Variant report

Variant	nsv1043683
Chromosome Location	chr9:140890714-140955547
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:140918133-140918313	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
3	BCL3	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
4	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
6	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
7	BRCA1	chr9:140910350-140910549	GM12878	blood:	n/a	n/a
8	CCNT2	chr9:140918130-140918232	K562	blood:	n/a	n/a
9	CCNT2	chr9:140928501-140928648	K562	blood:	n/a	n/a
10	CEBPB	chr9:140896195-140896462	K562	blood:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
11	CEBPB	chr9:140896197-140896470	Hela-S3	cervix:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
12	CEBPB	chr9:140896188-140896435	IMR90	lung:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
13	CEBPB	chr9:140942529-140942729	HepG2	liver:	n/a	chr9:140942603-140942614
14	CEBPB	chr9:140926106-140926306	K562	blood:	n/a	n/a
15	CEBPB	chr9:140926152-140926283	HepG2	liver:	n/a	n/a
16	CEBPB	chr9:140942551-140942648	Hela-S3	cervix:	n/a	chr9:140942603-140942614
17	CEBPB	chr9:140930573-140930631	K562	blood:	n/a	n/a
18	CEBPB	chr9:140896184-140896404	HepG2	liver:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
19	CEBPB	chr9:140896273-140896377	A549	lung:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
20	CEBPD	chr9:140928391-140928754	K562	blood:	n/a	n/a
21	CEBPD	chr9:140928434-140928784	K562	blood:	n/a	n/a
22	CTCF	chr9:140916754-140917063	K562	blood:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
23	CTCF	chr9:140949040-140949190	GM12864	blood:	n/a	chr9:140949100-140949118
24	CTCF	chr9:140916841-140917057	Pancreas_OC	pancreas:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
25	CTCF	chr9:140916846-140917054	Hela-S3	cervix:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
26	CTCF	chr9:140916840-140916990	AG09319	gingival:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
27	CTCF	chr9:140948992-140949160	A549	lung:	n/a	chr9:140949100-140949118
28	CTCF	chr9:140949031-140949174	LNCaP	prostate:	n/a	chr9:140949100-140949118
29	CTCF	chr9:140952811-140952824	MCF-7	breast:	n/a	n/a
30	CTCF	chr9:140948940-140949090	A549	lung:	n/a	n/a
31	CTCF	chr9:140949039-140949159	GM12891	blood:	n/a	chr9:140949100-140949118
32	CTCF	chr9:140916880-140917030	HRPEpiC	eye:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
33	CTCF	chr9:140916880-140917030	A549	lung:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
34	CTCF	chr9:140916840-140916990	SAEC	small airway:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
35	CTCF	chr9:140916880-140917030	HCPEpiC	choroid plexus:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
36	CTCF	chr9:140949100-140949250	K562	blood:	n/a	chr9:140949100-140949118
37	CTCF	chr9:140916820-140916970	HFF-Myc	foreskin:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
38	CTCF	chr9:140916872-140917027	GM10266	blood:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
39	CTCF	chr9:140916574-140917291	A549	lung:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916662-140916675 chr9:140916934-140916947 chr9:140916659-140916677
40	CTCF	chr9:140909361-140909522	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:140916903-140916973	GM20000	blood:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
42	CTCF	chr9:140916920-140917070	HFF	foreskin:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
43	CTCF	chr9:140916880-140917030	GM12874	blood:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
44	CTCF	chr9:140916820-140916970	Hela-S3	cervix:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
45	CTCF	chr9:140949060-140949210	NB4	blood:	n/a	chr9:140949100-140949118
46	CTCF	chr9:140902340-140902490	GM12874	blood:	n/a	chr9:140902429-140902438
47	CTCF	chr9:140916900-140917050	SAEC	small airway:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
48	CTCF	chr9:140949040-140949190	GM12875	blood:	n/a	chr9:140949100-140949118
49	CTCF	chr9:140916868-140917012	MCF-7	breast:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
50	CTCF	chr9:140949003-140949218	HepG2	liver:	n/a	chr9:140949100-140949118

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140920003-140920053	AG09319	gingival:	n/a
2	chr9:140916980-140917030	T-47D	breast:	n/a
3	chr9:140917413-140917463	NT2-D1	testis:	n/a
4	chr9:140917431-140917481	Jurkat	blood:	n/a
5	chr9:140916078-140916128	HMEC	breast:	n/a
6	chr9:140942584-140942634	SKMC	muscle:	n/a
7	chr9:140944087-140944137	HIPEpiC	eye:	n/a
8	chr9:140937920-140937970	GM19239	blood:	n/a
9	chr9:140916078-140916128	NH-A	brain:	n/a
10	chr9:140939579-140939629	ECC-1	luminal epithelium:	n/a
11	chr9:140916078-140916128	HRCEpiC	kidney:	n/a
12	chr9:140916980-140917030	GM06990	blood:	n/a
13	chr9:140917413-140917463	SK-N-MC	brain:	n/a
14	chr9:140939579-140939629	AG09309	skin:	n/a
15	chr9:140916078-140916128	AG04449	skin:	fetal
16	chr9:140917431-140917481	GM06990	blood:	n/a
17	chr9:140920003-140920053	PFSK-1	brain:	n/a
18	chr9:140916078-140916128	HEEpiC	esophagus:	n/a
19	chr9:140917413-140917463	NH-A	brain:	n/a
20	chr9:140939579-140939629	Jurkat	blood:	n/a
21	chr9:140942584-140942634	AoSMC	blood vessel:	n/a
22	chr9:140944087-140944137	AG10803	skin:	n/a
23	chr9:140917413-140917463	PANC-1	pancreas:	n/a
24	chr9:140937920-140937970	GM12891	blood:	n/a
25	chr9:140944087-140944137	HUVEC	blood vessel:	n/a
26	chr9:140917431-140917481	HL-60	blood:	n/a
27	chr9:140942584-140942634	ovcar-3	ovarian:	n/a
28	chr9:140917413-140917463	CMK	blood:	n/a
29	chr9:140939374-140939424	BJ	skin:	n/a
30	chr9:140916980-140917030	Hela-S3	cervix:	n/a
31	chr9:140939374-140939424	HNPCEpiC	eye:	n/a
32	chr9:140917431-140917481	GM19239	blood:	n/a
33	chr9:140917413-140917463	SAEC	small airway:	n/a
34	chr9:140920003-140920053	HRE	kidney:	n/a
35	chr9:140942584-140942634	H1-hESC	embryonic stem cell:	embryo
36	chr9:140916980-140917030	GM12892	blood:	n/a
37	chr9:140917431-140917481	SK-N-MC	brain:	n/a
38	chr9:140937920-140937970	T-47D	breast:	n/a
39	chr9:140939374-140939424	A549	lung:	n/a
40	chr9:140917413-140917463	NB4	blood:	n/a
41	chr9:140944087-140944137	SK-N-MC	brain:	n/a
42	chr9:140917413-140917463	HCT-116	colon:	n/a
43	chr9:140939579-140939629	PrEC	prostate:	n/a
44	chr9:140939579-140939629	BE2_C	brain:	n/a
45	chr9:140917431-140917481	BJ	skin:	n/a
46	chr9:140937920-140937970	HNPCEpiC	eye:	n/a
47	chr9:140916078-140916128	LNCaP	prostate:	n/a
48	chr9:140937920-140937970	Jurkat	blood:	n/a
49	chr9:140916980-140917030	A549	lung:	n/a
50	chr9:140916078-140916128	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
2	chr9:140769881..140772281-chr9:140919838..140921575,2	K562	blood:
3	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
4	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
5	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
6	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
7	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
8	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
9	chr9:140867124..140870002-chr9:140953480..140955243,2	MCF-7	breast:
10	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
11	chr22:50714431..50715299-chr9:140947514..140948493,3	MCF-7	breast:
12	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
13	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
14	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
15	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
16	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
17	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
18	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
19	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
20	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
21	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
22	chr9:140909435..140911470-chr9:140917464..140919841,2	MCF-7	breast:
23	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
24	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
25	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
26	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
27	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
28	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
29	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
30	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
31	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
32	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
33	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
34	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:

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

Variant related genes	Relation type
CACNA1B	TF binding region
CACNA1B	CpG island
ENSG00000148408	chromatin interactions

Extended variants
information (count: 2687 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:2687 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114138014	chr9:140890721-140890722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs545450659	chr9:140890849-140890850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553280615	chr9:140890851-140890852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs189522633	chr9:140890950-140890951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs75895970	chr9:140890997-140890998	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
6	rs542073382	chr9:140890998-140890999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373573328	chr9:140891001-140891002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs182272443	chr9:140891015-140891016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527954096	chr9:140891028-140891029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs376843694	chr9:140891088-140891089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548113459	chr9:140891186-140891187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570820680	chr9:140891285-140891286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574505363	chr9:140891289-140891290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs545213732	chr9:140891312-140891313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs533369059	chr9:140891324-140891325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs114871069	chr9:140891345-140891346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186765772	chr9:140891352-140891353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191655343	chr9:140891354-140891355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117229770	chr9:140891386-140891387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568295168	chr9:140891434-140891435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs1378955	chr9:140891465-140891466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141914101	chr9:140891534-140891535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs376142357	chr9:140891549-140891550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80060049	chr9:140891594-140891595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs34919108	chr9:140891642-140891643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545413946	chr9:140891681-140891682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs555803302	chr9:140891683-140891684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181686906	chr9:140891760-140891761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs73669835	chr9:140891816-140891817	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs117382617	chr9:140891818-140891819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572637994	chr9:140891898-140891899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541317532	chr9:140891911-140891912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564793296	chr9:140891919-140891920	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533332044	chr9:140891959-140891960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs118171672	chr9:140891971-140891972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544740421	chr9:140891985-140891986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568337000	chr9:140892123-140892124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529369131	chr9:140892129-140892130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549499056	chr9:140892230-140892231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141534173	chr9:140892231-140892232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs117138852	chr9:140892232-140892233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547259347	chr9:140892247-140892248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150464028	chr9:140892248-140892249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539379054	chr9:140892251-140892252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12555003	chr9:140892292-140892293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138264443	chr9:140892304-140892305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535190106	chr9:140892308-140892309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555448677	chr9:140892342-140892343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536993957	chr9:140892345-140892346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572519995	chr9:140892374-140892375	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:475 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140874600-140904600	Weak transcription	Brain Angular Gyrus	brain
2	chr9:140879800-140904600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr9:140885400-140900800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr9:140894600-140916600	Weak transcription	Brain Anterior Caudate	brain
5	chr9:140896800-140898600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr9:140896800-140903800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr9:140897200-140900800	Weak transcription	Brain Germinal Matrix	brain
8	chr9:140898200-140901200	Weak transcription	Fetal Brain Female	brain
9	chr9:140900800-140901400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:140900800-140901600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr9:140900800-140904800	Strong transcription	Brain Germinal Matrix	brain
12	chr9:140901200-140901800	Strong transcription	Fetal Brain Female	brain
13	chr9:140901600-140902600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:140901800-140902400	Weak transcription	Fetal Brain Female	brain
15	chr9:140902400-140905600	Strong transcription	Fetal Brain Female	brain
16	chr9:140902400-140917000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr9:140902600-140902800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr9:140902600-140916800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr9:140902800-140903000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr9:140902800-140917600	Weak transcription	Right Atrium	heart
21	chr9:140903000-140903200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr9:140903000-140905600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr9:140903200-140904000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:140903800-140905200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
25	chr9:140903800-140905800	Enhancers	Fetal Muscle Leg	muscle
26	chr9:140903800-140917000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr9:140904000-140904600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:140904000-140904800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr9:140904000-140905400	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr9:140904400-140904600	Enhancers	Spleen	Spleen
31	chr9:140904400-140905200	Enhancers	Right Ventricle	heart
32	chr9:140904600-140904800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr9:140904600-140905000	Enhancers	Brain Angular Gyrus	brain
34	chr9:140904600-140905000	Enhancers	Brain Cingulate Gyrus	brain
35	chr9:140904600-140905400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr9:140904600-140908600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr9:140904600-140917000	Weak transcription	Spleen	Spleen
38	chr9:140904800-140905000	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chr9:140904800-140906200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:140904800-140909400	Weak transcription	Brain Germinal Matrix	brain
41	chr9:140904800-140917000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr9:140905000-140911800	Weak transcription	Brain Cingulate Gyrus	brain
43	chr9:140905000-140915600	Weak transcription	Brain Angular Gyrus	brain
44	chr9:140905200-140907800	Weak transcription	Right Ventricle	heart
45	chr9:140905200-140917000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr9:140905400-140909200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr9:140905400-140910200	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr9:140905600-140909400	Weak transcription	Fetal Brain Female	brain
49	chr9:140905800-140907800	Weak transcription	Fetal Muscle Leg	muscle
50	chr9:140906200-140906800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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