Variant report

Variant	nsv1053762
Chromosome Location	chr9:98208542-98232120
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:518)
CpG islands
(count:366)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:518 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:98224854-98225426	K562	blood:	n/a	n/a
2	ARID3A	chr9:98215314-98215388	K562	blood:	n/a	n/a
3	ARID3A	chr9:98214579-98214712	K562	blood:	n/a	n/a
4	ATF1	chr9:98224654-98225251	K562	blood:	n/a	n/a
5	ATF2	chr9:98224649-98225239	GM12878	blood:	n/a	n/a
6	ATF2	chr9:98224457-98225273	GM12878	blood:	n/a	n/a
7	ATF3	chr9:98224774-98225257	K562	blood:	n/a	n/a
8	BACH1	chr9:98224894-98225069	K562	blood:	n/a	n/a
9	BACH1	chr9:98227166-98227236	K562	blood:	n/a	n/a
10	BATF	chr9:98224831-98225171	GM12878	blood:	n/a	n/a
11	BATF	chr9:98208520-98208810	GM12878	blood:	n/a	n/a
12	BATF	chr9:98208505-98208801	GM12878	blood:	n/a	n/a
13	BATF	chr9:98224780-98225220	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:98224740-98225225	GM12878	blood:	n/a	chr9:98225195-98225204
15	BCL11A	chr9:98224728-98225264	GM12878	blood:	n/a	chr9:98225195-98225204
16	BCL3	chr9:98224832-98225231	GM12878	blood:	n/a	chr9:98225195-98225204
17	BCL3	chr9:98224804-98225467	K562	blood:	n/a	chr9:98225195-98225204
18	BCLAF1	chr9:98224502-98225248	GM12878	blood:	n/a	chr9:98225195-98225204
19	BCLAF1	chr9:98224534-98225309	GM12878	blood:	n/a	chr9:98225195-98225204
20	BHLHE40	chr9:98215350-98215409	K562	blood:	n/a	n/a
21	BHLHE40	chr9:98223976-98224105	K562	blood:	n/a	n/a
22	BHLHE40	chr9:98208583-98208944	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:98224564-98225398	K562	blood:	n/a	n/a
24	BHLHE40	chr9:98210286-98210522	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:98214485-98214824	K562	blood:	n/a	n/a
26	BHLHE40	chr9:98224478-98225574	GM12878	blood:	n/a	n/a
27	CBX3	chr9:98224396-98225508	K562	blood:	n/a	n/a
28	CBX3	chr9:98224692-98225259	K562	blood:	n/a	n/a
29	CCNT2	chr9:98224778-98225492	K562	blood:	n/a	chr9:98225171-98225191 chr9:98225271-98225280
30	CEBPB	chr9:98224783-98225209	K562	blood:	n/a	n/a
31	CEBPB	chr9:98214152-98214240	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:98224798-98225320	K562	blood:	n/a	n/a
33	CEBPB	chr9:98219991-98220380	IMR90	lung:	n/a	chr9:98220176-98220193 chr9:98220177-98220190
34	CEBPB	chr9:98215326-98215541	K562	blood:	n/a	n/a
35	CEBPB	chr9:98221567-98221811	IMR90	lung:	n/a	n/a
36	CEBPB	chr9:98216885-98217055	K562	blood:	n/a	n/a
37	CEBPB	chr9:98224660-98225226	GM12878	blood:	n/a	n/a
38	CEBPB	chr9:98210387-98210708	H1-hESC	embryonic stem cell:	n/a	chr9:98210634-98210647
39	CEBPB	chr9:98224804-98225223	GM12878	blood:	n/a	n/a
40	CEBPD	chr9:98224641-98225442	K562	blood:	n/a	n/a
41	CEBPD	chr9:98224818-98225434	K562	blood:	n/a	n/a
42	CHD1	chr9:98225475-98225550	GM12878	blood:	n/a	n/a
43	CHD1	chr9:98224386-98225214	GM12878	blood:	n/a	n/a
44	CHD2	chr9:98210337-98210627	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr9:98224930-98225160	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr9:98224440-98225583	GM12878	blood:	n/a	chr9:98225271-98225281
47	CHD2	chr9:98224863-98225284	K562	blood:	n/a	chr9:98225271-98225281
48	CREB1	chr9:98224682-98225302	GM12878	blood:	n/a	n/a
49	CREB1	chr9:98224680-98225316	K562	blood:	n/a	n/a
50	CTCF	chr9:98224520-98224670	GM12871	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:98221619-98221669	H1-hESC	embryonic stem cell:	embryo
2	chr9:98212061-98212111	HIPEpiC	eye:	n/a
3	chr9:98213755-98213805	GM12878	blood:	n/a
4	chr9:98213755-98213805	HIPEpiC	eye:	n/a
5	chr9:98212061-98212111	CMK	blood:	n/a
6	chr9:98221619-98221669	AG04449	skin:	fetal
7	chr9:98221619-98221669	SK-N-SH	brain:	n/a
8	chr9:98215821-98215871	RPTEC	kidney:	n/a
9	chr9:98221975-98222025	HRPEpiC	eye:	n/a
10	chr9:98221975-98222025	NB4	blood:	n/a
11	chr9:98221975-98222025	PANC-1	pancreas:	n/a
12	chr9:98212061-98212111	GM12892	blood:	n/a
13	chr9:98213755-98213805	GM06990	blood:	n/a
14	chr9:98221975-98222025	HepG2	liver:	n/a
15	chr9:98221975-98222025	NHBE	bronchial:	n/a
16	chr9:98210236-98210286	AoSMC	blood vessel:	n/a
17	chr9:98215821-98215871	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:98221619-98221669	HRCEpiC	kidney:	n/a
19	chr9:98213755-98213805	HEK293	kidney:	embryo
20	chr9:98212061-98212111	A549	lung:	n/a
21	chr9:98221619-98221669	GM06990	blood:	n/a
22	chr9:98221619-98221669	BJ	skin:	n/a
23	chr9:98212061-98212111	PFSK-1	brain:	n/a
24	chr9:98210236-98210286	HepG2	liver:	n/a
25	chr9:98210236-98210286	HRE	kidney:	n/a
26	chr9:98210236-98210286	HUVEC	blood vessel:	n/a
27	chr9:98221975-98222025	LNCaP	prostate:	n/a
28	chr9:98213755-98213805	NHBE	bronchial:	n/a
29	chr9:98221619-98221669	T-47D	breast:	n/a
30	chr9:98213755-98213805	MCF10A-Er-Src	breast:	n/a
31	chr9:98212061-98212111	AG10803	skin:	n/a
32	chr9:98210236-98210286	MCF-7	breast:	n/a
33	chr9:98213755-98213805	HCT-116	colon:	n/a
34	chr9:98213755-98213805	AoSMC	blood vessel:	n/a
35	chr9:98213755-98213805	Jurkat	blood:	n/a
36	chr9:98215821-98215871	AG09309	skin:	n/a
37	chr9:98213755-98213805	SAEC	small airway:	n/a
38	chr9:98221975-98222025	HNPCEpiC	eye:	n/a
39	chr9:98213755-98213805	PrEC	prostate:	n/a
40	chr9:98212061-98212111	NH-A	brain:	n/a
41	chr9:98213755-98213805	RPTEC	kidney:	n/a
42	chr9:98210236-98210286	BE2_C	brain:	n/a
43	chr9:98212061-98212111	H1-hESC	embryonic stem cell:	embryo
44	chr9:98221619-98221669	ovcar-3	ovarian:	n/a
45	chr9:98212061-98212111	NT2-D1	testis:	n/a
46	chr9:98221619-98221669	K562	blood:	n/a
47	chr9:98221619-98221669	GM19239	blood:	n/a
48	chr9:98221619-98221669	HCPEpiC	choroid plexus:	n/a
49	chr9:98210236-98210286	PFSK-1	brain:	n/a
50	chr9:98213755-98213805	HRCEpiC	kidney:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:98187807..98190501-chr9:98217714..98219257,2	MCF-7	breast:
2	chr9:98207334..98210169-chr9:98211282..98214476,3	K562	blood:
3	chr9:98202595..98206584-chr9:98206995..98209232,3	MCF-7	breast:
4	chr9:98228127..98229820-chr9:98239088..98240889,2	K562	blood:
5	chr9:98222888..98225027-chr9:98277335..98280257,3	K562	blood:
6	chr9:98218003..98222058-chr9:98271885..98274474,3	K562	blood:
7	chr9:98141744..98142409-chr9:98210461..98211518,3	MCF-7	breast:
8	chr9:98201937..98203643-chr9:98208903..98210438,2	K562	blood:
9	chr9:98227014..98229023-chr9:98271434..98274318,2	MCF-7	breast:
10	chr9:98210280..98213178-chr9:98213473..98216650,4	K562	blood:
11	chr9:98223864..98226761-chr9:98228381..98231062,3	K562	blood:
12	chr9:98211125..98213950-chr9:98219693..98221314,2	MCF-7	breast:
13	chr12:53297243..53298949-chr9:98222802..98225552,2	MCF-7	breast:
14	chr9:98223412..98227347-chr9:98253313..98257210,3	K562	blood:
15	chr9:98209521..98214013-chr9:98214744..98218073,4	K562	blood:
16	chr9:98227321..98228997-chr9:98229888..98232177,2	K562	blood:
17	chr9:98218196..98221051-chr9:98231021..98232882,2	K562	blood:
18	chr9:98214310..98216415-chr9:98227721..98230889,3	MCF-7	breast:
19	chr9:98187259..98193172-chr9:98208629..98217669,12	MCF-7	breast:
20	chr9:98222977..98229750-chr9:98267050..98274823,12	K562	blood:
21	chr9:98202143..98207025-chr9:98207845..98211987,5	K562	blood:
22	chr9:98223555..98229775-chr9:98269693..98275962,10	K562	blood:
23	chr9:98218910..98222494-chr9:98224731..98227835,5	K562	blood:
24	chr9:98223181..98225027-chr9:98277335..98280257,2	K562	blood:
25	chr9:98195732..98198631-chr9:98215123..98217873,2	K562	blood:
26	chr9:98197131..98198876-chr9:98214885..98216623,2	K562	blood:
27	chr9:98199109..98200665-chr9:98217953..98219861,2	K562	blood:
28	chr9:98223864..98226761-chr9:98228381..98231062,3	K562	blood:
29	chr9:98206913..98208735-chr9:98254383..98256847,2	MCF-7	breast:
30	chr9:98077820..98081322-chr9:98214829..98218712,4	K562	blood:
31	chr9:98210481..98212145-chr9:98266993..98269582,2	K562	blood:
32	chr9:98210232..98214386-chr9:98264282..98269915,4	K562	blood:
33	chr9:98222216..98224760-chr9:98225950..98227870,2	MCF-7	breast:
34	chr9:98214310..98216415-chr9:98227721..98230889,3	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PTCH1	hsa-miR-212-3p	chr9:98208705-98208699

Variant related genes	Relation type
PTCH1	TF binding region
PTCH1	CpG island
ENSG00000271155	chromatin interactions
ENSG00000271314	chromatin interactions
ENSG00000185920	chromatin interactions
ENSG00000158169	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000237857	chromatin interactions

Extended variants
information (count: 1110 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1110 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142840663	chr9:98208570-98208571	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs371565232	chr9:98208588-98208589	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs147428149	chr9:98208590-98208591	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35853197	chr9:98208633-98208634	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs563305974	chr9:98208652-98208653	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189667531	chr9:98208674-98208675	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs549817079	chr9:98208691-98208692	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs571418312	chr9:98208692-98208693	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs199541400	chr9:98208695-98208696	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs532516217	chr9:98208719-98208720	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs547364687	chr9:98208726-98208727	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs139801496	chr9:98208787-98208788	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs180910391	chr9:98208790-98208791	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs377349141	chr9:98208832-98208833	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183664296	chr9:98208838-98208839	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs116870287	chr9:98208853-98208854	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs571055004	chr9:98208854-98208855	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs538461949	chr9:98208860-98208861	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs79038600	chr9:98208866-98208867	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs541157672	chr9:98208941-98208942	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs189547730	chr9:98208948-98208949	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs114296708	chr9:98208954-98208955	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111532669	chr9:98208964-98208965	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563602531	chr9:98208975-98208976	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs568950108	chr9:98208987-98208988	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs181845728	chr9:98208990-98208991	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs372443101	chr9:98208993-98208994	Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs375424308	chr9:98209006-98209007	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs73540189	chr9:98209055-98209056	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574213014	chr9:98209067-98209068	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs45593537	chr9:98209078-98209079	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs142023898	chr9:98209085-98209086	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs149694348	chr9:98209090-98209091	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs552815682	chr9:98209091-98209092	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs548555988	chr9:98209094-98209095	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570317228	chr9:98209095-98209096	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs537791155	chr9:98209107-98209108	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs552784979	chr9:98209108-98209109	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374921697	chr9:98209143-98209144	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs367959747	chr9:98209149-98209150	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs56237839	chr9:98209156-98209157	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs201959324	chr9:98209186-98209187	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs56023271	chr9:98209213-98209214	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs143464326	chr9:98209214-98209215	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs150696398	chr9:98209225-98209226	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs368571026	chr9:98209227-98209228	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201357130	chr9:98209236-98209237	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs556722778	chr9:98209249-98209250	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs575473447	chr9:98209277-98209278	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372686352	chr9:98209282-98209283	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Chordoma	18071362	CNVD
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
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	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
Leukemia	18688285	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
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Neurodevelopmental disorder	22521361	CNVD
Basal cell carcinoma	21518781	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1272 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98189600-98210800	Weak transcription	Right Atrium	heart
2	chr9:98197200-98208800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr9:98197800-98209400	Weak transcription	Fetal Heart	heart
4	chr9:98200800-98211800	Weak transcription	Fetal Brain Male	brain
5	chr9:98202000-98224600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr9:98203200-98208800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr9:98203400-98208600	Weak transcription	Colonic Mucosa	Colon
8	chr9:98203600-98211200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr9:98204400-98209600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:98204400-98220400	Strong transcription	Fetal Intestine Large	intestine
11	chr9:98204600-98209000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr9:98204600-98209800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr9:98204600-98212800	Strong transcription	Fetal Lung	lung
14	chr9:98204600-98214400	Weak transcription	Osteobl	bone
15	chr9:98204800-98224400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr9:98205000-98209600	Strong transcription	HUES64 Cell Line	embryonic stem cell
17	chr9:98205000-98210000	Strong transcription	HUES48 Cell Line	embryonic stem cell
18	chr9:98205200-98209000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr9:98205200-98218000	Weak transcription	Small Intestine	intestine
20	chr9:98205400-98208800	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr9:98205600-98208600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr9:98205600-98212600	Weak transcription	Colon Smooth Muscle	Colon
23	chr9:98206000-98210800	Weak transcription	K562	blood
24	chr9:98206000-98216000	Weak transcription	Primary T cells from cord blood	blood
25	chr9:98206000-98224400	Weak transcription	HUVEC	blood vessel
26	chr9:98206000-98237600	Weak transcription	Psoas Muscle	Psoas
27	chr9:98206200-98221400	Strong transcription	Fetal Intestine Small	intestine
28	chr9:98206400-98210200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr9:98206400-98217600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr9:98206400-98218400	Weak transcription	NHEK	skin
31	chr9:98206600-98209600	Strong transcription	H1 Cell Line	embryonic stem cell
32	chr9:98206600-98209600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr9:98206600-98209600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr9:98206600-98209600	Strong transcription	Stomach Smooth Muscle	stomach
35	chr9:98206600-98209800	Strong transcription	HUES6 Cell Line	embryonic stem cell
36	chr9:98206600-98209800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr9:98206600-98209800	Strong transcription	Brain Cingulate Gyrus	brain
38	chr9:98206600-98209800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr9:98206600-98209800	Strong transcription	Fetal Muscle Leg	muscle
40	chr9:98206600-98209800	Strong transcription	Left Ventricle	heart
41	chr9:98206600-98210000	Strong transcription	Brain Anterior Caudate	brain
42	chr9:98206600-98210000	Strong transcription	Right Ventricle	heart
43	chr9:98206600-98210200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
44	chr9:98206600-98210400	Strong transcription	Fetal Muscle Trunk	muscle
45	chr9:98206600-98211400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr9:98206600-98212400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr9:98206600-98212600	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr9:98206600-98213200	Strong transcription	Lung	lung
49	chr9:98206600-98217200	Strong transcription	Liver	Liver
50	chr9:98206600-98220200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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