Variant report

Variant	nsv559005
Chromosome Location	chr12:56117570-56120934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:183)
Chromatin interactive
region (count:31)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:56118241-56118809	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr12:56118650-56118657	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr12:56117805-56118681	A549	lung:	n/a	n/a
4	BCL3	chr12:56118024-56119418	A549	lung:	n/a	n/a
5	BCLAF1	chr12:56118327-56118796	GM12878	blood:	n/a	n/a
6	BHLHE40	chr12:56117983-56118100	K562	blood:	n/a	n/a
7	BHLHE40	chr12:56118552-56118623	GM12878	blood:	n/a	n/a
8	CHD1	chr12:56120323-56124349	IMR90	lung:	n/a	n/a
9	CHD2	chr12:56118495-56118713	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr12:56118497-56118740	GM12878	blood:	n/a	n/a
11	CTCF	chr12:56119203-56119484	T-47D	breast:	n/a	n/a
12	CTCF	chr12:56118456-56118694	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr12:56118520-56118670	GM06990	blood:	n/a	n/a
14	CTCF	chr12:56118458-56118703	A549	lung:	n/a	n/a
15	CTCF	chr12:56118464-56118704	HUVEC	blood vessel:	n/a	n/a
16	CTCF	chr12:56118440-56118590	A549	lung:	n/a	n/a
17	CTCF	chr12:56118399-56118693	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr12:56118464-56118695	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr12:56118477-56118665	Fibrobl	skin:	n/a	n/a
20	CTCF	chr12:56118460-56118610	GM12866	blood:	n/a	n/a
21	CTCF	chr12:56118500-56118650	HPAF	blood vessel:	n/a	n/a
22	CTCF	chr12:56118405-56118762	IMR90	lung:	n/a	n/a
23	CTCF	chr12:56118460-56118610	HCT-116	colon:	n/a	n/a
24	CTCF	chr12:56118392-56118789	K562	blood:	n/a	n/a
25	CTCF	chr12:56118359-56118770	A549	lung:	n/a	n/a
26	CTCF	chr12:56118372-56118790	GM12878	blood:	n/a	n/a
27	CTCF	chr12:56118188-56118276	GM19239	blood:	n/a	n/a
28	CTCF	chr12:56118520-56118670	GM12865	blood:	n/a	n/a
29	CTCF	chr12:56118500-56118650	HPF	lung:	n/a	n/a
30	CTCF	chr12:56118920-56119070	HEK293	kidney:	n/a	n/a
31	CTCF	chr12:56118464-56118717	Pancreas_OC	pancreas:	n/a	n/a
32	CTCF	chr12:56118461-56118686	MCF-7	breast:	n/a	n/a
33	CTCF	chr12:56118940-56119090	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr12:56118457-56118711	GM19239	blood:	n/a	n/a
35	CTCF	chr12:56118293-56118841	K562	blood:	n/a	n/a
36	CTCF	chr12:56118378-56118791	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr12:56118040-56118190	GM12873	blood:	n/a	n/a
38	CTCF	chr12:56118500-56118650	BJ	skin:	n/a	n/a
39	CTCF	chr12:56118466-56118697	Gliobla	brain:	n/a	n/a
40	CTCF	chr12:56118500-56118650	AG04449	skin:	n/a	n/a
41	CTCF	chr12:56118500-56118650	HVMF	connective:	n/a	n/a
42	CTCF	chr12:56118438-56118717	K562	blood:	n/a	n/a
43	CTCF	chr12:56118100-56118250	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr12:56118443-56118713	GM12891	blood:	n/a	n/a
45	CTCF	chr12:56118218-56118294	GM19238	blood:	n/a	n/a
46	CTCF	chr12:56118500-56118650	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr12:56118020-56118170	HVMF	connective:	n/a	n/a
48	CTCF	chr12:56118480-56118630	GM12866	blood:	n/a	n/a
49	CTCF	chr12:56118520-56118670	NHDF-neo	bronchial:	n/a	n/a
50	CTCF	chr12:56118480-56118630	GM12872	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56120816-56120866	HCF	heart:	n/a
2	chr12:56119258-56119308	AG09309	skin:	n/a
3	chr12:56120816-56120866	HEK293	kidney:	embryo
4	chr12:56118524-56118574	NHDF-neo	bronchial:	n/a
5	chr12:56118524-56118574	BE2_C	brain:	n/a
6	chr12:56120816-56120866	MCF-7	breast:	n/a
7	chr12:56118524-56118574	SAEC	small airway:	n/a
8	chr12:56119258-56119308	A549	lung:	n/a
9	chr12:56120816-56120866	Hela-S3	cervix:	n/a
10	chr12:56119258-56119308	NH-A	brain:	n/a
11	chr12:56120816-56120866	BJ	skin:	n/a
12	chr12:56118524-56118574	AG04450	lung:	fetal
13	chr12:56119258-56119308	PrEC	prostate:	n/a
14	chr12:56120816-56120866	AG10803	skin:	n/a
15	chr12:56119258-56119308	T-47D	breast:	n/a
16	chr12:56120816-56120866	ProgFib	skin:	n/a
17	chr12:56118524-56118574	AG09319	gingival:	n/a
18	chr12:56119258-56119308	MCF10A-Er-Src	breast:	n/a
19	chr12:56119258-56119308	U87	brain:	n/a
20	chr12:56118524-56118574	HepG2	liver:	n/a
21	chr12:56118524-56118574	ovcar-3	ovarian:	n/a
22	chr12:56120816-56120866	SK-N-SH	brain:	n/a
23	chr12:56120816-56120866	GM12892	blood:	n/a
24	chr12:56119258-56119308	HRPEpiC	eye:	n/a
25	chr12:56120816-56120866	NH-A	brain:	n/a
26	chr12:56120816-56120866	Hepatocyte	liver:	n/a
27	chr12:56119258-56119308	H1-hESC	embryonic stem cell:	embryo
28	chr12:56119258-56119308	NT2-D1	testis:	n/a
29	chr12:56120816-56120866	T-47D	breast:	n/a
30	chr12:56118524-56118574	HIPEpiC	eye:	n/a
31	chr12:56118524-56118574	HRE	kidney:	n/a
32	chr12:56120816-56120866	ECC-1	luminal epithelium:	n/a
33	chr12:56119258-56119308	SK-N-SH	brain:	n/a
34	chr12:56120816-56120866	K562	blood:	n/a
35	chr12:56120816-56120866	A549	lung:	n/a
36	chr12:56118524-56118574	IMR90	lung:	fetal
37	chr12:56120816-56120866	SKMC	muscle:	n/a
38	chr12:56118524-56118574	HRPEpiC	eye:	n/a
39	chr12:56118524-56118574	SKMC	muscle:	n/a
40	chr12:56119258-56119308	RPTEC	kidney:	n/a
41	chr12:56118524-56118574	NT2-D1	testis:	n/a
42	chr12:56120816-56120866	AG09319	gingival:	n/a
43	chr12:56120816-56120866	HUVEC	blood vessel:	n/a
44	chr12:56120816-56120866	LNCaP	prostate:	n/a
45	chr12:56118524-56118574	A549	lung:	n/a
46	chr12:56118524-56118574	BJ	skin:	n/a
47	chr12:56120816-56120866	PrEC	prostate:	n/a
48	chr12:56119258-56119308	HCM	heart:	n/a
49	chr12:56118524-56118574	H1-hESC	embryonic stem cell:	embryo
50	chr12:56118524-56118574	GM12892	blood:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56120533..56123958-chr12:56496918..56499602,3	K562	blood:
2	chr12:56120734..56123554-chr12:56508983..56512643,4	K562	blood:
3	chr12:56120505..56122635-chr12:56345271..56347933,2	K562	blood:
4	chr12:56117197..56125255-chr12:56135299..56142277,21	K562	blood:
5	chr12:56120591..56123197-chr12:56472700..56474357,3	MCF-7	breast:
6	chr12:56098994..56103683-chr12:56119699..56126107,8	MCF-7	breast:
7	chr12:56119665..56125098-chr12:56220794..56225708,11	MCF-7	breast:
8	chr12:56104896..56106917-chr12:56120568..56123344,2	MCF-7	breast:
9	chr12:56118190..56119080-chr12:56130780..56131563,6	MCF-7	breast:
10	chr12:56119294..56126638-chr12:56434111..56441706,13	K562	blood:
11	chr12:56117825..56119634-chr17:57178406..57181247,2	MCF-7	breast:
12	chr12:56115949..56118195-chr12:56224037..56226803,2	MCF-7	breast:
13	chr12:56088490..56090282-chr12:56117395..56118988,2	MCF-7	breast:
14	chr12:56115280..56117661-chr12:56434487..56437125,2	MCF-7	breast:
15	chr12:56118429..56118954-chr12:56190727..56191514,2	K562	blood:
16	chr12:56120093..56124486-chr12:56434488..56437037,3	K562	blood:
17	chr12:56118075..56119434-chr12:56130540..56132004,12	MCF-7	breast:
18	chr12:56075054..56077566-chr12:56115620..56119645,3	MCF-7	breast:
19	chr12:56120240..56124369-chr12:56508983..56513755,7	K562	blood:
20	chr12:56120515..56122201-chr12:56332595..56334238,2	K562	blood:
21	chr12:56037529..56040108-chr12:56117252..56119317,2	K562	blood:
22	chr12:56119684..56120517-chr7:23338542..23339053,2	NB4	blood:
23	chr12:56119392..56124555-chr12:56134719..56139155,10	MCF-7	breast:
24	chr12:56120851..56123825-chr12:56659216..56662167,3	K562	blood:
25	chr12:56118355..56119078-chr12:56130717..56131614,5	K562	blood:
26	chr12:56110479..56111014-chr12:56118069..56118640,2	K562	blood:
27	chr12:56118873..56123597-chr12:56135421..56141775,11	K562	blood:
28	chr12:56120003..56122736-chr12:56659216..56661326,3	K562	blood:
29	chr12:56099553..56102772-chr12:56120884..56124385,4	K562	blood:
30	chr12:56120864..56122982-chr12:56435772..56437272,2	MCF-7	breast:
31	chr12:56120587..56125243-chr12:56320195..56323478,6	MCF-7	breast:

No data

Variant related genes	Relation type
CD63	TF binding region
ENSG00000258056	TF binding region
CD63	CpG island
ENSG00000258056	CpG island
ENSG00000065357	chromatin interactions
ENSG00000229117	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000170515	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000135469	chromatin interactions
ENSG00000065361	chromatin interactions
ENSG00000156928	chromatin interactions
ENSG00000257390	chromatin interactions
ENSG00000170473	chromatin interactions
ENSG00000182796	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000135424	chromatin interactions
ENSG00000258345	chromatin interactions
ENSG00000135414	chromatin interactions
ENSG00000170439	chromatin interactions
ENSG00000135392	chromatin interactions
ENSG00000197728	chromatin interactions

Extended variants
information (count: 175 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:175 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3138136	chr12:56117570-56117571	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs542661978	chr12:56117619-56117620	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs186400692	chr12:56117644-56117645	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs57751631	chr12:56117648-56117649	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs3138135	chr12:56117652-56117653	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs367574522	chr12:56117656-56117657	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs544466160	chr12:56117659-56117660	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs556112230	chr12:56117661-56117662	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs143431876	chr12:56117662-56117663	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs367757406	chr12:56117672-56117673	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs200846937	chr12:56117696-56117697	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs13193	chr12:56117700-56117701	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs376530065	chr12:56117707-56117708	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs375135224	chr12:56117725-56117726	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs527371486	chr12:56117731-56117732	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs1058641	chr12:56117743-56117744	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs548708935	chr12:56117758-56117759	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs567205022	chr12:56117774-56117775	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs571658392	chr12:56117783-56117784	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs538179042	chr12:56117792-56117793	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs199865350	chr12:56117811-56117812	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs62638191	chr12:56117812-56117813	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs368073596	chr12:56117832-56117833	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs538878371	chr12:56117944-56117945	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs553945466	chr12:56117993-56117994	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs541639945	chr12:56118006-56118007	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs572247598	chr12:56118008-56118009	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs570871726	chr12:56118045-56118046	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs376854849	chr12:56118062-56118063	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs201807174	chr12:56118071-56118072	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs554685831	chr12:56118073-56118074	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs371942312	chr12:56118094-56118095	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs376583199	chr12:56118120-56118121	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs545045941	chr12:56118124-56118125	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs141783438	chr12:56118125-56118126	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs543433718	chr12:56118149-56118150	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs368653792	chr12:56118169-56118170	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs146041022	chr12:56118210-56118211	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs62638193	chr12:56118211-56118212	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs62638194	chr12:56118213-56118214	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs111033593	chr12:56118252-56118253	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs147986326	chr12:56118295-56118296	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs267607006	chr12:56118300-56118301	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs375455813	chr12:56118333-56118334	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs577996458	chr12:56118405-56118406	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs183719917	chr12:56118432-56118433	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs560347706	chr12:56118447-56118448	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs150493825	chr12:56118459-56118460	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs527384653	chr12:56118524-56118525	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs549034947	chr12:56118536-56118537	Strong transcription Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Multiple myeloma	16616336	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	19115005	CNVD
early-passage human iPS cells	21368824	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56111200-56120400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:56111600-56118400	Strong transcription	Thymus	Thymus
3	chr12:56112000-56117800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr12:56112200-56118000	Weak transcription	Fetal Lung	lung
5	chr12:56112400-56118000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr12:56112600-56117600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:56112600-56118200	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr12:56112600-56118800	Weak transcription	Small Intestine	intestine
9	chr12:56112800-56120800	Weak transcription	Fetal Brain Male	brain
10	chr12:56112800-56121000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr12:56113200-56118000	Weak transcription	Ovary	ovary
12	chr12:56113200-56118600	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr12:56113200-56120000	Strong transcription	Brain Germinal Matrix	brain
14	chr12:56113200-56120800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr12:56114200-56117800	Strong transcription	Spleen	Spleen
16	chr12:56114200-56118600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr12:56114400-56117800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:56114400-56118000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr12:56114400-56118600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr12:56114400-56121000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr12:56114600-56118000	Weak transcription	Fetal Kidney	kidney
22	chr12:56114800-56118200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr12:56115000-56118600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr12:56115000-56118600	Weak transcription	Primary T helper cells fromperipheralblood	blood
25	chr12:56115000-56120400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr12:56115200-56118200	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr12:56115400-56117600	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr12:56115400-56117600	Weak transcription	Brain Substantia Nigra	brain
29	chr12:56115400-56117600	Weak transcription	Esophagus	oesophagus
30	chr12:56115400-56117600	Weak transcription	Pancreas	Pancrea
31	chr12:56115400-56117800	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr12:56115400-56118000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr12:56115400-56118000	Weak transcription	Brain Angular Gyrus	brain
34	chr12:56115400-56118400	Weak transcription	K562	blood
35	chr12:56115400-56118600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr12:56115400-56120400	Genic enhancers	Fetal Intestine Large	intestine
37	chr12:56115400-56120400	Strong transcription	Fetal Stomach	stomach
38	chr12:56115400-56120600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr12:56115400-56121000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr12:56115400-56121200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
41	chr12:56115600-56117600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr12:56115600-56117800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr12:56115600-56117800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr12:56115600-56117800	Weak transcription	Aorta	Aorta
45	chr12:56115600-56118000	Weak transcription	Hela-S3	cervix
46	chr12:56115600-56120400	Strong transcription	Lung	lung
47	chr12:56115600-56120600	Genic enhancers	Fetal Muscle Trunk	muscle
48	chr12:56115600-56120800	Genic enhancers	Fetal Muscle Leg	muscle
49	chr12:56115800-56117600	Weak transcription	Gastric	stomach
50	chr12:56115800-56117600	Weak transcription	Right Atrium	heart

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