:13491132..13493545-chr6:13494855..13497448,2	K562	blood:
36	chr6:13491132..13493545-chr6:13494855..13497448,2	K562	blood:
37	chr6:13421809..13424895-chr6:13440143..13443244,3	MCF-7	breast:
38	chr6:13463059..13465217-chr6:13614576..13616808,2	MCF-7	breast:
39	chr6:13406145..13408180-chr6:13453724..13455818,2	MCF-7	breast:
40	chr6:13509236..13512148-chr6:13513623..13517377,3	K562	blood:
41	chr6:13406818..13408886-chr6:13483840..13488220,5	MCF-7	breast:
42	chr6:13489026..13490564-chr6:13494155..13495687,2	K562	blood:
43	chr6:13465251..13472690-chr6:13481619..13489131,10	K562	blood:
44	chr6:13476458..13478204-chr6:13481195..13483832,3	K562	blood:
45	chr6:13515852..13517581-chr6:13613414..13615781,2	K562	blood:
46	chr6:13486149..13488629-chr6:13509157..13510950,2	MCF-7	breast:
47	chr6:13494194..13498063-chr6:13500323..13502186,3	K562	blood:
48	chr6:13489026..13490564-chr6:13494155..13495687,2	K562	blood:
49	chr6:13491035..13492887-chr6:13614298..13616529,2	MCF-7	breast:
50	chr6:13471062..13472931-chr6:13486374..13489089,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL583828.1-1	chr6:13469502-13470862	NONHSAT107806
2	lnc-AL583828.1-1	chr6:13472213-13472295	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
ENSG00000124523	chromatin interactions
ENSG00000261071	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000145990	chromatin interactions
ENSG00000237786	chromatin interactions
ENSG00000225921	chromatin interactions
ENSG00000215022	chromatin interactions
ENSG00000218265	chromatin interactions
ENSG00000187461	chromatin interactions

Extended variants
information (count: 3236 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:3236 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4715295	chr6:13441424-13441425	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544451719	chr6:13441452-13441453	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs143409906	chr6:13441464-13441465	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs145908401	chr6:13441472-13441473	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs540521932	chr6:13441473-13441474	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs115071189	chr6:13441518-13441519	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs529207328	chr6:13441554-13441555	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs1992385	chr6:13441556-13441557	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs77849619	chr6:13441558-13441559	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs28545473	chr6:13441585-13441586	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs531807516	chr6:13441591-13441592	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs571051486	chr6:13441604-13441605	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs550537284	chr6:13441618-13441619	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs570618500	chr6:13441623-13441624	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs539794596	chr6:13441630-13441631	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs367573279	chr6:13441641-13441642	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs138729084	chr6:13441690-13441691	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs566484408	chr6:13441693-13441694	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs371413698	chr6:13441711-13441712	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs574999716	chr6:13441732-13441733	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182793784	chr6:13441771-13441772	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs543658949	chr6:13441795-13441796	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs188258120	chr6:13441823-13441824	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs191759797	chr6:13441850-13441851	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs374751361	chr6:13441866-13441867	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs182988336	chr6:13441888-13441889	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs368131992	chr6:13441891-13441892	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs559832053	chr6:13441971-13441972	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs528554498	chr6:13441972-13441973	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs149260778	chr6:13442009-13442010	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs144556720	chr6:13442030-13442031	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs540532019	chr6:13442062-13442063	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs560377806	chr6:13442136-13442137	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs529269630	chr6:13442143-13442144	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs542639363	chr6:13442151-13442152	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs562886903	chr6:13442182-13442183	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs538178571	chr6:13442211-13442212	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs531754433	chr6:13442239-13442240	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs554784417	chr6:13442319-13442320	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs148448482	chr6:13442320-13442321	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs188006764	chr6:13442341-13442342	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs141803147	chr6:13442361-13442362	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs146025715	chr6:13442397-13442398	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs566746358	chr6:13442405-13442406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115846692	chr6:13442484-13442485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192434158	chr6:13442494-13442495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs545455159	chr6:13442512-13442513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182351177	chr6:13442540-13442541	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs139556531	chr6:13442547-13442548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs144201126	chr6:13442548-13442549	Weak transcription Enhancers	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
Cancer	16790693	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD

Chromatin state (count:2855 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13428800-13451200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:13430000-13445000	Weak transcription	NHEK	skin
3	chr6:13432600-13445400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:13433000-13454000	Weak transcription	Hela-S3	cervix
5	chr6:13433200-13442000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr6:13433200-13445200	Weak transcription	Brain Angular Gyrus	brain
7	chr6:13433600-13445400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:13434400-13445200	Weak transcription	Fetal Heart	heart
9	chr6:13434400-13445200	Weak transcription	Pancreas	Pancrea
10	chr6:13434400-13448000	Weak transcription	Esophagus	oesophagus
11	chr6:13435600-13445000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:13436400-13445000	Weak transcription	Primary B cells from peripheral blood	blood
13	chr6:13437200-13445000	Weak transcription	Duodenum Mucosa	Duodenum
14	chr6:13437200-13445200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr6:13437600-13445200	Weak transcription	Fetal Thymus	thymus
16	chr6:13437800-13444200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr6:13438000-13445200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr6:13438000-13445200	Weak transcription	GM12878-XiMat	blood
19	chr6:13438200-13448400	Weak transcription	Small Intestine	intestine
20	chr6:13438600-13462200	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr6:13439600-13445200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr6:13439800-13441800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:13440200-13442400	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr6:13440200-13443200	Enhancers	Fetal Lung	lung
25	chr6:13440200-13445400	Weak transcription	Psoas Muscle	Psoas
26	chr6:13440400-13441600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr6:13440400-13445000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr6:13440600-13442400	Enhancers	Adipose Nuclei	Adipose
29	chr6:13440600-13442400	Enhancers	Right Atrium	heart
30	chr6:13440800-13441600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:13440800-13441600	Enhancers	Liver	Liver
32	chr6:13440800-13441600	Enhancers	Colon Smooth Muscle	Colon
33	chr6:13440800-13441600	Enhancers	Right Ventricle	heart
34	chr6:13440800-13441600	Enhancers	NHLF	lung
35	chr6:13440800-13441800	Enhancers	Fetal Stomach	stomach
36	chr6:13440800-13441800	Enhancers	Left Ventricle	heart
37	chr6:13440800-13442800	Enhancers	Stomach Smooth Muscle	stomach
38	chr6:13441000-13441600	Enhancers	Brain Hippocampus Middle	brain
39	chr6:13441000-13441600	Enhancers	Rectal Smooth Muscle	rectum
40	chr6:13441000-13441600	Enhancers	NHDF-Ad	bronchial
41	chr6:13441000-13441800	Enhancers	Brain Anterior Caudate	brain
42	chr6:13441000-13441800	Enhancers	Fetal Muscle Leg	muscle
43	chr6:13441000-13441800	Enhancers	Rectal Mucosa Donor 29	rectum
44	chr6:13441000-13443000	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr6:13441200-13441600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr6:13441200-13441600	Enhancers	Fetal Muscle Trunk	muscle
47	chr6:13441200-13441800	Enhancers	Brain Inferior Temporal Lobe	brain
48	chr6:13441200-13442400	Active TSS	Fetal Brain Male	brain
49	chr6:13441200-13445200	Weak transcription	Brain Substantia Nigra	brain
50	chr6:13441400-13441600	Enhancers	Placenta	Placenta

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