Variant report

Variant	nsv878655
Chromosome Location	chr4:9384748-9609506
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1152)
CpG islands
(count:5130)
Chromatin interactive
region (count:3)
LncRNA
region (count:5)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:9454189-9454353	HepG2	liver:	n/a	n/a
2	BACH1	chr4:9605857-9606056	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
5	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
6	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
7	BATF	chr4:9606281-9606749	GM12878	blood:	n/a	n/a
8	BATF	chr4:9605704-9606128	GM12878	blood:	n/a	n/a
9	BATF	chr4:9606359-9606745	GM12878	blood:	n/a	n/a
10	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
11	BATF	chr4:9390689-9391024	GM12878	blood:	n/a	n/a
12	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
13	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
14	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
15	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
16	BATF	chr4:9431784-9432036	GM12878	blood:	n/a	n/a
17	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
18	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
19	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:9605779-9606088	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:9605814-9606174	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:9390780-9390984	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:9390633-9391020	GM12878	blood:	n/a	n/a
25	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
26	BCL11A	chr4:9606348-9606693	GM12878	blood:	n/a	n/a
27	BCL11A	chr4:9606478-9606683	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:9390742-9390935	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:9533811-9533913	K562	blood:	n/a	n/a
30	CBX3	chr4:9597420-9597667	K562	blood:	n/a	n/a
31	CCNT2	chr4:9533734-9533999	K562	blood:	n/a	n/a
32	CEBPB	chr4:9453481-9453664	HepG2	liver:	n/a	chr4:9453618-9453629
33	CEBPB	chr4:9530664-9530884	K562	blood:	n/a	n/a
34	CEBPB	chr4:9430641-9430768	HepG2	liver:	n/a	chr4:9430673-9430686 chr4:9430674-9430685
35	CEBPB	chr4:9585906-9586106	HepG2	liver:	n/a	chr4:9585991-9586002
36	CEBPB	chr4:9530676-9530843	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr4:9405864-9406123	A549	lung:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
38	CEBPB	chr4:9405866-9406215	HepG2	liver:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
39	CEBPB	chr4:9605743-9605929	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:9405910-9406125	K562	blood:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
41	CEBPB	chr4:9608408-9608590	K562	blood:	n/a	n/a
42	CEBPB	chr4:9596784-9597029	HepG2	liver:	n/a	chr4:9596883-9596894
43	CEBPB	chr4:9530595-9530856	K562	blood:	n/a	n/a
44	CEBPB	chr4:9531399-9531602	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr4:9387057-9387237	HepG2	liver:	n/a	chr4:9387117-9387128
46	CEBPB	chr4:9600979-9601222	K562	blood:	n/a	n/a
47	CEBPD	chr4:9608329-9608642	K562	blood:	n/a	n/a
48	CHD1	chr4:9533998-9534198	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr4:9533893-9534015	HepG2	liver:	n/a	chr4:9533994-9534004
50	CHD2	chr4:9533949-9534111	H1-hESC	embryonic stem cell:	n/a	chr4:9533994-9534004

(count:5130 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9533948-9533998	HIPEpiC	eye:	n/a
2	chr4:9481822-9481872	GM12892	blood:	n/a
3	chr4:9457681-9457731	HRPEpiC	eye:	n/a
4	chr4:9494211-9494261	U87	brain:	n/a
5	chr4:9534313-9534363	NHBE	bronchial:	n/a
6	chr4:9453084-9453134	MCF10A-Er-Src	breast:	n/a
7	chr4:9533948-9533998	HIPEpiC	eye:	n/a
8	chr4:9481822-9481872	GM12892	blood:	n/a
9	chr4:9457681-9457731	HRPEpiC	eye:	n/a
10	chr4:9494211-9494261	U87	brain:	n/a
11	chr4:9534313-9534363	NHBE	bronchial:	n/a
12	chr4:9453084-9453134	MCF10A-Er-Src	breast:	n/a
13	chr4:9604187-9604237	MCF-7	breast:	n/a
14	chr4:9457537-9457587	AG10803	skin:	n/a
15	chr4:9601996-9602046	HCF	heart:	n/a
16	chr4:9506681-9506731	ovcar-3	ovarian:	n/a
17	chr4:9484735-9484785	NHBE	bronchial:	n/a
18	chr4:9508976-9509026	HMEC	breast:	n/a
19	chr4:9475346-9475396	CMK	blood:	n/a
20	chr4:9479947-9479997	Caco-2	colon:	n/a
21	chr4:9494907-9494957	SK-N-MC	brain:	n/a
22	chr4:9534366-9534416	HRE	kidney:	n/a
23	chr4:9503404-9503454	HAEpiC	amniotic membrane:	n/a
24	chr4:9494211-9494261	GM12892	blood:	n/a
25	chr4:9453650-9453700	U87	brain:	n/a
26	chr4:9523653-9523703	HUVEC	blood vessel:	n/a
27	chr4:9506681-9506731	NB4	blood:	n/a
28	chr4:9499878-9499928	NH-A	brain:	n/a
29	chr4:9482074-9482124	GM19239	blood:	n/a
30	chr4:9533426-9533476	HIPEpiC	eye:	n/a
31	chr4:9505764-9505814	T-47D	breast:	n/a
32	chr4:9533948-9533998	AG04450	lung:	fetal
33	chr4:9484735-9484785	Hela-S3	cervix:	n/a
34	chr4:9445158-9445208	HRCEpiC	kidney:	n/a
35	chr4:9476719-9476769	HNPCEpiC	eye:	n/a
36	chr4:9494396-9494446	T-47D	breast:	n/a
37	chr4:9457681-9457731	HRE	kidney:	n/a
38	chr4:9495454-9495504	T-47D	breast:	n/a
39	chr4:9446084-9446134	Hela-S3	cervix:	n/a
40	chr4:9499878-9499928	K562	blood:	n/a
41	chr4:9450292-9450342	AG10803	skin:	n/a
42	chr4:9533426-9533476	PrEC	prostate:	n/a
43	chr4:9494487-9494537	ProgFib	skin:	n/a
44	chr4:9446084-9446134	AG10803	skin:	n/a
45	chr4:9499194-9499244	MCF-7	breast:	n/a
46	chr4:9485487-9485537	PrEC	prostate:	n/a
47	chr4:9601996-9602046	NT2-D1	testis:	n/a
48	chr4:9558753-9558803	HRPEpiC	eye:	n/a
49	chr4:9457537-9457587	ECC-1	luminal epithelium:	n/a
50	chr4:9509896-9509946	NHBE	bronchial:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:
2	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:
3	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137
2	lnc-DEFB131-1	chr4:9470746-9471694	NONHSAT095133
3	lnc-RP11-1396O13.13.1-1	chr4:9388003-9388085	XLOC_003878
4	lnc-RP11-1396O13.13.1-1	chr4:9387384-9387466	XLOC_003878
5	lnc-RP11-1396O13.13.1-2	chr4:9390589-9390785	l_2601_chr4:9381878-9390785_kidney

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr4:9557878-9557899	MIMAT0005935_1

No data

Variant related genes	Relation type
RNA5SP153	TF binding region
OR7E85P	TF binding region
ENSG00000266246	TF binding region
ENSG00000249799	TF binding region
ENSG00000232773	TF binding region
OR7E84P	TF binding region
OR7E86P	TF binding region
ENSG00000219492	TF binding region
MIR548I2	TF binding region
DEFB131	TF binding region
ENSG00000249443	TF binding region
UNC93B7	TF binding region
ENSG00000188438	TF binding region
OR7E83P	TF binding region
ENSG00000265901	TF binding region
ENSG00000242034	TF binding region
ENSG00000244004	TF binding region
RNA5SP153	CpG island
OR7E85P	CpG island
ENSG00000266246	CpG island
ENSG00000249799	CpG island
ENSG00000232773	CpG island
OR7E84P	CpG island
OR7E86P	CpG island
ENSG00000219492	CpG island
MIR548I2	CpG island
DEFB131	CpG island
ENSG00000249443	CpG island
UNC93B7	CpG island
ENSG00000188438	CpG island
OR7E83P	CpG island
ENSG00000265901	CpG island
ENSG00000242034	CpG island
ENSG00000244004	CpG island

Extended variants
information (count: 10082 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:10082 , 50 per page) page: 1 2 3 4 5 6 7 ... 202

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149432078	chr4:9387399-9387400	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs556293692	chr4:9387420-9387421	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs577828109	chr4:9387421-9387422	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs114800772	chr4:9387426-9387427	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs369558155	chr4:9387429-9387430	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs572729021	chr4:9387434-9387435	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs144817842	chr4:9387462-9387463	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs143989404	chr4:9388034-9388035	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs71612295	chr4:9388039-9388040	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs538764400	chr4:9388046-9388047	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs547648723	chr4:9388058-9388059	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs566271332	chr4:9388061-9388062	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs536486876	chr4:9388074-9388075	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs555240063	chr4:9388076-9388077	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs576834887	chr4:9388082-9388083	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs140889924	chr4:9390407-9390408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6834672	chr4:9390408-9390409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187308590	chr4:9390482-9390483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567474391	chr4:9390489-9390490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531597166	chr4:9390494-9390495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs192204645	chr4:9390504-9390505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571616855	chr4:9390520-9390521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs6846545	chr4:9390521-9390522	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs558147175	chr4:9390555-9390556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs539714544	chr4:9390559-9390560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184743700	chr4:9390561-9390562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534302274	chr4:9390584-9390585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs557670192	chr4:9390590-9390591	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
29	rs116427847	chr4:9390593-9390594	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
30	rs577256101	chr4:9390594-9390595	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
31	rs573883629	chr4:9390598-9390599	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
32	rs544448878	chr4:9390616-9390617	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs556416433	chr4:9390644-9390645	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs541551322	chr4:9390645-9390646	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs369147792	chr4:9390650-9390651	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs6851747	chr4:9390660-9390661	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs574965473	chr4:9390671-9390672	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs572001684	chr4:9390683-9390684	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs190006201	chr4:9390686-9390687	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs142501007	chr4:9390700-9390701	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs73801256	chr4:9390708-9390709	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs538143747	chr4:9390709-9390710	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs563691643	chr4:9390729-9390730	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs114291117	chr4:9390744-9390745	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs4318648	chr4:9390760-9390761	Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs551439396	chr4:9390762-9390763	Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs192728584	chr4:9390786-9390787	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs184346067	chr4:9390796-9390797	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs188347708	chr4:9390800-9390801	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs181884318	chr4:9390810-9390811	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	21858162	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:899 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9390400-9390800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr4:9390600-9391400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr4:9390800-9391400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:9391000-9391200	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr4:9391400-9391800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:9423000-9424400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr4:9424000-9424400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr4:9424400-9427800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr4:9426600-9428200	Enhancers	HSMM	muscle
10	chr4:9427800-9429000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:9429000-9429400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr4:9429400-9429800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:9438200-9438600	Enhancers	Primary B cells from cord blood	blood
14	chr4:9438200-9438600	Enhancers	Primary hematopoietic stem cells	blood
15	chr4:9452600-9453800	Enhancers	Small Intestine	intestine
16	chr4:9453000-9453800	Enhancers	Duodenum Mucosa	Duodenum
17	chr4:9453600-9454800	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr4:9453600-9456200	Enhancers	Fetal Intestine Large	intestine
19	chr4:9453600-9456800	Enhancers	Fetal Intestine Small	intestine
20	chr4:9453600-9457200	Enhancers	Stomach Mucosa	stomach
21	chr4:9453800-9454600	Weak transcription	Duodenum Mucosa	Duodenum
22	chr4:9454600-9454800	Enhancers	Duodenum Mucosa	Duodenum
23	chr4:9454800-9455200	Weak transcription	Duodenum Mucosa	Duodenum
24	chr4:9454800-9455800	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr4:9455200-9457200	Enhancers	Duodenum Mucosa	Duodenum
26	chr4:9455800-9456800	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr4:9455800-9457200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr4:9456400-9456800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:9456400-9457200	Enhancers	Gastric	stomach
30	chr4:9476200-9477000	Bivalent Enhancer	Fetal Brain Male	brain
31	chr4:9476600-9477000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
32	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
33	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Leg	muscle
34	chr4:9477000-9477400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr4:9481600-9482000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:9481600-9482000	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr4:9481800-9482000	Enhancers	Duodenum Mucosa	Duodenum
38	chr4:9484800-9503800	Weak transcription	Right Atrium	heart
39	chr4:9495800-9496800	Enhancers	Fetal Thymus	thymus
40	chr4:9496200-9496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:9496200-9496800	Enhancers	Thymus	Thymus
42	chr4:9496200-9497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr4:9496400-9496600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:9496400-9496800	Enhancers	Primary hematopoietic stem cells	blood
45	chr4:9496600-9499000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr4:9496800-9499600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr4:9499000-9499200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr4:9499000-9499200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
49	chr4:9499000-9499600	Enhancers	Liver	Liver
50	chr4:9499000-9500400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links