Variant report

Variant	esv3353515
Chromosome Location	chr5:75609996-75632294
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:185)
CpG islands
(count:122)
Chromatin interactive
region (count:20)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:185 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:75615436-75615941	K562	blood:	n/a	n/a
2	ARID3A	chr5:75610646-75610839	HepG2	liver:	n/a	n/a
3	ATF1	chr5:75615481-75615873	K562	blood:	n/a	n/a
4	ATF1	chr5:75627072-75627286	K562	blood:	n/a	n/a
5	BACH1	chr5:75622537-75622692	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr5:75615266-75615927	K562	blood:	n/a	n/a
7	CCNT2	chr5:75627056-75627331	K562	blood:	n/a	n/a
8	CCNT2	chr5:75615311-75615956	K562	blood:	n/a	chr5:75615724-75615744
9	CEBPB	chr5:75615490-75615945	K562	blood:	n/a	n/a
10	CEBPB	chr5:75625808-75626112	HepG2	liver:	n/a	n/a
11	CEBPB	chr5:75625787-75626036	K562	blood:	n/a	n/a
12	CEBPB	chr5:75625473-75625525	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPD	chr5:75615481-75616067	K562	blood:	n/a	n/a
14	CEBPD	chr5:75615314-75616027	K562	blood:	n/a	n/a
15	CTCF	chr5:75630340-75630490	HepG2	liver:	n/a	n/a
16	CTCF	chr5:75630360-75630510	GM12866	blood:	n/a	n/a
17	CTCF	chr5:75630300-75630450	GM12873	blood:	n/a	n/a
18	CTCF	chr5:75630300-75630450	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr5:75630380-75630530	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr5:75630280-75630430	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr5:75630320-75630470	Hela-S3	cervix:	n/a	n/a
22	CTCF	chr5:75630380-75630530	HEK293	kidney:	n/a	n/a
23	CTCF	chr5:75630340-75630490	WERI-Rb-1	eye:	n/a	n/a
24	CTCF	chr5:75630380-75630530	GM12873	blood:	n/a	n/a
25	CTCF	chr5:75630400-75630550	K562	blood:	n/a	n/a
26	CTCF	chr5:75630360-75630510	RPTEC	kidney:	n/a	n/a
27	CTCF	chr5:75630460-75630610	HPF	lung:	n/a	n/a
28	CTCF	chr5:75630280-75630430	AG09309	skin:	n/a	n/a
29	CTCF	chr5:75630580-75630730	GM12865	blood:	n/a	n/a
30	CTCF	chr5:75630333-75630543	K562	blood:	n/a	n/a
31	CTCF	chr5:75630360-75630510	GM12867	blood:	n/a	n/a
32	CTCF	chr5:75630700-75630850	GM12866	blood:	n/a	n/a
33	CTCF	chr5:75630320-75630470	GM12868	blood:	n/a	n/a
34	CTCF	chr5:75630340-75630490	GM12865	blood:	n/a	n/a
35	CTCF	chr5:75627300-75627450	Caco-2	colon:	n/a	n/a
36	CTCF	chr5:75630380-75630530	GM12875	blood:	n/a	n/a
37	CTCF	chr5:75617011-75617077	LNCaP	prostate:	n/a	n/a
38	CTCF	chr5:75630320-75630470	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr5:75630300-75630450	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr5:75630380-75630530	GM12871	blood:	n/a	n/a
41	CTCF	chr5:75630340-75630490	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr5:75630380-75630530	BE2_C	brain:	n/a	n/a
43	CTCF	chr5:75630380-75630530	GM12872	blood:	n/a	n/a
44	CTCF	chr5:75628154-75628200	Fibrobl	skin:	n/a	n/a
45	CTCF	chr5:75626940-75627090	HepG2	liver:	n/a	n/a
46	CTCF	chr5:75630320-75630470	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:75630340-75630490	HAc	cerebellar:	n/a	n/a
48	CTCF	chr5:75630300-75630450	GM12878	blood:	n/a	n/a
49	CTCF	chr5:75617929-75618027	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr5:75630400-75630550	GM12865	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:75632122-75632172	Hepatocyte	liver:	n/a
2	chr5:75621618-75621668	HIPEpiC	eye:	n/a
3	chr5:75632122-75632172	HCM	heart:	n/a
4	chr5:75632122-75632172	HepG2	liver:	n/a
5	chr5:75632122-75632172	IMR90	lung:	fetal
6	chr5:75621618-75621668	RPTEC	kidney:	n/a
7	chr5:75621618-75621668	HCPEpiC	choroid plexus:	n/a
8	chr5:75632122-75632172	PANC-1	pancreas:	n/a
9	chr5:75632122-75632172	GM19239	blood:	n/a
10	chr5:75621618-75621668	IMR90	lung:	fetal
11	chr5:75632122-75632172	PrEC	prostate:	n/a
12	chr5:75632122-75632172	GM12891	blood:	n/a
13	chr5:75632122-75632172	HEK293	kidney:	embryo
14	chr5:75621618-75621668	AG09319	gingival:	n/a
15	chr5:75632122-75632172	HAEpiC	amniotic membrane:	n/a
16	chr5:75632122-75632172	ProgFib	skin:	n/a
17	chr5:75621618-75621668	HPAEpiC	pulmonary alveolar:	n/a
18	chr5:75632122-75632172	A549	lung:	n/a
19	chr5:75632122-75632172	GM12892	blood:	n/a
20	chr5:75621618-75621668	NB4	blood:	n/a
21	chr5:75621618-75621668	AG09309	skin:	n/a
22	chr5:75621618-75621668	MCF-7	breast:	n/a
23	chr5:75621618-75621668	AG10803	skin:	n/a
24	chr5:75621618-75621668	HNPCEpiC	eye:	n/a
25	chr5:75621618-75621668	SK-N-SH	brain:	n/a
26	chr5:75621618-75621668	GM12892	blood:	n/a
27	chr5:75621618-75621668	GM12891	blood:	n/a
28	chr5:75632122-75632172	HCT-116	colon:	n/a
29	chr5:75632122-75632172	BJ	skin:	n/a
30	chr5:75632122-75632172	HCPEpiC	choroid plexus:	n/a
31	chr5:75621618-75621668	A549	lung:	n/a
32	chr5:75621618-75621668	HUVEC	blood vessel:	n/a
33	chr5:75621618-75621668	H1-hESC	embryonic stem cell:	embryo
34	chr5:75632122-75632172	HRE	kidney:	n/a
35	chr5:75621618-75621668	SAEC	small airway:	n/a
36	chr5:75621618-75621668	HMEC	breast:	n/a
37	chr5:75632122-75632172	AG09319	gingival:	n/a
38	chr5:75632122-75632172	U87	brain:	n/a
39	chr5:75632122-75632172	HL-60	blood:	n/a
40	chr5:75621618-75621668	AG04449	skin:	fetal
41	chr5:75621618-75621668	U87	brain:	n/a
42	chr5:75632122-75632172	RPTEC	kidney:	n/a
43	chr5:75632122-75632172	GM12878	blood:	n/a
44	chr5:75632122-75632172	Hela-S3	cervix:	n/a
45	chr5:75621618-75621668	NH-A	brain:	n/a
46	chr5:75632122-75632172	T-47D	breast:	n/a
47	chr5:75632122-75632172	BE2_C	brain:	n/a
48	chr5:75621618-75621668	Hepatocyte	liver:	n/a
49	chr5:75632122-75632172	GM06990	blood:	n/a
50	chr5:75621618-75621668	K562	blood:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:75608362..75610873-chr5:75614139..75616859,2	K562	blood:
2	chr5:75620579..75623947-chr5:75630745..75632949,3	K562	blood:
3	chr5:75608679..75610289-chr5:75610691..75612692,2	MCF-7	breast:
4	chr5:75621687..75623947-chr5:75631428..75633046,3	K562	blood:
5	chr5:75620781..75623735-chr5:75631052..75633279,2	MCF-7	breast:
6	chr5:75601594..75605692-chr5:75607686..75610680,4	K562	blood:
7	chr5:75608679..75610289-chr5:75610691..75612692,2	MCF-7	breast:
8	chr5:75607482..75610409-chr5:75610558..75612294,2	K562	blood:
9	chr5:75629494..75631233-chr5:75639125..75641980,2	K562	blood:
10	chr5:75613788..75615569-chr5:75621673..75623658,3	K562	blood:
11	chr5:75630696..75632382-chr5:75666521..75668676,2	K562	blood:
12	chr5:75613788..75615569-chr5:75621673..75623658,3	K562	blood:
13	chr5:75608362..75610873-chr5:75614139..75616859,2	K562	blood:
14	chr5:75624448..75626842-chr5:75628180..75631008,2	K562	blood:
15	chr5:75620781..75623735-chr5:75631052..75633279,2	MCF-7	breast:
16	chr5:75624448..75626842-chr5:75628180..75631008,2	K562	blood:
17	chr5:75621687..75623947-chr5:75631428..75633046,3	K562	blood:
18	chr5:75628819..75631136-chr5:75840007..75842103,2	K562	blood:
19	chr5:75620579..75623947-chr5:75630745..75632949,3	K562	blood:
20	chr5:75607482..75610409-chr5:75610558..75612294,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IQGAP2-1	chr5:75627662-75629781	ENSG00000266045.1

No data

Variant related genes	Relation type
ENSG00000266045	TF binding region
ENSG00000250348	TF binding region
ENSG00000266045	CpG island
ENSG00000250348	CpG island

Extended variants
information (count: 907 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:907 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543276989	chr5:75610002-75610003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113148849	chr5:75610021-75610022	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139963439	chr5:75610053-75610054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2937742	chr5:75610074-75610075	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs566038624	chr5:75610084-75610085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528518332	chr5:75610094-75610095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113624493	chr5:75610134-75610135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs151194459	chr5:75610209-75610210	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs564110488	chr5:75610210-75610211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs537760638	chr5:75610228-75610229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs541118702	chr5:75610235-75610236	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567865610	chr5:75610269-75610270	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564216597	chr5:75610278-75610279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs533139669	chr5:75610293-75610294	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11390567	chr5:75610294-75610295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536829100	chr5:75610313-75610314	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1863919	chr5:75610347-75610348	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs572024168	chr5:75610399-75610400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541054097	chr5:75610472-75610473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs557482810	chr5:75610523-75610524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549778593	chr5:75610611-75610612	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs543232230	chr5:75610616-75610617	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs563398045	chr5:75610619-75610620	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs529347437	chr5:75610705-75610706	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs115715893	chr5:75610723-75610724	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs140249310	chr5:75610734-75610735	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs529100131	chr5:75610748-75610749	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs34723138	chr5:75610758-75610759	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs559199684	chr5:75610789-75610790	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs542393871	chr5:75610794-75610795	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs7732296	chr5:75610874-75610875	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs528595111	chr5:75610899-75610900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs184535096	chr5:75610915-75610916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150221146	chr5:75610955-75610956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548357944	chr5:75610967-75610968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369474332	chr5:75611013-75611014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10606819	chr5:75611014-75611015	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs76547779	chr5:75611015-75611016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143179242	chr5:75611017-75611018	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs565979034	chr5:75611079-75611080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567954864	chr5:75611108-75611109	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs536864425	chr5:75611137-75611138	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528765031	chr5:75611140-75611141	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs551814135	chr5:75611150-75611151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550036679	chr5:75611171-75611172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs567019300	chr5:75611172-75611173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534440574	chr5:75611240-75611241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs557794762	chr5:75611241-75611242	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112717559	chr5:75611266-75611267	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569817735	chr5:75611282-75611283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75604200-75614200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr5:75605200-75613600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr5:75609600-75615200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr5:75610000-75610800	Enhancers	Left Ventricle	heart
5	chr5:75610000-75611600	Enhancers	Pancreas	Pancrea
6	chr5:75610600-75611200	Enhancers	HepG2	liver
7	chr5:75613600-75614400	Enhancers	Stomach Mucosa	stomach
8	chr5:75613600-75615200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr5:75613600-75615400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr5:75613600-75617800	Enhancers	Primary hematopoietic stem cells	blood
11	chr5:75614200-75615400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr5:75614400-75615200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr5:75614400-75615600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr5:75614600-75615200	Enhancers	K562	blood
15	chr5:75615000-75615200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
16	chr5:75615200-75615600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr5:75615200-75615800	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr5:75615200-75615800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
19	chr5:75615200-75616200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:75615200-75616200	Flanking Active TSS	K562	blood
21	chr5:75615400-75615600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
22	chr5:75615400-75615800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr5:75615400-75616000	Enhancers	Primary T cells from cord blood	blood
24	chr5:75615400-75616000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr5:75615600-75615800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr5:75615800-75616000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr5:75615800-75616800	Weak transcription	Monocytes-CD14+_RO01746	blood
28	chr5:75615800-75617400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr5:75615800-75621000	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr5:75616000-75617800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr5:75616000-75620000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr5:75616000-75620800	Weak transcription	Primary T cells from cord blood	blood
33	chr5:75616200-75617000	Enhancers	K562	blood
34	chr5:75616200-75617400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr5:75617000-75617200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:75617200-75618400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr5:75617400-75620600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr5:75617400-75621000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr5:75617800-75620600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr5:75617800-75620600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr5:75618400-75618800	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr5:75618800-75620800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr5:75620000-75625200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:75620200-75621200	Enhancers	Primary T helper naive cells from peripheral blood	blood
45	chr5:75620200-75621200	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr5:75620200-75621400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr5:75620200-75621400	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr5:75620200-75621800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr5:75620200-75624600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr5:75620400-75621600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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