Variant report

Variant	nsv894494
Chromosome Location	chr9:139783292-139820856
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1088)
CpG islands
(count:733)
Chromatin interactive
region (count:125)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1088 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:139785139-139785222	K562	blood:	n/a	n/a
2	ARID3A	chr9:139795759-139796262	HepG2	liver:	n/a	n/a
3	ATF2	chr9:139796219-139797399	GM12878	blood:	n/a	n/a
4	ATF2	chr9:139796801-139797132	GM12878	blood:	n/a	n/a
5	ATF2	chr9:139793565-139794189	GM12878	blood:	n/a	n/a
6	ATF3	chr9:139797607-139798157	A549	lung:	n/a	n/a
7	ATF3	chr9:139796786-139797264	A549	lung:	n/a	n/a
8	ATF3	chr9:139796775-139797366	A549	lung:	n/a	n/a
9	BCL11A	chr9:139796813-139797131	GM12878	blood:	n/a	n/a
10	BCL3	chr9:139797597-139798176	A549	lung:	n/a	chr9:139797816-139797829
11	BCL3	chr9:139786048-139786446	GM12878	blood:	n/a	n/a
12	BCL3	chr9:139795421-139797476	A549	lung:	n/a	chr9:139797347-139797356
13	BCL3	chr9:139784099-139784784	GM12878	blood:	n/a	n/a
14	BCL3	chr9:139797618-139798144	A549	lung:	n/a	chr9:139797816-139797829
15	BCL3	chr9:139795624-139797410	A549	lung:	n/a	chr9:139797347-139797356
16	BCL3	chr9:139784097-139784832	GM12878	blood:	n/a	n/a
17	BCL3	chr9:139796862-139797143	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:139793643-139794077	GM12878	blood:	n/a	n/a
19	BCLAF1	chr9:139796179-139797280	GM12878	blood:	n/a	n/a
20	BCLAF1	chr9:139796283-139797305	GM12878	blood:	n/a	n/a
21	BCLAF1	chr9:139793519-139794276	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:139796177-139797269	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:139800923-139801103	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:139796129-139796748	A549	lung:	n/a	n/a
25	BHLHE40	chr9:139793691-139794097	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:139795536-139795546	GM12878	blood:	n/a	n/a
27	CEBPB	chr9:139795490-139795837	A549	lung:	n/a	n/a
28	CEBPB	chr9:139806590-139806733	MCF-7	breast:	n/a	n/a
29	CEBPB	chr9:139796119-139797347	GM12878	blood:	n/a	n/a
30	CEBPB	chr9:139817921-139818099	K562	blood:	n/a	n/a
31	CEBPB	chr9:139817946-139818046	A549	lung:	n/a	n/a
32	CEBPB	chr9:139809028-139809108	K562	blood:	n/a	n/a
33	CEBPB	chr9:139806673-139806682	IMR90	lung:	n/a	n/a
34	CHD1	chr9:139793607-139793973	GM12878	blood:	n/a	n/a
35	CHD1	chr9:139795813-139797269	GM12878	blood:	n/a	n/a
36	CHD1	chr9:139801621-139801666	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr9:139796192-139797307	GM12878	blood:	n/a	n/a
38	CHD2	chr9:139795744-139795798	GM12878	blood:	n/a	n/a
39	CHD2	chr9:139793748-139793969	GM12878	blood:	n/a	n/a
40	CREB1	chr9:139796746-139797306	A549	lung:	n/a	n/a
41	CREB1	chr9:139797668-139798151	A549	lung:	n/a	n/a
42	CREB1	chr9:139795718-139796698	A549	lung:	n/a	n/a
43	CREB1	chr9:139797631-139798213	A549	lung:	n/a	n/a
44	CREB1	chr9:139795822-139796181	A549	lung:	n/a	n/a
45	CTCF	chr9:139783325-139783330	MCF-7	breast:	n/a	n/a
46	CTCF	chr9:139820720-139820870	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr9:139820680-139820830	MCF-7	breast:	n/a	n/a
48	CTCF	chr9:139820640-139820790	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr9:139820280-139820430	K562	blood:	n/a	n/a
50	CTCF	chr9:139820740-139820890	HCPEpiC	choroid plexus:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:139812357-139812407	GM19239	blood:	n/a
2	chr9:139812357-139812407	GM19239	blood:	n/a
3	chr9:139803690-139803740	Hepatocyte	liver:	n/a
4	chr9:139784946-139784996	SK-N-MC	brain:	n/a
5	chr9:139804179-139804229	MCF10A-Er-Src	breast:	n/a
6	chr9:139812357-139812407	NHDF-neo	bronchial:	n/a
7	chr9:139812357-139812407	GM12892	blood:	n/a
8	chr9:139801358-139801408	AoSMC	blood vessel:	n/a
9	chr9:139802044-139802094	HepG2	liver:	n/a
10	chr9:139803690-139803740	MCF10A-Er-Src	breast:	n/a
11	chr9:139801358-139801408	HepG2	liver:	n/a
12	chr9:139818362-139818412	AG09309	skin:	n/a
13	chr9:139818475-139818525	NH-A	brain:	n/a
14	chr9:139804179-139804229	GM06990	blood:	n/a
15	chr9:139784946-139784996	NH-A	brain:	n/a
16	chr9:139812357-139812407	SK-N-SH_RA	brain:	n/a
17	chr9:139812357-139812407	SK-N-SH	brain:	n/a
18	chr9:139801358-139801408	AG10803	skin:	n/a
19	chr9:139818475-139818525	GM19239	blood:	n/a
20	chr9:139801238-139801288	HIPEpiC	eye:	n/a
21	chr9:139801358-139801408	U87	brain:	n/a
22	chr9:139801358-139801408	HL-60	blood:	n/a
23	chr9:139803690-139803740	PANC-1	pancreas:	n/a
24	chr9:139796499-139796549	ProgFib	skin:	n/a
25	chr9:139802044-139802094	NH-A	brain:	n/a
26	chr9:139803690-139803740	Hela-S3	cervix:	n/a
27	chr9:139801358-139801408	MCF10A-Er-Src	breast:	n/a
28	chr9:139802603-139802653	BE2_C	brain:	n/a
29	chr9:139818362-139818412	HCF	heart:	n/a
30	chr9:139818362-139818412	IMR90	lung:	fetal
31	chr9:139818475-139818525	HMEC	breast:	n/a
32	chr9:139796499-139796549	RPTEC	kidney:	n/a
33	chr9:139812357-139812407	IMR90	lung:	fetal
34	chr9:139802603-139802653	HepG2	liver:	n/a
35	chr9:139784946-139784996	AG09309	skin:	n/a
36	chr9:139801358-139801408	HRPEpiC	eye:	n/a
37	chr9:139803690-139803740	AG10803	skin:	n/a
38	chr9:139784946-139784996	SK-N-SH	brain:	n/a
39	chr9:139801238-139801288	SKMC	muscle:	n/a
40	chr9:139796499-139796549	PFSK-1	brain:	n/a
41	chr9:139804179-139804229	Hela-S3	cervix:	n/a
42	chr9:139812357-139812407	RPTEC	kidney:	n/a
43	chr9:139796499-139796549	PANC-1	pancreas:	n/a
44	chr9:139802044-139802094	GM12891	blood:	n/a
45	chr9:139803690-139803740	BE2_C	brain:	n/a
46	chr9:139803690-139803740	HRPEpiC	eye:	n/a
47	chr9:139802044-139802094	HIPEpiC	eye:	n/a
48	chr9:139802603-139802653	H1-hESC	embryonic stem cell:	embryo
49	chr9:139818362-139818412	HCM	heart:	n/a
50	chr9:139801358-139801408	NT2-D1	testis:	n/a

(count:125 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:139803131..139806388-chr9:139920851..139924287,3	MCF-7	breast:
2	chr9:139778819..139780705-chr9:139810347..139812332,2	MCF-7	breast:
3	chr9:139783203..139785610-chr9:139794854..139797810,2	K562	blood:
4	chr9:139684905..139687555-chr9:139781430..139784355,2	MCF-7	breast:
5	chr9:139795540..139797953-chr9:139837525..139839445,2	K562	blood:
6	chr9:139782933..139784988-chr9:139802726..139805365,2	MCF-7	breast:
7	chr9:139800158..139801677-chr9:139804575..139806256,2	K562	blood:
8	chr9:139784208..139786582-chr9:139790103..139791762,2	K562	blood:
9	chr9:139819161..139823751-chr9:139833746..139841057,7	MCF-7	breast:
10	chr9:139785054..139785841-chr9:139839271..139839781,2	K562	blood:
11	chr9:139779239..139781768-chr9:139816821..139818478,2	MCF-7	breast:
12	chr9:139807603..139811077-chr9:139837719..139840774,3	MCF-7	breast:
13	chr9:139804263..139805797-chr9:140135581..140137582,2	K562	blood:
14	chr9:139811545..139813653-chr9:139815698..139818461,2	MCF-7	breast:
15	chr9:139747109..139749937-chr9:139802751..139806100,4	MCF-7	breast:
16	chr9:139760009..139761695-chr9:139817996..139820632,2	MCF-7	breast:
17	chr9:139779114..139781370-chr9:139820572..139822302,2	K562	blood:
18	chr9:139693022..139696090-chr9:139793195..139796394,4	MCF-7	breast:
19	chr9:139796638..139798632-chr9:139809456..139812141,2	MCF-7	breast:
20	chr9:139816083..139817704-chr9:139818126..139820060,2	MCF-7	breast:
21	chr9:139740736..139746036-chr9:139779239..139783690,13	K562	blood:
22	chr9:139739931..139767051-chr9:139773561..139787082,72	MCF-7	breast:
23	chr9:139792856..139794821-chr9:139800116..139802562,2	MCF-7	breast:
24	chr9:139685391..139688312-chr9:139795592..139798395,3	MCF-7	breast:
25	chr9:139759277..139762153-chr9:139804558..139806244,2	MCF-7	breast:
26	chr9:139756813..139762418-chr9:139794047..139799241,10	MCF-7	breast:
27	chr9:139794979..139797624-chr9:139802353..139803934,2	K562	blood:
28	chr9:139798690..139801469-chr9:139809287..139811887,2	K562	blood:
29	chr9:139818284..139824330-chr9:139824492..139828191,6	K562	blood:
30	chr17:56709084..56710651-chr9:139796688..139798205,2	MCF-7	breast:
31	chr9:139792507..139794136-chr9:139799233..139802028,2	K562	blood:
32	chr9:139795672..139799443-chr9:139799856..139804982,9	MCF-7	breast:
33	chr9:139792836..139799400-chr9:139842261..139846047,7	MCF-7	breast:
34	chr9:139769964..139771564-chr9:139789375..139792259,2	K562	blood:
35	chr9:139755534..139766605-chr9:139787339..139798569,18	MCF-7	breast:
36	chr1:179846415..179847120-chr9:139804027..139804720,2	NB4	blood:
37	chr9:139742293..139744367-chr9:139785112..139787540,2	K562	blood:
38	chr9:139722005..139723538-chr9:139789677..139791201,2	K562	blood:
39	chr9:139795672..139799443-chr9:139799856..139804982,9	MCF-7	breast:
40	chr9:139759393..139761898-chr9:139811485..139813607,2	MCF-7	breast:
41	chr9:139802369..139806544-chr9:139806670..139809687,5	MCF-7	breast:
42	chr9:139742261..139744866-chr9:139815519..139817769,2	MCF-7	breast:
43	chr9:139745735..139748667-chr9:139820327..139822508,2	MCF-7	breast:
44	chr9:139818737..139820243-chr9:139922964..139924917,2	MCF-7	breast:
45	chr9:139789514..139792273-chr9:139796475..139799525,3	K562	blood:
46	chr9:139741435..139745914-chr9:139791926..139799555,14	MCF-7	breast:
47	chr9:139780981..139783113-chr9:139815785..139818548,2	K562	blood:
48	chr9:139771650..139773172-chr9:139817828..139820638,2	MCF-7	breast:
49	chr9:139816554..139819143-chr9:139870621..139872528,2	K562	blood:
50	chr9:139741638..139745300-chr9:139796064..139800031,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAMDC4-3	chr9:139794255-139794736	expReg_chr9_9714_+

No data

Variant related genes	Relation type
TRAF2	TF binding region
TRAF2	CpG island
ENSG00000180539	chromatin interactions
ENSG00000177943	chromatin interactions
ENSG00000213213	chromatin interactions
ENSG00000107223	chromatin interactions
ENSG00000107331	chromatin interactions
ENSG00000272896	chromatin interactions
ENSG00000107281	chromatin interactions
ENSG00000184925	chromatin interactions
ENSG00000196642	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000169583	chromatin interactions
ENSG00000186193	chromatin interactions
ENSG00000159069	chromatin interactions
ENSG00000198569	chromatin interactions
ENSG00000169905	chromatin interactions
ENSG00000266507	chromatin interactions
ENSG00000273066	chromatin interactions
ENSG00000272679	chromatin interactions
ENSG00000244187	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000148362	chromatin interactions
ENSG00000127191	chromatin interactions
ENSG00000107317	chromatin interactions
ENSG00000054148	chromatin interactions
ENSG00000176919	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 2057 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2057 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2784069	chr9:139783292-139783293	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564479391	chr9:139783351-139783352	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs183565570	chr9:139783353-139783354	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs144269403	chr9:139783361-139783362	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs577853073	chr9:139783367-139783368	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs147354500	chr9:139783398-139783399	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs563643839	chr9:139783412-139783413	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs139403568	chr9:139783419-139783420	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs543101203	chr9:139783422-139783423	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs559989538	chr9:139783435-139783436	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs538832367	chr9:139783466-139783467	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs368874504	chr9:139783469-139783470	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs17250029	chr9:139783519-139783520	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs186827013	chr9:139783555-139783556	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs549389321	chr9:139783572-139783573	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs372435056	chr9:139783603-139783604	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs56162748	chr9:139783640-139783641	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs79343646	chr9:139783671-139783672	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs533626382	chr9:139783672-139783673	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs77131484	chr9:139783686-139783687	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs79184889	chr9:139783688-139783689	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs142508217	chr9:139783693-139783694	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
23	rs535185691	chr9:139783712-139783713	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs563313771	chr9:139783715-139783716	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs548622426	chr9:139783732-139783733	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs17250036	chr9:139783741-139783742	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs141087945	chr9:139783757-139783758	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs554775437	chr9:139783765-139783766	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs557911805	chr9:139783809-139783810	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs577880828	chr9:139783820-139783821	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs12348012	chr9:139783858-139783859	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs145796746	chr9:139783879-139783880	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs574034332	chr9:139783948-139783949	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs543037848	chr9:139783959-139783960	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs559629089	chr9:139784001-139784002	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs573274982	chr9:139784033-139784034	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs545304665	chr9:139784063-139784064	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs529272290	chr9:139784104-139784105	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs565450233	chr9:139784134-139784135	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs112106904	chr9:139784182-139784183	Weak transcription Strong transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs549239149	chr9:139784230-139784231	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs117299973	chr9:139784241-139784242	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs192460802	chr9:139784251-139784252	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs566162529	chr9:139784296-139784297	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs528903359	chr9:139784301-139784302	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs548560668	chr9:139784317-139784318	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs565666062	chr9:139784328-139784329	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs534686475	chr9:139784364-139784365	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs551300723	chr9:139784371-139784372	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs571378781	chr9:139784375-139784376	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Hepatocellular carcinoma	22174799	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Mantle cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
Epilepsy	22083797	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Developmental delay	20877625	CNVD
Hypoplastic	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
Palpebral fissures	20877625	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Autism	22495309	CNVD

Chromatin state (count:1635 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139782000-139784200	Weak transcription	Lung	lung
2	chr9:139782000-139784400	Weak transcription	Ovary	ovary
3	chr9:139782000-139790400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:139782000-139792600	Weak transcription	Small Intestine	intestine
5	chr9:139782000-139793800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr9:139782000-139794800	Weak transcription	Aorta	Aorta
7	chr9:139782200-139783400	Enhancers	Primary T cells fromperipheralblood	blood
8	chr9:139782200-139783400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr9:139782200-139783400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr9:139782200-139783400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
11	chr9:139782200-139783400	Enhancers	Liver	Liver
12	chr9:139782200-139783600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr9:139782200-139783600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr9:139782200-139784000	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr9:139782200-139784000	Weak transcription	Fetal Stomach	stomach
16	chr9:139782200-139784000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr9:139782200-139784000	Weak transcription	Thymus	Thymus
18	chr9:139782200-139784000	Weak transcription	NH-A	brain
19	chr9:139782200-139784200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr9:139782200-139784200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:139782200-139784200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr9:139782200-139784200	Weak transcription	Adipose Nuclei	Adipose
23	chr9:139782200-139784200	Weak transcription	Rectal Mucosa Donor 29	rectum
24	chr9:139782200-139784200	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr9:139782200-139784200	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr9:139782200-139784400	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr9:139782200-139784400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr9:139782200-139784400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr9:139782200-139784400	Weak transcription	Primary T cells from cord blood	blood
30	chr9:139782200-139784400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr9:139782200-139784400	Weak transcription	Esophagus	oesophagus
32	chr9:139782200-139784400	Weak transcription	Pancreas	Pancrea
33	chr9:139782200-139784600	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr9:139782200-139784600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr9:139782200-139784600	Weak transcription	Stomach Smooth Muscle	stomach
36	chr9:139782200-139784600	Weak transcription	Osteobl	bone
37	chr9:139782200-139784800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr9:139782200-139784800	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr9:139782200-139784800	Weak transcription	Brain Germinal Matrix	brain
40	chr9:139782200-139784800	Weak transcription	Rectal Smooth Muscle	rectum
41	chr9:139782200-139784800	Weak transcription	HMEC	breast
42	chr9:139782200-139785600	Weak transcription	Primary B cells from peripheral blood	blood
43	chr9:139782200-139787200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr9:139782200-139787400	Weak transcription	Primary monocytes fromperipheralblood	blood
45	chr9:139782200-139787400	Weak transcription	Placenta	Placenta
46	chr9:139782200-139787400	Weak transcription	Left Ventricle	heart
47	chr9:139782200-139787400	Weak transcription	HSMM	muscle
48	chr9:139782200-139787400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr9:139782200-139787400	Weak transcription	NHLF	lung
50	chr9:139782200-139788800	Weak transcription	Fetal Muscle Leg	muscle

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