Variant report

Variant	nsv615218
Chromosome Location	chr9:116365126-116391069
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:665)
CpG islands
(count:61)
Chromatin interactive
region (count:35)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:116376294-116376349	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:116372138-116372489	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:116382820-116383077	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:116384914-116385574	HepG2	liver:	n/a	n/a
5	ATF2	chr9:116385103-116385621	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:116385186-116385785	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:116382711-116383313	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr9:116382718-116383223	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr9:116382768-116383032	K562	blood:	n/a	n/a
10	ATF3	chr9:116382699-116383222	A549	lung:	n/a	n/a
11	ATF3	chr9:116366723-116366919	K562	blood:	n/a	n/a
12	ATF3	chr9:116382824-116383173	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr9:116385319-116385849	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:116372310-116372500	H1-hESC	embryonic stem cell:	n/a	n/a
15	BHLHE40	chr9:116377619-116377877	GM12878	blood:	n/a	n/a
16	BHLHE40	chr9:116364735-116365218	HepG2	liver:	n/a	n/a
17	CBX3	chr9:116366546-116366890	K562	blood:	n/a	n/a
18	CCNT2	chr9:116375263-116375436	K562	blood:	n/a	n/a
19	CEBPB	chr9:116382792-116383041	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr9:116377193-116377726	IMR90	lung:	n/a	n/a
21	CEBPB	chr9:116385265-116385559	IMR90	lung:	n/a	n/a
22	CEBPB	chr9:116385185-116385485	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr9:116382888-116383139	HepG2	liver:	n/a	n/a
24	CEBPB	chr9:116382840-116383098	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr9:116382813-116383073	IMR90	lung:	n/a	n/a
26	CHD2	chr9:116382848-116383196	Hela-S3	cervix:	n/a	n/a
27	CHD2	chr9:116385498-116385611	HepG2	liver:	n/a	n/a
28	CHD2	chr9:116372137-116372469	HepG2	liver:	n/a	n/a
29	CHD2	chr9:116385248-116385621	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr9:116382889-116383066	HepG2	liver:	n/a	n/a
31	CHD2	chr9:116371781-116372554	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr9:116377356-116377805	GM12878	blood:	n/a	n/a
33	CHD2	chr9:116382786-116383006	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr9:116385163-116385556	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr9:116370700-116370850	AG04449	skin:	n/a	n/a
36	CTCF	chr9:116370720-116370870	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr9:116370720-116370870	AG04449	skin:	n/a	n/a
38	CTCF	chr9:116370720-116370870	BJ	skin:	n/a	n/a
39	CTCF	chr9:116373760-116373910	HepG2	liver:	n/a	n/a
40	CTCF	chr9:116370680-116370830	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr9:116370640-116370790	HMF	breast:	n/a	n/a
42	CTCF	chr9:116373660-116373810	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr9:116370720-116370870	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr9:116370700-116370850	NHDF-neo	bronchial:	n/a	n/a
45	CTCF	chr9:116370700-116370850	AG04450	lung:	n/a	n/a
46	CTCF	chr9:116370740-116370890	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr9:116370720-116370870	HCT-116	colon:	n/a	n/a
48	CTCF	chr9:116383800-116383950	AG04449	skin:	n/a	n/a
49	CTCF	chr9:116379183-116379375	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr9:116370720-116370870	HBMEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116372034-116372084	SK-N-SH	brain:	n/a
2	chr9:116372034-116372084	BJ	skin:	n/a
3	chr9:116372034-116372084	NHBE	bronchial:	n/a
4	chr9:116372034-116372084	AG04450	lung:	fetal
5	chr9:116372034-116372084	LNCaP	prostate:	n/a
6	chr9:116372034-116372084	RPTEC	kidney:	n/a
7	chr9:116372034-116372084	HCM	heart:	n/a
8	chr9:116372034-116372084	ECC-1	luminal epithelium:	n/a
9	chr9:116372034-116372084	PFSK-1	brain:	n/a
10	chr9:116372034-116372084	HNPCEpiC	eye:	n/a
11	chr9:116372034-116372084	A549	lung:	n/a
12	chr9:116372034-116372084	HRE	kidney:	n/a
13	chr9:116372034-116372084	H1-hESC	embryonic stem cell:	embryo
14	chr9:116372034-116372084	AG09319	gingival:	n/a
15	chr9:116372034-116372084	PANC-1	pancreas:	n/a
16	chr9:116372034-116372084	SK-N-SH_RA	brain:	n/a
17	chr9:116372034-116372084	NB4	blood:	n/a
18	chr9:116372034-116372084	HEEpiC	esophagus:	n/a
19	chr9:116372034-116372084	GM12878	blood:	n/a
20	chr9:116372034-116372084	AG09309	skin:	n/a
21	chr9:116372034-116372084	AoSMC	blood vessel:	n/a
22	chr9:116372034-116372084	SKMC	muscle:	n/a
23	chr9:116372034-116372084	GM12891	blood:	n/a
24	chr9:116372034-116372084	HMEC	breast:	n/a
25	chr9:116372034-116372084	MCF-7	breast:	n/a
26	chr9:116372034-116372084	HIPEpiC	eye:	n/a
27	chr9:116372034-116372084	T-47D	breast:	n/a
28	chr9:116372034-116372084	HPAEpiC	pulmonary alveolar:	n/a
29	chr9:116372034-116372084	ovcar-3	ovarian:	n/a
30	chr9:116372034-116372084	SK-N-MC	brain:	n/a
31	chr9:116372034-116372084	IMR90	lung:	fetal
32	chr9:116372034-116372084	AG10803	skin:	n/a
33	chr9:116372034-116372084	SAEC	small airway:	n/a
34	chr9:116372034-116372084	GM19239	blood:	n/a
35	chr9:116372034-116372084	BE2_C	brain:	n/a
36	chr9:116372034-116372084	HEK293	kidney:	embryo
37	chr9:116372034-116372084	NHDF-neo	bronchial:	n/a
38	chr9:116372034-116372084	MCF10A-Er-Src	breast:	n/a
39	chr9:116372034-116372084	HCF	heart:	n/a
40	chr9:116372034-116372084	HRCEpiC	kidney:	n/a
41	chr9:116372034-116372084	K562	blood:	n/a
42	chr9:116372034-116372084	AG04449	skin:	fetal
43	chr9:116372034-116372084	Hepatocyte	liver:	n/a
44	chr9:116372034-116372084	HUVEC	blood vessel:	n/a
45	chr9:116372034-116372084	HCT-116	colon:	n/a
46	chr9:116372034-116372084	Hela-S3	cervix:	n/a
47	chr9:116372034-116372084	HCPEpiC	choroid plexus:	n/a
48	chr9:116372034-116372084	PrEC	prostate:	n/a
49	chr9:116372034-116372084	HAEpiC	amniotic membrane:	n/a
50	chr9:116372034-116372084	ProgFib	skin:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116357889..116361731-chr9:116362609..116366505,5	MCF-7	breast:
2	chr9:116364314..116366664-chr9:116377313..116378930,2	MCF-7	breast:
3	chr9:116388280..116391769-chr9:116395247..116396966,3	MCF-7	breast:
4	chr9:116382263..116386126-chr9:116386783..116389124,3	MCF-7	breast:
5	chr9:116384013..116386920-chr9:116410896..116413460,2	MCF-7	breast:
6	chr9:116385537..116387562-chr9:116409870..116412944,3	MCF-7	breast:
7	chr9:116354124..116355971-chr9:116365134..116366899,2	MCF-7	breast:
8	chr9:116371231..116372845-chr9:116374624..116376242,2	MCF-7	breast:
9	chr9:116373324..116375940-chr9:116380563..116382794,2	MCF-7	breast:
10	chr9:116385601..116388209-chr9:116407553..116409087,2	MCF-7	breast:
11	chr9:116362421..116364215-chr9:116382528..116385259,2	MCF-7	breast:
12	chr9:116376628..116378313-chr9:116382222..116384609,3	MCF-7	breast:
13	chr9:116383635..116386801-chr9:116393462..116397071,5	MCF-7	breast:
14	chr9:116386561..116388140-chr9:116399851..116401503,2	MCF-7	breast:
15	chr9:116368318..116370482-chr9:116376784..116379532,2	MCF-7	breast:
16	chr9:116368954..116370603-chr9:116373905..116376244,2	MCF-7	breast:
17	chr9:116368474..116370761-chr9:116371001..116373367,2	MCF-7	breast:
18	chr9:116383167..116386391-chr9:116389906..116398638,8	MCF-7	breast:
19	chr9:116356309..116357937-chr9:116375558..116377978,2	MCF-7	breast:
20	chr9:116387727..116389592-chr9:116393862..116395666,2	K562	blood:
21	chr9:116368474..116370761-chr9:116371001..116373367,2	MCF-7	breast:
22	chr9:116375318..116378265-chr9:116400477..116402122,2	K562	blood:
23	chr9:116368318..116370482-chr9:116376784..116379532,2	MCF-7	breast:
24	chr9:116368954..116370603-chr9:116373905..116376244,2	MCF-7	breast:
25	chr9:116378512..116381632-chr9:116384610..116387755,3	MCF-7	breast:
26	chr9:116172702..116174409-chr9:116381360..116383255,2	MCF-7	breast:
27	chr9:116364672..116367023-chr9:116368239..116370280,2	MCF-7	breast:
28	chr9:116382263..116386126-chr9:116386783..116389124,3	MCF-7	breast:
29	chr9:116382976..116384778-chr9:116398456..116400066,2	MCF-7	breast:
30	chr9:116364314..116366664-chr9:116377313..116378930,2	MCF-7	breast:
31	chr9:116364672..116367023-chr9:116368239..116370280,2	MCF-7	breast:
32	chr9:116376628..116378313-chr9:116382222..116384609,3	MCF-7	breast:
33	chr9:116383167..116386391-chr9:116389906..116398638,8	MCF-7	breast:
34	chr9:116371231..116372845-chr9:116374624..116376242,2	MCF-7	breast:
35	chr9:116376834..116379828-chr9:116381468..116382973,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RGS3-1	chr9:116382056-116384914	ENSG00000233817
2	lnc-RGS3-1	chr9:116381508-116381691	ENSG00000233817

No data

Variant related genes	Relation type
ENSG00000233817	TF binding region
ENSG00000233817	CpG island
ENSG00000233817	chromatin interactions
ENSG00000148229	chromatin interactions
ENSG00000227482	chromatin interactions
ENSG00000138835	chromatin interactions
ENSG00000157653	chromatin interactions
LPHN1	miRNA target sites
SIPA1L2	miRNA target sites

Extended variants
information (count: 1004 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568557	chr9:116365126-116365127	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs35158038	chr9:116365128-116365129	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs567743	chr9:116365188-116365189	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs34288422	chr9:116365225-116365226	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185669488	chr9:116365227-116365228	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547345938	chr9:116365232-116365233	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs567036086	chr9:116365239-116365240	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs142407755	chr9:116365257-116365258	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs532775257	chr9:116365277-116365278	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571427957	chr9:116365352-116365353	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs373949818	chr9:116365361-116365362	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555276256	chr9:116365363-116365364	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569342769	chr9:116365429-116365430	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs538944701	chr9:116365436-116365437	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs142420807	chr9:116365450-116365451	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs10817494	chr9:116365451-116365452	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
17	rs117550331	chr9:116365518-116365519	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs536123656	chr9:116365538-116365539	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552867718	chr9:116365545-116365546	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs151297823	chr9:116365565-116365566	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538451472	chr9:116365603-116365604	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs558330834	chr9:116365617-116365618	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs575290248	chr9:116365619-116365620	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs56187153	chr9:116365723-116365724	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs35508860	chr9:116365727-116365728	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139434960	chr9:116365786-116365787	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs572935312	chr9:116365812-116365813	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs144456706	chr9:116365865-116365866	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs540900115	chr9:116365936-116365937	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs558553297	chr9:116365947-116365948	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs542552621	chr9:116366082-116366083	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560770360	chr9:116366126-116366127	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532710926	chr9:116366185-116366186	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552728067	chr9:116366186-116366187	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs562985017	chr9:116366187-116366188	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs585689	chr9:116366188-116366189	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs545734309	chr9:116366211-116366212	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568081794	chr9:116366230-116366231	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs575000170	chr9:116366243-116366244	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs563822636	chr9:116366290-116366291	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs146549395	chr9:116366291-116366292	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141191654	chr9:116366334-116366335	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs34278541	chr9:116366377-116366378	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs538597177	chr9:116366401-116366402	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs558714794	chr9:116366409-116366410	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs575376837	chr9:116366491-116366492	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs542533450	chr9:116366572-116366573	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537931599	chr9:116366588-116366589	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs554727093	chr9:116366598-116366599	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587614	chr9:116366640-116366641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	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
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
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
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116358000-116371800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:116360200-116365400	Enhancers	Skeletal Muscle Female	skeletal muscle
3	chr9:116360200-116366400	Enhancers	Placenta	Placenta
4	chr9:116360400-116371800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr9:116360600-116365800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr9:116360600-116366000	Enhancers	Right Ventricle	heart
7	chr9:116360800-116366000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr9:116360800-116366000	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr9:116360800-116366000	Enhancers	NHDF-Ad	bronchial
10	chr9:116360800-116366600	Enhancers	Liver	Liver
11	chr9:116361000-116365600	Enhancers	Left Ventricle	heart
12	chr9:116361000-116366400	Enhancers	Fetal Muscle Leg	muscle
13	chr9:116361200-116365600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr9:116361200-116365800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr9:116361200-116366600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr9:116361400-116366000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr9:116361400-116366000	Enhancers	Fetal Lung	lung
18	chr9:116361400-116367000	Enhancers	Adipose Nuclei	Adipose
19	chr9:116361600-116365600	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr9:116361800-116365200	Enhancers	HSMMtube	muscle
21	chr9:116362000-116366000	Enhancers	HMEC	breast
22	chr9:116362000-116366600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr9:116362200-116365800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr9:116362400-116365400	Enhancers	Osteobl	bone
25	chr9:116362400-116365600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:116362400-116366000	Enhancers	Fetal Muscle Trunk	muscle
27	chr9:116362400-116366400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr9:116362600-116365200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr9:116362600-116365600	Enhancers	Muscle Satellite Cultured Cells	--
30	chr9:116362800-116365200	Enhancers	Ovary	ovary
31	chr9:116363000-116365600	Enhancers	NH-A	brain
32	chr9:116363000-116365800	Enhancers	Fetal Stomach	stomach
33	chr9:116363000-116366800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr9:116363400-116365400	Enhancers	Brain Hippocampus Middle	brain
35	chr9:116363400-116366000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr9:116363600-116365400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:116363600-116365600	Enhancers	H9 Cell Line	embryonic stem cell
38	chr9:116363600-116365600	Enhancers	Fetal Intestine Small	intestine
39	chr9:116363600-116366000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr9:116363600-116366200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr9:116363600-116366200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr9:116363600-116366400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr9:116363800-116365200	Enhancers	Fetal Kidney	kidney
44	chr9:116363800-116365200	Enhancers	K562	blood
45	chr9:116363800-116365400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr9:116363800-116365400	Enhancers	Brain Substantia Nigra	brain
47	chr9:116363800-116365400	Enhancers	Esophagus	oesophagus
48	chr9:116363800-116365600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:116363800-116365600	Enhancers	Pancreas	Pancrea
50	chr9:116363800-116365800	Enhancers	NHEK	skin

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