Variant report

Variant	nsv975403
Chromosome Location	chr12:9481646-9541991
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1385)
CpG islands
(count:428)
Chromatin interactive
region (count:42)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1385 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:9531284-9531477	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:9495326-9496012	HepG2	liver:	n/a	n/a
3	ARID3A	chr12:9493327-9493396	K562	blood:	n/a	n/a
4	ATF1	chr12:9492605-9492785	K562	blood:	n/a	n/a
5	ATF1	chr12:9519822-9520248	K562	blood:	n/a	n/a
6	ATF1	chr12:9515879-9516104	K562	blood:	n/a	n/a
7	ATF1	chr12:9500046-9500362	K562	blood:	n/a	n/a
8	ATF1	chr12:9493010-9493521	K562	blood:	n/a	n/a
9	ATF1	chr12:9520485-9520799	K562	blood:	n/a	n/a
10	ATF1	chr12:9517037-9517719	K562	blood:	n/a	n/a
11	ATF1	chr12:9499390-9499755	K562	blood:	n/a	n/a
12	ATF2	chr12:9514144-9518351	GM12878	blood:	n/a	n/a
13	ATF2	chr12:9516298-9518464	GM12878	blood:	n/a	n/a
14	ATF2	chr12:9515316-9516084	GM12878	blood:	n/a	n/a
15	ATF2	chr12:9514231-9515229	GM12878	blood:	n/a	n/a
16	ATF2	chr12:9483870-9484266	GM12878	blood:	n/a	n/a
17	ATF2	chr12:9483724-9484288	GM12878	blood:	n/a	n/a
18	BACH1	chr12:9507019-9507395	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr12:9486740-9486998	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr12:9516711-9516911	K562	blood:	n/a	n/a
21	BACH1	chr12:9496419-9496420	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr12:9490118-9490128	K562	blood:	n/a	n/a
23	BATF	chr12:9516818-9517792	GM12878	blood:	n/a	n/a
24	BATF	chr12:9506976-9507254	GM12878	blood:	n/a	n/a
25	BATF	chr12:9516696-9517884	GM12878	blood:	n/a	n/a
26	BATF	chr12:9515676-9516129	GM12878	blood:	n/a	chr12:9515939-9515950
27	BATF	chr12:9514492-9515074	GM12878	blood:	n/a	n/a
28	BATF	chr12:9507017-9507310	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:9506964-9507320	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:9514587-9514903	GM12878	blood:	n/a	n/a
31	BCL11A	chr12:9514518-9515013	GM12878	blood:	n/a	chr12:9514548-9514557
32	BCL11A	chr12:9507015-9507175	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:9516896-9517726	GM12878	blood:	n/a	n/a
34	BCL11A	chr12:9516825-9517859	GM12878	blood:	n/a	n/a
35	BCL3	chr12:9516906-9517768	GM12878	blood:	n/a	n/a
36	BCL3	chr12:9514536-9515106	GM12878	blood:	n/a	chr12:9514548-9514557
37	BCL3	chr12:9516773-9518016	GM12878	blood:	n/a	n/a
38	BCL3	chr12:9514179-9515157	GM12878	blood:	n/a	chr12:9514548-9514557
39	BCLAF1	chr12:9516321-9518443	GM12878	blood:	n/a	n/a
40	BCLAF1	chr12:9514439-9515090	GM12878	blood:	n/a	chr12:9514548-9514557
41	BCLAF1	chr12:9516391-9518359	GM12878	blood:	n/a	n/a
42	BCLAF1	chr12:9514268-9515127	GM12878	blood:	n/a	chr12:9514548-9514557
43	BHLHE40	chr12:9495267-9495730	HepG2	liver:	n/a	n/a
44	BHLHE40	chr12:9516856-9517910	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:9493114-9493281	K562	blood:	n/a	n/a
46	BHLHE40	chr12:9531137-9531362	K562	blood:	n/a	n/a
47	BHLHE40	chr12:9507035-9507312	HepG2	liver:	n/a	n/a
48	BHLHE40	chr12:9514468-9515061	GM12878	blood:	n/a	n/a
49	BHLHE40	chr12:9499426-9499609	K562	blood:	n/a	n/a
50	BHLHE40	chr12:9507008-9507323	HepG2	liver:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9489057-9489107	U87	brain:	n/a
2	chr12:9489057-9489107	U87	brain:	n/a
3	chr12:9517562-9517612	SAEC	small airway:	n/a
4	chr12:9489057-9489107	LNCaP	prostate:	n/a
5	chr12:9486542-9486592	GM19239	blood:	n/a
6	chr12:9486542-9486592	GM12891	blood:	n/a
7	chr12:9501915-9501965	SK-N-SH	brain:	n/a
8	chr12:9489057-9489107	AG10803	skin:	n/a
9	chr12:9501915-9501965	SK-N-SH_RA	brain:	n/a
10	chr12:9517562-9517612	Hela-S3	cervix:	n/a
11	chr12:9493259-9493309	H1-hESC	embryonic stem cell:	embryo
12	chr12:9501845-9501895	NHBE	bronchial:	n/a
13	chr12:9501845-9501895	SKMC	muscle:	n/a
14	chr12:9489057-9489107	IMR90	lung:	fetal
15	chr12:9493259-9493309	SKMC	muscle:	n/a
16	chr12:9501845-9501895	Caco-2	colon:	n/a
17	chr12:9501783-9501833	PFSK-1	brain:	n/a
18	chr12:9501783-9501833	K562	blood:	n/a
19	chr12:9501783-9501833	HUVEC	blood vessel:	n/a
20	chr12:9517562-9517612	Caco-2	colon:	n/a
21	chr12:9489057-9489107	HIPEpiC	eye:	n/a
22	chr12:9493259-9493309	CMK	blood:	n/a
23	chr12:9501845-9501895	GM12891	blood:	n/a
24	chr12:9501915-9501965	HepG2	liver:	n/a
25	chr12:9517562-9517612	HUVEC	blood vessel:	n/a
26	chr12:9493259-9493309	K562	blood:	n/a
27	chr12:9501915-9501965	HAEpiC	amniotic membrane:	n/a
28	chr12:9501915-9501965	CMK	blood:	n/a
29	chr12:9501845-9501895	SAEC	small airway:	n/a
30	chr12:9517562-9517612	ProgFib	skin:	n/a
31	chr12:9501915-9501965	HCF	heart:	n/a
32	chr12:9501783-9501833	NB4	blood:	n/a
33	chr12:9517562-9517612	RPTEC	kidney:	n/a
34	chr12:9489057-9489107	GM19239	blood:	n/a
35	chr12:9501915-9501965	LNCaP	prostate:	n/a
36	chr12:9486542-9486592	AG09309	skin:	n/a
37	chr12:9501783-9501833	GM12891	blood:	n/a
38	chr12:9489057-9489107	MCF10A-Er-Src	breast:	n/a
39	chr12:9517562-9517612	HEK293	kidney:	embryo
40	chr12:9501783-9501833	AG04449	skin:	fetal
41	chr12:9486542-9486592	SKMC	muscle:	n/a
42	chr12:9517562-9517612	HIPEpiC	eye:	n/a
43	chr12:9493259-9493309	NT2-D1	testis:	n/a
44	chr12:9501915-9501965	AG09319	gingival:	n/a
45	chr12:9489057-9489107	SK-N-SH	brain:	n/a
46	chr12:9501783-9501833	GM19239	blood:	n/a
47	chr12:9517562-9517612	PFSK-1	brain:	n/a
48	chr12:9493259-9493309	GM06990	blood:	n/a
49	chr12:9493259-9493309	NH-A	brain:	n/a
50	chr12:9501845-9501895	BJ	skin:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:9522809..9525392-chr12:9798242..9800347,2	K562	blood:
2	chr12:9499156..9500827-chr12:9501599..9503470,2	MCF-7	breast:
3	chr12:9526563..9529363-chr12:9530052..9533405,3	MCF-7	breast:
4	chr12:9493453..9495524-chr12:9502233..9505001,2	K562	blood:
5	chr12:9431917..9434887-chr12:9485752..9487325,2	MCF-7	breast:
6	chr12:9530894..9532008-chr12:9621312..9622244,4	MCF-7	breast:
7	chr12:9516871..9518767-chr12:9528942..9530878,2	MCF-7	breast:
8	chr12:9483381..9483965-chr12:9531043..9531743,2	MCF-7	breast:
9	chr12:9492767..9495377-chr12:9497278..9499065,2	K562	blood:
10	chr12:9215856..9217597-chr12:9482273..9484056,2	MCF-7	breast:
11	chr12:9530855..9531819-chr12:9772155..9773338,3	MCF-7	breast:
12	chr12:9526563..9529363-chr12:9530052..9533405,3	MCF-7	breast:
13	chr12:9514676..9517481-chr12:9908794..9910668,2	K562	blood:
14	chr12:9483967..9484695-chr12:9530892..9531873,3	MCF-7	breast:
15	chr12:9483413..9484009-chr12:9524583..9525215,2	MCF-7	breast:
16	chr12:9483413..9484009-chr12:9524583..9525215,2	MCF-7	breast:
17	chr12:9514472..9517285-chr12:9517571..9520331,3	K562	blood:
18	chr12:9499156..9500827-chr12:9501599..9503470,2	MCF-7	breast:
19	chr12:9494429..9497191-chr12:9497385..9498990,2	MCF-7	breast:
20	chr12:9216318..9217819-chr12:9520696..9522982,2	MCF-7	breast:
21	chr12:9516871..9518767-chr12:9528942..9530878,2	MCF-7	breast:
22	chr12:9532106..9535030-chr12:9800116..9802366,2	MCF-7	breast:
23	chr12:9494429..9497191-chr12:9497385..9498990,2	MCF-7	breast:
24	chr12:9536132..9537679-chr12:9542165..9544182,2	MCF-7	breast:
25	chr11:62379397..62380044-chr12:9496046..9496903,2	HCT-116	colon:
26	chr12:9531253..9531816-chr12:9860516..9861214,2	MCF-7	breast:
27	chr12:9492332..9494947-chr12:9501072..9502931,2	MCF-7	breast:
28	chr12:9492332..9494947-chr12:9501072..9502931,2	MCF-7	breast:
29	chr12:9216794..9217363-chr12:9524530..9525508,3	MCF-7	breast:
30	chr12:9539959..9542936-chr12:9543055..9546745,3	K562	blood:
31	chr12:9483967..9484695-chr12:9530892..9531873,3	MCF-7	breast:
32	chr12:9536927..9538446-chr12:9539967..9542011,2	K562	blood:
33	chr12:9493453..9495524-chr12:9502233..9505001,2	K562	blood:
34	chr12:9483381..9483965-chr12:9531043..9531743,2	MCF-7	breast:
35	chr12:9536927..9538446-chr12:9539967..9542011,2	K562	blood:
36	chr12:9216106..9218386-chr12:9489612..9493915,4	MCF-7	breast:
37	chr12:9483454..9485642-chr12:9487208..9489749,3	K562	blood:
38	chr12:9492767..9495377-chr12:9497278..9499065,2	K562	blood:
39	chr12:9475880..9477662-chr12:9479960..9482900,2	K562	blood:
40	chr12:9485621..9488613-chr17:57864279..57867030,2	MCF-7	breast:
41	chr12:9483454..9485642-chr12:9487208..9489749,3	K562	blood:
42	chr12:9512017..9514493-chr12:9517939..9520276,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLEC2D-3	chr12:9520060-9522192	ENSG00000260423.1
2	lnc-CLEC2D-3	chr12:9529770-9529807	NONHSAT026815
3	lnc-CLEC2D-3	chr12:9528454-9528682	ENSG00000260423.1
4	lnc-CLEC2D-7	chr12:9493053-9493304	XLOC_009649
5	lnc-CLEC2D-5	chr12:9504271-9504480	XLOC_009651
6	lnc-CLEC2D-5	chr12:9504271-9504944	NONHSAT026731
7	lnc-CLEC2D-5	chr12:9502422-9502713	XLOC_009651
8	lnc-CLEC2D-6	chr12:9500409-9501023	NONHSAT026706
9	lnc-CLEC2D-3	chr12:9528409-9528682	NONHSAT026815
10	lnc-CLEC2D-3	chr12:9520084-9522661	NONHSAT026811
11	lnc-CLEC2D-6	chr12:9498751-9498941	NONHSAT026706
12	lnc-PZP-10	chr12:9495983-9496596	NONHSAT026583
13	lnc-CLEC2D-5	chr12:9502564-9502713	NONHSAT026731
14	lnc-CLEC2D-3	chr12:9528409-9528682	NONHSAT026814
15	lnc-CLEC2D-4	chr12:9519787-9520002	XLOC_009652
16	lnc-PZP-11	chr12:9533948-9534263	NONHSAT026813
17	lnc-CLEC2D-6	chr12:9499308-9499722	NONHSAT026706
18	lnc-CLEC2D-6	chr12:9500555-9500599	XLOC_009650
19	lnc-PZP-10	chr12:9502714-9503413	NONHSAT026583
20	lnc-CLEC2D-4	chr12:9518908-9519370	XLOC_009652
21	lnc-PZP-11	chr12:9524266-9524628	NONHSAT026813
22	lnc-CLEC2D-7	chr12:9492506-9492537	XLOC_009649
23	lnc-PZP-10	chr12:9486480-9486891	NONHSAT026583
24	lnc-PZP-10	chr12:9494143-9494640	NONHSAT026583
25	lnc-PZP-10	chr12:9489902-9490170	NONHSAT026583
26	lnc-CLEC2D-6	chr12:9499309-9499722	XLOC_009650
27	lnc-PZP-10	chr12:9495275-9495398	NONHSAT026583
28	lnc-PZP-10	chr12:9489581-9489812	NONHSAT026583
29	lnc-PZP-10	chr12:9499320-9499524	NONHSAT026583
30	lnc-PZP-10	chr12:9500060-9500507	NONHSAT026583
31	lnc-PZP-4	chr12:9519832-9519991	XLOC_010009
32	lnc-PZP-4	chr12:9516719-9517139	XLOC_010009

No data

Variant related genes	Relation type
ENSG00000260423	TF binding region
ENSG00000260423	CpG island
ENSG00000256442	chromatin interactions
ENSG00000245105	chromatin interactions
ENSG00000149499	chromatin interactions
ENSG00000214851	chromatin interactions
ENSG00000256594	chromatin interactions
ENSG00000260423	chromatin interactions
ENSG00000149489	chromatin interactions
ANXA8L1	miRNA target sites
CNN3	miRNA target sites

Extended variants
information (count: 1708 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150358744	chr12:9481831-9481832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372661025	chr12:9481836-9481837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs535826737	chr12:9481888-9481889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184335851	chr12:9481889-9481890	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs3168554	chr12:9481897-9481898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138028622	chr12:9481906-9481907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372035501	chr12:9481911-9481912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs149600371	chr12:9481925-9481926	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs11611357	chr12:9481961-9481962	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs4883239	chr12:9482043-9482044	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs73239086	chr12:9482118-9482119	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs7962164	chr12:9482130-9482131	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs7975044	chr12:9482154-9482155	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs541286565	chr12:9482212-9482213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs144260370	chr12:9482213-9482214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140027664	chr12:9482214-9482215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141924564	chr12:9482234-9482235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78225272	chr12:9482256-9482257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187181499	chr12:9482271-9482272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs79230149	chr12:9482287-9482288	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs77727199	chr12:9482301-9482302	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs80234779	chr12:9482314-9482315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7975196	chr12:9482323-9482324	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs191260630	chr12:9482332-9482333	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146400544	chr12:9482428-9482429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550334110	chr12:9482444-9482445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184528543	chr12:9482513-9482514	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs6487833	chr12:9482544-9482545	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs535550476	chr12:9482553-9482554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7310995	chr12:9482615-9482616	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs6487835	chr12:9482771-9482772	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs7311245	chr12:9482817-9482818	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs139775160	chr12:9482970-9482971	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12308397	chr12:9482986-9482987	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs7315532	chr12:9483063-9483064	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs536432269	chr12:9483153-9483154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7966144	chr12:9483176-9483177	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs151100892	chr12:9483238-9483239	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs190267296	chr12:9483275-9483276	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386760172	chr12:9483284-9483285	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs7969273	chr12:9483285-9483286	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs193278304	chr12:9483290-9483291	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7979195	chr12:9483295-9483296	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs12302963	chr12:9483324-9483325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185116267	chr12:9483347-9483348	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576100803	chr12:9483368-9483369	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541519824	chr12:9483426-9483427	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189107584	chr12:9483438-9483439	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528423474	chr12:9483461-9483462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs181196601	chr12:9483525-9483526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21611746	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Obesity	21131291	CNVD
Incontinentia Pigmenti	22033527	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Cancer	21272361	CNVD
Schizophrenia	20967226	CNVD

Chromatin state (count:668 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9437200-9485200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:9457400-9485800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr12:9464600-9487600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr12:9464800-9490000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr12:9465000-9486400	Weak transcription	A549	lung
6	chr12:9465400-9485200	Weak transcription	Fetal Intestine Small	intestine
7	chr12:9465600-9484000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr12:9465600-9488000	Weak transcription	Dnd41	blood
9	chr12:9466000-9484000	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr12:9466200-9484000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr12:9466400-9485200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr12:9466400-9487200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr12:9466400-9487600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr12:9472800-9487600	Weak transcription	Thymus	Thymus
15	chr12:9473000-9484000	Weak transcription	GM12878-XiMat	blood
16	chr12:9479000-9486800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:9479200-9486600	Weak transcription	Fetal Muscle Leg	muscle
18	chr12:9480000-9485600	Weak transcription	HepG2	liver
19	chr12:9480200-9483800	Weak transcription	Fetal Muscle Trunk	muscle
20	chr12:9480400-9483800	Weak transcription	Primary B cells from peripheral blood	blood
21	chr12:9480400-9483800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr12:9480400-9483800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr12:9480400-9483800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr12:9480400-9484000	Weak transcription	Right Ventricle	heart
25	chr12:9480600-9484000	Weak transcription	Primary T cells from cord blood	blood
26	chr12:9481000-9483800	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr12:9481200-9484000	Weak transcription	Fetal Thymus	thymus
28	chr12:9481600-9484000	Weak transcription	Fetal Lung	lung
29	chr12:9483800-9484200	Enhancers	Primary B cells from peripheral blood	blood
30	chr12:9483800-9484200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr12:9483800-9484200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr12:9483800-9484200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr12:9483800-9484200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr12:9483800-9484200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr12:9483800-9484200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr12:9483800-9484800	Enhancers	Fetal Muscle Trunk	muscle
37	chr12:9483800-9485400	Enhancers	Primary T cells fromperipheralblood	blood
38	chr12:9484000-9484200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr12:9484000-9484200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:9484000-9484200	Enhancers	Primary T cells from cord blood	blood
41	chr12:9484000-9484200	Enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr12:9484000-9484200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr12:9484000-9484200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr12:9484000-9484200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr12:9484000-9484200	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr12:9484000-9484200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr12:9484000-9484200	Enhancers	Brain Cingulate Gyrus	brain
48	chr12:9484000-9484200	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr12:9484000-9484200	Enhancers	Duodenum Mucosa	Duodenum
50	chr12:9484000-9484200	Enhancers	Right Atrium	heart

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