Variant report

Variant	nsv593894
Chromosome Location	chr4:28738088-28872833
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:28823833-28823988	K562	blood:	n/a	n/a
2	BHLHE40	chr4:28789517-28789783	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:28746053-28746244	HepG2	liver:	n/a	chr4:28746141-28746152
4	CEBPB	chr4:28777649-28777964	Hela-S3	cervix:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
5	CEBPB	chr4:28777642-28778300	HepG2	liver:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
6	CEBPB	chr4:28828127-28828387	A549	lung:	n/a	chr4:28828324-28828337 chr4:28828253-28828264
7	CEBPB	chr4:28777624-28778013	IMR90	lung:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
8	CEBPB	chr4:28872677-28872783	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:28825839-28825873	K562	blood:	n/a	chr4:28825857-28825866 chr4:28825855-28825868 chr4:28825855-28825868 chr4:28825855-28825866 chr4:28825856-28825867
10	CEBPB	chr4:28825718-28826010	IMR90	lung:	n/a	chr4:28825857-28825866 chr4:28825855-28825868 chr4:28825855-28825868 chr4:28825855-28825866 chr4:28825856-28825867
11	CEBPB	chr4:28777638-28778005	H1-hESC	embryonic stem cell:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
12	CEBPB	chr4:28777638-28778001	K562	blood:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
13	CEBPB	chr4:28825761-28825987	A549	lung:	n/a	chr4:28825857-28825866 chr4:28825855-28825868 chr4:28825855-28825868 chr4:28825855-28825866 chr4:28825856-28825867
14	CEBPB	chr4:28828214-28828396	K562	blood:	n/a	chr4:28828324-28828337 chr4:28828253-28828264
15	CEBPB	chr4:28851851-28851992	HepG2	liver:	n/a	chr4:28851864-28851875
16	CEBPB	chr4:28777640-28777999	A549	lung:	n/a	chr4:28777661-28777672 chr4:28777821-28777830 chr4:28777784-28777795 chr4:28777821-28777830 chr4:28777819-28777832 chr4:28777784-28777793 chr4:28777821-28777830 chr4:28777820-28777831
17	CEBPB	chr4:28825684-28826029	HepG2	liver:	n/a	chr4:28825857-28825866 chr4:28825855-28825868 chr4:28825855-28825868 chr4:28825855-28825866 chr4:28825856-28825867
18	CEBPB	chr4:28828128-28828442	HepG2	liver:	n/a	chr4:28828324-28828337 chr4:28828253-28828264
19	CEBPB	chr4:28828136-28828421	IMR90	lung:	n/a	chr4:28828324-28828337 chr4:28828253-28828264
20	CTCF	chr4:28856539-28856579	GM20000	blood:	n/a	n/a
21	CTCF	chr4:28819582-28819601	GM10266	blood:	n/a	n/a
22	CTCF	chr4:28747436-28747506	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:28790836-28790838	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr4:28815240-28815390	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:28790814-28791029	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr4:28790864-28790938	LNCaP	prostate:	n/a	n/a
27	CTCF	chr4:28841783-28841844	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr4:28790879-28790884	LNCaP	prostate:	n/a	n/a
29	CTCF	chr4:28843880-28844030	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:28815270-28815358	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:28790887-28790963	MCF-7	breast:	n/a	n/a
32	CTCF	chr4:28815220-28815370	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr4:28815160-28815310	BE2_C	brain:	n/a	n/a
34	CTCF	chr4:28747422-28747485	GM13976	blood:	n/a	n/a
35	CTCF	chr4:28790901-28790904	LNCaP	prostate:	n/a	n/a
36	CTCF	chr4:28790835-28790945	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr4:28815220-28815389	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:28790860-28790940	GM12878	blood:	n/a	n/a
39	CTCF	chr4:28790818-28790928	ProgFib	skin:	n/a	n/a
40	CTCF	chr4:28815280-28815430	AG09309	skin:	n/a	n/a
41	CTCF	chr4:28790800-28790950	AG09309	skin:	n/a	n/a
42	CTCF	chr4:28790839-28790998	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr4:28790817-28790961	Fibrobl	skin:	n/a	n/a
44	CTCF	chr4:28790767-28791040	T-47D	breast:	n/a	n/a
45	CTCF	chr4:28790820-28790970	AG09309	skin:	n/a	n/a
46	CTCF	chr4:28815289-28815366	ProgFib	skin:	n/a	n/a
47	CTCF	chr4:28790760-28790910	A549	lung:	n/a	n/a
48	CTCF	chr4:28815260-28815410	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:28790900-28791050	NB4	blood:	n/a	n/a
50	CTCF	chr4:28790780-28790930	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:28829667-28829717	HL-60	blood:	n/a
2	chr4:28829667-28829717	AG04450	lung:	fetal
3	chr4:28829667-28829717	SAEC	small airway:	n/a
4	chr4:28829667-28829717	PFSK-1	brain:	n/a
5	chr4:28829667-28829717	Jurkat	blood:	n/a
6	chr4:28829667-28829717	SK-N-MC	brain:	n/a
7	chr4:28829667-28829717	HCPEpiC	choroid plexus:	n/a
8	chr4:28829667-28829717	HEEpiC	esophagus:	n/a
9	chr4:28829667-28829717	BE2_C	brain:	n/a
10	chr4:28829667-28829717	HNPCEpiC	eye:	n/a
11	chr4:28829667-28829717	HepG2	liver:	n/a
12	chr4:28829667-28829717	PANC-1	pancreas:	n/a
13	chr4:28829667-28829717	NB4	blood:	n/a
14	chr4:28829667-28829717	HCF	heart:	n/a
15	chr4:28829667-28829717	GM12892	blood:	n/a
16	chr4:28829667-28829717	NHBE	bronchial:	n/a
17	chr4:28829667-28829717	A549	lung:	n/a
18	chr4:28829667-28829717	ECC-1	luminal epithelium:	n/a
19	chr4:28829667-28829717	ProgFib	skin:	n/a
20	chr4:28829667-28829717	HUVEC	blood vessel:	n/a
21	chr4:28829667-28829717	K562	blood:	n/a
22	chr4:28829667-28829717	U87	brain:	n/a
23	chr4:28829667-28829717	HEK293	kidney:	embryo
24	chr4:28829667-28829717	GM19239	blood:	n/a
25	chr4:28829667-28829717	AG09309	skin:	n/a
26	chr4:28829667-28829717	HMEC	breast:	n/a
27	chr4:28829667-28829717	AG10803	skin:	n/a
28	chr4:28829667-28829717	NH-A	brain:	n/a
29	chr4:28829667-28829717	SK-N-SH_RA	brain:	n/a
30	chr4:28829667-28829717	H1-hESC	embryonic stem cell:	embryo
31	chr4:28829667-28829717	MCF-7	breast:	n/a
32	chr4:28829667-28829717	HCM	heart:	n/a
33	chr4:28829667-28829717	HIPEpiC	eye:	n/a
34	chr4:28829667-28829717	HRCEpiC	kidney:	n/a
35	chr4:28829667-28829717	T-47D	breast:	n/a
36	chr4:28829667-28829717	SKMC	muscle:	n/a
37	chr4:28829667-28829717	HPAEpiC	pulmonary alveolar:	n/a
38	chr4:28829667-28829717	AoSMC	blood vessel:	n/a
39	chr4:28829667-28829717	RPTEC	kidney:	n/a
40	chr4:28829667-28829717	AG09319	gingival:	n/a
41	chr4:28829667-28829717	HRPEpiC	eye:	n/a
42	chr4:28829667-28829717	AG04449	skin:	fetal
43	chr4:28829667-28829717	SK-N-SH	brain:	n/a
44	chr4:28829667-28829717	Caco-2	colon:	n/a
45	chr4:28829667-28829717	HRE	kidney:	n/a
46	chr4:28829667-28829717	HCT-116	colon:	n/a
47	chr4:28829667-28829717	GM06990	blood:	n/a
48	chr4:28829667-28829717	CMK	blood:	n/a
49	chr4:28829667-28829717	Hela-S3	cervix:	n/a
50	chr4:28829667-28829717	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:28756009..28757657-chr4:28759258..28762060,2	MCF-7	breast:
2	chr4:28756009..28757657-chr4:28759258..28762060,2	MCF-7	breast:
3	chr4:28778617..28781313-chr4:28801513..28803129,2	K562	blood:
4	chr4:28823073..28825418-chr4:28842573..28844204,2	MCF-7	breast:
5	chr4:28787492..28790119-chr4:28809128..28811907,2	K562	blood:
6	chr4:28797752..28800390-chr4:28800946..28802986,2	K562	blood:
7	chr4:28778617..28781313-chr4:28801513..28803129,2	K562	blood:
8	chr17:45078439..45078999-chr4:28740495..28741046,2	MCF-7	breast:
9	chr14:46737193..46737995-chr4:28770057..28770960,2	MCF-7	breast:
10	chr4:28787492..28790119-chr4:28809128..28811907,2	K562	blood:
11	chr4:28760216..28762213-chr4:28762423..28765367,2	K562	blood:
12	chr4:28823073..28825418-chr4:28842573..28844204,2	MCF-7	breast:
13	chr4:28805670..28808284-chr4:28808958..28811325,2	K562	blood:
14	chr4:28760216..28762213-chr4:28762423..28765367,2	K562	blood:
15	chr4:28797752..28800390-chr4:28800946..28802986,2	K562	blood:
16	chr4:28805670..28808284-chr4:28808958..28811325,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STIM2-5	chr4:28754781-28754905	XLOC_003488
2	lnc-STIM2-5	chr4:28754425-28754728	XLOC_003488

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4275	chr4:28821214-28821230	MIMAT0016905

Variant related genes	Relation type
MESTP3	TF binding region
MESTP3	CpG island
MTMR9	miRNA target sites

Extended variants
information (count: 1283 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563160276	chr4:28750803-28750804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529016648	chr4:28750824-28750825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs548277511	chr4:28750842-28750843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187242397	chr4:28750858-28750859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs16881041	chr4:28750923-28750924	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs547753352	chr4:28750927-28750928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191615693	chr4:28750928-28750929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34102253	chr4:28750951-28750952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143743355	chr4:28750964-28750965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553055304	chr4:28750966-28750967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562097537	chr4:28750972-28750973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550460623	chr4:28751021-28751022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570268074	chr4:28751068-28751069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536053838	chr4:28751077-28751078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs555211361	chr4:28751104-28751105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182713197	chr4:28751122-28751123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534352263	chr4:28751130-28751131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10025997	chr4:28751169-28751170	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541898573	chr4:28751181-28751182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187175881	chr4:28751187-28751188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543323861	chr4:28751225-28751226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs556788556	chr4:28751228-28751229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs16881042	chr4:28751256-28751257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10014265	chr4:28751306-28751307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs533582416	chr4:28751316-28751317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs75467502	chr4:28751333-28751334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191634103	chr4:28751343-28751344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182306065	chr4:28751375-28751376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546918770	chr4:28751383-28751384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533323964	chr4:28751384-28751385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs10014342	chr4:28751389-28751390	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187534300	chr4:28751390-28751391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192626893	chr4:28751444-28751445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549533867	chr4:28751485-28751486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185624640	chr4:28751497-28751498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571220332	chr4:28751510-28751511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566116761	chr4:28751516-28751517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190484616	chr4:28751518-28751519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151180800	chr4:28751532-28751533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564335629	chr4:28751550-28751551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192909497	chr4:28751597-28751598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs16881043	chr4:28751601-28751602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115553885	chr4:28751624-28751625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10026366	chr4:28751635-28751636	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs542484639	chr4:28751646-28751647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184523286	chr4:28751713-28751714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536599887	chr4:28751775-28751776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs115779381	chr4:28751776-28751777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs116349775	chr4:28751788-28751789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1038901	chr4:28751947-28751948	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	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
Lung cancer	18438408	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Cancer	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:28750800-28751200	Enhancers	H1 Cell Line	embryonic stem cell
2	chr4:28751200-28755600	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr4:28753400-28754200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr4:28754200-28756000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr4:28754800-28755400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:28755000-28756200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:28755000-28756400	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr4:28755000-28757200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr4:28755000-28757600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr4:28755200-28756000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:28755200-28756400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr4:28755200-28756400	Enhancers	Fetal Brain Female	brain
13	chr4:28755200-28756800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr4:28755200-28757600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:28755400-28755800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
16	chr4:28755600-28756400	Enhancers	H1 Cell Line	embryonic stem cell
17	chr4:28755600-28756400	Enhancers	Fetal Brain Male	brain
18	chr4:28755800-28756400	Enhancers	H9 Cell Line	embryonic stem cell
19	chr4:28755800-28756600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:28755800-28757200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:28755800-28757200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr4:28756000-28756400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:28756000-28756400	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr4:28756000-28757200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:28756200-28756400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
26	chr4:28756400-28756600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr4:28756600-28756800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
28	chr4:28756800-28757600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr4:28757200-28757400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:28757200-28760800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:28760800-28761200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:28765600-28766400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr4:28765800-28766200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:28766000-28766400	Active TSS	Gastric	stomach
35	chr4:28767200-28768000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:28772600-28773000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr4:28773000-28773400	Enhancers	Colon Smooth Muscle	Colon
38	chr4:28773000-28774400	Enhancers	HSMM	muscle
39	chr4:28773000-28774400	Enhancers	NH-A	brain
40	chr4:28773000-28774600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr4:28773400-28774600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr4:28773400-28774800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr4:28775200-28775400	Enhancers	Fetal Heart	heart
44	chr4:28775200-28775600	Active TSS	Ovary	ovary
45	chr4:28775400-28775800	Flanking Active TSS	Fetal Heart	heart
46	chr4:28775800-28777400	Enhancers	Fetal Heart	heart
47	chr4:28776400-28776800	Enhancers	Brain Germinal Matrix	brain
48	chr4:28794400-28795400	Enhancers	Fetal Heart	heart
49	chr4:28795400-28799200	Weak transcription	Fetal Heart	heart
50	chr4:28795800-28796000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links