Variant report

Variant	nsv538319
Chromosome Location	chr6:76410921-76960225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2585)
CpG islands
(count:1525)
Chromatin interactive
region (count:152)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:2585 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:76601370-76601603	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:76484978-76485281	K562	blood:	n/a	n/a
3	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:76532773-76532821	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
7	ARID3A	chr6:76562512-76562787	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:76643375-76643655	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
10	ATF1	chr6:76517943-76518107	K562	blood:	n/a	n/a
11	ATF1	chr6:76562615-76562871	K562	blood:	n/a	n/a
12	ATF1	chr6:76757267-76757352	K562	blood:	n/a	n/a
13	ATF2	chr6:76540625-76541135	GM12878	blood:	n/a	n/a
14	ATF2	chr6:76703028-76703778	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr6:76636098-76636563	GM12878	blood:	n/a	n/a
16	ATF2	chr6:76540581-76541147	GM12878	blood:	n/a	n/a
17	ATF2	chr6:76829884-76830418	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr6:76523240-76523470	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr6:76783055-76783343	K562	blood:	n/a	n/a
20	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
21	BACH1	chr6:76644723-76645282	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr6:76783062-76783350	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:76603125-76603698	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr6:76540656-76541080	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
27	BATF	chr6:76453741-76453966	GM12878	blood:	n/a	n/a
28	BATF	chr6:76641889-76642089	GM12878	blood:	n/a	n/a
29	BATF	chr6:76491591-76491869	GM12878	blood:	n/a	chr6:76491779-76491789
30	BATF	chr6:76713845-76714245	GM12878	blood:	n/a	chr6:76714006-76714015
31	BATF	chr6:76540606-76541165	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
32	BATF	chr6:76713883-76714156	GM12878	blood:	n/a	chr6:76714006-76714015
33	BATF	chr6:76468871-76469148	GM12878	blood:	n/a	chr6:76468983-76468994
34	BATF	chr6:76636006-76636350	GM12878	blood:	n/a	n/a
35	BCL11A	chr6:76830090-76830300	H1-hESC	embryonic stem cell:	n/a	n/a
36	BCL11A	chr6:76830105-76830388	H1-hESC	embryonic stem cell:	n/a	n/a
37	BCL11A	chr6:76540692-76541027	GM12878	blood:	n/a	chr6:76541003-76541012
38	BCL11A	chr6:76453680-76454055	GM12878	blood:	n/a	n/a
39	BCL11A	chr6:76540633-76541116	GM12878	blood:	n/a	chr6:76541003-76541012
40	BCL11A	chr6:76453638-76454028	GM12878	blood:	n/a	n/a
41	BCL3	chr6:76540681-76541141	GM12878	blood:	n/a	chr6:76541003-76541012
42	BCLAF1	chr6:76540594-76541163	GM12878	blood:	n/a	chr6:76541003-76541012
43	BCLAF1	chr6:76540610-76541170	GM12878	blood:	n/a	chr6:76541003-76541012
44	BHLHE40	chr6:76458636-76459158	GM12878	blood:	n/a	chr6:76459001-76459017
45	BHLHE40	chr6:76716529-76716801	GM12878	blood:	n/a	n/a
46	BHLHE40	chr6:76486318-76486449	K562	blood:	n/a	n/a
47	BHLHE40	chr6:76458636-76459067	K562	blood:	n/a	chr6:76459001-76459017
48	BHLHE40	chr6:76463942-76463968	GM12878	blood:	n/a	n/a
49	BHLHE40	chr6:76463949-76464065	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:76533999-76534219	GM12878	blood:	n/a	n/a

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76645123-76645173	AG09319	gingival:	n/a
2	chr6:76583931-76583981	HCM	heart:	n/a
3	chr6:76783470-76783520	NT2-D1	testis:	n/a
4	chr6:76626770-76626820	CMK	blood:	n/a
5	chr6:76702942-76702992	LNCaP	prostate:	n/a
6	chr6:76645008-76645058	HL-60	blood:	n/a
7	chr6:76645008-76645058	GM12878	blood:	n/a
8	chr6:76645016-76645066	GM19239	blood:	n/a
9	chr6:76458633-76458683	NB4	blood:	n/a
10	chr6:76644222-76644272	HL-60	blood:	n/a
11	chr6:76783470-76783520	LNCaP	prostate:	n/a
12	chr6:76631383-76631433	U87	brain:	n/a
13	chr6:76626770-76626820	HEEpiC	esophagus:	n/a
14	chr6:76583931-76583981	HCT-116	colon:	n/a
15	chr6:76783470-76783520	AG09309	skin:	n/a
16	chr6:76456187-76456237	BE2_C	brain:	n/a
17	chr6:76425457-76425507	Hepatocyte	liver:	n/a
18	chr6:76644790-76644840	AG09319	gingival:	n/a
19	chr6:76645123-76645173	HNPCEpiC	eye:	n/a
20	chr6:76459511-76459561	HNPCEpiC	eye:	n/a
21	chr6:76645008-76645058	HRCEpiC	kidney:	n/a
22	chr6:76456187-76456237	GM12878	blood:	n/a
23	chr6:76645008-76645058	LNCaP	prostate:	n/a
24	chr6:76644770-76644820	SK-N-SH	brain:	n/a
25	chr6:76702942-76702992	GM19239	blood:	n/a
26	chr6:76645008-76645058	GM12892	blood:	n/a
27	chr6:76459077-76459127	HRCEpiC	kidney:	n/a
28	chr6:76456187-76456237	GM06990	blood:	n/a
29	chr6:76644807-76644857	Caco-2	colon:	n/a
30	chr6:76696290-76696340	LNCaP	prostate:	n/a
31	chr6:76458005-76458055	HepG2	liver:	n/a
32	chr6:76459511-76459561	H1-hESC	embryonic stem cell:	embryo
33	chr6:76461321-76461371	HRPEpiC	eye:	n/a
34	chr6:76644770-76644820	Hepatocyte	liver:	n/a
35	chr6:76425457-76425507	GM12891	blood:	n/a
36	chr6:76603364-76603414	HCM	heart:	n/a
37	chr6:76626770-76626820	GM19239	blood:	n/a
38	chr6:76644807-76644857	HUVEC	blood vessel:	n/a
39	chr6:76645008-76645058	T-47D	breast:	n/a
40	chr6:76645123-76645173	IMR90	lung:	fetal
41	chr6:76458633-76458683	ovcar-3	ovarian:	n/a
42	chr6:76645008-76645058	HEK293	kidney:	embryo
43	chr6:76644222-76644272	Hela-S3	cervix:	n/a
44	chr6:76645123-76645173	SKMC	muscle:	n/a
45	chr6:76636725-76636775	NHBE	bronchial:	n/a
46	chr6:76626770-76626820	HCT-116	colon:	n/a
47	chr6:76644770-76644820	NHDF-neo	bronchial:	n/a
48	chr6:76644807-76644857	Hepatocyte	liver:	n/a
49	chr6:76459077-76459127	ovcar-3	ovarian:	n/a
50	chr6:76626770-76626820	GM12891	blood:	n/a

(count:152 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:76619396..76621824-chr6:76631745..76633699,2	K562	blood:
2	chr6:76443894..76445853-chr6:76451155..76454793,3	MCF-7	breast:
3	chr6:76423467..76426296-chr6:76461021..76463732,3	MCF-7	breast:
4	chr6:76469142..76471151-chr6:76480358..76482124,2	MCF-7	breast:
5	chr6:76307687..76309384-chr6:76493357..76494955,2	K562	blood:
6	chr6:76467679..76469997-chr6:76472807..76474955,2	K562	blood:
7	chr6:76458666..76460451-chr6:76537768..76540622,2	MCF-7	breast:
8	chr6:76641512..76643461-chr6:76645513..76648039,2	K562	blood:
9	chr6:76458766..76460644-chr6:76463670..76465363,2	MCF-7	breast:
10	chr6:76830629..76833133-chr6:77061823..77064593,2	K562	blood:
11	chr6:76641510..76642065-chr6:78167262..78168037,2	MCF-7	breast:
12	chr6:76528373..76531036-chr6:76535873..76538476,2	MCF-7	breast:
13	chr6:76620793..76623567-chr6:76626394..76629286,2	MCF-7	breast:
14	chr6:76641897..76642417-chr6:77570899..77571594,2	MCF-7	breast:
15	chr5:151542542..151543442-chr6:76603129..76603708,2	MCF-7	breast:
16	chr6:76535425..76537050-chr6:76550391..76553381,2	MCF-7	breast:
17	chr6:76446062..76448644-chr6:76456702..76459457,3	MCF-7	breast:
18	chr6:76613924..76617174-chr6:76621064..76625151,5	MCF-7	breast:
19	chr3:141205080..141206779-chr6:76458156..76460847,2	MCF-7	breast:
20	chr6:76461468..76463754-chr6:76469518..76472253,2	MCF-7	breast:
21	chr6:76405218..76407618-chr6:76430939..76433858,2	MCF-7	breast:
22	chr6:76426476..76430048-chr6:76457436..76461171,5	MCF-7	breast:
23	chr6:76711975..76713621-chr6:76719761..76721754,2	K562	blood:
24	chr6:76457017..76459821-chr6:76526945..76528874,2	MCF-7	breast:
25	chr6:76564297..76564995-chr6:76602725..76603462,2	MCF-7	breast:
26	chr6:76527031..76529550-chr6:76557950..76559452,2	MCF-7	breast:
27	chr6:76467679..76469997-chr6:76472807..76474955,2	K562	blood:
28	chr2:233562031..233562988-chr6:76458771..76459462,2	Hela-S3	cervix:
29	chr6:76617686..76620159-chr6:76629560..76631488,2	MCF-7	breast:
30	chr6:76456068..76458008-chr6:76564755..76567247,2	MCF-7	breast:
31	chr6:76519784..76521479-chr6:76528977..76530844,2	MCF-7	breast:
32	chr6:76457084..76458969-chr6:76538382..76540807,2	MCF-7	breast:
33	chr6:76600564..76603457-chr6:76615084..76617457,2	MCF-7	breast:
34	chr6:76626564..76629624-chr6:76630461..76633607,3	MCF-7	breast:
35	chr6:76310826..76313123-chr6:76469584..76471602,2	MCF-7	breast:
36	chr6:76655935..76657484-chr6:76657598..76659631,2	MCF-7	breast:
37	chr6:76416294..76419277-chr6:76420477..76423022,2	K562	blood:
38	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
39	chr6:76564297..76564995-chr6:76602725..76603462,2	MCF-7	breast:
40	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
41	chr6:76310119..76312323-chr6:76471979..76473614,2	MCF-7	breast:
42	chr6:76457612..76460537-chr6:76566433..76568411,2	MCF-7	breast:
43	chr6:76458966..76460939-chr6:76574214..76577179,2	MCF-7	breast:
44	chr6:76457614..76459414-chr6:76469003..76470756,2	K562	blood:
45	chr6:76460418..76462531-chr6:76558690..76560910,2	MCF-7	breast:
46	chr6:76572406..76574229-chr6:76576124..76578272,2	K562	blood:
47	chr6:76452171..76456681-chr6:76457096..76463079,8	MCF-7	breast:
48	chr6:76469142..76471151-chr6:76480358..76482124,2	MCF-7	breast:
49	chr6:76617686..76620159-chr6:76629560..76631488,2	MCF-7	breast:
50	chr6:76465841..76467549-chr6:76494669..76496179,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO6-4	chr6:76673631-76673965	expReg_chr6_7326_+
2	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632
3	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	MYO6	hsa-miR-145-5p	chr6:76625103-76625109
2	MYO6	hsa-miR-320a	chr6:76625812-76625831
3	MYO6	hsa-miR-145-5p	chr6:76625088-76625110
4	MYO6	hsa-miR-145-5p	chr6:76625538-76625544
5	MYO6	hsa-miR-143-3p	chr6:76625569-76625576
6	MYO6	hsa-miR-143-3p	chr6:76625556-76625576

Variant related genes	Relation type
IMPG1	TF binding region
ENSG00000200040	TF binding region
ENSG00000239132	TF binding region
RNU6-248P	TF binding region
MYO6	TF binding region
RNU6-155P	TF binding region
RNA5SP209	TF binding region
IMPG1	CpG island
ENSG00000200040	CpG island
ENSG00000239132	CpG island
RNU6-248P	CpG island
MYO6	CpG island
RNU6-155P	CpG island
RNA5SP209	CpG island
ENSG00000217488	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000239132	chromatin interactions
ENSG00000196586	chromatin interactions
ENSG00000124243	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000252156	chromatin interactions
ENSG00000204120	chromatin interactions
ENSG00000223169	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000143971	chromatin interactions

Extended variants
information (count: 13193 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:13193 , 50 per page) page: 1 2 3 4 5 6 7 ... 264

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185794475	chr6:76410925-76410926	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577136129	chr6:76410933-76410934	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189107097	chr6:76410936-76410937	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs140076923	chr6:76410948-76410949	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs574966264	chr6:76410961-76410962	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs542016120	chr6:76410975-76410976	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs77087071	chr6:76411031-76411032	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs147373435	chr6:76411033-76411034	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72654744	chr6:76411078-76411079	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs564053806	chr6:76411085-76411086	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531534444	chr6:76411094-76411095	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554063556	chr6:76411175-76411176	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs181053476	chr6:76411213-76411214	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186326550	chr6:76411284-76411285	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs34546289	chr6:76411293-76411294	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs568207247	chr6:76411298-76411299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs374775701	chr6:76411306-76411307	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200232003	chr6:76411312-76411313	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs35765068	chr6:76411350-76411351	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs60715314	chr6:76411372-76411373	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs71561437	chr6:76411386-76411387	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs71561438	chr6:76411394-76411395	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs111739881	chr6:76411449-76411450	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs572653567	chr6:76411460-76411461	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs34489326	chr6:76411481-76411482	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs371167576	chr6:76411487-76411488	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs558563026	chr6:76411500-76411501	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs570803973	chr6:76411501-76411502	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs544892128	chr6:76411513-76411514	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs556823986	chr6:76411575-76411576	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs574986197	chr6:76411602-76411603	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs542430896	chr6:76411608-76411609	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs34636573	chr6:76411645-76411646	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs372602888	chr6:76411681-76411682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576456219	chr6:76411700-76411701	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs143481800	chr6:76411723-76411724	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs543091144	chr6:76411728-76411729	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs67313187	chr6:76411781-76411782	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547825587	chr6:76411783-76411784	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs9343316	chr6:76411800-76411801	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs9343317	chr6:76411843-76411844	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs188547564	chr6:76411900-76411901	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs543012610	chr6:76411910-76411911	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs200531593	chr6:76411935-76411936	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs76507265	chr6:76411948-76411949	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181384371	chr6:76412003-76412004	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs118094425	chr6:76412075-76412076	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146736382	chr6:76412172-76412173	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185921391	chr6:76412177-76412178	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs527809755	chr6:76412213-76412214	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Prostate cancer	16573809	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Salivary gland tumor	18059337	CNVD
Lung cancer	16773561	CNVD
Glioblastoma multiforme	22286061	CNVD
Urothelial cell carcinoma	18451213	CNVD
Prostate cancer	16461572	CNVD
Mental retardation	21045960	CNVD
Obesity	21045960	CNVD
learning difficulties	21045960	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:3855 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76382000-76422800	Weak transcription	Stomach Mucosa	stomach
2	chr6:76391400-76417200	Weak transcription	Gastric	stomach
3	chr6:76391400-76421200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:76391400-76426600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:76391600-76419200	Weak transcription	Right Ventricle	heart
6	chr6:76391600-76427200	Weak transcription	Small Intestine	intestine
7	chr6:76392000-76412200	Weak transcription	HepG2	liver
8	chr6:76392000-76412400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr6:76392000-76421400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr6:76392000-76423400	Weak transcription	NHEK	skin
11	chr6:76392000-76423800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr6:76392200-76420400	Weak transcription	Fetal Heart	heart
13	chr6:76392200-76421000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:76392200-76426800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr6:76395200-76420200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr6:76396800-76414600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:76396800-76414600	Strong transcription	Duodenum Mucosa	Duodenum
18	chr6:76396800-76414800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:76397000-76411400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
20	chr6:76397000-76413400	Strong transcription	Fetal Thymus	thymus
21	chr6:76397200-76415800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr6:76397200-76418000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr6:76397400-76413600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr6:76397400-76414000	Strong transcription	Dnd41	blood
25	chr6:76397400-76415000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:76397400-76430800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr6:76398000-76421000	Weak transcription	K562	blood
28	chr6:76398000-76428200	Weak transcription	Colonic Mucosa	Colon
29	chr6:76398200-76417200	Weak transcription	Spleen	Spleen
30	chr6:76398400-76411400	Strong transcription	HUES64 Cell Line	embryonic stem cell
31	chr6:76398400-76425400	Weak transcription	Pancreas	Pancrea
32	chr6:76399800-76426200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr6:76400000-76412800	Weak transcription	Aorta	Aorta
34	chr6:76400000-76413800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr6:76401600-76413600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:76401600-76426400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr6:76402000-76414200	Strong transcription	Primary monocytes fromperipheralblood	blood
38	chr6:76402000-76414200	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr6:76402200-76411400	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr6:76402200-76411600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr6:76402200-76414200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr6:76402200-76415000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr6:76402200-76425400	Strong transcription	Fetal Intestine Large	intestine
44	chr6:76402600-76413800	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chr6:76402800-76417200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr6:76403400-76414400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:76403800-76411200	Strong transcription	Osteobl	bone
48	chr6:76404800-76411400	Strong transcription	GM12878-XiMat	blood
49	chr6:76404800-76415200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr6:76405000-76411000	Strong transcription	HUVEC	blood vessel

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