Variant report

Variant	nsv534573
Chromosome Location	chr9:140550908-140757122
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4583)
CpG islands
(count:4645)
Chromatin interactive
region (count:179)
LncRNA
region (count:3)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:4583 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:140579525-140580074	K562	blood:	n/a	n/a
2	ARID3A	chr9:140565343-140565821	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:140570924-140570976	K562	blood:	n/a	n/a
4	ARID3A	chr9:140589695-140589979	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:140567215-140567607	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:140584600-140584950	HepG2	liver:	n/a	n/a
7	ATF1	chr9:140579568-140579816	K562	blood:	n/a	n/a
8	ATF2	chr9:140653453-140654075	GM12878	blood:	n/a	n/a
9	ATF2	chr9:140639148-140639804	GM12878	blood:	n/a	n/a
10	ATF2	chr9:140632651-140633030	GM12878	blood:	n/a	n/a
11	ATF2	chr9:140632555-140633044	GM12878	blood:	n/a	n/a
12	ATF2	chr9:140641009-140641568	GM12878	blood:	n/a	chr9:140641502-140641509
13	ATF2	chr9:140651891-140652508	GM12878	blood:	n/a	n/a
14	ATF2	chr9:140653486-140653886	GM12878	blood:	n/a	n/a
15	ATF2	chr9:140573609-140574126	GM12878	blood:	n/a	n/a
16	ATF2	chr9:140561209-140561817	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr9:140710782-140711539	GM12878	blood:	n/a	n/a
18	ATF2	chr9:140641019-140641614	GM12878	blood:	n/a	chr9:140641502-140641509
19	ATF2	chr9:140615932-140616395	GM12878	blood:	n/a	n/a
20	ATF2	chr9:140615735-140616429	GM12878	blood:	n/a	n/a
21	ATF2	chr9:140656647-140657415	GM12878	blood:	n/a	n/a
22	ATF2	chr9:140561222-140562002	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr9:140639968-140640492	GM12878	blood:	n/a	n/a
24	ATF2	chr9:140655367-140655871	GM12878	blood:	n/a	n/a
25	ATF2	chr9:140656794-140657321	GM12878	blood:	n/a	n/a
26	ATF2	chr9:140639164-140639781	GM12878	blood:	n/a	n/a
27	ATF2	chr9:140703449-140703804	GM12878	blood:	n/a	n/a
28	ATF2	chr9:140710777-140711402	GM12878	blood:	n/a	n/a
29	ATF2	chr9:140655366-140655982	GM12878	blood:	n/a	n/a
30	ATF2	chr9:140599708-140600308	GM12878	blood:	n/a	n/a
31	ATF3	chr9:140563816-140564115	K562	blood:	n/a	n/a
32	BACH1	chr9:140563667-140564160	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr9:140610803-140610830	K562	blood:	n/a	n/a
34	BACH1	chr9:140567460-140567647	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr9:140640020-140640565	H1-hESC	embryonic stem cell:	n/a	chr9:140640362-140640376
36	BACH1	chr9:140589663-140589942	K562	blood:	n/a	n/a
37	BACH1	chr9:140561065-140561826	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr9:140573811-140574048	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr9:140563712-140564172	K562	blood:	n/a	n/a
40	BACH1	chr9:140570996-140571303	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr9:140640186-140640518	K562	blood:	n/a	chr9:140640362-140640376
42	BACH1	chr9:140560252-140560464	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr9:140618399-140618691	H1-hESC	embryonic stem cell:	n/a	n/a
44	BATF	chr9:140639192-140639625	GM12878	blood:	n/a	n/a
45	BATF	chr9:140731105-140731321	GM12878	blood:	n/a	n/a
46	BATF	chr9:140656857-140657244	GM12878	blood:	n/a	n/a
47	BATF	chr9:140615504-140615792	GM12878	blood:	n/a	n/a
48	BATF	chr9:140655479-140655850	GM12878	blood:	n/a	n/a
49	BATF	chr9:140610458-140611042	GM12878	blood:	n/a	n/a
50	BATF	chr9:140710900-140711326	GM12878	blood:	n/a	chr9:140711120-140711131

(count:4645 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140658436-140658486	HEEpiC	esophagus:	n/a
2	chr9:140647870-140647920	T-47D	breast:	n/a
3	chr9:140687144-140687194	AG09319	gingival:	n/a
4	chr9:140709033-140709083	CMK	blood:	n/a
5	chr9:140671632-140671682	IMR90	lung:	fetal
6	chr9:140658436-140658486	HCPEpiC	choroid plexus:	n/a
7	chr9:140725898-140725948	AG09319	gingival:	n/a
8	chr9:140681131-140681181	HCPEpiC	choroid plexus:	n/a
9	chr9:140612549-140612599	HCM	heart:	n/a
10	chr9:140658436-140658486	HEEpiC	esophagus:	n/a
11	chr9:140647870-140647920	T-47D	breast:	n/a
12	chr9:140687144-140687194	AG09319	gingival:	n/a
13	chr9:140709033-140709083	CMK	blood:	n/a
14	chr9:140671632-140671682	IMR90	lung:	fetal
15	chr9:140658436-140658486	HCPEpiC	choroid plexus:	n/a
16	chr9:140725898-140725948	AG09319	gingival:	n/a
17	chr9:140681131-140681181	HCPEpiC	choroid plexus:	n/a
18	chr9:140612549-140612599	HCM	heart:	n/a
19	chr9:140733714-140733764	HUVEC	blood vessel:	n/a
20	chr9:140725898-140725948	HIPEpiC	eye:	n/a
21	chr9:140727571-140727621	ProgFib	skin:	n/a
22	chr9:140712932-140712982	SAEC	small airway:	n/a
23	chr9:140673936-140673986	NT2-D1	testis:	n/a
24	chr9:140707378-140707428	AG09319	gingival:	n/a
25	chr9:140731445-140731495	NT2-D1	testis:	n/a
26	chr9:140647870-140647920	HPAEpiC	pulmonary alveolar:	n/a
27	chr9:140674013-140674063	NHDF-neo	bronchial:	n/a
28	chr9:140673936-140673986	ECC-1	luminal epithelium:	n/a
29	chr9:140656200-140656250	H1-hESC	embryonic stem cell:	embryo
30	chr9:140615230-140615280	HEEpiC	esophagus:	n/a
31	chr9:140683649-140683699	AG04450	lung:	fetal
32	chr9:140709558-140709608	GM12878	blood:	n/a
33	chr9:140652711-140652761	IMR90	lung:	fetal
34	chr9:140703588-140703638	Caco-2	colon:	n/a
35	chr9:140681206-140681256	NHBE	bronchial:	n/a
36	chr9:140611316-140611366	NT2-D1	testis:	n/a
37	chr9:140703637-140703687	LNCaP	prostate:	n/a
38	chr9:140681206-140681256	HepG2	liver:	n/a
39	chr9:140738145-140738195	CMK	blood:	n/a
40	chr9:140656200-140656250	AG09309	skin:	n/a
41	chr9:140683649-140683699	AG09309	skin:	n/a
42	chr9:140708214-140708264	SK-N-SH_RA	brain:	n/a
43	chr9:140652685-140652735	AG04449	skin:	fetal
44	chr9:140716770-140716820	HMEC	breast:	n/a
45	chr9:140727571-140727621	MCF10A-Er-Src	breast:	n/a
46	chr9:140671200-140671250	BE2_C	brain:	n/a
47	chr9:140568043-140568093	K562	blood:	n/a
48	chr9:140586201-140586251	ECC-1	luminal epithelium:	n/a
49	chr9:140731445-140731495	SK-N-SH	brain:	n/a
50	chr9:140612442-140612492	Jurkat	blood:	n/a

(count:179 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr9:140556948..140560022-chr9:140562318..140565265,4	K562	blood:
2	chr9:140576034..140577675-chr9:140577860..140579633,2	K562	blood:
3	chr9:140679440..140682132-chr9:140702994..140705523,2	K562	blood:
4	chr9:140616597..140619590-chr9:140626319..140628863,2	K562	blood:
5	chr9:140498546..140502613-chr9:140552404..140554090,3	K562	blood:
6	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
7	chr9:140511684..140515922-chr9:140563311..140567576,10	MCF-7	breast:
8	chr9:140567130..140567958-chr9:140589475..140590450,2	MCF-7	breast:
9	chr9:140567845..140570418-chr9:140651009..140653801,2	MCF-7	breast:
10	chr9:140478738..140480572-chr9:140563857..140565636,2	MCF-7	breast:
11	chr9:140510590..140512160-chr9:140570027..140572607,2	MCF-7	breast:
12	chr9:140567130..140567958-chr9:140589475..140590450,2	MCF-7	breast:
13	chr9:140485611..140487134-chr9:140558504..140560713,2	MCF-7	breast:
14	chr9:140699377..140703481-chr9:140712801..140716368,4	K562	blood:
15	chr9:140571698..140574262-chr9:140609421..140611418,2	K562	blood:
16	chr9:140598819..140601234-chr9:140602896..140605674,2	K562	blood:
17	chr9:140706148..140707731-chr9:140712808..140715644,2	K562	blood:
18	chr9:140700744..140703518-chr9:140712352..140715179,2	K562	blood:
19	chr9:140610530..140612311-chr9:140612330..140615282,2	K562	blood:
20	chr9:140689938..140692282-chr9:140694934..140697761,2	MCF-7	breast:
21	chr9:140497340..140502310-chr9:140563850..140568927,6	K562	blood:
22	chr9:140636490..140638088-chr9:140638645..140641455,2	MCF-7	breast:
23	chr9:140567845..140570418-chr9:140651009..140653801,2	MCF-7	breast:
24	chr9:140576034..140577675-chr9:140577860..140579633,2	K562	blood:
25	chr9:140499260..140502923-chr9:140667967..140671652,3	MCF-7	breast:
26	chr9:140700980..140705198-chr9:140707876..140710677,3	K562	blood:
27	chr9:140574379..140576037-chr9:140580035..140582050,2	K562	blood:
28	chr9:140639569..140641263-chr9:140644746..140647470,2	MCF-7	breast:
29	chr9:140589041..140590820-chr9:140640169..140641796,2	K562	blood:
30	chr9:140621172..140623675-chr9:140625261..140627208,2	MCF-7	breast:
31	chr9:140713786..140716725-chr9:140719882..140722951,3	K562	blood:
32	chr9:140701752..140704462-chr9:140707799..140711263,3	MCF-7	breast:
33	chr9:140575772..140578110-chr9:140581931..140583477,2	MCF-7	breast:
34	chr9:140541151..140543199-chr9:140557554..140559869,2	MCF-7	breast:
35	chr9:140504074..140505804-chr9:140564024..140565554,2	K562	blood:
36	chr9:140558471..140560077-chr9:140589640..140592131,2	K562	blood:
37	chr9:140563248..140567111-chr9:140567384..140570139,4	K562	blood:
38	chr9:140444806..140448001-chr9:140579096..140581277,3	MCF-7	breast:
39	chr9:140662415..140665334-chr9:140667330..140669473,2	MCF-7	breast:
40	chr9:140645397..140647015-chr9:140648908..140650692,2	K562	blood:
41	chr9:140566819..140568166-chr9:140589329..140590605,6	MCF-7	breast:
42	chr9:140567353..140567947-chr9:140589446..140590314,3	K562	blood:
43	chr9:140627655..140630177-chr9:140631904..140633862,2	K562	blood:
44	chr9:140572176..140574298-chr9:140582921..140584758,3	MCF-7	breast:
45	chr9:140648170..140652364-chr9:140652458..140655697,5	MCF-7	breast:
46	chr9:140705835..140707524-chr9:140709188..140711003,2	K562	blood:
47	chr9:140565648..140568027-chr9:140588903..140590884,2	MCF-7	breast:
48	chr9:140591766..140593331-chr9:140667353..140669493,2	K562	blood:
49	chr9:140567353..140567947-chr9:140589446..140590314,3	K562	blood:
50	chr9:140563812..140566450-chr9:140570445..140574038,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CACNA1B-4	chr9:140657474-140659224	NONHSAT135751
2	lnc-AL772363.1-5	chr9:140682117-140683139	NONHSAT135752
3	lnc-AL772363.1-4	chr9:140703295-140703875	NONHSAT135753

miRNA name	Chromosome Location	mirBase accession
hsa-miR-602	chr9:140732886-140732908	MIMAT0003270

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	EHMT1	hsa-miR-1	chr9:140730432-140730455
2	EHMT1	hsa-miR-30e-5p	chr9:140730456-140730473
3	EHMT1	hsa-miR-615-3p	chr9:140729903-140729924

Variant related genes	Relation type
MIR602	TF binding region
EHMT1	TF binding region
ENSG00000255585	TF binding region
MIR602	CpG island
EHMT1	CpG island
ENSG00000255585	CpG island
ENSG00000203993	chromatin interactions
ENSG00000207693	chromatin interactions
ENSG00000255585	chromatin interactions
ENSG00000181090	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000233998	chromatin interactions
ENSG00000197070	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000130653	chromatin interactions

Extended variants
information (count: 9554 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:9554 , 50 per page) page: 1 2 3 4 5 6 7 ... 192

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563604117	chr9:140550922-140550923	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541926309	chr9:140550925-140550926	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139266027	chr9:140550932-140550933	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559158467	chr9:140550980-140550981	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143173208	chr9:140551016-140551017	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551899914	chr9:140551031-140551032	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561954760	chr9:140551116-140551117	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530947155	chr9:140551130-140551131	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs180781396	chr9:140551175-140551176	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527464016	chr9:140551178-140551179	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143754704	chr9:140551219-140551220	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536978972	chr9:140551221-140551222	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547336291	chr9:140551225-140551226	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs185772583	chr9:140551249-140551250	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567115566	chr9:140551264-140551265	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377321025	chr9:140551314-140551315	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs75907113	chr9:140551482-140551483	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557843771	chr9:140551483-140551484	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189331197	chr9:140551490-140551491	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs543427192	chr9:140551491-140551492	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556649234	chr9:140551497-140551498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78898763	chr9:140551581-140551582	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542542781	chr9:140551643-140551644	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs374486306	chr9:140551697-140551698	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs528312234	chr9:140551737-140551738	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544838758	chr9:140551770-140551771	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376454065	chr9:140551804-140551805	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10867041	chr9:140551809-140551810	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs551036329	chr9:140551847-140551848	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567689700	chr9:140551859-140551860	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530112609	chr9:140551861-140551862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10780180	chr9:140551863-140551864	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs567129615	chr9:140551869-140551870	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539225156	chr9:140551876-140551877	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181618954	chr9:140551900-140551901	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545345887	chr9:140551950-140551951	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs563974476	chr9:140551951-140551952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs571334955	chr9:140551961-140551962	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs368382324	chr9:140552034-140552035	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535551538	chr9:140552047-140552048	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556998068	chr9:140552166-140552167	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141891515	chr9:140552225-140552226	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs71510838	chr9:140552242-140552243	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533347801	chr9:140552243-140552244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527238276	chr9:140552247-140552248	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150625848	chr9:140552269-140552270	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572756890	chr9:140552286-140552287	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs545201256	chr9:140552297-140552298	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs34591563	chr9:140552303-140552304	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs397745440	chr9:140552314-140552315	Weak transcription Strong transcription Enhancers	n/a	n/a	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:8244 , 50 per page) page: 1 2 3 4 5 6 7 ... 165

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140516200-140558800	Weak transcription	NH-A	brain
2	chr9:140523400-140563400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr9:140526600-140557800	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr9:140527400-140557600	Weak transcription	Fetal Kidney	kidney
5	chr9:140527600-140551400	Weak transcription	Pancreas	Pancrea
6	chr9:140527600-140563800	Weak transcription	Aorta	Aorta
7	chr9:140527800-140559200	Weak transcription	Brain Hippocampus Middle	brain
8	chr9:140528000-140560600	Weak transcription	HUVEC	blood vessel
9	chr9:140531000-140564800	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr9:140533400-140559400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr9:140534200-140559800	Weak transcription	NHLF	lung
12	chr9:140534400-140555000	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr9:140534400-140559200	Weak transcription	Colon Smooth Muscle	Colon
14	chr9:140534400-140563400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr9:140534600-140551200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr9:140534600-140551600	Weak transcription	Right Atrium	heart
17	chr9:140534600-140560400	Weak transcription	Colonic Mucosa	Colon
18	chr9:140534600-140572600	Weak transcription	Small Intestine	intestine
19	chr9:140535200-140553000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:140535600-140553000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
21	chr9:140535600-140559000	Weak transcription	Fetal Brain Male	brain
22	chr9:140536000-140551800	Strong transcription	Fetal Intestine Small	intestine
23	chr9:140537600-140559000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr9:140538800-140552400	Weak transcription	HSMMtube	muscle
25	chr9:140538800-140559800	Weak transcription	Rectal Smooth Muscle	rectum
26	chr9:140540200-140554600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr9:140540200-140560200	Weak transcription	Psoas Muscle	Psoas
28	chr9:140540200-140564800	Weak transcription	HMEC	breast
29	chr9:140540400-140554800	Weak transcription	Brain Substantia Nigra	brain
30	chr9:140540400-140559000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr9:140540400-140559200	Weak transcription	Brain Angular Gyrus	brain
32	chr9:140540800-140551800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr9:140541800-140557600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr9:140542000-140551400	Weak transcription	Right Ventricle	heart
35	chr9:140542000-140557600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr9:140542000-140559200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr9:140542000-140559800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr9:140542200-140552800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr9:140542400-140551600	Weak transcription	Lung	lung
40	chr9:140542600-140552600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr9:140543000-140558600	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr9:140543200-140553200	Weak transcription	Primary hematopoietic stem cells	blood
43	chr9:140543400-140552800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr9:140543400-140559200	Weak transcription	NHDF-Ad	bronchial
45	chr9:140543600-140564800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr9:140544200-140559200	Weak transcription	Gastric	stomach
47	chr9:140544400-140557600	Weak transcription	Stomach Mucosa	stomach
48	chr9:140544600-140551200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr9:140545000-140551800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr9:140545200-140551000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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