Variant report

Variant	nsv469920
Chromosome Location	chr9:140866189-141027939
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1331)
CpG islands
(count:1344)
Chromatin interactive
region (count:87)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1331 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

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	chr9:141020637-141020864	K562	blood:	n/a	n/a
3	ATF3	chr9:141020692-141020855	GM12878	blood:	n/a	n/a
4	ATF3	chr9:141020689-141020889	GM12878	blood:	n/a	n/a
5	BACH1	chr9:140918133-140918313	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr9:141020609-141020912	GM12878	blood:	n/a	n/a
7	BATF	chr9:141023409-141023594	GM12878	blood:	n/a	n/a
8	BCL11A	chr9:141023414-141023612	GM12878	blood:	n/a	n/a
9	BCL3	chr9:140910358-140910716	GM12878	blood:	n/a	n/a
10	BCL3	chr9:140910297-140910754	GM12878	blood:	n/a	n/a
11	BCL3	chr9:140993643-140993893	GM12878	blood:	n/a	n/a
12	BCL3	chr9:140904990-140905244	GM12878	blood:	n/a	n/a
13	BHLHE40	chr9:140948945-140949242	K562	blood:	n/a	n/a
14	BHLHE40	chr9:140948939-140949175	HepG2	liver:	n/a	n/a
15	BHLHE40	chr9:140879411-140879615	HepG2	liver:	n/a	n/a
16	BHLHE40	chr9:140993888-140994157	HepG2	liver:	n/a	n/a
17	BHLHE40	chr9:140993839-140994191	K562	blood:	n/a	n/a
18	BRCA1	chr9:140910350-140910549	GM12878	blood:	n/a	n/a
19	CBX3	chr9:141023337-141023724	K562	blood:	n/a	n/a
20	CBX3	chr9:140980110-140980451	HCT-116	colon:	n/a	n/a
21	CBX3	chr9:140980062-140980441	K562	blood:	n/a	n/a
22	CBX3	chr9:141023334-141023686	K562	blood:	n/a	n/a
23	CBX3	chr9:140980114-140980383	K562	blood:	n/a	n/a
24	CBX3	chr9:141020180-141021846	K562	blood:	n/a	n/a
25	CBX3	chr9:141020423-141021627	K562	blood:	n/a	n/a
26	CCNT2	chr9:140918130-140918232	K562	blood:	n/a	n/a
27	CCNT2	chr9:140928501-140928648	K562	blood:	n/a	n/a
28	CEBPB	chr9:140986585-140986794	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr9:140988747-140988822	K562	blood:	n/a	chr9:140988798-140988809
30	CEBPB	chr9:140990315-140990645	A549	lung:	n/a	chr9:140990481-140990492
31	CEBPB	chr9:140896197-140896470	Hela-S3	cervix:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
32	CEBPB	chr9:141021040-141021243	GM12878	blood:	n/a	n/a
33	CEBPB	chr9:140942551-140942648	Hela-S3	cervix:	n/a	chr9:140942603-140942614
34	CEBPB	chr9:141020544-141021559	GM12878	blood:	n/a	n/a
35	CEBPB	chr9:140926152-140926283	HepG2	liver:	n/a	n/a
36	CEBPB	chr9:141020616-141021529	K562	blood:	n/a	n/a
37	CEBPB	chr9:140986589-140986844	MCF-7	breast:	n/a	n/a
38	CEBPB	chr9:140988749-140988840	HepG2	liver:	n/a	chr9:140988798-140988809
39	CEBPB	chr9:140968573-140968696	A549	lung:	n/a	n/a
40	CEBPB	chr9:140990326-140990648	Hela-S3	cervix:	n/a	chr9:140990481-140990492
41	CEBPB	chr9:140986459-140986918	MCF-7	breast:	n/a	n/a
42	CEBPB	chr9:140968639-140968665	HepG2	liver:	n/a	n/a
43	CEBPB	chr9:140896188-140896435	IMR90	lung:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
44	CEBPB	chr9:140995470-140995766	HepG2	liver:	n/a	chr9:140995597-140995608
45	CEBPB	chr9:140995462-140995769	K562	blood:	n/a	chr9:140995597-140995608
46	CEBPB	chr9:140896273-140896377	A549	lung:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
47	CEBPB	chr9:140896184-140896404	HepG2	liver:	n/a	chr9:140896330-140896341 chr9:140896305-140896316
48	CEBPB	chr9:141020799-141021006	GM12878	blood:	n/a	n/a
49	CEBPB	chr9:140995545-140995733	IMR90	lung:	n/a	chr9:140995597-140995608
50	CEBPB	chr9:140968603-140968732	K562	blood:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140916078-140916128	Jurkat	blood:	n/a
2	chr9:141012312-141012362	HEEpiC	esophagus:	n/a
3	chr9:140916078-140916128	Jurkat	blood:	n/a
4	chr9:141012312-141012362	HEEpiC	esophagus:	n/a
5	chr9:140916078-140916128	HUVEC	blood vessel:	n/a
6	chr9:141017457-141017507	PrEC	prostate:	n/a
7	chr9:141013537-141013587	BJ	skin:	n/a
8	chr9:141012312-141012362	AoSMC	blood vessel:	n/a
9	chr9:140944087-140944137	AG09309	skin:	n/a
10	chr9:140944087-140944137	LNCaP	prostate:	n/a
11	chr9:140937920-140937970	CMK	blood:	n/a
12	chr9:141017457-141017507	AG09309	skin:	n/a
13	chr9:140942584-140942634	IMR90	lung:	fetal
14	chr9:140939579-140939629	HRCEpiC	kidney:	n/a
15	chr9:141016367-141016417	CMK	blood:	n/a
16	chr9:140920003-140920053	K562	blood:	n/a
17	chr9:140942584-140942634	Hepatocyte	liver:	n/a
18	chr9:140970188-140970238	HCT-116	colon:	n/a
19	chr9:140920003-140920053	BE2_C	brain:	n/a
20	chr9:140970188-140970238	NT2-D1	testis:	n/a
21	chr9:140939374-140939424	H1-hESC	embryonic stem cell:	embryo
22	chr9:141007633-141007683	NHDF-neo	bronchial:	n/a
23	chr9:141022253-141022303	SK-N-MC	brain:	n/a
24	chr9:140970188-140970238	HRPEpiC	eye:	n/a
25	chr9:141014674-141014724	NHDF-neo	bronchial:	n/a
26	chr9:141017001-141017051	AG09309	skin:	n/a
27	chr9:141014674-141014724	HCM	heart:	n/a
28	chr9:141017457-141017507	PFSK-1	brain:	n/a
29	chr9:140916078-140916128	AG10803	skin:	n/a
30	chr9:140920003-140920053	GM19239	blood:	n/a
31	chr9:141016791-141016841	AG04449	skin:	fetal
32	chr9:141007633-141007683	PFSK-1	brain:	n/a
33	chr9:141016791-141016841	BE2_C	brain:	n/a
34	chr9:140917431-140917481	SK-N-SH	brain:	n/a
35	chr9:140917431-140917481	GM06990	blood:	n/a
36	chr9:140942584-140942634	AG09319	gingival:	n/a
37	chr9:140917431-140917481	AG10803	skin:	n/a
38	chr9:141016367-141016417	NHBE	bronchial:	n/a
39	chr9:140917431-140917481	AoSMC	blood vessel:	n/a
40	chr9:141013112-141013162	AG10803	skin:	n/a
41	chr9:140957018-140957068	Caco-2	colon:	n/a
42	chr9:141016791-141016841	PANC-1	pancreas:	n/a
43	chr9:141017001-141017051	BE2_C	brain:	n/a
44	chr9:140970188-140970238	SK-N-SH	brain:	n/a
45	chr9:140939579-140939629	HepG2	liver:	n/a
46	chr9:141022253-141022303	HepG2	liver:	n/a
47	chr9:140916078-140916128	RPTEC	kidney:	n/a
48	chr9:141017457-141017507	IMR90	lung:	fetal
49	chr9:140917431-140917481	SK-N-MC	brain:	n/a
50	chr9:140957018-140957068	Hepatocyte	liver:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr9:140944821..140947749-chr9:140947953..140949469,2	K562	blood:
2	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
3	chr9:141011439..141013713-chr9:141015634..141018380,2	K562	blood:
4	chr9:140937242..140939994-chr9:140944412..140947223,2	K562	blood:
5	chr9:140914118..140916387-chr9:140964722..140966318,2	MCF-7	breast:
6	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
7	chr9:140862016..140865668-chr9:140879753..140883106,4	MCF-7	breast:
8	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:
9	chr9:140864855..140867051-chr9:140878528..140880494,2	K562	blood:
10	chr1:149223401..149224369-chr9:140873101..140874123,8	MCF-7	breast:
11	chr9:140966280..140969244-chr9:140971430..140973098,2	K562	blood:
12	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
13	chr22:50714431..50715299-chr9:140947514..140948493,3	MCF-7	breast:
14	chr9:140962197..140963909-chr9:140964440..140967429,2	K562	blood:
15	chr9:140875871..140879281-chr9:140879997..140882583,3	MCF-7	breast:
16	chr9:140955879..140956683-chr9:140995540..140996190,2	MCF-7	breast:
17	chr9:140952760..140954416-chr9:140956168..140957899,2	MCF-7	breast:
18	chr9:140969366..140972281-chr9:140974102..140976549,3	MCF-7	breast:
19	chr9:140919903..140921728-chr9:140923070..140927229,3	K562	blood:
20	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
21	chr9:140900561..140902093-chr9:140907866..140909465,2	MCF-7	breast:
22	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
23	chr9:140938244..140939922-chr9:140958739..140960627,2	K562	blood:
24	chr9:140948638..140949637-chr9:141008065..141008656,3	MCF-7	breast:
25	chr9:140963638..140966246-chr9:140975970..140978505,2	MCF-7	breast:
26	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
27	chr9:140900853..140903158-chr9:140909684..140912170,2	MCF-7	breast:
28	chr9:140954487..140957535-chr9:140966154..140968363,3	K562	blood:
29	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
30	chr9:140865657..140867593-chr9:140877024..140879679,2	MCF-7	breast:
31	chr9:140966280..140969244-chr9:140971233..140973098,3	K562	blood:
32	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
33	chr9:140920105..140921728-chr9:140924502..140927229,2	K562	blood:
34	chr9:140991128..140993433-chr9:140998381..141000455,2	K562	blood:
35	chr9:140954622..140956914-chr9:140961204..140963629,3	MCF-7	breast:
36	chr1:149222900..149224638-chr9:140873623..140875123,3	MCF-7	breast:
37	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
38	chr9:140952348..140955305-chr9:140964883..140967739,2	MCF-7	breast:
39	chr9:140870732..140873052-chr9:140876120..140877929,2	K562	blood:
40	chr9:140869140..140872298-chr9:140874733..140877130,3	MCF-7	breast:
41	chr9:140884223..140886209-chr9:140893112..140896030,2	K562	blood:
42	chr9:140937047..140939903-chr9:140943662..140945593,2	MCF-7	breast:
43	chr9:140889129..140892271-chr9:140900387..140902590,3	K562	blood:
44	chr9:140878818..140881702-chr9:140884301..140887041,2	MCF-7	breast:
45	chr9:140958325..140960613-chr9:140962095..140963626,2	K562	blood:
46	chr9:140930141..140932633-chr9:140940366..140943124,2	MCF-7	breast:
47	chr9:140878818..140881702-chr9:140884301..140887041,2	MCF-7	breast:
48	chr9:140955401..140958368-chr9:140960292..140962101,2	K562	blood:
49	chr1:149223037..149225339-chr9:140872123..140875123,7	MCF-7	breast:
50	chr9:137024514..137025058-chr9:141013083..141013583,2	HCT-116	colon:

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

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

No data

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

Extended variants
information (count: 7189 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:7189 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4412433	chr9:140866189-140866190	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112706344	chr9:140866218-140866219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555544471	chr9:140866224-140866225	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs572185002	chr9:140866225-140866226	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558858267	chr9:140866245-140866246	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374042806	chr9:140866318-140866319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183735208	chr9:140866327-140866328	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs554863285	chr9:140866354-140866355	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543028142	chr9:140866357-140866358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs563210101	chr9:140866364-140866365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs386739702	chr9:140866396-140866397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116289668	chr9:140866397-140866398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566253512	chr9:140866419-140866420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs142785811	chr9:140866471-140866472	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190702141	chr9:140866472-140866473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530146076	chr9:140866482-140866483	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs181987686	chr9:140866483-140866484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537409161	chr9:140866531-140866532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs186986697	chr9:140866548-140866549	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191421981	chr9:140866576-140866577	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540573915	chr9:140866594-140866595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553235963	chr9:140866617-140866618	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs572184335	chr9:140866620-140866621	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs534541225	chr9:140866621-140866622	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs150622508	chr9:140866636-140866637	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs532588611	chr9:140866641-140866642	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs552482098	chr9:140866645-140866646	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs10780195	chr9:140866689-140866690	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs181790848	chr9:140866762-140866763	Weak transcription Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs149547519	chr9:140866808-140866809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs542707393	chr9:140866822-140866823	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144140674	chr9:140866823-140866824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12352971	chr9:140866826-140866827	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553872569	chr9:140866837-140866838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552021362	chr9:140866912-140866913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565530326	chr9:140866913-140866914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531238987	chr9:140866914-140866915	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs185652580	chr9:140866920-140866921	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs113616139	chr9:140866945-140866946	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs567644825	chr9:140866956-140866957	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536278100	chr9:140867005-140867006	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547055864	chr9:140867023-140867024	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs144369731	chr9:140867084-140867085	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs534480475	chr9:140867118-140867119	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148174647	chr9:140867165-140867166	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200428196	chr9:140867167-140867168	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs147383418	chr9:140867220-140867221	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568930631	chr9:140867226-140867227	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539076209	chr9:140867227-140867228	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114552605	chr9:140867231-140867232	Weak transcription Strong transcription Enhancers	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:833 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140845200-140866200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr9:140849800-140873400	Weak transcription	Brain Angular Gyrus	brain
3	chr9:140851800-140871800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr9:140853000-140866600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr9:140855200-140881200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr9:140861600-140876000	Strong transcription	Fetal Brain Female	brain
7	chr9:140863000-140889400	Weak transcription	Brain Cingulate Gyrus	brain
8	chr9:140864200-140868800	Strong transcription	iPS-15b Cell Line	embryonic stem cell
9	chr9:140864400-140879200	Weak transcription	Brain Anterior Caudate	brain
10	chr9:140864600-140867000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr9:140864600-140874000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr9:140865600-140878600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr9:140865800-140870800	Strong transcription	Brain Germinal Matrix	brain
14	chr9:140866200-140866600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr9:140866600-140866800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
16	chr9:140866600-140867200	Strong transcription	Brain Inferior Temporal Lobe	brain
17	chr9:140866600-140878600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:140867000-140868000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr9:140867000-140880400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr9:140867200-140867600	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr9:140867600-140868400	Strong transcription	Brain Inferior Temporal Lobe	brain
22	chr9:140868000-140870000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr9:140868200-140871400	Weak transcription	Spleen	Spleen
24	chr9:140868400-140869400	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr9:140868800-140869200	Enhancers	Fetal Muscle Leg	muscle
26	chr9:140868800-140870000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr9:140869200-140869600	Weak transcription	Fetal Muscle Leg	muscle
28	chr9:140869200-140871200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr9:140869400-140871200	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr9:140869600-140871000	Enhancers	Fetal Muscle Leg	muscle
31	chr9:140870000-140870600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr9:140870000-140871000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
33	chr9:140870600-140878400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr9:140870800-140872200	Weak transcription	Brain Germinal Matrix	brain
35	chr9:140871000-140872800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr9:140871200-140884000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr9:140871800-140872400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr9:140871800-140873000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr9:140872000-140872400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr9:140872200-140875200	Strong transcription	Brain Germinal Matrix	brain
41	chr9:140872400-140878800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr9:140872800-140873400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
43	chr9:140872800-140884600	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr9:140873000-140873400	Strong transcription	HUES64 Cell Line	embryonic stem cell
45	chr9:140873400-140873600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
46	chr9:140873400-140874000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr9:140873400-140874600	Strong transcription	Brain Angular Gyrus	brain
48	chr9:140873600-140880800	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr9:140874000-140874600	Strong transcription	iPS-15b Cell Line	embryonic stem cell
50	chr9:140874000-140875400	Strong transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links