Variant report

Variant	nsv1046495
Chromosome Location	chr9:140862503-141018985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1197)
CpG islands
(count:1284)
Chromatin interactive
region (count:89)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1197 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	BACH1	chr9:140918133-140918313	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
4	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
5	BCL3	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
6	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
7	BHLHE40	chr9:140993888-140994157	HepG2	liver:	n/a	n/a
8	BHLHE40	chr9:140879411-140879615	HepG2	liver:	n/a	n/a
9	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
10	BHLHE40	chr9:140862896-140863013	K562	blood:	n/a	n/a
11	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
12	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
13	BRCA1	chr9:140910350-140910549	GM12878	blood:	n/a	n/a
14	CBX3	chr9:140980062-140980441	K562	blood:	n/a	n/a
15	CBX3	chr9:140980110-140980451	HCT-116	colon:	n/a	n/a
16	CBX3	chr9:140980114-140980383	K562	blood:	n/a	n/a
17	CCNT2	chr9:140918130-140918232	K562	blood:	n/a	n/a
18	CCNT2	chr9:140928501-140928648	K562	blood:	n/a	n/a
19	CEBPB	chr9:140968659-140968695	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:140896197-140896470	Hela-S3	cervix:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
21	CEBPB	chr9:140990326-140990648	Hela-S3	cervix:	n/a	chr9:140990481-140990492
22	CEBPB	chr9:140990305-140990642	HepG2	liver:	n/a	chr9:140990481-140990492
23	CEBPB	chr9:140926106-140926306	K562	blood:	n/a	n/a
24	CEBPB	chr9:140930573-140930631	K562	blood:	n/a	n/a
25	CEBPB	chr9:140896273-140896377	A549	lung:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
26	CEBPB	chr9:140995462-140995769	K562	blood:	n/a	chr9:140995597-140995608
27	CEBPB	chr9:140995552-140995750	H1-hESC	embryonic stem cell:	n/a	chr9:140995597-140995608
28	CEBPB	chr9:140896188-140896435	IMR90	lung:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
29	CEBPB	chr9:140995470-140995766	HepG2	liver:	n/a	chr9:140995597-140995608
30	CEBPB	chr9:140968639-140968665	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:140926152-140926283	HepG2	liver:	n/a	n/a
32	CEBPB	chr9:140995483-140995724	A549	lung:	n/a	chr9:140995597-140995608
33	CEBPB	chr9:140990421-140990624	K562	blood:	n/a	chr9:140990481-140990492
34	CEBPB	chr9:140995545-140995733	IMR90	lung:	n/a	chr9:140995597-140995608
35	CEBPB	chr9:140986589-140986844	MCF-7	breast:	n/a	n/a
36	CEBPB	chr9:140986585-140986794	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr9:140968573-140968696	A549	lung:	n/a	n/a
38	CEBPB	chr9:140968603-140968732	K562	blood:	n/a	n/a
39	CEBPB	chr9:140896195-140896462	K562	blood:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
40	CEBPB	chr9:140986459-140986918	MCF-7	breast:	n/a	n/a
41	CEBPB	chr9:140988749-140988840	HepG2	liver:	n/a	chr9:140988798-140988809
42	CEBPB	chr9:140990315-140990645	A549	lung:	n/a	chr9:140990481-140990492
43	CEBPB	chr9:140896184-140896404	HepG2	liver:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
44	CEBPB	chr9:140942551-140942648	Hela-S3	cervix:	n/a	chr9:140942603-140942614
45	CEBPB	chr9:140988747-140988822	K562	blood:	n/a	chr9:140988798-140988809
46	CEBPB	chr9:140942529-140942729	HepG2	liver:	n/a	chr9:140942603-140942614
47	CEBPD	chr9:140928391-140928754	K562	blood:	n/a	n/a
48	CEBPD	chr9:140928434-140928784	K562	blood:	n/a	n/a
49	CTCF	chr9:140916846-140917054	Hela-S3	cervix:	n/a	chr9:140916937-140916950 chr9:140917019-140917032 chr9:140916932-140916950 chr9:140916934-140916947
50	CTCF	chr9:140916840-140916990	HMEC	breast:	n/a	chr9:140916937-140916950 chr9:140916932-140916950 chr9:140916934-140916947

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:141017457-141017507	GM12891	blood:	n/a
2	chr9:140970188-140970238	HRCEpiC	kidney:	n/a
3	chr9:140917413-140917463	NH-A	brain:	n/a
4	chr9:141017457-141017507	GM12891	blood:	n/a
5	chr9:140970188-140970238	HRCEpiC	kidney:	n/a
6	chr9:140917413-140917463	NH-A	brain:	n/a
7	chr9:141007633-141007683	NH-A	brain:	n/a
8	chr9:141016791-141016841	NHBE	bronchial:	n/a
9	chr9:141017457-141017507	U87	brain:	n/a
10	chr9:140939579-140939629	Caco-2	colon:	n/a
11	chr9:141016367-141016417	HUVEC	blood vessel:	n/a
12	chr9:141012312-141012362	GM06990	blood:	n/a
13	chr9:140957018-140957068	HNPCEpiC	eye:	n/a
14	chr9:140942584-140942634	NHBE	bronchial:	n/a
15	chr9:140917431-140917481	NB4	blood:	n/a
16	chr9:141013537-141013587	U87	brain:	n/a
17	chr9:141016791-141016841	MCF-7	breast:	n/a
18	chr9:141016367-141016417	HRE	kidney:	n/a
19	chr9:140916980-140917030	SK-N-SH	brain:	n/a
20	chr9:140917431-140917481	ECC-1	luminal epithelium:	n/a
21	chr9:140916980-140917030	NHBE	bronchial:	n/a
22	chr9:141017001-141017051	GM12892	blood:	n/a
23	chr9:141013537-141013587	SK-N-SH_RA	brain:	n/a
24	chr9:140920003-140920053	HCPEpiC	choroid plexus:	n/a
25	chr9:140920003-140920053	AG04449	skin:	fetal
26	chr9:141012312-141012362	SKMC	muscle:	n/a
27	chr9:141016367-141016417	AoSMC	blood vessel:	n/a
28	chr9:140939374-140939424	NT2-D1	testis:	n/a
29	chr9:141016791-141016841	HCT-116	colon:	n/a
30	chr9:140917413-140917463	HEEpiC	esophagus:	n/a
31	chr9:141013112-141013162	HCF	heart:	n/a
32	chr9:140917431-140917481	HRE	kidney:	n/a
33	chr9:140916078-140916128	GM06990	blood:	n/a
34	chr9:140939579-140939629	HRCEpiC	kidney:	n/a
35	chr9:141014674-141014724	Hepatocyte	liver:	n/a
36	chr9:140916078-140916128	T-47D	breast:	n/a
37	chr9:141016791-141016841	PFSK-1	brain:	n/a
38	chr9:140917431-140917481	HUVEC	blood vessel:	n/a
39	chr9:140944087-140944137	AG04449	skin:	fetal
40	chr9:141017001-141017051	LNCaP	prostate:	n/a
41	chr9:140942584-140942634	NB4	blood:	n/a
42	chr9:141007633-141007683	NT2-D1	testis:	n/a
43	chr9:140942584-140942634	HRCEpiC	kidney:	n/a
44	chr9:141016791-141016841	NB4	blood:	n/a
45	chr9:141014674-141014724	NT2-D1	testis:	n/a
46	chr9:141016791-141016841	NHDF-neo	bronchial:	n/a
47	chr9:140916980-140917030	HCPEpiC	choroid plexus:	n/a
48	chr9:141012312-141012362	A549	lung:	n/a
49	chr9:140970188-140970238	ProgFib	skin:	n/a
50	chr9:141016791-141016841	SK-N-SH	brain:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
2	chr9:140769881..140772281-chr9:140919838..140921575,2	K562	blood:
3	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
4	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
5	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
6	chr9:140958325..140960613-chr9:140962095..140963626,2	K562	blood:
7	chr9:140955941..140956581-chr9:140995170..140996036,2	MCF-7	breast:
8	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
9	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
10	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
11	chr22:50714431..50715299-chr9:140947514..140948493,3	MCF-7	breast:
12	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
13	chr9:140928490..140931085-chr9:140933253..140936075,2	MCF-7	breast:
14	chr1:149223037..149225339-chr9:140872123..140875123,7	MCF-7	breast:
15	chr9:140865657..140867593-chr9:140877024..140879679,2	MCF-7	breast:
16	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
17	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
18	chr9:140860566..140865150-chr9:140867846..140870803,4	MCF-7	breast:
19	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
20	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
21	chr9:140909435..140911470-chr9:140917464..140919841,2	MCF-7	breast:
22	chr9:141007252..141009770-chr9:141014340..141016354,2	MCF-7	breast:
23	chr9:140878818..140881702-chr9:140884301..140887041,2	MCF-7	breast:
24	chr9:140969366..140972281-chr9:140974102..140976549,3	MCF-7	breast:
25	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
26	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
27	chr9:140862016..140865668-chr9:140879753..140883106,4	MCF-7	breast:
28	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
29	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
30	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
31	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
32	chr9:140966280..140969244-chr9:140971233..140973098,3	K562	blood:
33	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
34	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
35	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
36	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:
37	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
38	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
39	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
40	chr9:140949053..140949565-chr9:140995304..140996092,3	MCF-7	breast:
41	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:
42	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
43	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
44	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
45	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
46	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
47	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
48	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
49	chr9:140865657..140867593-chr9:140877024..140879679,2	MCF-7	breast:
50	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:

(count:6 , 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-AL772363.1-6	chr9:140937901-140938239	NONHSAT135763
4	lnc-AL772363.1-6	chr9:140939331-140939523	NONHSAT135763
5	lnc-AL772363.1-6	chr9:140934955-140937453	NONHSAT135763
6	lnc-AL772363.1-7	chr9:140954809-140955130	NONHSAT135765

No data

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

Extended variants
information (count: 6943 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:6943 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559826723	chr9:140862561-140862562	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs74312739	chr9:140862578-140862579	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77151226	chr9:140862584-140862585	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553037894	chr9:140862600-140862601	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141124146	chr9:140862601-140862602	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147115719	chr9:140862656-140862657	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564939900	chr9:140862659-140862660	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575429564	chr9:140862686-140862687	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148156528	chr9:140862691-140862692	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79195528	chr9:140862732-140862733	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376903510	chr9:140862782-140862783	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547269900	chr9:140862796-140862797	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560651841	chr9:140862810-140862811	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186602857	chr9:140862834-140862835	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141954422	chr9:140862931-140862932	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs568982167	chr9:140862941-140862942	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191510540	chr9:140862967-140862968	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs530917262	chr9:140862981-140862982	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182791937	chr9:140862994-140862995	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536083971	chr9:140863059-140863060	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553214915	chr9:140863076-140863077	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550708485	chr9:140863096-140863097	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567642867	chr9:140863100-140863101	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536286085	chr9:140863143-140863144	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573069563	chr9:140863158-140863159	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs59048050	chr9:140863181-140863182	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs558586052	chr9:140863209-140863210	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535695750	chr9:140863218-140863219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191438047	chr9:140863318-140863319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544313166	chr9:140863361-140863362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150251993	chr9:140863393-140863394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs574956370	chr9:140863397-140863398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540506825	chr9:140863470-140863471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560807925	chr9:140863472-140863473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs118183179	chr9:140863481-140863482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs555555112	chr9:140863487-140863488	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs545745902	chr9:140863559-140863560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs111463707	chr9:140863598-140863599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138883042	chr9:140863600-140863601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs142078647	chr9:140863615-140863616	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs548253521	chr9:140863642-140863643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368641773	chr9:140863666-140863667	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs146331214	chr9:140863687-140863688	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529862683	chr9:140863720-140863721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538803327	chr9:140863749-140863750	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113535841	chr9:140863761-140863762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182188852	chr9:140863765-140863766	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs538941453	chr9:140863772-140863773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558931642	chr9:140863797-140863798	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575361422	chr9:140863847-140863848	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:851 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140845200-140866200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:140847400-140864000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr9:140849800-140873400	Weak transcription	Brain Angular Gyrus	brain
4	chr9:140850600-140862600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr9:140851800-140871800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr9:140853000-140866600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr9:140855200-140864000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr9:140855200-140864200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:140855200-140881200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr9:140855400-140864200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr9:140861600-140876000	Strong transcription	Fetal Brain Female	brain
12	chr9:140861800-140863000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr9:140861800-140863000	Strong transcription	Brain Germinal Matrix	brain
14	chr9:140861800-140864000	Weak transcription	Brain Anterior Caudate	brain
15	chr9:140862000-140863000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:140862600-140863000	Enhancers	Brain Cingulate Gyrus	brain
17	chr9:140862600-140863200	Enhancers	Spleen	Spleen
18	chr9:140863000-140864200	Weak transcription	Brain Germinal Matrix	brain
19	chr9:140863000-140865000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr9:140863000-140865000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr9:140863000-140889400	Weak transcription	Brain Cingulate Gyrus	brain
22	chr9:140863200-140864200	Weak transcription	Spleen	Spleen
23	chr9:140864000-140864400	Enhancers	Brain Anterior Caudate	brain
24	chr9:140864000-140864600	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr9:140864000-140865600	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr9:140864200-140864400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr9:140864200-140864600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
28	chr9:140864200-140864600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr9:140864200-140864600	Strong transcription	Brain Germinal Matrix	brain
30	chr9:140864200-140868800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
31	chr9:140864400-140879200	Weak transcription	Brain Anterior Caudate	brain
32	chr9:140864600-140865800	Weak transcription	Brain Germinal Matrix	brain
33	chr9:140864600-140867000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr9:140864600-140874000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr9:140865000-140865600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:140865000-140865800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr9:140865200-140865400	Bivalent Enhancer	Placenta	Placenta
38	chr9:140865600-140878600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr9:140865800-140870800	Strong transcription	Brain Germinal Matrix	brain
40	chr9:140866200-140866600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:140866600-140866800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
42	chr9:140866600-140867200	Strong transcription	Brain Inferior Temporal Lobe	brain
43	chr9:140866600-140878600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr9:140867000-140868000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr9:140867000-140880400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr9:140867200-140867600	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr9:140867600-140868400	Strong transcription	Brain Inferior Temporal Lobe	brain
48	chr9:140868000-140870000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:140868200-140871400	Weak transcription	Spleen	Spleen
50	chr9:140868400-140869400	Weak transcription	Brain Inferior Temporal Lobe	brain

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