Variant report

Variant	nsv892234
Chromosome Location	chr9:8645448-8703733
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:114)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:114 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:8682086-8682098	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr9:8653957-8654156	H1-hESC	embryonic stem cell:	n/a	chr9:8654056-8654067
3	CEBPB	chr9:8649914-8650117	HepG2	liver:	n/a	chr9:8649972-8649983
4	CEBPB	chr9:8653894-8654241	HepG2	liver:	n/a	chr9:8654056-8654067
5	CTCF	chr9:8673900-8674050	Caco-2	colon:	n/a	n/a
6	CTCF	chr9:8653200-8653350	AoAF	blood vessel:	n/a	n/a
7	CTCF	chr9:8692320-8692470	RPTEC	kidney:	n/a	chr9:8692426-8692444
8	CTCF	chr9:8692409-8692456	GM13976	blood:	n/a	chr9:8692426-8692444
9	CTCF	chr9:8673860-8674010	HepG2	liver:	n/a	n/a
10	CTCF	chr9:8653380-8653530	HPF	lung:	n/a	n/a
11	CTCF	chr9:8673820-8674074	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr9:8673840-8673990	HAc	cerebellar:	n/a	n/a
13	CTCF	chr9:8673920-8674070	HEK293	kidney:	n/a	n/a
14	CTCF	chr9:8673880-8674154	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr9:8673960-8674110	RPTEC	kidney:	n/a	n/a
16	CTCF	chr9:8673920-8674070	Caco-2	colon:	n/a	n/a
17	CTCF	chr9:8692391-8692455	MCF-7	breast:	n/a	chr9:8692426-8692444
18	CTCF	chr9:8692200-8692350	RPTEC	kidney:	n/a	n/a
19	CTCF	chr9:8673880-8674030	AoAF	blood vessel:	n/a	n/a
20	CTCF	chr9:8673951-8674062	HepG2	liver:	n/a	n/a
21	CTCF	chr9:8673938-8674054	HepG2	liver:	n/a	n/a
22	CTCF	chr9:8676726-8676782	GM13976	blood:	n/a	n/a
23	CTCF	chr9:8692420-8692458	GM13977	blood:	n/a	chr9:8692426-8692444
24	CTCF	chr9:8673860-8674010	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr9:8673980-8674130	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr9:8673940-8674090	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr9:8673880-8674030	HRE	kidney:	n/a	n/a
28	E2F4	chr9:8662176-8662553	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr9:8686572-8686864	MCF10A-Er-Src	breast:	n/a	chr9:8686752-8686763 chr9:8686753-8686762
30	FOS	chr9:8682014-8682234	MCF10A-Er-Src	breast:	n/a	chr9:8682155-8682164 chr9:8682156-8682165
31	FOS	chr9:8666215-8666375	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr9:8686652-8686852	MCF10A-Er-Src	breast:	n/a	chr9:8686752-8686763 chr9:8686753-8686762
33	FOS	chr9:8686675-8686806	MCF10A-Er-Src	breast:	n/a	chr9:8686752-8686763 chr9:8686753-8686762
34	FOS	chr9:8686659-8686805	MCF10A-Er-Src	breast:	n/a	chr9:8686752-8686763 chr9:8686753-8686762
35	GATA3	chr9:8664146-8664193	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr9:8695271-8695556	T-47D	breast:	n/a	chr9:8695539-8695546
37	GATA3	chr9:8695363-8695609	T-47D	breast:	n/a	chr9:8695539-8695546
38	GATA3	chr9:8652742-8652889	SH-SY5Y	brain:	n/a	chr9:8652763-8652779
39	GTF2F1	chr9:8647962-8648014	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr9:8682072-8682298	H1-hESC	embryonic stem cell:	n/a	chr9:8682155-8682164 chr9:8682154-8682165 chr9:8682156-8682165
41	JUND	chr9:8694993-8695272	H1-hESC	embryonic stem cell:	n/a	n/a
42	JUND	chr9:8682100-8682181	HepG2	liver:	n/a	chr9:8682155-8682164 chr9:8682154-8682165 chr9:8682156-8682165
43	JUND	chr9:8678303-8678348	H1-hESC	embryonic stem cell:	n/a	n/a
44	JUND	chr9:8647965-8648165	H1-hESC	embryonic stem cell:	n/a	n/a
45	JUND	chr9:8677792-8678002	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAFF	chr9:8668356-8668439	HepG2	liver:	n/a	n/a
47	MAFF	chr9:8666170-8666366	HepG2	liver:	n/a	chr9:8666254-8666272
48	MAFK	chr9:8681242-8681420	HepG2	liver:	n/a	n/a
49	MAFK	chr9:8687511-8687677	HepG2	liver:	n/a	n/a
50	MAFK	chr9:8668341-8668403	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:8683882-8683932	HAEpiC	amniotic membrane:	n/a
2	chr9:8683882-8683932	HepG2	liver:	n/a
3	chr9:8683882-8683932	U87	brain:	n/a
4	chr9:8683882-8683932	BJ	skin:	n/a
5	chr9:8683882-8683932	HCF	heart:	n/a
6	chr9:8683882-8683932	NB4	blood:	n/a
7	chr9:8683882-8683932	SK-N-MC	brain:	n/a
8	chr9:8683882-8683932	HPAEpiC	pulmonary alveolar:	n/a
9	chr9:8683882-8683932	AG09319	gingival:	n/a
10	chr9:8683882-8683932	AG10803	skin:	n/a
11	chr9:8683882-8683932	AoSMC	blood vessel:	n/a
12	chr9:8683882-8683932	NH-A	brain:	n/a
13	chr9:8683882-8683932	MCF-7	breast:	n/a
14	chr9:8683882-8683932	HRPEpiC	eye:	n/a
15	chr9:8683882-8683932	ProgFib	skin:	n/a
16	chr9:8683882-8683932	HRCEpiC	kidney:	n/a
17	chr9:8683882-8683932	ovcar-3	ovarian:	n/a
18	chr9:8683882-8683932	BE2_C	brain:	n/a
19	chr9:8683882-8683932	GM12892	blood:	n/a
20	chr9:8683882-8683932	Caco-2	colon:	n/a
21	chr9:8683882-8683932	GM06990	blood:	n/a
22	chr9:8683882-8683932	NHDF-neo	bronchial:	n/a
23	chr9:8683882-8683932	Hepatocyte	liver:	n/a
24	chr9:8683882-8683932	HEK293	kidney:	embryo
25	chr9:8683882-8683932	K562	blood:	n/a
26	chr9:8683882-8683932	GM12878	blood:	n/a
27	chr9:8683882-8683932	NT2-D1	testis:	n/a
28	chr9:8683882-8683932	PANC-1	pancreas:	n/a
29	chr9:8683882-8683932	MCF10A-Er-Src	breast:	n/a
30	chr9:8683882-8683932	A549	lung:	n/a
31	chr9:8683882-8683932	AG04450	lung:	fetal
32	chr9:8683882-8683932	HUVEC	blood vessel:	n/a
33	chr9:8683882-8683932	Jurkat	blood:	n/a
34	chr9:8683882-8683932	ECC-1	luminal epithelium:	n/a
35	chr9:8683882-8683932	GM19239	blood:	n/a
36	chr9:8683882-8683932	HIPEpiC	eye:	n/a
37	chr9:8683882-8683932	SK-N-SH_RA	brain:	n/a
38	chr9:8683882-8683932	AG09309	skin:	n/a
39	chr9:8683882-8683932	HCPEpiC	choroid plexus:	n/a
40	chr9:8683882-8683932	NHBE	bronchial:	n/a
41	chr9:8683882-8683932	H1-hESC	embryonic stem cell:	embryo
42	chr9:8683882-8683932	T-47D	breast:	n/a
43	chr9:8683882-8683932	HMEC	breast:	n/a
44	chr9:8683882-8683932	PFSK-1	brain:	n/a
45	chr9:8683882-8683932	HNPCEpiC	eye:	n/a
46	chr9:8683882-8683932	SKMC	muscle:	n/a
47	chr9:8683882-8683932	HRE	kidney:	n/a
48	chr9:8683882-8683932	LNCaP	prostate:	n/a
49	chr9:8683882-8683932	Hela-S3	cervix:	n/a
50	chr9:8683882-8683932	HCM	heart:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:14628744..14629586-chr9:8657312..8657812,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf123-6	chr9:8701390-8701552	ENSG00000235389.1
2	lnc-C9orf123-6	chr9:8700595-8700902	ENSG00000235389.2
3	lnc-C9orf123-6	chr9:8700595-8700916	ENSG00000235389.1
4	lnc-C9orf123-6	chr9:8701375-8701552	ENSG00000235389.2

No data

Variant related genes	Relation type
ENSG00000235389	TF binding region
ENSG00000235389	CpG island
ENSG00000132002	chromatin interactions

Extended variants
information (count: 3079 )
Associated
traits (count: 113 )

Variant overlapped rSNPs/rCNVs (count:3079 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16928234	chr9:8645448-8645449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs77963583	chr9:8645481-8645482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs140779595	chr9:8645487-8645488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs72698299	chr9:8645502-8645503	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs62530718	chr9:8645544-8645545	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs533474927	chr9:8645560-8645561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75554334	chr9:8645583-8645584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs35901971	chr9:8645603-8645604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs80201079	chr9:8645609-8645610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546690187	chr9:8645634-8645635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138688470	chr9:8645651-8645652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs72698301	chr9:8645659-8645660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs76757259	chr9:8645661-8645662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs570352072	chr9:8645701-8645702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185510207	chr9:8645703-8645704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537770895	chr9:8645718-8645719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529553953	chr9:8645738-8645739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs189927218	chr9:8645764-8645765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180729737	chr9:8645769-8645770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs141729161	chr9:8645791-8645792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556813603	chr9:8645796-8645797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79428060	chr9:8645827-8645828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538818870	chr9:8645850-8645851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72698302	chr9:8645861-8645862	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs4369050	chr9:8645887-8645888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72700303	chr9:8645903-8645904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs542546913	chr9:8645945-8645946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72700305	chr9:8645965-8645966	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs371780930	chr9:8645993-8645994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs72700307	chr9:8646008-8646009	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs564999147	chr9:8646023-8646024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187353129	chr9:8646055-8646056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74994538	chr9:8646061-8646062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375623228	chr9:8646062-8646063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563704993	chr9:8646069-8646070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200425619	chr9:8646070-8646071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs7855592	chr9:8646098-8646099	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs16928238	chr9:8646183-8646184	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs374916431	chr9:8646191-8646192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531197885	chr9:8646204-8646205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146286661	chr9:8646210-8646211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs567620734	chr9:8646212-8646213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs372371249	chr9:8646222-8646223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535028484	chr9:8646234-8646235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs192196085	chr9:8646245-8646246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138119079	chr9:8646253-8646254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149525582	chr9:8646254-8646255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs556678021	chr9:8646305-8646306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573384544	chr9:8646328-8646329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542484592	chr9:8646335-8646336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:113)

Disease	PMID	Source
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	21811587	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	20668451	CNVD
Schizophrenia	20838587	CNVD
Glioblastoma	18772890	CNVD
Glioblastoma multiforme	21390271	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:738 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8616800-8648000	Weak transcription	Fetal Kidney	kidney
2	chr9:8622000-8648600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr9:8623400-8647800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr9:8629800-8651600	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr9:8630200-8652400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr9:8631000-8649800	Weak transcription	Ovary	ovary
7	chr9:8634600-8648000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr9:8638000-8648000	Weak transcription	Fetal Brain Male	brain
9	chr9:8642600-8647800	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr9:8643800-8647800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr9:8644000-8651800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr9:8644400-8647800	Weak transcription	Brain Hippocampus Middle	brain
13	chr9:8644400-8660400	Weak transcription	Aorta	Aorta
14	chr9:8644600-8651200	Weak transcription	Fetal Muscle Leg	muscle
15	chr9:8644800-8647800	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr9:8645000-8646800	Weak transcription	Brain Substantia Nigra	brain
17	chr9:8645000-8647800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr9:8645000-8651200	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr9:8645200-8651200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr9:8646800-8647000	Enhancers	Brain Angular Gyrus	brain
21	chr9:8646800-8649000	Enhancers	Brain Substantia Nigra	brain
22	chr9:8647000-8647600	Weak transcription	Brain Angular Gyrus	brain
23	chr9:8647600-8649400	Enhancers	Brain Angular Gyrus	brain
24	chr9:8647800-8648000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr9:8647800-8648200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr9:8647800-8648200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr9:8647800-8648200	Enhancers	Placenta Amnion	Placenta Amnion
28	chr9:8647800-8648400	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr9:8647800-8648400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr9:8647800-8648800	Enhancers	Fetal Brain Female	brain
31	chr9:8647800-8649200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr9:8647800-8649600	Enhancers	Brain Anterior Caudate	brain
33	chr9:8647800-8650000	Enhancers	Primary hematopoietic stem cells	blood
34	chr9:8647800-8650200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr9:8647800-8650200	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr9:8647800-8651200	Enhancers	Brain Hippocampus Middle	brain
37	chr9:8647800-8651200	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr9:8648000-8648200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr9:8648000-8648400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr9:8648000-8648400	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr9:8648000-8649200	Enhancers	Brain Cingulate Gyrus	brain
42	chr9:8648000-8649400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:8648000-8649600	Enhancers	NH-A	brain
44	chr9:8648000-8651400	Enhancers	Fetal Brain Male	brain
45	chr9:8648200-8648600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:8648200-8648600	Weak transcription	Placenta Amnion	Placenta Amnion
47	chr9:8648200-8649400	Enhancers	Fetal Heart	heart
48	chr9:8648200-8649600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr9:8648200-8652400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:8648400-8649200	Enhancers	Primary B cells from cord blood	blood

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