Variant report

Variant	nsv1015892
Chromosome Location	chr5:101633610-101730439
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr5:101697133-101697334	A549	lung:	n/a	chr5:101697241-101697252
2	CEBPB	chr5:101697172-101697382	HepG2	liver:	n/a	chr5:101697241-101697252
3	CEBPB	chr5:101697160-101697335	H1-hESC	embryonic stem cell:	n/a	chr5:101697241-101697252
4	CEBPB	chr5:101697180-101697573	Hela-S3	cervix:	n/a	chr5:101697241-101697252
5	CEBPB	chr5:101634700-101635037	HepG2	liver:	n/a	chr5:101634861-101634872
6	CEBPB	chr5:101677430-101678074	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr5:101711009-101711381	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr5:101707622-101707804	HepG2	liver:	n/a	n/a
9	CEBPB	chr5:101634828-101635028	A549	lung:	n/a	chr5:101634861-101634872
10	CEBPB	chr5:101648276-101648476	HepG2	liver:	n/a	n/a
11	CTCF	chr5:101656210-101656244	Lung_OC	lung:	n/a	n/a
12	CTCF	chr5:101635940-101635968	GM19239	blood:	n/a	n/a
13	CTCF	chr5:101713573-101713670	GM10248	blood:	n/a	n/a
14	CTCF	chr5:101691750-101691798	Medullo	brain:	n/a	n/a
15	CTCF	chr5:101635957-101635977	A549	lung:	n/a	n/a
16	CTCF	chr5:101680400-101680550	GM12874	blood:	n/a	n/a
17	CTCF	chr5:101705640-101705746	Kidney_OC	kidney:	n/a	n/a
18	CTCF	chr5:101664920-101665070	GM12870	blood:	n/a	n/a
19	CTCF	chr5:101649235-101649271	GM13976	blood:	n/a	n/a
20	CTCF	chr5:101635941-101635978	MCF-7	breast:	n/a	n/a
21	CTCF	chr5:101655625-101655678	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr5:101721932-101721948	GM10266	blood:	n/a	n/a
23	CTCF	chr5:101635941-101635977	GM12891	blood:	n/a	n/a
24	CTCF	chr5:101675920-101676070	GM12869	blood:	n/a	n/a
25	CTCF	chr5:101635940-101636030	MCF-7	breast:	n/a	n/a
26	CTCF	chr5:101680427-101680490	GM13977	blood:	n/a	n/a
27	CTCF	chr5:101655320-101655470	RPTEC	kidney:	n/a	n/a
28	CTCF	chr5:101706800-101706950	AG09309	skin:	n/a	n/a
29	CTCF	chr5:101682904-101682957	GM10248	blood:	n/a	n/a
30	CTCF	chr5:101655640-101655790	RPTEC	kidney:	n/a	n/a
31	CTCF	chr5:101722500-101722650	GM12869	blood:	n/a	n/a
32	CTCF	chr5:101680400-101680550	RPTEC	kidney:	n/a	n/a
33	CTCF	chr5:101652802-101652851	GM10248	blood:	n/a	n/a
34	CTCF	chr5:101680500-101680650	RPTEC	kidney:	n/a	n/a
35	E2F4	chr5:101648320-101648506	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr5:101633554-101633663	MCF10A-Er-Src	breast:	n/a	n/a
37	E2F4	chr5:101672740-101672851	MCF10A-Er-Src	breast:	n/a	n/a
38	EP300	chr5:101677481-101678036	SK-N-SH_RA	brain:	n/a	n/a
39	EP300	chr5:101660326-101660817	SK-N-SH_RA	brain:	n/a	n/a
40	EP300	chr5:101649530-101650039	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr5:101660114-101661341	SK-N-SH	brain:	n/a	chr5:101661239-101661253 chr5:101661240-101661254 chr5:101660176-101660183
42	EP300	chr5:101711063-101711367	Hela-S3	cervix:	n/a	n/a
43	EP300	chr5:101649599-101649991	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr5:101697306-101697564	Hela-S3	cervix:	n/a	chr5:101697421-101697429
45	EP300	chr5:101639500-101639514	K562	blood:	n/a	n/a
46	EP300	chr5:101660426-101660868	SK-N-SH_RA	brain:	n/a	n/a
47	EP300	chr5:101677473-101678071	SK-N-SH_RA	brain:	n/a	n/a
48	EP300	chr5:101676659-101678367	SK-N-SH	brain:	n/a	n/a
49	EP300	chr5:101649301-101651275	SK-N-SH	brain:	n/a	chr5:101650291-101650301
50	FOS	chr5:101715881-101716150	MCF10A-Er-Src	breast:	n/a	chr5:101716057-101716067 chr5:101716056-101716068 chr5:101716058-101716067 chr5:101716058-101716066 chr5:101716059-101716066 chr5:101716057-101716066

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:101634495-101634545	HIPEpiC	eye:	n/a
2	chr5:101634495-101634545	SKMC	muscle:	n/a
3	chr5:101634495-101634545	Jurkat	blood:	n/a
4	chr5:101634495-101634545	SK-N-MC	brain:	n/a
5	chr5:101634495-101634545	HL-60	blood:	n/a
6	chr5:101634495-101634545	NHBE	bronchial:	n/a
7	chr5:101634495-101634545	HNPCEpiC	eye:	n/a
8	chr5:101634495-101634545	LNCaP	prostate:	n/a
9	chr5:101634495-101634545	GM19239	blood:	n/a
10	chr5:101634495-101634545	HEEpiC	esophagus:	n/a
11	chr5:101634495-101634545	NHDF-neo	bronchial:	n/a
12	chr5:101634495-101634545	HCF	heart:	n/a
13	chr5:101634495-101634545	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:101634495-101634545	GM12891	blood:	n/a
15	chr5:101634495-101634545	ProgFib	skin:	n/a
16	chr5:101634495-101634545	H1-hESC	embryonic stem cell:	embryo
17	chr5:101634495-101634545	IMR90	lung:	fetal
18	chr5:101634495-101634545	HAEpiC	amniotic membrane:	n/a
19	chr5:101634495-101634545	HCT-116	colon:	n/a
20	chr5:101634495-101634545	PANC-1	pancreas:	n/a
21	chr5:101634495-101634545	MCF-7	breast:	n/a
22	chr5:101634495-101634545	AG04450	lung:	fetal
23	chr5:101634495-101634545	SK-N-SH_RA	brain:	n/a
24	chr5:101634495-101634545	GM12878	blood:	n/a
25	chr5:101634495-101634545	MCF10A-Er-Src	breast:	n/a
26	chr5:101634495-101634545	NB4	blood:	n/a
27	chr5:101634495-101634545	RPTEC	kidney:	n/a
28	chr5:101634495-101634545	U87	brain:	n/a
29	chr5:101634495-101634545	HRE	kidney:	n/a
30	chr5:101634495-101634545	PrEC	prostate:	n/a
31	chr5:101634495-101634545	HRCEpiC	kidney:	n/a
32	chr5:101634495-101634545	BJ	skin:	n/a
33	chr5:101634495-101634545	T-47D	breast:	n/a
34	chr5:101634495-101634545	GM12892	blood:	n/a
35	chr5:101634495-101634545	HCPEpiC	choroid plexus:	n/a
36	chr5:101634495-101634545	HCM	heart:	n/a
37	chr5:101634495-101634545	SK-N-SH	brain:	n/a
38	chr5:101634495-101634545	GM06990	blood:	n/a
39	chr5:101634495-101634545	Hela-S3	cervix:	n/a
40	chr5:101634495-101634545	ovcar-3	ovarian:	n/a
41	chr5:101634495-101634545	CMK	blood:	n/a
42	chr5:101634495-101634545	HepG2	liver:	n/a
43	chr5:101634495-101634545	HMEC	breast:	n/a
44	chr5:101634495-101634545	ECC-1	luminal epithelium:	n/a
45	chr5:101634495-101634545	AG10803	skin:	n/a
46	chr5:101634495-101634545	AG09309	skin:	n/a
47	chr5:101634495-101634545	HRPEpiC	eye:	n/a
48	chr5:101634495-101634545	A549	lung:	n/a
49	chr5:101634495-101634545	NH-A	brain:	n/a
50	chr5:101634495-101634545	AG09319	gingival:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:101695964..101697659-chr5:101699587..101702225,2	K562	blood:
2	chr5:101725894..101726537-chr6:67534604..67535331,2	MCF-7	breast:
3	chr5:101709356..101712161-chr5:101716526..101719065,2	MCF-7	breast:
4	chr5:101709356..101712161-chr5:101716526..101719065,2	MCF-7	breast:
5	chr5:101695964..101697659-chr5:101699587..101702225,2	K562	blood:
6	chr5:101721756..101723696-chr5:101735841..101738611,2	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLCO4C1-1	chr5:101709041-101709198	NONHSAT103025
2	lnc-SLCO4C1-1	chr5:101707649-101707775	NONHSAT103025
3	lnc-SLCO4C1-1	chr5:101726685-101726933	NONHSAT103025
4	lnc-PAM-7	chr5:101638208-101638514	NONHSAT103024
5	lnc-SLCO4C1-1	chr5:101724392-101724529	NONHSAT103025

No data

Variant related genes	Relation type
RN7SKP68	TF binding region
SLCO6A1	TF binding region
SLCO4C1	TF binding region
RN7SKP68	CpG island
SLCO6A1	CpG island
SLCO4C1	CpG island

Extended variants
information (count: 1258 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1258 , 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	rs896545	chr5:101633610-101633611	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs569974071	chr5:101633643-101633644	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs144609197	chr5:101633664-101633665	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs529198058	chr5:101633747-101633748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547268123	chr5:101633751-101633752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565931054	chr5:101633793-101633794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs543158119	chr5:101633841-101633842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188062469	chr5:101633867-101633868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs192650213	chr5:101633869-101633870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184491235	chr5:101633871-101633872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569780504	chr5:101633885-101633886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564528522	chr5:101633953-101633954	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs536612628	chr5:101633963-101633964	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs555342494	chr5:101633967-101633968	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs190601470	chr5:101634015-101634016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536184793	chr5:101634022-101634023	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553941368	chr5:101634045-101634046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572331362	chr5:101634053-101634054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546004420	chr5:101634058-101634059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs532016658	chr5:101634111-101634112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78081330	chr5:101634112-101634113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs138355209	chr5:101634160-101634161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373445110	chr5:101634169-101634170	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs559413039	chr5:101634252-101634253	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs10479191	chr5:101634271-101634272	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs562155778	chr5:101634274-101634275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs529174498	chr5:101634306-101634307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192687626	chr5:101634390-101634391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371095740	chr5:101634435-101634436	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs184937754	chr5:101634436-101634437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs533124651	chr5:101634482-101634483	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs551622362	chr5:101634511-101634512	Weak transcription Enhancers Flanking Active TSS	CpG island	2 gene(s)	Overlapped CNVs	n/a
33	rs188921750	chr5:101634541-101634542	Weak transcription Enhancers Flanking Active TSS	CpG island	2 gene(s)	Overlapped CNVs	n/a
34	rs57977588	chr5:101634545-101634546	Weak transcription Enhancers Flanking Active TSS	CpG island	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs570118146	chr5:101634560-101634561	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs181657155	chr5:101634572-101634573	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs59934563	chr5:101634575-101634576	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs62372171	chr5:101634577-101634578	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs535751670	chr5:101634641-101634642	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs73774617	chr5:101634645-101634646	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs185601307	chr5:101634646-101634647	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs553596687	chr5:101634655-101634656	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs149276384	chr5:101634710-101634711	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs537347579	chr5:101634716-101634717	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs189722176	chr5:101634758-101634759	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs56881277	chr5:101634770-101634771	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs180847575	chr5:101634771-101634772	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs569521575	chr5:101634784-101634785	Weak transcription Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs555456036	chr5:101634801-101634802	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs574015315	chr5:101634894-101634895	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
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
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101632600-101649200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:101632800-101634200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr5:101632800-101634200	Weak transcription	Liver	Liver
4	chr5:101632800-101634400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr5:101633000-101634400	Weak transcription	HepG2	liver
6	chr5:101633200-101634200	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr5:101633200-101635000	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr5:101634200-101634400	Enhancers	Liver	Liver
9	chr5:101634200-101635000	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr5:101634400-101634800	Flanking Active TSS	Liver	Liver
11	chr5:101634400-101635000	Enhancers	HepG2	liver
12	chr5:101634800-101635400	Enhancers	Liver	Liver
13	chr5:101642200-101643200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr5:101642200-101643800	Enhancers	Brain Germinal Matrix	brain
15	chr5:101647400-101649400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:101647800-101648800	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr5:101647800-101651600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr5:101648000-101648800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:101648000-101649000	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr5:101648000-101649800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:101648200-101648600	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr5:101648400-101648600	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr5:101648400-101650800	Enhancers	Primary hematopoietic stem cells	blood
24	chr5:101648600-101649600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr5:101648600-101654000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr5:101648800-101653800	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr5:101649000-101654200	Weak transcription	Primary monocytes fromperipheralblood	blood
28	chr5:101649200-101649800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr5:101649600-101649800	Enhancers	Placenta	Placenta
30	chr5:101649600-101649800	Enhancers	Left Ventricle	heart
31	chr5:101649600-101650800	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr5:101649800-101650200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr5:101649800-101650200	Enhancers	Hela-S3	cervix
34	chr5:101650200-101651200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:101650800-101651800	Weak transcription	Primary hematopoietic stem cells	blood
36	chr5:101651200-101651600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr5:101651600-101652000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:101652000-101652200	Enhancers	Primary hematopoietic stem cells	blood
39	chr5:101653800-101654400	Enhancers	Primary neutrophils fromperipheralblood	blood
40	chr5:101654000-101654200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
41	chr5:101654200-101654400	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr5:101654200-101656000	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr5:101654400-101654600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
44	chr5:101654400-101655000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
45	chr5:101654600-101655800	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr5:101655000-101656600	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr5:101660400-101660800	Enhancers	Brain Germinal Matrix	brain
48	chr5:101660400-101660800	Enhancers	Fetal Muscle Leg	muscle
49	chr5:101664800-101665000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr5:101664800-101665000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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