Variant report

Variant	nsv917477
Chromosome Location	chr9:140796572-141073897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2351)
CpG islands
(count:2138)
Chromatin interactive
region (count:101)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2351 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr9:140884817-140885010	K562	blood:	n/a	n/a
2	ATF3	chr9:141020689-141020889	GM12878	blood:	n/a	n/a
3	ATF3	chr9:141020637-141020864	K562	blood:	n/a	n/a
4	ATF3	chr9:141054176-141054450	A549	lung:	n/a	n/a
5	ATF3	chr9:141020692-141020855	GM12878	blood:	n/a	n/a
6	ATF3	chr9:140851195-140851422	K562	blood:	n/a	n/a
7	BACH1	chr9:140918133-140918313	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr9:141064102-141064298	GM12878	blood:	n/a	n/a
9	BATF	chr9:141054182-141054368	GM12878	blood:	n/a	n/a
10	BATF	chr9:141050185-141050584	GM12878	blood:	n/a	n/a
11	BATF	chr9:141023409-141023594	GM12878	blood:	n/a	n/a
12	BATF	chr9:141020609-141020912	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:141054141-141054402	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:141067698-141067987	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:141023414-141023612	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:141054194-141054361	GM12878	blood:	n/a	n/a
17	BCL3	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
18	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
19	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
20	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:140851240-140851513	HepG2	liver:	n/a	n/a
22	BHLHE40	chr9:141061417-141061666	HepG2	liver:	n/a	n/a
23	BHLHE40	chr9:140851159-140851515	K562	blood:	n/a	n/a
24	BHLHE40	chr9:140862896-140863013	K562	blood:	n/a	n/a
25	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
26	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
27	BHLHE40	chr9:140851209-140851501	GM12878	blood:	n/a	n/a
28	BHLHE40	chr9:140993888-140994157	HepG2	liver:	n/a	n/a
29	BHLHE40	chr9:140879411-140879615	HepG2	liver:	n/a	n/a
30	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
31	BHLHE40	chr9:141044398-141044667	HepG2	liver:	n/a	n/a
32	BRCA1	chr9:140910350-140910549	GM12878	blood:	n/a	n/a
33	BRCA1	chr9:140841105-140841139	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr9:141023334-141023686	K562	blood:	n/a	n/a
35	CBX3	chr9:140980062-140980441	K562	blood:	n/a	n/a
36	CBX3	chr9:140980114-140980383	K562	blood:	n/a	n/a
37	CBX3	chr9:140839953-140840442	HCT-116	colon:	n/a	n/a
38	CBX3	chr9:140980110-140980451	HCT-116	colon:	n/a	n/a
39	CBX3	chr9:141020180-141021846	K562	blood:	n/a	n/a
40	CBX3	chr9:141023337-141023724	K562	blood:	n/a	n/a
41	CBX3	chr9:141020423-141021627	K562	blood:	n/a	n/a
42	CBX3	chr9:140851178-140851459	K562	blood:	n/a	n/a
43	CBX3	chr9:141041994-141042355	K562	blood:	n/a	n/a
44	CBX3	chr9:141044327-141044724	K562	blood:	n/a	n/a
45	CCNT2	chr9:140918130-140918232	K562	blood:	n/a	n/a
46	CCNT2	chr9:140928501-140928648	K562	blood:	n/a	n/a
47	CEBPB	chr9:140986585-140986794	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr9:140896184-140896404	HepG2	liver:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
49	CEBPB	chr9:140995483-140995724	A549	lung:	n/a	chr9:140995597-140995608
50	CEBPB	chr9:140926106-140926306	K562	blood:	n/a	n/a

(count:2138 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140916078-140916128	Hepatocyte	liver:	n/a
2	chr9:140916980-140917030	MCF-7	breast:	n/a
3	chr9:140939374-140939424	PrEC	prostate:	n/a
4	chr9:140916078-140916128	Hepatocyte	liver:	n/a
5	chr9:140916980-140917030	MCF-7	breast:	n/a
6	chr9:140939374-140939424	PrEC	prostate:	n/a
7	chr9:140916078-140916128	AoSMC	blood vessel:	n/a
8	chr9:141007633-141007683	U87	brain:	n/a
9	chr9:140970188-140970238	NHDF-neo	bronchial:	n/a
10	chr9:140818325-140818375	Hepatocyte	liver:	n/a
11	chr9:140816336-140816386	HCT-116	colon:	n/a
12	chr9:141013537-141013587	HPAEpiC	pulmonary alveolar:	n/a
13	chr9:140814587-140814637	HCF	heart:	n/a
14	chr9:140815010-140815060	Caco-2	colon:	n/a
15	chr9:140937920-140937970	NHDF-neo	bronchial:	n/a
16	chr9:140937920-140937970	HCM	heart:	n/a
17	chr9:141016791-141016841	HCT-116	colon:	n/a
18	chr9:141017001-141017051	SK-N-MC	brain:	n/a
19	chr9:141042453-141042503	ECC-1	luminal epithelium:	n/a
20	chr9:141017001-141017051	PFSK-1	brain:	n/a
21	chr9:140917431-140917481	HRPEpiC	eye:	n/a
22	chr9:141012312-141012362	HRPEpiC	eye:	n/a
23	chr9:140917431-140917481	HCPEpiC	choroid plexus:	n/a
24	chr9:141069847-141069897	GM12892	blood:	n/a
25	chr9:140814587-140814637	HPAEpiC	pulmonary alveolar:	n/a
26	chr9:140944087-140944137	MCF-7	breast:	n/a
27	chr9:141017001-141017051	HEK293	kidney:	embryo
28	chr9:141017457-141017507	T-47D	breast:	n/a
29	chr9:140937920-140937970	MCF-7	breast:	n/a
30	chr9:140917431-140917481	GM12892	blood:	n/a
31	chr9:140917431-140917481	NH-A	brain:	n/a
32	chr9:141013537-141013587	GM12878	blood:	n/a
33	chr9:140937920-140937970	NH-A	brain:	n/a
34	chr9:141042435-141042485	Caco-2	colon:	n/a
35	chr9:140916078-140916128	HUVEC	blood vessel:	n/a
36	chr9:140850133-140850183	HCF	heart:	n/a
37	chr9:141017457-141017507	NT2-D1	testis:	n/a
38	chr9:141014674-141014724	LNCaP	prostate:	n/a
39	chr9:140957018-140957068	GM19239	blood:	n/a
40	chr9:141069847-141069897	AG09319	gingival:	n/a
41	chr9:141045017-141045067	Jurkat	blood:	n/a
42	chr9:141013537-141013587	HRPEpiC	eye:	n/a
43	chr9:140850133-140850183	GM12891	blood:	n/a
44	chr9:140815010-140815060	NHDF-neo	bronchial:	n/a
45	chr9:141044509-141044559	Caco-2	colon:	n/a
46	chr9:140917431-140917481	ECC-1	luminal epithelium:	n/a
47	chr9:140816336-140816386	A549	lung:	n/a
48	chr9:140917431-140917481	HRE	kidney:	n/a
49	chr9:141017001-141017051	HRE	kidney:	n/a
50	chr9:140957018-140957068	AG10803	skin:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr9:140867124..140870002-chr9:140953480..140955243,2	MCF-7	breast:
2	chr9:140844057..140846982-chr9:140852715..140855154,2	MCF-7	breast:
3	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
4	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
5	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
6	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
7	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
8	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
9	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
10	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:
11	chr1:149223401..149224369-chr9:140873101..140874123,8	MCF-7	breast:
12	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:
13	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
14	chr9:140796431..140799040-chr9:140804864..140806682,2	K562	blood:
15	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
16	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
17	chr9:140955941..140956581-chr9:140995170..140996036,2	MCF-7	breast:
18	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
19	chr9:140966280..140969244-chr9:140971233..140973098,3	K562	blood:
20	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
21	chr9:140862016..140865668-chr9:140879753..140883106,4	MCF-7	breast:
22	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
23	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
24	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
25	chr1:149223037..149225339-chr9:140872123..140875123,7	MCF-7	breast:
26	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
27	chr9:140841179..140843467-chr9:140845016..140846625,2	K562	blood:
28	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
29	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
30	chr9:140796431..140799040-chr9:140804864..140806682,2	K562	blood:
31	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
32	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
33	chr9:140841179..140843467-chr9:140845016..140846625,2	K562	blood:
34	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
35	chr10:122225..122779-chr9:141041705..141042205,2	MCF-7	breast:
36	chr9:140860566..140865150-chr9:140867846..140870803,4	MCF-7	breast:
37	chr9:140797540..140799636-chr9:140804864..140807689,2	K562	blood:
38	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
39	chr22:50714431..50715299-chr9:140947514..140948493,3	MCF-7	breast:
40	chr9:140962197..140963909-chr9:140964440..140967429,2	K562	blood:
41	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
42	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
43	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:
44	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
45	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
46	chr1:149222900..149224638-chr9:140873623..140875123,3	MCF-7	breast:
47	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
48	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
49	chr9:140844057..140846982-chr9:140852715..140855154,2	MCF-7	breast:
50	chr9:140955941..140956581-chr9:140995170..140996036,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL772363.1-7	chr9:140955477-140955599	NONHSAT135765
2	lnc-AL772363.1-7	chr9:140954806-140956852	NONHSAT135764
3	lnc-AL772363.1-7	chr9:140954809-140955130	NONHSAT135765
4	lnc-AL772363.1-6	chr9:140934955-140937453	NONHSAT135763
5	lnc-AL772363.1-3	chr9:140843115-140843211	NONHSAT135761
6	lnc-AL772363.1-6	chr9:140939331-140939523	NONHSAT135763
7	lnc-AL772363.1-6	chr9:140937901-140938239	NONHSAT135763
8	lnc-AL772363.1-3	chr9:140843618-140844002	NONHSAT135761

No data

Variant related genes	Relation type
TUBBP5	TF binding region
CACNA1B	TF binding region
ENSG00000229926	TF binding region
TUBBP5	CpG island
CACNA1B	CpG island
ENSG00000229926	CpG island
ENSG00000230368	chromatin interactions
ENSG00000148408	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 11634 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:11634 , 50 per page) page: 1 2 3 4 5 6 7 ... 233

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13293511	chr9:140796702-140796703	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555280958	chr9:140796732-140796733	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs145416874	chr9:140796748-140796749	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs534217203	chr9:140796767-140796768	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs554272736	chr9:140796927-140796928	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs541707199	chr9:140797000-140797001	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs529447211	chr9:140797042-140797043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577422740	chr9:140797092-140797093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs549300654	chr9:140797122-140797123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565070175	chr9:140797129-140797130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115132743	chr9:140797134-140797135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs149211644	chr9:140797161-140797162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs56376782	chr9:140797198-140797199	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs543926604	chr9:140797214-140797215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529623910	chr9:140797246-140797247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs546199195	chr9:140797259-140797260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs372182058	chr9:140797264-140797265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559770350	chr9:140797265-140797266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532077191	chr9:140797276-140797277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563618832	chr9:140797291-140797292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375904644	chr9:140797308-140797309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs182286036	chr9:140797316-140797317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145151950	chr9:140797322-140797323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112595129	chr9:140797331-140797332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73668499	chr9:140797338-140797339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540084585	chr9:140797340-140797341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs533898575	chr9:140797351-140797352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529131430	chr9:140797383-140797384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373806642	chr9:140797385-140797386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7045802	chr9:140797401-140797402	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs577357355	chr9:140797542-140797543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541021081	chr9:140797545-140797546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539931069	chr9:140797561-140797562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556728523	chr9:140797562-140797563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs369052310	chr9:140797564-140797565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145741998	chr9:140797590-140797591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371100219	chr9:140797624-140797625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544411782	chr9:140797632-140797633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs560986256	chr9:140797699-140797700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs574680430	chr9:140797710-140797711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs540184306	chr9:140797711-140797712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192563170	chr9:140797723-140797724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532016780	chr9:140797724-140797725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551837408	chr9:140797761-140797762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148102530	chr9:140797787-140797788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111743962	chr9:140797792-140797793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531775212	chr9:140797875-140797876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141847557	chr9:140797887-140797888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372621821	chr9:140797902-140797903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527986612	chr9:140797905-140797906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:19)

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

Chromatin state (count:1322 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140787000-140807400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr9:140787400-140796600	Weak transcription	Fetal Brain Female	brain
3	chr9:140795000-140818200	Weak transcription	Fetal Brain Male	brain
4	chr9:140795400-140800200	Weak transcription	Brain Angular Gyrus	brain
5	chr9:140795400-140808800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr9:140796600-140797000	ZNF genes & repeats	Fetal Brain Female	brain
7	chr9:140797000-140806800	Weak transcription	Fetal Brain Female	brain
8	chr9:140798600-140807000	Weak transcription	Brain Germinal Matrix	brain
9	chr9:140800200-140800800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:140800200-140801000	Enhancers	Brain Angular Gyrus	brain
11	chr9:140800200-140801200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr9:140800200-140801200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr9:140800600-140801200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr9:140801000-140801200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
15	chr9:140801000-140808800	Weak transcription	Brain Angular Gyrus	brain
16	chr9:140801200-140808200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr9:140801200-140808400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr9:140802200-140807600	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr9:140802800-140806200	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr9:140805400-140813000	Weak transcription	Brain Anterior Caudate	brain
21	chr9:140806200-140806400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
22	chr9:140806200-140809000	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr9:140806200-140811600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr9:140806400-140807200	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr9:140806400-140817200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr9:140806800-140818800	Strong transcription	Fetal Brain Female	brain
27	chr9:140807000-140807600	Active TSS	Spleen	Spleen
28	chr9:140807000-140810000	Strong transcription	Brain Germinal Matrix	brain
29	chr9:140807200-140808000	Strong transcription	H9 Cell Line	embryonic stem cell
30	chr9:140807400-140810000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
31	chr9:140807600-140807800	Flanking Active TSS	Spleen	Spleen
32	chr9:140807600-140809200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr9:140807600-140809400	Strong transcription	HUES48 Cell Line	embryonic stem cell
34	chr9:140807600-140816600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr9:140807600-140829600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr9:140807800-140819400	Weak transcription	Spleen	Spleen
37	chr9:140808000-140809000	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr9:140808200-140809800	Strong transcription	Brain Inferior Temporal Lobe	brain
39	chr9:140808200-140821000	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr9:140808400-140809400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr9:140808800-140809000	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:140808800-140809200	Strong transcription	Brain Angular Gyrus	brain
43	chr9:140809000-140809200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr9:140809000-140809400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr9:140809000-140809400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
46	chr9:140809000-140809400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr9:140809000-140809800	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr9:140809200-140809400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:140809200-140809800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
50	chr9:140809200-140810800	Weak transcription	Brain Angular Gyrus	brain

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