Variant report

Variant	rs153873
Chromosome Location	chr5:61713663-61713664
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:61)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:61713646-61713696	ovcar-3	ovarian:	n/a
2	chr5:61713646-61713696	MCF10A-Er-Src	breast:	n/a
3	chr5:61713646-61713696	AG10803	skin:	n/a
4	chr5:61713646-61713696	AG04449	skin:	fetal
5	chr5:61713646-61713696	AG09319	gingival:	n/a
6	chr5:61713646-61713696	IMR90	lung:	fetal
7	chr5:61713646-61713696	HCPEpiC	choroid plexus:	n/a
8	chr5:61713646-61713696	GM12892	blood:	n/a
9	chr5:61713646-61713696	AoSMC	blood vessel:	n/a
10	chr5:61713646-61713696	MCF-7	breast:	n/a
11	chr5:61713646-61713696	SAEC	small airway:	n/a
12	chr5:61713646-61713696	LNCaP	prostate:	n/a
13	chr5:61713646-61713696	HNPCEpiC	eye:	n/a
14	chr5:61713646-61713696	K562	blood:	n/a
15	chr5:61713646-61713696	SK-N-MC	brain:	n/a
16	chr5:61713646-61713696	PFSK-1	brain:	n/a
17	chr5:61713646-61713696	RPTEC	kidney:	n/a
18	chr5:61713646-61713696	GM12891	blood:	n/a
19	chr5:61713646-61713696	Caco-2	colon:	n/a
20	chr5:61713646-61713696	AG09309	skin:	n/a
21	chr5:61713646-61713696	HCF	heart:	n/a
22	chr5:61713646-61713696	HRPEpiC	eye:	n/a
23	chr5:61713646-61713696	PANC-1	pancreas:	n/a
24	chr5:61713646-61713696	ECC-1	luminal epithelium:	n/a
25	chr5:61713646-61713696	HRE	kidney:	n/a
26	chr5:61713646-61713696	A549	lung:	n/a
27	chr5:61713646-61713696	HUVEC	blood vessel:	n/a
28	chr5:61713646-61713696	HAEpiC	amniotic membrane:	n/a
29	chr5:61713646-61713696	SK-N-SH_RA	brain:	n/a
30	chr5:61713646-61713696	ProgFib	skin:	n/a
31	chr5:61713646-61713696	NHDF-neo	bronchial:	n/a
32	chr5:61713646-61713696	NH-A	brain:	n/a
33	chr5:61713646-61713696	HCM	heart:	n/a
34	chr5:61713646-61713696	NB4	blood:	n/a
35	chr5:61713646-61713696	HMEC	breast:	n/a
36	chr5:61713646-61713696	GM12878	blood:	n/a
37	chr5:61713646-61713696	HL-60	blood:	n/a
38	chr5:61713646-61713696	NT2-D1	testis:	n/a
39	chr5:61713646-61713696	SK-N-SH	brain:	n/a
40	chr5:61713646-61713696	HRCEpiC	kidney:	n/a
41	chr5:61713646-61713696	CMK	blood:	n/a
42	chr5:61713646-61713696	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:61713646-61713696	HepG2	liver:	n/a
44	chr5:61713646-61713696	H1-hESC	embryonic stem cell:	embryo
45	chr5:61713646-61713696	AG04450	lung:	fetal
46	chr5:61713646-61713696	NHBE	bronchial:	n/a
47	chr5:61713646-61713696	T-47D	breast:	n/a
48	chr5:61713646-61713696	U87	brain:	n/a
49	chr5:61713646-61713696	HCT-116	colon:	n/a
50	chr5:61713646-61713696	Hela-S3	cervix:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:61699505..61701541-chr5:61711615..61714547,2	K562	blood:
2	chr5:61712841..61714503-chr5:61724688..61726349,2	K562	blood:
3	chr5:61711964..61713989-chr5:61715756..61717777,2	MCF-7	breast:
4	chr5:61708374..61709879-chr5:61712891..61715060,2	MCF-7	breast:

No data

Variant related genes	Relation type
IPO11	CpG island
ENSG00000086200	Chromatin interaction
ENSG00000086189	Chromatin interaction

Extended variants
information (count: 93 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs1108158	0.90[CHB][hapmap]
rs11747516	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs12654936	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap]
rs13155253	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs13156073	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs13180572	0.85[AMR][1000 genomes]
rs13189446	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[GIH][hapmap];0.82[TSI][hapmap]
rs13190153	0.85[ASN][1000 genomes]
rs153859	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs153860	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs153864	1.00[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs153866	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs153869	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs16890613	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs16890618	1.00[CEU][hapmap];0.90[CHB][hapmap]
rs16890634	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[GIH][hapmap];0.87[TSI][hapmap]
rs16890651	1.00[CEU][hapmap];0.81[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];0.82[TSI][hapmap]
rs16890869	0.85[AMR][1000 genomes]
rs173530	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs17382217	1.00[CEU][hapmap];0.94[TSI][hapmap];0.89[EUR][1000 genomes]
rs181784	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs187624	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes]
rs190445	0.90[AMR][1000 genomes]
rs2272291	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.84[MKK][hapmap];0.87[TSI][hapmap];0.91[ASN][1000 genomes]
rs2441115	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs246198	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs246200	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2463079	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs247477	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs247480	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs247481	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs247484	0.82[ASN][1000 genomes]
rs255391	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs255392	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs2650500	0.82[ASN][1000 genomes]
rs26619	0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs26620	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs26626	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs26627	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs27090	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs32047	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs32053	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs32148	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.96[MKK][hapmap];0.94[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs32149	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[LWK][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes]
rs32151	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs32152	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs32153	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs32156	0.90[AMR][1000 genomes]
rs32159	0.86[AMR][1000 genomes]
rs32162	0.87[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.86[MKK][hapmap];0.88[TSI][hapmap];0.90[AMR][1000 genomes]
rs32165	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.93[MKK][hapmap];1.00[TSI][hapmap];0.82[AMR][1000 genomes]
rs32167	0.86[AMR][1000 genomes]
rs32169	0.82[AMR][1000 genomes]
rs32170	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs32172	0.90[AMR][1000 genomes]
rs32173	0.90[AMR][1000 genomes]
rs32176	0.86[AMR][1000 genomes]
rs32177	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs32178	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs32180	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs32183	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs32184	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs32185	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs32189	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs35011	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35012	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs35054	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35055	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35058	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35961924	0.81[AMR][1000 genomes]
rs369624	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs3822487	1.00[CEU][hapmap];0.90[CHB][hapmap];0.85[ASN][1000 genomes]
rs40109	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs40290	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs40579	0.90[AMR][1000 genomes]
rs417822	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6893243	0.85[AMR][1000 genomes]
rs785665	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs785666	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs785667	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs814169	1.00[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.82[ASN][1000 genomes]
rs971965	0.90[CHB][hapmap];1.00[GIH][hapmap];0.82[TSI][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024090	chr5:61258759-61921150	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	esv2759345	chr5:61403138-61748912	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv1020255	chr5:61451792-62031365	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv1027539	chr5:61457762-62000008	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv1033578	chr5:61606610-61911153	Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv1025145	chr5:61624735-61824265	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv1029708	chr5:61625813-61877628	Bivalent/Poised TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
8	nsv881728	chr5:61630879-61857577	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	esv2757117	chr5:61649403-61748912	Weak transcription Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
10	nsv598348	chr5:61650843-61895124	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
11	esv35035	chr5:61657943-61792243	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs153873	KIF2A	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:84 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:61709200-61770800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr5:61709400-61727400	Weak transcription	Placenta	Placenta
3	chr5:61709400-61727400	Weak transcription	Pancreas	Pancrea
4	chr5:61709400-61763400	Weak transcription	Aorta	Aorta
5	chr5:61709600-61713800	Weak transcription	Left Ventricle	heart
6	chr5:61709600-61719400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr5:61709600-61723000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr5:61709600-61724600	Weak transcription	Fetal Stomach	stomach
9	chr5:61709600-61726400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr5:61709600-61728000	Weak transcription	Gastric	stomach
11	chr5:61709600-61738800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr5:61709600-61738800	Weak transcription	Fetal Muscle Trunk	muscle
13	chr5:61709600-61739800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr5:61709600-61744000	Weak transcription	Primary T cells fromperipheralblood	blood
15	chr5:61709800-61714600	Weak transcription	Primary B cells from peripheral blood	blood
16	chr5:61709800-61727400	Weak transcription	HSMM	muscle
17	chr5:61709800-61728000	Weak transcription	Fetal Lung	lung
18	chr5:61709800-61728000	Weak transcription	Right Ventricle	heart
19	chr5:61709800-61728000	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr5:61709800-61728200	Weak transcription	Brain Hippocampus Middle	brain
21	chr5:61709800-61738800	Weak transcription	Fetal Kidney	kidney
22	chr5:61709800-61743800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr5:61709800-61746000	Weak transcription	Primary hematopoietic stem cells	blood
24	chr5:61709800-61746600	Weak transcription	Fetal Thymus	thymus
25	chr5:61709800-61769000	Weak transcription	NH-A	brain
26	chr5:61709800-61809200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr5:61710000-61714200	Weak transcription	Adipose Nuclei	Adipose
28	chr5:61710000-61714200	Weak transcription	Psoas Muscle	Psoas
29	chr5:61710000-61715800	Weak transcription	HUVEC	blood vessel
30	chr5:61710000-61716200	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr5:61710000-61717200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr5:61710000-61718400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr5:61710000-61721200	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr5:61710000-61721400	Weak transcription	Duodenum Mucosa	Duodenum
35	chr5:61710000-61727000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr5:61710000-61727200	Weak transcription	Fetal Muscle Leg	muscle
37	chr5:61710000-61727600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr5:61710000-61729000	Weak transcription	Duodenum Smooth Muscle	Duodenum
39	chr5:61710000-61734200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
40	chr5:61710000-61734200	Weak transcription	Fetal Intestine Small	intestine
41	chr5:61710000-61737400	Weak transcription	Fetal Intestine Large	intestine
42	chr5:61710000-61739000	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr5:61710000-61746000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr5:61710200-61720400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr5:61710200-61728000	Weak transcription	Stomach Smooth Muscle	stomach
46	chr5:61710200-61733400	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr5:61710200-61738800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr5:61710200-61746000	Weak transcription	Primary B cells from cord blood	blood
49	chr5:61710400-61713800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:61710400-61718400	Weak transcription	NHDF-Ad	bronchial

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