Variant report

Variant	nsv830824
Chromosome Location	chr6:142361107-142544929
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2312)
CpG islands
(count:1891)
Chromatin interactive
region (count:131)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2312 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:142467802-142468560	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:142492534-142492795	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:142467784-142468437	K562	blood:	n/a	n/a
4	ARID3A	chr6:142528607-142528900	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:142509681-142509718	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:142433634-142433971	HepG2	liver:	n/a	n/a
7	ATF1	chr6:142468043-142468605	K562	blood:	n/a	n/a
8	ATF2	chr6:142468046-142468707	GM12878	blood:	n/a	n/a
9	ATF2	chr6:142409951-142410378	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr6:142468022-142468453	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr6:142467959-142468503	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr6:142467908-142468724	GM12878	blood:	n/a	n/a
13	ATF3	chr6:142467960-142468496	A549	lung:	n/a	n/a
14	ATF3	chr6:142468119-142468361	K562	blood:	n/a	n/a
15	ATF3	chr6:142467971-142468588	A549	lung:	n/a	chr6:142468553-142468562
16	ATF3	chr6:142468001-142468494	K562	blood:	n/a	n/a
17	BACH1	chr6:142409357-142409582	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:142468027-142468472	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:142409948-142410277	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr6:142468038-142468452	GM12878	blood:	n/a	n/a
21	BATF	chr6:142413816-142414046	GM12878	blood:	n/a	chr6:142413927-142413938
22	BATF	chr6:142413775-142414012	GM12878	blood:	n/a	chr6:142413927-142413938
23	BATF	chr6:142376411-142376651	GM12878	blood:	n/a	n/a
24	BCLAF1	chr6:142467910-142468518	K562	blood:	n/a	chr6:142468374-142468383
25	BCLAF1	chr6:142467900-142468691	GM12878	blood:	n/a	chr6:142468374-142468383
26	BCLAF1	chr6:142467983-142468766	K562	blood:	n/a	chr6:142468374-142468383
27	BCLAF1	chr6:142467982-142468621	GM12878	blood:	n/a	chr6:142468374-142468383
28	BHLHE40	chr6:142467972-142468783	K562	blood:	n/a	n/a
29	BHLHE40	chr6:142468016-142468729	HepG2	liver:	n/a	n/a
30	BHLHE40	chr6:142468001-142468591	GM12878	blood:	n/a	n/a
31	BHLHE40	chr6:142366125-142366500	HepG2	liver:	n/a	n/a
32	BHLHE40	chr6:142366123-142366493	GM12878	blood:	n/a	n/a
33	BRCA1	chr6:142467983-142468692	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr6:142468138-142468553	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:142477078-142477284	H1-hESC	embryonic stem cell:	n/a	n/a
36	BRCA1	chr6:142366297-142366496	GM12878	blood:	n/a	n/a
37	CBX3	chr6:142534533-142534958	HCT-116	colon:	n/a	n/a
38	CBX3	chr6:142534506-142534916	K562	blood:	n/a	n/a
39	CBX3	chr6:142467944-142468815	K562	blood:	n/a	n/a
40	CBX3	chr6:142528405-142528875	K562	blood:	n/a	n/a
41	CBX3	chr6:142467860-142468694	HCT-116	colon:	n/a	n/a
42	CBX3	chr6:142467973-142468795	HCT-116	colon:	n/a	n/a
43	CBX3	chr6:142534568-142534854	K562	blood:	n/a	n/a
44	CBX3	chr6:142467960-142468578	K562	blood:	n/a	n/a
45	CCNT2	chr6:142468141-142468647	K562	blood:	n/a	chr6:142468620-142468629
46	CCNT2	chr6:142504511-142504674	K562	blood:	n/a	n/a
47	CEBPB	chr6:142422323-142422633	HepG2	liver:	n/a	chr6:142422474-142422485
48	CEBPB	chr6:142433545-142433953	K562	blood:	n/a	n/a
49	CEBPB	chr6:142433569-142433930	IMR90	lung:	n/a	n/a
50	CEBPB	chr6:142366530-142366818	HepG2	liver:	n/a	chr6:142366690-142366701 chr6:142366685-142366702 chr6:142366688-142366701 chr6:142366688-142366699 chr6:142366690-142366701

(count:1891 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:142410098-142410148	IMR90	lung:	fetal
2	chr6:142410221-142410271	SKMC	muscle:	n/a
3	chr6:142468356-142468406	T-47D	breast:	n/a
4	chr6:142409202-142409252	SAEC	small airway:	n/a
5	chr6:142409939-142409989	AG04450	lung:	fetal
6	chr6:142468362-142468412	Caco-2	colon:	n/a
7	chr6:142476640-142476690	IMR90	lung:	fetal
8	chr6:142465233-142465283	HCF	heart:	n/a
9	chr6:142468512-142468562	ProgFib	skin:	n/a
10	chr6:142540447-142540497	NB4	blood:	n/a
11	chr6:142410098-142410148	RPTEC	kidney:	n/a
12	chr6:142465233-142465283	NHBE	bronchial:	n/a
13	chr6:142409630-142409680	AG09309	skin:	n/a
14	chr6:142468656-142468706	ECC-1	luminal epithelium:	n/a
15	chr6:142468197-142468247	SK-N-MC	brain:	n/a
16	chr6:142409993-142410043	PrEC	prostate:	n/a
17	chr6:142540447-142540497	HCM	heart:	n/a
18	chr6:142409417-142409467	A549	lung:	n/a
19	chr6:142409630-142409680	GM12891	blood:	n/a
20	chr6:142409939-142409989	HRCEpiC	kidney:	n/a
21	chr6:142468432-142468482	AG04449	skin:	fetal
22	chr6:142410221-142410271	HRE	kidney:	n/a
23	chr6:142468191-142468241	HIPEpiC	eye:	n/a
24	chr6:142410221-142410271	AG09319	gingival:	n/a
25	chr6:142410221-142410271	HRPEpiC	eye:	n/a
26	chr6:142468346-142468396	AG04450	lung:	fetal
27	chr6:142476640-142476690	NH-A	brain:	n/a
28	chr6:142409417-142409467	HNPCEpiC	eye:	n/a
29	chr6:142409756-142409806	SK-N-SH	brain:	n/a
30	chr6:142468318-142468368	HPAEpiC	pulmonary alveolar:	n/a
31	chr6:142410235-142410285	Hepatocyte	liver:	n/a
32	chr6:142409630-142409680	GM12892	blood:	n/a
33	chr6:142468656-142468706	PANC-1	pancreas:	n/a
34	chr6:142468191-142468241	SK-N-SH_RA	brain:	n/a
35	chr6:142468346-142468396	MCF-7	breast:	n/a
36	chr6:142410098-142410148	Caco-2	colon:	n/a
37	chr6:142410098-142410148	AG10803	skin:	n/a
38	chr6:142540447-142540497	PANC-1	pancreas:	n/a
39	chr6:142476640-142476690	SK-N-MC	brain:	n/a
40	chr6:142476640-142476690	Caco-2	colon:	n/a
41	chr6:142410100-142410150	BE2_C	brain:	n/a
42	chr6:142413804-142413854	BJ	skin:	n/a
43	chr6:142409939-142409989	NHBE	bronchial:	n/a
44	chr6:142468512-142468562	HNPCEpiC	eye:	n/a
45	chr6:142468656-142468706	HNPCEpiC	eye:	n/a
46	chr6:142468346-142468396	Jurkat	blood:	n/a
47	chr6:142476640-142476690	HNPCEpiC	eye:	n/a
48	chr6:142410098-142410148	ProgFib	skin:	n/a
49	chr6:142409756-142409806	SK-N-SH_RA	brain:	n/a
50	chr6:142468350-142468400	GM12892	blood:	n/a

(count:131 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:18028840..18030359-chr6:142364797..142366321,2	K562	blood:
2	chr6:142476386..142478985-chr6:142483280..142485789,2	MCF-7	breast:
3	chr6:142470687..142472679-chr6:142481549..142483699,2	K562	blood:
4	chr11:62607617..62609155-chr6:142364815..142367815,4	K562	blood:
5	chr6:141998840..141999399-chr6:142365802..142366506,2	MCF-7	breast:
6	chr6:4691449..4692204-chr6:142470501..142471255,2	MCF-7	breast:
7	chr6:142481873..142484319-chr6:142484922..142487226,2	MCF-7	breast:
8	chr3:73160094..73162090-chr6:142364795..142366316,3	MCF-7	breast:
9	chr3:73159958..73160528-chr6:142365797..142366324,3	HCT-116	colon:
10	chr17:41391026..41393127-chr6:142366322..142367825,2	K562	blood:
11	chr6:142481873..142484319-chr6:142484922..142487226,2	MCF-7	breast:
12	chr5:96695823..96698804-chr6:142366314..142367822,2	K562	blood:
13	chr6:142470533..142472236-chr6:142476885..142478577,2	K562	blood:
14	chr6:106716720..106717223-chr6:142365820..142366802,2	Hela-S3	cervix:
15	chr6:142388215..142391078-chr6:142393829..142396159,2	K562	blood:
16	chr17:41398699..41402637-chr6:142364804..142367821,8	MCF-7	breast:
17	chr12:77377724..77379224-chr6:142364821..142367801,2	K562	blood:
18	chr11:62607617..62610628-chr6:142364795..142367820,5	K562	blood:
19	chr6:142509860..142511893-chr6:142513753..142515292,2	K562	blood:
20	chr12:46766043..46766884-chr6:142365797..142366324,2	Hela-S3	cervix:
21	chr3:73160527..73161088-chr6:142365825..142366825,2	Hela-S3	cervix:
22	chr6:142477371..142478101-chr6:142709070..142709995,3	K562	blood:
23	chr13:58066693..58068213-chr6:142366296..142367819,2	K562	blood:
24	chr3:73160568..73161090-chr6:142365795..142366302,2	HCT-116	colon:
25	chr3:73158440..73161632-chr6:142364819..142367821,7	K562	blood:
26	chr6:142510733..142514047-chr6:142522766..142526301,3	K562	blood:
27	chr6:142460806..142463212-chr6:142465589..142468326,2	K562	blood:
28	chr2:169365158..169366659-chr6:142366300..142367803,2	K562	blood:
29	chr6:142366297..142366805-chr8:21899435..21899935,2	Hela-S3	cervix:
30	chr17:41462135..41468687-chr6:142364795..142367816,19	K562	blood:
31	chr6:142467676..142468644-chr6:142527890..142529634,6	MCF-7	breast:
32	chr6:142365543..142367464-chr6:142370102..142372383,2	K562	blood:
33	chr10:111980949..111982469-chr6:142364799..142366321,4	K562	blood:
34	chr6:142489018..142492180-chr6:142492773..142495963,3	K562	blood:
35	chr6:142366316..142367825-chrX:77930343..77931843,2	K562	blood:
36	chr6:141998374..141999368-chr6:142433353..142434249,2	MCF-7	breast:
37	chr17:41398742..41402600-chr6:142364799..142367825,21	K562	blood:
38	chr6:142310101..142311090-chr6:142528288..142529452,4	K562	blood:
39	chr6:142466713..142469829-chr6:142527405..142530920,3	K562	blood:
40	chr6:142475480..142479893-chr6:142481592..142484800,4	K562	blood:
41	chr22:50800361..50801881-chr6:142366303..142367821,2	K562	blood:
42	chr6:142366315..142366817-chr9:100684493..100685268,2	Hela-S3	cervix:
43	chr6:142366299..142366821-chrX:77931323..77931843,2	Hela-S3	cervix:
44	chr21:43172983..43173483-chr6:142366294..142366805,2	Hela-S3	cervix:
45	chr19:13218616..13221596-chr6:142366317..142367817,2	K562	blood:
46	chr3:73159944..73162090-chr6:142364797..142366302,3	MCF-7	breast:
47	chr19:49943464..49943982-chr6:142365804..142366321,2	Hela-S3	cervix:
48	chr19:49942462..49943984-chr6:142364795..142366315,3	K562	blood:
49	chr3:115770645..115772165-chr6:142364804..142366315,2	MCF-7	breast:
50	chr6:142475480..142479893-chr6:142481592..142484800,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJE1-4	chr6:142495920-142496027	NONHSAT115305
2	lnc-GJE1-6	chr6:142383854-142384190	NONHSAT115302
3	lnc-GJE1-4	chr6:142497360-142497981	NONHSAT115305
4	lnc-GJE1-4	chr6:142496680-142496862	NONHSAT115305

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	VTA1	hsa-miR-455-5p	chr6:142510580-142510603

Variant related genes	Relation type
ENSG00000270983	TF binding region
GJE1	TF binding region
VTA1	TF binding region
ENSG00000236822	TF binding region
NMBR	TF binding region
ENSG00000270983	CpG island
GJE1	CpG island
VTA1	CpG island
ENSG00000236822	CpG island
NMBR	CpG island
ENSG00000104888	chromatin interactions
ENSG00000136932	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000257199	chromatin interactions
ENSG00000147454	chromatin interactions
ENSG00000135521	chromatin interactions
ENSG00000112414	chromatin interactions
ENSG00000270983	chromatin interactions
ENSG00000009844	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000104907	chromatin interactions
ENSG00000158815	chromatin interactions
ENSG00000223247	chromatin interactions

Extended variants
information (count: 4182 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4182 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4130452	chr6:142361144-142361145	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144172532	chr6:142361153-142361154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573854056	chr6:142361159-142361160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146033514	chr6:142361163-142361164	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5880523	chr6:142361166-142361167	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571532153	chr6:142361210-142361211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577389417	chr6:142361244-142361245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs142073398	chr6:142361264-142361265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559849611	chr6:142361275-142361276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4130453	chr6:142361296-142361297	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs4130454	chr6:142361304-142361305	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs189238210	chr6:142361314-142361315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531923838	chr6:142361330-142361331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151160749	chr6:142361357-142361358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs567591932	chr6:142361368-142361369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs571893968	chr6:142361377-142361378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs192623756	chr6:142361391-142361392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547998097	chr6:142361540-142361541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371091217	chr6:142361541-142361542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114856693	chr6:142361556-142361557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536701868	chr6:142361569-142361570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554673805	chr6:142361570-142361571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184894854	chr6:142361582-142361583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7452468	chr6:142361594-142361595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536800770	chr6:142361613-142361614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs537771439	chr6:142361616-142361617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75708450	chr6:142361649-142361650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114273739	chr6:142361769-142361770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544845351	chr6:142361792-142361793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs188625330	chr6:142361839-142361840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs571812944	chr6:142361846-142361847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72983867	chr6:142361852-142361853	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs560739967	chr6:142361904-142361905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531311133	chr6:142361908-142361909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77815823	chr6:142362039-142362040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181740117	chr6:142362096-142362097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs532849710	chr6:142362183-142362184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs199681590	chr6:142362203-142362204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140228851	chr6:142362272-142362273	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566234682	chr6:142362277-142362278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567174403	chr6:142362321-142362322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537528695	chr6:142362359-142362360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186093322	chr6:142362362-142362363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530150357	chr6:142362369-142362370	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144801145	chr6:142362380-142362381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147942416	chr6:142362381-142362382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538812320	chr6:142362467-142362468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs4607449	chr6:142362548-142362549	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs558519310	chr6:142362584-142362585	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs571255156	chr6:142362721-142362722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	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
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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Breast cancer	21364760	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Burkitt''s lymphoma	19759907	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:2681 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142359600-142361200	Enhancers	HSMM	muscle
2	chr6:142360000-142361200	Enhancers	HSMMtube	muscle
3	chr6:142360400-142361800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:142360600-142361800	Weak transcription	HMEC	breast
5	chr6:142360600-142366200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:142360600-142366200	Weak transcription	Osteobl	bone
7	chr6:142360800-142366200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:142360800-142366200	Weak transcription	NHLF	lung
9	chr6:142361000-142366200	Weak transcription	NHDF-Ad	bronchial
10	chr6:142361800-142362200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:142361800-142362200	Enhancers	HMEC	breast
12	chr6:142361800-142362400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr6:142362000-142362400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:142362200-142363200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:142362200-142376600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr6:142362400-142362800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:142362400-142363000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:142362400-142363200	Enhancers	Brain Germinal Matrix	brain
19	chr6:142366200-142366400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:142366200-142366400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr6:142366200-142366400	Flanking Active TSS	Osteobl	bone
22	chr6:142366200-142366600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:142366200-142366600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:142366200-142366600	Enhancers	Adipose Nuclei	Adipose
25	chr6:142366200-142366600	Enhancers	Liver	Liver
26	chr6:142366200-142366800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr6:142366200-142367000	Enhancers	NHDF-Ad	bronchial
28	chr6:142366200-142367200	Enhancers	NHLF	lung
29	chr6:142366400-142366600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:142366400-142366800	Active TSS	Osteobl	bone
31	chr6:142366600-142367400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr6:142366800-142369000	Weak transcription	Osteobl	bone
33	chr6:142367000-142367200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:142367200-142370600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:142369000-142369600	Active TSS	Osteobl	bone
36	chr6:142369400-142369600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr6:142369400-142369800	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr6:142369600-142370000	Active TSS	Brain Angular Gyrus	brain
39	chr6:142376600-142377400	Enhancers	Fetal Stomach	stomach
40	chr6:142376600-142377400	Enhancers	HMEC	breast
41	chr6:142376600-142377600	Enhancers	Stomach Smooth Muscle	stomach
42	chr6:142376600-142377600	Enhancers	NHEK	skin
43	chr6:142376600-142377800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:142377600-142378000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr6:142377800-142382000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:142378000-142378200	Enhancers	Stomach Smooth Muscle	stomach
47	chr6:142378200-142379600	Weak transcription	Stomach Smooth Muscle	stomach
48	chr6:142379000-142379200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:142379200-142379400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr6:142379200-142379600	Active TSS	NHDF-Ad	bronchial

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