Variant report

Variant	nsv892084
Chromosome Location	chr9:2853103-2909883
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	chr9:2859915-2860115	HepG2	liver:	n/a	n/a
2	BACH1	chr9:2854677-2854892	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr9:2857478-2857878	GM12878	blood:	n/a	n/a
4	BATF	chr9:2857493-2857881	GM12878	blood:	n/a	n/a
5	BCLAF1	chr9:2857522-2857882	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:2857542-2857876	GM12878	blood:	n/a	n/a
7	BRCA1	chr9:2859836-2860152	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr9:2853641-2854039	MCF-7	breast:	n/a	n/a
9	CEBPB	chr9:2853813-2854018	A549	lung:	n/a	n/a
10	CEBPB	chr9:2872639-2872932	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr9:2872628-2872897	A549	lung:	n/a	n/a
12	CEBPB	chr9:2857680-2857985	IMR90	lung:	n/a	n/a
13	CEBPB	chr9:2857657-2858022	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr9:2872618-2872913	HepG2	liver:	n/a	n/a
15	CEBPB	chr9:2857672-2857994	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr9:2853734-2854018	IMR90	lung:	n/a	n/a
17	CHD2	chr9:2859954-2860009	HepG2	liver:	n/a	n/a
18	CTCF	chr9:2859851-2860106	K562	blood:	n/a	n/a
19	CTCF	chr9:2859732-2860086	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr9:2859900-2860050	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr9:2859920-2860070	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr9:2857740-2857890	K562	blood:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
23	CTCF	chr9:2872711-2872789	GM19240	blood:	n/a	n/a
24	CTCF	chr9:2857700-2857850	HFF-Myc	foreskin:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
25	CTCF	chr9:2857640-2857908	K562	blood:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
26	CTCF	chr9:2857605-2857948	HUVEC	blood vessel:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
27	CTCF	chr9:2859867-2860082	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr9:2859735-2860205	IMR90	lung:	n/a	n/a
29	CTCF	chr9:2858040-2858190	GM12864	blood:	n/a	n/a
30	CTCF	chr9:2859900-2860050	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr9:2859100-2859250	HMEC	breast:	n/a	n/a
32	CTCF	chr9:2857713-2857877	GM12891	blood:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
33	CTCF	chr9:2857680-2857830	HA-sp	spinal cord:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
34	CTCF	chr9:2857720-2857870	BE2_C	brain:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
35	CTCF	chr9:2859855-2860097	HepG2	liver:	n/a	n/a
36	CTCF	chr9:2857700-2857850	NB4	blood:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
37	CTCF	chr9:2872700-2872850	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr9:2858020-2858170	NHLF	lung:	n/a	n/a
39	CTCF	chr9:2859900-2860050	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr9:2859860-2860010	WI-38	lung:	n/a	n/a
41	CTCF	chr9:2857636-2857911	Gliobla	brain:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
42	CTCF	chr9:2857635-2857922	Kidney_OC	kidney:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
43	CTCF	chr9:2857621-2857947	Medullo	brain:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
44	CTCF	chr9:2859880-2860030	HFF-Myc	foreskin:	n/a	n/a
45	CTCF	chr9:2859846-2860117	NHEK	skin:	n/a	n/a
46	CTCF	chr9:2872645-2872857	MCF-7	breast:	n/a	n/a
47	CTCF	chr9:2859805-2860095	T-47D	breast:	n/a	n/a
48	CTCF	chr9:2857680-2857830	HCT-116	colon:	n/a	chr9:2857781-2857791 chr9:2857778-2857799 chr9:2857776-2857794 chr9:2857777-2857793 chr9:2857779-2857792
49	CTCF	chr9:2872680-2872830	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr9:2872463-2873037	HCT-116	colon:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:2859483..2860540-chr9:2991100..2991795,3	MCF-7	breast:
2	chr9:2859516..2860444-chr9:3181439..3182223,3	MCF-7	breast:
3	chr9:2872228..2873219-chr9:2989491..2990582,3	MCF-7	breast:
4	chr9:2889601..2892216-chr9:2916356..2918847,2	MCF-7	breast:
5	chr9:2850970..2853898-chr9:2855220..2856868,2	MCF-7	breast:
6	chr9:2857569..2858353-chr9:4117438..4118399,2	K562	blood:
7	chr9:2845302..2847142-chr9:2852039..2853784,2	K562	blood:
8	chr9:2857345..2858204-chr9:2991199..2991973,2	MCF-7	breast:
9	chr9:2872359..2873181-chr9:3181414..3182245,4	MCF-7	breast:
10	chr9:2857339..2858217-chr9:3181318..3182235,6	MCF-7	breast:
11	chr9:2843846..2845987-chr9:2855145..2859412,4	MCF-7	breast:
12	chr9:2850970..2853898-chr9:2855220..2856868,2	MCF-7	breast:
13	chr9:2842938..2845767-chr9:2851253..2855268,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIAA0020-5	chr9:2900320-2900804	NONHSAT130014

Variant related genes	Relation type
ENSG00000229184	TF binding region
ENSG00000236496	TF binding region
ENSG00000107249	chromatin interactions
ENSG00000080608	chromatin interactions
ENSG00000236511	chromatin interactions

Extended variants
information (count: 1424 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:1424 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13300111	chr9:2853103-2853104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs149278665	chr9:2853122-2853123	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs575735392	chr9:2853133-2853134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201917523	chr9:2853144-2853145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531854569	chr9:2853172-2853173	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs558490156	chr9:2853176-2853177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs577753088	chr9:2853204-2853205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs540195123	chr9:2853235-2853236	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143508031	chr9:2853298-2853299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528956831	chr9:2853305-2853306	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115640806	chr9:2853313-2853314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs147971229	chr9:2853360-2853361	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs553954405	chr9:2853371-2853372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143426140	chr9:2853375-2853376	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571165515	chr9:2853385-2853386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7857816	chr9:2853392-2853393	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546559873	chr9:2853393-2853394	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs566865545	chr9:2853394-2853395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs535981478	chr9:2853403-2853404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs555560049	chr9:2853444-2853445	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs569483621	chr9:2853465-2853466	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs538048337	chr9:2853466-2853467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs185274527	chr9:2853495-2853496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs578238324	chr9:2853501-2853502	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs533792672	chr9:2853502-2853503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs189686074	chr9:2853542-2853543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532957936	chr9:2853543-2853544	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs539652725	chr9:2853544-2853545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs79325616	chr9:2853549-2853550	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs73379806	chr9:2853554-2853555	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs374655456	chr9:2853556-2853557	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370872131	chr9:2853583-2853584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs147312821	chr9:2853593-2853594	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs544754204	chr9:2853633-2853634	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139401418	chr9:2853636-2853637	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545004532	chr9:2853642-2853643	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs375593667	chr9:2853662-2853663	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs180893027	chr9:2853675-2853676	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs547272728	chr9:2853690-2853691	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs143202395	chr9:2853710-2853711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs529271257	chr9:2853748-2853749	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs150888065	chr9:2853758-2853759	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs549499135	chr9:2853759-2853760	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs569214049	chr9:2853767-2853768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs139295530	chr9:2853776-2853777	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs185590905	chr9:2853799-2853800	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150002264	chr9:2853807-2853808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs576685695	chr9:2853814-2853815	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191242856	chr9:2853815-2853816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs183594321	chr9:2853891-2853892	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Gastric cancer	16715143	CNVD
Glioblastoma multiforme	22286061	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	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
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
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
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	20531469	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	21373258	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Ovarian cancer	22355333	CNVD
Schizophrenia	20967226	CNVD
Renal cell carcinoma	21215367	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:2850400-2854800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr9:2854400-2855200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr9:2854800-2855000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr9:2854800-2855200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr9:2855200-2855400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:2855400-2857200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:2857200-2857800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:2857400-2857600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
9	chr9:2857400-2857600	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr9:2857400-2857600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:2857400-2857600	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr9:2857400-2857600	Enhancers	NHDF-Ad	bronchial
13	chr9:2857400-2857800	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr9:2857400-2857800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr9:2857400-2857800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
16	chr9:2857600-2857800	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:2857600-2857800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr9:2857600-2857800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr9:2857600-2857800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
20	chr9:2857600-2857800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr9:2857600-2857800	Bivalent Enhancer	Fetal Heart	heart
22	chr9:2857600-2857800	Bivalent Enhancer	Fetal Kidney	kidney
23	chr9:2857600-2857800	Flanking Active TSS	NHDF-Ad	bronchial
24	chr9:2857600-2858000	Enhancers	Brain Anterior Caudate	brain
25	chr9:2857600-2858000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
26	chr9:2857600-2858000	Bivalent Enhancer	Fetal Brain Male	brain
27	chr9:2857600-2858200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr9:2857800-2858000	Enhancers	Fetal Stomach	stomach
29	chr9:2857800-2858200	Enhancers	Brain Hippocampus Middle	brain
30	chr9:2858000-2858200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr9:2860000-2860200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr9:2860200-2865200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr9:2865200-2865600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:2865200-2865600	Enhancers	Osteobl	bone
35	chr9:2866600-2867000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:2866600-2867400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr9:2866600-2867600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr9:2866800-2867600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr9:2868200-2869000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr9:2869000-2869800	Enhancers	Ovary	ovary
41	chr9:2870400-2873000	Enhancers	Primary T cells from cord blood	blood
42	chr9:2870800-2871400	Enhancers	Primary T helper cells PMA-I stimulated	--
43	chr9:2871200-2871400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr9:2871400-2871600	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr9:2871400-2871600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:2871400-2872400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr9:2871600-2873000	Enhancers	HepG2	liver
48	chr9:2871800-2872200	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr9:2872000-2872800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr9:2872200-2873200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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