Variant report

Variant	nsv10284
Chromosome Location	chr1:76079955-76082780
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:376)
CpG islands
(count:855)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:376 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76082080-76082152	HepG2	liver:	n/a	n/a
2	ATF1	chr1:76082531-76082931	K562	blood:	n/a	n/a
3	ATF1	chr1:76080039-76080344	K562	blood:	n/a	n/a
4	BACH1	chr1:76080097-76080757	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr1:76082259-76082774	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr1:76082516-76082778	K562	blood:	n/a	n/a
7	CCNT2	chr1:76081434-76081868	K562	blood:	n/a	n/a
8	CEBPB	chr1:76080265-76080779	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:76080295-76080590	HepG2	liver:	n/a	n/a
10	CHD1	chr1:76080578-76080604	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD1	chr1:76081541-76081550	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr1:76080646-76080799	K562	blood:	n/a	n/a
13	CHD2	chr1:76080382-76080944	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr1:76080347-76082590	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr1:76080820-76080970	NHLF	lung:	n/a	n/a
16	CTCF	chr1:76080660-76080810	A549	lung:	n/a	n/a
17	CTCF	chr1:76080500-76080650	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr1:76080445-76080689	GM19238	blood:	n/a	n/a
19	CTCF	chr1:76080680-76080830	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr1:76081260-76081410	GM12873	blood:	n/a	n/a
21	CTCF	chr1:76081860-76082010	HepG2	liver:	n/a	n/a
22	CTCF	chr1:76080350-76080839	MCF-7	breast:	n/a	n/a
23	CTCF	chr1:76080499-76080644	GM12892	blood:	n/a	n/a
24	CTCF	chr1:76080300-76080450	A549	lung:	n/a	n/a
25	CTCF	chr1:76081780-76081930	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr1:76080180-76080330	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr1:76080408-76080765	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:76080433-76080721	IMR90	lung:	n/a	n/a
29	CTCF	chr1:76080500-76080650	K562	blood:	n/a	n/a
30	CTCF	chr1:76080456-76080696	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:76080480-76080630	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr1:76080520-76080670	RPTEC	kidney:	n/a	n/a
33	CTCF	chr1:76079517-76082489	SK-N-SH	brain:	n/a	chr1:76082042-76082055
34	CTCF	chr1:76080860-76081010	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr1:76080480-76080630	AG04450	lung:	n/a	n/a
36	CTCF	chr1:76080920-76081070	HAc	cerebellar:	n/a	n/a
37	CTCF	chr1:76080460-76080653	GM10266	blood:	n/a	n/a
38	CTCF	chr1:76080498-76080632	GM19239	blood:	n/a	n/a
39	CTCF	chr1:76080445-76080656	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr1:76081300-76081450	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr1:76080500-76080650	BJ	skin:	n/a	n/a
42	CTCF	chr1:76080420-76080570	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr1:76080471-76080646	GM13977	blood:	n/a	n/a
44	CTCF	chr1:76081760-76081910	HepG2	liver:	n/a	n/a
45	CTCF	chr1:76080500-76080650	AoAF	blood vessel:	n/a	n/a
46	CTCF	chr1:76080480-76080630	RPTEC	kidney:	n/a	n/a
47	CTCF	chr1:76080321-76080675	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr1:76080540-76080690	GM12878	blood:	n/a	n/a
49	CTCF	chr1:76080447-76080681	A549	lung:	n/a	n/a
50	CTCF	chr1:76080500-76080650	GM12871	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76081408-76081458	HMEC	breast:	n/a
2	chr1:76081408-76081458	HMEC	breast:	n/a
3	chr1:76080924-76080974	HUVEC	blood vessel:	n/a
4	chr1:76082066-76082116	HRE	kidney:	n/a
5	chr1:76081962-76082012	Hepatocyte	liver:	n/a
6	chr1:76081408-76081458	GM19239	blood:	n/a
7	chr1:76082173-76082223	HCM	heart:	n/a
8	chr1:76081408-76081458	Jurkat	blood:	n/a
9	chr1:76081272-76081322	ECC-1	luminal epithelium:	n/a
10	chr1:76081272-76081322	NT2-D1	testis:	n/a
11	chr1:76081408-76081458	HNPCEpiC	eye:	n/a
12	chr1:76080684-76080734	Caco-2	colon:	n/a
13	chr1:76081408-76081458	BJ	skin:	n/a
14	chr1:76080410-76080460	NHDF-neo	bronchial:	n/a
15	chr1:76080684-76080734	HPAEpiC	pulmonary alveolar:	n/a
16	chr1:76081272-76081322	GM12878	blood:	n/a
17	chr1:76081962-76082012	BJ	skin:	n/a
18	chr1:76080727-76080777	SK-N-MC	brain:	n/a
19	chr1:76080727-76080777	HCT-116	colon:	n/a
20	chr1:76082066-76082116	GM19239	blood:	n/a
21	chr1:76081272-76081322	HCM	heart:	n/a
22	chr1:76080410-76080460	GM12878	blood:	n/a
23	chr1:76082173-76082223	Hela-S3	cervix:	n/a
24	chr1:76080924-76080974	NB4	blood:	n/a
25	chr1:76080727-76080777	HCPEpiC	choroid plexus:	n/a
26	chr1:76081408-76081458	MCF10A-Er-Src	breast:	n/a
27	chr1:76080727-76080777	RPTEC	kidney:	n/a
28	chr1:76081272-76081322	AG04450	lung:	fetal
29	chr1:76081408-76081458	HRPEpiC	eye:	n/a
30	chr1:76081379-76081429	SK-N-SH	brain:	n/a
31	chr1:76081962-76082012	HIPEpiC	eye:	n/a
32	chr1:76081962-76082012	AG04449	skin:	fetal
33	chr1:76081272-76081322	K562	blood:	n/a
34	chr1:76082173-76082223	HL-60	blood:	n/a
35	chr1:76081962-76082012	SAEC	small airway:	n/a
36	chr1:76081408-76081458	H1-hESC	embryonic stem cell:	embryo
37	chr1:76080684-76080734	HCT-116	colon:	n/a
38	chr1:76082173-76082223	ProgFib	skin:	n/a
39	chr1:76082690-76082740	MCF-7	breast:	n/a
40	chr1:76081272-76081322	SAEC	small airway:	n/a
41	chr1:76081408-76081458	K562	blood:	n/a
42	chr1:76082568-76082618	SK-N-SH	brain:	n/a
43	chr1:76080684-76080734	HAEpiC	amniotic membrane:	n/a
44	chr1:76082690-76082740	MCF10A-Er-Src	breast:	n/a
45	chr1:76080410-76080460	AG09309	skin:	n/a
46	chr1:76080684-76080734	PrEC	prostate:	n/a
47	chr1:76082568-76082618	RPTEC	kidney:	n/a
48	chr1:76082066-76082116	HRPEpiC	eye:	n/a
49	chr1:76081408-76081458	IMR90	lung:	fetal
50	chr1:76082568-76082618	GM06990	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76081387..76082907-chr17:41398843..41401870,3	K562	blood:
2	chr1:76079906..76082887-chr11:62607618..62609123,2	K562	blood:
3	chr1:76079591..76081611-chr1:76189875..76191572,2	MCF-7	breast:
4	chr1:76066835..76069254-chr1:76079406..76081859,2	MCF-7	breast:
5	chr1:76073216..76076150-chr1:76081319..76083961,2	MCF-7	breast:
6	chr1:76080604..76083289-chr1:76094142..76096069,2	K562	blood:
7	chr1:76081802..76083861-chr1:76085137..76086923,2	K562	blood:
8	chr1:76071710..76074403-chr1:76079679..76081378,2	K562	blood:
9	chr1:76081387..76082907-chr17:41398843..41400712,2	K562	blood:
10	chr1:75984267..75985784-chr1:76081741..76084002,2	K562	blood:
11	chr1:76081387..76081887-chr15:39080643..39081147,2	Hela-S3	cervix:
12	chr1:76080033..76082466-chr1:76250224..76251859,2	MCF-7	breast:
13	chr1:76079931..76081989-chr1:76083963..76086787,2	K562	blood:
14	chr1:76070009..76076148-chr1:76078248..76081967,7	K562	blood:
15	chr1:76079907..76082887-chr11:62607623..62609125,2	K562	blood:

No data

Variant related genes	Relation type
SLC44A5	TF binding region
SLC44A5	CpG island
ENSG00000117054	chromatin interactions
ENSG00000133316	chromatin interactions

Extended variants
information (count: 99 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:99 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180891239	chr1:76079971-76079972	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs532472891	chr1:76079996-76079997	Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs140792860	chr1:76080069-76080070	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs150111284	chr1:76080071-76080072	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs6593584	chr1:76080162-76080163	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs548915679	chr1:76080205-76080206	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs369394032	chr1:76080246-76080247	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs567441695	chr1:76080294-76080295	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs7355133	chr1:76080298-76080299	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552663884	chr1:76080313-76080314	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs571332825	chr1:76080328-76080329	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs531744749	chr1:76080341-76080342	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs111555912	chr1:76080464-76080465	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs557069100	chr1:76080485-76080486	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs575955418	chr1:76080492-76080493	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs372006283	chr1:76080520-76080521	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs543234652	chr1:76080582-76080583	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs185841502	chr1:76080588-76080589	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs573410403	chr1:76080600-76080601	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs576296708	chr1:76080606-76080607	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs369522929	chr1:76080642-76080643	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs149231943	chr1:76080702-76080703	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs147436176	chr1:76080723-76080724	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs555244803	chr1:76080768-76080769	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs565447714	chr1:76080798-76080799	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs544328068	chr1:76080824-76080825	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs562641741	chr1:76080828-76080829	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs530660895	chr1:76080947-76080948	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs74812527	chr1:76081047-76081048	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs548728755	chr1:76081052-76081053	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs12744080	chr1:76081070-76081071	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs561241562	chr1:76081080-76081081	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs112356533	chr1:76081089-76081090	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs112574817	chr1:76081102-76081103	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs546856591	chr1:76081103-76081104	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs3031479	chr1:76081114-76081115	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs76602034	chr1:76081115-76081116	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs77080011	chr1:76081117-76081118	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs141100798	chr1:76081119-76081120	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs571180859	chr1:76081120-76081121	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs61797277	chr1:76081121-76081122	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs71707527	chr1:76081122-76081123	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs79884901	chr1:76081125-76081126	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs149517579	chr1:76081129-76081130	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs376402490	chr1:76081131-76081132	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs147248334	chr1:76081133-76081134	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs369983288	chr1:76081135-76081136	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs56337760	chr1:76081148-76081149	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534493083	chr1:76081150-76081151	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs377397836	chr1:76081170-76081171	Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76078800-76080600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr1:76079400-76081400	Active TSS	Fetal Brain Male	brain
3	chr1:76079600-76080000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:76079600-76080000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr1:76079600-76080000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
6	chr1:76079600-76080200	Enhancers	Fetal Heart	heart
7	chr1:76079600-76080400	Flanking Active TSS	Brain Germinal Matrix	brain
8	chr1:76079600-76080600	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
9	chr1:76079800-76080000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
10	chr1:76079800-76080000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr1:76079800-76080000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
12	chr1:76079800-76080000	Flanking Active TSS	Brain Anterior Caudate	brain
13	chr1:76079800-76080000	Flanking Active TSS	Brain Substantia Nigra	brain
14	chr1:76079800-76080200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:76079800-76080200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr1:76079800-76080200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr1:76079800-76080200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr1:76079800-76080200	Active TSS	Brain Angular Gyrus	brain
19	chr1:76079800-76080200	Enhancers	Brain Cingulate Gyrus	brain
20	chr1:76079800-76080200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
21	chr1:76079800-76080400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
22	chr1:76079800-76080400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
23	chr1:76079800-76080400	Bivalent Enhancer	Stomach Mucosa	stomach
24	chr1:76079800-76081200	Active TSS	Fetal Brain Female	brain
25	chr1:76079800-76082200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
26	chr1:76079800-76082600	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr1:76080000-76080200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
28	chr1:76080000-76080200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
29	chr1:76080000-76080200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
30	chr1:76080000-76080200	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
31	chr1:76080000-76080200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr1:76080000-76080200	Active TSS	Brain Inferior Temporal Lobe	brain
33	chr1:76080000-76080200	Active TSS	Brain Substantia Nigra	brain
34	chr1:76080000-76080200	Bivalent Enhancer	Fetal Kidney	kidney
35	chr1:76080000-76080200	Enhancers	Pancreas	Pancrea
36	chr1:76080000-76080200	Enhancers	HepG2	liver
37	chr1:76080000-76080200	Enhancers	HUVEC	blood vessel
38	chr1:76080000-76080200	Bivalent Enhancer	NH-A	brain
39	chr1:76080000-76080400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
40	chr1:76080000-76080600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
41	chr1:76080000-76080600	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr1:76080000-76081400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
43	chr1:76080000-76082000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr1:76080000-76082200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr1:76080000-76082400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr1:76080000-76082600	Active TSS	Brain Anterior Caudate	brain
47	chr1:76080000-76082800	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
48	chr1:76080000-76082800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:76080200-76080400	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr1:76080200-76080400	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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