Variant report

Variant	esv1826079
Chromosome Location	chr5:1416646-1432825
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	BACH1	chr5:1421027-1421032	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr5:1416591-1416857	GM12878	blood:	n/a	n/a
3	CBX3	chr5:1428170-1428728	HCT-116	colon:	n/a	chr5:1428634-1428645
4	CEBPB	chr5:1426831-1427104	A549	lung:	n/a	chr5:1426982-1426993
5	CEBPB	chr5:1426842-1427119	HepG2	liver:	n/a	chr5:1426982-1426993
6	CEBPB	chr5:1426891-1427088	K562	blood:	n/a	chr5:1426982-1426993
7	CTCF	chr5:1424360-1424510	HepG2	liver:	n/a	chr5:1424474-1424483
8	CTCF	chr5:1424492-1424510	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr5:1424380-1424530	WERI-Rb-1	eye:	n/a	chr5:1424474-1424483
10	CTCF	chr5:1422580-1422661	GM13976	blood:	n/a	n/a
11	CTCF	chr5:1424400-1424550	Hela-S3	cervix:	n/a	chr5:1424474-1424483
12	CTCF	chr5:1417162-1417185	LNCaP	prostate:	n/a	n/a
13	CTCF	chr5:1422688-1422768	GM20000	blood:	n/a	n/a
14	CTCF	chr5:1424476-1424485	H1-hESC	embryonic stem cell:	n/a	n/a
15	CUX1	chr5:1418482-1418682	K562	blood:	n/a	n/a
16	EBF1	chr5:1422322-1423581	GM12878	blood:	n/a	chr5:1423516-1423525
17	EBF1	chr5:1422409-1422700	GM12878	blood:	n/a	n/a
18	EGR1	chr5:1424474-1424732	K562	blood:	n/a	chr5:1424614-1424624 chr5:1424614-1424625 chr5:1424612-1424627 chr5:1424613-1424626 chr5:1424613-1424626 chr5:1424614-1424623 chr5:1424612-1424626 chr5:1424614-1424625 chr5:1424614-1424624 chr5:1424613-1424626 chr5:1424613-1424626 chr5:1424608-1424630
19	EP300	chr5:1422421-1422819	GM12878	blood:	n/a	chr5:1422447-1422456
20	FOSL2	chr5:1422476-1422779	HepG2	liver:	n/a	n/a
21	GABPA	chr5:1422950-1423127	Hela-S3	cervix:	n/a	n/a
22	GABPA	chr5:1422503-1422745	GM12878	blood:	n/a	n/a
23	GABPA	chr5:1422507-1422756	Hela-S3	cervix:	n/a	n/a
24	GATA3	chr5:1429533-1429888	MCF-7	breast:	n/a	n/a
25	GATA3	chr5:1425757-1426001	SH-SY5Y	brain:	n/a	n/a
26	JUND	chr5:1422535-1422670	HepG2	liver:	n/a	n/a
27	JUND	chr5:1422486-1422733	HepG2	liver:	n/a	n/a
28	KAP1	chr5:1428317-1428588	HEK293	kidney:	n/a	n/a
29	MAFK	chr5:1420945-1420977	HepG2	liver:	n/a	n/a
30	MAFK	chr5:1424711-1424728	HepG2	liver:	n/a	n/a
31	MAFK	chr5:1424832-1424865	HepG2	liver:	n/a	chr5:1424835-1424855
32	MAX	chr5:1421706-1421959	NB4	blood:	n/a	n/a
33	MAX	chr5:1429570-1429732	K562	blood:	n/a	chr5:1429621-1429634 chr5:1429625-1429632 chr5:1429621-1429634 chr5:1429618-1429637 chr5:1429623-1429630
34	MAX	chr5:1429743-1429897	Hela-S3	cervix:	n/a	n/a
35	MAX	chr5:1429370-1429658	K562	blood:	n/a	chr5:1429502-1429513 chr5:1429621-1429634 chr5:1429625-1429632 chr5:1429502-1429513 chr5:1429503-1429513 chr5:1429621-1429634 chr5:1429503-1429512 chr5:1429618-1429637 chr5:1429503-1429512 chr5:1429504-1429511 chr5:1429623-1429630
36	MAX	chr5:1421608-1421908	K562	blood:	n/a	n/a
37	MAX	chr5:1429518-1429985	MCF-7	breast:	n/a	chr5:1429621-1429634 chr5:1429625-1429632 chr5:1429621-1429634 chr5:1429618-1429637 chr5:1429623-1429630
38	MYC	chr5:1417987-1418055	H1-hESC	embryonic stem cell:	n/a	chr5:1418044-1418054
39	MYC	chr5:1429739-1429828	MCF-7	breast:	n/a	n/a
40	MYC	chr5:1418757-1418806	HUVEC	blood vessel:	n/a	n/a
41	NR2F2	chr5:1416894-1417180	K562	blood:	n/a	n/a
42	NR3C1	chr5:1416622-1417023	A549	lung:	n/a	n/a
43	NR3C1	chr5:1416450-1417188	A549	lung:	n/a	n/a
44	NR3C1	chr5:1416414-1417224	A549	lung:	n/a	n/a
45	NR3C1	chr5:1416623-1417048	A549	lung:	n/a	n/a
46	NR3C1	chr5:1416405-1417123	A549	lung:	n/a	n/a
47	NR3C1	chr5:1416584-1417068	A549	lung:	n/a	n/a
48	PAX5	chr5:1422262-1423267	GM12878	blood:	n/a	n/a
49	RCOR1	chr5:1419240-1419271	K562	blood:	n/a	n/a
50	RCOR1	chr5:1419124-1419559	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:1431115-1431165	IMR90	lung:	fetal
2	chr5:1431115-1431165	IMR90	lung:	fetal
3	chr5:1430421-1430471	HCPEpiC	choroid plexus:	n/a
4	chr5:1417706-1417756	SK-N-SH_RA	brain:	n/a
5	chr5:1430867-1430917	Jurkat	blood:	n/a
6	chr5:1417003-1417053	LNCaP	prostate:	n/a
7	chr5:1430526-1430576	Jurkat	blood:	n/a
8	chr5:1430526-1430576	ovcar-3	ovarian:	n/a
9	chr5:1430526-1430576	LNCaP	prostate:	n/a
10	chr5:1430526-1430576	GM12891	blood:	n/a
11	chr5:1430421-1430471	ProgFib	skin:	n/a
12	chr5:1420305-1420355	U87	brain:	n/a
13	chr5:1430421-1430471	PANC-1	pancreas:	n/a
14	chr5:1430421-1430471	NT2-D1	testis:	n/a
15	chr5:1416958-1417008	AG10803	skin:	n/a
16	chr5:1431115-1431165	HMEC	breast:	n/a
17	chr5:1416793-1416843	PrEC	prostate:	n/a
18	chr5:1416958-1417008	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:1431115-1431165	SK-N-SH_RA	brain:	n/a
20	chr5:1416793-1416843	NT2-D1	testis:	n/a
21	chr5:1417706-1417756	HRE	kidney:	n/a
22	chr5:1417706-1417756	RPTEC	kidney:	n/a
23	chr5:1416793-1416843	HCM	heart:	n/a
24	chr5:1416793-1416843	HRE	kidney:	n/a
25	chr5:1431115-1431165	Caco-2	colon:	n/a
26	chr5:1430526-1430576	K562	blood:	n/a
27	chr5:1431115-1431165	NB4	blood:	n/a
28	chr5:1416958-1417008	HEK293	kidney:	embryo
29	chr5:1416793-1416843	T-47D	breast:	n/a
30	chr5:1417003-1417053	NHBE	bronchial:	n/a
31	chr5:1416873-1416923	NHBE	bronchial:	n/a
32	chr5:1416873-1416923	NB4	blood:	n/a
33	chr5:1430867-1430917	Hela-S3	cervix:	n/a
34	chr5:1416793-1416843	Hepatocyte	liver:	n/a
35	chr5:1431238-1431288	MCF10A-Er-Src	breast:	n/a
36	chr5:1430867-1430917	HL-60	blood:	n/a
37	chr5:1431115-1431165	GM12892	blood:	n/a
38	chr5:1416958-1417008	GM06990	blood:	n/a
39	chr5:1431238-1431288	GM06990	blood:	n/a
40	chr5:1430867-1430917	HCT-116	colon:	n/a
41	chr5:1430526-1430576	NH-A	brain:	n/a
42	chr5:1430421-1430471	PrEC	prostate:	n/a
43	chr5:1431115-1431165	MCF10A-Er-Src	breast:	n/a
44	chr5:1430526-1430576	U87	brain:	n/a
45	chr5:1431238-1431288	HRE	kidney:	n/a
46	chr5:1416958-1417008	SKMC	muscle:	n/a
47	chr5:1417003-1417053	GM12878	blood:	n/a
48	chr5:1416873-1416923	MCF-7	breast:	n/a
49	chr5:1416958-1417008	LNCaP	prostate:	n/a
50	chr5:1430526-1430576	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:1384483..1386901-chr5:1428744..1431153,3	MCF-7	breast:
2	chr5:1419115..1421419-chr5:1423950..1425563,2	K562	blood:
3	chr5:1425253..1427437-chr5:1431949..1434089,2	K562	blood:
4	chr5:1418661..1420754-chr5:1423796..1425538,2	MCF-7	breast:
5	chr5:1423809..1426140-chr5:1429007..1431319,2	MCF-7	breast:
6	chr5:1418661..1420754-chr5:1423796..1425538,2	MCF-7	breast:
7	chr5:1402687..1404889-chr5:1416990..1419588,2	K562	blood:
8	chr5:1422138..1425666-chr5:1426022..1429297,4	MCF-7	breast:
9	chr5:1430665..1432675-chr5:1438992..1440879,2	K562	blood:
10	chr5:1425253..1427437-chr5:1431949..1434089,2	K562	blood:
11	chr12:125405517..125406294-chr5:1426175..1426675,2	NB4	blood:
12	chr5:1392518..1394719-chr5:1425978..1428854,2	MCF-7	breast:
13	chr5:1422138..1425666-chr5:1426022..1429297,4	MCF-7	breast:
14	chr5:1423809..1426140-chr5:1429007..1431319,2	MCF-7	breast:
15	chr5:1419494..1421652-chr5:1421677..1423510,2	MCF-7	breast:
16	chr5:1429909..1432338-chr5:1439837..1441600,2	MCF-7	breast:
17	chr5:1419494..1421652-chr5:1421677..1423510,2	MCF-7	breast:
18	chr5:1419115..1421419-chr5:1423950..1425563,2	K562	blood:
19	chr5:1425948..1427546-chr5:1434317..1436496,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC6A18-3	chr5:1432580-1432743	NONHSAT100027
2	lnc-SLC6A18-3	chr5:1422018-1422129	NONHSAT100027

Variant related genes	Relation type
SLC6A3	TF binding region
SLC6A3	CpG island

Extended variants
information (count: 708 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2042449	chr5:1416646-1416647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs557524141	chr5:1416679-1416680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs575760136	chr5:1416794-1416795	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs187639860	chr5:1416803-1416804	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs190999831	chr5:1416809-1416810	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs528456927	chr5:1416810-1416811	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
7	rs567356275	chr5:1416823-1416824	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs558089810	chr5:1416839-1416840	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs538089855	chr5:1416843-1416844	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs550118158	chr5:1416851-1416852	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs540614799	chr5:1416873-1416874	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs561966427	chr5:1416874-1416875	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs529997026	chr5:1416879-1416880	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs571225423	chr5:1416886-1416887	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs28382252	chr5:1416894-1416895	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs28382251	chr5:1416898-1416899	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs182844675	chr5:1416903-1416904	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs551821291	chr5:1416904-1416905	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs538622572	chr5:1416928-1416929	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374326523	chr5:1416929-1416930	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs534441063	chr5:1416949-1416950	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs552546547	chr5:1416953-1416954	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs568006602	chr5:1416961-1416962	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs187520063	chr5:1416973-1416974	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs557376621	chr5:1416974-1416975	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs575763220	chr5:1416975-1416976	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs2652524	chr5:1416981-1416982	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs537230412	chr5:1416983-1416984	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs28382250	chr5:1416984-1416985	Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs137989291	chr5:1416989-1416990	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs555877244	chr5:1416999-1417000	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs191676337	chr5:1417004-1417005	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs2617612	chr5:1417007-1417008	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs368585439	chr5:1417037-1417038	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs2963252	chr5:1417047-1417048	Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542060163	chr5:1417050-1417051	Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs2652523	chr5:1417061-1417062	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs563451980	chr5:1417066-1417067	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs530747747	chr5:1417093-1417094	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536002239	chr5:1417095-1417096	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs143574024	chr5:1417103-1417104	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs528166157	chr5:1417109-1417110	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs2859607	chr5:1417116-1417117	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs541425061	chr5:1417149-1417150	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs546389286	chr5:1417164-1417165	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs112611577	chr5:1417186-1417187	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs2735922	chr5:1417187-1417188	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs535129698	chr5:1417211-1417212	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs13161905	chr5:1417212-1417213	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs569552884	chr5:1417214-1417215	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:116)

Disease	PMID	Source
Lung squamous cell carcinoma	22363434	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16608533	CNVD
Cervical cancer	16585170	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	17925434	CNVD
Ovarian cancer	20844748	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	21829676	CNVD
Intracranial ependymoma	16609018	CNVD
Breast cancer	19181860	CNVD
prenatal diagnosis	20453657	CNVD
Developmental delay	19490664	CNVD
Human papillomavirus	17975027	CNVD
Acute monocytic leukemia	16498392	CNVD
Gastric cancer	16891809	CNVD
Intracranial aneurysm	16715129	CNVD
Emphysema	19352772	CNVD
Chordoma	18071362	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Lung cancer	21911935	CNVD
Cri-du chat syndrome	21549014	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
abnormal development	18461090	CNVD
Lung cancer	19547694	CNVD
Cri-du chat syndrome	22283845	CNVD
Disorders of sex development	21048976	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Cancer	16751803	CNVD
Breast cancer	17133270	CNVD
Hepatocellular carcinoma	22174799	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	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
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21509527	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Oral cancer	22144094	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Intellectual disability	22102821	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Multiple myeloma	17550852	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Developmental delay	21147756	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
Ovarian cancer	21720365	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
Prostate cancer	18632612	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Melanoma	22183965	CNVD
Epilepsy	20502679	CNVD
Lung adenocarcinoma	17982442	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Schizophrenia	21346763	CNVD
lymphocytic leukemia	21291569	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1412600-1417200	Weak transcription	Spleen	Spleen
2	chr5:1415600-1418000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:1417200-1417400	Enhancers	Spleen	Spleen
4	chr5:1417400-1417800	Bivalent Enhancer	Right Ventricle	heart
5	chr5:1417400-1418200	ZNF genes & repeats	Spleen	Spleen
6	chr5:1418000-1418400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:1418400-1419800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:1418600-1419200	Active TSS	Fetal Lung	lung
9	chr5:1418800-1419200	Enhancers	Fetal Kidney	kidney
10	chr5:1419800-1420200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:1420000-1421400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr5:1420200-1420600	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:1420200-1421400	Enhancers	Fetal Muscle Leg	muscle
14	chr5:1420400-1421000	Enhancers	Fetal Thymus	thymus
15	chr5:1420400-1421200	Enhancers	HSMMtube	muscle
16	chr5:1420400-1421400	Enhancers	Adipose Nuclei	Adipose
17	chr5:1420600-1420800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr5:1420600-1420800	Active TSS	Gastric	stomach
19	chr5:1420600-1421200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:1420600-1421200	Enhancers	Spleen	Spleen
21	chr5:1420600-1421400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:1420800-1421000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr5:1420800-1421000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
24	chr5:1420800-1421200	Bivalent Enhancer	Placenta	Placenta
25	chr5:1420800-1421200	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr5:1420800-1421400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
27	chr5:1420800-1422000	Weak transcription	Gastric	stomach
28	chr5:1421200-1421800	Weak transcription	Spleen	Spleen
29	chr5:1421600-1422600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr5:1421800-1422200	Active TSS	Spleen	Spleen
31	chr5:1421800-1422400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr5:1422000-1422200	Enhancers	Gastric	stomach
33	chr5:1422200-1424400	Weak transcription	Spleen	Spleen
34	chr5:1422400-1423400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr5:1422600-1424400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr5:1423400-1425200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr5:1423800-1424000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
38	chr5:1424400-1424600	ZNF genes & repeats	Spleen	Spleen
39	chr5:1424400-1424800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:1424800-1425400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr5:1427400-1429400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr5:1428600-1429400	ZNF genes & repeats	Colon Smooth Muscle	Colon
43	chr5:1428600-1429600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
44	chr5:1428600-1429800	ZNF genes & repeats	Adipose Nuclei	Adipose
45	chr5:1428600-1430200	ZNF genes & repeats	Liver	Liver
46	chr5:1428800-1429000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr5:1429200-1429400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr5:1429200-1429400	Bivalent Enhancer	Hela-S3	cervix
49	chr5:1431400-1433000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:1431600-1431800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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