Variant report

Variant	nsv830652
Chromosome Location	chr6:45187467-45328983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:581)
CpG islands
(count:183)
Chromatin interactive
region (count:45)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45261866-45262573	K562	blood:	n/a	n/a
2	ARID3A	chr6:45232739-45233458	HepG2	liver:	n/a	chr6:45232952-45232968
3	ARID3A	chr6:45269375-45269397	HepG2	liver:	n/a	n/a
4	ATF1	chr6:45281948-45282153	K562	blood:	n/a	n/a
5	ATF1	chr6:45190091-45190279	K562	blood:	n/a	n/a
6	ATF1	chr6:45262037-45262466	K562	blood:	n/a	n/a
7	ATF3	chr6:45319495-45319856	K562	blood:	n/a	n/a
8	BACH1	chr6:45319062-45319882	K562	blood:	n/a	n/a
9	BACH1	chr6:45247706-45247721	K562	blood:	n/a	n/a
10	BACH1	chr6:45319488-45319837	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr6:45262157-45262334	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:45262140-45262391	K562	blood:	n/a	n/a
13	CBX3	chr6:45261984-45262477	K562	blood:	n/a	n/a
14	CBX3	chr6:45210390-45210813	HCT-116	colon:	n/a	n/a
15	CBX3	chr6:45259589-45259993	K562	blood:	n/a	n/a
16	CBX3	chr6:45207452-45207700	K562	blood:	n/a	n/a
17	CBX3	chr6:45208754-45209051	K562	blood:	n/a	n/a
18	CBX3	chr6:45208754-45209148	K562	blood:	n/a	n/a
19	CBX3	chr6:45199417-45199794	K562	blood:	n/a	n/a
20	CBX3	chr6:45199449-45199702	K562	blood:	n/a	n/a
21	CCNT2	chr6:45262135-45262467	K562	blood:	n/a	n/a
22	CCNT2	chr6:45320737-45320938	K562	blood:	n/a	n/a
23	CEBPB	chr6:45268295-45268493	K562	blood:	n/a	n/a
24	CEBPB	chr6:45319502-45319784	K562	blood:	n/a	n/a
25	CEBPB	chr6:45200403-45200505	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:45255417-45255508	H1-hESC	embryonic stem cell:	n/a	chr6:45255432-45255443
27	CEBPB	chr6:45268225-45268538	K562	blood:	n/a	n/a
28	CEBPB	chr6:45255287-45255589	K562	blood:	n/a	chr6:45255432-45255443
29	CEBPB	chr6:45233106-45233415	HepG2	liver:	n/a	chr6:45233290-45233301
30	CEBPB	chr6:45266930-45267130	A549	lung:	n/a	n/a
31	CEBPB	chr6:45257386-45257633	HepG2	liver:	n/a	n/a
32	CEBPB	chr6:45255347-45255571	A549	lung:	n/a	chr6:45255432-45255443
33	CEBPB	chr6:45319430-45319835	K562	blood:	n/a	n/a
34	CEBPB	chr6:45233172-45233354	HepG2	liver:	n/a	chr6:45233290-45233301
35	CEBPB	chr6:45255313-45255603	HepG2	liver:	n/a	chr6:45255432-45255443
36	CEBPB	chr6:45210528-45210647	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr6:45266943-45267153	K562	blood:	n/a	n/a
38	CEBPB	chr6:45268239-45268562	K562	blood:	n/a	n/a
39	CEBPB	chr6:45269073-45269435	HepG2	liver:	n/a	chr6:45269237-45269248
40	CEBPB	chr6:45319479-45319852	K562	blood:	n/a	n/a
41	CEBPB	chr6:45233125-45233428	IMR90	lung:	n/a	chr6:45233290-45233301
42	CEBPD	chr6:45262060-45262575	K562	blood:	n/a	n/a
43	CEBPD	chr6:45262093-45262474	K562	blood:	n/a	n/a
44	CHD2	chr6:45238010-45238307	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr6:45238008-45238362	K562	blood:	n/a	n/a
46	CTCF	chr6:45193990-45194048	GM12878	blood:	n/a	chr6:45194005-45194014
47	CTCF	chr6:45265226-45265302	LNCaP	prostate:	n/a	n/a
48	CTCF	chr6:45193980-45194130	HEK293	kidney:	n/a	chr6:45194005-45194014
49	CTCF	chr6:45193980-45194130	AG04450	lung:	n/a	chr6:45194005-45194014
50	CTCF	chr6:45278140-45278290	GM12873	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45296101-45296151	H1-hESC	embryonic stem cell:	embryo
2	chr6:45295718-45295768	H1-hESC	embryonic stem cell:	embryo
3	chr6:45296101-45296151	PFSK-1	brain:	n/a
4	chr6:45295718-45295768	MCF-7	breast:	n/a
5	chr6:45295718-45295768	HCF	heart:	n/a
6	chr6:45296101-45296151	SK-N-SH_RA	brain:	n/a
7	chr6:45296101-45296151	AG09309	skin:	n/a
8	chr6:45294599-45294649	RPTEC	kidney:	n/a
9	chr6:45294599-45294649	BE2_C	brain:	n/a
10	chr6:45295718-45295768	GM12878	blood:	n/a
11	chr6:45296101-45296151	GM12891	blood:	n/a
12	chr6:45294599-45294649	IMR90	lung:	fetal
13	chr6:45296101-45296151	NHBE	bronchial:	n/a
14	chr6:45296101-45296151	SAEC	small airway:	n/a
15	chr6:45295718-45295768	A549	lung:	n/a
16	chr6:45296101-45296151	HPAEpiC	pulmonary alveolar:	n/a
17	chr6:45296101-45296151	AG10803	skin:	n/a
18	chr6:45295718-45295768	AG09319	gingival:	n/a
19	chr6:45294599-45294649	BJ	skin:	n/a
20	chr6:45295718-45295768	AG04449	skin:	fetal
21	chr6:45294599-45294649	AG04449	skin:	fetal
22	chr6:45296101-45296151	AG04450	lung:	fetal
23	chr6:45294599-45294649	NT2-D1	testis:	n/a
24	chr6:45296101-45296151	BE2_C	brain:	n/a
25	chr6:45295718-45295768	HCM	heart:	n/a
26	chr6:45296101-45296151	GM06990	blood:	n/a
27	chr6:45296101-45296151	HRE	kidney:	n/a
28	chr6:45296101-45296151	HRPEpiC	eye:	n/a
29	chr6:45295718-45295768	NH-A	brain:	n/a
30	chr6:45295718-45295768	HMEC	breast:	n/a
31	chr6:45294599-45294649	HCF	heart:	n/a
32	chr6:45294599-45294649	HepG2	liver:	n/a
33	chr6:45294599-45294649	K562	blood:	n/a
34	chr6:45296101-45296151	LNCaP	prostate:	n/a
35	chr6:45295718-45295768	SKMC	muscle:	n/a
36	chr6:45294599-45294649	SK-N-SH	brain:	n/a
37	chr6:45296101-45296151	NT2-D1	testis:	n/a
38	chr6:45296101-45296151	SKMC	muscle:	n/a
39	chr6:45294599-45294649	PANC-1	pancreas:	n/a
40	chr6:45295718-45295768	LNCaP	prostate:	n/a
41	chr6:45295718-45295768	PrEC	prostate:	n/a
42	chr6:45295718-45295768	T-47D	breast:	n/a
43	chr6:45295718-45295768	NB4	blood:	n/a
44	chr6:45296101-45296151	HIPEpiC	eye:	n/a
45	chr6:45295718-45295768	SK-N-SH_RA	brain:	n/a
46	chr6:45294599-45294649	GM12891	blood:	n/a
47	chr6:45295718-45295768	Hela-S3	cervix:	n/a
48	chr6:45296101-45296151	SK-N-MC	brain:	n/a
49	chr6:45294599-45294649	HCPEpiC	choroid plexus:	n/a
50	chr6:45294599-45294649	AG10803	skin:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:45301898..45307330-chr6:45307475..45313805,9	K562	blood:
2	chr6:45292654..45296444-chr6:45296488..45298804,3	K562	blood:
3	chr6:45316969..45324602-chr6:45343747..45347622,7	K562	blood:
4	chr6:45260561..45262170-chr6:45267835..45269561,2	K562	blood:
5	chr6:45226327..45228586-chr6:45230289..45234245,4	K562	blood:
6	chr6:45293709..45297564-chr6:45344489..45347736,3	K562	blood:
7	chr6:45263673..45265578-chr6:45288685..45291243,2	K562	blood:
8	chr6:45235925..45238854-chr6:45344533..45347145,2	K562	blood:
9	chr6:45320886..45324665-chr6:45343747..45345679,4	K562	blood:
10	chr6:45220520..45222060-chr6:45226309..45228939,2	MCF-7	breast:
11	chr6:45301898..45307330-chr6:45307475..45313805,9	K562	blood:
12	chr6:45200553..45203015-chr6:45211837..45214861,3	K562	blood:
13	chr6:13328120..13330665-chr6:45294928..45297649,2	MCF-7	breast:
14	chr6:45226327..45228586-chr6:45230289..45234245,4	K562	blood:
15	chr6:45232941..45235847-chr6:45236328..45239058,2	MCF-7	breast:
16	chr6:45220520..45222060-chr6:45226309..45228939,2	MCF-7	breast:
17	chr6:45305783..45308112-chr6:45339812..45341818,2	K562	blood:
18	chr6:45304794..45307348-chr6:45311162..45312827,2	MCF-7	breast:
19	chr6:45294783..45298304-chr6:45298765..45304802,5	K562	blood:
20	chr6:45271340..45273940-chr6:45277312..45279261,2	K562	blood:
21	chr6:45302590..45306713-chr6:45309297..45313421,5	K562	blood:
22	chr6:45310690..45313113-chr6:45345352..45347822,2	K562	blood:
23	chr6:45271340..45273940-chr6:45277312..45279261,2	K562	blood:
24	chr6:45200553..45203015-chr6:45211837..45214861,3	K562	blood:
25	chr6:45213921..45216260-chr6:45230809..45233624,3	K562	blood:
26	chr6:45232941..45235847-chr6:45236328..45239058,2	MCF-7	breast:
27	chr6:45296736..45299376-chr6:45345158..45347288,2	MCF-7	breast:
28	chr6:45285385..45288934-chr6:45291924..45295475,3	K562	blood:
29	chr20:59263227..59263735-chr6:45242300..45243068,2	MCF-7	breast:
30	chr6:45294565..45296467-chr6:45297982..45300166,3	MCF-7	breast:
31	chr6:45213921..45216260-chr6:45230809..45233624,3	K562	blood:
32	chr6:45304794..45307348-chr6:45311162..45312827,2	MCF-7	breast:
33	chr6:45328959..45331419-chr6:45344647..45347032,2	MCF-7	breast:
34	chr6:44928658..44930221-chr6:45326668..45328264,2	K562	blood:
35	chr6:45290102..45292496-chr6:45343857..45345735,2	K562	blood:
36	chr6:45271337..45274007-chr6:45344284..45348156,3	K562	blood:
37	chr6:45285385..45288934-chr6:45291924..45295475,3	K562	blood:
38	chr6:45260561..45262170-chr6:45267835..45269561,2	K562	blood:
39	chr6:45321773..45324627-chr6:45328640..45330333,2	K562	blood:
40	chr6:45317245..45320523-chr6:45344222..45346971,4	K562	blood:
41	chr6:45302590..45306713-chr6:45309297..45313421,5	K562	blood:
42	chr6:45293709..45295327-chr6:45344477..45346734,2	K562	blood:
43	chr6:45325121..45327435-chr6:45334510..45336608,2	K562	blood:
44	chr6:45312353..45317699-chr6:45329934..45333110,5	K562	blood:
45	chr6:45278640..45281374-chr6:45290172..45292607,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ENPP4-3	chr6:45296398-45296521	NONHSAT112978
2	lnc-ENPP4-3	chr6:45296054-45296197	NONHSAT112978
3	lnc-ENPP4-3	chr6:45296054-45296232	NONHSAT112979
4	lnc-CLIC5-2	chr6:45227949-45228305	ENSG00000230554.1
5	lnc-CLIC5-2	chr6:45227825-45227890	ENSG00000230554.1
6	lnc-CLIC5-3	chr6:45218692-45218873	NONHSAT112976
7	lnc-ENPP4-3	chr6:45296398-45296521	NONHSAT112979

No data

Variant related genes	Relation type
SUPT3H	TF binding region
RUNX2	TF binding region
SUPT3H	CpG island
RUNX2	CpG island
ENSG00000124813	chromatin interactions
ENSG00000145979	chromatin interactions
ENSG00000196284	chromatin interactions

Extended variants
information (count: 5285 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:5285 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538819351	chr6:45187477-45187478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190824124	chr6:45187495-45187496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142205126	chr6:45187515-45187516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146749320	chr6:45187543-45187544	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140359363	chr6:45187545-45187546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9349317	chr6:45187548-45187549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs13340453	chr6:45187551-45187552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184924240	chr6:45187554-45187555	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558215898	chr6:45187555-45187556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs10948216	chr6:45187556-45187557	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs558534267	chr6:45187611-45187612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs10948217	chr6:45187618-45187619	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs189780026	chr6:45187639-45187640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs531981468	chr6:45187652-45187653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs530380389	chr6:45187653-45187654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs535226852	chr6:45187679-45187680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs560483819	chr6:45187690-45187691	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527704914	chr6:45187691-45187692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376865687	chr6:45187732-45187733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112983096	chr6:45187733-45187734	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181098941	chr6:45187735-45187736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs80340644	chr6:45187777-45187778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554697216	chr6:45187778-45187779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75034354	chr6:45187779-45187780	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs67960187	chr6:45187802-45187803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs202007034	chr6:45187804-45187805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186696328	chr6:45187825-45187826	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191528914	chr6:45187897-45187898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554080295	chr6:45187915-45187916	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12660963	chr6:45187976-45187977	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs536499860	chr6:45188075-45188076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372406612	chr6:45188077-45188078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548099568	chr6:45188115-45188116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566096378	chr6:45188134-45188135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371792030	chr6:45188144-45188145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs533524652	chr6:45188196-45188197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376439798	chr6:45188206-45188207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs558178918	chr6:45188212-45188213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs553154392	chr6:45188219-45188220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs370405396	chr6:45188251-45188252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146469602	chr6:45188315-45188316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537553293	chr6:45188318-45188319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs373804466	chr6:45188322-45188323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs183812195	chr6:45188326-45188327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140750224	chr6:45188394-45188395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542476132	chr6:45188397-45188398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116000338	chr6:45188403-45188404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572803171	chr6:45188417-45188418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535847060	chr6:45188454-45188455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs188751519	chr6:45188475-45188476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Osteosarcoma	16790693	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
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Ovarian cancer	20844748	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:768 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45186200-45189200	Weak transcription	HSMM	muscle
2	chr6:45186800-45188000	Enhancers	Dnd41	blood
3	chr6:45189800-45192800	Weak transcription	Primary B cells from cord blood	blood
4	chr6:45190000-45190400	Enhancers	K562	blood
5	chr6:45190200-45190800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:45190600-45191000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:45196600-45199600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:45196800-45207600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:45197400-45198800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:45198800-45200400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:45198800-45200400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr6:45199000-45200800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr6:45199600-45200200	Weak transcription	Ovary	ovary
14	chr6:45199600-45201200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:45199600-45201400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
16	chr6:45199600-45201400	ZNF genes & repeats	Dnd41	blood
17	chr6:45199600-45201600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr6:45199800-45200400	ZNF genes & repeats	Brain Angular Gyrus	brain
19	chr6:45199800-45201000	Weak transcription	Fetal Heart	heart
20	chr6:45199800-45201200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
21	chr6:45199800-45201400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr6:45200000-45200400	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
23	chr6:45200000-45200600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
24	chr6:45200000-45201200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr6:45200000-45201200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:45200000-45201200	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr6:45200200-45200400	ZNF genes & repeats	Ovary	ovary
28	chr6:45200200-45200600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr6:45200200-45201600	ZNF genes & repeats	Fetal Intestine Large	intestine
30	chr6:45200400-45201200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr6:45200400-45201200	ZNF genes & repeats	Fetal Stomach	stomach
32	chr6:45200400-45201200	Strong transcription	Ovary	ovary
33	chr6:45200400-45201400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:45200400-45201400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:45200400-45201400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr6:45200600-45200800	ZNF genes & repeats	Primary B cells from cord blood	blood
37	chr6:45200600-45201200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr6:45200600-45201200	ZNF genes & repeats	Esophagus	oesophagus
39	chr6:45200600-45201200	ZNF genes & repeats	Lung	lung
40	chr6:45200800-45201000	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:45200800-45201200	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr6:45200800-45201400	Strong transcription	Primary B cells from cord blood	blood
43	chr6:45201000-45201400	ZNF genes & repeats	Aorta	Aorta
44	chr6:45201000-45201400	ZNF genes & repeats	Fetal Heart	heart
45	chr6:45201000-45201600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:45201000-45203400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr6:45201200-45201800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:45201200-45203400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:45201200-45203800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:45201200-45204800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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