Variant report

Variant	nsv982178
Chromosome Location	chr9:104290227-104293633
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104292514-104292714	HepG2	liver:	n/a	n/a
2	ATF2	chr9:104292374-104292716	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr9:104292401-104292766	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr9:104292317-104292714	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:104292414-104292743	GM12878	blood:	n/a	n/a
6	CEBPB	chr9:104292355-104292675	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr9:104292458-104292635	HepG2	liver:	n/a	n/a
8	CTCF	chr9:104292860-104293010	BJ	skin:	n/a	n/a
9	CTCF	chr9:104292500-104292650	HA-sp	spinal cord:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
10	CTCF	chr9:104292480-104292630	GM12865	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
11	CTCF	chr9:104292520-104292670	HPAF	blood vessel:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
12	CTCF	chr9:104292900-104293050	HVMF	connective:	n/a	n/a
13	CTCF	chr9:104292448-104292721	Medullo	brain:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
14	CTCF	chr9:104292500-104292650	HCPEpiC	choroid plexus:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
15	CTCF	chr9:104292500-104292650	GM12870	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
16	CTCF	chr9:104292444-104292706	GM13976	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
17	CTCF	chr9:104292431-104292745	A549	lung:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
18	CTCF	chr9:104292480-104292630	GM12872	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
19	CTCF	chr9:104292500-104292650	BJ	skin:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
20	CTCF	chr9:104292452-104292724	HUVEC	blood vessel:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
21	CTCF	chr9:104292399-104292742	K562	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
22	CTCF	chr9:104292940-104293090	AG04449	skin:	n/a	n/a
23	CTCF	chr9:104292500-104292650	BE2_C	brain:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
24	CTCF	chr9:104292800-104292950	SAEC	small airway:	n/a	n/a
25	CTCF	chr9:104291913-104293204	A549	lung:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
26	CTCF	chr9:104292865-104292965	GM10248	blood:	n/a	n/a
27	CTCF	chr9:104292347-104292692	A549	lung:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
28	CTCF	chr9:104292479-104292683	GM20000	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
29	CTCF	chr9:104292500-104292650	HAc	cerebellar:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
30	CTCF	chr9:104292480-104292630	GM12870	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
31	CTCF	chr9:104292900-104293050	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr9:104292499-104292659	H1-hESC	embryonic stem cell:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
33	CTCF	chr9:104292500-104292650	RPTEC	kidney:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
34	CTCF	chr9:104292291-104292732	MCF-7	breast:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
35	CTCF	chr9:104292500-104292650	WI-38	lung:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
36	CTCF	chr9:104292451-104292700	Gliobla	brain:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
37	CTCF	chr9:104292451-104292694	NHEK	skin:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
38	CTCF	chr9:104292520-104292670	HRPEpiC	eye:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
39	CTCF	chr9:104292000-104292150	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr9:104292880-104293030	HVMF	connective:	n/a	n/a
41	CTCF	chr9:104292520-104292670	AoAF	blood vessel:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
42	CTCF	chr9:104292480-104292694	GM10248	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
43	CTCF	chr9:104292458-104292704	LNCaP	prostate:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
44	CTCF	chr9:104292480-104292630	HL-60	blood:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
45	CTCF	chr9:104292600-104292750	HCT-116	colon:	n/a	n/a
46	CTCF	chr9:104292520-104292670	Hela-S3	cervix:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
47	CTCF	chr9:104292560-104292710	HRPEpiC	eye:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
48	CTCF	chr9:104292461-104292685	Fibrobl	skin:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
49	CTCF	chr9:104292480-104292630	BE2_C	brain:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588
50	CTCF	chr9:104292500-104292650	HRE	kidney:	n/a	chr9:104292572-104292590 chr9:104292573-104292589 chr9:104292567-104292588

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104292242-104292292	LNCaP	prostate:	n/a
2	chr9:104292242-104292292	SK-N-SH	brain:	n/a
3	chr9:104292242-104292292	AG04450	lung:	fetal
4	chr9:104292242-104292292	PFSK-1	brain:	n/a
5	chr9:104292242-104292292	AG09319	gingival:	n/a
6	chr9:104292242-104292292	HEK293	kidney:	embryo
7	chr9:104292242-104292292	IMR90	lung:	fetal
8	chr9:104292242-104292292	HRCEpiC	kidney:	n/a
9	chr9:104292242-104292292	AoSMC	blood vessel:	n/a
10	chr9:104292242-104292292	Jurkat	blood:	n/a
11	chr9:104292242-104292292	A549	lung:	n/a
12	chr9:104292242-104292292	ECC-1	luminal epithelium:	n/a
13	chr9:104292242-104292292	AG04449	skin:	fetal
14	chr9:104292242-104292292	T-47D	breast:	n/a
15	chr9:104292242-104292292	H1-hESC	embryonic stem cell:	embryo
16	chr9:104292242-104292292	U87	brain:	n/a
17	chr9:104292242-104292292	BE2_C	brain:	n/a
18	chr9:104292242-104292292	HMEC	breast:	n/a
19	chr9:104292242-104292292	HIPEpiC	eye:	n/a
20	chr9:104292242-104292292	SK-N-SH_RA	brain:	n/a
21	chr9:104292242-104292292	HCT-116	colon:	n/a
22	chr9:104292242-104292292	HCPEpiC	choroid plexus:	n/a
23	chr9:104292242-104292292	Hepatocyte	liver:	n/a
24	chr9:104292242-104292292	HRE	kidney:	n/a
25	chr9:104292242-104292292	NH-A	brain:	n/a
26	chr9:104292242-104292292	GM12878	blood:	n/a
27	chr9:104292242-104292292	GM06990	blood:	n/a
28	chr9:104292242-104292292	MCF10A-Er-Src	breast:	n/a
29	chr9:104292242-104292292	SAEC	small airway:	n/a
30	chr9:104292242-104292292	MCF-7	breast:	n/a
31	chr9:104292242-104292292	HCF	heart:	n/a
32	chr9:104292242-104292292	GM12891	blood:	n/a
33	chr9:104292242-104292292	ProgFib	skin:	n/a
34	chr9:104292242-104292292	ovcar-3	ovarian:	n/a
35	chr9:104292242-104292292	SK-N-MC	brain:	n/a
36	chr9:104292242-104292292	PrEC	prostate:	n/a
37	chr9:104292242-104292292	GM12892	blood:	n/a
38	chr9:104292242-104292292	CMK	blood:	n/a
39	chr9:104292242-104292292	NB4	blood:	n/a
40	chr9:104292242-104292292	AG10803	skin:	n/a
41	chr9:104292242-104292292	AG09309	skin:	n/a
42	chr9:104292242-104292292	Caco-2	colon:	n/a
43	chr9:104292242-104292292	HAEpiC	amniotic membrane:	n/a
44	chr9:104292242-104292292	BJ	skin:	n/a
45	chr9:104292242-104292292	Hela-S3	cervix:	n/a
46	chr9:104292242-104292292	HNPCEpiC	eye:	n/a
47	chr9:104292242-104292292	NT2-D1	testis:	n/a
48	chr9:104292242-104292292	HL-60	blood:	n/a
49	chr9:104292242-104292292	HepG2	liver:	n/a
50	chr9:104292242-104292292	PANC-1	pancreas:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:104211181..104212704-chr9:104292065..104293358,10	K562	blood:
2	chr9:104210777..104212299-chr9:104292128..104293102,7	MCF-7	breast:
3	chr9:104292076..104294018-chr9:104296144..104297763,2	K562	blood:
4	chr9:104227401..104228428-chr9:104292031..104293031,5	K562	blood:
5	chr9:104246363..104248786-chr9:104290917..104293044,2	K562	blood:
6	chr9:104220056..104222734-chr9:104292272..104293989,2	K562	blood:
7	chr9:103476641..103477292-chr9:104292118..104293044,2	K562	blood:
8	chr9:104221051..104221944-chr9:104292075..104293445,6	MCF-7	breast:
9	chr9:104220969..104222009-chr9:104292098..104293000,3	K562	blood:
10	chr9:104226892..104228195-chr9:104292114..104293047,7	MCF-7	breast:
11	chr9:104219436..104220096-chr9:104292310..104293060,2	MCF-7	breast:
12	chr9:104221027..104221969-chr9:104291863..104293035,11	MCF-7	breast:
13	chr9:104208004..104209865-chr9:104292464..104295242,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf125-1	chr9:104293517-104293841	NONHSAT133742

Variant related genes	Relation type
RNF20	TF binding region
RNF20	CpG island
ENSG00000155827	chromatin interactions
ENSG00000270982	chromatin interactions

Extended variants
information (count: 149 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:149 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191204908	chr9:104290266-104290267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs551837938	chr9:104290268-104290269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140185648	chr9:104290342-104290343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534378571	chr9:104290345-104290346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs183367028	chr9:104290414-104290415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554089628	chr9:104290420-104290421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528508271	chr9:104290436-104290437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573957148	chr9:104290439-104290440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs79728660	chr9:104290457-104290458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs78810137	chr9:104290464-104290465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186294435	chr9:104290489-104290490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34002208	chr9:104290575-104290576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544706885	chr9:104290612-104290613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532495358	chr9:104290696-104290697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7019395	chr9:104290707-104290708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs189891187	chr9:104290711-104290712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541178733	chr9:104290717-104290718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs368571420	chr9:104290745-104290746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs371423021	chr9:104290808-104290809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs28605156	chr9:104290814-104290815	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550090128	chr9:104290844-104290845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563609947	chr9:104290895-104290896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531712791	chr9:104290919-104290920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569518883	chr9:104290940-104290941	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368082398	chr9:104290959-104290960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182679543	chr9:104291031-104291032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530592569	chr9:104291047-104291048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188071419	chr9:104291068-104291069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201196657	chr9:104291077-104291078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs534045940	chr9:104291095-104291096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371571609	chr9:104291125-104291126	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs553670656	chr9:104291174-104291175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566982965	chr9:104291193-104291194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs77153735	chr9:104291220-104291221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs535945692	chr9:104291242-104291243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191338513	chr9:104291249-104291250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs146323705	chr9:104291258-104291259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs538594416	chr9:104291260-104291261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150064710	chr9:104291272-104291273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs558275745	chr9:104291301-104291302	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs572058574	chr9:104291320-104291321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs555974758	chr9:104291324-104291325	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554747481	chr9:104291326-104291327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs12350648	chr9:104291328-104291329	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs534346688	chr9:104291381-104291382	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs111375622	chr9:104291393-104291394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532323075	chr9:104291432-104291433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs575729372	chr9:104291433-104291434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs36069212	chr9:104291436-104291437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545346945	chr9:104291437-104291438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	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
Gastrointestinal stromal cancer	20877625	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
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104286800-104295200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr9:104286800-104295200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr9:104287200-104295200	Weak transcription	Adipose Nuclei	Adipose
4	chr9:104287600-104290800	Weak transcription	Brain Hippocampus Middle	brain
5	chr9:104289600-104295200	Weak transcription	Brain Anterior Caudate	brain
6	chr9:104289800-104295400	Weak transcription	NHEK	skin
7	chr9:104290200-104295400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr9:104290600-104290800	Enhancers	Brain Cingulate Gyrus	brain
9	chr9:104290600-104291400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr9:104290800-104291000	Enhancers	Brain Hippocampus Middle	brain
11	chr9:104290800-104291400	Enhancers	Brain Angular Gyrus	brain
12	chr9:104290800-104292400	Enhancers	Fetal Heart	heart
13	chr9:104290800-104295200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr9:104291000-104295400	Weak transcription	Brain Hippocampus Middle	brain
15	chr9:104291400-104295200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
16	chr9:104291400-104295200	Weak transcription	Brain Angular Gyrus	brain
17	chr9:104291400-104295400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr9:104291600-104295800	Weak transcription	Small Intestine	intestine
19	chr9:104292000-104292400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr9:104292200-104292400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr9:104292200-104292400	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr9:104292200-104292400	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr9:104292200-104292600	Enhancers	Stomach Mucosa	stomach
24	chr9:104292400-104292600	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr9:104292400-104292600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr9:104292400-104295200	Weak transcription	Fetal Heart	heart
27	chr9:104292400-104295400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr9:104292600-104295200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr9:104292600-104295200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr9:104292600-104295200	Weak transcription	Stomach Mucosa	stomach
31	chr9:104292800-104295200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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