Variant report

Variant	nsv1043466
Chromosome Location	chr9:107950174-108001988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:61)
Chromatin interactive
region (count:30)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:107969161-107969616	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:107978784-107979057	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:107953817-107954397	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:107950180-107950379	HepG2	liver:	n/a	n/a
5	ATF2	chr9:107954003-107954505	GM12878	blood:	n/a	n/a
6	ATF3	chr9:107953867-107954425	A549	lung:	n/a	n/a
7	ATF3	chr9:107949976-107950492	A549	lung:	n/a	n/a
8	BATF	chr9:107954036-107954383	GM12878	blood:	n/a	n/a
9	BATF	chr9:107954047-107954323	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:107954062-107954392	GM12878	blood:	n/a	n/a
11	BCL11A	chr9:107954065-107954307	GM12878	blood:	n/a	n/a
12	BCL3	chr9:107953890-107954501	A549	lung:	n/a	n/a
13	BCL3	chr9:107949887-107950563	A549	lung:	n/a	n/a
14	BCL3	chr9:107953770-107954476	A549	lung:	n/a	n/a
15	BHLHE40	chr9:107954014-107954389	HepG2	liver:	n/a	n/a
16	BHLHE40	chr9:107969191-107969452	HepG2	liver:	n/a	n/a
17	BRCA1	chr9:107954498-107954618	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr9:107984446-107984482	GM12878	blood:	n/a	n/a
19	CBX3	chr9:107985839-107986132	K562	blood:	n/a	n/a
20	CBX3	chr9:107985862-107986159	K562	blood:	n/a	n/a
21	CBX3	chr9:107985775-107986244	HCT-116	colon:	n/a	n/a
22	CEBPB	chr9:107969096-107969642	A549	lung:	n/a	n/a
23	CEBPB	chr9:107953936-107954457	GM12878	blood:	n/a	chr9:107954242-107954253
24	CEBPB	chr9:107982627-107982983	HepG2	liver:	n/a	chr9:107982790-107982801
25	CEBPB	chr9:107950090-107950388	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:107954026-107954446	MCF-7	breast:	n/a	chr9:107954242-107954253
27	CEBPB	chr9:107976518-107976606	K562	blood:	n/a	n/a
28	CEBPB	chr9:107953974-107954458	HepG2	liver:	n/a	chr9:107954242-107954253
29	CEBPB	chr9:107950067-107950506	MCF-7	breast:	n/a	n/a
30	CEBPB	chr9:107953987-107954510	MCF-7	breast:	n/a	chr9:107954242-107954253
31	CEBPB	chr9:107954003-107954468	HepG2	liver:	n/a	chr9:107954242-107954253
32	CEBPB	chr9:107956525-107956889	K562	blood:	n/a	chr9:107956702-107956713
33	CEBPB	chr9:107956515-107956877	Hela-S3	cervix:	n/a	chr9:107956702-107956713
34	CEBPB	chr9:107995472-107995676	K562	blood:	n/a	chr9:107995547-107995558
35	CEBPB	chr9:107949972-107950541	MCF-7	breast:	n/a	n/a
36	CEBPB	chr9:107950055-107950481	A549	lung:	n/a	n/a
37	CEBPB	chr9:107982718-107982869	HepG2	liver:	n/a	chr9:107982790-107982801
38	CEBPB	chr9:107953881-107954443	HepG2	liver:	n/a	chr9:107954242-107954253
39	CEBPB	chr9:107982713-107982975	MCF-7	breast:	n/a	chr9:107982790-107982801
40	CEBPB	chr9:107969058-107969531	IMR90	lung:	n/a	n/a
41	CEBPB	chr9:107995434-107995695	IMR90	lung:	n/a	chr9:107995547-107995558
42	CEBPB	chr9:107964931-107965027	HepG2	liver:	n/a	chr9:107964968-107964979
43	CEBPB	chr9:107995431-107995632	A549	lung:	n/a	chr9:107995547-107995558
44	CEBPB	chr9:107969270-107969639	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:107950070-107950440	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:107995429-107995678	Hela-S3	cervix:	n/a	chr9:107995547-107995558
47	CEBPB	chr9:107956491-107956964	A549	lung:	n/a	chr9:107956702-107956713
48	CEBPB	chr9:107956523-107956882	A549	lung:	n/a	chr9:107956702-107956713
49	CEBPB	chr9:107956517-107956896	HepG2	liver:	n/a	chr9:107956702-107956713
50	CEBPB	chr9:107982645-107982988	H1-hESC	embryonic stem cell:	n/a	chr9:107982790-107982801

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:107979587-107979637	Hepatocyte	liver:	n/a
2	chr9:107979587-107979637	BE2_C	brain:	n/a
3	chr9:107979587-107979637	NH-A	brain:	n/a
4	chr9:107979587-107979637	HepG2	liver:	n/a
5	chr9:107979587-107979637	NB4	blood:	n/a
6	chr9:107979587-107979637	ProgFib	skin:	n/a
7	chr9:107979587-107979637	Caco-2	colon:	n/a
8	chr9:107979587-107979637	GM12878	blood:	n/a
9	chr9:107979587-107979637	HNPCEpiC	eye:	n/a
10	chr9:107979587-107979637	NT2-D1	testis:	n/a
11	chr9:107979587-107979637	U87	brain:	n/a
12	chr9:107979587-107979637	HRCEpiC	kidney:	n/a
13	chr9:107979587-107979637	ovcar-3	ovarian:	n/a
14	chr9:107979587-107979637	SK-N-SH	brain:	n/a
15	chr9:107979587-107979637	HIPEpiC	eye:	n/a
16	chr9:107979587-107979637	NHDF-neo	bronchial:	n/a
17	chr9:107979587-107979637	SK-N-SH_RA	brain:	n/a
18	chr9:107979587-107979637	AG04450	lung:	fetal
19	chr9:107979587-107979637	SK-N-MC	brain:	n/a
20	chr9:107979587-107979637	GM06990	blood:	n/a
21	chr9:107979587-107979637	MCF10A-Er-Src	breast:	n/a
22	chr9:107979587-107979637	BJ	skin:	n/a
23	chr9:107979587-107979637	HPAEpiC	pulmonary alveolar:	n/a
24	chr9:107979587-107979637	Jurkat	blood:	n/a
25	chr9:107979587-107979637	GM12892	blood:	n/a
26	chr9:107979587-107979637	HEEpiC	esophagus:	n/a
27	chr9:107979587-107979637	GM12891	blood:	n/a
28	chr9:107979587-107979637	PrEC	prostate:	n/a
29	chr9:107979587-107979637	HRE	kidney:	n/a
30	chr9:107979587-107979637	LNCaP	prostate:	n/a
31	chr9:107979587-107979637	AG09309	skin:	n/a
32	chr9:107979587-107979637	NHBE	bronchial:	n/a
33	chr9:107979587-107979637	HRPEpiC	eye:	n/a
34	chr9:107979587-107979637	T-47D	breast:	n/a
35	chr9:107979587-107979637	HMEC	breast:	n/a
36	chr9:107979587-107979637	AG10803	skin:	n/a
37	chr9:107979587-107979637	AG09319	gingival:	n/a
38	chr9:107979587-107979637	Hela-S3	cervix:	n/a
39	chr9:107979587-107979637	PFSK-1	brain:	n/a
40	chr9:107979587-107979637	AG04449	skin:	fetal
41	chr9:107979587-107979637	HCM	heart:	n/a
42	chr9:107979587-107979637	A549	lung:	n/a
43	chr9:107979587-107979637	K562	blood:	n/a
44	chr9:107979587-107979637	IMR90	lung:	fetal
45	chr9:107979587-107979637	HCF	heart:	n/a
46	chr9:107979587-107979637	HEK293	kidney:	embryo
47	chr9:107979587-107979637	GM19239	blood:	n/a
48	chr9:107979587-107979637	HAEpiC	amniotic membrane:	n/a
49	chr9:107979587-107979637	HUVEC	blood vessel:	n/a
50	chr9:107979587-107979637	RPTEC	kidney:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:107983423..107986241-chr9:107988114..107989665,2	K562	blood:
2	chr9:107979211..107982587-chr9:107983640..107987366,3	MCF-7	breast:
3	chr9:107971630..107974403-chr9:107994725..107996879,2	MCF-7	breast:
4	chr9:107951628..107955432-chr9:108005280..108008809,4	MCF-7	breast:
5	chr9:107990853..107992925-chr9:108005176..108007091,2	MCF-7	breast:
6	chr9:107979211..107982587-chr9:107983640..107987366,3	MCF-7	breast:
7	chr9:107971630..107974403-chr9:107994725..107996879,2	MCF-7	breast:
8	chr9:107950713..107951349-chr9:108177451..108178322,2	MCF-7	breast:
9	chr9:107989785..107992485-chr9:107999468..108001014,2	MCF-7	breast:
10	chr9:107984198..107987905-chr9:108005262..108007467,3	MCF-7	breast:
11	chr9:107953178..107956116-chr9:107958984..107960617,2	MCF-7	breast:
12	chr9:107940503..107943393-chr9:108000733..108002997,2	MCF-7	breast:
13	chr9:107976686..107978196-chr9:108005195..108008055,2	MCF-7	breast:
14	chr9:107949926..107956747-chr9:108004908..108009966,10	MCF-7	breast:
15	chr9:107983423..107986241-chr9:107988114..107989665,2	K562	blood:
16	chr9:107964013..107966115-chr9:108007069..108009049,2	MCF-7	breast:
17	chr9:107983271..107985398-chr9:108006121..108008052,2	MCF-7	breast:
18	chr9:107999147..108002971-chr9:108003945..108007816,6	MCF-7	breast:
19	chr9:107953178..107956116-chr9:107958984..107960617,2	MCF-7	breast:
20	chr9:107993075..107994603-chr9:107998043..108000828,2	MCF-7	breast:
21	chr9:107948857..107951560-chr9:108005097..108008240,3	MCF-7	breast:
22	chr9:107986434..107988530-chr9:108007277..108010113,2	MCF-7	breast:
23	chr9:107966411..107971365-chr9:108005584..108009070,6	MCF-7	breast:
24	chr9:107993075..107994603-chr9:107998043..108000828,2	MCF-7	breast:
25	chr9:107986788..107989562-chr9:108004560..108006596,2	K562	blood:
26	chr9:107989785..107992485-chr9:107999468..108001014,2	MCF-7	breast:
27	chr9:107967440..107970602-chr9:108006099..108010242,5	MCF-7	breast:
28	chr9:107993056..107995506-chr9:107999251..108000803,2	MCF-7	breast:
29	chr9:107993056..107995506-chr9:107999251..108000803,2	MCF-7	breast:
30	chr9:107997912..108002258-chr9:108004974..108009513,7	MCF-7	breast:

No data

Variant related genes	Relation type
SLC44A1	TF binding region
ENSG00000238208	TF binding region
SLC44A1	CpG island
ENSG00000238208	CpG island
ENSG00000070214	chromatin interactions

Extended variants
information (count: 1863 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1863 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7866760	chr9:107950174-107950175	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10118180	chr9:107950275-107950276	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189507880	chr9:107950308-107950309	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs566445155	chr9:107950323-107950324	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs77347958	chr9:107950335-107950336	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs192401655	chr9:107950345-107950346	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs533195743	chr9:107950419-107950420	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371955949	chr9:107950474-107950475	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375690244	chr9:107950484-107950485	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs71364073	chr9:107950485-107950486	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs112174880	chr9:107950494-107950495	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11521647	chr9:107950496-107950497	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs140425549	chr9:107950519-107950520	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548833533	chr9:107950534-107950535	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144285534	chr9:107950538-107950539	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs147833405	chr9:107950543-107950544	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs139142485	chr9:107950568-107950569	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs535963781	chr9:107950613-107950614	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs184613861	chr9:107950615-107950616	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs10991578	chr9:107950648-107950649	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs557607820	chr9:107950699-107950700	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs576218082	chr9:107950706-107950707	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs149102705	chr9:107950710-107950711	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs190346976	chr9:107950736-107950737	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145649172	chr9:107950761-107950762	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562167620	chr9:107950805-107950806	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs573627242	chr9:107950821-107950822	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs540660982	chr9:107950947-107950948	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs148698572	chr9:107950957-107950958	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181676048	chr9:107950974-107950975	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs71364074	chr9:107950975-107950976	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs142213364	chr9:107950976-107950977	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs553067320	chr9:107951010-107951011	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs373856438	chr9:107951045-107951046	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs146540154	chr9:107951051-107951052	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs141314933	chr9:107951052-107951053	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs145048583	chr9:107951054-107951055	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs559344886	chr9:107951089-107951090	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs185035078	chr9:107951091-107951092	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs34001298	chr9:107951093-107951094	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs560837334	chr9:107951129-107951130	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs189548610	chr9:107951133-107951134	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs528518559	chr9:107951146-107951147	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs546654779	chr9:107951152-107951153	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs34834796	chr9:107951162-107951163	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs551493559	chr9:107951197-107951198	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs571586371	chr9:107951209-107951210	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs569800562	chr9:107951242-107951243	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs141525030	chr9:107951251-107951252	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs551052359	chr9:107951342-107951343	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:107949000-107951200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr9:107949400-107950800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr9:107949600-107951400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:107949600-107958200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr9:107949800-107950200	Flanking Active TSS	A549	lung
6	chr9:107949800-107950400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:107949800-107950400	Enhancers	NH-A	brain
8	chr9:107949800-107950600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr9:107949800-107950600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:107949800-107950800	Enhancers	NHDF-Ad	bronchial
11	chr9:107949800-107950800	Enhancers	Osteobl	bone
12	chr9:107949800-107951000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr9:107949800-107951200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:107949800-107951200	Enhancers	Muscle Satellite Cultured Cells	--
15	chr9:107949800-107952400	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr9:107950000-107950400	Enhancers	HepG2	liver
17	chr9:107950000-107950400	Enhancers	HUVEC	blood vessel
18	chr9:107950000-107950600	Enhancers	HSMM	muscle
19	chr9:107950000-107951200	Enhancers	Hela-S3	cervix
20	chr9:107950200-107950800	Enhancers	Liver	Liver
21	chr9:107950200-107951400	Enhancers	Stomach Mucosa	stomach
22	chr9:107950200-107951600	Enhancers	A549	lung
23	chr9:107950400-107952800	Weak transcription	HepG2	liver
24	chr9:107950600-107951000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr9:107950600-107953800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr9:107950800-107951200	Weak transcription	Liver	Liver
27	chr9:107950800-107953800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr9:107950800-107953800	Weak transcription	Osteobl	bone
29	chr9:107951000-107953600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr9:107951200-107951400	Enhancers	Liver	Liver
31	chr9:107951200-107953600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr9:107951200-107953600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:107951200-107953600	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr9:107951400-107953600	Weak transcription	Liver	Liver
35	chr9:107951600-107951800	Enhancers	Primary B cells from cord blood	blood
36	chr9:107951600-107952800	Weak transcription	A549	lung
37	chr9:107951800-107952800	Weak transcription	Primary B cells from cord blood	blood
38	chr9:107952200-107952400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
39	chr9:107952200-107952600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr9:107952400-107953000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr9:107952400-107953000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr9:107952800-107953000	Enhancers	HepG2	liver
43	chr9:107952800-107953400	Enhancers	Primary B cells from cord blood	blood
44	chr9:107952800-107953800	Enhancers	A549	lung
45	chr9:107953000-107953400	Weak transcription	HepG2	liver
46	chr9:107953000-107953600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr9:107953400-107955600	Enhancers	HepG2	liver
48	chr9:107953600-107953800	Enhancers	Liver	Liver
49	chr9:107953600-107954000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr9:107953600-107954000	Enhancers	Spleen	Spleen

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