Variant report

Variant	nsv430454
Chromosome Location	chr12:7954033-8117073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3987)
CpG islands
(count:1832)
Chromatin interactive
region (count:78)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3987 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:7959548-7959804	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:8059700-8060067	K562	blood:	n/a	n/a
3	ARID3A	chr12:8059547-8060068	HepG2	liver:	n/a	n/a
4	ARID3A	chr12:8088653-8089277	HepG2	liver:	n/a	n/a
5	ARID3A	chr12:8085795-8086124	K562	blood:	n/a	n/a
6	ARID3A	chr12:8115662-8116416	K562	blood:	n/a	n/a
7	ARID3A	chr12:7959526-7959828	K562	blood:	n/a	n/a
8	ARID3A	chr12:8090479-8091378	K562	blood:	n/a	n/a
9	ARID3A	chr12:8003917-8004749	HepG2	liver:	n/a	n/a
10	ARID3A	chr12:8043247-8043927	HepG2	liver:	n/a	n/a
11	ARID3A	chr12:7984707-7984990	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:8088187-8089350	K562	blood:	n/a	n/a
13	ARID3A	chr12:7984728-7985022	K562	blood:	n/a	n/a
14	ARID3A	chr12:8090642-8091063	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:8113305-8113722	HepG2	liver:	n/a	n/a
16	ARID3A	chr12:8057729-8058351	HepG2	liver:	n/a	n/a
17	ARID3A	chr12:8111282-8111525	K562	blood:	n/a	n/a
18	ARID3A	chr12:8085786-8086136	HepG2	liver:	n/a	n/a
19	ARID3A	chr12:8113289-8113981	K562	blood:	n/a	n/a
20	ATF1	chr12:8017264-8017507	K562	blood:	n/a	n/a
21	ATF1	chr12:8090846-8091129	K562	blood:	n/a	n/a
22	ATF1	chr12:8085836-8086220	K562	blood:	n/a	n/a
23	ATF1	chr12:7996816-7996880	K562	blood:	n/a	n/a
24	ATF1	chr12:8059740-8060026	K562	blood:	n/a	n/a
25	ATF1	chr12:8113284-8113661	K562	blood:	n/a	chr12:8113469-8113483
26	ATF1	chr12:8111308-8111508	K562	blood:	n/a	n/a
27	ATF1	chr12:8043615-8043923	K562	blood:	n/a	n/a
28	ATF1	chr12:8021845-8022067	K562	blood:	n/a	n/a
29	ATF1	chr12:8115657-8116051	K562	blood:	n/a	n/a
30	ATF2	chr12:8058108-8058451	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr12:8012580-8013428	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr12:8085753-8086276	GM12878	blood:	n/a	n/a
33	ATF2	chr12:8113247-8113725	H1-hESC	embryonic stem cell:	n/a	chr12:8113469-8113483
34	ATF2	chr12:8113268-8113696	GM12878	blood:	n/a	chr12:8113469-8113483
35	ATF2	chr12:8012535-8013325	H1-hESC	embryonic stem cell:	n/a	n/a
36	ATF2	chr12:8058648-8058932	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr12:8085669-8086239	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr12:8088400-8088859	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF2	chr12:8059068-8059314	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr12:8113135-8113746	GM12878	blood:	n/a	chr12:8113469-8113483
41	ATF2	chr12:8059682-8059979	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr12:8058161-8058458	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr12:8042996-8043524	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF3	chr12:8059696-8059961	K562	blood:	n/a	n/a
45	ATF3	chr12:8111301-8111571	K562	blood:	n/a	n/a
46	ATF3	chr12:8043693-8043923	K562	blood:	n/a	n/a
47	ATF3	chr12:8113305-8113574	K562	blood:	n/a	n/a
48	BACH1	chr12:8009353-8009400	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr12:8085950-8086044	K562	blood:	n/a	n/a
50	BACH1	chr12:8113365-8113616	K562	blood:	n/a	n/a

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8025593-8025643	HEK293	kidney:	embryo
2	chr12:8012926-8012976	A549	lung:	n/a
3	chr12:8025593-8025643	HEK293	kidney:	embryo
4	chr12:8012926-8012976	A549	lung:	n/a
5	chr12:8090274-8090324	PANC-1	pancreas:	n/a
6	chr12:8015103-8015153	ECC-1	luminal epithelium:	n/a
7	chr12:8090274-8090324	SK-N-SH	brain:	n/a
8	chr12:8090274-8090324	HEK293	kidney:	embryo
9	chr12:8088931-8088981	HepG2	liver:	n/a
10	chr12:8025593-8025643	CMK	blood:	n/a
11	chr12:8012926-8012976	Hela-S3	cervix:	n/a
12	chr12:8015903-8015953	NHDF-neo	bronchial:	n/a
13	chr12:8112512-8112562	HepG2	liver:	n/a
14	chr12:8015791-8015841	BE2_C	brain:	n/a
15	chr12:8012926-8012976	GM12892	blood:	n/a
16	chr12:8089207-8089257	A549	lung:	n/a
17	chr12:8015103-8015153	AG04450	lung:	fetal
18	chr12:8025567-8025617	A549	lung:	n/a
19	chr12:8088818-8088868	HEK293	kidney:	embryo
20	chr12:8025646-8025696	HCM	heart:	n/a
21	chr12:8025640-8025690	MCF-7	breast:	n/a
22	chr12:8088937-8088987	SAEC	small airway:	n/a
23	chr12:8015103-8015153	BE2_C	brain:	n/a
24	chr12:8022108-8022158	GM12878	blood:	n/a
25	chr12:8043600-8043650	HNPCEpiC	eye:	n/a
26	chr12:8068706-8068756	HAEpiC	amniotic membrane:	n/a
27	chr12:8015903-8015953	Jurkat	blood:	n/a
28	chr12:8089207-8089257	T-47D	breast:	n/a
29	chr12:8015103-8015153	LNCaP	prostate:	n/a
30	chr12:8088937-8088987	HMEC	breast:	n/a
31	chr12:8015103-8015153	SKMC	muscle:	n/a
32	chr12:8085898-8085948	PANC-1	pancreas:	n/a
33	chr12:8025593-8025643	SK-N-SH_RA	brain:	n/a
34	chr12:8025861-8025911	HEK293	kidney:	embryo
35	chr12:8043600-8043650	ProgFib	skin:	n/a
36	chr12:8012926-8012976	HRCEpiC	kidney:	n/a
37	chr12:8089207-8089257	GM12892	blood:	n/a
38	chr12:8025861-8025911	GM06990	blood:	n/a
39	chr12:8025394-8025444	Hepatocyte	liver:	n/a
40	chr12:8025567-8025617	HRCEpiC	kidney:	n/a
41	chr12:8090274-8090324	ProgFib	skin:	n/a
42	chr12:8023676-8023726	ProgFib	skin:	n/a
43	chr12:8023676-8023726	NHDF-neo	bronchial:	n/a
44	chr12:8025646-8025696	HNPCEpiC	eye:	n/a
45	chr12:8025593-8025643	HepG2	liver:	n/a
46	chr12:8089331-8089381	NB4	blood:	n/a
47	chr12:8025567-8025617	Hela-S3	cervix:	n/a
48	chr12:8025646-8025696	HEEpiC	esophagus:	n/a
49	chr12:8089207-8089257	Jurkat	blood:	n/a
50	chr12:8068600-8068650	LNCaP	prostate:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:8087187..8090473-chr12:8145986..8149446,6	K562	blood:
2	chr1:110527259..110528065-chr12:8112015..8112963,2	Hela-S3	cervix:
3	chr12:8078079..8079745-chr12:8081820..8084687,2	K562	blood:
4	chr12:8036991..8037615-chr12:8067883..8068385,2	MCF-7	breast:
5	chr12:8010803..8012757-chr12:8088381..8089897,2	K562	blood:
6	chr12:7985856..7986361-chr12:8086765..8087460,2	Hela-S3	cervix:
7	chr12:7868671..7869617-chr12:7959225..7960025,4	MCF-7	breast:
8	chr12:8088375..8088982-chr9:91933247..91933918,2	Hela-S3	cervix:
9	chr12:8012407..8013335-chr12:8085608..8086866,5	MCF-7	breast:
10	chr12:7869134..7869702-chr12:7959145..7959716,2	MCF-7	breast:
11	chr12:7830039..7830628-chr12:7959515..7960112,3	K562	blood:
12	chr12:8070443..8072854-chr12:8088308..8090486,2	K562	blood:
13	chr12:8084020..8086848-chr12:8141207..8142977,3	K562	blood:
14	chr12:8083967..8091170-chr12:8109520..8119614,46	K562	blood:
15	chr12:8059520..8061435-chr12:8069662..8071830,2	K562	blood:
16	chr12:8070261..8071764-chr12:8135788..8138437,2	K562	blood:
17	chr12:8037350..8037880-chr12:8072256..8073016,2	MCF-7	breast:
18	chr12:7829622..7830601-chr12:7959144..7960112,6	MCF-7	breast:
19	chr12:8078175..8078721-chr12:52540417..52541265,2	Hela-S3	cervix:
20	chr12:8078026..8081783-chr12:8085460..8087380,4	K562	blood:
21	chr12:8078059..8078559-chr9:128909058..128909559,2	Hela-S3	cervix:
22	chr12:8113497..8114011-chr15:83680023..83680548,2	Hela-S3	cervix:
23	chr12:8043777..8046059-chr12:8052507..8054935,2	K562	blood:
24	chr12:8078362..8080559-chr12:8146575..8149430,3	K562	blood:
25	chr12:8012297..8013140-chr12:8147611..8148236,3	K562	blood:
26	chr12:8085816..8086359-chr12:8113371..8113882,2	MCF-7	breast:
27	chr12:8088485..8089092-chr20:34542395..34543185,2	Hela-S3	cervix:
28	chr12:8059520..8061435-chr12:8069662..8071830,2	K562	blood:
29	chr12:8079295..8080034-chr3:52017052..52017578,2	Hela-S3	cervix:
30	chr12:8078355..8080764-chr12:8088312..8090126,3	K562	blood:
31	chr12:8104344..8105975-chr12:8113594..8115153,2	K562	blood:
32	chr12:8111834..8114370-chr12:8114927..8116487,2	K562	blood:
33	chr12:8086230..8090473-chr12:8145838..8149446,6	K562	blood:
34	chr12:8083967..8091864-chr12:8109862..8120659,42	K562	blood:
35	chr12:8085519..8086564-chr12:8147572..8148265,4	MCF-7	breast:
36	chr12:8079264..8080792-chr12:8088312..8090277,2	K562	blood:
37	chr12:8088047..8090687-chr12:8184432..8186364,2	K562	blood:
38	chr12:8088407..8089259-chr17:41465310..41465894,2	Hela-S3	cervix:
39	chr12:8083329..8085520-chr12:8141366..8142977,2	K562	blood:
40	chr12:8085591..8086340-chr12:8147548..8148474,2	K562	blood:
41	chr12:8104344..8105975-chr12:8113594..8115153,2	K562	blood:
42	chr12:7053329..7056206-chr12:8086714..8089278,2	K562	blood:
43	chr12:8086764..8088671-chr12:8089424..8092121,2	K562	blood:
44	chr12:8070443..8072854-chr12:8088308..8090486,2	K562	blood:
45	chr12:8083356..8086081-chr12:8183722..8185622,2	K562	blood:
46	chr12:8053022..8053940-chr12:8067825..8068746,2	MCF-7	breast:
47	chr12:8090828..8092674-chr12:8101690..8105270,3	K562	blood:
48	chr12:8111834..8114370-chr12:8114927..8116487,2	K562	blood:
49	chr12:8088424..8089028-chr2:220042726..220043324,2	Hela-S3	cervix:
50	chr12:8078026..8081783-chr12:8085460..8087380,4	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NANOGP1-2	chr12:8013033-8013360	NONHSAT026271
2	lnc-SLC2A14-2	chr12:8072262-8072346	NONHSAT026275
3	lnc-SLC2A14-2	chr12:8071827-8072124	NONHSAT026275
4	lnc-SLC2A3-2	chr12:8025403-8025460	NONHSAT026272
5	lnc-SLC2A3-2	chr12:8023775-8023879	NONHSAT026272
6	lnc-NANOGP1-1	chr12:8052070-8052674	NONHSAT026274
7	lnc-SLC2A3-2	chr12:8024469-8024544	NONHSAT026272
8	lnc-SLC2A14-1	chr12:8049210-8049554	NONHSAT026273
9	lnc-SLC2A3-2	chr12:8023446-8023658	NONHSAT026272

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC2A3	hsa-miR-195-5p	chr12:8073905-8073927
2	SLC2A3	hsa-miR-195-5p	chr12:8073911-8073904
3	SLC2A3	hsa-miR-148a-3p	chr12:8072526-8072548
4	SLC2A3	hsa-miR-24-3p	chr12:8072331-8072354
5	SLC2A3	hsa-miR-148a-3p	chr12:8072532-8072526

Variant related genes	Relation type
ENSG00000201663	TF binding region
SLC2A14	TF binding region
ENSG00000222978	TF binding region
ENSG00000255885	TF binding region
ENSG00000241828	TF binding region
SLC2A3	TF binding region
NANOGP1	TF binding region
ENSG00000255356	TF binding region
ENSG00000199912	TF binding region
ENSG00000201663	CpG island
SLC2A14	CpG island
ENSG00000222978	CpG island
ENSG00000255885	CpG island
ENSG00000241828	CpG island
SLC2A3	CpG island
NANOGP1	CpG island
ENSG00000255356	CpG island
ENSG00000199912	CpG island
ENSG00000136854	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000255885	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000065970	chromatin interactions
ENSG00000173660	chromatin interactions
ENSG00000059804	chromatin interactions
ENSG00000115649	chromatin interactions
ENSG00000155957	chromatin interactions
ENSG00000240739	chromatin interactions
ENSG00000111679	chromatin interactions
ENSG00000144567	chromatin interactions
ENSG00000173262	chromatin interactions
ENSG00000176654	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000169609	chromatin interactions
ENSG00000171222	chromatin interactions
ENSG00000168710	chromatin interactions
ENSG00000108294	chromatin interactions
ENSG00000181873	chromatin interactions
ENSG00000241828	chromatin interactions
ENSG00000136044	chromatin interactions
ENSG00000132128	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000100836	chromatin interactions
ENSG00000243989	chromatin interactions

Extended variants
information (count: 4939 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4939 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2110088	chr12:7954035-7954036	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs74058873	chr12:7954039-7954040	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs111636037	chr12:7954043-7954044	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs1990482	chr12:7954051-7954052	Strong transcription Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs187345477	chr12:7954170-7954171	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs386760034	chr12:7954220-7954221	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs192144629	chr12:7954222-7954223	Strong transcription Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs5796289	chr12:7954330-7954331	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34951409	chr12:7954357-7954358	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs1990481	chr12:7954360-7954361	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs183080964	chr12:7954376-7954377	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs5796290	chr12:7954459-7954460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs3040870	chr12:7954460-7954461	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566748517	chr12:7954461-7954462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139787435	chr12:7954462-7954463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375425920	chr12:7954472-7954473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115370398	chr12:7954561-7954562	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141544126	chr12:7954573-7954574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs150535582	chr12:7954574-7954575	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs200367118	chr12:7954584-7954585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188075560	chr12:7954649-7954650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2377096	chr12:7954679-7954680	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs142689106	chr12:7954707-7954708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200413369	chr12:7954714-7954715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs7488453	chr12:7954742-7954743	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs192579412	chr12:7954756-7954757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs139479400	chr12:7954852-7954853	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145270582	chr12:7954855-7954856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147220783	chr12:7954856-7954857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148661392	chr12:7954886-7954887	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs34951846	chr12:7954913-7954914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201701688	chr12:7954939-7954940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs142340849	chr12:7954942-7954943	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200327675	chr12:7954943-7954944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371558982	chr12:7955003-7955004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184252972	chr12:7955035-7955036	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2377095	chr12:7955052-7955053	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187967589	chr12:7955057-7955058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530665744	chr12:7955060-7955061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12580130	chr12:7955083-7955084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs5796293	chr12:7955095-7955096	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs397726774	chr12:7955106-7955107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs58529449	chr12:7955132-7955133	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs11055860	chr12:7955193-7955194	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs192502102	chr12:7955219-7955220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11055861	chr12:7955263-7955264	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs151270722	chr12:7955292-7955293	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546451351	chr12:7955296-7955297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185073162	chr12:7955316-7955317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs140481703	chr12:7955319-7955320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
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
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21364760	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
Medullary thyroid carcinoma	18765511	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Nasopharyngeal cancer	20548289	CNVD
Type 2 diabetes	21526130	CNVD
Autism	22495309	CNVD
Bipolar disorder	19214233	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Ependymoma	20639864	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3026 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7947400-7956800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr12:7950400-7960800	Weak transcription	Stomach Mucosa	stomach
3	chr12:7951000-7957600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:7951000-7959800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr12:7951200-7969200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr12:7951800-7957800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr12:7952400-7955600	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr12:7952400-7955800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr12:7953200-7954200	Weak transcription	HepG2	liver
10	chr12:7953200-7954800	Strong transcription	HUES6 Cell Line	embryonic stem cell
11	chr12:7953200-7957600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr12:7953200-7957600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:7953600-7987400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:7953800-7954200	Strong transcription	H1 Cell Line	embryonic stem cell
15	chr12:7954000-7954400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
16	chr12:7954000-7959200	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr12:7954000-7959800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
18	chr12:7954200-7954400	Enhancers	HepG2	liver
19	chr12:7954200-7957600	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr12:7954400-7957600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr12:7954800-7957600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr12:7955600-7957600	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr12:7955800-7956400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr12:7956400-7956600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
25	chr12:7956600-7958000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr12:7957600-7957800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr12:7957600-7957800	Enhancers	H1 Cell Line	embryonic stem cell
28	chr12:7957600-7957800	Enhancers	H9 Cell Line	embryonic stem cell
29	chr12:7957600-7957800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr12:7957600-7958000	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr12:7957600-7958000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr12:7957600-7958200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:7957600-7958400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr12:7957600-7958400	Enhancers	NH-A	brain
35	chr12:7957600-7959200	Enhancers	NHDF-Ad	bronchial
36	chr12:7957600-7959400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr12:7957600-7959600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr12:7957600-7959800	Enhancers	HMEC	breast
39	chr12:7957800-7958000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr12:7957800-7958200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr12:7957800-7958200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr12:7957800-7958200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr12:7957800-7958600	Enhancers	Osteobl	bone
44	chr12:7957800-7958800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:7957800-7958800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr12:7957800-7958800	Enhancers	NHEK	skin
47	chr12:7958000-7958200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr12:7958000-7958400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr12:7958000-7958600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr12:7958000-7958800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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