Variant report

Variant	nsv886664
Chromosome Location	chr6:131443843-131754930
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1952)
CpG islands
(count:1468)
Chromatin interactive
region (count:48)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1952 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:131688478-131688702	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:131457111-131457634	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:131504139-131504291	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:131459690-131459766	K562	blood:	n/a	n/a
5	ARID3A	chr6:131485073-131485283	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:131456357-131456657	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:131481625-131481806	HepG2	liver:	n/a	n/a
8	ATF2	chr6:131689359-131689878	GM12878	blood:	n/a	n/a
9	ATF2	chr6:131520738-131521260	GM12878	blood:	n/a	n/a
10	ATF2	chr6:131602635-131603046	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:131614880-131615112	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:131456427-131456648	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr6:131451051-131451309	GM12878	blood:	n/a	chr6:131451179-131451189 chr6:131451178-131451189
14	BATF	chr6:131451078-131451303	GM12878	blood:	n/a	chr6:131451179-131451189 chr6:131451178-131451189
15	BATF	chr6:131520913-131521168	GM12878	blood:	n/a	n/a
16	BCLAF1	chr6:131520780-131521237	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:131456349-131457263	HepG2	liver:	n/a	chr6:131456953-131456969 chr6:131456961-131456977
18	BHLHE40	chr6:131520903-131521363	GM12878	blood:	n/a	n/a
19	BHLHE40	chr6:131457013-131457179	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:131457109-131457125	K562	blood:	n/a	n/a
21	BHLHE40	chr6:131615330-131615434	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:131658375-131658379	HepG2	liver:	n/a	n/a
23	BHLHE40	chr6:131638814-131638816	HepG2	liver:	n/a	n/a
24	BRCA1	chr6:131721187-131722017	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr6:131456609-131456644	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr6:131456401-131456653	HepG2	liver:	n/a	n/a
27	BRCA1	chr6:131455939-131456362	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr6:131520861-131521007	GM12878	blood:	n/a	n/a
29	BRCA1	chr6:131600918-131600951	GM12878	blood:	n/a	n/a
30	CBX3	chr6:131456323-131456630	K562	blood:	n/a	n/a
31	CBX3	chr6:131721613-131722328	HCT-116	colon:	n/a	n/a
32	CCNT2	chr6:131456367-131457090	K562	blood:	n/a	n/a
33	CEBPB	chr6:131641602-131641645	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr6:131493447-131493669	Hela-S3	cervix:	n/a	chr6:131493545-131493556
35	CEBPB	chr6:131711535-131711716	K562	blood:	n/a	chr6:131711661-131711678
36	CEBPB	chr6:131582226-131582427	ECC-1	luminal epithelium:	n/a	chr6:131582286-131582297
37	CEBPB	chr6:131486177-131486413	IMR90	lung:	n/a	chr6:131486384-131486396 chr6:131486322-131486333
38	CEBPB	chr6:131577153-131577476	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr6:131713735-131713978	IMR90	lung:	n/a	chr6:131713872-131713883
40	CEBPB	chr6:131451086-131451422	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:131659493-131659557	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr6:131456112-131456482	IMR90	lung:	n/a	chr6:131456292-131456305 chr6:131456294-131456305 chr6:131456292-131456303 chr6:131456294-131456305
43	CEBPB	chr6:131721441-131721949	A549	lung:	n/a	n/a
44	CEBPB	chr6:131477600-131477888	K562	blood:	n/a	n/a
45	CEBPB	chr6:131576868-131577048	HepG2	liver:	n/a	chr6:131576977-131576988
46	CEBPB	chr6:131713721-131714007	A549	lung:	n/a	chr6:131713872-131713883
47	CEBPB	chr6:131456011-131456610	A549	lung:	n/a	chr6:131456292-131456305 chr6:131456294-131456305 chr6:131456292-131456303 chr6:131456294-131456305
48	CEBPB	chr6:131511033-131511126	A549	lung:	n/a	chr6:131511073-131511084 chr6:131511073-131511086 chr6:131511073-131511086 chr6:131511073-131511086
49	CEBPB	chr6:131577143-131577459	MCF-7	breast:	n/a	n/a
50	CEBPB	chr6:131485004-131485348	IMR90	lung:	n/a	chr6:131485179-131485190

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:131745773-131745823	BJ	skin:	n/a
2	chr6:131456780-131456830	HCM	heart:	n/a
3	chr6:131642853-131642903	AoSMC	blood vessel:	n/a
4	chr6:131642853-131642903	NH-A	brain:	n/a
5	chr6:131745773-131745823	BJ	skin:	n/a
6	chr6:131456780-131456830	HCM	heart:	n/a
7	chr6:131642853-131642903	AoSMC	blood vessel:	n/a
8	chr6:131642853-131642903	NH-A	brain:	n/a
9	chr6:131456780-131456830	GM06990	blood:	n/a
10	chr6:131690266-131690316	MCF10A-Er-Src	breast:	n/a
11	chr6:131722497-131722547	HRE	kidney:	n/a
12	chr6:131504781-131504831	IMR90	lung:	fetal
13	chr6:131456365-131456415	PrEC	prostate:	n/a
14	chr6:131548063-131548113	SAEC	small airway:	n/a
15	chr6:131481003-131481053	HEK293	kidney:	embryo
16	chr6:131613706-131613756	Caco-2	colon:	n/a
17	chr6:131722497-131722547	SK-N-SH	brain:	n/a
18	chr6:131571669-131571719	HUVEC	blood vessel:	n/a
19	chr6:131457146-131457196	AG04450	lung:	fetal
20	chr6:131456365-131456415	A549	lung:	n/a
21	chr6:131456780-131456830	CMK	blood:	n/a
22	chr6:131613706-131613756	AG09319	gingival:	n/a
23	chr6:131613706-131613756	HMEC	breast:	n/a
24	chr6:131456780-131456830	HIPEpiC	eye:	n/a
25	chr6:131705123-131705173	NH-A	brain:	n/a
26	chr6:131455450-131455500	ECC-1	luminal epithelium:	n/a
27	chr6:131456365-131456415	MCF10A-Er-Src	breast:	n/a
28	chr6:131705123-131705173	NHDF-neo	bronchial:	n/a
29	chr6:131657922-131657972	A549	lung:	n/a
30	chr6:131745773-131745823	NB4	blood:	n/a
31	chr6:131484138-131484188	HCPEpiC	choroid plexus:	n/a
32	chr6:131571669-131571719	SK-N-SH_RA	brain:	n/a
33	chr6:131602870-131602920	NB4	blood:	n/a
34	chr6:131456785-131456835	LNCaP	prostate:	n/a
35	chr6:131457506-131457556	MCF10A-Er-Src	breast:	n/a
36	chr6:131455450-131455500	SK-N-MC	brain:	n/a
37	chr6:131456785-131456835	AG09309	skin:	n/a
38	chr6:131548063-131548113	HL-60	blood:	n/a
39	chr6:131457146-131457196	GM12878	blood:	n/a
40	chr6:131457146-131457196	NB4	blood:	n/a
41	chr6:131456785-131456835	GM12892	blood:	n/a
42	chr6:131457146-131457196	BE2_C	brain:	n/a
43	chr6:131571669-131571719	NB4	blood:	n/a
44	chr6:131613706-131613756	NH-A	brain:	n/a
45	chr6:131481003-131481053	A549	lung:	n/a
46	chr6:131602870-131602920	GM12892	blood:	n/a
47	chr6:131481003-131481053	H1-hESC	embryonic stem cell:	embryo
48	chr6:131456785-131456835	NB4	blood:	n/a
49	chr6:131613706-131613756	HUVEC	blood vessel:	n/a
50	chr6:131456785-131456835	Caco-2	colon:	n/a

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:131456917..131458462-chr6:131459846..131461723,2	MCF-7	breast:
2	chr15:69744952..69745682-chr6:131456347..131457188,2	Hela-S3	cervix:
3	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:
4	chr6:131206634..131207291-chr6:131489082..131489592,2	K562	blood:
5	chr6:131738927..131740867-chr6:131743230..131745826,2	K562	blood:
6	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
7	chr6:131562493..131564861-chr6:131566716..131568915,2	MCF-7	breast:
8	chr6:131452705..131454330-chr6:131455080..131456599,2	K562	blood:
9	chr11:62609119..62609619-chr6:131456326..131457092,2	HCT-116	colon:
10	chr6:131526816..131527805-chr6:131855115..131855774,2	MCF-7	breast:
11	chr6:131731836..131734655-chr6:131749824..131752389,2	K562	blood:
12	chr6:131614360..131616508-chr6:131705803..131707677,2	K562	blood:
13	chr6:131591823..131594173-chr6:131613820..131615536,2	K562	blood:
14	chr6:131456917..131458462-chr6:131459846..131461723,2	MCF-7	breast:
15	chr6:131715833..131718825-chr6:131734370..131736424,2	K562	blood:
16	chr6:131591823..131594173-chr6:131613820..131615536,2	K562	blood:
17	chr6:131443799..131447689-chr6:131455563..131459446,5	K562	blood:
18	chr6:131698297..131700688-chr6:131701676..131704606,3	K562	blood:
19	chr6:131455039..131456597-chr6:131460458..131462514,2	K562	blood:
20	chr6:131453607..131455513-chr6:131455602..131457616,2	MCF-7	breast:
21	chr6:131614360..131616508-chr6:131705803..131707677,2	K562	blood:
22	chr6:131715833..131718825-chr6:131734370..131736424,2	K562	blood:
23	chr6:131743564..131746106-chr6:131750332..131753297,3	MCF-7	breast:
24	chr6:131743564..131746106-chr6:131750332..131753297,3	MCF-7	breast:
25	chr6:131482888..131484884-chr6:131488327..131490881,2	MCF-7	breast:
26	chr6:131503963..131504691-chr6:131855024..131855989,3	MCF-7	breast:
27	chr6:131449929..131453503-chr6:131455186..131458213,3	MCF-7	breast:
28	chr6:131504234..131504890-chr8:67976530..67977471,2	MCF-7	breast:
29	chr4:105398713..105399471-chr6:131472742..131473607,2	MCF-7	breast:
30	chr6:131452705..131454330-chr6:131455080..131456599,2	K562	blood:
31	chr6:131731836..131734655-chr6:131749824..131752389,2	K562	blood:
32	chr6:131709683..131711909-chr6:131717715..131719994,2	MCF-7	breast:
33	chr6:131709683..131711909-chr6:131717715..131719994,2	MCF-7	breast:
34	chr6:131465952..131467796-chr6:131470590..131473026,2	MCF-7	breast:
35	chr1:1509737..1510642-chr6:131456190..131456991,2	Hela-S3	cervix:
36	chr6:131451653..131454218-chr6:131455902..131457884,2	MCF-7	breast:
37	chr6:131526933..131527448-chr6:131918295..131918857,2	MCF-7	breast:
38	chr6:131482888..131484884-chr6:131488327..131490881,2	MCF-7	breast:
39	chr6:131455039..131456597-chr6:131460458..131462514,2	K562	blood:
40	chr6:131455097..131458948-chr6:131460458..131462191,4	K562	blood:
41	chr6:131448808..131452691-chr6:131455777..131458768,3	K562	blood:
42	chr6:131520473..131521448-chr6:131582980..131583832,4	MCF-7	breast:
43	chr6:131738927..131740867-chr6:131743230..131745826,2	K562	blood:
44	chr6:131456092..131458598-chr6:131462926..131464450,2	K562	blood:
45	chr6:131206207..131207173-chr6:131488628..131489910,7	MCF-7	breast:
46	chr6:131698297..131700688-chr6:131701676..131704606,3	K562	blood:
47	chr6:131445229..131447238-chr6:131455740..131457874,2	K562	blood:
48	chr6:131574679..131577194-chr6:131577773..131580608,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EPB41L2-1	chr6:131465390-131465456	l_3256_chr6:131447706-131492675_testes
2	lnc-AKAP7-1	chr6:131619214-131619459	NONHSAT114915
3	lnc-EPB41L2-1	chr6:131447707-131447861	l_3256_chr6:131447706-131492675_testes
4	lnc-MED23-1	chr6:131649280-131649342	NONHSAT114916
5	lnc-AKAP7-1	chr6:131630402-131630414	NONHSAT114915
6	lnc-MED23-1	chr6:131652426-131652634	NONHSAT114916
7	lnc-EPB41L2-1	chr6:131492570-131492675	l_3256_chr6:131447706-131492675_testes

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AKAP7	hsa-miR-375	chr6:131604183-131604206
2	AKAP7	hsa-miR-375	chr6:131604029-131604050

Variant related genes	Relation type
AKAP7	TF binding region
ENSG00000218857	TF binding region
AKAP7	CpG island
ENSG00000218857	CpG island
ENSG00000118507	chromatin interactions
ENSG00000160075	chromatin interactions
ENSG00000137818	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000215014	chromatin interactions

Extended variants
information (count: 11798 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:11798 , 50 per page) page: 1 2 3 4 5 6 7 ... 236

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs516473	chr6:131443843-131443844	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs533090621	chr6:131443874-131443875	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35659530	chr6:131443894-131443895	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs79259851	chr6:131443931-131443932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs72989868	chr6:131443932-131443933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs538428474	chr6:131443968-131443969	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556757144	chr6:131443984-131443985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201709225	chr6:131443985-131443986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs199923101	chr6:131443986-131443987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs376310895	chr6:131443991-131443992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555720882	chr6:131444011-131444012	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs645550	chr6:131444116-131444117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs533025187	chr6:131444132-131444133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201921280	chr6:131444133-131444134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs398002835	chr6:131444144-131444145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs57189640	chr6:131444158-131444159	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs554143879	chr6:131444214-131444215	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs532108688	chr6:131444223-131444224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs375666968	chr6:131444306-131444307	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs551998854	chr6:131444345-131444346	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs189331711	chr6:131444348-131444349	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192377635	chr6:131444351-131444352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs560705156	chr6:131444381-131444382	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs527971484	chr6:131444396-131444397	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575866774	chr6:131444403-131444404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs78380698	chr6:131444412-131444413	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs561500353	chr6:131444428-131444429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs57208456	chr6:131444451-131444452	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs79510578	chr6:131444500-131444501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369617930	chr6:131444510-131444511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532771594	chr6:131444511-131444512	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs577760	chr6:131444538-131444539	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs563250844	chr6:131444542-131444543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530591058	chr6:131444563-131444564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550399367	chr6:131444564-131444565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs568627816	chr6:131444586-131444587	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs139025077	chr6:131444700-131444701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369483133	chr6:131444705-131444706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189383268	chr6:131444713-131444714	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs547771280	chr6:131444745-131444746	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566092947	chr6:131444746-131444747	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539435358	chr6:131444775-131444776	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs372210176	chr6:131444784-131444785	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs576132881	chr6:131444787-131444788	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs9492834	chr6:131444797-131444798	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs9492835	chr6:131444808-131444809	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs563805004	chr6:131444837-131444838	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541346941	chr6:131444863-131444864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs559374017	chr6:131444947-131444948	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577836917	chr6:131444965-131444966	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

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
Colorectal cancer	16272173	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
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
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	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
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4076 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131443000-131444000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:131443400-131444200	Enhancers	Brain Germinal Matrix	brain
3	chr6:131443600-131445600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr6:131443600-131446600	Weak transcription	NHDF-Ad	bronchial
5	chr6:131443600-131451000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:131443800-131445600	Weak transcription	Brain Angular Gyrus	brain
7	chr6:131443800-131446600	Weak transcription	NHLF	lung
8	chr6:131444000-131445000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr6:131444000-131445200	Weak transcription	NHEK	skin
10	chr6:131445000-131446000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr6:131445200-131447200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:131445200-131447200	Enhancers	NHEK	skin
13	chr6:131445400-131447200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr6:131445400-131447200	Enhancers	HMEC	breast
15	chr6:131445600-131445800	Enhancers	Brain Angular Gyrus	brain
16	chr6:131445600-131445800	Enhancers	HSMMtube	muscle
17	chr6:131445600-131446000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:131445600-131446000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr6:131445800-131446600	Weak transcription	HSMMtube	muscle
20	chr6:131446000-131451000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr6:131446000-131456200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr6:131446400-131446800	Enhancers	A549	lung
23	chr6:131446400-131447200	Enhancers	Muscle Satellite Cultured Cells	--
24	chr6:131446400-131447200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr6:131446600-131446800	Enhancers	HSMMtube	muscle
26	chr6:131446600-131447000	Enhancers	HSMM	muscle
27	chr6:131446600-131447000	Enhancers	NH-A	brain
28	chr6:131446600-131447000	Enhancers	NHDF-Ad	bronchial
29	chr6:131446600-131447000	Enhancers	NHLF	lung
30	chr6:131446800-131451200	Weak transcription	HSMMtube	muscle
31	chr6:131447000-131451200	Weak transcription	HSMM	muscle
32	chr6:131447200-131450800	Weak transcription	NHEK	skin
33	chr6:131447200-131451000	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr6:131447200-131451000	Weak transcription	HMEC	breast
35	chr6:131447200-131455800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr6:131449000-131456000	Weak transcription	Fetal Brain Male	brain
37	chr6:131450200-131451800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:131450800-131451200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr6:131450800-131451600	Enhancers	HepG2	liver
40	chr6:131450800-131451600	Enhancers	NHEK	skin
41	chr6:131450800-131452000	Enhancers	Liver	Liver
42	chr6:131451000-131451400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:131451000-131451400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:131451000-131451400	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr6:131451000-131451600	Enhancers	Muscle Satellite Cultured Cells	--
46	chr6:131451000-131451600	Enhancers	HMEC	breast
47	chr6:131451000-131452000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr6:131451200-131451600	Enhancers	HSMMtube	muscle
49	chr6:131451200-131452400	Enhancers	HSMM	muscle
50	chr6:131451200-131455800	Weak transcription	Monocytes-CD14+_RO01746	blood

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