Variant report

Variant	esv3692850
Chromosome Location	chr4:165868229-165879381
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:457)
CpG islands
(count:732)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:457 , 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	chr4:165877987-165878027	K562	blood:	n/a	n/a
4	BHLHE40	chr4:165877853-165878275	GM12878	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	CREB1	chr4:165877817-165878316	A549	lung:	n/a	n/a
9	CREB1	chr4:165877796-165878486	GM12878	blood:	n/a	n/a
10	CREB1	chr4:165877895-165878381	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr4:165877837-165878615	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr4:165870720-165870870	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr4:165870665-165871238	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr4:165878100-165878250	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr4:165870680-165870830	GM12872	blood:	n/a	n/a
16	CTCF	chr4:165878118-165878216	MCF-7	breast:	n/a	n/a
17	CTCF	chr4:165870738-165870854	A549	lung:	n/a	n/a
18	CTCF	chr4:165870760-165870910	HAc	cerebellar:	n/a	n/a
19	CTCF	chr4:165870660-165870810	HRE	kidney:	n/a	n/a
20	CTCF	chr4:165878180-165878330	HRE	kidney:	n/a	n/a
21	CTCF	chr4:165878086-165878277	GM12891	blood:	n/a	n/a
22	CTCF	chr4:165878100-165878250	GM12872	blood:	n/a	n/a
23	CTCF	chr4:165870717-165870862	LNCaP	prostate:	n/a	n/a
24	CTCF	chr4:165870700-165870850	NB4	blood:	n/a	n/a
25	CTCF	chr4:165871000-165871150	AG09319	gingival:	n/a	n/a
26	CTCF	chr4:165870800-165870950	GM12868	blood:	n/a	n/a
27	CTCF	chr4:165870760-165870910	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr4:165871000-165871150	AG10803	skin:	n/a	n/a
29	CTCF	chr4:165870962-165871192	ProgFib	skin:	n/a	n/a
30	CTCF	chr4:165870700-165870850	GM12801	blood:	n/a	n/a
31	CTCF	chr4:165878000-165878150	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr4:165870720-165870870	HMEC	breast:	n/a	n/a
33	CTCF	chr4:165870700-165870850	HPF	lung:	n/a	n/a
34	CTCF	chr4:165870737-165870855	Medullo	brain:	n/a	n/a
35	CTCF	chr4:165870923-165870928	NHEK	skin:	n/a	n/a
36	CTCF	chr4:165878020-165878170	HMEC	breast:	n/a	n/a
37	CTCF	chr4:165878260-165878410	AG10803	skin:	n/a	n/a
38	CTCF	chr4:165870760-165870910	AG10803	skin:	n/a	n/a
39	CTCF	chr4:165870700-165870850	GM12867	blood:	n/a	n/a
40	CTCF	chr4:165870720-165871010	NHLF	lung:	n/a	n/a
41	CTCF	chr4:165878160-165878310	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr4:165870700-165870850	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr4:165870740-165870890	BJ	skin:	n/a	n/a
44	CTCF	chr4:165870999-165871158	GM12892	blood:	n/a	n/a
45	CTCF	chr4:165870720-165870870	GM12872	blood:	n/a	n/a
46	CTCF	chr4:165870680-165870830	GM12874	blood:	n/a	n/a
47	CTCF	chr4:165870976-165871180	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:165878374-165878449	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:165870700-165870850	GM12878	blood:	n/a	n/a
50	CTCF	chr4:165870686-165870927	GM19238	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165876955-165877005	AG09319	gingival:	n/a
2	chr4:165875543-165875593	NB4	blood:	n/a
3	chr4:165877875-165877925	K562	blood:	n/a
4	chr4:165878037-165878087	PANC-1	pancreas:	n/a
5	chr4:165878136-165878186	ECC-1	luminal epithelium:	n/a
6	chr4:165876955-165877005	GM12878	blood:	n/a
7	chr4:165877875-165877925	ovcar-3	ovarian:	n/a
8	chr4:165878091-165878141	Caco-2	colon:	n/a
9	chr4:165878742-165878792	NH-A	brain:	n/a
10	chr4:165878317-165878367	PANC-1	pancreas:	n/a
11	chr4:165877875-165877925	PrEC	prostate:	n/a
12	chr4:165878219-165878269	HRE	kidney:	n/a
13	chr4:165877875-165877925	H1-hESC	embryonic stem cell:	embryo
14	chr4:165878219-165878269	HNPCEpiC	eye:	n/a
15	chr4:165878219-165878269	AG09319	gingival:	n/a
16	chr4:165878055-165878105	HCM	heart:	n/a
17	chr4:165878742-165878792	BE2_C	brain:	n/a
18	chr4:165878742-165878792	ProgFib	skin:	n/a
19	chr4:165876955-165877005	Jurkat	blood:	n/a
20	chr4:165876955-165877005	BJ	skin:	n/a
21	chr4:165878091-165878141	ProgFib	skin:	n/a
22	chr4:165878317-165878367	GM19239	blood:	n/a
23	chr4:165878136-165878186	RPTEC	kidney:	n/a
24	chr4:165878742-165878792	HCPEpiC	choroid plexus:	n/a
25	chr4:165878037-165878087	HCF	heart:	n/a
26	chr4:165877875-165877925	AG09309	skin:	n/a
27	chr4:165878055-165878105	ProgFib	skin:	n/a
28	chr4:165877045-165877095	BJ	skin:	n/a
29	chr4:165878037-165878087	PFSK-1	brain:	n/a
30	chr4:165878085-165878135	HEEpiC	esophagus:	n/a
31	chr4:165878136-165878186	HCPEpiC	choroid plexus:	n/a
32	chr4:165878085-165878135	A549	lung:	n/a
33	chr4:165876955-165877005	PANC-1	pancreas:	n/a
34	chr4:165878055-165878105	RPTEC	kidney:	n/a
35	chr4:165878742-165878792	H1-hESC	embryonic stem cell:	embryo
36	chr4:165878742-165878792	AG04450	lung:	fetal
37	chr4:165878136-165878186	A549	lung:	n/a
38	chr4:165878317-165878367	HEEpiC	esophagus:	n/a
39	chr4:165878317-165878367	HRCEpiC	kidney:	n/a
40	chr4:165878091-165878141	HRPEpiC	eye:	n/a
41	chr4:165875543-165875593	MCF-7	breast:	n/a
42	chr4:165878085-165878135	AG09309	skin:	n/a
43	chr4:165878219-165878269	PANC-1	pancreas:	n/a
44	chr4:165877045-165877095	CMK	blood:	n/a
45	chr4:165875543-165875593	A549	lung:	n/a
46	chr4:165876955-165877005	HRE	kidney:	n/a
47	chr4:165878037-165878087	BJ	skin:	n/a
48	chr4:165878091-165878141	AG04449	skin:	fetal
49	chr4:165877045-165877095	AG10803	skin:	n/a
50	chr4:165875543-165875593	SKMC	muscle:	n/a

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

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

(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
FAM218A	TF binding region
ENSG00000236941	CpG island
FAM218A	CpG island
ENSG00000199347	chromatin interactions
ENSG00000250486	chromatin interactions
ENSG00000236941	chromatin interactions

Extended variants
information (count: 424 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:424 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10016502	chr4:165868229-165868230	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs369403083	chr4:165868231-165868232	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs182967583	chr4:165868235-165868236	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs187342108	chr4:165868271-165868272	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs540344213	chr4:165868282-165868283	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs561749896	chr4:165868299-165868300	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs144412006	chr4:165868305-165868306	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs577255811	chr4:165868306-165868307	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs550747710	chr4:165868339-165868340	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs148796053	chr4:165868356-165868357	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs56126121	chr4:165868363-165868364	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs190217173	chr4:165868371-165868372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs544749172	chr4:165868393-165868394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs566544956	chr4:165868424-165868425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs77113509	chr4:165868437-165868438	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs397879249	chr4:165868449-165868450	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541796911	chr4:165868458-165868459	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs183112018	chr4:165868460-165868461	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs143591131	chr4:165868466-165868467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567748162	chr4:165868467-165868468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs538098924	chr4:165868501-165868502	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112370342	chr4:165868531-165868532	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543050465	chr4:165868557-165868558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571700374	chr4:165868573-165868574	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs377438808	chr4:165868622-165868623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs187608551	chr4:165868637-165868638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs554469328	chr4:165868638-165868639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572909452	chr4:165868647-165868648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113549251	chr4:165868655-165868656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548026403	chr4:165868721-165868722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563390118	chr4:165868743-165868744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540211557	chr4:165868750-165868751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192618298	chr4:165868788-165868789	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185618343	chr4:165868790-165868791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs56410348	chr4:165868812-165868813	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs557510615	chr4:165868825-165868826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577548501	chr4:165868862-165868863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs13116412	chr4:165868976-165868977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200781123	chr4:165868984-165868985	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374717212	chr4:165868985-165868986	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532929404	chr4:165868991-165868992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs544937212	chr4:165869025-165869026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs386681635	chr4:165869027-165869028	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs79370093	chr4:165869028-165869029	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs527728592	chr4:165869031-165869032	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs548958606	chr4:165869042-165869043	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567515495	chr4:165869045-165869046	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs531833389	chr4:165869046-165869047	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188965837	chr4:165869047-165869048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs13143461	chr4:165869055-165869056	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	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:340 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165859200-165869200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:165864600-165869200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr4:165864800-165869000	Weak transcription	Fetal Muscle Leg	muscle
4	chr4:165864800-165869200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr4:165866600-165868400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr4:165866800-165869200	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr4:165866800-165870800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr4:165867000-165870800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:165867600-165869400	Enhancers	GM12878-XiMat	blood
10	chr4:165869000-165869600	Enhancers	Fetal Muscle Trunk	muscle
11	chr4:165869000-165871200	Enhancers	Fetal Muscle Leg	muscle
12	chr4:165869200-165869400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:165869200-165869400	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr4:165869200-165869600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr4:165869200-165869600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr4:165869200-165869600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:165869400-165870200	Weak transcription	GM12878-XiMat	blood
18	chr4:165869600-165870200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr4:165869600-165870800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:165870200-165871200	Enhancers	GM12878-XiMat	blood
21	chr4:165870800-165871000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr4:165870800-165871000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr4:165870800-165871200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr4:165870800-165871200	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr4:165870800-165871200	Bivalent Enhancer	Psoas Muscle	Psoas
26	chr4:165870800-165871400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:165870800-165871400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr4:165871000-165874800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr4:165871000-165877800	Weak transcription	Spleen	Spleen
30	chr4:165871200-165875000	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr4:165871200-165877600	Weak transcription	GM12878-XiMat	blood
32	chr4:165873400-165875000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:165873800-165874000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:165873800-165874000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr4:165874000-165874200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr4:165874000-165877800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr4:165874000-165878000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:165874200-165877800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr4:165874800-165875200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr4:165875000-165875200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr4:165875000-165875400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:165875000-165875600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr4:165875200-165875600	Active TSS	ES-I3 Cell Line	embryonic stem cell
44	chr4:165875400-165877600	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr4:165875600-165877800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr4:165875600-165877800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr4:165876400-165877600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr4:165876800-165877000	Enhancers	H1 Cell Line	embryonic stem cell
49	chr4:165876800-165877000	Enhancers	HSMM	muscle
50	chr4:165877000-165877600	Weak transcription	HSMM	muscle

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