Variant report

Variant	nsv1034311
Chromosome Location	chr5:59193517-59257171
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:201)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:201 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr5:59254698-59255037	GM12878	blood:	n/a	n/a
2	BATF	chr5:59233475-59233811	GM12878	blood:	n/a	n/a
3	BATF	chr5:59233497-59233778	GM12878	blood:	n/a	n/a
4	BCL11A	chr5:59200990-59201371	GM12878	blood:	n/a	n/a
5	CEBPB	chr5:59219392-59219534	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr5:59248870-59248976	A549	lung:	n/a	n/a
7	CEBPB	chr5:59206397-59206520	Hela-S3	cervix:	n/a	chr5:59206458-59206469 chr5:59206458-59206467
8	CHD2	chr5:59218334-59218341	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr5:59217708-59217917	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr5:59217858-59217860	GM12878	blood:	n/a	n/a
11	CHD2	chr5:59232866-59232942	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr5:59219440-59219590	AG10803	skin:	n/a	n/a
13	CTCF	chr5:59219400-59219550	HAc	cerebellar:	n/a	n/a
14	CTCF	chr5:59219413-59219568	Medullo	brain:	n/a	n/a
15	CTCF	chr5:59219260-59219410	HMEC	breast:	n/a	n/a
16	CTCF	chr5:59219420-59219552	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr5:59219380-59219530	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr5:59219440-59219590	HMEC	breast:	n/a	n/a
19	CTCF	chr5:59249985-59250027	GM20000	blood:	n/a	n/a
20	CTCF	chr5:59219420-59219570	Caco-2	colon:	n/a	n/a
21	CTCF	chr5:59219640-59219790	AG10803	skin:	n/a	n/a
22	CTCF	chr5:59219440-59219590	MCF-7	breast:	n/a	n/a
23	CTCF	chr5:59219400-59219550	AG04449	skin:	n/a	n/a
24	CTCF	chr5:59219416-59219561	A549	lung:	n/a	n/a
25	CTCF	chr5:59219244-59219693	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:59219400-59219550	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr5:59219340-59219490	HFF-Myc	foreskin:	n/a	n/a
28	CTCF	chr5:59219374-59219622	Gliobla	brain:	n/a	n/a
29	CTCF	chr5:59219360-59219510	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr5:59219378-59219606	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr5:59219413-59219606	MCF-7	breast:	n/a	n/a
32	CTCF	chr5:59219400-59219550	HFF	foreskin:	n/a	n/a
33	CTCF	chr5:59219400-59219550	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr5:59219400-59219550	AG09319	gingival:	n/a	n/a
35	CTCF	chr5:59219540-59219690	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr5:59219440-59219590	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr5:59219400-59219550	HCM	heart:	n/a	n/a
38	CTCF	chr5:59219455-59219536	Lung_OC	lung:	n/a	n/a
39	CTCF	chr5:59219500-59219650	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr5:59219438-59219533	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr5:59219380-59219530	SAEC	small airway:	n/a	n/a
42	CTCF	chr5:59219400-59219550	BJ	skin:	n/a	n/a
43	CTCF	chr5:59219225-59219615	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:59219440-59219590	AG09319	gingival:	n/a	n/a
45	CTCF	chr5:59219400-59219550	HPF	lung:	n/a	n/a
46	CTCF	chr5:59219420-59219547	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:59219380-59219530	HEK293	kidney:	n/a	n/a
48	CTCF	chr5:59219440-59219590	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr5:59219433-59219568	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:59219440-59219590	BE2_C	brain:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:59193490-59193540	MCF10A-Er-Src	breast:	n/a
2	chr5:59193490-59193540	Caco-2	colon:	n/a
3	chr5:59193490-59193540	ovcar-3	ovarian:	n/a
4	chr5:59193490-59193540	GM19239	blood:	n/a
5	chr5:59193490-59193540	HIPEpiC	eye:	n/a
6	chr5:59193490-59193540	H1-hESC	embryonic stem cell:	embryo
7	chr5:59193490-59193540	HAEpiC	amniotic membrane:	n/a
8	chr5:59193490-59193540	SK-N-SH_RA	brain:	n/a
9	chr5:59193490-59193540	HCF	heart:	n/a
10	chr5:59193490-59193540	A549	lung:	n/a
11	chr5:59193490-59193540	U87	brain:	n/a
12	chr5:59193490-59193540	RPTEC	kidney:	n/a
13	chr5:59193490-59193540	HEEpiC	esophagus:	n/a
14	chr5:59193490-59193540	HCT-116	colon:	n/a
15	chr5:59193490-59193540	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:59193490-59193540	GM06990	blood:	n/a
17	chr5:59193490-59193540	GM12891	blood:	n/a
18	chr5:59193490-59193540	K562	blood:	n/a
19	chr5:59193490-59193540	HMEC	breast:	n/a
20	chr5:59193490-59193540	Hela-S3	cervix:	n/a
21	chr5:59193490-59193540	PrEC	prostate:	n/a
22	chr5:59193490-59193540	GM12892	blood:	n/a
23	chr5:59193490-59193540	HRCEpiC	kidney:	n/a
24	chr5:59193490-59193540	CMK	blood:	n/a
25	chr5:59193490-59193540	HRPEpiC	eye:	n/a
26	chr5:59193490-59193540	HUVEC	blood vessel:	n/a
27	chr5:59193490-59193540	PANC-1	pancreas:	n/a
28	chr5:59193490-59193540	AG09309	skin:	n/a
29	chr5:59193490-59193540	AG10803	skin:	n/a
30	chr5:59193490-59193540	IMR90	lung:	fetal
31	chr5:59193490-59193540	Jurkat	blood:	n/a
32	chr5:59193490-59193540	AG04450	lung:	fetal
33	chr5:59193490-59193540	Hepatocyte	liver:	n/a
34	chr5:59193490-59193540	HL-60	blood:	n/a
35	chr5:59193490-59193540	SK-N-MC	brain:	n/a
36	chr5:59193490-59193540	HRE	kidney:	n/a
37	chr5:59193490-59193540	SKMC	muscle:	n/a
38	chr5:59193490-59193540	HepG2	liver:	n/a
39	chr5:59193490-59193540	NB4	blood:	n/a
40	chr5:59193490-59193540	AoSMC	blood vessel:	n/a
41	chr5:59193490-59193540	GM12878	blood:	n/a
42	chr5:59193490-59193540	HNPCEpiC	eye:	n/a
43	chr5:59193490-59193540	NHBE	bronchial:	n/a
44	chr5:59193490-59193540	HCPEpiC	choroid plexus:	n/a
45	chr5:59193490-59193540	HEK293	kidney:	embryo
46	chr5:59193490-59193540	NH-A	brain:	n/a
47	chr5:59193490-59193540	SAEC	small airway:	n/a
48	chr5:59193490-59193540	AG04449	skin:	fetal
49	chr5:59193490-59193540	NT2-D1	testis:	n/a
50	chr5:59193490-59193540	T-47D	breast:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:59109451..59110017-chr5:59219079..59219734,2	MCF-7	breast:
2	chr5:59196889..59199265-chr5:59202553..59204106,2	K562	blood:
3	chr5:59235055..59237552-chr5:59238015..59240745,2	MCF-7	breast:
4	chr5:59200694..59202492-chr5:59202727..59205702,2	K562	blood:
5	chr5:59204919..59207898-chr5:59228269..59230906,2	K562	blood:
6	chr5:59196889..59199265-chr5:59202553..59204106,2	K562	blood:
7	chr5:59235055..59237552-chr5:59238015..59240745,2	MCF-7	breast:
8	chr5:59200694..59202492-chr5:59202727..59205702,2	K562	blood:
9	chr5:59204919..59207898-chr5:59228269..59230906,2	K562	blood:

No data

Variant related genes	Relation type
PDE4D	TF binding region
PDE4D	CpG island

Extended variants
information (count: 2070 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:2070 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6894929	chr5:59193517-59193518	Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs173942	chr5:59193562-59193563	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs547248547	chr5:59193573-59193574	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs567083341	chr5:59193598-59193599	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs568972523	chr5:59193618-59193619	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs189400237	chr5:59193640-59193641	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs374540975	chr5:59193647-59193648	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs60359678	chr5:59193678-59193679	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs181371490	chr5:59193680-59193681	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs537088766	chr5:59193700-59193701	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs6868845	chr5:59193702-59193703	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs556681638	chr5:59193763-59193764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs576900614	chr5:59193802-59193803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1546364	chr5:59193824-59193825	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs546756916	chr5:59193869-59193870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367998294	chr5:59193870-59193871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs185829571	chr5:59193886-59193887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs73761040	chr5:59193973-59193974	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs541580337	chr5:59193988-59193989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113643639	chr5:59193989-59193990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs74430042	chr5:59193997-59193998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575442122	chr5:59193998-59193999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369904646	chr5:59194017-59194018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77473969	chr5:59194091-59194092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs558320497	chr5:59194104-59194105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs544619839	chr5:59194176-59194177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564306397	chr5:59194180-59194181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs533328123	chr5:59194229-59194230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs568520485	chr5:59194262-59194263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73761042	chr5:59194263-59194264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs75601850	chr5:59194274-59194275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549300370	chr5:59194296-59194297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs537411972	chr5:59194303-59194304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569580367	chr5:59194307-59194308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75295972	chr5:59194331-59194332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs550586952	chr5:59194361-59194362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570129605	chr5:59194366-59194367	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs143284926	chr5:59194394-59194395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs552655350	chr5:59194426-59194427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566192245	chr5:59194470-59194471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535308587	chr5:59194544-59194545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374817827	chr5:59194553-59194554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74395775	chr5:59194679-59194680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554833345	chr5:59194683-59194684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs151132687	chr5:59194721-59194722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544193761	chr5:59194774-59194775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566694867	chr5:59194775-59194776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs558001526	chr5:59194776-59194777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533942653	chr5:59194783-59194784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs578072323	chr5:59194801-59194802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	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
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	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
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:59193000-59200800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:59194200-59194400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:59197000-59197200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr5:59200800-59201200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr5:59201200-59202000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr5:59201200-59202200	Active TSS	Pancreatic Islets	Pancreatic Islet
7	chr5:59202200-59202400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr5:59206400-59278800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr5:59209000-59210600	Weak transcription	Aorta	Aorta
10	chr5:59210600-59210800	Enhancers	Aorta	Aorta
11	chr5:59215000-59215600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr5:59215000-59215600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:59215000-59215800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr5:59215200-59215600	Enhancers	Primary hematopoietic stem cells	blood
15	chr5:59215600-59218200	Weak transcription	Primary hematopoietic stem cells	blood
16	chr5:59216400-59216800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr5:59216800-59217200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr5:59217000-59218600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr5:59217200-59218600	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr5:59217400-59218200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr5:59217400-59218800	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr5:59217400-59218800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr5:59217600-59218200	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr5:59217600-59218600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr5:59217800-59218400	Enhancers	H1 Cell Line	embryonic stem cell
26	chr5:59217800-59218400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:59217800-59218400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:59217800-59218600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr5:59217800-59218600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr5:59217800-59219000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr5:59218000-59218400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr5:59218200-59218600	Enhancers	Primary hematopoietic stem cells	blood
33	chr5:59218200-59218600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr5:59218200-59218800	Enhancers	Adipose Nuclei	Adipose
35	chr5:59218400-59219200	Enhancers	Hela-S3	cervix
36	chr5:59218600-59219400	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr5:59219400-59221000	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr5:59223200-59223800	Enhancers	Fetal Brain Male	brain
39	chr5:59223200-59224000	Enhancers	Brain Germinal Matrix	brain
40	chr5:59223600-59224000	Enhancers	Cortex derived primary cultured neurospheres	brain
41	chr5:59232200-59232800	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr5:59232600-59232800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr5:59232600-59233400	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:59237600-59238800	Enhancers	Adipose Nuclei	Adipose
45	chr5:59238400-59242800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr5:59238800-59239600	Weak transcription	Adipose Nuclei	Adipose
47	chr5:59239400-59239800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr5:59239400-59240000	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr5:59239400-59240000	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr5:59239600-59239800	Active TSS	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links