Variant report

Variant	nsv517554
Chromosome Location	chr4:165859951-165878335
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:459)
CpG islands
(count:671)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	BCLAF1	chr4:165877809-165878342	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:165877853-165878275	GM12878	blood:	n/a	n/a
4	BHLHE40	chr4:165877987-165878027	K562	blood:	n/a	n/a
5	CBX3	chr4:165877855-165878292	K562	blood:	n/a	n/a
6	CHD2	chr4:165877860-165878562	GM12878	blood:	n/a	n/a
7	CHD2	chr4:165877922-165878553	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr4:165867270-165867286	GM12878	blood:	n/a	n/a
9	CREB1	chr4:165877895-165878381	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr4:165877817-165878316	A549	lung:	n/a	n/a
11	CREB1	chr4:165877796-165878486	GM12878	blood:	n/a	n/a
12	CTBP2	chr4:165877837-165878615	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr4:165870670-165870920	GM12878	blood:	n/a	n/a
14	CTCF	chr4:165870962-165871181	GM19239	blood:	n/a	n/a
15	CTCF	chr4:165878329-165878443	MCF-7	breast:	n/a	n/a
16	CTCF	chr4:165870880-165871030	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr4:165870700-165870850	GM12878	blood:	n/a	n/a
18	CTCF	chr4:165871043-165871120	HepG2	liver:	n/a	n/a
19	CTCF	chr4:165870680-165870915	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr4:165870680-165870830	GM12874	blood:	n/a	n/a
21	CTCF	chr4:165878000-165878150	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr4:165870970-165871179	Gliobla	brain:	n/a	n/a
23	CTCF	chr4:165869324-165869372	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:165870740-165870890	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr4:165870660-165870810	AG09309	skin:	n/a	n/a
26	CTCF	chr4:165870962-165871192	ProgFib	skin:	n/a	n/a
27	CTCF	chr4:165870760-165870910	HCT-116	colon:	n/a	n/a
28	CTCF	chr4:165870740-165870890	GM12873	blood:	n/a	n/a
29	CTCF	chr4:165870700-165870850	GM12866	blood:	n/a	n/a
30	CTCF	chr4:165870712-165870893	GM12892	blood:	n/a	n/a
31	CTCF	chr4:165878280-165878430	WERI-Rb-1	eye:	n/a	n/a
32	CTCF	chr4:165878220-165878370	BJ	skin:	n/a	n/a
33	CTCF	chr4:165870720-165870870	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr4:165870620-165870770	HFF-Myc	foreskin:	n/a	n/a
35	CTCF	chr4:165870680-165870830	GM12872	blood:	n/a	n/a
36	CTCF	chr4:165870720-165870870	HPF	lung:	n/a	n/a
37	CTCF	chr4:165871064-165871101	GM12891	blood:	n/a	n/a
38	CTCF	chr4:165870700-165870850	NB4	blood:	n/a	n/a
39	CTCF	chr4:165870740-165870890	K562	blood:	n/a	n/a
40	CTCF	chr4:165870680-165870830	HCT-116	colon:	n/a	n/a
41	CTCF	chr4:165871020-165871170	AG10803	skin:	n/a	n/a
42	CTCF	chr4:165871027-165871181	GM12878	blood:	n/a	n/a
43	CTCF	chr4:165870725-165870851	GM13977	blood:	n/a	n/a
44	CTCF	chr4:165870720-165870870	HMEC	breast:	n/a	n/a
45	CTCF	chr4:165870700-165870850	GM12869	blood:	n/a	n/a
46	CTCF	chr4:165870709-165870876	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:165878085-165878209	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:165870896-165870899	GM10248	blood:	n/a	n/a
49	CTCF	chr4:165870640-165870790	HVMF	connective:	n/a	n/a
50	CTCF	chr4:165870720-165870870	HCPEpiC	choroid plexus:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165878085-165878135	NB4	blood:	n/a
2	chr4:165876955-165877005	K562	blood:	n/a
3	chr4:165877045-165877095	Hepatocyte	liver:	n/a
4	chr4:165878055-165878105	AG04449	skin:	fetal
5	chr4:165878055-165878105	ECC-1	luminal epithelium:	n/a
6	chr4:165878085-165878135	SKMC	muscle:	n/a
7	chr4:165877045-165877095	HEK293	kidney:	embryo
8	chr4:165878136-165878186	PANC-1	pancreas:	n/a
9	chr4:165878085-165878135	CMK	blood:	n/a
10	chr4:165877875-165877925	HL-60	blood:	n/a
11	chr4:165878037-165878087	GM19239	blood:	n/a
12	chr4:165878136-165878186	CMK	blood:	n/a
13	chr4:165877875-165877925	NB4	blood:	n/a
14	chr4:165878317-165878367	GM12892	blood:	n/a
15	chr4:165878091-165878141	HEEpiC	esophagus:	n/a
16	chr4:165878085-165878135	ovcar-3	ovarian:	n/a
17	chr4:165876955-165877005	HEEpiC	esophagus:	n/a
18	chr4:165877875-165877925	BE2_C	brain:	n/a
19	chr4:165878317-165878367	AG04450	lung:	fetal
20	chr4:165878055-165878105	SK-N-MC	brain:	n/a
21	chr4:165878091-165878141	ovcar-3	ovarian:	n/a
22	chr4:165878037-165878087	PFSK-1	brain:	n/a
23	chr4:165875543-165875593	CMK	blood:	n/a
24	chr4:165878055-165878105	U87	brain:	n/a
25	chr4:165876955-165877005	HEK293	kidney:	embryo
26	chr4:165878219-165878269	IMR90	lung:	fetal
27	chr4:165876955-165877005	AG04449	skin:	fetal
28	chr4:165878317-165878367	HCPEpiC	choroid plexus:	n/a
29	chr4:165877045-165877095	SAEC	small airway:	n/a
30	chr4:165878085-165878135	HCT-116	colon:	n/a
31	chr4:165878055-165878105	BJ	skin:	n/a
32	chr4:165878317-165878367	HRE	kidney:	n/a
33	chr4:165878317-165878367	RPTEC	kidney:	n/a
34	chr4:165878091-165878141	U87	brain:	n/a
35	chr4:165877045-165877095	HCT-116	colon:	n/a
36	chr4:165877045-165877095	T-47D	breast:	n/a
37	chr4:165877045-165877095	SK-N-SH	brain:	n/a
38	chr4:165878055-165878105	ovcar-3	ovarian:	n/a
39	chr4:165876955-165877005	ovcar-3	ovarian:	n/a
40	chr4:165877875-165877925	RPTEC	kidney:	n/a
41	chr4:165878085-165878135	NHBE	bronchial:	n/a
42	chr4:165878037-165878087	Jurkat	blood:	n/a
43	chr4:165878091-165878141	RPTEC	kidney:	n/a
44	chr4:165875543-165875593	HNPCEpiC	eye:	n/a
45	chr4:165875543-165875593	AoSMC	blood vessel:	n/a
46	chr4:165878091-165878141	HCT-116	colon:	n/a
47	chr4:165878219-165878269	HRPEpiC	eye:	n/a
48	chr4:165878055-165878105	HCF	heart:	n/a
49	chr4:165876955-165877005	NHDF-neo	bronchial:	n/a
50	chr4:165878037-165878087	Hela-S3	cervix:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:165876074..165878048-chr4:165892405..165894471,2	MCF-7	breast:
2	chr4:165868495..165870203-chr4:165872665..165874987,2	MCF-7	breast:
3	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
4	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
5	chr4:165866322..165867965-chr4:165877072..165879577,2	MCF-7	breast:
6	chr1:11966992..11968590-chr4:165867023..165868624,2	K562	blood:
7	chr4:165874581..165877460-chr4:165878651..165880772,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf39-3	chr4:165869231-165869699	NONHSAT099093

No data

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

Extended variants
information (count: 715 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:715 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4359860	chr4:165859951-165859952	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553263614	chr4:165859955-165859956	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs374177008	chr4:165859990-165859991	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs187702155	chr4:165859993-165859994	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs535342174	chr4:165859997-165859998	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs575661192	chr4:165860008-165860009	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546297700	chr4:165860012-165860013	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564389393	chr4:165860033-165860034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76404122	chr4:165860045-165860046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546855464	chr4:165860046-165860047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs144815376	chr4:165860062-165860063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7663962	chr4:165860063-165860064	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs370448433	chr4:165860072-165860073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193181408	chr4:165860141-165860142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114452495	chr4:165860147-165860148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536609253	chr4:165860148-165860149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7664173	chr4:165860158-165860159	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs367673485	chr4:165860159-165860160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183418651	chr4:165860191-165860192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4691137	chr4:165860211-165860212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs574642596	chr4:165860224-165860225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535749305	chr4:165860237-165860238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs374879952	chr4:165860247-165860248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs7664752	chr4:165860277-165860278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs575722559	chr4:165860288-165860289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188417782	chr4:165860293-165860294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs539531134	chr4:165860306-165860307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564631944	chr4:165860310-165860311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192727498	chr4:165860346-165860347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556354767	chr4:165860352-165860353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183972148	chr4:165860369-165860370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535780179	chr4:165860399-165860400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs561949659	chr4:165860403-165860404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs529420821	chr4:165860411-165860412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554514465	chr4:165860419-165860420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs372920919	chr4:165860420-165860421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56192412	chr4:165860435-165860436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs71618426	chr4:165860438-165860439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs57625117	chr4:165860440-165860441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200472306	chr4:165860441-165860442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576538865	chr4:165860442-165860443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs7681048	chr4:165860443-165860444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs116479139	chr4:165860529-165860530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115737297	chr4:165860550-165860551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs76340045	chr4:165860567-165860568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188361612	chr4:165860634-165860635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs60663651	chr4:165860638-165860639	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546670620	chr4:165860709-165860710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568281796	chr4:165860743-165860744	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs535608609	chr4:165860840-165860841	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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

Chromatin state (count:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165859000-165860000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr4:165859200-165864400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:165859200-165869200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:165859400-165861000	Weak transcription	Fetal Muscle Leg	muscle
5	chr4:165859800-165860800	Weak transcription	GM12878-XiMat	blood
6	chr4:165860800-165861000	Enhancers	GM12878-XiMat	blood
7	chr4:165861200-165861400	Enhancers	Fetal Muscle Leg	muscle
8	chr4:165864200-165864600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:165864200-165864800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:165864400-165864600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:165864400-165864600	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr4:165864400-165864800	Enhancers	NHEK	skin
13	chr4:165864600-165864800	Enhancers	Fetal Muscle Leg	muscle
14	chr4:165864600-165865000	Enhancers	HSMMtube	muscle
15	chr4:165864600-165865200	Enhancers	Placenta Amnion	Placenta Amnion
16	chr4:165864600-165869200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:165864800-165869000	Weak transcription	Fetal Muscle Leg	muscle
18	chr4:165864800-165869200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:165865800-165867000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:165866200-165866600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr4:165866200-165866800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr4:165866200-165866800	Enhancers	iPS-20b Cell Line	embryonic stem cell
23	chr4:165866600-165866800	Enhancers	HMEC	breast
24	chr4:165866600-165868400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr4:165866800-165869200	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr4:165866800-165870800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr4:165867000-165870800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr4:165867600-165869400	Enhancers	GM12878-XiMat	blood
29	chr4:165869000-165869600	Enhancers	Fetal Muscle Trunk	muscle
30	chr4:165869000-165871200	Enhancers	Fetal Muscle Leg	muscle
31	chr4:165869200-165869400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr4:165869200-165869400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr4:165869200-165869600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr4:165869200-165869600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:165869200-165869600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr4:165869400-165870200	Weak transcription	GM12878-XiMat	blood
37	chr4:165869600-165870200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:165869600-165870800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:165870200-165871200	Enhancers	GM12878-XiMat	blood
40	chr4:165870800-165871000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr4:165870800-165871000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr4:165870800-165871200	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr4:165870800-165871200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:165870800-165871200	Bivalent Enhancer	Psoas Muscle	Psoas
45	chr4:165870800-165871400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:165870800-165871400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr4:165871000-165874800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr4:165871000-165877800	Weak transcription	Spleen	Spleen
49	chr4:165871200-165875000	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr4:165871200-165877600	Weak transcription	GM12878-XiMat	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links