Variant report

Variant	rs2515241
Chromosome Location	chr11:63975331-63975332
allele	A/G
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	MYC	chr11:63975238-63975491	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:63973771-63976077	U87	brain:	n/a	n/a
3	POLR2A	chr11:63972847-63976061	GM12891	blood:	n/a	n/a
4	EP300	chr11:63975195-63975610	GM12878	blood:	n/a	n/a
5	EP300	chr11:63974997-63975347	K562	blood:	n/a	chr11:63975062-63975069
6	TBP	chr11:63973889-63975530	K562	blood:	n/a	n/a
7	CEBPD	chr11:63974613-63975779	K562	blood:	n/a	n/a
8	MAFF	chr11:63974923-63975435	K562	blood:	n/a	n/a
9	CTCF	chr11:63975200-63975350	K562	blood:	n/a	n/a
10	POLR2A	chr11:63973087-63975757	GM12878	blood:	n/a	n/a
11	TAF1	chr11:63974706-63975665	GM12878	blood:	n/a	n/a
12	EBF1	chr11:63975014-63975581	GM12878	blood:	n/a	n/a
13	POU2F2	chr11:63974077-63975564	GM12891	blood:	n/a	n/a
14	CTCF	chr11:63975150-63975388	K562	blood:	n/a	n/a
15	PML	chr11:63973613-63975622	K562	blood:	n/a	chr11:63975049-63975057 chr11:63975106-63975115
16	MYC	chr11:63973624-63975764	K562	blood:	n/a	chr11:63973884-63973893 chr11:63973992-63974002
17	CCNT2	chr11:63973900-63975557	K562	blood:	n/a	chr11:63974266-63974275 chr11:63975509-63975518
18	POLR2A	chr11:63972904-63976551	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:63973231-63976656	GM12878	blood:	n/a	n/a
20	NR2F2	chr11:63973768-63975984	K562	blood:	n/a	n/a
21	POLR2A	chr11:63972968-63979020	GM12878	blood:	n/a	n/a
22	POLR2A	chr11:63973082-63976238	K562	blood:	n/a	n/a
23	POLR2A	chr11:63972926-63975688	HL-60	blood:	n/a	n/a
24	ATF2	chr11:63974901-63975597	GM12878	blood:	n/a	n/a
25	EGR1	chr11:63975226-63975626	GM12878	blood:	n/a	chr11:63975411-63975421 chr11:63975510-63975523 chr11:63975513-63975523 chr11:63975408-63975422 chr11:63975337-63975347
26	ELF1	chr11:63972952-63975775	GM12878	blood:	n/a	chr11:63973154-63973165 chr11:63975062-63975071 chr11:63975061-63975072 chr11:63973114-63973127
27	BATF	chr11:63974989-63975561	GM12878	blood:	n/a	n/a
28	TAF1	chr11:63974681-63975619	GM12891	blood:	n/a	n/a
29	TCF12	chr11:63975174-63975575	GM12878	blood:	n/a	chr11:63975535-63975545
30	POLR2A	chr11:63975027-63975648	PANC-1	pancreas:	n/a	n/a
31	RELA	chr11:63974839-63975837	GM19193	blood:	n/a	n/a
32	TAF1	chr11:63974760-63975628	GM12891	blood:	n/a	n/a
33	POLR2A	chr11:63974910-63975551	ProgFib	skin:	n/a	n/a
34	POLR2A	chr11:63972869-63978649	K562	blood:	n/a	n/a
35	PAX5	chr11:63973738-63975649	GM12878	blood:	n/a	n/a
36	EP300	chr11:63974969-63975525	GM12878	blood:	n/a	chr11:63975062-63975069
37	USF1	chr11:63975080-63975603	K562	blood:	n/a	n/a
38	RCOR1	chr11:63973840-63975581	K562	blood:	n/a	n/a
39	POLR2A	chr11:63972859-63975682	PFSK-1	brain:	n/a	n/a
40	BHLHE40	chr11:63973937-63975538	K562	blood:	n/a	chr11:63974489-63974505
41	YY1	chr11:63974398-63975720	K562	blood:	n/a	chr11:63974822-63974836 chr11:63975036-63975050
42	MAFK	chr11:63974769-63975484	K562	blood:	n/a	chr11:63975154-63975169
43	YY1	chr11:63974496-63975654	GM12891	blood:	n/a	chr11:63974822-63974836 chr11:63975036-63975050
44	STAT5A	chr11:63972958-63975971	GM12878	blood:	n/a	chr11:63974138-63974150 chr11:63973245-63973256 chr11:63973221-63973228
45	POLR2A	chr11:63973192-63976000	HUVEC	blood vessel:	n/a	n/a
46	MYC	chr11:63973745-63975597	NB4	blood:	n/a	chr11:63973884-63973893 chr11:63973992-63974002
47	POU2F2	chr11:63974853-63975663	GM12891	blood:	n/a	n/a
48	CEBPD	chr11:63974680-63975705	K562	blood:	n/a	n/a
49	EBF1	chr11:63973775-63975565	GM12878	blood:	n/a	chr11:63974054-63974063 chr11:63974054-63974064 chr11:63974390-63974399 chr11:63974053-63974064
50	MYC	chr11:63973905-63975590	K562	blood:	n/a	chr11:63973992-63974002

No.	Distal block	Cell Line	Cell type
1	chr11:63975145..63975836-chr11:63993483..63994123,2	K562	blood:
2	chr11:63972047..63977847-chr11:64122012..64128099,8	K562	blood:
3	chr11:63969363..63977705-chr11:64080619..64088284,16	K562	blood:
4	chr11:63972230..63976425-chr11:64106710..64112651,7	K562	blood:
5	chr11:63951359..63955952-chr11:63973161..63976481,4	MCF-7	breast:
6	chr11:63973802..63976476-chr11:64070377..64073257,2	MCF-7	breast:
7	chr11:63974393..63980083-chr11:64051080..64055862,5	MCF-7	breast:
8	chr11:63740485..63742258-chr11:63973387..63975999,2	K562	blood:
9	chr11:63973628..63976272-chr11:64056827..64059574,2	MCF-7	breast:
10	chr11:63973691..63975490-chr11:64083933..64085958,2	MCF-7	breast:
11	chr11:63932241..63934493-chr11:63974004..63976708,3	K562	blood:
12	chr11:63930981..63933673-chr11:63971506..63975446,4	K562	blood:
13	chr11:63975166..63977422-chr11:63978356..63981165,2	MCF-7	breast:
14	chr11:63972384..63977847-chr11:64121311..64126015,8	K562	blood:

Variant related genes	Relation type
FERMT3	TF binding region
ENSG00000133315	Chromatin interaction
ENSG00000149761	Chromatin interaction
ENSG00000168439	Chromatin interaction
ENSG00000173153	Chromatin interaction
ENSG00000149781	Chromatin interaction
ENSG00000173264	Chromatin interaction
ENSG00000162302	Chromatin interaction
ENSG00000168071	Chromatin interaction
ENSG00000126432	Chromatin interaction
ENSG00000173113	Chromatin interaction
ENSG00000219435	Chromatin interaction
ENSG00000257069	Chromatin interaction
ENSG00000182450	Chromatin interaction
ENSG00000149743	Chromatin interaction
ENSG00000176340	Chromatin interaction
ENSG00000256100	Chromatin interaction
ENSG00000002330	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs11231722	0.89[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs11601522	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11603042	0.83[CHB][hapmap]
rs11603192	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11603384	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11603538	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11604782	0.92[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12418535	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12420070	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12787945	0.80[CHB][hapmap];0.91[YRI][hapmap];0.88[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs1860368	0.92[CEU][hapmap];0.83[CHB][hapmap];0.94[JPT][hapmap];0.85[EUR][1000 genomes]
rs2236648	0.80[CHB][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs2282491	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2282492	0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2429455	0.92[CEU][hapmap];0.87[JPT][hapmap];0.87[YRI][hapmap];0.84[EUR][1000 genomes]
rs2845597	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3888316	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4980508	0.80[CHB][hapmap]
rs4980524	0.81[CHB][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs594942	0.87[CEU][hapmap];0.94[CHB][hapmap];0.88[JPT][hapmap];0.87[YRI][hapmap]
rs604203	0.80[JPT][hapmap]
rs60452247	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6591836	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7102177	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7111753	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7112960	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7938819	0.81[CHB][hapmap]
rs882147	0.81[CHB][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897631	chr11:63664882-64129722	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	254 gene(s)	inside rSNPs	diseases
2	esv1802079	chr11:63746066-64151373	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	247 gene(s)	inside rSNPs	diseases
3	nsv897646	chr11:63754986-64150370	Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
4	nsv1035875	chr11:63800238-64132030	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	234 gene(s)	inside rSNPs	diseases
5	nsv469961	chr11:63822940-64085967	Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	224 gene(s)	inside rSNPs	diseases
6	nsv897660	chr11:63860826-64125142	Weak transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	231 gene(s)	inside rSNPs	diseases
7	nsv897661	chr11:63863405-64129722	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	233 gene(s)	inside rSNPs	diseases
8	nsv897662	chr11:63889749-64150370	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
9	nsv897664	chr11:63919742-64150370	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	237 gene(s)	inside rSNPs	diseases
10	nsv468592	chr11:63924446-64042997	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
11	nsv555184	chr11:63924446-64042997	Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	166 gene(s)	inside rSNPs	diseases
12	nsv897665	chr11:63927695-64026144	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
13	nsv897666	chr11:63929493-64026144	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	155 gene(s)	inside rSNPs	diseases
14	nsv869944	chr11:63932152-64123062	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	227 gene(s)	inside rSNPs	diseases
15	nsv468593	chr11:63941734-64089874	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
16	nsv555185	chr11:63941734-64089874	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
17	nsv555186	chr11:63949095-64097233	Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	212 gene(s)	inside rSNPs	diseases
18	nsv468595	chr11:63953121-64027888	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
19	nsv555187	chr11:63953121-64027888	Strong transcription Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases
20	nsv897667	chr11:63964657-64078380	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	141 gene(s)	inside rSNPs	diseases
21	nsv897668	chr11:63964657-64085298	Weak transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	163 gene(s)	inside rSNPs	diseases
22	nsv897669	chr11:63964657-64089874	Genic enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
23	nsv897670	chr11:63964657-64097233	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
24	nsv897671	chr11:63964657-64150370	Active TSS Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	179 gene(s)	inside rSNPs	diseases
25	nsv541061	chr11:63970174-64010995	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	76 gene(s)	inside rSNPs	diseases
26	nsv832186	chr11:63972260-64170059	Active TSS Genic enhancers Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	180 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2515241	NUDT22	Cis_1M	lymphoblastoid	RTeQTL
rs2515241	TRPT1	cis	Muscle Skeletal	GTEx
rs2515241	PPP1R14B	cis	Muscle Skeletal	GTEx

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63955800-63975400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr11:63957400-63975800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr11:63959600-63976000	Strong transcription	Fetal Brain Female	brain
4	chr11:63959600-63977000	Strong transcription	iPS-15b Cell Line	embryonic stem cell
5	chr11:63959800-63976000	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr11:63960000-63975400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
7	chr11:63960000-63975600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:63960000-63976200	Strong transcription	H1 Cell Line	embryonic stem cell
9	chr11:63967200-63975600	Strong transcription	Placenta Amnion	Placenta Amnion
10	chr11:63967400-63976200	Strong transcription	Brain Germinal Matrix	brain
11	chr11:63970200-63979000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:63971600-63992800	Weak transcription	Fetal Kidney	kidney
13	chr11:63972000-63980000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr11:63972000-63990000	Weak transcription	Ovary	ovary
15	chr11:63972400-63975400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:63972400-63976200	Strong transcription	A549	lung
17	chr11:63973000-63975400	Strong transcription	H9 Cell Line	embryonic stem cell
18	chr11:63973000-63975600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
19	chr11:63973000-63976000	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr11:63973000-63976000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr11:63973000-63976200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:63973000-63976400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:63973200-63978600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:63973200-63987800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr11:63973400-63975400	Genic enhancers	HUES6 Cell Line	embryonic stem cell
26	chr11:63973400-63975800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
27	chr11:63973400-63976000	Transcr. at gene 5' and 3'	Dnd41	blood
28	chr11:63973400-63983000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:63973600-63975400	Flanking Active TSS	Primary hematopoietic stem cells	blood
30	chr11:63973600-63975800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:63973600-63975800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
32	chr11:63973600-63976000	Flanking Active TSS	Colonic Mucosa	Colon
33	chr11:63973600-63976200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr11:63973600-63993000	Weak transcription	Aorta	Aorta
35	chr11:63973800-63975600	Active TSS	Duodenum Smooth Muscle	Duodenum
36	chr11:63973800-63976000	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:63973800-63976400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr11:63973800-63982600	Weak transcription	Hela-S3	cervix
39	chr11:63974000-63975400	Active TSS	Primary T killer memory cells from peripheral blood	blood
40	chr11:63974000-63975600	Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr11:63974000-63975600	Transcr. at gene 5' and 3'	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr11:63974000-63975800	Active TSS	Primary T cells from cord blood	blood
43	chr11:63974000-63975800	Transcr. at gene 5' and 3'	Placenta	Placenta
44	chr11:63974000-63975800	Active TSS	Rectal Smooth Muscle	rectum
45	chr11:63974000-63975800	Active TSS	Thymus	Thymus
46	chr11:63974000-63976200	Flanking Active TSS	HUVEC	blood vessel
47	chr11:63974000-63976200	Genic enhancers	NHLF	lung
48	chr11:63974000-63976600	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
49	chr11:63974000-63986400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr11:63974200-63975400	Active TSS	Primary monocytes fromperipheralblood	blood

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