Variant report

Variant	nsv540362
Chromosome Location	chr9:140401645-140452700
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2320)
CpG islands
(count:1466)
Chromatin interactive
region (count:158)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:140406300-140406534	K562	blood:	n/a	n/a
2	ARID3A	chr9:140431001-140431055	K562	blood:	n/a	n/a
3	ARID3A	chr9:140429317-140429674	K562	blood:	n/a	n/a
4	ATF1	chr9:140406110-140406643	K562	blood:	n/a	n/a
5	ATF1	chr9:140413661-140413862	K562	blood:	n/a	n/a
6	ATF3	chr9:140406167-140406614	K562	blood:	n/a	n/a
7	ATF3	chr9:140429242-140429797	HepG2	liver:	n/a	n/a
8	ATF3	chr9:140411303-140411539	K562	blood:	n/a	n/a
9	ATF3	chr9:140429329-140429663	K562	blood:	n/a	n/a
10	ATF3	chr9:140429318-140429660	HepG2	liver:	n/a	n/a
11	ATF3	chr9:140429282-140429618	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr9:140429357-140429545	GM12878	blood:	n/a	n/a
13	ATF3	chr9:140412120-140413744	K562	blood:	n/a	n/a
14	ATF3	chr9:140411269-140411670	K562	blood:	n/a	n/a
15	ATF3	chr9:140444794-140445032	K562	blood:	n/a	n/a
16	ATF3	chr9:140429244-140429721	GM12878	blood:	n/a	n/a
17	ATF3	chr9:140429268-140429655	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF3	chr9:140406275-140406755	K562	blood:	n/a	n/a
19	BACH1	chr9:140445891-140445908	K562	blood:	n/a	n/a
20	BACH1	chr9:140445812-140446093	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr9:140444871-140445043	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr9:140405284-140405477	K562	blood:	n/a	n/a
23	BATF	chr9:140406312-140406518	GM12878	blood:	n/a	n/a
24	BATF	chr9:140440190-140440437	GM12878	blood:	n/a	n/a
25	BATF	chr9:140419827-140420433	GM12878	blood:	n/a	n/a
26	BATF	chr9:140406195-140406475	GM12878	blood:	n/a	n/a
27	BCL11A	chr9:140431189-140431465	GM12878	blood:	n/a	n/a
28	BCL11A	chr9:140429186-140429489	GM12878	blood:	n/a	n/a
29	BCL11A	chr9:140420033-140420454	GM12878	blood:	n/a	n/a
30	BCL3	chr9:140446495-140447277	A549	lung:	n/a	chr9:140446514-140446527
31	BCL3	chr9:140446470-140447336	A549	lung:	n/a	chr9:140446514-140446527
32	BCL3	chr9:140403490-140404024	GM12878	blood:	n/a	n/a
33	BCLAF1	chr9:140446664-140447061	GM12878	blood:	n/a	n/a
34	BHLHE40	chr9:140429271-140429664	A549	lung:	n/a	n/a
35	BHLHE40	chr9:140413599-140414372	K562	blood:	n/a	n/a
36	BHLHE40	chr9:140445842-140446042	GM12878	blood:	n/a	chr9:140445881-140445897
37	BHLHE40	chr9:140444689-140445061	HepG2	liver:	n/a	n/a
38	BHLHE40	chr9:140444679-140445082	K562	blood:	n/a	n/a
39	BHLHE40	chr9:140444730-140445039	GM12878	blood:	n/a	n/a
40	BHLHE40	chr9:140429259-140429660	K562	blood:	n/a	n/a
41	BHLHE40	chr9:140406121-140406881	K562	blood:	n/a	n/a
42	BHLHE40	chr9:140429269-140429634	GM12878	blood:	n/a	n/a
43	BHLHE40	chr9:140419864-140420058	GM12878	blood:	n/a	n/a
44	BHLHE40	chr9:140446341-140446464	K562	blood:	n/a	n/a
45	BHLHE40	chr9:140444731-140445029	A549	lung:	n/a	n/a
46	BHLHE40	chr9:140445821-140446098	K562	blood:	n/a	chr9:140445881-140445897
47	BHLHE40	chr9:140429303-140429729	HepG2	liver:	n/a	n/a
48	BRCA1	chr9:140445938-140446071	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr9:140444741-140444956	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr9:140405434-140405481	Hela-S3	cervix:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140447608-140447658	K562	blood:	n/a
2	chr9:140446240-140446290	HEEpiC	esophagus:	n/a
3	chr9:140447608-140447658	K562	blood:	n/a
4	chr9:140446240-140446290	HEEpiC	esophagus:	n/a
5	chr9:140446458-140446508	HL-60	blood:	n/a
6	chr9:140409915-140409965	NB4	blood:	n/a
7	chr9:140408634-140408684	SAEC	small airway:	n/a
8	chr9:140444966-140445016	BE2_C	brain:	n/a
9	chr9:140417855-140417905	GM12891	blood:	n/a
10	chr9:140425395-140425445	HEEpiC	esophagus:	n/a
11	chr9:140406894-140406944	H1-hESC	embryonic stem cell:	embryo
12	chr9:140406894-140406944	HUVEC	blood vessel:	n/a
13	chr9:140446240-140446290	HCM	heart:	n/a
14	chr9:140419935-140419985	NHBE	bronchial:	n/a
15	chr9:140447608-140447658	MCF10A-Er-Src	breast:	n/a
16	chr9:140446458-140446508	AG09309	skin:	n/a
17	chr9:140444966-140445016	SK-N-SH	brain:	n/a
18	chr9:140418776-140418826	MCF-7	breast:	n/a
19	chr9:140437281-140437331	HL-60	blood:	n/a
20	chr9:140419935-140419985	PANC-1	pancreas:	n/a
21	chr9:140446656-140446706	HCF	heart:	n/a
22	chr9:140446993-140447043	NB4	blood:	n/a
23	chr9:140444966-140445016	HRPEpiC	eye:	n/a
24	chr9:140406645-140406695	SKMC	muscle:	n/a
25	chr9:140437771-140437821	MCF-7	breast:	n/a
26	chr9:140446240-140446290	AoSMC	blood vessel:	n/a
27	chr9:140406123-140406173	AG09309	skin:	n/a
28	chr9:140446823-140446873	GM12892	blood:	n/a
29	chr9:140444378-140444428	GM12891	blood:	n/a
30	chr9:140437281-140437331	HNPCEpiC	eye:	n/a
31	chr9:140437017-140437067	BJ	skin:	n/a
32	chr9:140409915-140409965	HCPEpiC	choroid plexus:	n/a
33	chr9:140444966-140445016	NHBE	bronchial:	n/a
34	chr9:140437771-140437821	H1-hESC	embryonic stem cell:	embryo
35	chr9:140406645-140406695	GM19239	blood:	n/a
36	chr9:140446823-140446873	HCM	heart:	n/a
37	chr9:140446458-140446508	SK-N-SH_RA	brain:	n/a
38	chr9:140449460-140449510	AG10803	skin:	n/a
39	chr9:140409915-140409965	HRCEpiC	kidney:	n/a
40	chr9:140444966-140445016	GM12892	blood:	n/a
41	chr9:140406645-140406695	SAEC	small airway:	n/a
42	chr9:140406645-140406695	H1-hESC	embryonic stem cell:	embryo
43	chr9:140444378-140444428	HEEpiC	esophagus:	n/a
44	chr9:140406123-140406173	MCF-7	breast:	n/a
45	chr9:140437281-140437331	SK-N-MC	brain:	n/a
46	chr9:140425395-140425445	Hepatocyte	liver:	n/a
47	chr9:140406123-140406173	BE2_C	brain:	n/a
48	chr9:140417855-140417905	LNCaP	prostate:	n/a
49	chr9:140437281-140437331	PrEC	prostate:	n/a
50	chr9:140447608-140447658	NB4	blood:	n/a

(count:158 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr17:41464359..41467817-chr9:140403952..140405475,5	MCF-7	breast:
2	chr9:140447442..140450048-chr9:140483763..140485400,2	MCF-7	breast:
3	chr9:140352080..140354787-chr9:140444624..140448715,3	MCF-7	breast:
4	chr17:41380386..41382219-chr9:140405478..140406978,2	MCF-7	breast:
5	chr9:140444055..140447780-chr9:140498087..140502451,7	MCF-7	breast:
6	chr9:140428970..140429596-chr9:140445585..140446090,2	MCF-7	breast:
7	chr17:41466027..41467892-chr9:140403958..140405470,2	MCF-7	breast:
8	chr9:140317304..140318861-chr9:140444413..140447408,2	K562	blood:
9	chr9:140406090..140408073-chr9:140408484..140412188,3	K562	blood:
10	chr9:140385602..140387946-chr9:140412336..140414686,2	K562	blood:
11	chr3:73158225..73159978-chr9:140403956..140405478,2	K562	blood:
12	chr9:140428683..140431076-chr9:140437788..140439883,2	K562	blood:
13	chr17:41398704..41402669-chr9:140403952..140406979,22	K562	blood:
14	chr9:140397655..140400167-chr9:140400822..140403662,2	K562	blood:
15	chr9:140204438..140205971-chr9:140437533..140440193,2	MCF-7	breast:
16	chr10:88699240..88699757-chr9:140425167..140425667,2	MCF-7	breast:
17	chr9:140431100..140433802-chr9:140474645..140476543,2	K562	blood:
18	chr9:140406492..140409440-chr9:140417122..140420049,2	MCF-7	breast:
19	chr9:140450468..140452580-chr9:140456810..140458829,2	MCF-7	breast:
20	chr9:140448023..140449747-chr9:140465385..140467974,2	K562	blood:
21	chr9:140432353..140434549-chr9:140437572..140440082,2	K562	blood:
22	chr9:140430947..140433586-chr9:140435095..140437160,2	K562	blood:
23	chr9:140434775..140436378-chr9:140438386..140440079,2	K562	blood:
24	chr17:41464701..41468607-chr9:140403951..140406971,9	K562	blood:
25	chr9:140317630..140318209-chr9:140420130..140421092,2	MCF-7	breast:
26	chr9:140189647..140191629-chr9:140408835..140411014,2	MCF-7	breast:
27	chr9:140431806..140435662-chr9:140440796..140444107,4	K562	blood:
28	chr9:140419598..140421857-chr9:140445264..140447853,2	MCF-7	breast:
29	chr9:140420711..140423726-chr9:140426984..140429291,3	K562	blood:
30	chr9:140118466..140120300-chr9:140443395..140446342,2	MCF-7	breast:
31	chr9:140446439..140449718-chr9:140469897..140473461,3	K562	blood:
32	chr9:140430080..140431601-chr9:140437966..140440152,2	MCF-7	breast:
33	chr9:140444528..140447263-chr9:140504669..140508200,5	MCF-7	breast:
34	chr9:140444557..140448587-chr9:140470804..140473699,6	MCF-7	breast:
35	chr9:140427918..140430895-chr9:140433135..140434802,2	K562	blood:
36	chr9:140418643..140420555-chr9:140421259..140423904,2	K562	blood:
37	chr9:140354790..140356755-chr9:140406317..140408071,2	K562	blood:
38	chr3:73158225..73161441-chr9:140403956..140406956,4	K562	blood:
39	chr9:140426937..140428831-chr9:140509967..140512178,2	K562	blood:
40	chr9:140332825..140334847-chr9:140416477..140418783,2	MCF-7	breast:
41	chr9:140170828..140173620-chr9:140446274..140448338,3	K562	blood:
42	chr9:140192004..140196032-chr9:140413457..140417425,3	MCF-7	breast:
43	chr11:62607627..62609127-chr9:140403971..140406953,2	K562	blood:
44	chr9:140433778..140436154-chr9:140439881..140442046,2	MCF-7	breast:
45	chr9:140423153..140425130-chr9:140444999..140447899,2	MCF-7	breast:
46	chr9:140402660..140405211-chr9:140405983..140408009,2	MCF-7	breast:
47	chr9:140332776..140334313-chr9:140412829..140415749,2	MCF-7	breast:
48	chr9:140434663..140439673-chr9:140442906..140447183,7	MCF-7	breast:
49	chr9:140401353..140403296-chr9:140405117..140407444,2	K562	blood:
50	chr9:140323536..140326071-chr9:140429160..140430978,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR85-1	chr9:140412889-140412899	NONHSAT135734
2	lnc-WDR85-1	chr9:140411319-140412418	NONHSAT135734

No data

Variant related genes	Relation type
ENSG00000263933	TF binding region
PNPLA7	TF binding region
MRPL41	TF binding region
ENSG00000263933	CpG island
PNPLA7	CpG island
MRPL41	CpG island
ENSG00000133316	chromatin interactions
ENSG00000187609	chromatin interactions
ENSG00000176101	chromatin interactions
ENSG00000176248	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000178980	chromatin interactions
ENSG00000263933	chromatin interactions
ENSG00000165417	chromatin interactions
ENSG00000197191	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000188747	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000198113	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000203993	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2469 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:2469 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557772382	chr9:140401646-140401647	Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs191897506	chr9:140401673-140401674	Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs149619548	chr9:140401797-140401798	Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs555865086	chr9:140401815-140401816	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs557300186	chr9:140401822-140401823	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs573849149	chr9:140401823-140401824	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs572170587	chr9:140401981-140401982	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs541178686	chr9:140401982-140401983	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564263368	chr9:140401994-140401995	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs542867804	chr9:140402005-140402006	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs533252021	chr9:140402058-140402059	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs559866521	chr9:140402061-140402062	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs528620812	chr9:140402075-140402076	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs545065555	chr9:140402095-140402096	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs565328084	chr9:140402123-140402124	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs543040091	chr9:140402147-140402148	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs530814235	chr9:140402152-140402153	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs115572089	chr9:140402168-140402169	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs183757362	chr9:140402189-140402190	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs188478601	chr9:140402191-140402192	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs372856629	chr9:140402276-140402277	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs144357203	chr9:140402277-140402278	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs180893278	chr9:140402296-140402297	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562925476	chr9:140402371-140402372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546823328	chr9:140402397-140402398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs79626304	chr9:140402423-140402424	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565627189	chr9:140402425-140402426	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs534759970	chr9:140402480-140402481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557569687	chr9:140402492-140402493	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs187016773	chr9:140402592-140402593	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114391885	chr9:140402741-140402742	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557267389	chr9:140402748-140402749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574014447	chr9:140402795-140402796	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372719510	chr9:140402799-140402800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs190702294	chr9:140402802-140402803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542831151	chr9:140402804-140402805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371943308	chr9:140402815-140402816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181571115	chr9:140402846-140402847	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs545438651	chr9:140402847-140402848	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs565245289	chr9:140402861-140402862	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs35508998	chr9:140402863-140402864	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187107156	chr9:140402875-140402876	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs12351541	chr9:140402881-140402882	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs543728438	chr9:140402890-140402891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141494424	chr9:140402913-140402914	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs546784288	chr9:140402915-140402916	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146329747	chr9:140402932-140402933	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563453960	chr9:140402996-140402997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191141531	chr9:140403007-140403008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs139524924	chr9:140403011-140403012	Weak transcription	Chromatin interactive region	1 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:1859 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140376800-140444000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:140377000-140437000	Weak transcription	Left Ventricle	heart
3	chr9:140377200-140420200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr9:140386600-140403200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:140386600-140403400	Weak transcription	Aorta	Aorta
6	chr9:140388400-140404000	Weak transcription	Brain Hippocampus Middle	brain
7	chr9:140388400-140425200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr9:140389000-140403800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:140392000-140425800	Weak transcription	Primary T cells from cord blood	blood
10	chr9:140393000-140417800	Weak transcription	Fetal Brain Female	brain
11	chr9:140393000-140429400	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr9:140393800-140403400	Weak transcription	Primary B cells from cord blood	blood
13	chr9:140394000-140419800	Weak transcription	Primary B cells from peripheral blood	blood
14	chr9:140394000-140429200	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr9:140394800-140415600	Weak transcription	Brain Angular Gyrus	brain
16	chr9:140395000-140414000	Weak transcription	Brain Substantia Nigra	brain
17	chr9:140395200-140409400	Weak transcription	Spleen	Spleen
18	chr9:140396000-140404000	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr9:140396200-140403400	Weak transcription	Brain Cingulate Gyrus	brain
20	chr9:140396200-140403600	Weak transcription	Pancreas	Pancrea
21	chr9:140396200-140409200	Weak transcription	Right Ventricle	heart
22	chr9:140396400-140403400	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr9:140396400-140429200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr9:140396600-140403400	Weak transcription	Brain Anterior Caudate	brain
25	chr9:140396600-140403600	Weak transcription	Liver	Liver
26	chr9:140396800-140406200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr9:140400000-140401800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr9:140400200-140403400	Weak transcription	Adipose Nuclei	Adipose
29	chr9:140400400-140402000	Enhancers	NHLF	lung
30	chr9:140400400-140403400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr9:140400800-140401800	Enhancers	NHDF-Ad	bronchial
32	chr9:140400800-140406200	Weak transcription	Stomach Mucosa	stomach
33	chr9:140401400-140401800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr9:140401400-140403400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr9:140401400-140413600	Weak transcription	Gastric	stomach
36	chr9:140401600-140401800	Enhancers	HSMMtube	muscle
37	chr9:140401600-140402000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr9:140401600-140403400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr9:140401600-140406400	Weak transcription	Ovary	ovary
40	chr9:140401800-140402000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr9:140401800-140403800	Weak transcription	HSMMtube	muscle
42	chr9:140402000-140409400	Weak transcription	Fetal Stomach	stomach
43	chr9:140403200-140404000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr9:140403400-140403600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
45	chr9:140403400-140403800	Strong transcription	Brain Cingulate Gyrus	brain
46	chr9:140403400-140404200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr9:140403400-140404200	Strong transcription	Primary B cells from cord blood	blood
48	chr9:140403400-140404200	Strong transcription	Adipose Nuclei	Adipose
49	chr9:140403400-140404200	Strong transcription	Aorta	Aorta
50	chr9:140403400-140404200	Strong transcription	Brain Anterior Caudate	brain

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