Variant report

Variant	nsv528486
Chromosome Location	chr8:103279922-103373304
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:932)
CpG islands
(count:122)
Chromatin interactive
region (count:139)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:932 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:103343336-103343763	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:103343488-103343707	K562	blood:	n/a	n/a
3	ARID3A	chr8:103284645-103284984	HepG2	liver:	n/a	n/a
4	ATF1	chr8:103299547-103299848	K562	blood:	n/a	n/a
5	ATF1	chr8:103343461-103343696	K562	blood:	n/a	n/a
6	ATF2	chr8:103299500-103299977	GM12878	blood:	n/a	n/a
7	ATF2	chr8:103301688-103303049	GM12878	blood:	n/a	n/a
8	ATF2	chr8:103299368-103300512	GM12878	blood:	n/a	n/a
9	ATF2	chr8:103288897-103289336	GM12878	blood:	n/a	n/a
10	ATF2	chr8:103301985-103303010	GM12878	blood:	n/a	n/a
11	ATF3	chr8:103343445-103343629	K562	blood:	n/a	n/a
12	BACH1	chr8:103337377-103337406	K562	blood:	n/a	n/a
13	BACH1	chr8:103327016-103327019	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr8:103299509-103299836	GM12878	blood:	n/a	n/a
15	BATF	chr8:103302047-103302733	GM12878	blood:	n/a	chr8:103302295-103302303
16	BATF	chr8:103300273-103300492	GM12878	blood:	n/a	chr8:103300344-103300355
17	BATF	chr8:103343381-103343729	GM12878	blood:	n/a	n/a
18	BATF	chr8:103302065-103302744	GM12878	blood:	n/a	chr8:103302295-103302303
19	BATF	chr8:103358907-103359195	GM12878	blood:	n/a	chr8:103359042-103359053 chr8:103359043-103359053
20	BATF	chr8:103300240-103300512	GM12878	blood:	n/a	chr8:103300344-103300355
21	BCL11A	chr8:103299538-103299770	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:103302041-103302785	GM12878	blood:	n/a	chr8:103302298-103302307
23	BCL11A	chr8:103299534-103299899	GM12878	blood:	n/a	chr8:103299851-103299858
24	BCL11A	chr8:103302050-103302733	GM12878	blood:	n/a	chr8:103302298-103302307
25	BCL3	chr8:103302189-103302463	GM12878	blood:	n/a	chr8:103302298-103302307
26	BCL3	chr8:103302028-103302755	GM12878	blood:	n/a	chr8:103302298-103302307
27	BCLAF1	chr8:103302013-103302991	GM12878	blood:	n/a	chr8:103302298-103302307
28	BCLAF1	chr8:103302024-103303075	GM12878	blood:	n/a	chr8:103302298-103302307
29	BCLAF1	chr8:103325205-103325661	GM12878	blood:	n/a	n/a
30	BCLAF1	chr8:103299424-103299979	GM12878	blood:	n/a	chr8:103299851-103299858
31	BCLAF1	chr8:103299501-103300078	GM12878	blood:	n/a	chr8:103299851-103299858
32	BHLHE40	chr8:103371463-103371490	GM12878	blood:	n/a	n/a
33	BHLHE40	chr8:103325302-103325629	GM12878	blood:	n/a	n/a
34	BHLHE40	chr8:103284818-103284897	K562	blood:	n/a	n/a
35	BHLHE40	chr8:103288977-103289511	GM12878	blood:	n/a	n/a
36	BHLHE40	chr8:103302003-103302926	GM12878	blood:	n/a	n/a
37	BRCA1	chr8:103293627-103293631	GM12878	blood:	n/a	n/a
38	BRCA1	chr8:103336597-103336661	Hela-S3	cervix:	n/a	n/a
39	CCNT2	chr8:103343433-103343624	K562	blood:	n/a	n/a
40	CEBPB	chr8:103299425-103300123	GM12878	blood:	n/a	chr8:103299583-103299600
41	CEBPB	chr8:103284700-103284984	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:103284574-103285076	MCF-7	breast:	n/a	n/a
43	CEBPB	chr8:103284646-103285013	K562	blood:	n/a	n/a
44	CEBPB	chr8:103284635-103285019	K562	blood:	n/a	n/a
45	CEBPB	chr8:103284702-103284889	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:103284499-103285143	MCF-7	breast:	n/a	n/a
47	CEBPB	chr8:103280083-103280228	K562	blood:	n/a	n/a
48	CEBPB	chr8:103284661-103285013	IMR90	lung:	n/a	n/a
49	CEBPB	chr8:103305764-103306161	MCF-7	breast:	n/a	chr8:103305989-103306000
50	CEBPB	chr8:103284651-103285025	Hela-S3	cervix:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:103344822-103344872	LNCaP	prostate:	n/a
2	chr8:103344822-103344872	SKMC	muscle:	n/a
3	chr8:103293724-103293774	AG04449	skin:	fetal
4	chr8:103293724-103293774	HEK293	kidney:	embryo
5	chr8:103293724-103293774	MCF-7	breast:	n/a
6	chr8:103293724-103293774	SK-N-MC	brain:	n/a
7	chr8:103293724-103293774	AG04450	lung:	fetal
8	chr8:103344822-103344872	Hela-S3	cervix:	n/a
9	chr8:103344822-103344872	HUVEC	blood vessel:	n/a
10	chr8:103293724-103293774	A549	lung:	n/a
11	chr8:103293724-103293774	HMEC	breast:	n/a
12	chr8:103344822-103344872	Caco-2	colon:	n/a
13	chr8:103344822-103344872	H1-hESC	embryonic stem cell:	embryo
14	chr8:103344822-103344872	GM12891	blood:	n/a
15	chr8:103344822-103344872	SK-N-MC	brain:	n/a
16	chr8:103293724-103293774	BJ	skin:	n/a
17	chr8:103344822-103344872	A549	lung:	n/a
18	chr8:103293724-103293774	Hepatocyte	liver:	n/a
19	chr8:103293724-103293774	SKMC	muscle:	n/a
20	chr8:103293724-103293774	AG09309	skin:	n/a
21	chr8:103293724-103293774	PANC-1	pancreas:	n/a
22	chr8:103293724-103293774	CMK	blood:	n/a
23	chr8:103293724-103293774	HepG2	liver:	n/a
24	chr8:103344822-103344872	K562	blood:	n/a
25	chr8:103344822-103344872	HNPCEpiC	eye:	n/a
26	chr8:103293724-103293774	Hela-S3	cervix:	n/a
27	chr8:103344822-103344872	GM12892	blood:	n/a
28	chr8:103293724-103293774	Jurkat	blood:	n/a
29	chr8:103293724-103293774	MCF10A-Er-Src	breast:	n/a
30	chr8:103293724-103293774	SAEC	small airway:	n/a
31	chr8:103344822-103344872	NT2-D1	testis:	n/a
32	chr8:103344822-103344872	HRPEpiC	eye:	n/a
33	chr8:103293724-103293774	NH-A	brain:	n/a
34	chr8:103344822-103344872	HCPEpiC	choroid plexus:	n/a
35	chr8:103293724-103293774	Caco-2	colon:	n/a
36	chr8:103344822-103344872	HIPEpiC	eye:	n/a
37	chr8:103293724-103293774	SK-N-SH	brain:	n/a
38	chr8:103293724-103293774	U87	brain:	n/a
39	chr8:103293724-103293774	RPTEC	kidney:	n/a
40	chr8:103293724-103293774	HCF	heart:	n/a
41	chr8:103293724-103293774	GM12878	blood:	n/a
42	chr8:103293724-103293774	NB4	blood:	n/a
43	chr8:103344822-103344872	NB4	blood:	n/a
44	chr8:103344822-103344872	GM06990	blood:	n/a
45	chr8:103344822-103344872	PFSK-1	brain:	n/a
46	chr8:103293724-103293774	HCT-116	colon:	n/a
47	chr8:103344822-103344872	NHBE	bronchial:	n/a
48	chr8:103344822-103344872	Jurkat	blood:	n/a
49	chr8:103293724-103293774	AoSMC	blood vessel:	n/a
50	chr8:103344822-103344872	U87	brain:	n/a

(count:139 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:103354174..103356522-chr8:103413215..103415897,2	MCF-7	breast:
2	chr8:103343757..103347850-chr8:103350455..103353849,3	MCF-7	breast:
3	chr8:103289581..103292045-chr8:103294238..103296259,2	MCF-7	breast:
4	chr8:103286886..103288922-chr8:103301773..103304069,2	MCF-7	breast:
5	chr8:103316263..103319023-chr8:103321772..103324552,2	K562	blood:
6	chr8:103354163..103355932-chr8:103355988..103358425,2	MCF-7	breast:
7	chr8:103314765..103317133-chr8:103323557..103325616,2	MCF-7	breast:
8	chr8:103310657..103313440-chr8:103423670..103425525,2	MCF-7	breast:
9	chr8:103335858..103340204-chr8:103341217..103345311,4	MCF-7	breast:
10	chr8:103363341..103365795-chr8:103374362..103376186,2	K562	blood:
11	chr8:103320694..103323615-chr8:103327057..103329412,3	K562	blood:
12	chr8:103351534..103353891-chr8:103354616..103356190,2	K562	blood:
13	chr8:103298686..103300294-chr8:103304892..103306650,2	K562	blood:
14	chr8:103321724..103323932-chr8:103666261..103668059,2	MCF-7	breast:
15	chr8:103135779..103136619-chr8:103284753..103285336,2	MCF-7	breast:
16	chr8:103302801..103305090-chr8:103317702..103319684,2	K562	blood:
17	chr8:103300987..103303610-chr8:103310069..103313635,3	K562	blood:
18	chr8:103371293..103374711-chr8:103423320..103425587,3	K562	blood:
19	chr8:103351132..103353034-chr8:103354690..103357157,2	K562	blood:
20	chr8:103339200..103341368-chr8:103346324..103348716,2	MCF-7	breast:
21	chr8:103302801..103305090-chr8:103317702..103319684,2	K562	blood:
22	chr8:103265116..103266649-chr8:103292317..103294443,2	MCF-7	breast:
23	chr8:103327893..103330442-chr8:103665150..103667023,2	MCF-7	breast:
24	chr8:103298397..103300610-chr8:103306655..103309037,2	MCF-7	breast:
25	chr8:103291796..103293789-chr8:103308408..103310782,2	MCF-7	breast:
26	chr8:103322726..103324564-chr8:103335535..103337396,2	MCF-7	breast:
27	chr8:103341661..103343308-chr8:103345011..103347065,2	K562	blood:
28	chr8:103308388..103310812-chr8:103313420..103315385,2	MCF-7	breast:
29	chr8:103304151..103307358-chr8:103314933..103318460,5	MCF-7	breast:
30	chr8:103270085..103274841-chr8:103276076..103281465,7	K562	blood:
31	chr8:103359154..103362889-chr8:103423110..103427139,3	K562	blood:
32	chr8:103315506..103318243-chr8:103326156..103330411,3	MCF-7	breast:
33	chr8:103320694..103323615-chr8:103327057..103329412,3	K562	blood:
34	chr8:103351917..103354522-chr8:103402313..103404781,2	K562	blood:
35	chr8:103314765..103317133-chr8:103323557..103325616,2	MCF-7	breast:
36	chr8:103283887..103286372-chr8:103287473..103290307,2	K562	blood:
37	chr8:103308012..103310056-chr8:103311769..103313826,2	K562	blood:
38	chr8:103281266..103283853-chr8:103291011..103293055,2	MCF-7	breast:
39	chr8:103322301..103325413-chr8:103327690..103330553,4	MCF-7	breast:
40	chr8:103320295..103322347-chr8:103361195..103362875,2	MCF-7	breast:
41	chr8:103328642..103330645-chr8:103421922..103425963,5	MCF-7	breast:
42	chr8:103270450..103272206-chr8:103296928..103298886,2	MCF-7	breast:
43	chr8:103291796..103293789-chr8:103308408..103310782,2	MCF-7	breast:
44	chr8:103342633..103344961-chr8:103423576..103425389,2	MCF-7	breast:
45	chr8:103354048..103356355-chr8:103421459..103423886,2	MCF-7	breast:
46	chr8:103292940..103295048-chr8:103868980..103871435,2	K562	blood:
47	chr8:103286886..103288922-chr8:103301773..103304069,2	MCF-7	breast:
48	chr8:103364849..103366619-chr8:103423307..103426264,2	MCF-7	breast:
49	chr8:103342878..103344564-chr8:103375467..103378106,2	MCF-7	breast:
50	chr17:56707742..56710113-chr8:103317617..103319699,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KB-1980E6.3.1-5	chr8:103333203-103334737	ucscGeneNc_uc003ykp_1
2	lnc-KB-1980E6.3.1-5	chr8:103325013-103325525	ucscGeneNc_uc003ykp_1
3	lnc-RRM2B-2	chr8:103279321-103280946	NONHSAT128085

No data

Variant related genes	Relation type
UBR5	TF binding region
UBR5	CpG island
ENSG00000155096	chromatin interactions
ENSG00000048392	chromatin interactions
ENSG00000104490	chromatin interactions
ENSG00000155090	chromatin interactions
ENSG00000246263	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000104517	chromatin interactions

Extended variants
information (count: 3459 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:3459 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13261195	chr8:103279922-103279923	Strong transcription Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs187792552	chr8:103279987-103279988	Strong transcription Weak transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs193175675	chr8:103280027-103280028	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs145476648	chr8:103280062-103280063	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs184400767	chr8:103280065-103280066	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs537388764	chr8:103280071-103280072	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs146902228	chr8:103280082-103280083	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs573980065	chr8:103280128-103280129	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs28680306	chr8:103280131-103280132	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs181842396	chr8:103280145-103280146	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs138949643	chr8:103280180-103280181	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs546007642	chr8:103280224-103280225	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs577809815	chr8:103280241-103280242	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs564315210	chr8:103280246-103280247	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs531635856	chr8:103280300-103280301	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs550053991	chr8:103280308-103280309	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs183957071	chr8:103280421-103280422	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs528899583	chr8:103280422-103280423	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs547149548	chr8:103280486-103280487	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs565415630	chr8:103280535-103280536	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs34297513	chr8:103280583-103280584	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs201098712	chr8:103280602-103280603	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs189412982	chr8:103280613-103280614	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs180724177	chr8:103280618-103280619	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs569960494	chr8:103280622-103280623	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs143669015	chr8:103280623-103280624	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs148105280	chr8:103280633-103280634	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs377240670	chr8:103280656-103280657	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs200002154	chr8:103280678-103280679	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs534997753	chr8:103280679-103280680	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs186575525	chr8:103280714-103280715	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs113807594	chr8:103280718-103280719	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs554153120	chr8:103280721-103280722	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs11782288	chr8:103280771-103280772	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs141885384	chr8:103280784-103280785	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs542677163	chr8:103280792-103280793	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs545568383	chr8:103280892-103280893	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs564227354	chr8:103280936-103280937	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs111759102	chr8:103280939-103280940	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs576315254	chr8:103280946-103280947	Weak transcription Strong transcription Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs117385805	chr8:103280947-103280948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562038022	chr8:103280977-103280978	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs16869318	chr8:103281024-103281025	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs191079149	chr8:103281040-103281041	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558962917	chr8:103281043-103281044	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532859191	chr8:103281099-103281100	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551062021	chr8:103281161-103281162	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs143124130	chr8:103281207-103281208	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs151177011	chr8:103281209-103281210	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs373017857	chr8:103281339-103281340	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Sezary syndrome	18413736	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Urothelial cell carcinoma	18451213	CNVD
Colorectal cancer	21645411	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	16912164	CNVD
Breast cancer	20409316	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Breast cancer	21611746	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Autism	22495309	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22844521	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Gastric cancer	22014070	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:2813 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:103252200-103292800	Weak transcription	Gastric	stomach
2	chr8:103252200-103318800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:103252400-103280200	Weak transcription	Aorta	Aorta
4	chr8:103252400-103292400	Weak transcription	Psoas Muscle	Psoas
5	chr8:103252600-103280000	Weak transcription	Fetal Brain Male	brain
6	chr8:103256000-103299000	Strong transcription	Primary B cells from peripheral blood	blood
7	chr8:103256000-103299000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr8:103256000-103299600	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr8:103256200-103285000	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr8:103256200-103299600	Strong transcription	Primary monocytes fromperipheralblood	blood
11	chr8:103257400-103299400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr8:103262400-103299400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:103262600-103281600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:103262600-103288200	Strong transcription	GM12878-XiMat	blood
15	chr8:103262600-103299600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:103262600-103329800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr8:103262800-103285200	Strong transcription	NHDF-Ad	bronchial
18	chr8:103262800-103286800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
19	chr8:103262800-103296000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:103262800-103299600	Strong transcription	HSMM	muscle
21	chr8:103263000-103294000	Strong transcription	Skeletal Muscle Female	skeletal muscle
22	chr8:103263000-103299000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
23	chr8:103263000-103299000	Strong transcription	Liver	Liver
24	chr8:103263000-103299000	Strong transcription	Fetal Thymus	thymus
25	chr8:103263200-103284000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr8:103263200-103286800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr8:103263200-103292800	Strong transcription	Placenta	Placenta
28	chr8:103263200-103298800	Strong transcription	Duodenum Mucosa	Duodenum
29	chr8:103263400-103285000	Strong transcription	Adipose Nuclei	Adipose
30	chr8:103263400-103295600	Strong transcription	Rectal Mucosa Donor 29	rectum
31	chr8:103263400-103298200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr8:103263400-103299000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr8:103263400-103299000	Strong transcription	Dnd41	blood
34	chr8:103263400-103327800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr8:103263400-103327800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr8:103263800-103284600	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr8:103263800-103285200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr8:103264000-103299000	Strong transcription	Primary T helper cells fromperipheralblood	blood
39	chr8:103264200-103299000	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr8:103264800-103298800	Strong transcription	Primary T helper cells PMA-I stimulated	--
41	chr8:103265000-103280600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:103265000-103284400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr8:103265200-103284800	Strong transcription	Fetal Lung	lung
44	chr8:103265600-103285200	Strong transcription	NH-A	brain
45	chr8:103266200-103285200	Strong transcription	Brain Anterior Caudate	brain
46	chr8:103266200-103285600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr8:103266200-103299400	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr8:103266800-103329000	Strong transcription	HUES6 Cell Line	embryonic stem cell
49	chr8:103267400-103327800	Strong transcription	HUES48 Cell Line	embryonic stem cell
50	chr8:103267400-103329000	Strong transcription	iPS-20b Cell Line	embryonic stem cell

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