Variant report

Variant	nsv932201
Chromosome Location	chr6:76365548-77219650
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3596)
CpG islands
(count:1589)
Chromatin interactive
region (count:195)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:3596 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

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	chr6:76562512-76562787	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:76445315-76446019	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:76458622-76458651	K562	blood:	n/a	n/a
6	ARID3A	chr6:76532773-76532821	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:76383585-76383961	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:76458528-76458682	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:76457201-76457496	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:76643375-76643655	HepG2	liver:	n/a	n/a
11	ATF1	chr6:76757267-76757352	K562	blood:	n/a	n/a
12	ATF1	chr6:76517943-76518107	K562	blood:	n/a	n/a
13	ATF1	chr6:77032417-77032606	K562	blood:	n/a	n/a
14	ATF1	chr6:76562615-76562871	K562	blood:	n/a	n/a
15	ATF2	chr6:77151557-77151935	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:76829884-76830418	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:77151494-77151955	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr6:76703028-76703778	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr6:76636098-76636563	GM12878	blood:	n/a	n/a
20	ATF2	chr6:76540625-76541135	GM12878	blood:	n/a	n/a
21	ATF2	chr6:76540581-76541147	GM12878	blood:	n/a	n/a
22	ATF3	chr6:76400719-76401129	HCT-116	colon:	n/a	n/a
23	ATF3	chr6:77151504-77151916	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr6:77151627-77151935	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr6:77148487-77148871	H1-hESC	embryonic stem cell:	n/a	chr6:77148663-77148677
26	BACH1	chr6:76644723-76645282	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr6:76407134-76407232	K562	blood:	n/a	n/a
28	BACH1	chr6:76459213-76459671	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr6:76783062-76783350	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:76783055-76783343	K562	blood:	n/a	n/a
31	BACH1	chr6:76458435-76458631	K562	blood:	n/a	n/a
32	BACH1	chr6:76458387-76458719	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:76603125-76603698	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:77113127-77113151	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:76523240-76523470	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr6:76713883-76714156	GM12878	blood:	n/a	chr6:76714006-76714015
37	BATF	chr6:77176056-77176337	GM12878	blood:	n/a	chr6:77176197-77176208
38	BATF	chr6:76641889-76642089	GM12878	blood:	n/a	n/a
39	BATF	chr6:77219241-77219437	GM12878	blood:	n/a	chr6:77219332-77219343
40	BATF	chr6:76491591-76491869	GM12878	blood:	n/a	chr6:76491779-76491789
41	BATF	chr6:76540656-76541080	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
42	BATF	chr6:76540606-76541165	GM12878	blood:	n/a	chr6:76540850-76540861 chr6:76540956-76540965 chr6:76540847-76540857
43	BATF	chr6:76636006-76636350	GM12878	blood:	n/a	n/a
44	BATF	chr6:76468871-76469148	GM12878	blood:	n/a	chr6:76468983-76468994
45	BATF	chr6:77176105-77176301	GM12878	blood:	n/a	chr6:77176197-77176208
46	BATF	chr6:76453741-76453966	GM12878	blood:	n/a	n/a
47	BATF	chr6:76713845-76714245	GM12878	blood:	n/a	chr6:76714006-76714015
48	BCL11A	chr6:76540633-76541116	GM12878	blood:	n/a	chr6:76541003-76541012
49	BCL11A	chr6:76453638-76454028	GM12878	blood:	n/a	n/a
50	BCL11A	chr6:76830105-76830388	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:76603364-76603414	SK-N-SH_RA	brain:	n/a
2	chr6:76696290-76696340	SK-N-MC	brain:	n/a
3	chr6:76583931-76583981	NHDF-neo	bronchial:	n/a
4	chr6:76603364-76603414	SK-N-SH_RA	brain:	n/a
5	chr6:76696290-76696340	SK-N-MC	brain:	n/a
6	chr6:76583931-76583981	NHDF-neo	bronchial:	n/a
7	chr6:76458005-76458055	SK-N-MC	brain:	n/a
8	chr6:76644790-76644840	BE2_C	brain:	n/a
9	chr6:76644222-76644272	AG09319	gingival:	n/a
10	chr6:76626770-76626820	AG04450	lung:	fetal
11	chr6:76458633-76458683	AG04450	lung:	fetal
12	chr6:76459511-76459561	SAEC	small airway:	n/a
13	chr6:76724431-76724481	NHDF-neo	bronchial:	n/a
14	chr6:76626770-76626820	Hela-S3	cervix:	n/a
15	chr6:76636725-76636775	CMK	blood:	n/a
16	chr6:76583931-76583981	PrEC	prostate:	n/a
17	chr6:76702942-76702992	HRPEpiC	eye:	n/a
18	chr6:76762173-76762223	AG09309	skin:	n/a
19	chr6:76655983-76656033	SKMC	muscle:	n/a
20	chr6:76458633-76458683	HUVEC	blood vessel:	n/a
21	chr6:76762173-76762223	AG04449	skin:	fetal
22	chr6:76461321-76461371	HCPEpiC	choroid plexus:	n/a
23	chr6:76645123-76645173	SAEC	small airway:	n/a
24	chr6:76425457-76425507	HCF	heart:	n/a
25	chr6:76458633-76458683	HepG2	liver:	n/a
26	chr6:76425457-76425507	AG04449	skin:	fetal
27	chr6:76724431-76724481	PANC-1	pancreas:	n/a
28	chr6:76645123-76645173	HRCEpiC	kidney:	n/a
29	chr6:76702942-76702992	AG10803	skin:	n/a
30	chr6:76631383-76631433	HUVEC	blood vessel:	n/a
31	chr6:76783470-76783520	SK-N-SH_RA	brain:	n/a
32	chr6:76425457-76425507	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:76644222-76644272	HEK293	kidney:	embryo
34	chr6:76644222-76644272	SK-N-SH	brain:	n/a
35	chr6:76459511-76459561	HCT-116	colon:	n/a
36	chr6:76762173-76762223	HRPEpiC	eye:	n/a
37	chr6:76603364-76603414	MCF10A-Er-Src	breast:	n/a
38	chr6:76636725-76636775	U87	brain:	n/a
39	chr6:77036802-77036852	HAEpiC	amniotic membrane:	n/a
40	chr6:76631383-76631433	HIPEpiC	eye:	n/a
41	chr6:76425457-76425507	NT2-D1	testis:	n/a
42	chr6:76655983-76656033	HAEpiC	amniotic membrane:	n/a
43	chr6:76644790-76644840	HIPEpiC	eye:	n/a
44	chr6:76644222-76644272	RPTEC	kidney:	n/a
45	chr6:76459511-76459561	NHDF-neo	bronchial:	n/a
46	chr6:76696290-76696340	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:76603364-76603414	K562	blood:	n/a
48	chr6:76626770-76626820	SAEC	small airway:	n/a
49	chr6:76645123-76645173	PrEC	prostate:	n/a
50	chr6:76425457-76425507	AG10803	skin:	n/a

(count:195 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:76985498..76986021-chr6:77586428..77587326,2	MCF-7	breast:
2	chr6:76405218..76407618-chr6:76430939..76433858,2	MCF-7	breast:
3	chr6:76406647..76409621-chr6:76410785..76413589,2	K562	blood:
4	chr6:76461153..76463947-chr6:76466842..76469998,3	MCF-7	breast:
5	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
6	chr6:76655935..76657484-chr6:76657598..76659631,2	MCF-7	breast:
7	chr6:76457017..76459821-chr6:76526945..76528874,2	MCF-7	breast:
8	chr6:76370677..76372880-chr6:76377007..76378733,2	K562	blood:
9	chr6:76397986..76399777-chr6:76458759..76460559,2	MCF-7	breast:
10	chr6:76619396..76621824-chr6:76631745..76633699,2	K562	blood:
11	chr6:76530548..76533502-chr6:76541265..76544166,2	K562	blood:
12	chr6:76361046..76364656-chr6:76366287..76368782,3	K562	blood:
13	chr6:76416294..76419277-chr6:76420477..76423022,2	K562	blood:
14	chr6:76373474..76375579-chr6:76380760..76383330,2	K562	blood:
15	chr6:76711975..76713621-chr6:76719761..76721754,2	K562	blood:
16	chr6:76310342..76312305-chr6:76373129..76377244,3	K562	blood:
17	chr6:76369470..76371755-chr6:76372281..76373933,2	K562	blood:
18	chr6:76457060..76461197-chr6:76473704..76478813,6	MCF-7	breast:
19	chr2:44363492..44364046-chr6:76624126..76624909,2	MCF-7	breast:
20	chr6:76600564..76603457-chr6:76615084..76617457,2	MCF-7	breast:
21	chr6:76457826..76459890-chr6:76553422..76554950,2	MCF-7	breast:
22	chr6:76426836..76429906-chr6:76458673..76460595,3	MCF-7	breast:
23	chr6:76522682..76525185-chr6:76527621..76531483,3	MCF-7	breast:
24	chr6:76456068..76458008-chr6:76564755..76567247,2	MCF-7	breast:
25	chr6:77172267..77174922-chr6:77177230..77180103,2	K562	blood:
26	chr6:76467657..76469847-chr6:76559756..76561654,2	MCF-7	breast:
27	chr6:76450359..76452041-chr6:76457600..76459670,2	MCF-7	breast:
28	chr6:76530548..76533502-chr6:76541265..76544166,2	K562	blood:
29	chr6:76312246..76314943-chr6:76370644..76373354,2	MCF-7	breast:
30	chr6:76416198..76418365-chr6:76457940..76460718,3	MCF-7	breast:
31	chr6:76620793..76623567-chr6:76626394..76629286,2	MCF-7	breast:
32	chr6:76469142..76471151-chr6:76480358..76482124,2	MCF-7	breast:
33	chr6:76373474..76375579-chr6:76380760..76383330,2	K562	blood:
34	chr6:76948100..76950177-chr6:76951701..76954019,2	MCF-7	breast:
35	chr6:76402029..76404149-chr6:76408590..76410105,2	MCF-7	breast:
36	chr6:76446062..76448644-chr6:76456702..76459457,3	MCF-7	breast:
37	chr6:76644344..76645305-chr6:77060589..77061466,9	MCF-7	breast:
38	chr6:76423467..76426296-chr6:76461021..76463732,3	MCF-7	breast:
39	chr6:76356613..76358787-chr6:76370587..76373323,2	K562	blood:
40	chr6:76310227..76312452-chr6:76481370..76483085,2	K562	blood:
41	chr3:141205080..141206779-chr6:76458156..76460847,2	MCF-7	breast:
42	chr6:76443894..76445853-chr6:76451155..76454793,3	MCF-7	breast:
43	chr6:76465841..76467549-chr6:76494669..76496179,2	MCF-7	breast:
44	chr6:76564297..76564995-chr6:76602725..76603462,2	MCF-7	breast:
45	chr6:76386546..76388318-chr6:76399041..76401218,2	K562	blood:
46	chr6:76424414..76426953-chr6:76430333..76433018,2	MCF-7	breast:
47	chr6:76459743..76462264-chr6:76558072..76560658,3	MCF-7	breast:
48	chr6:76310925..76313590-chr6:76457201..76459634,2	K562	blood:
49	chr20:49411019..49411554-chr6:76942200..76943162,2	MCF-7	breast:
50	chr6:76458193..76461486-chr6:76482230..76486067,4	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYO6-6	chr6:76368978-76369123	NONHSAT113627
2	lnc-SENP6-5	chr6:76434955-76435356	NONHSAT113632
3	lnc-SENP6-4	chr6:76433669-76434665	NONHSAT113631
4	lnc-MYO6-4	chr6:76673631-76673965	expReg_chr6_7326_+
5	lnc-MYO6-6	chr6:76372937-76373221	NONHSAT113627

No data

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

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

Variant related genes	Relation type
IMPG1	TF binding region
ENSG00000200040	TF binding region
ENSG00000239132	TF binding region
RNU6-248P	TF binding region
RN7SKP163	TF binding region
SENP6	TF binding region
MYO6	TF binding region
RNU6-155P	TF binding region
RNU6-261P	TF binding region
RNA5SP209	TF binding region
IMPG1	CpG island
ENSG00000200040	CpG island
ENSG00000239132	CpG island
RNU6-248P	CpG island
RN7SKP163	CpG island
SENP6	CpG island
MYO6	CpG island
RNU6-155P	CpG island
RNU6-261P	CpG island
RNA5SP209	CpG island
ENSG00000196586	chromatin interactions
ENSG00000124243	chromatin interactions
ENSG00000252156	chromatin interactions
ENSG00000217488	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000204120	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000124596	chromatin interactions
ENSG00000001167	chromatin interactions
ENSG00000223169	chromatin interactions
ENSG00000112697	chromatin interactions
ENSG00000143971	chromatin interactions
ENSG00000112701	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000239132	chromatin interactions
ENSG00000112706	chromatin interactions

Extended variants
information (count: 17642 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:17642 , 50 per page) page: 1 2 3 4 5 6 7 ... 353

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143078316	chr6:76365548-76365549	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs112837534	chr6:76365550-76365551	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs368207965	chr6:76365551-76365552	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs369643822	chr6:76365564-76365565	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs556856824	chr6:76365615-76365616	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs189790761	chr6:76365651-76365652	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs542047249	chr6:76365702-76365703	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs62415579	chr6:76365769-76365770	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs534775879	chr6:76365800-76365801	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572274011	chr6:76365820-76365821	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs545517115	chr6:76365835-76365836	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs563980987	chr6:76365840-76365841	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs531376350	chr6:76365885-76365886	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs543045474	chr6:76365896-76365897	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141104792	chr6:76365909-76365910	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs529184356	chr6:76365924-76365925	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139475726	chr6:76365930-76365931	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78057771	chr6:76365932-76365933	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs5877459	chr6:76365947-76365948	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553226432	chr6:76365979-76365980	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182463310	chr6:76366006-76366007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs187145336	chr6:76366007-76366008	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191797384	chr6:76366011-76366012	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116515352	chr6:76366024-76366025	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs147016958	chr6:76366105-76366106	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs538286599	chr6:76366150-76366151	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs182888778	chr6:76366157-76366158	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs199670923	chr6:76366164-76366165	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138176861	chr6:76366247-76366248	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188744280	chr6:76366256-76366257	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs62415580	chr6:76366266-76366267	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs572310688	chr6:76366274-76366275	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs545950808	chr6:76366322-76366323	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs558010180	chr6:76366330-76366331	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs557878724	chr6:76366350-76366351	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs576032826	chr6:76366379-76366380	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs543437098	chr6:76366386-76366387	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs561543391	chr6:76366391-76366392	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs373034380	chr6:76366431-76366432	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141741934	chr6:76366442-76366443	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs192958593	chr6:76366461-76366462	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559644269	chr6:76366570-76366571	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533202367	chr6:76366682-76366683	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs570939	chr6:76366724-76366725	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs564633948	chr6:76366792-76366793	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150129675	chr6:76366886-76366887	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs550217434	chr6:76366926-76366927	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs568140524	chr6:76366927-76366928	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs535412718	chr6:76366953-76366954	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs543478230	chr6:76366962-76366963	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Chronic lymphocytic leukemia	21546498	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD

Chromatin state (count:5193 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76320200-76391600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:76321800-76370400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr6:76330600-76368600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr6:76330600-76369800	Weak transcription	Right Ventricle	heart
5	chr6:76330600-76370200	Weak transcription	Aorta	Aorta
6	chr6:76330600-76381600	Weak transcription	Stomach Mucosa	stomach
7	chr6:76330600-76390400	Weak transcription	Gastric	stomach
8	chr6:76332000-76368400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr6:76332800-76389000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr6:76333000-76365800	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr6:76333000-76366000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr6:76333200-76391000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr6:76335200-76370600	Weak transcription	Psoas Muscle	Psoas
14	chr6:76335400-76388800	Weak transcription	Small Intestine	intestine
15	chr6:76335600-76370400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:76339200-76366400	Strong transcription	Dnd41	blood
17	chr6:76339400-76402000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:76340200-76390400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr6:76340400-76374600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:76340400-76390400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr6:76341400-76369400	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr6:76342200-76387200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr6:76342400-76366800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr6:76342400-76367000	Weak transcription	Brain Angular Gyrus	brain
25	chr6:76342800-76391200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
26	chr6:76348800-76370400	Weak transcription	Fetal Brain Female	brain
27	chr6:76349200-76368400	Weak transcription	HepG2	liver
28	chr6:76350000-76370600	Weak transcription	NHEK	skin
29	chr6:76350200-76369800	Weak transcription	Colonic Mucosa	Colon
30	chr6:76351400-76390400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:76352000-76368800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
32	chr6:76352200-76370000	Weak transcription	Rectal Smooth Muscle	rectum
33	chr6:76353200-76369600	Weak transcription	Fetal Heart	heart
34	chr6:76354000-76366400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr6:76354400-76377600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr6:76354600-76391200	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr6:76355000-76370200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr6:76356600-76366600	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr6:76356800-76366000	Strong transcription	Primary T helper cells fromperipheralblood	blood
40	chr6:76356800-76391800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:76357200-76390000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:76358200-76366400	Strong transcription	Primary B cells from peripheral blood	blood
43	chr6:76358200-76388000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:76358200-76392200	Strong transcription	Primary T helper cells PMA-I stimulated	--
45	chr6:76358400-76375400	Strong transcription	Fetal Intestine Large	intestine
46	chr6:76358400-76391000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:76359000-76369600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr6:76359400-76369000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr6:76360000-76367000	Weak transcription	Brain Hippocampus Middle	brain
50	chr6:76360000-76369400	Weak transcription	Brain Anterior Caudate	brain

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