Variant report

Variant	esv2759145
Chromosome Location	chr3:46016464-46120400
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1616)
CpG islands
(count:1468)
Chromatin interactive
region (count:103)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:46022962-46023285	K562	blood:	n/a	n/a
2	ARID3A	chr3:46037100-46037950	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:46064529-46064778	K562	blood:	n/a	n/a
4	ATF1	chr3:46053741-46054031	K562	blood:	n/a	n/a
5	ATF1	chr3:46059273-46059575	K562	blood:	n/a	n/a
6	ATF1	chr3:46055293-46055475	K562	blood:	n/a	n/a
7	ATF1	chr3:46037183-46037522	K562	blood:	n/a	n/a
8	ATF1	chr3:46027941-46028138	K562	blood:	n/a	n/a
9	ATF1	chr3:46022873-46023180	K562	blood:	n/a	n/a
10	ATF1	chr3:46064475-46064783	K562	blood:	n/a	n/a
11	ATF2	chr3:46037097-46037668	GM12878	blood:	n/a	n/a
12	ATF2	chr3:46106504-46107307	GM12878	blood:	n/a	n/a
13	ATF2	chr3:46100787-46101392	GM12878	blood:	n/a	n/a
14	ATF2	chr3:46037009-46037697	GM12878	blood:	n/a	n/a
15	ATF2	chr3:46106617-46107309	GM12878	blood:	n/a	n/a
16	ATF3	chr3:46037224-46037518	HepG2	liver:	n/a	n/a
17	ATF3	chr3:46120302-46120624	K562	blood:	n/a	n/a
18	ATF3	chr3:46120322-46120602	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr3:46120225-46120692	GM12878	blood:	n/a	n/a
20	BACH1	chr3:46120140-46120660	K562	blood:	n/a	n/a
21	BACH1	chr3:46037156-46037636	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr3:46120272-46120690	GM12878	blood:	n/a	n/a
23	BATF	chr3:46035115-46035491	GM12878	blood:	n/a	n/a
24	BATF	chr3:46061207-46061552	GM12878	blood:	n/a	chr3:46061394-46061405
25	BATF	chr3:46061290-46061524	GM12878	blood:	n/a	chr3:46061394-46061405
26	BATF	chr3:46100968-46101221	GM12878	blood:	n/a	n/a
27	BATF	chr3:46106622-46107287	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:46061258-46061555	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:46100932-46101296	GM12878	blood:	n/a	chr3:46101170-46101179
30	BCL11A	chr3:46106945-46107200	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:46106614-46107280	GM12878	blood:	n/a	chr3:46106756-46106765 chr3:46106916-46106925
32	BCL11A	chr3:46071476-46071833	GM12878	blood:	n/a	n/a
33	BCL3	chr3:46059227-46059572	GM12878	blood:	n/a	n/a
34	BCL3	chr3:46106576-46107260	GM12878	blood:	n/a	chr3:46106756-46106765 chr3:46106916-46106925
35	BCL3	chr3:46105248-46105539	GM12878	blood:	n/a	n/a
36	BCL3	chr3:46059187-46059621	GM12878	blood:	n/a	n/a
37	BCL3	chr3:46106690-46107094	GM12878	blood:	n/a	chr3:46106756-46106765 chr3:46106916-46106925
38	BCLAF1	chr3:46106649-46107168	GM12878	blood:	n/a	chr3:46106756-46106765 chr3:46106916-46106925
39	BCLAF1	chr3:46100805-46101396	GM12878	blood:	n/a	chr3:46101170-46101179
40	BCLAF1	chr3:46036715-46037642	GM12878	blood:	n/a	n/a
41	BCLAF1	chr3:46106571-46107314	GM12878	blood:	n/a	chr3:46106756-46106765 chr3:46106916-46106925
42	BHLHE40	chr3:46120189-46120725	K562	blood:	n/a	n/a
43	BHLHE40	chr3:46106934-46106943	K562	blood:	n/a	n/a
44	BHLHE40	chr3:46037177-46037946	HepG2	liver:	n/a	n/a
45	BHLHE40	chr3:46100956-46101356	GM12878	blood:	n/a	n/a
46	BHLHE40	chr3:46036201-46036351	K562	blood:	n/a	n/a
47	BHLHE40	chr3:46035959-46036718	GM12878	blood:	n/a	n/a
48	BHLHE40	chr3:46120328-46120693	GM12878	blood:	n/a	n/a
49	BHLHE40	chr3:46037062-46037788	K562	blood:	n/a	n/a
50	BHLHE40	chr3:46106656-46107265	GM12878	blood:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46037014-46037064	H1-hESC	embryonic stem cell:	embryo
2	chr3:46036571-46036621	BJ	skin:	n/a
3	chr3:46062881-46062931	HCM	heart:	n/a
4	chr3:46065328-46065378	K562	blood:	n/a
5	chr3:46037014-46037064	H1-hESC	embryonic stem cell:	embryo
6	chr3:46036571-46036621	BJ	skin:	n/a
7	chr3:46062881-46062931	HCM	heart:	n/a
8	chr3:46065328-46065378	K562	blood:	n/a
9	chr3:46037592-46037642	SK-N-SH	brain:	n/a
10	chr3:46037942-46037992	AG04450	lung:	fetal
11	chr3:46064611-46064661	HepG2	liver:	n/a
12	chr3:46065328-46065378	ECC-1	luminal epithelium:	n/a
13	chr3:46065762-46065812	AoSMC	blood vessel:	n/a
14	chr3:46037014-46037064	NT2-D1	testis:	n/a
15	chr3:46069366-46069416	GM06990	blood:	n/a
16	chr3:46029278-46029328	ovcar-3	ovarian:	n/a
17	chr3:46037942-46037992	HIPEpiC	eye:	n/a
18	chr3:46037496-46037546	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:46033800-46033850	HAEpiC	amniotic membrane:	n/a
20	chr3:46037470-46037520	HPAEpiC	pulmonary alveolar:	n/a
21	chr3:46037496-46037546	A549	lung:	n/a
22	chr3:46070399-46070449	BE2_C	brain:	n/a
23	chr3:46065328-46065378	HCT-116	colon:	n/a
24	chr3:46062588-46062638	LNCaP	prostate:	n/a
25	chr3:46037496-46037546	Jurkat	blood:	n/a
26	chr3:46037496-46037546	GM06990	blood:	n/a
27	chr3:46036571-46036621	NHBE	bronchial:	n/a
28	chr3:46064611-46064661	MCF-7	breast:	n/a
29	chr3:46064611-46064661	CMK	blood:	n/a
30	chr3:46070399-46070449	NH-A	brain:	n/a
31	chr3:46036571-46036621	NT2-D1	testis:	n/a
32	chr3:46069366-46069416	NB4	blood:	n/a
33	chr3:46062881-46062931	PFSK-1	brain:	n/a
34	chr3:46069693-46069743	HRE	kidney:	n/a
35	chr3:46037496-46037546	GM12891	blood:	n/a
36	chr3:46037592-46037642	GM19239	blood:	n/a
37	chr3:46037014-46037064	SK-N-SH_RA	brain:	n/a
38	chr3:46033800-46033850	SK-N-SH	brain:	n/a
39	chr3:46068932-46068982	AG09319	gingival:	n/a
40	chr3:46062662-46062712	SAEC	small airway:	n/a
41	chr3:46070399-46070449	HEEpiC	esophagus:	n/a
42	chr3:46062881-46062931	GM12892	blood:	n/a
43	chr3:46036571-46036621	HEK293	kidney:	embryo
44	chr3:46062588-46062638	SKMC	muscle:	n/a
45	chr3:46069693-46069743	SK-N-MC	brain:	n/a
46	chr3:46069693-46069743	HAEpiC	amniotic membrane:	n/a
47	chr3:46037470-46037520	GM19239	blood:	n/a
48	chr3:46069366-46069416	HepG2	liver:	n/a
49	chr3:46029278-46029328	NH-A	brain:	n/a
50	chr3:46069366-46069416	HRPEpiC	eye:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:45971111..45971673-chr3:46120113..46120665,2	MCF-7	breast:
2	chr3:46064588..46066447-chr3:46080025..46081697,2	K562	blood:
3	chr3:46103249..46106082-chr3:46119956..46121890,2	K562	blood:
4	chr3:45970362..45970959-chr3:46120109..46120778,2	MCF-7	breast:
5	chr3:46017706..46019852-chr3:46035209..46037613,2	K562	blood:
6	chr3:45801846..45803268-chr3:46119981..46120996,10	K562	blood:
7	chr3:46048434..46050837-chr3:46053075..46054735,2	K562	blood:
8	chr3:46056098..46058529-chr3:46065218..46067707,2	K562	blood:
9	chr3:45970536..45971214-chr3:46120157..46120881,2	MCF-7	breast:
10	chr3:46038061..46039576-chr3:46044215..46045732,2	K562	blood:
11	chr3:46106956..46110561-chr3:46110945..46113902,3	K562	blood:
12	chr3:46014022..46017742-chr3:46018515..46020350,3	MCF-7	breast:
13	chr3:45978760..45981889-chr3:46119716..46121321,25	MCF-7	breast:
14	chr3:46026501..46029475-chr3:46032165..46035137,4	MCF-7	breast:
15	chr3:45992659..45994641-chr3:46028942..46030792,2	K562	blood:
16	chr3:46095387..46098200-chr3:46100479..46102760,2	K562	blood:
17	chr3:46036059..46037983-chr3:46447594..46449867,2	K562	blood:
18	chr3:45987551..45988458-chr3:46119930..46120914,4	MCF-7	breast:
19	chr3:45881509..45882298-chr3:46120089..46120945,2	MCF-7	breast:
20	chr3:46038061..46039576-chr3:46044215..46045732,2	K562	blood:
21	chr3:45816597..45817280-chr3:46120013..46120834,2	K562	blood:
22	chr3:45970248..45970774-chr3:46120086..46120929,2	K562	blood:
23	chr3:45997101..45998721-chr3:46017987..46020675,2	K562	blood:
24	chr3:45979895..45980974-chr3:46119979..46120805,8	MCF-7	breast:
25	chr3:45979007..45979682-chr3:46117842..46118764,2	MCF-7	breast:
26	chr3:46019979..46023374-chr3:46034093..46037294,5	K562	blood:
27	chr3:46049509..46051650-chr3:46061569..46063331,2	K562	blood:
28	chr3:45980561..45981539-chr3:46118125..46119072,2	MCF-7	breast:
29	chr3:46028019..46029570-chr3:46035343..46037600,2	MCF-7	breast:
30	chr3:45965432..45966076-chr3:46120033..46120908,2	K562	blood:
31	chr3:46021917..46024700-chr3:46027716..46030169,2	MCF-7	breast:
32	chr3:46019151..46021048-chr3:46024338..46027316,2	K562	blood:
33	chr3:46120227..46120919-chr3:46249276..46249992,2	K562	blood:
34	chr3:45874102..45874933-chr3:46120010..46120588,2	MCF-7	breast:
35	chr3:46020688..46022439-chr3:46080709..46083125,2	K562	blood:
36	chr3:46011530..46014566-chr3:46015264..46018457,3	K562	blood:
37	chr3:46008363..46011066-chr3:46026720..46029201,2	MCF-7	breast:
38	chr3:46058613..46061881-chr3:46065109..46067652,3	K562	blood:
39	chr3:46022722..46024858-chr3:46024939..46027896,2	K562	blood:
40	chr3:46013767..46016030-chr3:46019815..46022441,2	K562	blood:
41	chr3:45979673..45982315-chr3:46020948..46022553,2	K562	blood:
42	chr3:46019490..46020101-chr3:46029374..46029909,2	MCF-7	breast:
43	chr3:46044700..46047149-chr3:46047918..46051696,3	K562	blood:
44	chr3:46034481..46038695-chr3:46049566..46055289,5	K562	blood:
45	chr17:5389674..5390238-chr3:46037073..46037659,2	Hela-S3	cervix:
46	chr3:46020688..46022439-chr3:46080709..46083125,2	K562	blood:
47	chr3:45639893..45641594-chr3:46034221..46037019,2	K562	blood:
48	chr3:46015505..46018391-chr3:46024106..46026296,2	K562	blood:
49	chr3:46035149..46036764-chr3:46100668..46103208,2	K562	blood:
50	chr3:46024602..46026106-chr3:46028613..46030507,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FYCO1-2	chr3:46063649-46063769	NONHSAT089427
2	lnc-FYCO1-2	chr3:46063333-46063470	NONHSAT089427
3	lnc-FYCO1-2	chr3:46068910-46068979	NONHSAT089427
4	lnc-XCR1-1	chr3:46058516-46062157	NONHSAT089426
5	lnc-FYCO1-1	chr3:46026073-46026514	NONHSAT089425
6	lnc-XCR1-2	chr3:46033520-46037161	ucscGeneNc_uc003cpd_1
7	lnc-FYCO1-1	chr3:46037214-46037316	NONHSAT089425

No data

Variant related genes	Relation type
XCR1	TF binding region
NRBF2P2	TF binding region
FYCO1	TF binding region
XCR1	CpG island
NRBF2P2	CpG island
FYCO1	CpG island
ENSG00000172215	chromatin interactions
ENSG00000249992	chromatin interactions
ENSG00000168071	chromatin interactions
ENSG00000226933	chromatin interactions
ENSG00000223552	chromatin interactions
ENSG00000167842	chromatin interactions
ENSG00000072849	chromatin interactions
ENSG00000121797	chromatin interactions
ENSG00000163823	chromatin interactions
ENSG00000163820	chromatin interactions
ENSG00000173578	chromatin interactions

Extended variants
information (count: 3493 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3493 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12639598	chr3:46016464-46016465	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147747923	chr3:46016481-46016482	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs140873519	chr3:46016548-46016549	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564337332	chr3:46016551-46016552	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140062438	chr3:46016564-46016565	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71756916	chr3:46016565-46016566	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs3821884	chr3:46016599-46016600	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs144873702	chr3:46016687-46016688	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369490186	chr3:46016693-46016694	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372930369	chr3:46016694-46016695	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs147795043	chr3:46016698-46016699	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375889330	chr3:46016708-46016709	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs369204352	chr3:46016722-46016723	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372485725	chr3:46016723-46016724	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569096080	chr3:46016769-46016770	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs140695972	chr3:46016774-46016775	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs530538817	chr3:46016785-46016786	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145897969	chr3:46016789-46016790	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552223395	chr3:46016795-46016796	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs570357544	chr3:46016798-46016799	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372180748	chr3:46016840-46016841	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs751552	chr3:46016851-46016852	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs367925220	chr3:46016853-46016854	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370400873	chr3:46016857-46016858	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368235039	chr3:46016867-46016868	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs568411256	chr3:46016892-46016893	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115435184	chr3:46016893-46016894	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs751553	chr3:46016944-46016945	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs575360767	chr3:46016963-46016964	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs140228956	chr3:46016969-46016970	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs374510137	chr3:46016974-46016975	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112717422	chr3:46017007-46017008	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558182371	chr3:46017038-46017039	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573162315	chr3:46017078-46017079	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs540660347	chr3:46017165-46017166	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150291219	chr3:46017186-46017187	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529579549	chr3:46017246-46017247	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs904634	chr3:46017304-46017305	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs562765838	chr3:46017323-46017324	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533523739	chr3:46017324-46017325	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531677555	chr3:46017337-46017338	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182792369	chr3:46017371-46017372	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs187306725	chr3:46017388-46017389	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs753110	chr3:46017393-46017394	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs546646260	chr3:46017408-46017409	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs73830672	chr3:46017417-46017418	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs568010282	chr3:46017418-46017419	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12629722	chr3:46017422-46017423	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535763347	chr3:46017480-46017481	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs528903675	chr3:46017579-46017580	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2101 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:45981600-46025000	Strong transcription	Fetal Intestine Large	intestine
2	chr3:45986400-46026600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:45986600-46026800	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr3:45987200-46027200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr3:45987400-46026600	Strong transcription	HUES6 Cell Line	embryonic stem cell
6	chr3:45987800-46026400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr3:45987800-46026800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr3:45987800-46027200	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr3:45988000-46026600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr3:45990600-46017200	Strong transcription	Rectal Mucosa Donor 29	rectum
11	chr3:45991200-46017400	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr3:45996200-46025400	Strong transcription	Liver	Liver
13	chr3:45999400-46018200	Strong transcription	Fetal Lung	lung
14	chr3:46000000-46029600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr3:46002200-46018600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr3:46002600-46025000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:46002600-46027200	Weak transcription	A549	lung
18	chr3:46007800-46024200	Weak transcription	Fetal Kidney	kidney
19	chr3:46008600-46026400	Strong transcription	Hela-S3	cervix
20	chr3:46009000-46027800	Weak transcription	Fetal Brain Male	brain
21	chr3:46009200-46017000	Weak transcription	Stomach Mucosa	stomach
22	chr3:46009600-46018000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr3:46010200-46021000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr3:46010200-46022600	Weak transcription	Brain Angular Gyrus	brain
25	chr3:46010200-46024200	Strong transcription	Left Ventricle	heart
26	chr3:46010200-46027000	Weak transcription	Fetal Brain Female	brain
27	chr3:46010200-46029600	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr3:46010200-46033000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:46010600-46017400	Strong transcription	Fetal Muscle Leg	muscle
30	chr3:46010600-46020800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr3:46010800-46022400	Weak transcription	Fetal Heart	heart
32	chr3:46011400-46020800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr3:46012000-46020800	Weak transcription	Ovary	ovary
34	chr3:46012800-46016600	Genic enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr3:46013000-46017200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
36	chr3:46013000-46019200	Strong transcription	Adipose Nuclei	Adipose
37	chr3:46013000-46026200	Weak transcription	Brain Germinal Matrix	brain
38	chr3:46013200-46017000	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr3:46013200-46017600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:46013600-46017600	Genic enhancers	Primary T cells fromperipheralblood	blood
41	chr3:46013600-46017800	Genic enhancers	Thymus	Thymus
42	chr3:46013600-46018000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
43	chr3:46013600-46021000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr3:46013600-46023000	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr3:46013600-46025000	Strong transcription	Fetal Intestine Small	intestine
46	chr3:46013600-46025400	Strong transcription	Fetal Muscle Trunk	muscle
47	chr3:46013600-46025600	Strong transcription	Fetal Stomach	stomach
48	chr3:46013600-46034000	Genic enhancers	Fetal Thymus	thymus
49	chr3:46013800-46016800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr3:46013800-46017600	Genic enhancers	Dnd41	blood

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