Variant report

Variant	nsv615242
Chromosome Location	chr9:117047121-117103973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1762)
CpG islands
(count:611)
Chromatin interactive
region (count:65)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1762 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:117084358-117084903	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:117091599-117091832	HepG2	liver:	n/a	n/a
3	ATF1	chr9:117080165-117080332	K562	blood:	n/a	n/a
4	ATF2	chr9:117050503-117050900	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr9:117050431-117050865	A549	lung:	n/a	n/a
6	ATF3	chr9:117080162-117080453	K562	blood:	n/a	n/a
7	BACH1	chr9:117050529-117050848	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr9:117069753-117069785	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr9:117047663-117048091	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr9:117050371-117050932	A549	lung:	n/a	chr9:117050674-117050683
11	BCL3	chr9:117080178-117080438	GM12878	blood:	n/a	n/a
12	BCL3	chr9:117050379-117050786	A549	lung:	n/a	chr9:117050674-117050683
13	BCL3	chr9:117080117-117080458	GM12878	blood:	n/a	n/a
14	BCL3	chr9:117094659-117095275	GM12878	blood:	n/a	n/a
15	BCL3	chr9:117094739-117094968	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:117068113-117068430	HepG2	liver:	n/a	n/a
17	BHLHE40	chr9:117068161-117068341	GM12878	blood:	n/a	n/a
18	BHLHE40	chr9:117047758-117047982	K562	blood:	n/a	chr9:117047959-117047975
19	BHLHE40	chr9:117085114-117085542	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:117101399-117101695	K562	blood:	n/a	n/a
21	BHLHE40	chr9:117053342-117053611	K562	blood:	n/a	n/a
22	BHLHE40	chr9:117102654-117102933	K562	blood:	n/a	chr9:117102783-117102792 chr9:117102776-117102797 chr9:117102782-117102791 chr9:117102782-117102791
23	BHLHE40	chr9:117068003-117068369	K562	blood:	n/a	n/a
24	BHLHE40	chr9:117091885-117092313	HepG2	liver:	n/a	n/a
25	BHLHE40	chr9:117084718-117085030	HepG2	liver:	n/a	n/a
26	BRCA1	chr9:117101433-117101581	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr9:117068353-117068553	HepG2	liver:	n/a	n/a
28	BRCA1	chr9:117053310-117053516	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr9:117068164-117068380	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr9:117089360-117089769	K562	blood:	n/a	n/a
31	CBX3	chr9:117096067-117096511	K562	blood:	n/a	n/a
32	CCNT2	chr9:117098534-117098959	K562	blood:	n/a	n/a
33	CEBPB	chr9:117084769-117085000	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:117080094-117080477	HepG2	liver:	n/a	chr9:117080273-117080284
35	CEBPB	chr9:117080214-117080319	HepG2	liver:	n/a	chr9:117080273-117080284
36	CEBPB	chr9:117080097-117080535	Hela-S3	cervix:	n/a	chr9:117080273-117080284
37	CEBPB	chr9:117080115-117080579	A549	lung:	n/a	chr9:117080273-117080284
38	CEBPB	chr9:117080094-117080487	K562	blood:	n/a	chr9:117080273-117080284
39	CEBPB	chr9:117091524-117091772	HepG2	liver:	n/a	n/a
40	CEBPB	chr9:117091567-117091727	HepG2	liver:	n/a	n/a
41	CEBPB	chr9:117084690-117085081	HepG2	liver:	n/a	n/a
42	CEBPB	chr9:117077405-117077763	HepG2	liver:	n/a	chr9:117077571-117077582 chr9:117077573-117077582 chr9:117077571-117077584
43	CEBPB	chr9:117091269-117091840	HepG2	liver:	n/a	n/a
44	CEBPB	chr9:117103181-117103338	HepG2	liver:	n/a	chr9:117103287-117103298
45	CEBPB	chr9:117080082-117080511	IMR90	lung:	n/a	chr9:117080273-117080284
46	CEBPB	chr9:117080205-117080383	K562	blood:	n/a	chr9:117080273-117080284
47	CEBPB	chr9:117077520-117077679	IMR90	lung:	n/a	chr9:117077571-117077582 chr9:117077573-117077582 chr9:117077571-117077584
48	CEBPB	chr9:117091468-117091849	HepG2	liver:	n/a	n/a
49	CEBPB	chr9:117084795-117084978	HepG2	liver:	n/a	n/a
50	CEBPB	chr9:117053422-117053529	Hela-S3	cervix:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117085966-117086016	SK-N-SH	brain:	n/a
2	chr9:117085966-117086016	SK-N-SH	brain:	n/a
3	chr9:117084602-117084652	GM12892	blood:	n/a
4	chr9:117068532-117068582	H1-hESC	embryonic stem cell:	embryo
5	chr9:117093052-117093102	SAEC	small airway:	n/a
6	chr9:117090924-117090974	GM12891	blood:	n/a
7	chr9:117096902-117096952	HL-60	blood:	n/a
8	chr9:117090924-117090974	SK-N-SH	brain:	n/a
9	chr9:117096902-117096952	IMR90	lung:	fetal
10	chr9:117068532-117068582	HEEpiC	esophagus:	n/a
11	chr9:117096902-117096952	GM12878	blood:	n/a
12	chr9:117047688-117047738	AG09309	skin:	n/a
13	chr9:117096902-117096952	ProgFib	skin:	n/a
14	chr9:117085966-117086016	HCM	heart:	n/a
15	chr9:117090924-117090974	HRCEpiC	kidney:	n/a
16	chr9:117093175-117093225	HRCEpiC	kidney:	n/a
17	chr9:117096902-117096952	SK-N-SH_RA	brain:	n/a
18	chr9:117068532-117068582	ECC-1	luminal epithelium:	n/a
19	chr9:117084602-117084652	MCF10A-Er-Src	breast:	n/a
20	chr9:117090924-117090974	AG09319	gingival:	n/a
21	chr9:117093052-117093102	BE2_C	brain:	n/a
22	chr9:117068159-117068209	MCF10A-Er-Src	breast:	n/a
23	chr9:117068532-117068582	SAEC	small airway:	n/a
24	chr9:117084602-117084652	HCPEpiC	choroid plexus:	n/a
25	chr9:117093052-117093102	MCF10A-Er-Src	breast:	n/a
26	chr9:117068361-117068411	HAEpiC	amniotic membrane:	n/a
27	chr9:117093175-117093225	AG10803	skin:	n/a
28	chr9:117084602-117084652	AG04450	lung:	fetal
29	chr9:117090924-117090974	AG04450	lung:	fetal
30	chr9:117068532-117068582	PFSK-1	brain:	n/a
31	chr9:117093052-117093102	HL-60	blood:	n/a
32	chr9:117068532-117068582	HAEpiC	amniotic membrane:	n/a
33	chr9:117093175-117093225	NB4	blood:	n/a
34	chr9:117093052-117093102	AG09319	gingival:	n/a
35	chr9:117090924-117090974	HIPEpiC	eye:	n/a
36	chr9:117096902-117096952	SK-N-MC	brain:	n/a
37	chr9:117047688-117047738	HPAEpiC	pulmonary alveolar:	n/a
38	chr9:117068532-117068582	AG09319	gingival:	n/a
39	chr9:117068361-117068411	PFSK-1	brain:	n/a
40	chr9:117068159-117068209	AG04449	skin:	fetal
41	chr9:117096902-117096952	LNCaP	prostate:	n/a
42	chr9:117093175-117093225	NHDF-neo	bronchial:	n/a
43	chr9:117090924-117090974	GM19239	blood:	n/a
44	chr9:117096902-117096952	HRCEpiC	kidney:	n/a
45	chr9:117084602-117084652	A549	lung:	n/a
46	chr9:117068532-117068582	SKMC	muscle:	n/a
47	chr9:117084602-117084652	HRPEpiC	eye:	n/a
48	chr9:117090924-117090974	NHDF-neo	bronchial:	n/a
49	chr9:117096902-117096952	HNPCEpiC	eye:	n/a
50	chr9:117096902-117096952	BE2_C	brain:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:117101580..117103166-chr9:117103266..117105308,2	MCF-7	breast:
2	chr9:116844678..116846349-chr9:117050619..117053590,2	MCF-7	breast:
3	chr9:116916702..116920015-chr9:117048012..117051881,4	K562	blood:
4	chr9:117001198..117001897-chr9:117053004..117053908,2	MCF-7	breast:
5	chr9:117060520..117062937-chr9:117065825..117069499,4	MCF-7	breast:
6	chr9:117062219..117064212-chr9:117064334..117066027,2	MCF-7	breast:
7	chr9:116917096..116918203-chr9:117052981..117053630,5	MCF-7	breast:
8	chr9:116844851..116845417-chr9:117067843..117068379,2	MCF-7	breast:
9	chr9:117033926..117037136-chr9:117049130..117052892,3	MCF-7	breast:
10	chr9:116869923..116871115-chr9:117053002..117053726,3	K562	blood:
11	chr9:117103384..117106313-chr9:117156764..117158345,2	MCF-7	breast:
12	chr9:117101497..117102031-chr9:117424117..117425066,2	K562	blood:
13	chr9:117101788..117104585-chr9:117150273..117152104,2	MCF-7	breast:
14	chr9:116869934..116871127-chr9:117052704..117054035,13	MCF-7	breast:
15	chr6:13696678..13697254-chr9:117099459..117100279,2	MCF-7	breast:
16	chr9:117102977..117106643-chr9:117157703..117161882,4	K562	blood:
17	chr9:116869935..116870873-chr9:117052125..117052932,3	K562	blood:
18	chr9:117099812..117101508-chr9:117113315..117115822,2	MCF-7	breast:
19	chr9:116917252..116918213-chr9:117052941..117053917,4	K562	blood:
20	chr9:116870303..116871233-chr9:117051501..117052146,3	MCF-7	breast:
21	chr9:117048708..117051555-chr9:117052234..117055024,3	MCF-7	breast:
22	chr9:117103574..117106536-chr9:117108537..117110176,2	MCF-7	breast:
23	chr9:116869916..116870857-chr9:117067860..117068426,2	K562	blood:
24	chr9:116917422..116918284-chr9:117067805..117069207,4	K562	blood:
25	chr9:116917474..116919144-chr9:117052623..117055969,3	MCF-7	breast:
26	chr9:116869895..116870973-chr9:117052879..117053661,10	MCF-7	breast:
27	chr9:117102242..117104116-chr9:117108408..117110413,2	K562	blood:
28	chr9:117065267..117067834-chr9:117158317..117161019,2	MCF-7	breast:
29	chr9:117068040..117068779-chr9:117101087..117101920,2	MCF-7	breast:
30	chr9:117101454..117102367-chr9:117485164..117485846,2	K562	blood:
31	chr9:117100634..117103007-chr9:117108442..117110444,2	MCF-7	breast:
32	chr9:117073544..117075822-chr9:117160051..117162438,2	K562	blood:
33	chr9:117068239..117069211-chr9:117101111..117102006,2	K562	blood:
34	chr9:117066557..117068874-chr9:117077753..117079545,2	MCF-7	breast:
35	chr9:116844247..116845566-chr9:117052560..117054100,7	MCF-7	breast:
36	chr9:116845927..116847866-chr9:117052148..117055626,3	MCF-7	breast:
37	chr9:117053392..117053933-chr9:117067853..117068400,2	K562	blood:
38	chr9:117060520..117062937-chr9:117065825..117069499,4	MCF-7	breast:
39	chr9:117101434..117102012-chr9:117415923..117416790,3	K562	blood:
40	chr9:117101442..117101963-chr9:117167919..117168430,2	K562	blood:
41	chr9:116499791..116500371-chr9:117053010..117053583,4	K562	blood:
42	chr9:117102552..117105205-chr9:117109835..117112398,2	K562	blood:
43	chr9:117101198..117101979-chr9:117111299..117111941,2	MCF-7	breast:
44	chr9:117101149..117102026-chr9:117196751..117197558,2	MCF-7	breast:
45	chr9:116569447..116570300-chr9:117052628..117053509,2	MCF-7	breast:
46	chr9:117052909..117055629-chr9:117066648..117068962,2	MCF-7	breast:
47	chr9:116774861..116777762-chr9:117046301..117047948,2	MCF-7	breast:
48	chr9:116843600..116846294-chr9:117069884..117072218,2	MCF-7	breast:
49	chr9:117101534..117102049-chr9:117270024..117270719,2	MCF-7	breast:
50	chr9:117086796..117090916-chr9:117093612..117097049,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ORM1-1	chr9:117063564-117063599	NONHSAT134374
2	lnc-ORM1-1	chr9:117063725-117063822	NONHSAT134374
3	lnc-ORM1-1	chr9:117062642-117062967	NONHSAT134374
4	lnc-ORM1-1	chr9:117063352-117063405	NONHSAT134374

No data

Variant related genes	Relation type
ORM2	TF binding region
COL27A1	TF binding region
ORM1	TF binding region
ORM2	CpG island
COL27A1	CpG island
ORM1	CpG island
ENSG00000230054	chromatin interactions
ENSG00000106948	chromatin interactions
ENSG00000196739	chromatin interactions
ENSG00000235119	chromatin interactions

Extended variants
information (count: 2780 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2780 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13291199	chr9:117047121-117047122	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs567471830	chr9:117047125-117047126	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568071544	chr9:117047143-117047144	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376366481	chr9:117047156-117047157	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546654002	chr9:117047192-117047193	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs111492876	chr9:117047198-117047199	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376664977	chr9:117047199-117047200	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116186465	chr9:117047208-117047209	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538640589	chr9:117047223-117047224	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184671364	chr9:117047224-117047225	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs571448367	chr9:117047253-117047254	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537305978	chr9:117047261-117047262	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535459327	chr9:117047277-117047278	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs72762670	chr9:117047283-117047284	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs565676423	chr9:117047290-117047291	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553079379	chr9:117047300-117047301	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs76579901	chr9:117047313-117047314	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187584533	chr9:117047316-117047317	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141429521	chr9:117047407-117047408	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs531114194	chr9:117047417-117047418	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs544463160	chr9:117047438-117047439	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs561161633	chr9:117047499-117047500	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs4381012	chr9:117047502-117047503	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs546723588	chr9:117047519-117047520	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs566843759	chr9:117047539-117047540	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs150820273	chr9:117047551-117047552	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs139234588	chr9:117047552-117047553	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs192519603	chr9:117047581-117047582	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs570301925	chr9:117047637-117047638	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs557267446	chr9:117047689-117047690	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs567494558	chr9:117047714-117047715	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs536433014	chr9:117047724-117047725	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs374154689	chr9:117047743-117047744	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs374352229	chr9:117047758-117047759	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs572845889	chr9:117047768-117047769	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs112699155	chr9:117047783-117047784	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs545040290	chr9:117047801-117047802	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs558275722	chr9:117047803-117047804	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs575142759	chr9:117047812-117047813	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs144316597	chr9:117047831-117047832	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs561231757	chr9:117047875-117047876	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs2130722	chr9:117047888-117047889	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs555512699	chr9:117047913-117047914	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs573635643	chr9:117047941-117047942	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs116591696	chr9:117047957-117047958	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs560690209	chr9:117047965-117047966	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs185068288	chr9:117047974-117047975	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs552608421	chr9:117048014-117048015	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs562766769	chr9:117048028-117048029	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs531719222	chr9:117048034-117048035	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Retinoblastoma	19183342	CNVD

Chromatin state (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:117005000-117050200	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr9:117012400-117054400	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr9:117013400-117067800	Weak transcription	Right Ventricle	heart
4	chr9:117016200-117047400	Weak transcription	Fetal Kidney	kidney
5	chr9:117026600-117057000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr9:117026800-117050000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr9:117027600-117047600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:117027800-117056800	Weak transcription	Colon Smooth Muscle	Colon
9	chr9:117028200-117077000	Weak transcription	Gastric	stomach
10	chr9:117038200-117052800	Weak transcription	Stomach Mucosa	stomach
11	chr9:117039400-117049400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:117039800-117047400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr9:117039800-117047600	Weak transcription	Adipose Nuclei	Adipose
14	chr9:117039800-117076600	Weak transcription	Lung	lung
15	chr9:117040200-117047600	Weak transcription	HUVEC	blood vessel
16	chr9:117040200-117053000	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr9:117041600-117047600	Weak transcription	Esophagus	oesophagus
18	chr9:117041800-117061800	Weak transcription	Aorta	Aorta
19	chr9:117042000-117050000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:117043000-117047600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr9:117043000-117051000	Strong transcription	HepG2	liver
22	chr9:117043200-117051800	Strong transcription	Liver	Liver
23	chr9:117043400-117051800	Genic enhancers	Fetal Muscle Leg	muscle
24	chr9:117043400-117053800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr9:117043600-117047600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr9:117043600-117047600	Strong transcription	Stomach Smooth Muscle	stomach
27	chr9:117043800-117053800	Genic enhancers	Fetal Muscle Trunk	muscle
28	chr9:117043800-117074800	Strong transcription	Fetal Intestine Large	intestine
29	chr9:117043800-117075200	Weak transcription	Rectal Smooth Muscle	rectum
30	chr9:117044200-117047600	Weak transcription	Duodenum Mucosa	Duodenum
31	chr9:117044200-117057600	Weak transcription	Right Atrium	heart
32	chr9:117044400-117057000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr9:117044800-117055000	Strong transcription	Fetal Intestine Small	intestine
34	chr9:117045000-117047400	Weak transcription	Ovary	ovary
35	chr9:117045400-117048200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr9:117045600-117047200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:117045600-117047200	Weak transcription	Brain Hippocampus Middle	brain
38	chr9:117045600-117047400	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr9:117045600-117047400	Weak transcription	HSMM	muscle
40	chr9:117045600-117048000	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr9:117045600-117049200	Weak transcription	Fetal Thymus	thymus
42	chr9:117045600-117050000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr9:117045800-117047400	Weak transcription	Osteobl	bone
44	chr9:117045800-117047600	Weak transcription	HSMMtube	muscle
45	chr9:117045800-117050200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:117046000-117047200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr9:117046000-117047200	Weak transcription	NH-A	brain
48	chr9:117046000-117047400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr9:117046000-117047400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr9:117046000-117048200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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