Variant report

Variant	esv3410287
Chromosome Location	chr12:32142734-32219420
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1415)
CpG islands
(count:183)
Chromatin interactive
region (count:39)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1415 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:32192858-32193616	K562	blood:	n/a	n/a
2	ARID3A	chr12:32187062-32187394	K562	blood:	n/a	n/a
3	ARID3A	chr12:32213606-32213852	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:32173938-32174440	K562	blood:	n/a	n/a
5	ARID3A	chr12:32173008-32173640	K562	blood:	n/a	chr12:32173009-32173025 chr12:32173012-32173028
6	ARID3A	chr12:32158464-32158892	K562	blood:	n/a	n/a
7	ARID3A	chr12:32213547-32213848	K562	blood:	n/a	n/a
8	ARID3A	chr12:32183690-32184712	K562	blood:	n/a	n/a
9	ARID3A	chr12:32153228-32153727	K562	blood:	n/a	n/a
10	ARID3A	chr12:32204432-32204885	K562	blood:	n/a	n/a
11	ARID3A	chr12:32182766-32182776	K562	blood:	n/a	n/a
12	ARID3A	chr12:32200362-32201261	K562	blood:	n/a	n/a
13	ARID3A	chr12:32207151-32207474	K562	blood:	n/a	n/a
14	ARID3A	chr12:32183003-32183359	K562	blood:	n/a	n/a
15	ATF1	chr12:32203036-32203105	K562	blood:	n/a	n/a
16	ATF1	chr12:32200324-32201255	K562	blood:	n/a	n/a
17	ATF1	chr12:32153310-32153625	K562	blood:	n/a	n/a
18	ATF1	chr12:32204425-32204862	K562	blood:	n/a	n/a
19	ATF1	chr12:32205355-32205521	K562	blood:	n/a	n/a
20	ATF1	chr12:32187095-32187402	K562	blood:	n/a	n/a
21	ATF1	chr12:32173951-32174406	K562	blood:	n/a	n/a
22	ATF1	chr12:32184012-32184492	K562	blood:	n/a	n/a
23	ATF1	chr12:32158405-32158812	K562	blood:	n/a	n/a
24	ATF2	chr12:32169809-32170266	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr12:32144700-32145155	GM12878	blood:	n/a	n/a
26	ATF2	chr12:32213450-32213857	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr12:32213411-32213812	GM12878	blood:	n/a	n/a
28	ATF2	chr12:32213478-32213885	GM12878	blood:	n/a	n/a
29	ATF2	chr12:32166327-32166733	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr12:32166251-32166794	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF3	chr12:32158396-32158863	K562	blood:	n/a	n/a
32	ATF3	chr12:32183911-32184420	K562	blood:	n/a	n/a
33	ATF3	chr12:32200736-32201209	K562	blood:	n/a	n/a
34	ATF3	chr12:32153295-32153579	K562	blood:	n/a	n/a
35	ATF3	chr12:32204374-32204872	A549	lung:	n/a	n/a
36	BACH1	chr12:32184763-32184780	K562	blood:	n/a	n/a
37	BACH1	chr12:32183772-32184220	K562	blood:	n/a	n/a
38	BACH1	chr12:32200505-32200661	K562	blood:	n/a	n/a
39	BACH1	chr12:32158509-32158692	K562	blood:	n/a	n/a
40	BACH1	chr12:32153330-32153648	K562	blood:	n/a	n/a
41	BATF	chr12:32144632-32145114	GM12878	blood:	n/a	chr12:32144945-32144955
42	BATF	chr12:32144766-32145106	GM12878	blood:	n/a	chr12:32144945-32144955
43	BCL11A	chr12:32178851-32179186	GM12878	blood:	n/a	n/a
44	BCL11A	chr12:32166387-32166762	H1-hESC	embryonic stem cell:	n/a	n/a
45	BCL3	chr12:32158395-32158935	K562	blood:	n/a	n/a
46	BCLAF1	chr12:32184003-32184545	K562	blood:	n/a	n/a
47	BCLAF1	chr12:32183892-32184490	K562	blood:	n/a	n/a
48	BCLAF1	chr12:32200286-32201277	K562	blood:	n/a	n/a
49	BCLAF1	chr12:32153236-32153777	K562	blood:	n/a	n/a
50	BCLAF1	chr12:32213479-32213920	GM12878	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	chr12:32145672-32145722	NHDF-neo	bronchial:	n/a
2	chr12:32185731-32185781	AoSMC	blood vessel:	n/a
3	chr12:32192489-32192539	HUVEC	blood vessel:	n/a
4	chr12:32145672-32145722	IMR90	lung:	fetal
5	chr12:32185731-32185781	NB4	blood:	n/a
6	chr12:32145672-32145722	NT2-D1	testis:	n/a
7	chr12:32145672-32145722	AG04449	skin:	fetal
8	chr12:32185731-32185781	MCF-7	breast:	n/a
9	chr12:32185731-32185781	SK-N-MC	brain:	n/a
10	chr12:32145672-32145722	PANC-1	pancreas:	n/a
11	chr12:32145672-32145722	AoSMC	blood vessel:	n/a
12	chr12:32145672-32145722	GM12878	blood:	n/a
13	chr12:32192489-32192539	NHDF-neo	bronchial:	n/a
14	chr12:32185731-32185781	Hela-S3	cervix:	n/a
15	chr12:32145672-32145722	HEEpiC	esophagus:	n/a
16	chr12:32185731-32185781	HNPCEpiC	eye:	n/a
17	chr12:32192489-32192539	HRE	kidney:	n/a
18	chr12:32192489-32192539	NT2-D1	testis:	n/a
19	chr12:32192489-32192539	AG10803	skin:	n/a
20	chr12:32145672-32145722	HCM	heart:	n/a
21	chr12:32192489-32192539	PFSK-1	brain:	n/a
22	chr12:32192489-32192539	AoSMC	blood vessel:	n/a
23	chr12:32192489-32192539	BJ	skin:	n/a
24	chr12:32192489-32192539	HEK293	kidney:	embryo
25	chr12:32145672-32145722	HNPCEpiC	eye:	n/a
26	chr12:32185731-32185781	AG04449	skin:	fetal
27	chr12:32145672-32145722	GM12892	blood:	n/a
28	chr12:32185731-32185781	H1-hESC	embryonic stem cell:	embryo
29	chr12:32145672-32145722	GM12891	blood:	n/a
30	chr12:32185731-32185781	RPTEC	kidney:	n/a
31	chr12:32145672-32145722	HEK293	kidney:	embryo
32	chr12:32145672-32145722	ProgFib	skin:	n/a
33	chr12:32185731-32185781	HCF	heart:	n/a
34	chr12:32185731-32185781	U87	brain:	n/a
35	chr12:32185731-32185781	Hepatocyte	liver:	n/a
36	chr12:32192489-32192539	GM19239	blood:	n/a
37	chr12:32145672-32145722	MCF10A-Er-Src	breast:	n/a
38	chr12:32192489-32192539	BE2_C	brain:	n/a
39	chr12:32192489-32192539	GM06990	blood:	n/a
40	chr12:32192489-32192539	A549	lung:	n/a
41	chr12:32185731-32185781	SK-N-SH_RA	brain:	n/a
42	chr12:32145672-32145722	MCF-7	breast:	n/a
43	chr12:32185731-32185781	IMR90	lung:	fetal
44	chr12:32192489-32192539	H1-hESC	embryonic stem cell:	embryo
45	chr12:32192489-32192539	NH-A	brain:	n/a
46	chr12:32145672-32145722	HCF	heart:	n/a
47	chr12:32145672-32145722	HCPEpiC	choroid plexus:	n/a
48	chr12:32192489-32192539	HL-60	blood:	n/a
49	chr12:32185731-32185781	LNCaP	prostate:	n/a
50	chr12:32145672-32145722	HRCEpiC	kidney:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:32146985..32148655-chr12:32151850..32154209,2	MCF-7	breast:
2	chr12:32173013..32175537-chr12:32177292..32179791,2	K562	blood:
3	chr12:32146985..32148655-chr12:32151850..32154209,2	MCF-7	breast:
4	chr12:32192092..32194335-chr12:32198674..32200576,2	K562	blood:
5	chr12:32184129..32186800-chr12:32198545..32200849,2	K562	blood:
6	chr12:32173443..32176016-chr12:32188514..32190413,2	K562	blood:
7	chr12:32173443..32176016-chr12:32188514..32190413,2	K562	blood:
8	chr12:32175862..32178406-chr12:32179354..32181196,2	K562	blood:
9	chr12:32185942..32189585-chr12:32195326..32198101,3	K562	blood:
10	chr12:32213439..32214241-chr12:32496597..32497332,2	MCF-7	breast:
11	chr12:32199482..32202478-chr12:32260191..32262626,2	K562	blood:
12	chr12:32184129..32187066-chr12:32199349..32202275,2	K562	blood:
13	chr12:32111364..32113470-chr12:32143202..32145757,3	K562	blood:
14	chr12:32168121..32171020-chr12:32184096..32185622,2	K562	blood:
15	chr12:32175862..32178406-chr12:32179354..32181196,2	K562	blood:
16	chr12:32116205..32118530-chr12:32174123..32177069,2	K562	blood:
17	chr12:31881091..31882971-chr12:32206555..32209474,2	K562	blood:
18	chr12:32167636..32169968-chr12:32184518..32186741,2	K562	blood:
19	chr12:32192092..32194335-chr12:32198674..32200576,2	K562	blood:
20	chr12:32110978..32112717-chr12:32158767..32160498,2	K562	blood:
21	chr12:32213222..32214189-chr12:32464699..32465690,4	MCF-7	breast:
22	chr12:32112309..32113815-chr12:32205277..32207073,2	K562	blood:
23	chr12:31835175..31835818-chr12:32213320..32214060,2	MCF-7	breast:
24	chr12:32184129..32187066-chr12:32199349..32202275,2	K562	blood:
25	chr12:32167636..32169968-chr12:32184518..32186741,2	K562	blood:
26	chr12:32193881..32196557-chr12:32221966..32223576,2	MCF-7	breast:
27	chr12:32185942..32189585-chr12:32195326..32198101,3	K562	blood:
28	chr12:31880053..31882994-chr12:32145779..32148383,2	K562	blood:
29	chr12:31867484..31869953-chr12:32200460..32203745,3	K562	blood:
30	chr12:32168121..32171020-chr12:32184096..32185622,2	K562	blood:
31	chr12:32112365..32113214-chr12:32213234..32213824,2	MCF-7	breast:
32	chr12:32138789..32140299-chr12:32142028..32144820,2	K562	blood:
33	chr12:32185942..32188780-chr12:32195326..32198101,2	K562	blood:
34	chr12:32184129..32186800-chr12:32198545..32200849,2	K562	blood:
35	chr12:32213625..32214125-chr9:122632674..122633194,2	MCF-7	breast:
36	chr12:32111704..32113744-chr12:32185448..32187261,2	K562	blood:
37	chr12:32185942..32188780-chr12:32195326..32198101,2	K562	blood:
38	chr12:32213140..32214101-chr12:32454772..32455510,3	MCF-7	breast:
39	chr12:32173013..32175537-chr12:32177292..32179791,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BICD1-2	chr12:32204371-32204515	NONHSAT027603
2	lnc-BICD1-2	chr12:32204070-32204143	NONHSAT027603
3	lnc-C12orf35-3	chr12:32152004-32152447	expReg_chr12_2826_+
4	lnc-C12orf35-7	chr12:32160061-32160369	NONHSAT027602
5	lnc-C12orf35-4	chr12:32154358-32155125	NONHSAT027600
6	lnc-C12orf35-6	chr12:32155165-32157256	NONHSAT027601

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	C12orf35	hsa-miR-23a-3p	chr12:32145867-32145889
2	C12orf35	hsa-miR-21-5p	chr12:32145825-32145845

Variant related genes	Relation type
ENSG00000257094	TF binding region
ENSG00000257094	CpG island
ENSG00000257530	chromatin interactions
ENSG00000151746	chromatin interactions
ENSG00000174718	chromatin interactions
ENSG00000151743	chromatin interactions

Extended variants
information (count: 3646 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3646 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145235750	chr12:32142740-32142741	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs149177552	chr12:32142764-32142765	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536466721	chr12:32142790-32142791	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs147491705	chr12:32142798-32142799	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs555393447	chr12:32142817-32142818	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527758865	chr12:32142838-32142839	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs567018557	chr12:32142900-32142901	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs575253495	chr12:32142928-32142929	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs142161192	chr12:32142931-32142932	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs146713495	chr12:32142935-32142936	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs138050111	chr12:32142981-32142982	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4931001	chr12:32143000-32143001	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs185677856	chr12:32143004-32143005	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140342125	chr12:32143010-32143011	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116188813	chr12:32143025-32143026	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs542468403	chr12:32143072-32143073	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs555848517	chr12:32143136-32143137	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536014480	chr12:32143158-32143159	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs4931002	chr12:32143169-32143170	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs531841234	chr12:32143174-32143175	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551929766	chr12:32143175-32143176	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs145529309	chr12:32143181-32143182	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs527700895	chr12:32143187-32143188	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs112129031	chr12:32143199-32143200	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs140688147	chr12:32143271-32143272	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs10844084	chr12:32143277-32143278	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs4931003	chr12:32143302-32143303	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs376734016	chr12:32143353-32143354	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs369780361	chr12:32143359-32143360	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537533411	chr12:32143372-32143373	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs188577534	chr12:32143374-32143375	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs150799616	chr12:32143376-32143377	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570884024	chr12:32143435-32143436	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs113758781	chr12:32143444-32143445	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544091618	chr12:32143485-32143486	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs553996349	chr12:32143543-32143544	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs377441204	chr12:32143573-32143574	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs4931004	chr12:32143652-32143653	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542958719	chr12:32143653-32143654	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556060058	chr12:32143665-32143666	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138447512	chr12:32143680-32143681	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576336491	chr12:32143703-32143704	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs545482615	chr12:32143751-32143752	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6488022	chr12:32143791-32143792	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs149261242	chr12:32143797-32143798	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs111529813	chr12:32143831-32143832	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541594577	chr12:32143843-32143844	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529828894	chr12:32143858-32143859	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs79421115	chr12:32143867-32143868	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs543892223	chr12:32143878-32143879	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Chronic lymphocytic leukemia	21546498	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	21509527	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Cancer	21129771	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17899364	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
microdeletion syndrome	16199537	CNVD
Chordoma	18071362	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32114000-32150800	Weak transcription	NHLF	lung
2	chr12:32116400-32143200	ZNF genes & repeats	GM12878-XiMat	blood
3	chr12:32123200-32143800	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
4	chr12:32123400-32143200	ZNF genes & repeats	Primary T helper cells PMA-I stimulated	--
5	chr12:32123800-32143200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
6	chr12:32128800-32150600	Weak transcription	Hela-S3	cervix
7	chr12:32130400-32150200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr12:32132800-32147200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr12:32134800-32149400	Weak transcription	Esophagus	oesophagus
10	chr12:32134800-32149800	Weak transcription	Pancreas	Pancrea
11	chr12:32134800-32151000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr12:32134800-32155400	Weak transcription	NHDF-Ad	bronchial
13	chr12:32135000-32143000	Weak transcription	Spleen	Spleen
14	chr12:32135000-32147800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr12:32135000-32148600	Weak transcription	Brain Hippocampus Middle	brain
16	chr12:32135000-32149200	Weak transcription	Brain Substantia Nigra	brain
17	chr12:32135000-32149800	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr12:32135000-32149800	Weak transcription	Colon Smooth Muscle	Colon
19	chr12:32135000-32150000	Weak transcription	Right Ventricle	heart
20	chr12:32135000-32150200	Weak transcription	Rectal Smooth Muscle	rectum
21	chr12:32135000-32150800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
22	chr12:32135000-32156000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr12:32135000-32156400	Weak transcription	Gastric	stomach
24	chr12:32135200-32148200	Weak transcription	Brain Angular Gyrus	brain
25	chr12:32135600-32148800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr12:32135800-32142800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr12:32136000-32142800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr12:32136000-32150000	Weak transcription	Aorta	Aorta
29	chr12:32136000-32150600	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr12:32136000-32155000	Weak transcription	HSMMtube	muscle
31	chr12:32136200-32144200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:32136200-32150600	Weak transcription	Psoas Muscle	Psoas
33	chr12:32136200-32155400	Weak transcription	Osteobl	bone
34	chr12:32136400-32143600	Strong transcription	Dnd41	blood
35	chr12:32136400-32151000	Weak transcription	NH-A	brain
36	chr12:32136600-32144800	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr12:32136600-32149600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr12:32136600-32150800	Weak transcription	HSMM	muscle
39	chr12:32137200-32143000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr12:32137200-32158600	Weak transcription	HUVEC	blood vessel
41	chr12:32137400-32143000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr12:32137400-32143000	Weak transcription	Left Ventricle	heart
43	chr12:32137600-32143200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr12:32137600-32151400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr12:32137800-32142800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr12:32137800-32143000	Weak transcription	Fetal Brain Male	brain
47	chr12:32137800-32147400	Weak transcription	Primary hematopoietic stem cells	blood
48	chr12:32138200-32146600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr12:32138200-32147800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr12:32138400-32143000	Weak transcription	Adipose Nuclei	Adipose

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