Variant report

Variant	nsv468995
Chromosome Location	chr12:7961576-8123306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4163)
CpG islands
(count:1956)
Chromatin interactive
region (count:88)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:4163 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:8090642-8091063	HepG2	liver:	n/a	n/a
2	ARID3A	chr12:8123121-8123440	K562	blood:	n/a	n/a
3	ARID3A	chr12:8113289-8113981	K562	blood:	n/a	n/a
4	ARID3A	chr12:8059700-8060067	K562	blood:	n/a	n/a
5	ARID3A	chr12:8085795-8086124	K562	blood:	n/a	n/a
6	ARID3A	chr12:8043247-8043927	HepG2	liver:	n/a	n/a
7	ARID3A	chr12:7984728-7985022	K562	blood:	n/a	n/a
8	ARID3A	chr12:8111282-8111525	K562	blood:	n/a	n/a
9	ARID3A	chr12:8115662-8116416	K562	blood:	n/a	n/a
10	ARID3A	chr12:8088187-8089350	K562	blood:	n/a	n/a
11	ARID3A	chr12:8085786-8086136	HepG2	liver:	n/a	n/a
12	ARID3A	chr12:8003917-8004749	HepG2	liver:	n/a	n/a
13	ARID3A	chr12:8057729-8058351	HepG2	liver:	n/a	n/a
14	ARID3A	chr12:8113305-8113722	HepG2	liver:	n/a	n/a
15	ARID3A	chr12:8088653-8089277	HepG2	liver:	n/a	n/a
16	ARID3A	chr12:8059547-8060068	HepG2	liver:	n/a	n/a
17	ARID3A	chr12:7984707-7984990	HepG2	liver:	n/a	n/a
18	ARID3A	chr12:8090479-8091378	K562	blood:	n/a	n/a
19	ATF1	chr12:8113284-8113661	K562	blood:	n/a	chr12:8113469-8113483
20	ATF1	chr12:8115657-8116051	K562	blood:	n/a	n/a
21	ATF1	chr12:8123138-8123571	K562	blood:	n/a	n/a
22	ATF1	chr12:8043615-8043923	K562	blood:	n/a	n/a
23	ATF1	chr12:8021845-8022067	K562	blood:	n/a	n/a
24	ATF1	chr12:8059740-8060026	K562	blood:	n/a	n/a
25	ATF1	chr12:7996816-7996880	K562	blood:	n/a	n/a
26	ATF1	chr12:8111308-8111508	K562	blood:	n/a	n/a
27	ATF1	chr12:8085836-8086220	K562	blood:	n/a	n/a
28	ATF1	chr12:8017264-8017507	K562	blood:	n/a	n/a
29	ATF1	chr12:8090846-8091129	K562	blood:	n/a	n/a
30	ATF2	chr12:8042996-8043524	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr12:8058108-8058451	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr12:8058648-8058932	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF2	chr12:8012535-8013325	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr12:8059068-8059314	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr12:8113135-8113746	GM12878	blood:	n/a	chr12:8113469-8113483
36	ATF2	chr12:8058161-8058458	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr12:8088400-8088859	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr12:8113268-8113696	GM12878	blood:	n/a	chr12:8113469-8113483
39	ATF2	chr12:8085669-8086239	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr12:8012580-8013428	H1-hESC	embryonic stem cell:	n/a	n/a
41	ATF2	chr12:8123061-8123858	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr12:8059682-8059979	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr12:8113247-8113725	H1-hESC	embryonic stem cell:	n/a	chr12:8113469-8113483
44	ATF2	chr12:8085753-8086276	GM12878	blood:	n/a	n/a
45	ATF3	chr12:8059696-8059961	K562	blood:	n/a	n/a
46	ATF3	chr12:8111301-8111571	K562	blood:	n/a	n/a
47	ATF3	chr12:8043693-8043923	K562	blood:	n/a	n/a
48	ATF3	chr12:8123044-8123595	A549	lung:	n/a	n/a
49	ATF3	chr12:8123054-8123695	A549	lung:	n/a	n/a
50	ATF3	chr12:8113305-8113574	K562	blood:	n/a	n/a

(count:1956 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:8088931-8088981	HCF	heart:	n/a
2	chr12:8085898-8085948	AG04450	lung:	fetal
3	chr12:8088741-8088791	HUVEC	blood vessel:	n/a
4	chr12:8025640-8025690	PFSK-1	brain:	n/a
5	chr12:8088931-8088981	HCF	heart:	n/a
6	chr12:8085898-8085948	AG04450	lung:	fetal
7	chr12:8088741-8088791	HUVEC	blood vessel:	n/a
8	chr12:8025640-8025690	PFSK-1	brain:	n/a
9	chr12:8023676-8023726	AoSMC	blood vessel:	n/a
10	chr12:8085898-8085948	SAEC	small airway:	n/a
11	chr12:8068627-8068677	AG10803	skin:	n/a
12	chr12:8015103-8015153	HEK293	kidney:	embryo
13	chr12:8025567-8025617	MCF10A-Er-Src	breast:	n/a
14	chr12:8025567-8025617	A549	lung:	n/a
15	chr12:8089331-8089381	BE2_C	brain:	n/a
16	chr12:8068627-8068677	HAEpiC	amniotic membrane:	n/a
17	chr12:8025567-8025617	BJ	skin:	n/a
18	chr12:8068706-8068756	SK-N-SH	brain:	n/a
19	chr12:8025861-8025911	HCPEpiC	choroid plexus:	n/a
20	chr12:8025582-8025632	ProgFib	skin:	n/a
21	chr12:8068627-8068677	HNPCEpiC	eye:	n/a
22	chr12:8043600-8043650	SK-N-SH	brain:	n/a
23	chr12:8025517-8025567	Hepatocyte	liver:	n/a
24	chr12:8043600-8043650	AG09319	gingival:	n/a
25	chr12:8025646-8025696	NHBE	bronchial:	n/a
26	chr12:8026515-8026565	HRCEpiC	kidney:	n/a
27	chr12:8089331-8089381	K562	blood:	n/a
28	chr12:8022108-8022158	ProgFib	skin:	n/a
29	chr12:8022108-8022158	T-47D	breast:	n/a
30	chr12:7966784-7966834	AG09319	gingival:	n/a
31	chr12:8025517-8025567	BE2_C	brain:	n/a
32	chr12:8022108-8022158	ovcar-3	ovarian:	n/a
33	chr12:8089207-8089257	HRCEpiC	kidney:	n/a
34	chr12:8121010-8121060	SK-N-SH	brain:	n/a
35	chr12:8068627-8068677	NB4	blood:	n/a
36	chr12:8122787-8122837	HCT-116	colon:	n/a
37	chr12:8121010-8121060	NB4	blood:	n/a
38	chr12:8088818-8088868	HNPCEpiC	eye:	n/a
39	chr12:8068706-8068756	GM12878	blood:	n/a
40	chr12:8025861-8025911	HRPEpiC	eye:	n/a
41	chr12:8090274-8090324	Jurkat	blood:	n/a
42	chr12:8023676-8023726	K562	blood:	n/a
43	chr12:8025861-8025911	HCT-116	colon:	n/a
44	chr12:8089207-8089257	Jurkat	blood:	n/a
45	chr12:8068627-8068677	ProgFib	skin:	n/a
46	chr12:8088931-8088981	SAEC	small airway:	n/a
47	chr12:8085898-8085948	RPTEC	kidney:	n/a
48	chr12:8068706-8068756	PANC-1	pancreas:	n/a
49	chr12:8122787-8122837	BE2_C	brain:	n/a
50	chr12:8023676-8023726	IMR90	lung:	fetal

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:7985856..7986361-chr12:8086765..8087460,2	Hela-S3	cervix:
2	chr12:8113559..8117732-chr12:8120758..8122349,3	K562	blood:
3	chr12:8070443..8072854-chr12:8088308..8090486,2	K562	blood:
4	chr12:8121881..8123482-chr12:8179287..8181428,2	MCF-7	breast:
5	chr12:8043777..8046059-chr12:8052507..8054935,2	K562	blood:
6	chr12:8037350..8037880-chr12:8072256..8073016,2	MCF-7	breast:
7	chr12:8078079..8079745-chr12:8081820..8084687,2	K562	blood:
8	chr12:8078026..8081783-chr12:8085460..8087380,4	K562	blood:
9	chr12:8083581..8086103-chr12:8144653..8146389,2	K562	blood:
10	chr12:8123158..8123849-chr9:123605368..123605903,2	Hela-S3	cervix:
11	chr12:8081132..8084096-chr12:8120749..8123406,2	K562	blood:
12	chr12:8088282..8089244-chr14:23790396..23791050,2	Hela-S3	cervix:
13	chr12:8012482..8013075-chr12:8147622..8148284,2	MCF-7	breast:
14	chr12:8086230..8090473-chr12:8145838..8149446,6	K562	blood:
15	chr12:8070261..8071764-chr12:8135788..8138437,2	K562	blood:
16	chr12:8104344..8105975-chr12:8113594..8115153,2	K562	blood:
17	chr12:8078059..8078559-chr9:128909058..128909559,2	Hela-S3	cervix:
18	chr12:8087187..8090473-chr12:8145986..8149446,6	K562	blood:
19	chr12:8059520..8061435-chr12:8069662..8071830,2	K562	blood:
20	chr12:8088695..8090780-chr12:8106535..8108288,2	K562	blood:
21	chr12:8122799..8123468-chr2:114514128..114514983,2	Hela-S3	cervix:
22	chr12:8088424..8089028-chr2:220042726..220043324,2	Hela-S3	cervix:
23	chr12:8122338..8125451-chr12:8144270..8148107,3	MCF-7	breast:
24	chr12:8088360..8089072-chr12:105629548..105630374,2	Hela-S3	cervix:
25	chr12:8119439..8121044-chr12:8122365..8125023,2	MCF-7	breast:
26	chr12:8110467..8113364-chr12:8121918..8123445,2	K562	blood:
27	chr12:8012297..8013140-chr12:8147611..8148236,3	K562	blood:
28	chr12:8086985..8090687-chr12:8184864..8188373,3	K562	blood:
29	chr12:8086764..8088671-chr12:8089424..8092121,2	K562	blood:
30	chr12:7053329..7056206-chr12:8086714..8089278,2	K562	blood:
31	chr12:8053022..8053940-chr12:8067825..8068746,2	MCF-7	breast:
32	chr12:8072655..8075503-chr12:8080387..8083295,2	K562	blood:
33	chr12:8085519..8086564-chr12:8147572..8148265,4	MCF-7	breast:
34	chr12:8121840..8124690-chr12:8146278..8148330,2	MCF-7	breast:
35	chr12:8070443..8072854-chr12:8088308..8090486,2	K562	blood:
36	chr12:8083329..8085520-chr12:8141366..8142977,2	K562	blood:
37	chr12:8086764..8088671-chr12:8089424..8092121,2	K562	blood:
38	chr12:8123186..8125071-chr12:8144664..8146577,2	K562	blood:
39	chr12:8012407..8013335-chr12:8085608..8086866,5	MCF-7	breast:
40	chr12:8104344..8105975-chr12:8113594..8115153,2	K562	blood:
41	chr12:8078175..8078721-chr12:52540417..52541265,2	Hela-S3	cervix:
42	chr12:8085591..8086340-chr12:8147548..8148474,2	K562	blood:
43	chr12:8088047..8090687-chr12:8184432..8186364,2	K562	blood:
44	chr12:8088485..8089092-chr20:34542395..34543185,2	Hela-S3	cervix:
45	chr12:8010803..8012757-chr12:8088381..8089897,2	K562	blood:
46	chr12:8083967..8091170-chr12:8109520..8119614,46	K562	blood:
47	chr12:8113559..8117732-chr12:8120758..8122349,3	K562	blood:
48	chr12:8119439..8121044-chr12:8122365..8125023,2	MCF-7	breast:
49	chr12:8090828..8092674-chr12:8101690..8105270,3	K562	blood:
50	chr12:8120815..8122769-chr12:8135785..8138000,2	K562	blood:

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

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

No data

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

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

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
ENSG00000201663	CpG island
SLC2A14	CpG island
ENSG00000222978	CpG island
ENSG00000255885	CpG island
ENSG00000241828	CpG island
SLC2A3	CpG island
NANOGP1	CpG island
ENSG00000255356	CpG island
ENSG00000115084	chromatin interactions
ENSG00000115649	chromatin interactions
ENSG00000132128	chromatin interactions
ENSG00000226752	chromatin interactions
ENSG00000111679	chromatin interactions
ENSG00000171222	chromatin interactions
ENSG00000187742	chromatin interactions
ENSG00000114779	chromatin interactions
ENSG00000065970	chromatin interactions
ENSG00000059804	chromatin interactions
ENSG00000272173	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000144567	chromatin interactions
ENSG00000168710	chromatin interactions
ENSG00000173262	chromatin interactions
ENSG00000108294	chromatin interactions
ENSG00000137203	chromatin interactions
ENSG00000155957	chromatin interactions
ENSG00000240739	chromatin interactions
ENSG00000176654	chromatin interactions
ENSG00000169609	chromatin interactions
ENSG00000136044	chromatin interactions
ENSG00000243989	chromatin interactions
ENSG00000241828	chromatin interactions
ENSG00000173660	chromatin interactions
ENSG00000181873	chromatin interactions
ENSG00000255885	chromatin interactions
ENSG00000100836	chromatin interactions
ENSG00000136854	chromatin interactions

Extended variants
information (count: 4842 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:4842 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7312589	chr12:7961576-7961577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371891843	chr12:7961594-7961595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs57404073	chr12:7961611-7961612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573163062	chr12:7961648-7961649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550129805	chr12:7961651-7961652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9738765	chr12:7961657-7961658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541204422	chr12:7961711-7961712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138169004	chr12:7961732-7961733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs58357422	chr12:7961733-7961734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs11055909	chr12:7961756-7961757	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs35263181	chr12:7961763-7961764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140332504	chr12:7961783-7961784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186736590	chr12:7961807-7961808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555701638	chr12:7961844-7961845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs549222408	chr12:7961877-7961878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192038486	chr12:7961888-7961889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs182804579	chr12:7961889-7961890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs111344785	chr12:7961892-7961893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371657617	chr12:7961914-7961915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534884116	chr12:7962029-7962030	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557968717	chr12:7962037-7962038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575363160	chr12:7962044-7962045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187181477	chr12:7962069-7962070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189736755	chr12:7962084-7962085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544099627	chr12:7962117-7962118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182346393	chr12:7962131-7962132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186904836	chr12:7962137-7962138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10845950	chr12:7962167-7962168	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs532534726	chr12:7962173-7962174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10845951	chr12:7962186-7962187	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs10845952	chr12:7962208-7962209	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs10845953	chr12:7962230-7962231	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs548431815	chr12:7962245-7962246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs116009377	chr12:7962283-7962284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116758679	chr12:7962302-7962303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535445975	chr12:7962305-7962306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71038769	chr12:7962322-7962323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs114801501	chr12:7962366-7962367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs145990038	chr12:7962402-7962403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10845956	chr12:7962446-7962447	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs71038770	chr12:7962489-7962490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141443346	chr12:7962597-7962598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193093966	chr12:7962708-7962709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184217142	chr12:7962714-7962715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76437302	chr12:7962784-7962785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188216714	chr12:7962855-7962856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs35943098	chr12:7962987-7962988	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546613571	chr12:7963021-7963022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12370306	chr12:7963052-7963053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543520864	chr12:7963132-7963133	Weak 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:3241 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:7951200-7969200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr12:7953600-7987400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:7958200-7963400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:7958400-7978800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr12:7959600-7964400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr12:7959800-7964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr12:7960000-7964200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr12:7963400-7963600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr12:7963600-7964000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:7964200-7964600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr12:7964200-7965000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:7964200-7965400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:7964400-7964800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr12:7964400-7965000	Enhancers	Primary hematopoietic stem cells	blood
15	chr12:7964400-7965400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr12:7964800-7965400	Enhancers	Placenta	Placenta
17	chr12:7965000-7973200	Weak transcription	Ovary	ovary
18	chr12:7965200-7965400	Enhancers	HepG2	liver
19	chr12:7965400-7984800	Weak transcription	HepG2	liver
20	chr12:7969200-7972000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr12:7972000-7973000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr12:7972200-7978400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:7973000-7974000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
24	chr12:7974000-7976000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr12:7976000-7983200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr12:7977400-7979800	Enhancers	Placenta	Placenta
27	chr12:7977800-7978200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:7978200-7978600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:7978200-7979400	Enhancers	HMEC	breast
30	chr12:7978200-7979400	Enhancers	NHEK	skin
31	chr12:7978400-7978600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr12:7978400-7978800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr12:7978400-7979400	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr12:7978600-7979400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:7978600-7979600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr12:7978800-7979200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr12:7978800-7979200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr12:7978800-7979200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr12:7978800-7979400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr12:7978800-7979400	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr12:7978800-7979400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr12:7978800-7979400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr12:7979000-7979200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr12:7979000-7979400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr12:7979000-7979600	Enhancers	Placenta Amnion	Placenta Amnion
46	chr12:7979400-7979800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:7979400-7979800	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
48	chr12:7979600-7986600	Weak transcription	Placenta Amnion	Placenta Amnion
49	chr12:7979800-7985200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr12:7983200-7986600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland

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