Variant report

Variant	nsv540360
Chromosome Location	chr9:140360372-140391898
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:447)
CpG islands
(count:793)
Chromatin interactive
region (count:71)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:447 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:140388745-140388839	K562	blood:	n/a	n/a
2	ATF1	chr9:140385237-140385607	K562	blood:	n/a	n/a
3	ATF1	chr9:140386077-140386838	K562	blood:	n/a	n/a
4	ATF1	chr9:140376674-140377053	K562	blood:	n/a	n/a
5	ATF2	chr9:140376547-140376853	GM12878	blood:	n/a	n/a
6	ATF3	chr9:140376711-140377025	K562	blood:	n/a	n/a
7	ATF3	chr9:140376631-140377006	K562	blood:	n/a	n/a
8	BACH1	chr9:140376512-140377007	K562	blood:	n/a	n/a
9	BCL11A	chr9:140376611-140376765	GM12878	blood:	n/a	n/a
10	BCL3	chr9:140366048-140366259	GM12878	blood:	n/a	n/a
11	BHLHE40	chr9:140376543-140377273	K562	blood:	n/a	n/a
12	BHLHE40	chr9:140376682-140377094	HepG2	liver:	n/a	n/a
13	BHLHE40	chr9:140376746-140376930	GM12878	blood:	n/a	n/a
14	BHLHE40	chr9:140386093-140386833	K562	blood:	n/a	n/a
15	BHLHE40	chr9:140388628-140388967	K562	blood:	n/a	n/a
16	BHLHE40	chr9:140387537-140387771	K562	blood:	n/a	n/a
17	BHLHE40	chr9:140376779-140377018	A549	lung:	n/a	n/a
18	CBX3	chr9:140370180-140370445	K562	blood:	n/a	n/a
19	CBX3	chr9:140376496-140377104	K562	blood:	n/a	n/a
20	CBX3	chr9:140388579-140388820	K562	blood:	n/a	n/a
21	CBX3	chr9:140370108-140370501	K562	blood:	n/a	n/a
22	CBX3	chr9:140386246-140386901	K562	blood:	n/a	n/a
23	CBX3	chr9:140387464-140387854	K562	blood:	n/a	n/a
24	CBX3	chr9:140388325-140388963	K562	blood:	n/a	n/a
25	CBX3	chr9:140367397-140367722	K562	blood:	n/a	n/a
26	CCNT2	chr9:140388585-140388851	K562	blood:	n/a	n/a
27	CCNT2	chr9:140376819-140377100	K562	blood:	n/a	n/a
28	CCNT2	chr9:140386132-140386794	K562	blood:	n/a	chr9:140386518-140386538
29	CEBPB	chr9:140376448-140377055	MCF-7	breast:	n/a	n/a
30	CEBPB	chr9:140386116-140386476	K562	blood:	n/a	n/a
31	CEBPB	chr9:140376550-140376937	IMR90	lung:	n/a	n/a
32	CEBPB	chr9:140376575-140377018	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr9:140376623-140376842	A549	lung:	n/a	n/a
34	CEBPB	chr9:140376625-140377105	K562	blood:	n/a	n/a
35	CEBPB	chr9:140376555-140377066	MCF-7	breast:	n/a	n/a
36	CHD2	chr9:140386271-140386726	K562	blood:	n/a	n/a
37	CHD2	chr9:140382416-140382938	HepG2	liver:	n/a	n/a
38	CHD2	chr9:140376726-140376945	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr9:140373800-140373950	HepG2	liver:	n/a	n/a
40	CTCF	chr9:140360360-140360510	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr9:140374540-140374690	HepG2	liver:	n/a	chr9:140374587-140374596
42	CTCF	chr9:140389273-140389292	GM13976	blood:	n/a	n/a
43	CTCF	chr9:140373760-140373910	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr9:140374543-140374563	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr9:140375780-140375930	HepG2	liver:	n/a	n/a
46	CTCF	chr9:140390180-140390330	HepG2	liver:	n/a	chr9:140390299-140390312
47	CTCF	chr9:140388521-140388744	K562	blood:	n/a	n/a
48	CUX1	chr9:140388561-140388734	K562	blood:	n/a	n/a
49	CUX1	chr9:140386282-140386862	K562	blood:	n/a	n/a
50	E2F6	chr9:140387535-140387899	K562	blood:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140380767-140380817	U87	brain:	n/a
2	chr9:140361383-140361433	SK-N-SH	brain:	n/a
3	chr9:140380767-140380817	HCT-116	colon:	n/a
4	chr9:140388604-140388654	HCF	heart:	n/a
5	chr9:140374463-140374513	MCF-7	breast:	n/a
6	chr9:140372956-140373006	PrEC	prostate:	n/a
7	chr9:140361383-140361433	HRCEpiC	kidney:	n/a
8	chr9:140388523-140388573	SK-N-SH	brain:	n/a
9	chr9:140375580-140375630	IMR90	lung:	fetal
10	chr9:140375580-140375630	HUVEC	blood vessel:	n/a
11	chr9:140389750-140389800	SKMC	muscle:	n/a
12	chr9:140388604-140388654	HepG2	liver:	n/a
13	chr9:140372956-140373006	MCF-7	breast:	n/a
14	chr9:140374285-140374335	NH-A	brain:	n/a
15	chr9:140374285-140374335	AG09319	gingival:	n/a
16	chr9:140374463-140374513	Caco-2	colon:	n/a
17	chr9:140374285-140374335	HCT-116	colon:	n/a
18	chr9:140375580-140375630	HMEC	breast:	n/a
19	chr9:140361383-140361433	A549	lung:	n/a
20	chr9:140377789-140377839	NHBE	bronchial:	n/a
21	chr9:140388604-140388654	ProgFib	skin:	n/a
22	chr9:140388604-140388654	AG09309	skin:	n/a
23	chr9:140375757-140375807	NH-A	brain:	n/a
24	chr9:140380767-140380817	BE2_C	brain:	n/a
25	chr9:140369012-140369062	U87	brain:	n/a
26	chr9:140361383-140361433	NH-A	brain:	n/a
27	chr9:140377789-140377839	U87	brain:	n/a
28	chr9:140374463-140374513	BE2_C	brain:	n/a
29	chr9:140380767-140380817	K562	blood:	n/a
30	chr9:140369012-140369062	BJ	skin:	n/a
31	chr9:140369012-140369062	RPTEC	kidney:	n/a
32	chr9:140377789-140377839	HUVEC	blood vessel:	n/a
33	chr9:140375757-140375807	AG04449	skin:	fetal
34	chr9:140388604-140388654	NHBE	bronchial:	n/a
35	chr9:140391480-140391530	Jurkat	blood:	n/a
36	chr9:140372956-140373006	A549	lung:	n/a
37	chr9:140374463-140374513	SKMC	muscle:	n/a
38	chr9:140380767-140380817	HepG2	liver:	n/a
39	chr9:140372956-140373006	GM12878	blood:	n/a
40	chr9:140372956-140373006	HIPEpiC	eye:	n/a
41	chr9:140361383-140361433	ovcar-3	ovarian:	n/a
42	chr9:140372956-140373006	HMEC	breast:	n/a
43	chr9:140374285-140374335	HRE	kidney:	n/a
44	chr9:140361383-140361433	HRE	kidney:	n/a
45	chr9:140380767-140380817	Caco-2	colon:	n/a
46	chr9:140391480-140391530	IMR90	lung:	fetal
47	chr9:140375757-140375807	AG10803	skin:	n/a
48	chr9:140391480-140391530	HEK293	kidney:	embryo
49	chr9:140375757-140375807	HCM	heart:	n/a
50	chr9:140380767-140380817	GM06990	blood:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:140381904..140384229-chr9:140391274..140393120,2	MCF-7	breast:
2	chr9:140195115..140197812-chr9:140370800..140372324,2	MCF-7	breast:
3	chr9:140366440..140369385-chr9:140386495..140388983,2	K562	blood:
4	chr9:140358518..140361237-chr9:140374816..140376548,2	K562	blood:
5	chr9:140355434..140357921-chr9:140362408..140364687,2	K562	blood:
6	chr9:140386948..140388697-chr9:140392621..140394758,2	K562	blood:
7	chr9:140193294..140197517-chr9:140375531..140379734,5	K562	blood:
8	chr9:140366776..140369288-chr9:140374545..140377101,2	K562	blood:
9	chr9:140347395..140351065-chr9:140385610..140390076,3	K562	blood:
10	chr9:140195239..140196828-chr9:140374464..140377100,2	MCF-7	breast:
11	chr9:140333557..140336034-chr9:140380943..140382564,2	MCF-7	breast:
12	chr9:140361859..140363963-chr9:140372248..140374801,2	K562	blood:
13	chr9:140352543..140355351-chr9:140391040..140393280,2	K562	blood:
14	chr9:140352137..140355481-chr9:140359120..140360959,3	MCF-7	breast:
15	chr9:140369670..140372957-chr9:140374398..140376940,3	K562	blood:
16	chr9:140366440..140369385-chr9:140386495..140388983,2	K562	blood:
17	chr9:140170582..140172704-chr9:140385378..140387482,2	K562	blood:
18	chr9:140352296..140354160-chr9:140364137..140366294,2	K562	blood:
19	chr9:140138434..140140488-chr9:140371095..140373101,2	MCF-7	breast:
20	chr9:140358054..140360809-chr9:140375764..140378242,2	MCF-7	breast:
21	chr9:140194392..140197374-chr9:140369400..140371103,2	K562	blood:
22	chr9:140195654..140197517-chr9:140377821..140379734,2	K562	blood:
23	chr9:140374520..140376870-chr9:140381387..140383269,3	MCF-7	breast:
24	chr9:140347395..140349788-chr9:140384770..140388598,3	K562	blood:
25	chr9:140368012..140372188-chr9:140372653..140377700,7	MCF-7	breast:
26	chr9:140358080..140361646-chr9:140366206..140369326,3	K562	blood:
27	chr9:140377265..140380212-chr9:140382477..140384358,2	MCF-7	breast:
28	chr9:140374954..140376826-chr9:140380949..140383700,2	K562	blood:
29	chr9:140374712..140376719-chr9:140389156..140391051,2	MCF-7	breast:
30	chr9:140381904..140384229-chr9:140391274..140393120,2	MCF-7	breast:
31	chr9:140385602..140387946-chr9:140412336..140414686,2	K562	blood:
32	chr9:140353655..140356104-chr9:140385846..140387400,2	MCF-7	breast:
33	chr9:140209677..140212013-chr9:140385479..140387034,2	K562	blood:
34	chr9:140352396..140354372-chr9:140365202..140367744,2	MCF-7	breast:
35	chr9:140345509..140349478-chr9:140382824..140385336,3	K562	blood:
36	chr9:140385364..140389907-chr9:140391534..140397085,5	MCF-7	breast:
37	chr9:140354317..140357067-chr9:140368182..140370239,2	MCF-7	breast:
38	chr9:140353780..140356340-chr9:140380016..140383276,3	K562	blood:
39	chr9:140385694..140388620-chr9:140402959..140406743,3	K562	blood:
40	chr9:140361462..140363724-chr9:140374237..140376572,2	MCF-7	breast:
41	chr9:140374535..140376997-chr9:140379595..140382767,4	MCF-7	breast:
42	chr9:140390861..140392833-chr9:140394887..140396541,2	MCF-7	breast:
43	chr9:140328788..140330687-chr9:140382717..140384936,2	K562	blood:
44	chr9:140358518..140361237-chr9:140374816..140376548,2	K562	blood:
45	chr9:140385373..140390339-chr9:140393084..140398390,8	MCF-7	breast:
46	chr9:140361836..140364169-chr9:140371733..140373898,2	K562	blood:
47	chr9:140195867..140198276-chr9:140376571..140378475,2	MCF-7	breast:
48	chr9:140377045..140378867-chr9:140380603..140382500,2	K562	blood:
49	chr9:140192588..140195747-chr9:140385238..140387979,3	MCF-7	breast:
50	chr9:140353788..140359040-chr9:140385385..140389520,8	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOXA1-2	chr9:140383407-140384391	NONHSAT135733
2	lnc-NOXA1-2	chr9:140383507-140383567	NONHSAT135732
3	lnc-NELF-2	chr9:140385913-140386550	NONHSAT135731
4	lnc-NOXA1-2	chr9:140383224-140383341	NONHSAT135733
5	lnc-NELF-2	chr9:140382990-140383726	NONHSAT135731
6	lnc-NOXA1-2	chr9:140383003-140383341	NONHSAT135732

No data

Variant related genes	Relation type
PNPLA7	TF binding region
PNPLA7	CpG island
ENSG00000260996	chromatin interactions
ENSG00000198113	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000188833	chromatin interactions
ENSG00000188229	chromatin interactions

Extended variants
information (count: 1410 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:1410 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76844712	chr9:140360399-140360400	Weak transcription ZNF genes & repeats Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs371969138	chr9:140360466-140360467	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs551559070	chr9:140360496-140360497	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs567975528	chr9:140360499-140360500	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs565423331	chr9:140360547-140360548	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs375734889	chr9:140360548-140360549	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs530800605	chr9:140360576-140360577	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs370084262	chr9:140360586-140360587	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs550913701	chr9:140360588-140360589	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs567668057	chr9:140360611-140360612	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs542466116	chr9:140360617-140360618	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs552738436	chr9:140360620-140360621	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs536920109	chr9:140360626-140360627	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs572848666	chr9:140360636-140360637	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs536899903	chr9:140360699-140360700	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs79610359	chr9:140360783-140360784	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs567054752	chr9:140360845-140360846	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs539250337	chr9:140360867-140360868	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs118014901	chr9:140360870-140360871	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs577708696	chr9:140360944-140360945	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs544880429	chr9:140360948-140360949	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs375812369	chr9:140360963-140360964	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs79284093	chr9:140360992-140360993	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs80320455	chr9:140361002-140361003	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186954414	chr9:140361013-140361014	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542497869	chr9:140361051-140361052	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs371851351	chr9:140361060-140361061	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs552875715	chr9:140361067-140361068	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs572946424	chr9:140361079-140361080	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs201466544	chr9:140361082-140361083	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs545227687	chr9:140361116-140361117	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs28641033	chr9:140361121-140361122	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs556692533	chr9:140361126-140361127	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564939200	chr9:140361147-140361148	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs530990246	chr9:140361164-140361165	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs28628583	chr9:140361170-140361171	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs28407939	chr9:140361188-140361189	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs28376262	chr9:140361195-140361196	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs28410086	chr9:140361198-140361199	Weak transcription ZNF genes & repeats Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs544402236	chr9:140361213-140361214	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs9414732	chr9:140361224-140361225	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561234567	chr9:140361252-140361253	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs530153476	chr9:140361262-140361263	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs547293645	chr9:140361269-140361270	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs56231361	chr9:140361273-140361274	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs532589065	chr9:140361279-140361280	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs552691345	chr9:140361285-140361286	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs28540352	chr9:140361293-140361294	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs28552828	chr9:140361296-140361297	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs569372275	chr9:140361311-140361312	Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140354200-140370200	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:140354400-140362600	Weak transcription	Right Atrium	heart
3	chr9:140354400-140369600	Weak transcription	Aorta	Aorta
4	chr9:140354400-140369600	Weak transcription	Liver	Liver
5	chr9:140354400-140370200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:140354400-140370200	Weak transcription	Brain Angular Gyrus	brain
7	chr9:140354600-140370200	Weak transcription	Brain Anterior Caudate	brain
8	chr9:140354600-140370200	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr9:140354600-140370200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr9:140354600-140370400	Weak transcription	Ovary	ovary
11	chr9:140354800-140369600	Weak transcription	Adipose Nuclei	Adipose
12	chr9:140355800-140361000	Enhancers	Fetal Brain Male	brain
13	chr9:140356400-140360800	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr9:140356600-140377000	Weak transcription	Rectal Smooth Muscle	rectum
15	chr9:140357600-140360400	Flanking Active TSS	HepG2	liver
16	chr9:140358200-140361800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
17	chr9:140358400-140370200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr9:140358600-140361400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr9:140358800-140360600	Weak transcription	Fetal Brain Female	brain
20	chr9:140359000-140361400	Weak transcription	Gastric	stomach
21	chr9:140359000-140370200	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr9:140359000-140372400	Weak transcription	Pancreas	Pancrea
23	chr9:140359000-140373200	Weak transcription	Right Ventricle	heart
24	chr9:140359600-140369600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
25	chr9:140359800-140360400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
26	chr9:140359800-140360400	Enhancers	Spleen	Spleen
27	chr9:140359800-140369400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr9:140360000-140361400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr9:140360400-140360800	Enhancers	HepG2	liver
30	chr9:140360400-140365400	Weak transcription	Spleen	Spleen
31	chr9:140360600-140361200	Enhancers	Fetal Brain Female	brain
32	chr9:140360800-140361000	Bivalent Enhancer	HepG2	liver
33	chr9:140361000-140362600	Weak transcription	Fetal Brain Male	brain
34	chr9:140361200-140362600	Weak transcription	Fetal Brain Female	brain
35	chr9:140361400-140361600	Genic enhancers	Gastric	stomach
36	chr9:140361400-140362000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:140361400-140362000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr9:140361600-140362000	Strong transcription	Gastric	stomach
39	chr9:140361800-140362000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:140361800-140363000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr9:140362000-140368200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:140362000-140373800	Weak transcription	Gastric	stomach
43	chr9:140362600-140363800	Enhancers	Fetal Brain Female	brain
44	chr9:140362600-140364400	Enhancers	Fetal Brain Male	brain
45	chr9:140363000-140364400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:140363000-140366400	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr9:140363600-140365800	Enhancers	Primary hematopoietic stem cells	blood
48	chr9:140363600-140365800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr9:140363800-140368400	Weak transcription	Fetal Brain Female	brain
50	chr9:140364200-140364400	Bivalent Enhancer	Dnd41	blood

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