Variant report

Variant	esv2762526
Chromosome Location	chr5:76134777-76153934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:244)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 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	ARID3A	chr5:76145750-76146088	K562	blood:	n/a	n/a
2	ARID3A	chr5:76147455-76147464	HepG2	liver:	n/a	n/a
3	ATF1	chr5:76152591-76152875	K562	blood:	n/a	n/a
4	ATF3	chr5:76145745-76146124	K562	blood:	n/a	n/a
5	BHLHE40	chr5:76145717-76145893	GM12878	blood:	n/a	n/a
6	BHLHE40	chr5:76145594-76146150	K562	blood:	n/a	n/a
7	BHLHE40	chr5:76152823-76152904	K562	blood:	n/a	n/a
8	BHLHE40	chr5:76145340-76145346	K562	blood:	n/a	n/a
9	BRCA1	chr5:76142105-76142119	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr5:76151671-76152135	K562	blood:	n/a	n/a
11	CBX3	chr5:76145548-76146197	K562	blood:	n/a	n/a
12	CBX3	chr5:76145641-76146136	K562	blood:	n/a	n/a
13	CCNT2	chr5:76145582-76146271	K562	blood:	n/a	chr5:76145946-76145966 chr5:76146151-76146160 chr5:76146143-76146152
14	CEBPB	chr5:76134470-76135001	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr5:76145587-76146120	K562	blood:	n/a	n/a
16	CEBPB	chr5:76145621-76146014	K562	blood:	n/a	n/a
17	CEBPD	chr5:76145629-76146138	K562	blood:	n/a	n/a
18	CEBPD	chr5:76145662-76146271	K562	blood:	n/a	n/a
19	CHD2	chr5:76146401-76146435	K562	blood:	n/a	n/a
20	CHD2	chr5:76145837-76146041	K562	blood:	n/a	n/a
21	CTCF	chr5:76139980-76140130	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:76137480-76137630	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr5:76145320-76145470	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr5:76137534-76137608	K562	blood:	n/a	n/a
25	CTCF	chr5:76145340-76145490	HEK293	kidney:	n/a	n/a
26	CTCF	chr5:76137460-76137610	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr5:76137520-76137670	NHEK	skin:	n/a	n/a
28	CTCF	chr5:76137520-76137670	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:76139880-76140030	HEK293	kidney:	n/a	n/a
30	CTCF	chr5:76137420-76137570	HEK293	kidney:	n/a	n/a
31	CTCF	chr5:76152020-76152170	GM12873	blood:	n/a	n/a
32	CTCF	chr5:76139920-76140070	HPAF	blood vessel:	n/a	n/a
33	CTCF	chr5:76137519-76137710	K562	blood:	n/a	n/a
34	CTCF	chr5:76139860-76140010	RPTEC	kidney:	n/a	n/a
35	CTCF	chr5:76145760-76145910	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr5:76152060-76152210	GM12867	blood:	n/a	n/a
37	CTCF	chr5:76137560-76137710	HRE	kidney:	n/a	n/a
38	CTCF	chr5:76139880-76140030	HVMF	connective:	n/a	n/a
39	CTCF	chr5:76139960-76140110	A549	lung:	n/a	n/a
40	CTCF	chr5:76137500-76137650	HCT-116	colon:	n/a	n/a
41	CTCF	chr5:76145700-76146120	K562	blood:	n/a	n/a
42	CTCF	chr5:76137460-76137610	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr5:76145748-76146056	K562	blood:	n/a	n/a
44	CTCF	chr5:76137500-76137650	A549	lung:	n/a	n/a
45	CTCF	chr5:76145760-76145910	HCPEpiC	choroid plexus:	n/a	n/a
46	CUX1	chr5:76151934-76152037	K562	blood:	n/a	n/a
47	E2F4	chr5:76134753-76135031	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F6	chr5:76145595-76146063	K562	blood:	n/a	chr5:76145787-76145798
49	E2F6	chr5:76145605-76145967	K562	blood:	n/a	chr5:76145787-76145798
50	E2F6	chr5:76145659-76146043	K562	blood:	n/a	chr5:76145787-76145798

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:76145809-76145859	HNPCEpiC	eye:	n/a
2	chr5:76145903-76145953	HUVEC	blood vessel:	n/a
3	chr5:76144940-76144990	ovcar-3	ovarian:	n/a
4	chr5:76145809-76145859	ovcar-3	ovarian:	n/a
5	chr5:76145809-76145859	NH-A	brain:	n/a
6	chr5:76145809-76145859	AG04449	skin:	fetal
7	chr5:76146148-76146198	HCT-116	colon:	n/a
8	chr5:76144940-76144990	LNCaP	prostate:	n/a
9	chr5:76145903-76145953	HCM	heart:	n/a
10	chr5:76144940-76144990	K562	blood:	n/a
11	chr5:76144940-76144990	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:76145809-76145859	GM12878	blood:	n/a
13	chr5:76146148-76146198	AG04449	skin:	fetal
14	chr5:76145809-76145859	NT2-D1	testis:	n/a
15	chr5:76144940-76144990	NB4	blood:	n/a
16	chr5:76146148-76146198	HL-60	blood:	n/a
17	chr5:76146148-76146198	Hepatocyte	liver:	n/a
18	chr5:76145903-76145953	SK-N-MC	brain:	n/a
19	chr5:76145809-76145859	PFSK-1	brain:	n/a
20	chr5:76145903-76145953	HMEC	breast:	n/a
21	chr5:76145809-76145859	MCF10A-Er-Src	breast:	n/a
22	chr5:76145809-76145859	Hela-S3	cervix:	n/a
23	chr5:76145903-76145953	HEEpiC	esophagus:	n/a
24	chr5:76146148-76146198	ProgFib	skin:	n/a
25	chr5:76145809-76145859	A549	lung:	n/a
26	chr5:76145809-76145859	PANC-1	pancreas:	n/a
27	chr5:76145903-76145953	PrEC	prostate:	n/a
28	chr5:76145809-76145859	GM12892	blood:	n/a
29	chr5:76144940-76144990	SKMC	muscle:	n/a
30	chr5:76146148-76146198	SKMC	muscle:	n/a
31	chr5:76144940-76144990	BJ	skin:	n/a
32	chr5:76146148-76146198	HRCEpiC	kidney:	n/a
33	chr5:76146148-76146198	HEK293	kidney:	embryo
34	chr5:76145809-76145859	Caco-2	colon:	n/a
35	chr5:76145903-76145953	SKMC	muscle:	n/a
36	chr5:76145903-76145953	ovcar-3	ovarian:	n/a
37	chr5:76146148-76146198	AG10803	skin:	n/a
38	chr5:76144940-76144990	NT2-D1	testis:	n/a
39	chr5:76145809-76145859	RPTEC	kidney:	n/a
40	chr5:76145809-76145859	BE2_C	brain:	n/a
41	chr5:76145903-76145953	Hela-S3	cervix:	n/a
42	chr5:76145809-76145859	BJ	skin:	n/a
43	chr5:76144940-76144990	GM12878	blood:	n/a
44	chr5:76144940-76144990	MCF10A-Er-Src	breast:	n/a
45	chr5:76146148-76146198	ovcar-3	ovarian:	n/a
46	chr5:76145903-76145953	HAEpiC	amniotic membrane:	n/a
47	chr5:76146148-76146198	K562	blood:	n/a
48	chr5:76144940-76144990	HCM	heart:	n/a
49	chr5:76145903-76145953	RPTEC	kidney:	n/a
50	chr5:76145903-76145953	HCF	heart:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:76132665..76134749-chr5:76137165..76139299,2	K562	blood:
2	chr5:76113078..76116046-chr5:76145704..76148210,2	K562	blood:
3	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
4	chr5:76149093..76150688-chr5:76152808..76155326,2	K562	blood:
5	chr5:76127088..76128697-chr5:76136604..76139100,2	K562	blood:
6	chr5:76144979..76147946-chr5:76325039..76327688,2	K562	blood:
7	chr5:76135978..76138972-chr5:76140477..76142942,2	MCF-7	breast:
8	chr5:75973826..75975865-chr5:76141935..76143640,2	MCF-7	breast:
9	chr5:76149093..76150688-chr5:76152808..76155326,2	K562	blood:
10	chr5:76136037..76139434-chr5:76141594..76145921,5	K562	blood:
11	chr5:76145559..76148481-chr5:76149405..76151711,4	K562	blood:
12	chr5:76150968..76153966-chr5:76157599..76160236,2	K562	blood:

No data

Variant related genes	Relation type
RN7SL208P	TF binding region
S100Z	TF binding region
RN7SL208P	CpG island
S100Z	CpG island
ENSG00000164252	chromatin interactions
ENSG00000264391	chromatin interactions
ENSG00000171643	chromatin interactions
ENSG00000164251	chromatin interactions

Extended variants
information (count: 748 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:748 , 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	rs6453253	chr5:76134777-76134778	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs369762001	chr5:76134813-76134814	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs576763159	chr5:76134829-76134830	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs539500297	chr5:76134841-76134842	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs35228744	chr5:76134924-76134925	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs556308351	chr5:76134944-76134945	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs183405535	chr5:76134977-76134978	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542468823	chr5:76135008-76135009	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs562360227	chr5:76135023-76135024	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572745812	chr5:76135026-76135027	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs550720658	chr5:76135061-76135062	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs541364541	chr5:76135062-76135063	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs34959623	chr5:76135081-76135082	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs188466952	chr5:76135116-76135117	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs6880329	chr5:76135124-76135125	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs12186357	chr5:76135153-76135154	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs549837530	chr5:76135178-76135179	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs563471579	chr5:76135184-76135185	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs548695784	chr5:76135185-76135186	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs531388070	chr5:76135219-76135220	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs116254619	chr5:76135220-76135221	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs568259083	chr5:76135222-76135223	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs534043602	chr5:76135260-76135261	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs547381940	chr5:76135263-76135264	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs10059976	chr5:76135277-76135278	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs539461042	chr5:76135306-76135307	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs556271333	chr5:76135312-76135313	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs576247314	chr5:76135333-76135334	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs536053773	chr5:76135348-76135349	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs555882725	chr5:76135360-76135361	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs572561371	chr5:76135382-76135383	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs374307730	chr5:76135426-76135427	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs192942876	chr5:76135431-76135432	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs183905978	chr5:76135475-76135476	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577950547	chr5:76135508-76135509	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs10058498	chr5:76135511-76135512	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs563430677	chr5:76135512-76135513	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs187881931	chr5:76135533-76135534	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs34404650	chr5:76135576-76135577	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs70982646	chr5:76135595-76135596	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs549066727	chr5:76135606-76135607	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs561878519	chr5:76135641-76135642	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs527510170	chr5:76135642-76135643	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377338136	chr5:76135645-76135646	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs371113077	chr5:76135646-76135647	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs551094267	chr5:76135658-76135659	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs570682590	chr5:76135696-76135697	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs532939954	chr5:76135697-76135698	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs549851116	chr5:76135747-76135748	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs569672650	chr5:76135764-76135765	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Spinal muscular atrophy	21762474	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
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
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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	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
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Spinal muscular atrophy	15981080	CNVD
Spinal muscular atrophy	18839960	CNVD
Spinal muscular atrophy	19716110	CNVD
Glioblastoma multiforme	22286061	CNVD
craniofacial dysmorphism	21918468	CNVD
Multiple myeloma	16616336	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17133270	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Schizophrenia	23813976	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:354 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:76117400-76135200	Weak transcription	Colonic Mucosa	Colon
2	chr5:76129200-76134800	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr5:76129400-76134800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:76129800-76135800	Weak transcription	Pancreas	Pancrea
5	chr5:76130200-76134800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr5:76130200-76135800	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr5:76130200-76137200	Weak transcription	Esophagus	oesophagus
8	chr5:76130400-76135600	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr5:76130400-76140400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr5:76130800-76134800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr5:76132200-76135400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr5:76132200-76145800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:76132800-76136800	Enhancers	Fetal Intestine Large	intestine
14	chr5:76133000-76134800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr5:76133000-76135000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr5:76133000-76135000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr5:76133600-76136800	Enhancers	Fetal Intestine Small	intestine
18	chr5:76133800-76135000	Enhancers	NHEK	skin
19	chr5:76133800-76135200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr5:76133800-76135200	Enhancers	HUVEC	blood vessel
21	chr5:76134000-76135200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr5:76134000-76135200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr5:76134000-76136000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr5:76134000-76136000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:76134200-76134800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr5:76134200-76135000	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr5:76134200-76135000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr5:76134200-76135000	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr5:76134200-76135000	Enhancers	Fetal Kidney	kidney
30	chr5:76134200-76135000	Enhancers	HMEC	breast
31	chr5:76134200-76135000	Flanking Active TSS	NH-A	brain
32	chr5:76134200-76135200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:76134200-76135200	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr5:76134200-76135200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr5:76134200-76135200	Enhancers	Muscle Satellite Cultured Cells	--
36	chr5:76134200-76135200	Enhancers	Stomach Mucosa	stomach
37	chr5:76134200-76135400	Enhancers	NHDF-Ad	bronchial
38	chr5:76134200-76135400	Enhancers	Osteobl	bone
39	chr5:76134200-76135800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr5:76134200-76136000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr5:76134200-76136000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:76134200-76136200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr5:76134200-76136800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr5:76134400-76134800	Weak transcription	Gastric	stomach
45	chr5:76134400-76134800	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr5:76134400-76134800	Enhancers	A549	lung
47	chr5:76134400-76135000	Enhancers	Primary hematopoietic stem cells	blood
48	chr5:76134400-76135200	Flanking Active TSS	Hela-S3	cervix
49	chr5:76134400-76135200	Enhancers	NHLF	lung
50	chr5:76134400-76135400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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