Variant report

Variant	nsv967698
Chromosome Location	chr4:165898469-165911460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:157)
CpG islands
(count:673)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:157 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:165898293-165899043	GM12878	blood:	n/a	n/a
2	BCLAF1	chr4:165898340-165899117	GM12878	blood:	n/a	chr4:165898823-165898832
3	BHLHE40	chr4:165898610-165899070	GM12878	blood:	n/a	n/a
4	BRCA1	chr4:165898635-165898831	GM12878	blood:	n/a	n/a
5	CHD2	chr4:165898446-165899204	GM12878	blood:	n/a	n/a
6	CTCF	chr4:165898840-165898990	GM12864	blood:	n/a	n/a
7	CTCF	chr4:165898840-165898990	GM12865	blood:	n/a	n/a
8	CTCF	chr4:165898827-165898924	Fibrobl	skin:	n/a	n/a
9	CTCF	chr4:165898840-165898990	GM12878	blood:	n/a	n/a
10	CTCF	chr4:165898782-165899055	GM12878	blood:	n/a	n/a
11	CTCF	chr4:165898820-165898970	AG04449	skin:	n/a	n/a
12	CTCF	chr4:165898800-165898950	GM12870	blood:	n/a	n/a
13	CTCF	chr4:165898820-165898970	GM06990	blood:	n/a	n/a
14	CTCF	chr4:165898737-165899203	GM19239	blood:	n/a	n/a
15	CTCF	chr4:165899100-165899250	GM12864	blood:	n/a	n/a
16	CTCF	chr4:165898840-165898990	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr4:165898760-165898910	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr4:165898800-165898950	GM12867	blood:	n/a	n/a
19	CTCF	chr4:165899025-165899026	GM12892	blood:	n/a	n/a
20	CTCF	chr4:165898800-165898950	HPAF	blood vessel:	n/a	n/a
21	CTCF	chr4:165898980-165899130	GM12869	blood:	n/a	n/a
22	CTCF	chr4:165898815-165898916	GM13976	blood:	n/a	n/a
23	CTCF	chr4:165898980-165899130	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr4:165898788-165899015	GM19240	blood:	n/a	n/a
25	CTCF	chr4:165898880-165899030	BE2_C	brain:	n/a	n/a
26	CTCF	chr4:165898803-165898806	GM13976	blood:	n/a	n/a
27	CTCF	chr4:165898860-165899010	GM06990	blood:	n/a	n/a
28	CTCF	chr4:165898760-165898910	AG04449	skin:	n/a	n/a
29	CTCF	chr4:165898840-165898990	BJ	skin:	n/a	n/a
30	CTCF	chr4:165898860-165899010	GM12872	blood:	n/a	n/a
31	CTCF	chr4:165898800-165898950	GM12865	blood:	n/a	n/a
32	CTCF	chr4:165898884-165898889	NHEK	skin:	n/a	n/a
33	CTCF	chr4:165906080-165906230	GM12864	blood:	n/a	n/a
34	CTCF	chr4:165898900-165899050	HCM	heart:	n/a	n/a
35	CTCF	chr4:165898820-165898970	GM12872	blood:	n/a	n/a
36	CTCF	chr4:165898860-165899010	GM12873	blood:	n/a	n/a
37	CTCF	chr4:165898860-165899010	HRPEpiC	eye:	n/a	n/a
38	CTCF	chr4:165898820-165898970	GM12873	blood:	n/a	n/a
39	CTCF	chr4:165898920-165899070	AG10803	skin:	n/a	n/a
40	CTCF	chr4:165898880-165899030	HPF	lung:	n/a	n/a
41	CTCF	chr4:165898800-165898950	GM12878	blood:	n/a	n/a
42	CTCF	chr4:165898634-165899119	GM12878	blood:	n/a	n/a
43	CTCF	chr4:165898880-165899030	GM12872	blood:	n/a	n/a
44	CTCF	chr4:165898894-165898909	NHEK	skin:	n/a	n/a
45	CTCF	chr4:165898800-165898950	GM12869	blood:	n/a	n/a
46	CTCF	chr4:165898870-165898944	Spleen_OC	spleen:	n/a	n/a
47	CTCF	chr4:165898800-165898950	AG09319	gingival:	n/a	n/a
48	CTCF	chr4:165899020-165899170	HRE	kidney:	n/a	n/a
49	CTCF	chr4:165898855-165898995	GM20000	blood:	n/a	n/a
50	CTCF	chr4:165898800-165898950	GM12874	blood:	n/a	n/a

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165898666-165898716	PANC-1	pancreas:	n/a
2	chr4:165898707-165898757	AG09319	gingival:	n/a
3	chr4:165898666-165898716	PANC-1	pancreas:	n/a
4	chr4:165898707-165898757	AG09319	gingival:	n/a
5	chr4:165898967-165899017	HCPEpiC	choroid plexus:	n/a
6	chr4:165899396-165899446	SKMC	muscle:	n/a
7	chr4:165898926-165898976	H1-hESC	embryonic stem cell:	embryo
8	chr4:165898666-165898716	CMK	blood:	n/a
9	chr4:165898848-165898898	HCF	heart:	n/a
10	chr4:165898967-165899017	GM06990	blood:	n/a
11	chr4:165900224-165900274	HMEC	breast:	n/a
12	chr4:165899396-165899446	U87	brain:	n/a
13	chr4:165900224-165900274	RPTEC	kidney:	n/a
14	chr4:165900285-165900335	AG09319	gingival:	n/a
15	chr4:165898666-165898716	SKMC	muscle:	n/a
16	chr4:165898967-165899017	NH-A	brain:	n/a
17	chr4:165898967-165899017	AoSMC	blood vessel:	n/a
18	chr4:165898707-165898757	ProgFib	skin:	n/a
19	chr4:165898835-165898885	AG04450	lung:	fetal
20	chr4:165898835-165898885	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:165900285-165900335	HCT-116	colon:	n/a
22	chr4:165898825-165898875	K562	blood:	n/a
23	chr4:165898835-165898885	HIPEpiC	eye:	n/a
24	chr4:165898835-165898885	AG10803	skin:	n/a
25	chr4:165899396-165899446	HEK293	kidney:	embryo
26	chr4:165898967-165899017	GM12878	blood:	n/a
27	chr4:165898666-165898716	HRPEpiC	eye:	n/a
28	chr4:165898848-165898898	GM12878	blood:	n/a
29	chr4:165898848-165898898	A549	lung:	n/a
30	chr4:165899396-165899446	AG10803	skin:	n/a
31	chr4:165898825-165898875	SK-N-SH_RA	brain:	n/a
32	chr4:165898825-165898875	Hela-S3	cervix:	n/a
33	chr4:165898825-165898875	MCF10A-Er-Src	breast:	n/a
34	chr4:165898825-165898875	U87	brain:	n/a
35	chr4:165898707-165898757	MCF10A-Er-Src	breast:	n/a
36	chr4:165899396-165899446	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:165900224-165900274	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:165898835-165898885	Hepatocyte	liver:	n/a
39	chr4:165898707-165898757	HCT-116	colon:	n/a
40	chr4:165898707-165898757	BE2_C	brain:	n/a
41	chr4:165898825-165898875	HEK293	kidney:	embryo
42	chr4:165898967-165899017	AG04449	skin:	fetal
43	chr4:165900285-165900335	SAEC	small airway:	n/a
44	chr4:165898848-165898898	BE2_C	brain:	n/a
45	chr4:165900285-165900335	HL-60	blood:	n/a
46	chr4:165898967-165899017	IMR90	lung:	fetal
47	chr4:165898926-165898976	MCF10A-Er-Src	breast:	n/a
48	chr4:165898825-165898875	HEEpiC	esophagus:	n/a
49	chr4:165898825-165898875	PFSK-1	brain:	n/a
50	chr4:165900285-165900335	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:165896605..165899172-chr4:165907116..165908745,2	MCF-7	breast:
2	chr4:165896605..165899172-chr4:165907116..165908745,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf39-5	chr4:165911021-165911093	l_2770_chr4:165894766-165911093_prostate
2	lnc-C4orf39-4	chr4:165908417-165908939	NONHSAT099095
3	lnc-C4orf39-3	chr4:165899902-165899980	NONHSAT099093

No data

Variant related genes	Relation type
ENSG00000248229	TF binding region
TRIM61	TF binding region
ENSG00000248229	CpG island
TRIM61	CpG island
ENSG00000183439	chromatin interactions
ENSG00000248229	chromatin interactions

Extended variants
information (count: 280 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34505099	chr4:165898478-165898479	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs56231925	chr4:165898502-165898503	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs567570985	chr4:165898505-165898506	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs537724682	chr4:165898574-165898575	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146577558	chr4:165898670-165898671	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs74651789	chr4:165898682-165898683	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539178351	chr4:165898718-165898719	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553966856	chr4:165898742-165898743	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554305688	chr4:165898764-165898765	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs572526760	chr4:165898830-165898831	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs543215516	chr4:165898872-165898873	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs373382831	chr4:165899043-165899044	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs114080664	chr4:165899060-165899061	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs141275956	chr4:165899078-165899079	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs543735959	chr4:165899114-165899115	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs76571840	chr4:165899170-165899171	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs73001978	chr4:165899171-165899172	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs7680569	chr4:165899225-165899226	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs559816674	chr4:165899266-165899267	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs371031697	chr4:165899325-165899326	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs116756804	chr4:165899348-165899349	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs549184625	chr4:165899352-165899353	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs567329549	chr4:165899367-165899368	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs577863159	chr4:165899371-165899372	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs531668382	chr4:165899372-165899373	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs369598553	chr4:165899397-165899398	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs549799268	chr4:165899459-165899460	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571717415	chr4:165899501-165899502	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186741766	chr4:165899505-165899506	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs191134654	chr4:165899528-165899529	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554994123	chr4:165899530-165899531	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs149686384	chr4:165899538-165899539	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544721293	chr4:165899551-165899552	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539039420	chr4:165899566-165899567	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554168701	chr4:165899569-165899570	Active TSS Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183117775	chr4:165899617-165899618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536320863	chr4:165899678-165899679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144105010	chr4:165899686-165899687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185974452	chr4:165899692-165899693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373012135	chr4:165899725-165899726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544134638	chr4:165899729-165899730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574970542	chr4:165899763-165899764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558818963	chr4:165899765-165899766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577072979	chr4:165899785-165899786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544610677	chr4:165899787-165899788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs559694971	chr4:165899790-165899791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs189615535	chr4:165899831-165899832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201523793	chr4:165899864-165899865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs13144910	chr4:165899865-165899866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113414445	chr4:165899868-165899869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165897600-165899000	Active TSS	GM12878-XiMat	blood
2	chr4:165897600-165899400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:165897600-165899400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr4:165897800-165898600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr4:165897800-165898800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:165897800-165898800	Active TSS	Fetal Muscle Trunk	muscle
7	chr4:165897800-165899000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr4:165897800-165899200	Active TSS	H9 Cell Line	embryonic stem cell
9	chr4:165897800-165899200	Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr4:165897800-165899200	Active TSS	Right Ventricle	heart
11	chr4:165897800-165899200	Active TSS	HSMM	muscle
12	chr4:165897800-165899400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr4:165897800-165899400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:165897800-165899400	Active TSS	HUES64 Cell Line	embryonic stem cell
15	chr4:165897800-165899400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr4:165897800-165899400	Active TSS	Primary hematopoietic stem cells short term culture	blood
17	chr4:165897800-165899400	Active TSS	Fetal Stomach	stomach
18	chr4:165897800-165899400	Active TSS	Right Atrium	heart
19	chr4:165897800-165899600	Active TSS	ES-I3 Cell Line	embryonic stem cell
20	chr4:165898000-165898600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:165898000-165898800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
22	chr4:165898000-165898800	Active TSS	NH-A	brain
23	chr4:165898000-165899000	Active TSS	H1 Cell Line	embryonic stem cell
24	chr4:165898000-165899000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:165898000-165899000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr4:165898000-165899000	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
27	chr4:165898000-165899000	Active TSS	Fetal Intestine Small	intestine
28	chr4:165898000-165899000	Active TSS	Fetal Lung	lung
29	chr4:165898000-165899000	Active TSS	NHLF	lung
30	chr4:165898000-165899200	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:165898000-165899200	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr4:165898000-165899200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:165898000-165899200	Active TSS	Primary T cells from cord blood	blood
34	chr4:165898000-165899200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr4:165898000-165899200	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr4:165898000-165899200	Active TSS	Colon Smooth Muscle	Colon
37	chr4:165898000-165899200	Active TSS	Duodenum Mucosa	Duodenum
38	chr4:165898000-165899200	Active TSS	Fetal Brain Female	brain
39	chr4:165898000-165899200	Active TSS	Left Ventricle	heart
40	chr4:165898000-165899200	Active TSS	Psoas Muscle	Psoas
41	chr4:165898000-165899400	Active TSS	Primary B cells from cord blood	blood
42	chr4:165898000-165899400	Active TSS	Brain Anterior Caudate	brain
43	chr4:165898000-165899400	Active TSS	Brain Hippocampus Middle	brain
44	chr4:165898000-165899400	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr4:165898000-165899400	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr4:165898000-165899400	Active TSS	Rectal Smooth Muscle	rectum
47	chr4:165898200-165898600	Active TSS	Lung	lung
48	chr4:165898200-165898800	Flanking Active TSS	Primary hematopoietic stem cells	blood
49	chr4:165898200-165898800	Active TSS	Primary T helper cells fromperipheralblood	blood
50	chr4:165898200-165898800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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