Variant report

Variant	nsv967697
Chromosome Location	chr4:165843736-165889668
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1015)
CpG islands
(count:1221)
Chromatin interactive
region (count:14)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1015 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:165877669-165878118	GM12878	blood:	n/a	n/a
2	BATF	chr4:165857047-165857297	GM12878	blood:	n/a	n/a
3	BATF	chr4:165856995-165857356	GM12878	blood:	n/a	n/a
4	BCL11A	chr4:165857038-165857347	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:165856980-165857343	GM12878	blood:	n/a	n/a
6	BCLAF1	chr4:165877809-165878342	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:165857075-165857535	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:165877853-165878275	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:165877987-165878027	K562	blood:	n/a	n/a
10	BHLHE40	chr4:165880700-165880797	HepG2	liver:	n/a	n/a
11	BRCA1	chr4:165859210-165859241	GM12878	blood:	n/a	n/a
12	CBX3	chr4:165877855-165878292	K562	blood:	n/a	n/a
13	CEBPB	chr4:165846118-165846395	HepG2	liver:	n/a	chr4:165846274-165846285
14	CEBPB	chr4:165846154-165846243	K562	blood:	n/a	n/a
15	CHD1	chr4:165857436-165858121	GM12878	blood:	n/a	n/a
16	CHD1	chr4:165858664-165859460	GM12878	blood:	n/a	n/a
17	CHD2	chr4:165858814-165859380	GM12878	blood:	n/a	n/a
18	CHD2	chr4:165877860-165878562	GM12878	blood:	n/a	n/a
19	CHD2	chr4:165877922-165878553	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:165867270-165867286	GM12878	blood:	n/a	n/a
21	CHD2	chr4:165857085-165858018	GM12878	blood:	n/a	n/a
22	CREB1	chr4:165877817-165878316	A549	lung:	n/a	n/a
23	CREB1	chr4:165877895-165878381	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr4:165877796-165878486	GM12878	blood:	n/a	n/a
25	CTBP2	chr4:165877837-165878615	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr4:165859200-165859350	GM12865	blood:	n/a	n/a
27	CTCF	chr4:165870695-165870917	GM12891	blood:	n/a	n/a
28	CTCF	chr4:165856450-165856931	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:165856660-165856810	GM12871	blood:	n/a	n/a
30	CTCF	chr4:165870738-165870854	A549	lung:	n/a	n/a
31	CTCF	chr4:165870720-165870870	GM12875	blood:	n/a	n/a
32	CTCF	chr4:165857620-165857770	GM12872	blood:	n/a	n/a
33	CTCF	chr4:165856491-165856832	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:165859185-165859288	LNCaP	prostate:	n/a	n/a
35	CTCF	chr4:165878057-165878441	GM12878	blood:	n/a	n/a
36	CTCF	chr4:165870633-165871252	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:165858820-165858980	GM19240	blood:	n/a	n/a
38	CTCF	chr4:165870640-165870790	RPTEC	kidney:	n/a	n/a
39	CTCF	chr4:165859760-165859910	GM12878	blood:	n/a	n/a
40	CTCF	chr4:165858820-165858970	GM12873	blood:	n/a	n/a
41	CTCF	chr4:165856690-165856794	GM13976	blood:	n/a	n/a
42	CTCF	chr4:165859157-165859350	ProgFib	skin:	n/a	n/a
43	CTCF	chr4:165870680-165870830	MCF-7	breast:	n/a	n/a
44	CTCF	chr4:165864520-165864670	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:165858840-165858990	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr4:165870880-165871030	NHDF-neo	bronchial:	n/a	n/a
47	CTCF	chr4:165856700-165856850	GM06990	blood:	n/a	n/a
48	CTCF	chr4:165859160-165859310	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:165858847-165858942	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:165878000-165878150	HBMEC	blood vessel:	n/a	n/a

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165878037-165878087	HCPEpiC	choroid plexus:	n/a
2	chr4:165878037-165878087	HCPEpiC	choroid plexus:	n/a
3	chr4:165850972-165851022	AoSMC	blood vessel:	n/a
4	chr4:165851186-165851236	GM19239	blood:	n/a
5	chr4:165878055-165878105	NH-A	brain:	n/a
6	chr4:165878085-165878135	SAEC	small airway:	n/a
7	chr4:165878317-165878367	ECC-1	luminal epithelium:	n/a
8	chr4:165876955-165877005	U87	brain:	n/a
9	chr4:165875543-165875593	GM12878	blood:	n/a
10	chr4:165854181-165854231	U87	brain:	n/a
11	chr4:165877045-165877095	PFSK-1	brain:	n/a
12	chr4:165878091-165878141	H1-hESC	embryonic stem cell:	embryo
13	chr4:165854181-165854231	AG10803	skin:	n/a
14	chr4:165878742-165878792	HRPEpiC	eye:	n/a
15	chr4:165851186-165851236	LNCaP	prostate:	n/a
16	chr4:165878136-165878186	NH-A	brain:	n/a
17	chr4:165851186-165851236	GM12892	blood:	n/a
18	chr4:165851186-165851236	ProgFib	skin:	n/a
19	chr4:165878317-165878367	MCF10A-Er-Src	breast:	n/a
20	chr4:165878091-165878141	GM12891	blood:	n/a
21	chr4:165850972-165851022	BJ	skin:	n/a
22	chr4:165851859-165851909	T-47D	breast:	n/a
23	chr4:165877045-165877095	SKMC	muscle:	n/a
24	chr4:165875543-165875593	SKMC	muscle:	n/a
25	chr4:165851859-165851909	HCM	heart:	n/a
26	chr4:165881424-165881474	HRCEpiC	kidney:	n/a
27	chr4:165878091-165878141	GM19239	blood:	n/a
28	chr4:165854246-165854296	NH-A	brain:	n/a
29	chr4:165851859-165851909	IMR90	lung:	fetal
30	chr4:165877875-165877925	SK-N-MC	brain:	n/a
31	chr4:165878136-165878186	CMK	blood:	n/a
32	chr4:165877045-165877095	HEEpiC	esophagus:	n/a
33	chr4:165854181-165854231	NT2-D1	testis:	n/a
34	chr4:165854181-165854231	NHDF-neo	bronchial:	n/a
35	chr4:165878219-165878269	CMK	blood:	n/a
36	chr4:165851859-165851909	GM19239	blood:	n/a
37	chr4:165878037-165878087	NHBE	bronchial:	n/a
38	chr4:165878219-165878269	MCF-7	breast:	n/a
39	chr4:165878091-165878141	SAEC	small airway:	n/a
40	chr4:165876955-165877005	AG10803	skin:	n/a
41	chr4:165877045-165877095	GM19239	blood:	n/a
42	chr4:165876955-165877005	PANC-1	pancreas:	n/a
43	chr4:165878219-165878269	AG04449	skin:	fetal
44	chr4:165851186-165851236	GM06990	blood:	n/a
45	chr4:165851186-165851236	NH-A	brain:	n/a
46	chr4:165851077-165851127	PANC-1	pancreas:	n/a
47	chr4:165875543-165875593	HIPEpiC	eye:	n/a
48	chr4:165878037-165878087	HL-60	blood:	n/a
49	chr4:165851859-165851909	ProgFib	skin:	n/a
50	chr4:165858544-165858594	HCM	heart:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:165874581..165877460-chr4:165878651..165880772,2	K562	blood:
2	chr4:165866322..165867965-chr4:165877072..165879577,2	MCF-7	breast:
3	chr4:165876074..165878048-chr4:165892405..165894471,2	MCF-7	breast:
4	chr4:165874581..165877460-chr4:165878651..165880772,2	K562	blood:
5	chr4:165877542..165879531-chr4:165880684..165882237,2	MCF-7	breast:
6	chr4:165876835..165879626-chr4:165882281..165885476,4	MCF-7	breast:
7	chr4:165701014..165701543-chr4:165856051..165856573,2	MCF-7	breast:
8	chr4:165699281..165700032-chr4:165856272..165857241,2	MCF-7	breast:
9	chr1:11966992..11968590-chr4:165867023..165868624,2	K562	blood:
10	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
11	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
12	chr4:165868495..165870203-chr4:165872665..165874987,2	MCF-7	breast:
13	chr4:165856166..165858715-chr4:165877906..165879898,2	MCF-7	breast:
14	chr4:165877284..165881205-chr4:165885674..165889440,5	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM61-2	chr4:165856103-165856321	NONHSAT099091
2	lnc-C4orf39-3	chr4:165883229-165883240	NONHSAT099093
3	lnc-C4orf39-3	chr4:165882287-165882345	NONHSAT099093
4	lnc-C4orf39-3	chr4:165869231-165869699	NONHSAT099093
5	lnc-TRIM61-4	chr4:165850646-165851103	NONHSAT099089

No data

Variant related genes	Relation type
ENSG00000236941	TF binding region
ENSG00000270960	TF binding region
NACA3P	TF binding region
FAM218BP	TF binding region
FAM218A	TF binding region
ENSG00000248645	TF binding region
ENSG00000244146	TF binding region
ENSG00000236941	CpG island
ENSG00000270960	CpG island
NACA3P	CpG island
FAM218BP	CpG island
FAM218A	CpG island
ENSG00000248645	CpG island
ENSG00000244146	CpG island
ENSG00000250486	chromatin interactions
ENSG00000236941	chromatin interactions
ENSG00000199347	chromatin interactions

Extended variants
information (count: 1798 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1798 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539032909	chr4:165845069-165845070	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs182153694	chr4:165845093-165845094	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs187325278	chr4:165845158-165845159	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs13106523	chr4:165845165-165845166	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs564080169	chr4:165845208-165845209	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs140221373	chr4:165845254-165845255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs573880509	chr4:165845302-165845303	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs114966088	chr4:165845338-165845339	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs145378997	chr4:165845373-165845374	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs577988003	chr4:165845382-165845383	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs146449617	chr4:165845402-165845403	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs192281608	chr4:165845411-165845412	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs527772909	chr4:165845427-165845428	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs549792473	chr4:165845454-165845455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs542862470	chr4:165845501-165845502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561127081	chr4:165845515-165845516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs79845118	chr4:165845539-165845540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183603337	chr4:165845560-165845561	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs6856935	chr4:165845582-165845583	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs141369930	chr4:165845617-165845618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532948617	chr4:165845677-165845678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs188670753	chr4:165845703-165845704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192041672	chr4:165845708-165845709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs114684525	chr4:165845716-165845717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs72631697	chr4:165845746-165845747	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs112368958	chr4:165845789-165845790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76177238	chr4:165845840-165845841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138944246	chr4:165845892-165845893	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs116826127	chr4:165845932-165845933	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs538690331	chr4:165845949-165845950	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs553749208	chr4:165846011-165846012	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs572238106	chr4:165846013-165846014	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs115051695	chr4:165846086-165846087	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs566145306	chr4:165846095-165846096	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs112276690	chr4:165846121-165846122	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs114232803	chr4:165846152-165846153	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs77994931	chr4:165846186-165846187	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs550399274	chr4:165846191-165846192	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs182727060	chr4:165846295-165846296	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs532850037	chr4:165846299-165846300	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs113547106	chr4:165846310-165846311	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs187099629	chr4:165846377-165846378	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs527245686	chr4:165846383-165846384	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs147281277	chr4:165846454-165846455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567203514	chr4:165846461-165846462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs112164749	chr4:165846529-165846530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549702551	chr4:165846536-165846537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571565930	chr4:165846547-165846548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs75528990	chr4:165846553-165846554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs538526403	chr4:165846560-165846561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165845400-165845600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:165845400-165848400	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:165845800-165847000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:165846000-165846400	Enhancers	GM12878-XiMat	blood
5	chr4:165847000-165848400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:165847200-165848400	Enhancers	NHEK	skin
7	chr4:165847200-165848600	Enhancers	HMEC	breast
8	chr4:165847600-165848600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:165847600-165848600	Enhancers	HSMM	muscle
10	chr4:165848200-165849200	Enhancers	NHDF-Ad	bronchial
11	chr4:165848400-165851800	Weak transcription	NHEK	skin
12	chr4:165848400-165852400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr4:165848600-165852200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:165851800-165852200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:165851800-165852200	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr4:165851800-165853400	Enhancers	NHEK	skin
17	chr4:165852000-165854200	Enhancers	HSMMtube	muscle
18	chr4:165852200-165852600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:165852200-165853400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr4:165852400-165853800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr4:165852400-165854200	Enhancers	HSMM	muscle
22	chr4:165852600-165852800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:165852600-165853000	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr4:165852800-165853400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr4:165852800-165854000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr4:165853000-165853400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr4:165853200-165854000	Enhancers	GM12878-XiMat	blood
28	chr4:165853400-165853600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr4:165853400-165856800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:165853600-165857800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr4:165854000-165855200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:165854000-165855400	ZNF genes & repeats	GM12878-XiMat	blood
33	chr4:165854200-165858600	Weak transcription	HSMMtube	muscle
34	chr4:165855200-165858800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr4:165855400-165855600	Weak transcription	GM12878-XiMat	blood
36	chr4:165855600-165856800	Enhancers	GM12878-XiMat	blood
37	chr4:165855800-165857200	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:165856400-165856600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr4:165856600-165858000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr4:165856800-165857000	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr4:165856800-165857000	Flanking Active TSS	GM12878-XiMat	blood
42	chr4:165856800-165857600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr4:165857000-165857400	Enhancers	GM12878-XiMat	blood
44	chr4:165857000-165857800	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr4:165857200-165857600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr4:165857400-165859400	Flanking Active TSS	GM12878-XiMat	blood
47	chr4:165857600-165859200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr4:165857600-165859200	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr4:165857600-165859200	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr4:165857600-165859200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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