Variant report

Variant	esv3329093
Chromosome Location	chr9:140338364-140364635
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1727)
CpG islands
(count:1833)
Chromatin interactive
region (count:114)
LncRNA
region (count:0)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1727 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:140339716-140339973	K562	blood:	n/a	n/a
2	ARID3A	chr9:140353775-140353946	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:140349264-140349724	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:140339748-140340324	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:140349505-140349575	K562	blood:	n/a	n/a
6	ATF1	chr9:140353686-140354042	K562	blood:	n/a	n/a
7	ATF2	chr9:140339754-140340081	GM12878	blood:	n/a	n/a
8	ATF2	chr9:140339651-140340225	GM12878	blood:	n/a	n/a
9	ATF2	chr9:140353700-140354020	GM12878	blood:	n/a	n/a
10	ATF2	chr9:140356259-140356799	GM12878	blood:	n/a	n/a
11	ATF3	chr9:140353730-140354018	K562	blood:	n/a	chr9:140353933-140353942
12	ATF3	chr9:140339807-140340056	K562	blood:	n/a	n/a
13	ATF3	chr9:140339735-140340110	K562	blood:	n/a	n/a
14	BACH1	chr9:140353567-140353571	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr9:140348915-140348937	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr9:140339767-140340162	GM12878	blood:	n/a	n/a
17	BATF	chr9:140339791-140340143	GM12878	blood:	n/a	n/a
18	BCLAF1	chr9:140339683-140340185	GM12878	blood:	n/a	chr9:140340123-140340136
19	BHLHE40	chr9:140360026-140360264	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:140349078-140349719	HepG2	liver:	n/a	n/a
21	BHLHE40	chr9:140339661-140340154	K562	blood:	n/a	n/a
22	BHLHE40	chr9:140354272-140354390	K562	blood:	n/a	n/a
23	BHLHE40	chr9:140344849-140345128	GM12878	blood:	n/a	n/a
24	BHLHE40	chr9:140340634-140340642	K562	blood:	n/a	n/a
25	BHLHE40	chr9:140356258-140356800	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:140339639-140340255	GM12878	blood:	n/a	n/a
27	BHLHE40	chr9:140344739-140345154	HepG2	liver:	n/a	n/a
28	BHLHE40	chr9:140345383-140345496	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:140353589-140353958	HepG2	liver:	n/a	chr9:140353759-140353775 chr9:140353733-140353749
30	BHLHE40	chr9:140349306-140349664	K562	blood:	n/a	n/a
31	BHLHE40	chr9:140353464-140354014	K562	blood:	n/a	chr9:140353759-140353775 chr9:140353733-140353749
32	BHLHE40	chr9:140353600-140354010	GM12878	blood:	n/a	chr9:140353759-140353775 chr9:140353733-140353749
33	BHLHE40	chr9:140356194-140356914	K562	blood:	n/a	n/a
34	BHLHE40	chr9:140339825-140340146	HepG2	liver:	n/a	n/a
35	BRCA1	chr9:140348268-140348306	GM12878	blood:	n/a	n/a
36	BRCA1	chr9:140353762-140354035	GM12878	blood:	n/a	n/a
37	BRCA1	chr9:140353673-140354305	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr9:140351138-140351173	HepG2	liver:	n/a	n/a
39	BRCA1	chr9:140353726-140353910	H1-hESC	embryonic stem cell:	n/a	n/a
40	BRCA1	chr9:140339618-140340058	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr9:140356266-140356324	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr9:140353715-140353990	HepG2	liver:	n/a	n/a
43	CBX3	chr9:140339698-140340095	K562	blood:	n/a	n/a
44	CBX3	chr9:140344575-140344848	K562	blood:	n/a	n/a
45	CBX3	chr9:140356110-140356583	K562	blood:	n/a	n/a
46	CCNT2	chr9:140348445-140348786	K562	blood:	n/a	chr9:140348741-140348750
47	CCNT2	chr9:140353203-140354400	K562	blood:	n/a	chr9:140353933-140353942
48	CCNT2	chr9:140356212-140356612	K562	blood:	n/a	n/a
49	CCNT2	chr9:140347892-140348046	K562	blood:	n/a	n/a
50	CEBPB	chr9:140358583-140358740	HepG2	liver:	n/a	chr9:140358621-140358632

(count:1833 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140356757-140356807	NHBE	bronchial:	n/a
2	chr9:140352318-140352368	ECC-1	luminal epithelium:	n/a
3	chr9:140340778-140340828	HEEpiC	esophagus:	n/a
4	chr9:140356757-140356807	NHBE	bronchial:	n/a
5	chr9:140352318-140352368	ECC-1	luminal epithelium:	n/a
6	chr9:140340778-140340828	HEEpiC	esophagus:	n/a
7	chr9:140343325-140343375	T-47D	breast:	n/a
8	chr9:140341606-140341656	NH-A	brain:	n/a
9	chr9:140343617-140343667	ovcar-3	ovarian:	n/a
10	chr9:140343325-140343375	SKMC	muscle:	n/a
11	chr9:140359477-140359527	Caco-2	colon:	n/a
12	chr9:140361383-140361433	IMR90	lung:	fetal
13	chr9:140349128-140349178	SAEC	small airway:	n/a
14	chr9:140355163-140355213	GM12892	blood:	n/a
15	chr9:140353134-140353184	A549	lung:	n/a
16	chr9:140352910-140352960	HEEpiC	esophagus:	n/a
17	chr9:140356757-140356807	SAEC	small airway:	n/a
18	chr9:140356757-140356807	HEK293	kidney:	embryo
19	chr9:140356757-140356807	AG09319	gingival:	n/a
20	chr9:140346864-140346914	NB4	blood:	n/a
21	chr9:140342917-140342967	ECC-1	luminal epithelium:	n/a
22	chr9:140357706-140357756	SK-N-SH	brain:	n/a
23	chr9:140346899-140346949	HRPEpiC	eye:	n/a
24	chr9:140353961-140354011	GM12878	blood:	n/a
25	chr9:140346899-140346949	HEK293	kidney:	embryo
26	chr9:140353134-140353184	AG09309	skin:	n/a
27	chr9:140343854-140343904	HPAEpiC	pulmonary alveolar:	n/a
28	chr9:140341606-140341656	IMR90	lung:	fetal
29	chr9:140356757-140356807	ECC-1	luminal epithelium:	n/a
30	chr9:140349944-140349994	GM12892	blood:	n/a
31	chr9:140346899-140346949	MCF-7	breast:	n/a
32	chr9:140354043-140354093	Hela-S3	cervix:	n/a
33	chr9:140353961-140354011	IMR90	lung:	fetal
34	chr9:140359477-140359527	HepG2	liver:	n/a
35	chr9:140353475-140353525	NHBE	bronchial:	n/a
36	chr9:140356475-140356525	HL-60	blood:	n/a
37	chr9:140349128-140349178	AG04450	lung:	fetal
38	chr9:140353134-140353184	SKMC	muscle:	n/a
39	chr9:140353961-140354011	AG04450	lung:	fetal
40	chr9:140354043-140354093	IMR90	lung:	fetal
41	chr9:140355163-140355213	NT2-D1	testis:	n/a
42	chr9:140348014-140348064	NT2-D1	testis:	n/a
43	chr9:140352188-140352238	AoSMC	blood vessel:	n/a
44	chr9:140353475-140353525	SAEC	small airway:	n/a
45	chr9:140361383-140361433	HCF	heart:	n/a
46	chr9:140352188-140352238	HAEpiC	amniotic membrane:	n/a
47	chr9:140340778-140340828	BE2_C	brain:	n/a
48	chr9:140341606-140341656	SK-N-SH	brain:	n/a
49	chr9:140352910-140352960	HCF	heart:	n/a
50	chr9:140359477-140359527	HCPEpiC	choroid plexus:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:140358518..140361237-chr9:140374816..140376548,2	K562	blood:
2	chr9:140352557..140355387-chr9:140371788..140374935,3	MCF-7	breast:
3	chr9:140156032..140157606-chr9:140354181..140356478,2	MCF-7	breast:
4	chr9:140317349..140318505-chr9:140339431..140340433,7	K562	blood:
5	chr9:140116174..140118873-chr9:140338820..140340591,2	MCF-7	breast:
6	chr7:100472348..100473128-chr9:140353098..140353655,2	Hela-S3	cervix:
7	chr9:140361836..140364169-chr9:140371733..140373898,2	K562	blood:
8	chr9:140322555..140324613-chr9:140354689..140356322,2	MCF-7	breast:
9	chr9:140077620..140079519-chr9:140351621..140354134,2	K562	blood:
10	chr9:140169668..140172993-chr9:140345187..140348460,4	K562	blood:
11	chr9:140354790..140356755-chr9:140406317..140408071,2	K562	blood:
12	chr1:182808509..182809054-chr9:140353928..140354794,2	Hela-S3	cervix:
13	chr9:140193764..140196943-chr9:140350718..140357972,9	K562	blood:
14	chr9:140352080..140354787-chr9:140444624..140448715,3	MCF-7	breast:
15	chr9:140331075..140334517-chr9:140343053..140345567,3	K562	blood:
16	chr9:140336153..140338452-chr9:140342014..140345176,3	MCF-7	breast:
17	chr9:140138699..140141466-chr9:140349196..140351989,2	K562	blood:
18	chr9:140189738..140190666-chr9:140339488..140340122,3	MCF-7	breast:
19	chr9:140194341..140197966-chr9:140350520..140353803,7	MCF-7	breast:
20	chr9:140340048..140342300-chr9:140352355..140353867,2	MCF-7	breast:
21	chr9:140355853..140357358-chr9:140357603..140359754,2	MCF-7	breast:
22	chr9:140158177..140160283-chr9:140341405..140343127,2	K562	blood:
23	chr9:140189492..140190310-chr9:140339405..140340198,3	MCF-7	breast:
24	chr14:103800123..103800887-chr9:140353475..140354015,2	HCT-116	colon:
25	chr2:676897..677660-chr9:140353219..140353959,2	Hela-S3	cervix:
26	chr9:140328603..140331524-chr9:140339859..140341815,2	MCF-7	breast:
27	chr9:140195671..140196210-chr9:140339702..140340361,2	MCF-7	breast:
28	chr9:140196649..140197437-chr9:140339458..140340157,2	MCF-7	breast:
29	chr1:108185908..108186619-chr9:140340323..140340878,2	MCF-7	breast:
30	chr9:140317389..140318271-chr9:140339648..140340812,5	MCF-7	breast:
31	chr9:140191336..140198265-chr9:140351106..140355775,13	MCF-7	breast:
32	chr9:140142023..140145002-chr9:140350817..140354805,3	K562	blood:
33	chr9:140355434..140357921-chr9:140362408..140364687,2	K562	blood:
34	chr3:128902432..128903203-chr9:140352919..140353757,2	NB4	blood:
35	chr9:140245725..140246694-chr9:140339428..140340337,3	MCF-7	breast:
36	chr1:153939505..153940159-chr9:140353647..140354212,2	HCT-116	colon:
37	chr9:140316329..140318019-chr9:140348495..140350237,2	K562	blood:
38	chr9:140189676..140191205-chr9:140348837..140351487,2	MCF-7	breast:
39	chr9:140189561..140190480-chr9:140339770..140340606,3	K562	blood:
40	chr9:140188855..140198797-chr9:140328049..140340935,26	K562	blood:
41	chr9:140081774..140084608-chr9:140352899..140355217,2	MCF-7	breast:
42	chr9:140317565..140318277-chr9:140339425..140340227,3	MCF-7	breast:
43	chr9:140320511..140322623-chr9:140338358..140341178,2	MCF-7	breast:
44	chr9:140189903..140198274-chr9:140327279..140342312,31	MCF-7	breast:
45	chr9:140135678..140137635-chr9:140352214..140353821,2	K562	blood:
46	chr9:140134025..140136288-chr9:140347230..140351135,3	MCF-7	breast:
47	chr9:140316257..140317769-chr9:140352568..140355064,2	K562	blood:
48	chr9:140316974..140319739-chr9:140351873..140353918,3	MCF-7	breast:
49	chr9:140336000..140341073-chr9:140346212..140348839,4	MCF-7	breast:
50	chr9:140322924..140326598-chr9:140339996..140343918,4	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7114-5p	chr9:140344513-140344533	MIMAT0028125
hsa-miR-7114-3p	chr9:140344478-140344498	MIMAT0028126

No data

Variant related genes	Relation type
PNPLA7	TF binding region
ENTPD8	TF binding region
NSMF	TF binding region
PNPLA7	CpG island
ENTPD8	CpG island
NSMF	CpG island
ENSG00000176101	chromatin interactions
ENSG00000087087	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000151353	chromatin interactions
ENSG00000135829	chromatin interactions
ENSG00000188833	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000268996	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000233296	chromatin interactions
ENSG00000188163	chromatin interactions
ENSG00000258890	chromatin interactions
ENSG00000108654	chromatin interactions
ENSG00000100664	chromatin interactions
ENSG00000143570	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000198435	chromatin interactions
ENSG00000165716	chromatin interactions
ENSG00000120889	chromatin interactions
ENSG00000188986	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000072401	chromatin interactions
ENSG00000187609	chromatin interactions
ENSG00000198113	chromatin interactions
ENSG00000177239	chromatin interactions
ENSG00000260996	chromatin interactions
ENSG00000130653	chromatin interactions
ENSG00000143578	chromatin interactions
ENSG00000124216	chromatin interactions
ENSG00000169714	chromatin interactions
ENSG00000176058	chromatin interactions
ENSG00000188747	chromatin interactions
ENSG00000176248	chromatin interactions
ENSG00000188229	chromatin interactions

Extended variants
information (count: 1396 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:1396 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143350088	chr9:140338382-140338383	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs144827508	chr9:140338391-140338392	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs530354692	chr9:140338392-140338393	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs542697012	chr9:140338465-140338466	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs545498052	chr9:140338481-140338482	Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs562785294	chr9:140338517-140338518	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs369900731	chr9:140338549-140338550	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs188778767	chr9:140338559-140338560	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs562659935	chr9:140338561-140338562	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs561904160	chr9:140338570-140338571	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs34027272	chr9:140338638-140338639	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs527489503	chr9:140338675-140338676	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs193026595	chr9:140338679-140338680	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs558460482	chr9:140338706-140338707	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs374907175	chr9:140338708-140338709	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs6606587	chr9:140338713-140338714	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs533321601	chr9:140338737-140338738	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs370453277	chr9:140338743-140338744	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs35876167	chr9:140338759-140338760	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs570328925	chr9:140338815-140338816	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs535814332	chr9:140338816-140338817	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs28395258	chr9:140338913-140338914	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs556036157	chr9:140338921-140338922	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs148571847	chr9:140338926-140338927	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs185221844	chr9:140338932-140338933	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs553417543	chr9:140338936-140338937	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs116562468	chr9:140338958-140338959	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs545761354	chr9:140339008-140339009	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs555933087	chr9:140339010-140339011	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs142917620	chr9:140339038-140339039	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs369789103	chr9:140339071-140339072	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs150642936	chr9:140339077-140339078	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs11516129	chr9:140339091-140339092	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs560382053	chr9:140339145-140339146	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs377580589	chr9:140339153-140339154	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs561964061	chr9:140339194-140339195	Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs188557914	chr9:140339223-140339224	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs560450416	chr9:140339278-140339279	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs541241242	chr9:140339333-140339334	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs140050373	chr9:140339340-140339341	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs533314306	chr9:140339343-140339344	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs143610889	chr9:140339360-140339361	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs181375503	chr9:140339376-140339377	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs529291935	chr9:140339377-140339378	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs7867154	chr9:140339386-140339387	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs7862271	chr9:140339430-140339431	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs368227468	chr9:140339440-140339441	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs532395189	chr9:140339480-140339481	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs534873802	chr9:140339522-140339523	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs146798358	chr9:140339538-140339539	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	7 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:1909 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140336000-140339600	Weak transcription	Placenta	Placenta
2	chr9:140336200-140339400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr9:140336200-140339600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr9:140336200-140340000	Weak transcription	Lung	lung
5	chr9:140336200-140340000	Weak transcription	Pancreas	Pancrea
6	chr9:140336200-140342600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr9:140336200-140343000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr9:140336200-140347800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:140336400-140339600	Weak transcription	HMEC	breast
10	chr9:140336400-140339800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr9:140336400-140348200	Weak transcription	Right Atrium	heart
12	chr9:140336600-140339400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr9:140336600-140339400	Weak transcription	NHEK	skin
14	chr9:140336600-140339600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr9:140336600-140339600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr9:140336600-140340000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr9:140336600-140340000	Weak transcription	Colonic Mucosa	Colon
18	chr9:140336600-140343600	Weak transcription	Right Ventricle	heart
19	chr9:140336600-140348600	Weak transcription	Left Ventricle	heart
20	chr9:140336800-140339400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr9:140336800-140339600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:140336800-140339600	Weak transcription	Primary B cells from cord blood	blood
23	chr9:140336800-140339600	Weak transcription	Primary T helper cells fromperipheralblood	blood
24	chr9:140336800-140339800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr9:140336800-140340000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr9:140336800-140340000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr9:140336800-140343200	Weak transcription	Ovary	ovary
28	chr9:140336800-140343400	Weak transcription	HUES48 Cell Line	embryonic stem cell
29	chr9:140336800-140343600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr9:140336800-140343600	Weak transcription	Aorta	Aorta
31	chr9:140336800-140352400	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr9:140337000-140339200	Weak transcription	Hela-S3	cervix
33	chr9:140337000-140339400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr9:140337000-140339400	Weak transcription	Fetal Intestine Large	intestine
35	chr9:140337000-140339400	Weak transcription	Fetal Intestine Small	intestine
36	chr9:140337000-140339400	Weak transcription	K562	blood
37	chr9:140337000-140339600	Weak transcription	Liver	Liver
38	chr9:140337000-140339600	Weak transcription	A549	lung
39	chr9:140337000-140339600	Weak transcription	HepG2	liver
40	chr9:140337000-140340000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr9:140338200-140346600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr9:140339200-140339600	Enhancers	Hela-S3	cervix
43	chr9:140339400-140340200	Enhancers	Duodenum Smooth Muscle	Duodenum
44	chr9:140339400-140340200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr9:140339400-140340200	Enhancers	Fetal Intestine Small	intestine
46	chr9:140339400-140340400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:140339400-140340400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:140339400-140340600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr9:140339400-140340600	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr9:140339400-140340600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--

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