Variant report

Variant	nsv880859
Chromosome Location	chr5:2159490-2190572
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	chr5:2166887-2167061	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr5:2165383-2165567	K562	blood:	n/a	n/a
3	BHLHE40	chr5:2165392-2165603	HepG2	liver:	n/a	n/a
4	CTCF	chr5:2165360-2165490	Fibrobl	skin:	n/a	n/a
5	CTCF	chr5:2166915-2167052	MCF-7	breast:	n/a	n/a
6	CTCF	chr5:2165460-2165499	GM10248	blood:	n/a	n/a
7	CTCF	chr5:2166943-2167028	MCF-7	breast:	n/a	n/a
8	CTCF	chr5:2166909-2167032	MCF-7	breast:	n/a	n/a
9	CTCF	chr5:2166880-2167030	WERI-Rb-1	eye:	n/a	n/a
10	CTCF	chr5:2164000-2164150	GM06990	blood:	n/a	chr5:2164072-2164085
11	CTCF	chr5:2170400-2170550	HEK293	kidney:	n/a	n/a
12	CTCF	chr5:2166891-2167027	MCF-7	breast:	n/a	n/a
13	CTCF	chr5:2164069-2164090	H1-hESC	embryonic stem cell:	n/a	chr5:2164072-2164085
14	CTCF	chr5:2166899-2167044	MCF-7	breast:	n/a	n/a
15	E2F4	chr5:2187356-2187570	MCF10A-Er-Src	breast:	n/a	n/a
16	ELF1	chr5:2183157-2183399	K562	blood:	n/a	chr5:2183276-2183289
17	FOS	chr5:2176782-2177103	MCF10A-Er-Src	breast:	n/a	chr5:2176957-2176965
18	FOS	chr5:2176913-2177002	MCF10A-Er-Src	breast:	n/a	chr5:2176957-2176965
19	FOS	chr5:2187311-2187598	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr5:2187334-2187578	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr5:2176804-2177087	MCF10A-Er-Src	breast:	n/a	chr5:2176957-2176965
22	FOS	chr5:2187322-2187614	MCF10A-Er-Src	breast:	n/a	n/a
23	FOSL2	chr5:2176728-2177211	MCF-7	breast:	n/a	chr5:2176957-2176965
24	GATA3	chr5:2176669-2177293	MCF-7	breast:	n/a	chr5:2176958-2176967 chr5:2176979-2176988
25	GATA3	chr5:2176526-2177427	MCF-7	breast:	n/a	chr5:2176958-2176967 chr5:2176979-2176988
26	GATA3	chr5:2176756-2177114	T-47D	breast:	n/a	chr5:2176958-2176967 chr5:2176979-2176988
27	MAFK	chr5:2184087-2184396	HepG2	liver:	n/a	chr5:2184245-2184256 chr5:2184240-2184256 chr5:2184244-2184255 chr5:2184240-2184255
28	MAFK	chr5:2184165-2184389	HepG2	liver:	n/a	chr5:2184245-2184256 chr5:2184240-2184256 chr5:2184244-2184255 chr5:2184240-2184255
29	MAX	chr5:2165274-2165584	NB4	blood:	n/a	chr5:2165482-2165492 chr5:2165446-2165456
30	MAX	chr5:2165339-2165572	K562	blood:	n/a	chr5:2165482-2165492 chr5:2165446-2165456
31	MAX	chr5:2189350-2189501	NB4	blood:	n/a	chr5:2189474-2189484
32	MAX	chr5:2165325-2165582	HepG2	liver:	n/a	chr5:2165482-2165492 chr5:2165446-2165456
33	MAX	chr5:2165390-2165503	Hela-S3	cervix:	n/a	chr5:2165482-2165492 chr5:2165446-2165456
34	MAX	chr5:2165280-2165637	A549	lung:	n/a	chr5:2165482-2165492 chr5:2165446-2165456
35	MYC	chr5:2165387-2165456	HUVEC	blood vessel:	n/a	chr5:2165446-2165456
36	NR2F2	chr5:2176811-2177129	MCF-7	breast:	n/a	n/a
37	POLR2A	chr5:2181458-2181483	Gliobla	brain:	n/a	n/a
38	POLR2A	chr5:2178135-2178290	MCF-7	breast:	n/a	n/a
39	POLR2A	chr5:2165453-2165464	MCF-7	breast:	n/a	n/a
40	POLR2A	chr5:2170486-2170600	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr5:2185032-2185260	H1-hESC	embryonic stem cell:	n/a	n/a
42	POLR2A	chr5:2185118-2185308	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr5:2165385-2165451	MCF-7	breast:	n/a	n/a
44	RAD21	chr5:2178834-2179147	H1-hESC	embryonic stem cell:	n/a	n/a
45	REST	chr5:2170507-2170678	H1-hESC	embryonic stem cell:	n/a	chr5:2170591-2170598 chr5:2170597-2170617 chr5:2170597-2170617 chr5:2170600-2170613 chr5:2170603-2170617 chr5:2170598-2170616
46	RFX5	chr5:2189616-2189659	K562	blood:	n/a	n/a
47	SRF	chr5:2180297-2180435	GM12878	blood:	n/a	n/a
48	TCF7L2	chr5:2176750-2177227	MCF-7	breast:	n/a	chr5:2176910-2176917
49	USF1	chr5:2183183-2183384	H1-hESC	embryonic stem cell:	n/a	n/a
50	USF1	chr5:2183179-2183419	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:2186856-2186906	HCPEpiC	choroid plexus:	n/a
2	chr5:2186856-2186906	HCPEpiC	choroid plexus:	n/a
3	chr5:2169402-2169452	BJ	skin:	n/a
4	chr5:2169769-2169819	HRPEpiC	eye:	n/a
5	chr5:2170036-2170086	Hepatocyte	liver:	n/a
6	chr5:2184062-2184112	NH-A	brain:	n/a
7	chr5:2179563-2179613	HAEpiC	amniotic membrane:	n/a
8	chr5:2179563-2179613	HCM	heart:	n/a
9	chr5:2176047-2176097	HCF	heart:	n/a
10	chr5:2187004-2187054	AoSMC	blood vessel:	n/a
11	chr5:2176047-2176097	NH-A	brain:	n/a
12	chr5:2169402-2169452	AG04449	skin:	fetal
13	chr5:2180505-2180555	HCPEpiC	choroid plexus:	n/a
14	chr5:2175315-2175365	AG04450	lung:	fetal
15	chr5:2180824-2180874	HCT-116	colon:	n/a
16	chr5:2186371-2186421	LNCaP	prostate:	n/a
17	chr5:2170490-2170540	HepG2	liver:	n/a
18	chr5:2165422-2165472	NB4	blood:	n/a
19	chr5:2187004-2187054	NB4	blood:	n/a
20	chr5:2169729-2169779	GM19239	blood:	n/a
21	chr5:2180505-2180555	GM06990	blood:	n/a
22	chr5:2176142-2176192	NHDF-neo	bronchial:	n/a
23	chr5:2170490-2170540	AG10803	skin:	n/a
24	chr5:2176047-2176097	NHDF-neo	bronchial:	n/a
25	chr5:2169371-2169421	NHBE	bronchial:	n/a
26	chr5:2175315-2175365	T-47D	breast:	n/a
27	chr5:2186972-2187022	HRE	kidney:	n/a
28	chr5:2180252-2180302	MCF-7	breast:	n/a
29	chr5:2177644-2177694	CMK	blood:	n/a
30	chr5:2165422-2165472	SAEC	small airway:	n/a
31	chr5:2170036-2170086	HCM	heart:	n/a
32	chr5:2184062-2184112	HEK293	kidney:	embryo
33	chr5:2169769-2169819	AG09319	gingival:	n/a
34	chr5:2184062-2184112	GM12891	blood:	n/a
35	chr5:2176142-2176192	BJ	skin:	n/a
36	chr5:2175315-2175365	U87	brain:	n/a
37	chr5:2186659-2186709	MCF-7	breast:	n/a
38	chr5:2180418-2180468	MCF-7	breast:	n/a
39	chr5:2169402-2169452	A549	lung:	n/a
40	chr5:2165422-2165472	T-47D	breast:	n/a
41	chr5:2169815-2169865	AG04449	skin:	fetal
42	chr5:2169769-2169819	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:2186659-2186709	HEEpiC	esophagus:	n/a
44	chr5:2180418-2180468	AG10803	skin:	n/a
45	chr5:2186371-2186421	PANC-1	pancreas:	n/a
46	chr5:2170490-2170540	AG04449	skin:	fetal
47	chr5:2169371-2169421	RPTEC	kidney:	n/a
48	chr5:2186659-2186709	SK-N-SH	brain:	n/a
49	chr5:2170490-2170540	NH-A	brain:	n/a
50	chr5:2180418-2180468	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:2157501..2159114-chr5:2160612..2162756,2	K562	blood:
2	chr5:2147549..2149132-chr5:2161047..2163097,2	K562	blood:
3	chr5:2176104..2179198-chr5:2180274..2184546,3	K562	blood:
4	chr5:2177408..2179073-chr5:2187197..2190154,2	MCF-7	breast:
5	chr5:2164885..2167443-chr5:2167494..2169230,2	K562	blood:
6	chr5:2158940..2162569-chr5:2167840..2169762,3	K562	blood:
7	chr5:2172730..2175692-chr5:2193909..2195679,2	K562	blood:
8	chr5:2176104..2179198-chr5:2180274..2184546,3	K562	blood:
9	chr5:2164885..2167443-chr5:2167494..2169230,2	K562	blood:
10	chr5:2158940..2162569-chr5:2167840..2169762,3	K562	blood:
11	chr5:2177408..2179073-chr5:2187197..2190154,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000201026	TF binding region
ENSG00000201026	CpG island

Extended variants
information (count: 1464 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10072352	chr5:2159490-2159491	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs548306135	chr5:2159494-2159495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs569860730	chr5:2159559-2159560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530656221	chr5:2159637-2159638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552427784	chr5:2159644-2159645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs544613557	chr5:2159674-2159675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs570628456	chr5:2159675-2159676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375166142	chr5:2159677-2159678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553374304	chr5:2159784-2159785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs562715622	chr5:2159785-2159786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10065776	chr5:2159807-2159808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs115643814	chr5:2159814-2159815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs536344364	chr5:2159818-2159819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554684939	chr5:2159821-2159822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145876093	chr5:2159854-2159855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543682032	chr5:2159870-2159871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs62328177	chr5:2159914-2159915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs376693701	chr5:2159938-2159939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557046139	chr5:2159954-2159955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558678736	chr5:2159965-2159966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370217022	chr5:2159967-2159968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190453157	chr5:2159993-2159994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149222025	chr5:2160016-2160017	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs559342566	chr5:2160020-2160021	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs529758459	chr5:2160026-2160027	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs576781380	chr5:2160031-2160032	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs182751439	chr5:2160037-2160038	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs113462284	chr5:2160057-2160058	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs530653270	chr5:2160063-2160064	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs552054513	chr5:2160085-2160086	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs570638561	chr5:2160088-2160089	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs186708301	chr5:2160098-2160099	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs147982738	chr5:2160117-2160118	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs565729373	chr5:2160119-2160120	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs536281398	chr5:2160123-2160124	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs4358531	chr5:2160134-2160135	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs191091913	chr5:2160145-2160146	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs537567852	chr5:2160179-2160180	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs183042297	chr5:2160212-2160213	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs370001070	chr5:2160214-2160215	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs577368807	chr5:2160235-2160236	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs143482876	chr5:2160240-2160241	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs147177800	chr5:2160244-2160245	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs12654394	chr5:2160336-2160337	Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs113840795	chr5:2160339-2160340	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs529664798	chr5:2160354-2160355	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs575120402	chr5:2160363-2160364	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs187569295	chr5:2160461-2160462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192542560	chr5:2160474-2160475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13162706	chr5:2160491-2160492	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:111)

Disease	PMID	Source
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	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	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
Breast cancer	21364760	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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:129 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:2150200-2160000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:2158000-2171000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr5:2159800-2160200	Weak transcription	Esophagus	oesophagus
4	chr5:2160000-2160400	Active TSS	Spleen	Spleen
5	chr5:2163200-2164600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:2163200-2166200	Enhancers	H1 Cell Line	embryonic stem cell
7	chr5:2163400-2163600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr5:2163400-2163600	Bivalent Enhancer	Right Ventricle	heart
9	chr5:2163400-2166200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr5:2163600-2164200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr5:2163600-2165000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr5:2163800-2164000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
13	chr5:2163800-2165200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr5:2163800-2165400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr5:2163800-2165600	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr5:2163800-2165800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr5:2164000-2164600	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
18	chr5:2164000-2165000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chr5:2164000-2166200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
20	chr5:2164200-2165200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr5:2164400-2165800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr5:2164600-2164800	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
23	chr5:2164600-2165000	Bivalent Enhancer	Fetal Stomach	stomach
24	chr5:2164600-2165400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr5:2164800-2165800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
26	chr5:2165000-2165400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:2165200-2165600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr5:2165400-2165600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
29	chr5:2165400-2165600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
30	chr5:2165400-2166800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:2165400-2171000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr5:2165600-2166000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr5:2165600-2176200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr5:2165800-2166000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
35	chr5:2165800-2166000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr5:2165800-2166400	Bivalent Enhancer	Right Ventricle	heart
37	chr5:2166200-2167200	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr5:2166800-2167400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:2167200-2167400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr5:2167400-2170400	Weak transcription	H1 Cell Line	embryonic stem cell
41	chr5:2167400-2170400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:2168800-2169000	Bivalent Enhancer	Hela-S3	cervix
43	chr5:2168800-2170600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
44	chr5:2169000-2169400	Bivalent Enhancer	Fetal Muscle Leg	muscle
45	chr5:2169200-2169400	Bivalent Enhancer	Fetal Kidney	kidney
46	chr5:2169200-2169400	Bivalent Enhancer	Fetal Lung	lung
47	chr5:2169200-2170200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr5:2169400-2170800	Bivalent Enhancer	Fetal Stomach	stomach
49	chr5:2170200-2170400	Bivalent Enhancer	Brain Germinal Matrix	brain
50	chr5:2170200-2170400	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland

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