Variant report

Variant	nsv832501
Chromosome Location	chr12:103463927-103648825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:741)
CpG islands
(count:122)
Chromatin interactive
region (count:35)
LncRNA
region (count:89)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:103522800-103523221	HepG2	liver:	n/a	n/a
2	ATF2	chr12:103499612-103500283	GM12878	blood:	n/a	n/a
3	ATF2	chr12:103495843-103496583	GM12878	blood:	n/a	n/a
4	ATF2	chr12:103507916-103508908	GM12878	blood:	n/a	n/a
5	ATF2	chr12:103537893-103538455	GM12878	blood:	n/a	n/a
6	ATF2	chr12:103537944-103538377	GM12878	blood:	n/a	n/a
7	ATF2	chr12:103575036-103575649	GM12878	blood:	n/a	n/a
8	ATF2	chr12:103499623-103500289	GM12878	blood:	n/a	n/a
9	ATF2	chr12:103575056-103575875	GM12878	blood:	n/a	n/a
10	ATF2	chr12:103507953-103508895	GM12878	blood:	n/a	n/a
11	ATF2	chr12:103495880-103496682	GM12878	blood:	n/a	n/a
12	BATF	chr12:103575105-103575605	GM12878	blood:	n/a	n/a
13	BATF	chr12:103499643-103500177	GM12878	blood:	n/a	n/a
14	BATF	chr12:103499635-103500155	GM12878	blood:	n/a	n/a
15	BATF	chr12:103495947-103496461	GM12878	blood:	n/a	n/a
16	BATF	chr12:103479340-103479597	GM12878	blood:	n/a	n/a
17	BATF	chr12:103508505-103508788	GM12878	blood:	n/a	chr12:103508653-103508664 chr12:103508654-103508664
18	BATF	chr12:103508062-103508483	GM12878	blood:	n/a	n/a
19	BATF	chr12:103495976-103496398	GM12878	blood:	n/a	n/a
20	BATF	chr12:103575153-103575536	GM12878	blood:	n/a	n/a
21	BATF	chr12:103479315-103479636	GM12878	blood:	n/a	n/a
22	BATF	chr12:103572542-103572768	GM12878	blood:	n/a	n/a
23	BCL11A	chr12:103499791-103500146	GM12878	blood:	n/a	n/a
24	BCL11A	chr12:103495927-103496447	GM12878	blood:	n/a	n/a
25	BCL11A	chr12:103575155-103575814	GM12878	blood:	n/a	chr12:103575205-103575214
26	BCL11A	chr12:103538047-103538352	GM12878	blood:	n/a	n/a
27	BCL11A	chr12:103575242-103575455	GM12878	blood:	n/a	n/a
28	BCL11A	chr12:103496064-103496349	GM12878	blood:	n/a	n/a
29	BCL11A	chr12:103508132-103508462	GM12878	blood:	n/a	n/a
30	BCL11A	chr12:103508026-103508941	GM12878	blood:	n/a	chr12:103508657-103508666 chr12:103508656-103508665
31	BCL11A	chr12:103499589-103500230	GM12878	blood:	n/a	n/a
32	BCL11A	chr12:103479338-103479673	GM12878	blood:	n/a	n/a
33	BCL11A	chr12:103479380-103479633	GM12878	blood:	n/a	n/a
34	BCL3	chr12:103508049-103508785	GM12878	blood:	n/a	chr12:103508657-103508666 chr12:103508656-103508665
35	BCL3	chr12:103575150-103575600	GM12878	blood:	n/a	chr12:103575205-103575214
36	BCL3	chr12:103508092-103508535	GM12878	blood:	n/a	n/a
37	BCL3	chr12:103499661-103500138	GM12878	blood:	n/a	n/a
38	BCL3	chr12:103495993-103496521	GM12878	blood:	n/a	n/a
39	BCLAF1	chr12:103575076-103575710	GM12878	blood:	n/a	chr12:103575205-103575214
40	BCLAF1	chr12:103508021-103508800	GM12878	blood:	n/a	chr12:103508657-103508666 chr12:103508656-103508665
41	BCLAF1	chr12:103507971-103508884	GM12878	blood:	n/a	chr12:103508657-103508666 chr12:103508656-103508665
42	BCLAF1	chr12:103575064-103575597	GM12878	blood:	n/a	chr12:103575205-103575214
43	BCLAF1	chr12:103499620-103500213	GM12878	blood:	n/a	n/a
44	BHLHE40	chr12:103575141-103576094	GM12878	blood:	n/a	n/a
45	BHLHE40	chr12:103538664-103538676	GM12878	blood:	n/a	n/a
46	BHLHE40	chr12:103479307-103479639	GM12878	blood:	n/a	n/a
47	BHLHE40	chr12:103496018-103496847	GM12878	blood:	n/a	n/a
48	BHLHE40	chr12:103499541-103500210	GM12878	blood:	n/a	n/a
49	BRCA1	chr12:103503705-103503927	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr12:103560752-103561092	MCF-7	breast:	n/a	chr12:103560906-103560917 chr12:103560907-103560916 chr12:103560907-103560916 chr12:103560905-103560918 chr12:103560907-103560916 chr12:103560907-103560916

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:103486047-103486097	GM12891	blood:	n/a
2	chr12:103591917-103591967	MCF10A-Er-Src	breast:	n/a
3	chr12:103591917-103591967	IMR90	lung:	fetal
4	chr12:103591917-103591967	HIPEpiC	eye:	n/a
5	chr12:103591917-103591967	SK-N-SH	brain:	n/a
6	chr12:103591917-103591967	HEEpiC	esophagus:	n/a
7	chr12:103486047-103486097	HCF	heart:	n/a
8	chr12:103486047-103486097	HCPEpiC	choroid plexus:	n/a
9	chr12:103486047-103486097	HMEC	breast:	n/a
10	chr12:103591917-103591967	NHBE	bronchial:	n/a
11	chr12:103591917-103591967	ProgFib	skin:	n/a
12	chr12:103486047-103486097	AG10803	skin:	n/a
13	chr12:103591917-103591967	NB4	blood:	n/a
14	chr12:103486047-103486097	PANC-1	pancreas:	n/a
15	chr12:103486047-103486097	Caco-2	colon:	n/a
16	chr12:103591917-103591967	GM12891	blood:	n/a
17	chr12:103486047-103486097	MCF10A-Er-Src	breast:	n/a
18	chr12:103486047-103486097	ovcar-3	ovarian:	n/a
19	chr12:103486047-103486097	SKMC	muscle:	n/a
20	chr12:103591917-103591967	SKMC	muscle:	n/a
21	chr12:103591917-103591967	CMK	blood:	n/a
22	chr12:103486047-103486097	MCF-7	breast:	n/a
23	chr12:103591917-103591967	HL-60	blood:	n/a
24	chr12:103591917-103591967	HMEC	breast:	n/a
25	chr12:103591917-103591967	Caco-2	colon:	n/a
26	chr12:103591917-103591967	AG10803	skin:	n/a
27	chr12:103486047-103486097	NHDF-neo	bronchial:	n/a
28	chr12:103591917-103591967	HCPEpiC	choroid plexus:	n/a
29	chr12:103486047-103486097	SK-N-SH_RA	brain:	n/a
30	chr12:103591917-103591967	HRE	kidney:	n/a
31	chr12:103591917-103591967	SK-N-MC	brain:	n/a
32	chr12:103486047-103486097	AG09319	gingival:	n/a
33	chr12:103591917-103591967	AG09319	gingival:	n/a
34	chr12:103591917-103591967	HRPEpiC	eye:	n/a
35	chr12:103591917-103591967	MCF-7	breast:	n/a
36	chr12:103486047-103486097	BE2_C	brain:	n/a
37	chr12:103486047-103486097	PrEC	prostate:	n/a
38	chr12:103486047-103486097	SK-N-MC	brain:	n/a
39	chr12:103591917-103591967	GM06990	blood:	n/a
40	chr12:103486047-103486097	LNCaP	prostate:	n/a
41	chr12:103591917-103591967	T-47D	breast:	n/a
42	chr12:103486047-103486097	NHBE	bronchial:	n/a
43	chr12:103591917-103591967	AG09309	skin:	n/a
44	chr12:103486047-103486097	GM06990	blood:	n/a
45	chr12:103486047-103486097	HepG2	liver:	n/a
46	chr12:103486047-103486097	HAEpiC	amniotic membrane:	n/a
47	chr12:103486047-103486097	GM12892	blood:	n/a
48	chr12:103591917-103591967	ECC-1	luminal epithelium:	n/a
49	chr12:103486047-103486097	NH-A	brain:	n/a
50	chr12:103486047-103486097	HCT-116	colon:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:103342479..103343468-chr12:103569109..103570109,23	MCF-7	breast:
2	chr12:103636638..103639088-chr12:103888091..103889982,2	MCF-7	breast:
3	chr12:103496611..103498948-chr12:103501564..103503561,3	K562	blood:
4	chr12:103473983..103476392-chr12:103479910..103481574,2	MCF-7	breast:
5	chr12:103473983..103476392-chr12:103479910..103481574,2	MCF-7	breast:
6	chr10:97805584..97806458-chr12:103575603..103576420,2	MCF-7	breast:
7	chr12:103342479..103343468-chr12:103569109..103570014,11	MCF-7	breast:
8	chr12:103349887..103352220-chr12:103642036..103643565,2	MCF-7	breast:
9	chr12:103643339..103643876-chr12:103766841..103767542,2	MCF-7	breast:
10	chr12:103567206..103569823-chr12:103663759..103665929,2	MCF-7	breast:
11	chr12:103569111..103570024-chr12:103918043..103919091,5	MCF-7	breast:
12	chr12:103632067..103634446-chr12:103637268..103639130,2	MCF-7	breast:
13	chr12:103569173..103569956-chr12:103896987..103897845,3	MCF-7	breast:
14	chr12:103567485..103570052-chr12:103761974..103764560,2	MCF-7	breast:
15	chr12:103343154..103347521-chr12:103565562..103568893,4	MCF-7	breast:
16	chr12:103600594..103603379-chr12:103611609..103613668,2	MCF-7	breast:
17	chr12:103644168..103646590-chr12:103650807..103653487,2	K562	blood:
18	chr12:103477948..103479966-chr12:103483211..103485459,2	MCF-7	breast:
19	chr12:103477948..103479966-chr12:103483211..103485459,2	MCF-7	breast:
20	chr12:103600594..103603379-chr12:103611609..103613668,2	MCF-7	breast:
21	chr12:103496611..103498948-chr12:103501564..103503561,3	K562	blood:
22	chr12:103344308..103344865-chr12:103569473..103570033,2	MCF-7	breast:
23	chr12:103567572..103571382-chr12:103642751..103645285,4	MCF-7	breast:
24	chr12:103569245..103570050-chr12:103639690..103640508,2	MCF-7	breast:
25	chr12:103345130..103346737-chr12:103603490..103605464,2	MCF-7	breast:
26	chr12:103342538..103343552-chr12:103569117..103569983,3	MCF-7	breast:
27	chr12:103346974..103348798-chr12:103634414..103635996,2	MCF-7	breast:
28	chr12:103569149..103570117-chr12:103917984..103918759,8	MCF-7	breast:
29	chr12:103639814..103640778-chr12:103766634..103767396,2	MCF-7	breast:
30	chr12:103569111..103570024-chr12:103918043..103918908,7	MCF-7	breast:
31	chr12:103567572..103571382-chr12:103642751..103645285,4	MCF-7	breast:
32	chr12:103569035..103569938-chr12:103766846..103767430,3	MCF-7	breast:
33	chr12:103355593..103357176-chr12:103566399..103568963,2	MCF-7	breast:
34	chr12:103569245..103570050-chr12:103639690..103640508,2	MCF-7	breast:
35	chr12:103350008..103351674-chr12:103594791..103596374,2	MCF-7	breast:

(count:89 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-552I14.1.1-1	chr12:103561816-103561962	XLOC_009858
2	lnc-RP11-552I14.1.1-1	chr12:103553237-103553361	XLOC_009858
3	lnc-RP11-552I14.1.1-1	chr12:103549877-103549986	XLOC_009858
4	lnc-RP11-552I14.1.1-1	chr12:103555359-103555408	XLOC_009858
5	lnc-RP11-552I14.1.1-1	chr12:103571827-103571987	XLOC_009858
6	lnc-RP11-552I14.1.1-1	chr12:103553237-103553361	XLOC_009858
7	lnc-RP11-552I14.1.1-1	chr12:103556689-103556728	NONHSAT030362
8	lnc-RP11-552I14.1.1-1	chr12:103555359-103555408	XLOC_009858
9	lnc-RP11-552I14.1.1-1	chr12:103545604-103545696	XLOC_009858
10	lnc-RP11-552I14.1.1-1	chr12:103571827-103571987	XLOC_009858
11	lnc-RP11-552I14.1.1-1	chr12:103549877-103549986	NONHSAT030355
12	lnc-RP11-552I14.1.1-1	chr12:103549877-103549986	XLOC_009858
13	lnc-C12orf42-1	chr12:103513592-103513788	XLOC_010177
14	lnc-RP11-552I14.1.1-1	chr12:103553237-103553361	XLOC_009858
15	lnc-RP11-552I14.1.1-1	chr12:103561816-103562108	XLOC_009858
16	lnc-RP11-552I14.1.1-1	chr12:103545604-103545696	XLOC_009858
17	lnc-RP11-552I14.1.1-1	chr12:103549877-103549986	XLOC_009858
18	lnc-RP11-552I14.1.1-1	chr12:103549006-103549047	XLOC_009858
19	lnc-RP11-552I14.1.1-1	chr12:103549877-103549986	XLOC_009858
20	lnc-RP11-552I14.1.1-1	chr12:103545621-103545696	XLOC_009858
21	lnc-RP11-552I14.1.1-1	chr12:103548925-103549047	NONHSAT030355
22	lnc-RP11-552I14.1.1-1	chr12:103553237-103553361	XLOC_009858
23	lnc-C12orf42-2	chr12:103572357-103572453	ENSG00000257703.1
24	lnc-RP11-552I14.1.1-1	chr12:103558178-103558215	NONHSAT140090
25	lnc-RP11-552I14.1.1-1	chr12:103549877-103549986	XLOC_009858
26	lnc-RP11-552I14.1.1-1	chr12:103555359-103555408	XLOC_009858
27	lnc-RP11-552I14.1.1-1	chr12:103556634-103556728	NONHSAT140090
28	lnc-RP11-552I14.1.1-1	chr12:103549877-103549986	XLOC_009858
29	lnc-RP11-552I14.1.1-1	chr12:103548775-103549047	NONHSAT030350
30	lnc-RP11-552I14.1.1-1	chr12:103556494-103556728	XLOC_009858
31	lnc-RP11-552I14.1.1-1	chr12:103561816-103561962	XLOC_009858
32	lnc-RP11-552I14.1.1-1	chr12:103553237-103553361	XLOC_009858
33	lnc-RP11-552I14.1.1-1	chr12:103561816-103562087	NONHSAT030362
34	lnc-RP11-552I14.1.1-1	chr12:103556494-103556728	XLOC_009858
35	lnc-RP11-552I14.1.1-1	chr12:103545603-103545696	NONHSAT030350
36	lnc-RP11-552I14.1.1-1	chr12:103571826-103571987	NONHSAT030350
37	lnc-RP11-552I14.1.1-1	chr12:103555358-103555408	NONHSAT030350
38	lnc-RP11-552I14.1.1-1	chr12:103545633-103545696	NONHSAT030355
39	lnc-RP11-552I14.1.1-1	chr12:103549006-103549047	XLOC_009858
40	lnc-RP11-552I14.1.1-1	chr12:103556494-103556728	XLOC_009858
41	lnc-RP11-552I14.1.1-1	chr12:103561816-103562087	NONHSAT140090
42	lnc-RP11-552I14.1.1-1	chr12:103549006-103549047	XLOC_009858
43	lnc-RP11-552I14.1.1-1	chr12:103556493-103556728	NONHSAT030350
44	lnc-RP11-552I14.1.1-1	chr12:103557340-103557394	XLOC_009858
45	lnc-RP11-552I14.1.1-1	chr12:103561815-103562108	NONHSAT030350
46	lnc-RP11-552I14.1.1-1	chr12:103558178-103558215	XLOC_009858
47	lnc-RP11-552I14.1.1-1	chr12:103548776-103549047	XLOC_009858
48	lnc-RP11-552I14.1.1-1	chr12:103556494-103556728	XLOC_009858
49	lnc-RP11-552I14.1.1-1	chr12:103549006-103549047	XLOC_009858
50	lnc-RP11-552I14.1.1-1	chr12:103556494-103556728	XLOC_009858

No data

Variant related genes	Relation type
ENSG00000238909	TF binding region
ENSG00000257703	TF binding region
ENSG00000257860	TF binding region
RNU7-184P	TF binding region
ENSG00000238909	CpG island
ENSG00000257703	CpG island
ENSG00000257860	CpG island
RNU7-184P	CpG island
ENSG00000257415	chromatin interactions
ENSG00000139352	chromatin interactions
ENSG00000171759	chromatin interactions
ENSG00000179088	chromatin interactions
ENSG00000238909	chromatin interactions
MTMR4	miRNA target sites
MTMR6	miRNA target sites
FAM57A	miRNA target sites
FAM49B	miRNA target sites
E2F6	miRNA target sites
FAM59A	miRNA target sites
MTMR9	miRNA target sites
RAVER1	miRNA target sites
EIF3A	miRNA target sites
CBR4	miRNA target sites
ZEB1	miRNA target sites
FAM46A	miRNA target sites
ZEB2	miRNA target sites
RAVER2	miRNA target sites
RB1	miRNA target sites
CAB39	miRNA target sites

Extended variants
information (count: 4042 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4042 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79680413	chr12:103469236-103469237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs114533910	chr12:103469252-103469253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189092666	chr12:103469266-103469267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551448130	chr12:103469270-103469271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17033418	chr12:103469295-103469296	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs73179703	chr12:103469296-103469297	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs551312022	chr12:103469322-103469323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs4764934	chr12:103469376-103469377	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs139916399	chr12:103469482-103469483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546709927	chr12:103469488-103469489	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566847156	chr12:103469564-103469565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538800929	chr12:103469585-103469586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558582731	chr12:103469611-103469612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577427219	chr12:103469612-103469613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536819549	chr12:103469632-103469633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78218173	chr12:103469701-103469702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs181436353	chr12:103469729-103469730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs542891657	chr12:103469781-103469782	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184146395	chr12:103469845-103469846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572751525	chr12:103469846-103469847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs189112689	chr12:103469854-103469855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143375684	chr12:103469873-103469874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs115389238	chr12:103469874-103469875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181447514	chr12:103469914-103469915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186508508	chr12:103469920-103469921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs377706467	chr12:103469945-103469946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557831265	chr12:103469946-103469947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530365037	chr12:103469961-103469962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145594745	chr12:103469982-103469983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192436627	chr12:103470029-103470030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371273474	chr12:103470061-103470062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs538608416	chr12:103470068-103470069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553317793	chr12:103470081-103470082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs527642033	chr12:103470107-103470108	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148909505	chr12:103470154-103470155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182002317	chr12:103470179-103470180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77186703	chr12:103470184-103470185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs73179704	chr12:103470191-103470192	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561430420	chr12:103470206-103470207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs556772336	chr12:103470218-103470219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143618937	chr12:103470222-103470223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555126844	chr12:103470224-103470225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs73183634	chr12:103470245-103470246	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs529129563	chr12:103470323-103470324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141588705	chr12:103470325-103470326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs186273227	chr12:103470331-103470332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541334812	chr12:103470345-103470346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76372057	chr12:103470392-103470393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182548114	chr12:103470433-103470434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs34749360	chr12:103470532-103470533	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	22032731	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
lymphocytic leukemia	21291569	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Neurocytoma	17123091	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103469200-103471800	Enhancers	Liver	Liver
2	chr12:103478600-103479800	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr12:103479000-103479800	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr12:103479200-103479600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr12:103479200-103479800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr12:103479200-103480000	Enhancers	Brain Germinal Matrix	brain
7	chr12:103479400-103479800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr12:103479600-103480000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr12:103479600-103484600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr12:103479800-103484000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr12:103479800-103484800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr12:103479800-103484800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr12:103480000-103480400	Weak transcription	Brain Germinal Matrix	brain
14	chr12:103480200-103480600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr12:103480400-103480600	Enhancers	Brain Germinal Matrix	brain
16	chr12:103480600-103483600	Weak transcription	Brain Germinal Matrix	brain
17	chr12:103480800-103481200	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr12:103483600-103486800	Enhancers	Brain Germinal Matrix	brain
19	chr12:103484000-103486200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr12:103484400-103485200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr12:103484600-103486600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr12:103484800-103485800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr12:103484800-103486200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr12:103484800-103486400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr12:103484800-103487400	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr12:103485000-103487200	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr12:103485800-103486400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr12:103485800-103486600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr12:103485800-103487400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr12:103486000-103486400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:103486000-103487200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr12:103486000-103487400	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr12:103486400-103487200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr12:103486400-103487400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr12:103486600-103488000	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr12:103486600-103489400	Enhancers	Fetal Intestine Large	intestine
37	chr12:103486600-103489400	Enhancers	Fetal Intestine Small	intestine
38	chr12:103486800-103487200	Enhancers	Duodenum Mucosa	Duodenum
39	chr12:103486800-103487400	Enhancers	Liver	Liver
40	chr12:103486800-103488600	Enhancers	Stomach Mucosa	stomach
41	chr12:103487000-103487200	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr12:103487000-103487600	Enhancers	Small Intestine	intestine
43	chr12:103487200-103487400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr12:103487200-103487600	Flanking Active TSS	Duodenum Mucosa	Duodenum
45	chr12:103487200-103488000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
46	chr12:103487400-103487600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr12:103487400-103487800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr12:103487400-103487800	Flanking Active TSS	Liver	Liver
49	chr12:103487400-103488000	Active TSS	Colonic Mucosa	Colon
50	chr12:103487400-103488000	Enhancers	HepG2	liver

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