Variant report

Variant	nsv428755
Chromosome Location	chr4:16366311-16528135
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:965)
CpG islands
(count:306)
Chromatin interactive
region (count:23)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:965 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:16445167-16445446	HepG2	liver:	n/a	n/a
2	BCL3	chr4:16426584-16426810	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:16445300-16445436	HepG2	liver:	n/a	n/a
4	CBX3	chr4:16510599-16510898	K562	blood:	n/a	n/a
5	CBX3	chr4:16510655-16510932	K562	blood:	n/a	n/a
6	CBX3	chr4:16510661-16511029	HCT-116	colon:	n/a	n/a
7	CEBPB	chr4:16500604-16500971	A549	lung:	n/a	chr4:16500786-16500797
8	CEBPB	chr4:16454922-16455045	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:16499276-16499557	HepG2	liver:	n/a	chr4:16499444-16499455
10	CEBPB	chr4:16379490-16379585	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:16420477-16420984	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr4:16440703-16441091	IMR90	lung:	n/a	chr4:16440998-16441011
13	CEBPB	chr4:16442800-16442951	HepG2	liver:	n/a	chr4:16442873-16442884 chr4:16442871-16442882
14	CEBPB	chr4:16526882-16527123	Hela-S3	cervix:	n/a	chr4:16527003-16527014
15	CEBPB	chr4:16500431-16500981	IMR90	lung:	n/a	chr4:16500786-16500797
16	CEBPB	chr4:16500643-16500976	H1-hESC	embryonic stem cell:	n/a	chr4:16500786-16500797
17	CEBPB	chr4:16500627-16500981	HepG2	liver:	n/a	chr4:16500786-16500797
18	CEBPB	chr4:16491284-16491371	HepG2	liver:	n/a	chr4:16491314-16491325 chr4:16491316-16491325 chr4:16491316-16491327
19	CEBPB	chr4:16498190-16498468	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:16499274-16499587	IMR90	lung:	n/a	chr4:16499444-16499455
21	CEBPB	chr4:16514603-16514774	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:16500696-16500952	Hela-S3	cervix:	n/a	chr4:16500786-16500797
23	CEBPB	chr4:16391458-16391785	H1-hESC	embryonic stem cell:	n/a	chr4:16391602-16391613 chr4:16391602-16391615 chr4:16391602-16391613
24	CEBPB	chr4:16420522-16420858	MCF-7	breast:	n/a	n/a
25	CEBPB	chr4:16499353-16499561	K562	blood:	n/a	chr4:16499444-16499455
26	CEBPB	chr4:16500599-16500976	K562	blood:	n/a	chr4:16500786-16500797
27	CEBPB	chr4:16393964-16394080	HepG2	liver:	n/a	chr4:16394022-16394033
28	CEBPB	chr4:16526786-16527203	IMR90	lung:	n/a	chr4:16527003-16527014
29	CEBPB	chr4:16526917-16527111	A549	lung:	n/a	chr4:16527003-16527014
30	CEBPB	chr4:16526858-16527104	HepG2	liver:	n/a	chr4:16527003-16527014
31	CEBPB	chr4:16472983-16473248	IMR90	lung:	n/a	n/a
32	CEBPB	chr4:16430989-16430994	HepG2	liver:	n/a	n/a
33	CEBPB	chr4:16466327-16466557	IMR90	lung:	n/a	n/a
34	CEBPB	chr4:16420521-16420852	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr4:16499312-16499609	H1-hESC	embryonic stem cell:	n/a	chr4:16499444-16499455
36	CTCF	chr4:16510740-16510890	BJ	skin:	n/a	chr4:16510780-16510801
37	CTCF	chr4:16445240-16445390	GM12865	blood:	n/a	chr4:16445310-16445326 chr4:16445316-16445324 chr4:16445304-16445325 chr4:16445309-16445327
38	CTCF	chr4:16507378-16507706	K562	blood:	n/a	n/a
39	CTCF	chr4:16510740-16510890	GM12869	blood:	n/a	chr4:16510780-16510801
40	CTCF	chr4:16445240-16445390	HCT-116	colon:	n/a	chr4:16445310-16445326 chr4:16445316-16445324 chr4:16445304-16445325 chr4:16445309-16445327
41	CTCF	chr4:16445220-16445370	AG10803	skin:	n/a	chr4:16445310-16445326 chr4:16445316-16445324 chr4:16445304-16445325 chr4:16445309-16445327
42	CTCF	chr4:16518560-16518710	HFF-Myc	foreskin:	n/a	n/a
43	CTCF	chr4:16507380-16507530	GM12865	blood:	n/a	n/a
44	CTCF	chr4:16445087-16445643	A549	lung:	n/a	chr4:16445310-16445326 chr4:16445316-16445324 chr4:16445304-16445325 chr4:16445309-16445327
45	CTCF	chr4:16445611-16445653	GM10266	blood:	n/a	n/a
46	CTCF	chr4:16445240-16445390	GM12868	blood:	n/a	chr4:16445310-16445326 chr4:16445316-16445324 chr4:16445304-16445325 chr4:16445309-16445327
47	CTCF	chr4:16507520-16507670	AG04450	lung:	n/a	n/a
48	CTCF	chr4:16518540-16518690	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr4:16452260-16452410	HCM	heart:	n/a	n/a
50	CTCF	chr4:16507440-16507590	NHLF	lung:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:16507312-16507362	Hela-S3	cervix:	n/a
2	chr4:16507312-16507362	Hela-S3	cervix:	n/a
3	chr4:16504379-16504429	K562	blood:	n/a
4	chr4:16504574-16504624	BJ	skin:	n/a
5	chr4:16507312-16507362	ProgFib	skin:	n/a
6	chr4:16366593-16366643	SAEC	small airway:	n/a
7	chr4:16504379-16504429	ovcar-3	ovarian:	n/a
8	chr4:16504574-16504624	NH-A	brain:	n/a
9	chr4:16504379-16504429	BE2_C	brain:	n/a
10	chr4:16504574-16504624	HUVEC	blood vessel:	n/a
11	chr4:16504643-16504693	LNCaP	prostate:	n/a
12	chr4:16507312-16507362	HCT-116	colon:	n/a
13	chr4:16366593-16366643	Caco-2	colon:	n/a
14	chr4:16504379-16504429	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:16504643-16504693	GM06990	blood:	n/a
16	chr4:16504379-16504429	NHBE	bronchial:	n/a
17	chr4:16504574-16504624	BE2_C	brain:	n/a
18	chr4:16507312-16507362	HMEC	breast:	n/a
19	chr4:16504643-16504693	RPTEC	kidney:	n/a
20	chr4:16504643-16504693	ProgFib	skin:	n/a
21	chr4:16504379-16504429	HNPCEpiC	eye:	n/a
22	chr4:16366593-16366643	SK-N-SH_RA	brain:	n/a
23	chr4:16504379-16504429	SK-N-MC	brain:	n/a
24	chr4:16504379-16504429	PrEC	prostate:	n/a
25	chr4:16507312-16507362	SK-N-MC	brain:	n/a
26	chr4:16366593-16366643	MCF-7	breast:	n/a
27	chr4:16366593-16366643	ovcar-3	ovarian:	n/a
28	chr4:16504643-16504693	HCF	heart:	n/a
29	chr4:16504379-16504429	AG04449	skin:	fetal
30	chr4:16504643-16504693	BJ	skin:	n/a
31	chr4:16507312-16507362	SAEC	small airway:	n/a
32	chr4:16504643-16504693	SK-N-MC	brain:	n/a
33	chr4:16366593-16366643	PFSK-1	brain:	n/a
34	chr4:16366593-16366643	HCF	heart:	n/a
35	chr4:16504574-16504624	H1-hESC	embryonic stem cell:	embryo
36	chr4:16507312-16507362	AoSMC	blood vessel:	n/a
37	chr4:16504643-16504693	HRE	kidney:	n/a
38	chr4:16504379-16504429	NH-A	brain:	n/a
39	chr4:16504643-16504693	AG10803	skin:	n/a
40	chr4:16366593-16366643	NHBE	bronchial:	n/a
41	chr4:16507312-16507362	HEEpiC	esophagus:	n/a
42	chr4:16504574-16504624	SK-N-SH	brain:	n/a
43	chr4:16504574-16504624	GM12891	blood:	n/a
44	chr4:16504574-16504624	HIPEpiC	eye:	n/a
45	chr4:16504574-16504624	MCF10A-Er-Src	breast:	n/a
46	chr4:16504643-16504693	AG04449	skin:	fetal
47	chr4:16504643-16504693	NHDF-neo	bronchial:	n/a
48	chr4:16507312-16507362	HIPEpiC	eye:	n/a
49	chr4:16507312-16507362	PrEC	prostate:	n/a
50	chr4:16507312-16507362	HRE	kidney:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:16360973..16364086-chr4:16365820..16368451,4	MCF-7	breast:
2	chr4:16464985..16467880-chr4:16480876..16482983,2	MCF-7	breast:
3	chr4:16361224..16363467-chr4:16364801..16367359,3	MCF-7	breast:
4	chr4:16291216..16292322-chr4:16444840..16445760,4	MCF-7	breast:
5	chr4:16363037..16365847-chr4:16366056..16368462,2	K562	blood:
6	chr4:16432922..16435405-chr4:16435500..16437482,2	MCF-7	breast:
7	chr4:16409590..16411758-chr4:16414173..16416975,2	MCF-7	breast:
8	chr4:16470332..16473137-chr4:16479314..16480841,2	MCF-7	breast:
9	chr4:16364655..16366735-chr4:16377619..16379236,2	K562	blood:
10	chr4:16464469..16467149-chr4:16468846..16471729,2	K562	blood:
11	chr4:16459198..16462112-chr4:16462228..16466168,3	MCF-7	breast:
12	chr4:16291175..16292655-chr4:16444905..16445780,4	MCF-7	breast:
13	chr4:16387221..16389892-chr4:16394899..16397221,2	K562	blood:
14	chr4:16409590..16411758-chr4:16414173..16416975,2	MCF-7	breast:
15	chr4:16470332..16473137-chr4:16479314..16480841,2	MCF-7	breast:
16	chr4:16432922..16435405-chr4:16435500..16437482,2	MCF-7	breast:
17	chr4:16464985..16467880-chr4:16480876..16482983,2	MCF-7	breast:
18	chr4:16292192..16292811-chr4:16446518..16447107,2	MCF-7	breast:
19	chr4:16464469..16467149-chr4:16468846..16471729,2	K562	blood:
20	chr4:16360699..16362829-chr4:16383139..16385452,2	MCF-7	breast:
21	chr4:16364655..16366735-chr4:16377619..16379236,2	K562	blood:
22	chr4:16459198..16462112-chr4:16462228..16466168,3	MCF-7	breast:
23	chr4:16387221..16389892-chr4:16394899..16397221,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD38-3	chr4:16427988-16428063	ENSG00000248138.1
2	lnc-CD38-3	chr4:16513556-16513810	ENSG00000248138.1
3	lnc-CD38-3	chr4:16435680-16435865	ENSG00000248138.1
4	lnc-CD38-3	chr4:16427988-16428063	ENSG00000248138.1
5	lnc-CD38-3	chr4:16403821-16403855	NONHSAT095690
6	lnc-CD38-3	chr4:16427988-16428063	NONHSAT095690
7	lnc-CD38-3	chr4:16422683-16422756	NONHSAT095690
8	lnc-TAPT1-3	chr4:16398154-16398946	NONHSAT095687
9	lnc-CD38-3	chr4:16422683-16422756	ENSG00000248138.1
10	lnc-CD38-3	chr4:16453975-16454393	NONHSAT095690
11	lnc-CD38-3	chr4:16435680-16435865	NONHSAT095690
12	lnc-CD38-3	chr4:16403821-16403855	ENSG00000248138.1
13	lnc-TAPT1-3	chr4:16389542-16389545	NONHSAT095687
14	lnc-CD38-3	chr4:16402053-16402156	ENSG00000248138.1

No data

Variant related genes	Relation type
ZEB2P1	TF binding region
ENSG00000248138	TF binding region
LDB2	TF binding region
ZEB2P1	CpG island
ENSG00000248138	CpG island
LDB2	CpG island
ENSG00000249506	chromatin interactions

Extended variants
information (count: 3630 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3630 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540036516	chr4:16366363-16366364	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs199706931	chr4:16366392-16366393	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs556500180	chr4:16366396-16366397	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs573539988	chr4:16366417-16366418	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs77910889	chr4:16366438-16366439	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs555773324	chr4:16366443-16366444	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs575575110	chr4:16366448-16366449	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs374891535	chr4:16366468-16366469	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187877091	chr4:16366474-16366475	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs549198364	chr4:16366518-16366519	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs564599092	chr4:16366616-16366617	Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs578034261	chr4:16366643-16366644	Enhancers	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs539996529	chr4:16366665-16366666	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559931026	chr4:16366678-16366679	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529122206	chr4:16366704-16366705	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs548843529	chr4:16366709-16366710	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs114121292	chr4:16366756-16366757	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs531328595	chr4:16366784-16366785	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs551137046	chr4:16366849-16366850	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs571275136	chr4:16366876-16366877	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs374411957	chr4:16366957-16366958	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149357179	chr4:16366966-16366967	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs80240739	chr4:16366981-16366982	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538984635	chr4:16367028-16367029	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373724530	chr4:16367034-16367035	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs567093134	chr4:16367063-16367064	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs144590623	chr4:16367075-16367076	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs556013227	chr4:16367077-16367078	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs575893671	chr4:16367091-16367092	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs538190213	chr4:16367122-16367123	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs115024035	chr4:16367141-16367142	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs577679703	chr4:16367193-16367194	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs574041460	chr4:16367217-16367218	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs540348456	chr4:16367230-16367231	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs139805549	chr4:16367247-16367248	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199796007	chr4:16367445-16367446	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs573485899	chr4:16367469-16367470	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs115138848	chr4:16367483-16367484	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs562797712	chr4:16367487-16367488	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192654581	chr4:16367523-16367524	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs576349530	chr4:16367526-16367527	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs551317204	chr4:16367599-16367600	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184371987	chr4:16367601-16367602	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs73239777	chr4:16367608-16367609	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs547496174	chr4:16367623-16367624	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113541791	chr4:16367646-16367647	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529503991	chr4:16367736-16367737	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs80040266	chr4:16367792-16367793	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188666281	chr4:16367820-16367821	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs67798922	chr4:16367827-16367828	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	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
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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	22183965	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:16366600-16367200	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr4:16366600-16367200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:16366800-16367200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:16367000-16367200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:16367000-16368200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr4:16377800-16378400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:16379400-16380000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:16379800-16380200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:16380600-16381200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr4:16380800-16381400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:16381000-16382000	Enhancers	Fetal Kidney	kidney
12	chr4:16381200-16384400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr4:16382000-16386400	Weak transcription	Fetal Kidney	kidney
14	chr4:16383400-16385600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:16384400-16384800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr4:16384800-16386000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr4:16385600-16385800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:16385600-16388000	Enhancers	Fetal Muscle Leg	muscle
19	chr4:16385800-16386800	Enhancers	Fetal Stomach	stomach
20	chr4:16386000-16386400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr4:16386000-16386800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr4:16386200-16386400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr4:16386400-16386600	Enhancers	Fetal Kidney	kidney
24	chr4:16388000-16388800	Weak transcription	Fetal Muscle Leg	muscle
25	chr4:16388600-16389200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:16388800-16389600	Enhancers	Fetal Muscle Leg	muscle
27	chr4:16391400-16391800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr4:16392800-16393200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr4:16396800-16397600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr4:16397600-16399000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr4:16399000-16399400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chr4:16413000-16413600	Enhancers	Fetal Stomach	stomach
33	chr4:16413200-16413400	Enhancers	Fetal Kidney	kidney
34	chr4:16413400-16417200	Weak transcription	Fetal Kidney	kidney
35	chr4:16413600-16414600	Weak transcription	Fetal Stomach	stomach
36	chr4:16414800-16415000	Enhancers	Fetal Stomach	stomach
37	chr4:16417200-16418600	Enhancers	Fetal Kidney	kidney
38	chr4:16418200-16421200	Enhancers	HUVEC	blood vessel
39	chr4:16419400-16419600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr4:16419600-16420600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:16419600-16421000	Enhancers	NHEK	skin
42	chr4:16420600-16421400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:16420800-16421000	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr4:16429800-16435200	Weak transcription	Fetal Brain Male	brain
45	chr4:16435200-16436400	Enhancers	Fetal Brain Male	brain
46	chr4:16436400-16441000	Weak transcription	Fetal Brain Male	brain
47	chr4:16439400-16441800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:16439800-16440400	Enhancers	NH-A	brain
49	chr4:16439800-16441400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:16439800-16441400	Enhancers	Osteobl	bone

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