Variant report

Variant	nsv831508
Chromosome Location	chr9:10584843-10769475
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	BACH1	chr9:10731396-10731463	K562	blood:	n/a	n/a
2	BACH1	chr9:10612811-10613185	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr9:10612838-10613346	K562	blood:	n/a	n/a
4	CEBPB	chr9:10646990-10647193	HepG2	liver:	n/a	chr9:10647078-10647089 chr9:10647078-10647091
5	CEBPB	chr9:10584890-10585155	A549	lung:	n/a	chr9:10585075-10585088 chr9:10585076-10585087 chr9:10585075-10585086
6	CEBPB	chr9:10605774-10606046	IMR90	lung:	n/a	chr9:10605898-10605911 chr9:10605898-10605911 chr9:10605895-10605912 chr9:10605898-10605909 chr9:10605900-10605911 chr9:10605898-10605911
7	CEBPB	chr9:10597829-10598144	IMR90	lung:	n/a	chr9:10597988-10598005
8	CEBPB	chr9:10597856-10598158	HepG2	liver:	n/a	chr9:10597988-10598005
9	CEBPB	chr9:10635667-10636010	A549	lung:	n/a	chr9:10635839-10635852 chr9:10635840-10635851 chr9:10635841-10635850
10	CEBPB	chr9:10631704-10631897	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr9:10678846-10679125	IMR90	lung:	n/a	n/a
12	CEBPB	chr9:10612917-10612934	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:10599520-10599740	IMR90	lung:	n/a	chr9:10599614-10599625 chr9:10599614-10599627
14	CEBPB	chr9:10605774-10606014	HepG2	liver:	n/a	chr9:10605898-10605911 chr9:10605898-10605911 chr9:10605895-10605912 chr9:10605898-10605909 chr9:10605900-10605911 chr9:10605898-10605911
15	CEBPB	chr9:10597948-10598030	H1-hESC	embryonic stem cell:	n/a	chr9:10597988-10598005
16	CEBPB	chr9:10599485-10599703	HepG2	liver:	n/a	chr9:10599614-10599625 chr9:10599614-10599627
17	CEBPB	chr9:10663860-10664105	A549	lung:	n/a	chr9:10663898-10663909
18	CEBPB	chr9:10597859-10598088	A549	lung:	n/a	chr9:10597988-10598005
19	CEBPB	chr9:10584953-10585136	HepG2	liver:	n/a	chr9:10585075-10585088 chr9:10585076-10585087 chr9:10585075-10585086
20	CEBPB	chr9:10635667-10636017	HepG2	liver:	n/a	chr9:10635839-10635852 chr9:10635840-10635851 chr9:10635841-10635850
21	CEBPB	chr9:10660565-10660834	IMR90	lung:	n/a	n/a
22	CEBPB	chr9:10635685-10636024	IMR90	lung:	n/a	chr9:10635839-10635852 chr9:10635840-10635851 chr9:10635841-10635850
23	CHD1	chr9:10612779-10612818	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr9:10613166-10613178	HepG2	liver:	n/a	n/a
25	CHD2	chr9:10697250-10697363	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr9:10612915-10613421	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTBP2	chr9:10612575-10613478	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:10612980-10613130	GM12866	blood:	n/a	chr9:10613024-10613037
29	CTCF	chr9:10744291-10744351	GM13976	blood:	n/a	n/a
30	CTCF	chr9:10613000-10613150	HA-sp	spinal cord:	n/a	chr9:10613024-10613037
31	CTCF	chr9:10612960-10613110	GM12867	blood:	n/a	chr9:10613024-10613037
32	CTCF	chr9:10612980-10613130	GM12870	blood:	n/a	chr9:10613024-10613037
33	CTCF	chr9:10612940-10613090	GM12870	blood:	n/a	chr9:10613024-10613037
34	CTCF	chr9:10612980-10613130	Caco-2	colon:	n/a	chr9:10613024-10613037
35	CTCF	chr9:10612980-10613130	HUVEC	blood vessel:	n/a	chr9:10613024-10613037
36	CTCF	chr9:10612960-10613110	HRPEpiC	eye:	n/a	chr9:10613024-10613037
37	CTCF	chr9:10612940-10613090	HPF	lung:	n/a	chr9:10613024-10613037
38	CTCF	chr9:10612965-10613176	GM13977	blood:	n/a	chr9:10613024-10613037
39	CTCF	chr9:10612911-10613244	H1-hESC	embryonic stem cell:	n/a	chr9:10613024-10613037
40	CTCF	chr9:10613024-10613139	K562	blood:	n/a	chr9:10613024-10613037
41	CTCF	chr9:10612911-10613212	HepG2	liver:	n/a	chr9:10613024-10613037
42	CTCF	chr9:10612743-10613360	A549	lung:	n/a	chr9:10613024-10613037 chr9:10612908-10612921 chr9:10612898-10612911
43	CTCF	chr9:10612940-10613090	AG04449	skin:	n/a	chr9:10613024-10613037
44	CTCF	chr9:10704820-10704970	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr9:10612982-10613067	GM13976	blood:	n/a	chr9:10613024-10613037
46	CTCF	chr9:10612960-10613110	GM06990	blood:	n/a	chr9:10613024-10613037
47	CTCF	chr9:10613020-10613170	GM12871	blood:	n/a	chr9:10613024-10613037
48	CTCF	chr9:10612980-10613130	GM12872	blood:	n/a	chr9:10613024-10613037
49	CTCF	chr9:10613000-10613150	HCM	heart:	n/a	chr9:10613024-10613037
50	CTCF	chr9:10612960-10613110	HBMEC	blood vessel:	n/a	chr9:10613024-10613037

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:10612700-10612750	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:10613328-10613378	ProgFib	skin:	n/a
3	chr9:10615205-10615255	K562	blood:	n/a
4	chr9:10613332-10613382	HCPEpiC	choroid plexus:	n/a
5	chr9:10615205-10615255	SK-N-SH	brain:	n/a
6	chr9:10615205-10615255	HRCEpiC	kidney:	n/a
7	chr9:10613328-10613378	IMR90	lung:	fetal
8	chr9:10613332-10613382	ECC-1	luminal epithelium:	n/a
9	chr9:10612700-10612750	SK-N-MC	brain:	n/a
10	chr9:10615205-10615255	GM06990	blood:	n/a
11	chr9:10615205-10615255	HL-60	blood:	n/a
12	chr9:10612700-10612750	HEK293	kidney:	embryo
13	chr9:10612700-10612750	HRCEpiC	kidney:	n/a
14	chr9:10612700-10612750	SK-N-SH_RA	brain:	n/a
15	chr9:10615205-10615255	HNPCEpiC	eye:	n/a
16	chr9:10613328-10613378	NB4	blood:	n/a
17	chr9:10613332-10613382	H1-hESC	embryonic stem cell:	embryo
18	chr9:10613328-10613378	LNCaP	prostate:	n/a
19	chr9:10613328-10613378	HCM	heart:	n/a
20	chr9:10613332-10613382	HRCEpiC	kidney:	n/a
21	chr9:10613332-10613382	GM12892	blood:	n/a
22	chr9:10612700-10612750	GM12878	blood:	n/a
23	chr9:10615205-10615255	AG04449	skin:	fetal
24	chr9:10613328-10613378	HUVEC	blood vessel:	n/a
25	chr9:10613332-10613382	GM06990	blood:	n/a
26	chr9:10615205-10615255	BJ	skin:	n/a
27	chr9:10613332-10613382	PrEC	prostate:	n/a
28	chr9:10613332-10613382	HRPEpiC	eye:	n/a
29	chr9:10613328-10613378	HRPEpiC	eye:	n/a
30	chr9:10612700-10612750	LNCaP	prostate:	n/a
31	chr9:10613328-10613378	GM12891	blood:	n/a
32	chr9:10615205-10615255	IMR90	lung:	fetal
33	chr9:10612700-10612750	HCPEpiC	choroid plexus:	n/a
34	chr9:10613328-10613378	ECC-1	luminal epithelium:	n/a
35	chr9:10615205-10615255	MCF10A-Er-Src	breast:	n/a
36	chr9:10612700-10612750	HCM	heart:	n/a
37	chr9:10613332-10613382	NB4	blood:	n/a
38	chr9:10612700-10612750	PrEC	prostate:	n/a
39	chr9:10615205-10615255	ECC-1	luminal epithelium:	n/a
40	chr9:10613328-10613378	MCF10A-Er-Src	breast:	n/a
41	chr9:10613328-10613378	HCPEpiC	choroid plexus:	n/a
42	chr9:10613328-10613378	AG09309	skin:	n/a
43	chr9:10612700-10612750	A549	lung:	n/a
44	chr9:10615205-10615255	AG09309	skin:	n/a
45	chr9:10615205-10615255	HRE	kidney:	n/a
46	chr9:10615205-10615255	NH-A	brain:	n/a
47	chr9:10612700-10612750	HAEpiC	amniotic membrane:	n/a
48	chr9:10613332-10613382	SK-N-MC	brain:	n/a
49	chr9:10615205-10615255	HepG2	liver:	n/a
50	chr9:10612700-10612750	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:10593948..10596046-chr9:10596166..10598402,2	MCF-7	breast:
2	chr9:10697506..10699235-chr9:10701323..10703741,2	K562	blood:
3	chr9:10656522..10658673-chr9:10675612..10678102,2	K562	blood:
4	chr9:10656522..10658673-chr9:10675612..10678102,2	K562	blood:
5	chr9:10593948..10596046-chr9:10596166..10598402,2	MCF-7	breast:
6	chr9:10697506..10699235-chr9:10701323..10703741,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PTPRD-1	chr9:10632083-10632203	ENSG00000232035
2	lnc-TYRP1-3	chr9:10616617-10616669	ENSG00000226717
3	lnc-TYRP1-3	chr9:10613186-10613426	NONHSAT130200
4	lnc-TYRP1-3	chr9:10617861-10618218	ENSG00000226717
5	lnc-TYRP1-3	chr9:10617861-10620420	ENSG00000226717.2
6	lnc-TYRP1-3	chr9:10616617-10616671	NONHSAT130200
7	lnc-TYRP1-3	chr9:10616617-10616663	NONHSAT130202
8	lnc-TYRP1-3	chr9:10613237-10613443	NONHSAT130202
9	lnc-TYRP1-3	chr9:10616617-10616669	ENSG00000226717.2
10	lnc-TYRP1-3	chr9:10613202-10613426	ENSG00000226717.2
11	lnc-TYRP1-3	chr9:10613202-10613426	ENSG00000226717
12	lnc-PTPRD-1	chr9:10631750-10631785	ENSG00000232035

Variant related genes	Relation type
ENSG00000226717	TF binding region
PTPRD	TF binding region
ENSG00000232035	TF binding region
ENSG00000226717	CpG island
PTPRD	CpG island
ENSG00000232035	CpG island
KIF5B	miRNA target sites
RPAP2	miRNA target sites

Extended variants
information (count: 2332 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:2332 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551165969	chr9:10586270-10586271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs369138497	chr9:10586308-10586309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544393029	chr9:10586310-10586311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs148261196	chr9:10586349-10586350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs181006173	chr9:10586401-10586402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546824879	chr9:10586409-10586410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186467823	chr9:10586435-10586436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370485569	chr9:10586455-10586456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114034114	chr9:10586457-10586458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552153389	chr9:10586458-10586459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569177992	chr9:10586481-10586482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538162115	chr9:10586489-10586490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13298283	chr9:10586527-10586528	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs190279233	chr9:10586535-10586536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181212054	chr9:10586539-10586540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185705121	chr9:10586545-10586546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190557039	chr9:10586549-10586550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544974292	chr9:10586565-10586566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558609669	chr9:10586570-10586571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs575577338	chr9:10586603-10586604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs76192663	chr9:10586605-10586606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568872069	chr9:10586610-10586611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553098436	chr9:10586618-10586619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561131776	chr9:10586639-10586640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141864270	chr9:10586661-10586662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs540431809	chr9:10586668-10586669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183936643	chr9:10586676-10586677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188919241	chr9:10586703-10586704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552116649	chr9:10586722-10586723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550123735	chr9:10586753-10586754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs5896406	chr9:10586786-10586787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556748202	chr9:10586787-10586788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs5896407	chr9:10586801-10586802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs536903976	chr9:10586807-10586808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs1341202	chr9:10586876-10586877	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs10959178	chr9:10586881-10586882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1555484	chr9:10586886-10586887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs568632929	chr9:10586898-10586899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs73398207	chr9:10586911-10586912	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs145413392	chr9:10586936-10586937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs190996572	chr9:10587083-10587084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538755285	chr9:10587092-10587093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111881038	chr9:10587096-10587097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs555829304	chr9:10587115-10587116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182760034	chr9:10587131-10587132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs544507957	chr9:10587144-10587145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs554526826	chr9:10587146-10587147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs142014913	chr9:10587154-10587155	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572671566	chr9:10587165-10587166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35287509	chr9:10594635-10594636	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:118)

Disease	PMID	Source
abnormal development	18461090	CNVD
Disorders of sex development	21048976	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
Glioblastoma multiforme	21080181	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
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
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Cancer	20164920	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
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	21764851	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Melanoma	22183965	CNVD
Barrett''s syndrome	19417022	CNVD
Renal cell carcinoma	21215367	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:10586200-10587200	Enhancers	NHEK	skin
2	chr9:10594600-10595000	Enhancers	Fetal Brain Male	brain
3	chr9:10595000-10606600	Weak transcription	Fetal Brain Male	brain
4	chr9:10605200-10606000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr9:10605200-10606000	Enhancers	NHEK	skin
6	chr9:10605400-10606000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:10606000-10609600	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr9:10606600-10607000	Enhancers	Fetal Brain Male	brain
9	chr9:10607000-10608600	Weak transcription	Fetal Brain Male	brain
10	chr9:10607400-10613600	Active TSS	Fetal Brain Female	brain
11	chr9:10608600-10614400	Active TSS	Fetal Brain Male	brain
12	chr9:10609200-10612200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr9:10609400-10610400	Active TSS	Brain Angular Gyrus	brain
14	chr9:10609600-10610200	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
15	chr9:10610000-10610200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr9:10610000-10610200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
17	chr9:10610000-10610200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
18	chr9:10610000-10610600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr9:10610000-10613400	Active TSS	Brain Inferior Temporal Lobe	brain
20	chr9:10610200-10613600	Active TSS	Pancreatic Islets	Pancreatic Islet
21	chr9:10610400-10611600	Weak transcription	Brain Angular Gyrus	brain
22	chr9:10610600-10611600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr9:10611200-10611800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr9:10611200-10611800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:10611400-10611600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
26	chr9:10611600-10611800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
27	chr9:10611600-10611800	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
28	chr9:10611600-10611800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
29	chr9:10611600-10612000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
30	chr9:10611600-10612000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
31	chr9:10611600-10613400	Active TSS	Brain Anterior Caudate	brain
32	chr9:10611600-10613400	Active TSS	Brain Cingulate Gyrus	brain
33	chr9:10611600-10613400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
34	chr9:10611600-10613800	Active TSS	Brain Angular Gyrus	brain
35	chr9:10611800-10612000	Flanking Bivalent TSS/Enh	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:10611800-10612000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
37	chr9:10611800-10612200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr9:10611800-10612200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
39	chr9:10611800-10612200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:10611800-10613400	Bivalent/Poised TSS	Brain Germinal Matrix	brain
41	chr9:10611800-10614000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
42	chr9:10612000-10612200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
43	chr9:10612000-10612200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
44	chr9:10612000-10612200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
45	chr9:10612000-10612200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr9:10612000-10612200	Enhancers	HMEC	breast
47	chr9:10612000-10612400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
48	chr9:10612000-10612400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr9:10612000-10612600	Flanking Active TSS	NHEK	skin
50	chr9:10612000-10613400	Active TSS	Brain Substantia Nigra	brain

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