Variant report

Variant	esv2762532
Chromosome Location	chr5:100041758-100136552
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	ATF2	chr5:100113239-100113801	GM12878	blood:	n/a	n/a
2	ATF2	chr5:100115814-100116618	GM12878	blood:	n/a	n/a
3	ATF2	chr5:100113254-100113986	GM12878	blood:	n/a	n/a
4	BACH1	chr5:100096973-100097266	K562	blood:	n/a	n/a
5	BACH1	chr5:100096929-100097209	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr5:100124193-100124393	GM12878	blood:	n/a	n/a
7	BATF	chr5:100113362-100113705	GM12878	blood:	n/a	n/a
8	BATF	chr5:100067561-100067816	GM12878	blood:	n/a	n/a
9	BATF	chr5:100113325-100113660	GM12878	blood:	n/a	n/a
10	BCL11A	chr5:100113452-100113629	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:100113380-100113701	GM12878	blood:	n/a	n/a
12	BCL3	chr5:100113343-100113674	GM12878	blood:	n/a	n/a
13	BCLAF1	chr5:100116020-100116573	GM12878	blood:	n/a	n/a
14	BCLAF1	chr5:100115920-100116600	GM12878	blood:	n/a	n/a
15	BCLAF1	chr5:100113279-100113876	GM12878	blood:	n/a	n/a
16	BCLAF1	chr5:100067447-100067934	GM12878	blood:	n/a	n/a
17	BCLAF1	chr5:100113272-100113938	GM12878	blood:	n/a	n/a
18	BHLHE40	chr5:100111359-100111795	GM12878	blood:	n/a	n/a
19	BHLHE40	chr5:100115802-100116582	GM12878	blood:	n/a	n/a
20	BHLHE40	chr5:100085721-100085891	K562	blood:	n/a	chr5:100085784-100085793 chr5:100085778-100085799 chr5:100085782-100085795 chr5:100085784-100085793 chr5:100085785-100085794
21	BHLHE40	chr5:100113363-100114175	GM12878	blood:	n/a	n/a
22	BRCA1	chr5:100115518-100115994	GM12878	blood:	n/a	n/a
23	BRCA1	chr5:100113499-100114105	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr5:100113268-100114079	HCT-116	colon:	n/a	n/a
25	CBX3	chr5:100113248-100113812	HCT-116	colon:	n/a	n/a
26	CEBPB	chr5:100042565-100042840	ECC-1	luminal epithelium:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
27	CEBPB	chr5:100125486-100126062	H1-hESC	embryonic stem cell:	n/a	chr5:100125637-100125650 chr5:100125637-100125648 chr5:100125638-100125649
28	CEBPB	chr5:100115670-100116002	Hela-S3	cervix:	n/a	chr5:100115850-100115863 chr5:100115850-100115863 chr5:100115823-100115834 chr5:100115852-100115863 chr5:100115850-100115861
29	CEBPB	chr5:100115663-100115976	A549	lung:	n/a	chr5:100115850-100115863 chr5:100115850-100115863 chr5:100115823-100115834 chr5:100115852-100115863 chr5:100115850-100115861
30	CEBPB	chr5:100133631-100133810	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:100042413-100042963	A549	lung:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
32	CEBPB	chr5:100042513-100042872	IMR90	lung:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
33	CEBPB	chr5:100113188-100113936	HCT-116	colon:	n/a	chr5:100113674-100113687
34	CEBPB	chr5:100098690-100099088	IMR90	lung:	n/a	chr5:100098892-100098903 chr5:100098893-100098902 chr5:100098891-100098904 chr5:100098891-100098902 chr5:100098891-100098904 chr5:100098893-100098902 chr5:100098893-100098902 chr5:100098893-100098902
35	CEBPB	chr5:100125481-100125713	IMR90	lung:	n/a	chr5:100125637-100125650 chr5:100125637-100125648 chr5:100125638-100125649
36	CEBPB	chr5:100042612-100042787	K562	blood:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
37	CEBPB	chr5:100098847-100098971	H1-hESC	embryonic stem cell:	n/a	chr5:100098892-100098903 chr5:100098893-100098902 chr5:100098891-100098904 chr5:100098891-100098902 chr5:100098891-100098904 chr5:100098893-100098902 chr5:100098893-100098902 chr5:100098893-100098902
38	CEBPB	chr5:100042431-100042911	Hela-S3	cervix:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
39	CEBPB	chr5:100056318-100056590	A549	lung:	n/a	chr5:100056471-100056482
40	CEBPB	chr5:100113288-100113693	HCT-116	colon:	n/a	chr5:100113674-100113687
41	CEBPB	chr5:100115696-100116027	MCF-7	breast:	n/a	chr5:100115850-100115863 chr5:100115850-100115863 chr5:100115823-100115834 chr5:100115852-100115863 chr5:100115850-100115861
42	CEBPB	chr5:100042520-100042894	K562	blood:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
43	CEBPB	chr5:100056315-100056624	IMR90	lung:	n/a	chr5:100056471-100056482
44	CEBPB	chr5:100113306-100114016	Hela-S3	cervix:	n/a	chr5:100113674-100113687
45	CEBPB	chr5:100112158-100112415	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr5:100056317-100056628	HepG2	liver:	n/a	chr5:100056471-100056482
47	CEBPB	chr5:100125570-100125685	K562	blood:	n/a	chr5:100125637-100125650 chr5:100125637-100125648 chr5:100125638-100125649
48	CEBPB	chr5:100042521-100042870	K562	blood:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
49	CEBPB	chr5:100042502-100042882	H1-hESC	embryonic stem cell:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650
50	CEBPB	chr5:100042462-100042862	MCF-7	breast:	n/a	chr5:100042694-100042705 chr5:100042693-100042706 chr5:100042639-100042650

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:100108624-100108674	AG10803	skin:	n/a
2	chr5:100108624-100108674	AG10803	skin:	n/a
3	chr5:100108624-100108674	NHDF-neo	bronchial:	n/a
4	chr5:100108624-100108674	HNPCEpiC	eye:	n/a
5	chr5:100108624-100108674	NT2-D1	testis:	n/a
6	chr5:100126093-100126143	SK-N-SH_RA	brain:	n/a
7	chr5:100108624-100108674	AG09309	skin:	n/a
8	chr5:100126093-100126143	Jurkat	blood:	n/a
9	chr5:100126093-100126143	IMR90	lung:	fetal
10	chr5:100108624-100108674	GM12891	blood:	n/a
11	chr5:100108624-100108674	NH-A	brain:	n/a
12	chr5:100126093-100126143	AG09319	gingival:	n/a
13	chr5:100126093-100126143	NHBE	bronchial:	n/a
14	chr5:100126093-100126143	AG10803	skin:	n/a
15	chr5:100126093-100126143	HL-60	blood:	n/a
16	chr5:100126093-100126143	NHDF-neo	bronchial:	n/a
17	chr5:100108624-100108674	Caco-2	colon:	n/a
18	chr5:100108624-100108674	SKMC	muscle:	n/a
19	chr5:100108624-100108674	NHBE	bronchial:	n/a
20	chr5:100126093-100126143	NH-A	brain:	n/a
21	chr5:100126093-100126143	SK-N-MC	brain:	n/a
22	chr5:100108624-100108674	AoSMC	blood vessel:	n/a
23	chr5:100126093-100126143	PANC-1	pancreas:	n/a
24	chr5:100108624-100108674	A549	lung:	n/a
25	chr5:100126093-100126143	H1-hESC	embryonic stem cell:	embryo
26	chr5:100126093-100126143	U87	brain:	n/a
27	chr5:100126093-100126143	HAEpiC	amniotic membrane:	n/a
28	chr5:100108624-100108674	HEK293	kidney:	embryo
29	chr5:100126093-100126143	AG04450	lung:	fetal
30	chr5:100126093-100126143	HUVEC	blood vessel:	n/a
31	chr5:100108624-100108674	HCF	heart:	n/a
32	chr5:100108624-100108674	HCM	heart:	n/a
33	chr5:100126093-100126143	PFSK-1	brain:	n/a
34	chr5:100108624-100108674	SK-N-SH	brain:	n/a
35	chr5:100108624-100108674	SAEC	small airway:	n/a
36	chr5:100126093-100126143	MCF10A-Er-Src	breast:	n/a
37	chr5:100108624-100108674	MCF-7	breast:	n/a
38	chr5:100108624-100108674	HEEpiC	esophagus:	n/a
39	chr5:100108624-100108674	GM12892	blood:	n/a
40	chr5:100108624-100108674	Hepatocyte	liver:	n/a
41	chr5:100108624-100108674	T-47D	breast:	n/a
42	chr5:100126093-100126143	HCF	heart:	n/a
43	chr5:100108624-100108674	MCF10A-Er-Src	breast:	n/a
44	chr5:100126093-100126143	GM12878	blood:	n/a
45	chr5:100108624-100108674	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:100108624-100108674	HCT-116	colon:	n/a
47	chr5:100108624-100108674	PrEC	prostate:	n/a
48	chr5:100126093-100126143	ovcar-3	ovarian:	n/a
49	chr5:100126093-100126143	GM19239	blood:	n/a
50	chr5:100108624-100108674	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:100079826..100081841-chr5:100089952..100091943,2	K562	blood:
2	chr5:99982875..99983980-chr5:100090231..100091716,20	MCF-7	breast:
3	chr5:100056227..100057850-chr5:100061884..100063603,2	K562	blood:
4	chr5:100043067..100045245-chr5:100047793..100049309,2	K562	blood:
5	chr5:100079826..100081841-chr5:100089952..100091943,2	K562	blood:
6	chr5:100129066..100130718-chr5:100133106..100136007,2	MCF-7	breast:
7	chr5:100084872..100087123-chr5:100099781..100102264,2	MCF-7	breast:
8	chr5:99982908..99983980-chr5:100090394..100091716,11	MCF-7	breast:
9	chr5:99983062..99983901-chr5:100090730..100091412,3	MCF-7	breast:
10	chr5:100073871..100076252-chrX:117692329..117695024,2	MCF-7	breast:
11	chr5:100091660..100093864-chr5:100095640..100097485,2	MCF-7	breast:
12	chr5:100084872..100087123-chr5:100099781..100102264,2	MCF-7	breast:
13	chr5:100088083..100090255-chr5:100094028..100097000,2	MCF-7	breast:
14	chr5:100043067..100045245-chr5:100047793..100049309,2	K562	blood:
15	chr5:100088083..100090255-chr5:100094028..100097000,2	MCF-7	breast:
16	chr5:100091660..100093864-chr5:100095640..100097485,2	MCF-7	breast:
17	chr5:100081411..100083893-chr5:100102856..100104705,2	MCF-7	breast:
18	chr5:100081411..100083893-chr5:100102856..100104705,2	MCF-7	breast:
19	chr5:100032298..100033924-chr5:100061965..100063557,2	K562	blood:
20	chr5:100056227..100057850-chr5:100061884..100063603,2	K562	blood:
21	chr5:99983045..99983930-chr5:100117214..100117742,2	MCF-7	breast:
22	chr20:52739790..52740546-chr5:100102888..100103739,2	MCF-7	breast:
23	chr5:100129066..100130718-chr5:100133106..100136007,2	MCF-7	breast:
24	chr5:100128599..100130272-chr5:100154288..100156292,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM174A-3	chr5:100128634-100128791	NONHSAT103010
2	lnc-FAM174A-2	chr5:100068762-100069090	NONHSAT103009
3	lnc-FAM174A-3	chr5:100117459-100117529	NONHSAT103010

Variant related genes	Relation type
RN7SKP62	TF binding region
RN7SKP62	CpG island

Extended variants
information (count: 2894 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2894 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs33966109	chr5:100041758-100041759	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs34612958	chr5:100041821-100041822	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs547179919	chr5:100041839-100041840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs200598446	chr5:100041883-100041884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567994257	chr5:100041931-100041932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115467105	chr5:100041956-100041957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190510163	chr5:100042007-100042008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558756161	chr5:100042009-100042010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570942224	chr5:100042055-100042056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368468608	chr5:100042056-100042057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562276112	chr5:100042060-100042061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556638596	chr5:100042133-100042134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372767247	chr5:100042183-100042184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575174232	chr5:100042194-100042195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs6887907	chr5:100042199-100042200	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs528456180	chr5:100042213-100042214	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs554508021	chr5:100042279-100042280	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs62387618	chr5:100042283-100042284	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs572517869	chr5:100042286-100042287	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs546391900	chr5:100042290-100042291	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs564011607	chr5:100042311-100042312	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs531463695	chr5:100042315-100042316	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs543011588	chr5:100042342-100042343	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs561386341	chr5:100042355-100042356	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs35019724	chr5:100042394-100042395	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs6873143	chr5:100042417-100042418	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs539647655	chr5:100042477-100042478	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs182414584	chr5:100042507-100042508	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs186948615	chr5:100042544-100042545	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs565988756	chr5:100042576-100042577	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs532951010	chr5:100042589-100042590	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs191540217	chr5:100042601-100042602	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs570851881	chr5:100042666-100042667	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs371448897	chr5:100042678-100042679	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs556701652	chr5:100042724-100042725	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs568417437	chr5:100042764-100042765	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535872026	chr5:100042765-100042766	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs9791168	chr5:100042766-100042767	Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs12153759	chr5:100042778-100042779	Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs546060003	chr5:100042796-100042797	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs182564906	chr5:100042808-100042809	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs368475042	chr5:100042818-100042819	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs149772449	chr5:100042857-100042858	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs73776637	chr5:100042897-100042898	Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs397938158	chr5:100042904-100042905	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs200481364	chr5:100042907-100042908	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs561452677	chr5:100042909-100042910	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs540194296	chr5:100042955-100042956	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs145740307	chr5:100042966-100042967	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs79352466	chr5:100043055-100043056	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:614 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:100041600-100042200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr5:100042000-100042200	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr5:100042000-100042600	Enhancers	Primary B cells from cord blood	blood
4	chr5:100042000-100043200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr5:100042200-100042600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr5:100042200-100042800	Enhancers	Dnd41	blood
7	chr5:100042200-100043000	Enhancers	Adipose Nuclei	Adipose
8	chr5:100042200-100043200	Enhancers	HUVEC	blood vessel
9	chr5:100042200-100043200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr5:100042400-100042800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr5:100042400-100043000	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr5:100042400-100043000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr5:100042400-100043200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:100042400-100043200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr5:100042400-100043200	Enhancers	Hela-S3	cervix
16	chr5:100042600-100043000	Active TSS	Primary hematopoietic stem cells	blood
17	chr5:100042600-100045000	Enhancers	Primary neutrophils fromperipheralblood	blood
18	chr5:100042800-100043000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr5:100042800-100043200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:100043000-100043200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr5:100043000-100044000	Weak transcription	Adipose Nuclei	Adipose
22	chr5:100043000-100044200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:100043200-100044200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:100043200-100044400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr5:100043200-100044800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr5:100044000-100044200	Enhancers	Adipose Nuclei	Adipose
27	chr5:100044000-100044400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr5:100044200-100044800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr5:100044200-100045400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr5:100044200-100045400	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr5:100044200-100046400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr5:100044400-100044800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr5:100044400-100044800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr5:100044400-100044800	Enhancers	Placenta	Placenta
35	chr5:100044600-100044800	Enhancers	Spleen	Spleen
36	chr5:100044600-100045200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:100044800-100045400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr5:100044800-100045400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr5:100045200-100045600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr5:100045200-100045600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:100045200-100045800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr5:100045200-100045800	Enhancers	Brain Anterior Caudate	brain
43	chr5:100045400-100045600	Enhancers	Adipose Nuclei	Adipose
44	chr5:100045800-100047200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr5:100046400-100049000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr5:100047400-100047600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:100049000-100049400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr5:100050400-100051200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr5:100050400-100051200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr5:100050400-100052000	Enhancers	Dnd41	blood

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