Variant report

Variant	nsv891945
Chromosome Location	chr9:102645-202118
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:944)
CpG islands
(count:1040)
Chromatin interactive
region (count:0)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:944 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr9:114203-114262	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr9:113631-113796	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:178645-179348	GM12878	blood:	n/a	chr9:179069-179082
4	BATF	chr9:184216-185020	GM12878	blood:	n/a	chr9:184501-184509
5	BATF	chr9:156921-157465	GM12878	blood:	n/a	n/a
6	BATF	chr9:183636-184093	GM12878	blood:	n/a	n/a
7	BATF	chr9:120835-121041	GM12878	blood:	n/a	n/a
8	BATF	chr9:164778-164998	GM12878	blood:	n/a	n/a
9	BATF	chr9:178082-178323	GM12878	blood:	n/a	n/a
10	BATF	chr9:122820-123095	GM12878	blood:	n/a	n/a
11	BATF	chr9:156608-156841	GM12878	blood:	n/a	n/a
12	BATF	chr9:160145-160379	GM12878	blood:	n/a	n/a
13	BATF	chr9:200387-200708	GM12878	blood:	n/a	chr9:200519-200530
14	BATF	chr9:183522-184128	GM12878	blood:	n/a	n/a
15	BATF	chr9:116510-116717	GM12878	blood:	n/a	n/a
16	BATF	chr9:199639-200066	GM12878	blood:	n/a	n/a
17	BATF	chr9:198874-199092	GM12878	blood:	n/a	chr9:198886-198895
18	BATF	chr9:198812-199262	GM12878	blood:	n/a	chr9:198886-198895
19	BATF	chr9:185844-186146	GM12878	blood:	n/a	n/a
20	BATF	chr9:178036-178376	GM12878	blood:	n/a	n/a
21	BATF	chr9:167629-168111	GM12878	blood:	n/a	n/a
22	BATF	chr9:152906-153110	GM12878	blood:	n/a	chr9:152982-152993
23	BATF	chr9:177184-177383	GM12878	blood:	n/a	n/a
24	BATF	chr9:194727-194900	GM12878	blood:	n/a	n/a
25	BATF	chr9:156926-157447	GM12878	blood:	n/a	n/a
26	BATF	chr9:185181-185422	GM12878	blood:	n/a	n/a
27	BATF	chr9:199669-200113	GM12878	blood:	n/a	n/a
28	BATF	chr9:185826-186168	GM12878	blood:	n/a	n/a
29	BATF	chr9:167541-168102	GM12878	blood:	n/a	n/a
30	BATF	chr9:184237-185449	GM12878	blood:	n/a	chr9:184501-184509
31	BATF	chr9:156635-156839	GM12878	blood:	n/a	n/a
32	BATF	chr9:178394-179363	GM12878	blood:	n/a	chr9:179069-179082
33	BCL11A	chr9:178003-179356	GM12878	blood:	n/a	n/a
34	BCL11A	chr9:185858-186302	GM12878	blood:	n/a	n/a
35	BCL11A	chr9:167581-168072	GM12878	blood:	n/a	n/a
36	BCL11A	chr9:164593-164855	GM12878	blood:	n/a	n/a
37	BCL11A	chr9:177609-177794	GM12878	blood:	n/a	n/a
38	BCL11A	chr9:135538-135849	GM12878	blood:	n/a	n/a
39	BCL11A	chr9:153305-153607	GM12878	blood:	n/a	n/a
40	BCL11A	chr9:160125-160430	GM12878	blood:	n/a	n/a
41	BCL11A	chr9:198891-199091	GM12878	blood:	n/a	n/a
42	BCL11A	chr9:154005-154265	GM12878	blood:	n/a	n/a
43	BCL11A	chr9:184302-184949	GM12878	blood:	n/a	n/a
44	BCL11A	chr9:183794-184108	GM12878	blood:	n/a	n/a
45	BCL11A	chr9:151681-151909	GM12878	blood:	n/a	n/a
46	BCL11A	chr9:117598-117759	GM12878	blood:	n/a	n/a
47	BCL11A	chr9:184246-185366	GM12878	blood:	n/a	n/a
48	BCL11A	chr9:178105-179362	GM12878	blood:	n/a	n/a
49	BCL11A	chr9:156917-157457	GM12878	blood:	n/a	n/a
50	BCL11A	chr9:152739-152922	GM12878	blood:	n/a	n/a

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:117044-117094	SAEC	small airway:	n/a
2	chr9:104568-104618	HCT-116	colon:	n/a
3	chr9:113530-113580	HCPEpiC	choroid plexus:	n/a
4	chr9:117044-117094	SAEC	small airway:	n/a
5	chr9:104568-104618	HCT-116	colon:	n/a
6	chr9:113530-113580	HCPEpiC	choroid plexus:	n/a
7	chr9:176893-176943	AG04450	lung:	fetal
8	chr9:104568-104618	Hepatocyte	liver:	n/a
9	chr9:109039-109089	MCF-7	breast:	n/a
10	chr9:118091-118141	HepG2	liver:	n/a
11	chr9:113530-113580	HNPCEpiC	eye:	n/a
12	chr9:117608-117658	SAEC	small airway:	n/a
13	chr9:113530-113580	RPTEC	kidney:	n/a
14	chr9:117044-117094	ovcar-3	ovarian:	n/a
15	chr9:168828-168878	NH-A	brain:	n/a
16	chr9:112937-112987	Caco-2	colon:	n/a
17	chr9:117608-117658	Hepatocyte	liver:	n/a
18	chr9:179409-179459	A549	lung:	n/a
19	chr9:114838-114888	PrEC	prostate:	n/a
20	chr9:109039-109089	AG10803	skin:	n/a
21	chr9:113530-113580	HEK293	kidney:	embryo
22	chr9:112937-112987	SK-N-SH_RA	brain:	n/a
23	chr9:114359-114409	NT2-D1	testis:	n/a
24	chr9:117608-117658	GM12891	blood:	n/a
25	chr9:118698-118748	IMR90	lung:	fetal
26	chr9:176893-176943	NB4	blood:	n/a
27	chr9:114838-114888	K562	blood:	n/a
28	chr9:179409-179459	SK-N-SH	brain:	n/a
29	chr9:118530-118580	SAEC	small airway:	n/a
30	chr9:114140-114190	SKMC	muscle:	n/a
31	chr9:179409-179459	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:114838-114888	CMK	blood:	n/a
33	chr9:117608-117658	H1-hESC	embryonic stem cell:	embryo
34	chr9:117044-117094	HRPEpiC	eye:	n/a
35	chr9:118091-118141	RPTEC	kidney:	n/a
36	chr9:104568-104618	PANC-1	pancreas:	n/a
37	chr9:104568-104618	HMEC	breast:	n/a
38	chr9:114359-114409	GM06990	blood:	n/a
39	chr9:114359-114409	ECC-1	luminal epithelium:	n/a
40	chr9:168828-168878	HEK293	kidney:	embryo
41	chr9:112937-112987	HEEpiC	esophagus:	n/a
42	chr9:112618-112668	GM12891	blood:	n/a
43	chr9:114140-114190	SAEC	small airway:	n/a
44	chr9:114838-114888	HMEC	breast:	n/a
45	chr9:112618-112668	HUVEC	blood vessel:	n/a
46	chr9:104568-104618	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:114140-114190	IMR90	lung:	fetal
48	chr9:118530-118580	HPAEpiC	pulmonary alveolar:	n/a
49	chr9:117608-117658	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:104568-104618	SK-N-SH	brain:	n/a

No data

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FOXD4-5	chr9:151745-152078	NONHSAT129910
2	lnc-FOXD4-3	chr9:113606-113656	NONHSAT129899
3	lnc-FOXD4-2	chr9:109596-109842	NONHSAT129897
4	lnc-FOXD4-2	chr9:108804-109469	NONHSAT129897
5	lnc-FOXD4-2	chr9:102740-102941	ENSG00000227917
6	lnc-FOXD4-1	chr9:113694-113754	ENSG00000231808
7	lnc-FOXD4-2	chr9:109316-109471	NONHSAT129895
8	lnc-FOXD4-2	chr9:103694-103754	NONHSAT129896
9	lnc-FOXD4-5	chr9:161567-161647	NONHSAT129910
10	lnc-FOXD4-3	chr9:114040-115772	NONHSAT129899
11	lnc-FOXD4-2	chr9:102716-103067	NONHSAT129896
12	lnc-FOXD4-2	chr9:102740-102850	NONHSAT129895
13	lnc-FOXD4-1	chr9:112716-113067	ENSG00000231808
14	lnc-FOXD4-5	chr9:154709-154795	NONHSAT129910
15	lnc-FOXD4-5	chr9:156481-156527	NONHSAT129910

No data

Variant related genes	Relation type
ENSG00000231808	TF binding region
FOXD4	TF binding region
ENSG00000227917	TF binding region
CBWD1	TF binding region
ENSG00000231808	CpG island
FOXD4	CpG island
ENSG00000227917	CpG island
CBWD1	CpG island

Extended variants
information (count: 3076 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:3076 , 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	rs2998976	chr9:102645-102646	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs150825601	chr9:102651-102652	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs571986250	chr9:102653-102654	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs77659105	chr9:102672-102673	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs182241000	chr9:102680-102681	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs571989840	chr9:102683-102684	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs62532145	chr9:102702-102703	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs543104467	chr9:102703-102704	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs564885664	chr9:102716-102717	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs10977639	chr9:102721-102722	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs552125930	chr9:102727-102728	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs2998975	chr9:102728-102729	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs139336184	chr9:102730-102731	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs144149065	chr9:102770-102771	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs10977640	chr9:102793-102794	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs186477530	chr9:102798-102799	ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs538346051	chr9:102814-102815	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs556205389	chr9:102827-102828	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs2811129	chr9:102831-102832	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs538674283	chr9:102832-102833	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs192603882	chr9:102839-102840	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs10977644	chr9:102843-102844	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs569659949	chr9:102886-102887	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs185413180	chr9:102940-102941	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs10977649	chr9:102950-102951	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs374628325	chr9:102972-102973	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs542554760	chr9:102996-102997	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs554752913	chr9:103010-103011	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs576118359	chr9:103045-103046	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs559397368	chr9:103722-103723	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs368833247	chr9:103723-103724	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs574316556	chr9:103735-103736	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs528548095	chr9:104569-104570	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs553116350	chr9:104571-104572	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs373116136	chr9:104578-104579	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs375426742	chr9:104599-104600	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs201290350	chr9:105133-105134	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs144660169	chr9:105136-105137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs535208549	chr9:105143-105144	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs556983936	chr9:105150-105151	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs76741984	chr9:105169-105170	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs79689957	chr9:105178-105179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs568535037	chr9:105186-105187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs531270547	chr9:105208-105209	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs201210595	chr9:105211-105212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs200784943	chr9:105233-105234	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs77456528	chr9:105260-105261	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs539076558	chr9:105281-105282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs199747667	chr9:105286-105287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs185712962	chr9:105300-105301	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	20164920	CNVD
Ovarian cancer	21720365	CNVD
Myelofibrosis	22110671	CNVD
Lynch syndrome	18415027	CNVD
Retinoblastoma	21504564	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	22286061	CNVD
Williams-beuren syndrome	18553513	CNVD
Disorders of sex development	21048976	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
prenatal diagnosis	20453657	CNVD
Gastric cancer	16715143	CNVD
Esophageal squamous carcinoma	18405350	CNVD
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
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
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
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
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
Intracranial ependymoma	16609018	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:782 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:102600-102800	ZNF genes & repeats	Lung	lung
2	chr9:108800-109000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
3	chr9:108800-109000	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
4	chr9:108800-109000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
5	chr9:108800-109000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr9:109200-109400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
7	chr9:109200-109400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr9:109200-109400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:109200-110000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
10	chr9:112800-113000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
11	chr9:112800-113000	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 2	blood
12	chr9:112800-113000	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
13	chr9:112800-113000	Bivalent Enhancer	Brain Hippocampus Middle	brain
14	chr9:112800-113000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
15	chr9:112800-113000	Bivalent Enhancer	K562	blood
16	chr9:112800-113200	Bivalent Enhancer	Fetal Muscle Leg	muscle
17	chr9:112800-113400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
18	chr9:112800-113400	Bivalent Enhancer	Primary T helper 17 cells PMA-I stimulated	--
19	chr9:112800-113400	Bivalent Enhancer	Primary T helper cells fromperipheralblood	blood
20	chr9:112800-113400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
21	chr9:112800-113400	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
22	chr9:112800-113400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr9:112800-113400	Bivalent Enhancer	Adipose Nuclei	Adipose
24	chr9:112800-113400	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
25	chr9:112800-113400	Bivalent/Poised TSS	Right Ventricle	heart
26	chr9:112800-113400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
27	chr9:112800-113600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr9:112800-113600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr9:112800-113800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
30	chr9:112800-113800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr9:112800-114000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
32	chr9:112800-115200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
33	chr9:112800-115400	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
34	chr9:113000-113200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr9:113000-113200	Active TSS	Primary hematopoietic stem cells short term culture	blood
36	chr9:113000-113200	Bivalent Enhancer	Fetal Intestine Large	intestine
37	chr9:113000-113400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:113000-113400	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
39	chr9:113000-113400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr9:113000-113400	Bivalent Enhancer	Brain Germinal Matrix	brain
41	chr9:113000-113800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
42	chr9:113000-113800	Bivalent Enhancer	Placenta	Placenta
43	chr9:113000-114400	Active TSS	K562	blood
44	chr9:113000-115200	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
45	chr9:113200-113400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr9:113200-113400	Bivalent/Poised TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr9:113200-113400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr9:113200-113400	Bivalent Enhancer	Colonic Mucosa	Colon
49	chr9:113200-113600	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
50	chr9:113200-113600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

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