Variant report

Variant	nsv540377
Chromosome Location	chr9:140900955-141018985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:931)
CpG islands
(count:1284)
Chromatin interactive
region (count:65)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:931 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

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	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
3	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
4	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
5	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:140993888-140994157	HepG2	liver:	n/a	n/a
7	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
8	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
10	BRCA1	chr9:140910350-140910549	GM12878	blood:	n/a	n/a
11	CBX3	chr9:140980114-140980383	K562	blood:	n/a	n/a
12	CBX3	chr9:140980062-140980441	K562	blood:	n/a	n/a
13	CBX3	chr9:140980110-140980451	HCT-116	colon:	n/a	n/a
14	CCNT2	chr9:140928501-140928648	K562	blood:	n/a	n/a
15	CCNT2	chr9:140918130-140918232	K562	blood:	n/a	n/a
16	CEBPB	chr9:140930573-140930631	K562	blood:	n/a	n/a
17	CEBPB	chr9:140968659-140968695	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:140995470-140995766	HepG2	liver:	n/a	chr9:140995597-140995608
19	CEBPB	chr9:140988747-140988822	K562	blood:	n/a	chr9:140988798-140988809
20	CEBPB	chr9:140986459-140986918	MCF-7	breast:	n/a	n/a
21	CEBPB	chr9:140988749-140988840	HepG2	liver:	n/a	chr9:140988798-140988809
22	CEBPB	chr9:140995483-140995724	A549	lung:	n/a	chr9:140995597-140995608
23	CEBPB	chr9:140995545-140995733	IMR90	lung:	n/a	chr9:140995597-140995608
24	CEBPB	chr9:140926106-140926306	K562	blood:	n/a	n/a
25	CEBPB	chr9:140990305-140990642	HepG2	liver:	n/a	chr9:140990481-140990492
26	CEBPB	chr9:140968639-140968665	HepG2	liver:	n/a	n/a
27	CEBPB	chr9:140990315-140990645	A549	lung:	n/a	chr9:140990481-140990492
28	CEBPB	chr9:140995552-140995750	H1-hESC	embryonic stem cell:	n/a	chr9:140995597-140995608
29	CEBPB	chr9:140986585-140986794	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:140942529-140942729	HepG2	liver:	n/a	chr9:140942603-140942614
31	CEBPB	chr9:140968603-140968732	K562	blood:	n/a	n/a
32	CEBPB	chr9:140990421-140990624	K562	blood:	n/a	chr9:140990481-140990492
33	CEBPB	chr9:140926152-140926283	HepG2	liver:	n/a	n/a
34	CEBPB	chr9:140995462-140995769	K562	blood:	n/a	chr9:140995597-140995608
35	CEBPB	chr9:140986589-140986844	MCF-7	breast:	n/a	n/a
36	CEBPB	chr9:140990326-140990648	Hela-S3	cervix:	n/a	chr9:140990481-140990492
37	CEBPB	chr9:140968573-140968696	A549	lung:	n/a	n/a
38	CEBPB	chr9:140942551-140942648	Hela-S3	cervix:	n/a	chr9:140942603-140942614
39	CEBPD	chr9:140928434-140928784	K562	blood:	n/a	n/a
40	CEBPD	chr9:140928391-140928754	K562	blood:	n/a	n/a
41	CTCF	chr9:140909361-140909529	MCF-7	breast:	n/a	n/a
42	CTCF	chr9:140916900-140917050	HCM	heart:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
43	CTCF	chr9:140916900-140917050	GM12868	blood:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
44	CTCF	chr9:140995580-140995730	HCT-116	colon:	n/a	n/a
45	CTCF	chr9:140916860-140917010	Hela-S3	cervix:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947
46	CTCF	chr9:140995600-140995750	GM12878	blood:	n/a	n/a
47	CTCF	chr9:140995542-140995721	Gliobla	brain:	n/a	n/a
48	CTCF	chr9:140995562-140995675	A549	lung:	n/a	n/a
49	CTCF	chr9:141007760-141007910	BE2_C	brain:	n/a	n/a
50	CTCF	chr9:140995540-140995690	GM12867	blood:	n/a	n/a

(count:1284 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140917431-140917481	Hela-S3	cervix:	n/a
2	chr9:141016791-141016841	LNCaP	prostate:	n/a
3	chr9:141016791-141016841	NT2-D1	testis:	n/a
4	chr9:140917431-140917481	Hela-S3	cervix:	n/a
5	chr9:141016791-141016841	LNCaP	prostate:	n/a
6	chr9:141016791-141016841	NT2-D1	testis:	n/a
7	chr9:140939579-140939629	BJ	skin:	n/a
8	chr9:140937920-140937970	NT2-D1	testis:	n/a
9	chr9:140957018-140957068	HPAEpiC	pulmonary alveolar:	n/a
10	chr9:140944087-140944137	HRCEpiC	kidney:	n/a
11	chr9:140916980-140917030	HCPEpiC	choroid plexus:	n/a
12	chr9:140920003-140920053	NHBE	bronchial:	n/a
13	chr9:140916078-140916128	NB4	blood:	n/a
14	chr9:141013112-141013162	GM12878	blood:	n/a
15	chr9:140916980-140917030	PFSK-1	brain:	n/a
16	chr9:141016791-141016841	IMR90	lung:	fetal
17	chr9:140916980-140917030	HRCEpiC	kidney:	n/a
18	chr9:141016791-141016841	NHBE	bronchial:	n/a
19	chr9:140942584-140942634	GM12891	blood:	n/a
20	chr9:140970188-140970238	GM12891	blood:	n/a
21	chr9:140920003-140920053	MCF-7	breast:	n/a
22	chr9:140920003-140920053	K562	blood:	n/a
23	chr9:141013112-141013162	GM12892	blood:	n/a
24	chr9:141017457-141017507	SAEC	small airway:	n/a
25	chr9:140944087-140944137	HCT-116	colon:	n/a
26	chr9:140937920-140937970	AG04450	lung:	fetal
27	chr9:141007633-141007683	PrEC	prostate:	n/a
28	chr9:140939374-140939424	AG04449	skin:	fetal
29	chr9:140939374-140939424	Caco-2	colon:	n/a
30	chr9:140920003-140920053	AoSMC	blood vessel:	n/a
31	chr9:141014674-141014724	GM12892	blood:	n/a
32	chr9:141017001-141017051	NB4	blood:	n/a
33	chr9:141014674-141014724	CMK	blood:	n/a
34	chr9:141013112-141013162	NHBE	bronchial:	n/a
35	chr9:141014674-141014724	NHDF-neo	bronchial:	n/a
36	chr9:140917413-140917463	BE2_C	brain:	n/a
37	chr9:140916078-140916128	SAEC	small airway:	n/a
38	chr9:140970188-140970238	HL-60	blood:	n/a
39	chr9:141016367-141016417	HUVEC	blood vessel:	n/a
40	chr9:141012312-141012362	AG09319	gingival:	n/a
41	chr9:141007633-141007683	H1-hESC	embryonic stem cell:	embryo
42	chr9:140937920-140937970	NHBE	bronchial:	n/a
43	chr9:140917413-140917463	HIPEpiC	eye:	n/a
44	chr9:140939374-140939424	HCF	heart:	n/a
45	chr9:140939579-140939629	AG04449	skin:	fetal
46	chr9:141007633-141007683	HUVEC	blood vessel:	n/a
47	chr9:141012312-141012362	ProgFib	skin:	n/a
48	chr9:141014674-141014724	LNCaP	prostate:	n/a
49	chr9:140920003-140920053	Hepatocyte	liver:	n/a
50	chr9:140939374-140939424	RPTEC	kidney:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
2	chr9:140955941..140956581-chr9:140995170..140996036,2	MCF-7	breast:
3	chr9:140909435..140911470-chr9:140917464..140919841,2	MCF-7	breast:
4	chr9:140867124..140870002-chr9:140953480..140955243,2	MCF-7	breast:
5	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
6	chr9:140966280..140969244-chr9:140971233..140973098,3	K562	blood:
7	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
8	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
9	chr9:140958325..140960613-chr9:140962095..140963626,2	K562	blood:
10	chr22:50714431..50715299-chr9:140947514..140948493,3	MCF-7	breast:
11	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
12	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
13	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
14	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
15	chr9:140955941..140956581-chr9:140995170..140996036,2	MCF-7	breast:
16	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
17	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
18	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
19	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
20	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
21	chr9:140966280..140969244-chr9:140971233..140973098,3	K562	blood:
22	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
23	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
24	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
25	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
26	chr9:140969366..140972281-chr9:140974102..140976549,3	MCF-7	breast:
27	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
28	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
29	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
30	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
31	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
32	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
33	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
34	chr9:140960893..140963806-chr9:140965235..140966903,2	K562	blood:
35	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
36	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
37	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
38	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
39	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
40	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
41	chr9:140769881..140772281-chr9:140919838..140921575,2	K562	blood:
42	chr9:140962197..140963909-chr9:140964440..140967429,2	K562	blood:
43	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
44	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:
45	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
46	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
47	chr9:140958325..140960613-chr9:140962095..140963626,2	K562	blood:
48	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
49	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
50	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 5421 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:5421 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs58086432	chr9:140900962-140900963	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs376987861	chr9:140901007-140901008	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555106023	chr9:140901045-140901046	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs567443093	chr9:140901061-140901062	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs536463927	chr9:140901066-140901067	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs553236572	chr9:140901118-140901119	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs143248798	chr9:140901119-140901120	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs538969071	chr9:140901120-140901121	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs558257315	chr9:140901125-140901126	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs575204029	chr9:140901126-140901127	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs190785156	chr9:140901130-140901131	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs560665141	chr9:140901145-140901146	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs2290580	chr9:140901146-140901147	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs148289826	chr9:140901173-140901174	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs11794499	chr9:140901176-140901177	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs71510864	chr9:140901177-140901178	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs200932694	chr9:140901178-140901179	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs201784946	chr9:140901179-140901180	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs199938582	chr9:140901189-140901190	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs200898118	chr9:140901212-140901213	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs146062420	chr9:140901227-140901228	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs552845454	chr9:140901255-140901256	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs200099852	chr9:140901257-140901258	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201096610	chr9:140901260-140901261	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs368450405	chr9:140901263-140901264	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs202184196	chr9:140901269-140901270	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200239452	chr9:140901293-140901294	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201000167	chr9:140901299-140901300	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs201843905	chr9:140901320-140901321	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs200273640	chr9:140901323-140901324	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201062476	chr9:140901329-140901330	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs199784241	chr9:140901344-140901345	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs200546797	chr9:140901346-140901347	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534314732	chr9:140901358-140901359	ZNF genes & repeats Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs78898109	chr9:140901405-140901406	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs566698392	chr9:140901433-140901434	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs116183563	chr9:140901438-140901439	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs558817584	chr9:140901450-140901451	Weak transcription Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs138872166	chr9:140901472-140901473	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550044393	chr9:140901493-140901494	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537432141	chr9:140901499-140901500	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554171987	chr9:140901561-140901562	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574192709	chr9:140901581-140901582	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539980508	chr9:140901595-140901596	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs560274674	chr9:140901613-140901614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115250203	chr9:140901678-140901679	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7876019	chr9:140901721-140901722	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558078805	chr9:140901727-140901728	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs541671699	chr9:140901756-140901757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs10718000	chr9:140901758-140901759	Weak transcription Strong 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:729 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

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	chr9:140894600-140916600	Weak transcription	Brain Anterior Caudate	brain
4	chr9:140896800-140903800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr9:140898200-140901200	Weak transcription	Fetal Brain Female	brain
6	chr9:140900800-140901400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:140900800-140901600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:140900800-140904800	Strong transcription	Brain Germinal Matrix	brain
9	chr9:140901200-140901800	Strong transcription	Fetal Brain Female	brain
10	chr9:140901600-140902600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr9:140901800-140902400	Weak transcription	Fetal Brain Female	brain
12	chr9:140902400-140905600	Strong transcription	Fetal Brain Female	brain
13	chr9:140902400-140917000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr9:140902600-140902800	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr9:140902600-140916800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr9:140902800-140903000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:140902800-140917600	Weak transcription	Right Atrium	heart
18	chr9:140903000-140903200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:140903000-140905600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr9:140903200-140904000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr9:140903800-140905200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
22	chr9:140903800-140905800	Enhancers	Fetal Muscle Leg	muscle
23	chr9:140903800-140917000	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr9:140904000-140904600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr9:140904000-140904800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr9:140904000-140905400	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr9:140904400-140904600	Enhancers	Spleen	Spleen
28	chr9:140904400-140905200	Enhancers	Right Ventricle	heart
29	chr9:140904600-140904800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr9:140904600-140905000	Enhancers	Brain Angular Gyrus	brain
31	chr9:140904600-140905000	Enhancers	Brain Cingulate Gyrus	brain
32	chr9:140904600-140905400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr9:140904600-140908600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr9:140904600-140917000	Weak transcription	Spleen	Spleen
35	chr9:140904800-140905000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr9:140904800-140906200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr9:140904800-140909400	Weak transcription	Brain Germinal Matrix	brain
38	chr9:140904800-140917000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr9:140905000-140911800	Weak transcription	Brain Cingulate Gyrus	brain
40	chr9:140905000-140915600	Weak transcription	Brain Angular Gyrus	brain
41	chr9:140905200-140907800	Weak transcription	Right Ventricle	heart
42	chr9:140905200-140917000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr9:140905400-140909200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr9:140905400-140910200	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr9:140905600-140909400	Weak transcription	Fetal Brain Female	brain
46	chr9:140905800-140907800	Weak transcription	Fetal Muscle Leg	muscle
47	chr9:140906200-140906800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr9:140906600-140906800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr9:140906800-140909200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr9:140907600-140908200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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