Variant report

Variant	nsv880722
Chromosome Location	chr5:29249544-29466930
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	chr5:29261746-29261789	K562	blood:	n/a	n/a
2	ATF1	chr5:29431656-29431817	K562	blood:	n/a	n/a
3	ATF1	chr5:29425063-29425178	K562	blood:	n/a	n/a
4	ATF1	chr5:29425986-29425989	K562	blood:	n/a	n/a
5	ATF1	chr5:29300805-29300808	K562	blood:	n/a	n/a
6	BACH1	chr5:29433080-29433172	K562	blood:	n/a	n/a
7	BCL3	chr5:29262604-29263216	A549	lung:	n/a	n/a
8	BRCA1	chr5:29307600-29307906	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr5:29263899-29264484	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr5:29262408-29263657	Hela-S3	cervix:	n/a	n/a
11	CCNT2	chr5:29256507-29256622	K562	blood:	n/a	n/a
12	CEBPB	chr5:29262615-29263342	A549	lung:	n/a	chr5:29262923-29262940 chr5:29263293-29263306
13	CEBPB	chr5:29282499-29282730	A549	lung:	n/a	chr5:29282672-29282683 chr5:29282673-29282684
14	CEBPB	chr5:29387050-29387411	IMR90	lung:	n/a	chr5:29387309-29387320 chr5:29387204-29387215
15	CEBPB	chr5:29433473-29433683	K562	blood:	n/a	chr5:29433543-29433554 chr5:29433541-29433552
16	CEBPB	chr5:29413274-29413380	A549	lung:	n/a	chr5:29413367-29413380 chr5:29413367-29413378
17	CEBPB	chr5:29262193-29263529	Hela-S3	cervix:	n/a	chr5:29262923-29262940 chr5:29263293-29263306
18	CEBPB	chr5:29298016-29298086	A549	lung:	n/a	chr5:29298021-29298032
19	CEBPB	chr5:29307586-29307932	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr5:29390980-29391087	K562	blood:	n/a	chr5:29391028-29391039
21	CEBPB	chr5:29425611-29425821	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:29266045-29266218	A549	lung:	n/a	n/a
23	CEBPB	chr5:29387025-29387424	HepG2	liver:	n/a	chr5:29387309-29387320 chr5:29387204-29387215
24	CEBPB	chr5:29293365-29293604	A549	lung:	n/a	chr5:29293483-29293494
25	CEBPB	chr5:29311019-29311308	Hela-S3	cervix:	n/a	chr5:29311159-29311176 chr5:29311160-29311173
26	CEBPB	chr5:29337911-29338232	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:29387041-29387392	A549	lung:	n/a	chr5:29387309-29387320 chr5:29387204-29387215
28	CEBPB	chr5:29262771-29263188	A549	lung:	n/a	chr5:29262923-29262940
29	CEBPB	chr5:29262929-29262971	K562	blood:	n/a	n/a
30	CEBPB	chr5:29337963-29338183	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:29310295-29310520	Hela-S3	cervix:	n/a	chr5:29310377-29310390 chr5:29310377-29310388
32	CEBPB	chr5:29265995-29266209	HepG2	liver:	n/a	n/a
33	CEBPB	chr5:29377734-29377818	HepG2	liver:	n/a	chr5:29377787-29377800 chr5:29377787-29377800 chr5:29377787-29377798 chr5:29377787-29377798 chr5:29377788-29377799
34	CEBPB	chr5:29459773-29459805	K562	blood:	n/a	n/a
35	CEBPB	chr5:29268187-29268501	A549	lung:	n/a	n/a
36	CEBPB	chr5:29351314-29351662	HepG2	liver:	n/a	chr5:29351485-29351496
37	CEBPB	chr5:29293316-29293607	Hela-S3	cervix:	n/a	chr5:29293483-29293494
38	CEBPB	chr5:29262798-29263210	A549	lung:	n/a	chr5:29262923-29262940
39	CEBPB	chr5:29387081-29387400	Hela-S3	cervix:	n/a	chr5:29387309-29387320 chr5:29387204-29387215
40	CEBPB	chr5:29433374-29433733	IMR90	lung:	n/a	chr5:29433543-29433554 chr5:29433541-29433552
41	CEBPB	chr5:29433358-29433700	HepG2	liver:	n/a	chr5:29433543-29433554 chr5:29433541-29433552
42	CEBPB	chr5:29387091-29387291	H1-hESC	embryonic stem cell:	n/a	chr5:29387204-29387215
43	CEBPB	chr5:29414090-29414343	K562	blood:	n/a	n/a
44	CEBPB	chr5:29263886-29264679	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr5:29293399-29293591	H1-hESC	embryonic stem cell:	n/a	chr5:29293483-29293494
46	CEBPB	chr5:29276960-29277157	HepG2	liver:	n/a	n/a
47	CEBPB	chr5:29337241-29337370	K562	blood:	n/a	chr5:29337327-29337338 chr5:29337343-29337354
48	CEBPB	chr5:29293312-29293657	K562	blood:	n/a	chr5:29293483-29293494
49	CEBPB	chr5:29351326-29351657	A549	lung:	n/a	chr5:29351485-29351496
50	CEBPB	chr5:29261400-29261648	A549	lung:	n/a	chr5:29261494-29261505 chr5:29261494-29261507

No.	Distal block	Cell Line	Cell type
1	chr5:29374107..29376875-chr5:29377791..29380634,2	K562	blood:
2	chr5:29367263..29368784-chr5:29811787..29812627,6	MCF-7	breast:
3	chr5:29367557..29368187-chr5:29811640..29812581,2	MCF-7	breast:
4	chr5:29374107..29376875-chr5:29377791..29380634,2	K562	blood:
5	chr5:29367148..29368248-chr5:29697562..29698574,8	MCF-7	breast:
6	chr5:29394432..29396496-chr5:29400311..29402057,2	MCF-7	breast:
7	chr5:29367229..29368191-chr5:29697633..29698544,4	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DROSHA-7	chr5:29380373-29380432	XLOC_004765
2	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
3	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
4	lnc-DROSHA-12	chr5:29399178-29399246	l_2897_chr5:29390052-29431912_testes
5	lnc-DROSHA-7	chr5:29389918-29390046	XLOC_004765
6	lnc-DROSHA-7	chr5:29383211-29383410	XLOC_004765
7	lnc-DROSHA-12	chr5:29425675-29425803	l_2897_chr5:29390052-29431912_testes
8	lnc-DROSHA-12	chr5:29415951-29416189	l_2897_chr5:29390052-29431912_testes
9	lnc-DROSHA-12	chr5:29417717-29417826	l_2897_chr5:29390052-29431912_testes
10	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
11	lnc-DROSHA-7	chr5:29380403-29380432	XLOC_004765
12	lnc-DROSHA-7	chr5:29395961-29396088	XLOC_004765
13	lnc-DROSHA-7	chr5:29363459-29363489	XLOC_004765
14	lnc-DROSHA-12	chr5:29391719-29391826	l_2897_chr5:29390052-29431912_testes
15	lnc-DROSHA-12	chr5:29431718-29431912	l_2897_chr5:29390052-29431912_testes
16	lnc-DROSHA-7	chr5:29384404-29384499	XLOC_004765
17	lnc-DROSHA-7	chr5:29389918-29390046	NR_104628
18	lnc-DROSHA-7	chr5:29389918-29390047	XLOC_004765
19	lnc-DROSHA-12	chr5:29390053-29390256	l_2897_chr5:29390052-29431912_testes
20	lnc-DROSHA-7	chr5:29384404-29384499	XLOC_004765
21	lnc-DROSHA-7	chr5:29355912-29356069	XLOC_004765
22	lnc-DROSHA-7	chr5:29395961-29396083	NR_104628
23	lnc-DROSHA-7	chr5:29380196-29380432	NR_104628
24	lnc-DROSHA-7	chr5:29381960-29382069	NR_104628
25	lnc-DROSHA-12	chr5:29420161-29420256	l_2897_chr5:29390052-29431912_testes
26	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765
27	lnc-DROSHA-7	chr5:29384427-29384499	NR_104628
28	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
29	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
30	lnc-DROSHA-7	chr5:29384427-29384499	XLOC_004765
31	lnc-DROSHA-7	chr5:29381960-29382069	XLOC_004765
32	lnc-DROSHA-7	chr5:29395961-29396100	XLOC_004765

Variant related genes	Relation type
ENSG00000248391	TF binding region
ENSG00000248391	chromatin interactions
SGMS1	miRNA target sites
AGK	miRNA target sites
AGXT2L1	miRNA target sites
AHCTF1	miRNA target sites
FMNL2	miRNA target sites
AGL	miRNA target sites
SERPINB2	miRNA target sites
AGPAT3	miRNA target sites
DGKA	miRNA target sites

Extended variants
information (count: 2015 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7717683	chr5:29249544-29249545	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs191175789	chr5:29249570-29249571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561811534	chr5:29249573-29249574	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112141399	chr5:29249582-29249583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559997598	chr5:29249635-29249636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs34023576	chr5:29249646-29249647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs540858163	chr5:29249648-29249649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530265777	chr5:29249676-29249677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs71608747	chr5:29249677-29249678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs548622615	chr5:29249691-29249692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs142079454	chr5:29249704-29249705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183305031	chr5:29249730-29249731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11951992	chr5:29249751-29249752	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs530840341	chr5:29249756-29249757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369346006	chr5:29249768-29249769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146702026	chr5:29249871-29249872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs140264425	chr5:29249892-29249893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs187596958	chr5:29249900-29249901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs560279184	chr5:29249916-29249917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568185610	chr5:29249934-29249935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs10940787	chr5:29250014-29250015	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs549884383	chr5:29250147-29250148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553888274	chr5:29250251-29250252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10940788	chr5:29250258-29250259	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs10940789	chr5:29250271-29250272	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs10940790	chr5:29250315-29250316	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs557777406	chr5:29250338-29250339	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs145249560	chr5:29250381-29250382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540332121	chr5:29250397-29250398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs561737632	chr5:29250421-29250422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574969895	chr5:29250446-29250447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs72743468	chr5:29250453-29250454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs563873364	chr5:29250463-29250464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531227668	chr5:29250493-29250494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs137877356	chr5:29250507-29250508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564145556	chr5:29250537-29250538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs149123555	chr5:29250544-29250545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370291717	chr5:29250585-29250586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546707044	chr5:29250596-29250597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73750008	chr5:29250629-29250630	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs535316042	chr5:29250665-29250666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539687926	chr5:29250683-29250684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191455820	chr5:29250705-29250706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs76207296	chr5:29250743-29250744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113259076	chr5:29250749-29250750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11441165	chr5:29250750-29250751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566625047	chr5:29250755-29250756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11416003	chr5:29250758-29250759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs558037332	chr5:29250815-29250816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572897341	chr5:29250858-29250859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29249400-29249600	Enhancers	Hela-S3	cervix
2	chr5:29249600-29250200	Weak transcription	Hela-S3	cervix
3	chr5:29250200-29250400	Enhancers	Hela-S3	cervix
4	chr5:29250400-29254800	Weak transcription	Hela-S3	cervix
5	chr5:29254800-29255000	Enhancers	Hela-S3	cervix
6	chr5:29255000-29255600	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr5:29255000-29258600	Weak transcription	Hela-S3	cervix
8	chr5:29255200-29255400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr5:29255400-29257200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr5:29258600-29258800	Enhancers	Hela-S3	cervix
11	chr5:29258800-29259600	Weak transcription	Hela-S3	cervix
12	chr5:29259600-29262600	Enhancers	Hela-S3	cervix
13	chr5:29262200-29263000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:29262400-29262600	Enhancers	A549	lung
15	chr5:29262600-29263000	Flanking Active TSS	Hela-S3	cervix
16	chr5:29262600-29263400	Active TSS	A549	lung
17	chr5:29263000-29264000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:29263000-29264200	Enhancers	Hela-S3	cervix
19	chr5:29263400-29264000	Weak transcription	A549	lung
20	chr5:29264000-29264600	Enhancers	Fetal Muscle Leg	muscle
21	chr5:29264200-29264400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr5:29264200-29264400	Enhancers	A549	lung
23	chr5:29264200-29264600	Enhancers	Fetal Muscle Trunk	muscle
24	chr5:29264200-29264600	Flanking Active TSS	Hela-S3	cervix
25	chr5:29264600-29266200	Enhancers	Hela-S3	cervix
26	chr5:29276600-29277000	Enhancers	Hela-S3	cervix
27	chr5:29295200-29297600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr5:29296600-29296800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:29304600-29305200	Enhancers	Hela-S3	cervix
30	chr5:29305200-29305600	Weak transcription	Hela-S3	cervix
31	chr5:29305600-29308400	Enhancers	Hela-S3	cervix
32	chr5:29342600-29343400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:29367400-29367800	Enhancers	Brain Cingulate Gyrus	brain
34	chr5:29367400-29368000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:29367400-29368200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:29382600-29383200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:29382600-29383200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr5:29383000-29383400	Active TSS	HepG2	liver
39	chr5:29408200-29408400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr5:29408400-29410800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:29410800-29411200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:29417600-29418000	Enhancers	Fetal Brain Male	brain
43	chr5:29417600-29418000	Enhancers	Psoas Muscle	Psoas
44	chr5:29429200-29429400	ZNF genes & repeats	Pancreas	Pancrea
45	chr5:29433000-29433200	Enhancers	Aorta	Aorta
46	chr5:29450400-29450800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr5:29456800-29461400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr5:29461200-29461600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr5:29461200-29461600	Enhancers	Brain Inferior Temporal Lobe	brain
50	chr5:29461400-29461800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links