Variant report

Variant	nsv1046491
Chromosome Location	chr9:85861492-86063992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1556)
CpG islands
(count:0)
Chromatin interactive
region (count:48)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1556 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:85995538-85995760	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:85881768-85882093	HepG2	liver:	n/a	n/a
3	ARID3A	chr9:86002256-86002974	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:86046640-86046862	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:86038820-86039458	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:85949209-85949566	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:86044088-86044496	HepG2	liver:	n/a	n/a
8	ARID3A	chr9:85886506-85886784	K562	blood:	n/a	n/a
9	ARID3A	chr9:86047116-86047302	HepG2	liver:	n/a	n/a
10	ATF2	chr9:85862749-85862994	GM12878	blood:	n/a	n/a
11	ATF3	chr9:86011356-86011553	K562	blood:	n/a	n/a
12	ATF3	chr9:86047065-86047627	A549	lung:	n/a	n/a
13	BACH1	chr9:86047143-86047418	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr9:85930593-85930942	H1-hESC	embryonic stem cell:	n/a	chr9:85930753-85930767
15	BACH1	chr9:85930601-85930913	K562	blood:	n/a	chr9:85930753-85930767
16	BATF	chr9:85862689-85863065	GM12878	blood:	n/a	n/a
17	BATF	chr9:85862776-85862983	GM12878	blood:	n/a	n/a
18	BCL3	chr9:86047054-86047650	A549	lung:	n/a	n/a
19	BHLHE40	chr9:85963083-85963094	HepG2	liver:	n/a	n/a
20	BHLHE40	chr9:85896193-85896215	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:85862652-85863002	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:86052764-86052990	K562	blood:	n/a	chr9:86052881-86052890 chr9:86052882-86052891 chr9:86052880-86052893 chr9:86052882-86052891
23	BHLHE40	chr9:85862793-85862798	K562	blood:	n/a	n/a
24	BRCA1	chr9:86047206-86047532	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr9:85949213-85949556	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr9:85949358-85949421	HepG2	liver:	n/a	n/a
27	BRCA1	chr9:85895869-85895924	Hela-S3	cervix:	n/a	n/a
28	CCNT2	chr9:85886465-85886913	K562	blood:	n/a	n/a
29	CEBPB	chr9:85949272-85949544	HepG2	liver:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
30	CEBPB	chr9:85949236-85949480	K562	blood:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
31	CEBPB	chr9:85949106-85949698	MCF-7	breast:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
32	CEBPB	chr9:85949286-85949453	HepG2	liver:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
33	CEBPB	chr9:85949234-85949592	IMR90	lung:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
34	CEBPB	chr9:86047253-86047600	A549	lung:	n/a	n/a
35	CEBPB	chr9:86046637-86047584	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr9:86029070-86029224	IMR90	lung:	n/a	chr9:86029138-86029149
37	CEBPB	chr9:85964486-85964500	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr9:85949199-85949616	A549	lung:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
39	CEBPB	chr9:85949144-85949696	ECC-1	luminal epithelium:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
40	CEBPB	chr9:85949180-85949648	ECC-1	luminal epithelium:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
41	CEBPB	chr9:85974235-85974258	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr9:85889614-85889867	HepG2	liver:	n/a	chr9:85889742-85889753
43	CEBPB	chr9:85949211-85949666	MCF-7	breast:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
44	CEBPB	chr9:86020223-86020328	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:85949161-85949663	A549	lung:	n/a	chr9:85949423-85949434 chr9:85949422-85949435
46	CEBPB	chr9:85914421-85914820	MCF-7	breast:	n/a	chr9:85914588-85914605
47	CEBPB	chr9:85969887-85970148	K562	blood:	n/a	n/a
48	CEBPB	chr9:86029083-86029277	HepG2	liver:	n/a	chr9:86029138-86029149
49	CEBPB	chr9:85947420-85947641	HepG2	liver:	n/a	chr9:85947517-85947528
50	CEBPB	chr9:85949233-85949585	H1-hESC	embryonic stem cell:	n/a	chr9:85949423-85949434 chr9:85949422-85949435

No data

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:85948851..85949820-chr9:86158705..86159977,11	MCF-7	breast:
2	chr9:86024808..86026717-chr9:86030447..86032295,2	K562	blood:
3	chr9:85813872..85814740-chr9:85944985..85945810,2	MCF-7	breast:
4	chr9:86046794..86050465-chr9:86050692..86054566,4	MCF-7	breast:
5	chr9:85978630..85980450-chr9:86151808..86153596,2	MCF-7	breast:
6	chr9:85833661..85835663-chr9:85859284..85862101,2	MCF-7	breast:
7	chr9:85948862..85949803-chr9:86138270..86139266,2	MCF-7	breast:
8	chr9:86011563..86014986-chr9:86016916..86020141,4	MCF-7	breast:
9	chr20:46718060..46720676-chr9:85907908..85910586,2	MCF-7	breast:
10	chr9:86046794..86050465-chr9:86050692..86054566,4	MCF-7	breast:
11	chr9:85834318..85834922-chr9:85942136..85942786,2	MCF-7	breast:
12	chr9:85948926..85949823-chr9:86159014..86160096,5	MCF-7	breast:
13	chr9:85996640..85999188-chr9:86152643..86154584,2	MCF-7	breast:
14	chr9:85947660..85948662-chr9:86159439..86160258,3	MCF-7	breast:
15	chr9:85833317..85835949-chr9:85882469..85885385,2	MCF-7	breast:
16	chr9:85936186..85938298-chr9:85939709..85942316,2	MCF-7	breast:
17	chr9:85954485..85956704-chr9:85957124..85959138,2	MCF-7	breast:
18	chr9:85985180..85988135-chr9:86151816..86155066,3	MCF-7	breast:
19	chr9:85944888..85945838-chr9:86153084..86153602,2	MCF-7	breast:
20	chr20:2450434..2451238-chr9:85908931..85909431,2	Hela-S3	cervix:
21	chr9:85997879..86001519-chr9:86002024..86006738,6	MCF-7	breast:
22	chr9:85948858..85949573-chr9:86197679..86198534,2	MCF-7	breast:
23	chr9:86046084..86048921-chr9:86138267..86141242,2	MCF-7	breast:
24	chr9:85954485..85956704-chr9:85957124..85959138,2	MCF-7	breast:
25	chr9:85908596..85911105-chr9:85914154..85916205,2	MCF-7	breast:
26	chr9:85954481..85956414-chr9:86152733..86154497,2	MCF-7	breast:
27	chr9:85910928..85912509-chr9:85920492..85923421,2	K562	blood:
28	chr9:86045543..86047511-chr9:86062619..86064900,2	MCF-7	breast:
29	chr9:85856974..85859342-chr9:85860363..85862242,2	MCF-7	breast:
30	chr9:85908596..85911105-chr9:85914154..85916205,2	MCF-7	breast:
31	chr9:85948847..85949772-chr9:86153221..86154500,7	MCF-7	breast:
32	chr9:86045543..86047511-chr9:86062619..86064900,2	MCF-7	breast:
33	chr9:85998150..86000418-chr9:86018604..86020788,2	MCF-7	breast:
34	chr9:85873280..85875908-chr9:85879895..85882458,2	K562	blood:
35	chr9:85998150..86000418-chr9:86018604..86020788,2	MCF-7	breast:
36	chr9:86011563..86014986-chr9:86016916..86020141,4	MCF-7	breast:
37	chr9:85910411..85912906-chr9:85925285..85927422,2	MCF-7	breast:
38	chr4:11914973..11915747-chr9:85898451..85899210,2	MCF-7	breast:
39	chr9:85948863..85949433-chr9:86153276..86154229,4	MCF-7	breast:
40	chr17:56708616..56709461-chr9:85924098..85925119,7	HCT-116	colon:
41	chr9:85997879..86001519-chr9:86002024..86006738,6	MCF-7	breast:
42	chr9:86009690..86011505-chr9:86151453..86153248,2	MCF-7	breast:
43	chr9:85884317..85887181-chr9:85896355..85898967,2	MCF-7	breast:
44	chr20:55780966..55782713-chr9:85914150..85917090,2	MCF-7	breast:
45	chr9:85910928..85912509-chr9:85920492..85923421,2	K562	blood:
46	chr9:86024808..86026717-chr9:86030447..86032295,2	K562	blood:
47	chr9:85936186..85938298-chr9:85939709..85942316,2	MCF-7	breast:
48	chr9:86054433..86056553-chr9:86066145..86068552,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf103-2	chr9:85894072-85894414	ENSG00000237529.1
2	lnc-C9orf103-5	chr9:85882090-85885748	NONHSAT132734
3	lnc-C9orf103-2	chr9:85891291-85891474	ENSG00000237529.1

No data

Variant related genes	Relation type
RNU4-29P	TF binding region
ENSG00000237529	TF binding region
FRMD3	TF binding region
ENSG00000238608	TF binding region
ENSG00000172159	chromatin interactions
ENSG00000229109	chromatin interactions
ENSG00000238608	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 7823 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:7823 , 50 per page) page: 1 2 3 4 5 6 7 ... 157

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149654125	chr9:85861515-85861516	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs139506236	chr9:85861556-85861557	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs145057363	chr9:85861557-85861558	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369361182	chr9:85861559-85861560	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs199534798	chr9:85861560-85861561	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs77652422	chr9:85861561-85861562	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375820261	chr9:85861582-85861583	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373107249	chr9:85861584-85861585	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs67837353	chr9:85861585-85861586	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201262764	chr9:85861586-85861587	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs142083422	chr9:85861598-85861599	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs58656596	chr9:85861599-85861600	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs199762598	chr9:85861600-85861601	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540914859	chr9:85861607-85861608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs145168669	chr9:85861654-85861655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs532530818	chr9:85861672-85861673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182590436	chr9:85861705-85861706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs562889951	chr9:85861744-85861745	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs17086111	chr9:85861761-85861762	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs548707721	chr9:85861767-85861768	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs558776444	chr9:85861768-85861769	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs147609403	chr9:85861795-85861796	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149098015	chr9:85861853-85861854	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs552423880	chr9:85861864-85861865	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs570687041	chr9:85861908-85861909	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs537765626	chr9:85861939-85861940	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs555713301	chr9:85861943-85861944	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376935449	chr9:85861958-85861959	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187151637	chr9:85861993-85861994	Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs567721530	chr9:85862079-85862080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs143180436	chr9:85862119-85862120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553630152	chr9:85862160-85862161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs551233584	chr9:85862217-85862218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573385227	chr9:85862246-85862247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10646229	chr9:85862299-85862300	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs35790064	chr9:85862300-85862301	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs540500619	chr9:85862306-85862307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs3029549	chr9:85862311-85862312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377128633	chr9:85862312-85862313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559190604	chr9:85862329-85862330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs577538648	chr9:85862342-85862343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs76131593	chr9:85862355-85862356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1056476	chr9:85862365-85862366	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs192015861	chr9:85862453-85862454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs181526732	chr9:85862481-85862482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530155213	chr9:85862565-85862566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs542306227	chr9:85862568-85862569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560409629	chr9:85862579-85862580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543956495	chr9:85862609-85862610	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148263096	chr9:85862653-85862654	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Melanoma	18172304	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
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Urothelial cell carcinoma	18451213	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Renal cell carcinoma	18765545	CNVD
Astrocytoma	22246337	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:1667 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85847200-85865400	Weak transcription	Ovary	ovary
2	chr9:85851400-85862800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:85854400-85862800	Weak transcription	Esophagus	oesophagus
4	chr9:85854400-85863000	Weak transcription	Pancreas	Pancrea
5	chr9:85854400-85865400	Weak transcription	Spleen	Spleen
6	chr9:85854400-85865600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr9:85854400-85865600	Weak transcription	Right Ventricle	heart
8	chr9:85854600-85864600	Weak transcription	Fetal Kidney	kidney
9	chr9:85854600-85866000	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr9:85854600-85866400	Weak transcription	Stomach Mucosa	stomach
11	chr9:85854800-85862600	Weak transcription	Skeletal Muscle Male	skeletal muscle
12	chr9:85854800-85867400	Weak transcription	HepG2	liver
13	chr9:85854800-85890400	Weak transcription	Primary neutrophils fromperipheralblood	blood
14	chr9:85855000-85865800	Weak transcription	Fetal Stomach	stomach
15	chr9:85855000-85881400	Weak transcription	Adipose Nuclei	Adipose
16	chr9:85856000-85866800	Weak transcription	Fetal Muscle Trunk	muscle
17	chr9:85856200-85910600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr9:85858600-85865600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr9:85858600-85866400	Weak transcription	Fetal Muscle Leg	muscle
20	chr9:85859000-85862800	Weak transcription	Left Ventricle	heart
21	chr9:85859400-85864200	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr9:85861200-85865800	Weak transcription	Aorta	Aorta
23	chr9:85861400-85861600	Flanking Active TSS	Fetal Heart	heart
24	chr9:85861400-85873000	Weak transcription	Psoas Muscle	Psoas
25	chr9:85861400-85873000	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr9:85861600-85861800	Enhancers	Fetal Heart	heart
27	chr9:85861600-85868000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:85861800-85862000	Flanking Active TSS	Fetal Heart	heart
29	chr9:85862000-85863000	Enhancers	Fetal Heart	heart
30	chr9:85862600-85863200	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr9:85862800-85863000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr9:85862800-85863200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr9:85862800-85863200	ZNF genes & repeats	Esophagus	oesophagus
34	chr9:85862800-85863400	Genic enhancers	Left Ventricle	heart
35	chr9:85863000-85863200	ZNF genes & repeats	Pancreas	Pancrea
36	chr9:85863000-85863400	ZNF genes & repeats	Gastric	stomach
37	chr9:85863000-85873000	Weak transcription	Fetal Heart	heart
38	chr9:85863200-85868000	Weak transcription	Pancreas	Pancrea
39	chr9:85863200-85873200	Weak transcription	Skeletal Muscle Male	skeletal muscle
40	chr9:85863400-85865600	Weak transcription	Left Ventricle	heart
41	chr9:85864200-85864400	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr9:85865400-85866000	Genic enhancers	Spleen	Spleen
43	chr9:85865600-85865800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr9:85865600-85865800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr9:85865600-85866000	Enhancers	Left Ventricle	heart
46	chr9:85865600-85866200	Genic enhancers	Right Ventricle	heart
47	chr9:85865800-85866000	ZNF genes & repeats	Fetal Stomach	stomach
48	chr9:85865800-85866200	ZNF genes & repeats	Aorta	Aorta
49	chr9:85866000-85866600	Weak transcription	Spleen	Spleen
50	chr9:85866000-85873000	Weak transcription	Left Ventricle	heart

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