Variant report

Variant	rs4910869
Chromosome Location	chr11:4006438-4006439
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr11:4006227-4006453	K562	blood:	n/a	n/a
2	CTCF	chr11:4006156-4006461	K562	blood:	n/a	n/a
3	MYC	chr11:4006199-4006446	K562	blood:	n/a	n/a
4	RAD21	chr11:4005996-4006735	SK-N-SH	brain:	n/a	n/a
5	RAD21	chr11:4006076-4006472	HCT-116	colon:	n/a	n/a
6	RAD21	chr11:4006029-4006588	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr11:4006142-4006492	H1-hESC	embryonic stem cell:	n/a	n/a
8	SIN3A	chr11:4006216-4006500	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr11:4006155-4006496	K562	blood:	n/a	n/a
10	RCOR1	chr11:4006202-4006544	K562	blood:	n/a	n/a
11	TEAD4	chr11:4006044-4006589	K562	blood:	n/a	n/a
12	RAD21	chr11:4006107-4006458	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr11:4006246-4006443	HUVEC	blood vessel:	n/a	n/a
14	SMC3	chr11:4006151-4006507	GM12878	blood:	n/a	n/a
15	RAD21	chr11:4006187-4006486	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr11:4006300-4006450	HRE	kidney:	n/a	n/a
17	RAD21	chr11:4006133-4006484	IMR90	lung:	n/a	n/a
18	CTCF	chr11:4006198-4006502	K562	blood:	n/a	n/a
19	CTCF	chr11:4006149-4006519	GM12878	blood:	n/a	n/a
20	EP300	chr11:4006219-4006486	K562	blood:	n/a	n/a
21	ZNF384	chr11:4006172-4006548	K562	blood:	n/a	n/a
22	CTCF	chr11:4006340-4006490	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr11:4006300-4006450	AG10803	skin:	n/a	n/a
24	RAD21	chr11:4006159-4006545	H1-hESC	embryonic stem cell:	n/a	n/a
25	ZNF143	chr11:4006217-4006469	K562	blood:	n/a	n/a
26	CTCF	chr11:4006360-4006510	HFF-Myc	foreskin:	n/a	n/a
27	CTCF	chr11:4006160-4006600	HCT-116	colon:	n/a	n/a
28	CTCF	chr11:4005977-4006664	SK-N-SH	brain:	n/a	n/a
29	RAD21	chr11:4006153-4006495	HCT-116	colon:	n/a	n/a
30	UBTF	chr11:4006227-4006462	K562	blood:	n/a	n/a
31	JUND	chr11:4006172-4006513	K562	blood:	n/a	n/a
32	CTCF	chr11:4006320-4006470	GM12866	blood:	n/a	n/a
33	RAD21	chr11:4006111-4006448	HepG2	liver:	n/a	n/a
34	CTCF	chr11:4006320-4006470	HVMF	connective:	n/a	n/a
35	RAD21	chr11:4006129-4006512	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr11:4006300-4006450	HUVEC	blood vessel:	n/a	n/a
37	CTCF	chr11:4006228-4006444	Spleen_OC	spleen:	n/a	n/a
38	ELK1	chr11:4006371-4006480	GM12878	blood:	n/a	n/a
39	RAD21	chr11:4006170-4006479	GM12878	blood:	n/a	n/a
40	CTCF	chr11:4006119-4006546	K562	blood:	n/a	n/a
41	MAZ	chr11:4006156-4006494	K562	blood:	n/a	n/a
42	TAL1	chr11:4006186-4006542	K562	blood:	n/a	chr11:4006333-4006348
43	RAD21	chr11:4006152-4006449	GM12878	blood:	n/a	n/a
44	CTCF	chr11:4006400-4006550	HFF	foreskin:	n/a	n/a
45	RCOR1	chr11:4006090-4006516	K562	blood:	n/a	n/a
46	CTCF	chr11:4006148-4006459	H1-hESC	embryonic stem cell:	n/a	n/a
47	SMC3	chr11:4006171-4006443	K562	blood:	n/a	n/a
48	CTCF	chr11:4006190-4006479	IMR90	lung:	n/a	n/a
49	CTCF	chr11:4006300-4006450	GM12865	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:4003558..4006551-chr11:4007203..4009019,2	K562	blood:
2	chr11:3873199..3875344-chr11:4005574..4008407,2	K562	blood:
3	chr11:3994046..3996108-chr11:4004247..4006936,2	K562	blood:
4	chr11:3873199..3875209-chr11:4005574..4007848,2	K562	blood:

No data

Variant related genes	Relation type
STIM1	TF binding region
ENSG00000255141	Chromatin interaction

Extended variants
information (count: 93 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1013351	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10500590	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10742200	0.83[EUR][1000 genomes]
rs10767702	0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10767713	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10767715	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10767767	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10767811	0.94[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.97[TSI][hapmap];0.82[ASN][1000 genomes]
rs10835311	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10835312	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10835331	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10835333	0.81[TSI][hapmap]
rs10835337	0.81[GIH][hapmap];0.90[TSI][hapmap]
rs10835340	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10835359	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10835390	0.82[EUR][1000 genomes]
rs10835399	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10835402	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10835403	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10835406	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10835407	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10835454	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10835474	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10835508	0.91[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10835521	0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes]
rs10835540	0.94[CHB][hapmap];0.81[EUR][1000 genomes]
rs10835556	0.86[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10835557	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10835561	0.82[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs10835596	1.00[ASW][hapmap];0.87[CEU][hapmap];0.94[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10835597	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10835601	0.81[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10835604	0.82[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs11030276	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11030404	0.87[GIH][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes]
rs11030579	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11030599	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11030627	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11030631	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11030639	0.91[CEU][hapmap];0.93[CHB][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11030660	0.94[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11030781	0.94[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.81[ASN][1000 genomes]
rs11030918	0.89[GIH][hapmap]
rs11493482	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11828337	0.80[EUR][1000 genomes]
rs12223176	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12281293	1.00[CHB][hapmap];0.86[JPT][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12283447	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12286710	0.90[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12290747	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12295138	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1349583	0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1442726	0.87[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1452047	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1452048	0.81[EUR][1000 genomes]
rs17081	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17279635	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1839910	0.81[EUR][1000 genomes]
rs2119987	1.00[AFR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2412338	0.82[EUR][1000 genomes]
rs28419002	0.82[ASN][1000 genomes]
rs2898947	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4910590	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4910596	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4910597	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4910598	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4910866	1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4910868	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4910875	0.91[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4910877	0.82[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4910880	0.93[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs6578424	0.83[GIH][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes]
rs66503725	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs66596383	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs67065286	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs67300156	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7102215	0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7113845	0.83[EUR][1000 genomes]
rs7128762	0.87[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7129444	0.91[GIH][hapmap]
rs714380	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs71466139	0.85[ASN][1000 genomes]
rs720571	0.91[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs750525	0.81[TSI][hapmap]
rs7924984	0.87[GIH][hapmap];0.90[TSI][hapmap];0.82[EUR][1000 genomes]
rs7935824	0.91[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7950153	0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs963998	1.00[ASW][hapmap];0.82[CEU][hapmap];0.94[CHB][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs995498	1.00[ASW][hapmap];0.87[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.93[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052744	chr11:3739162-4017601	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers 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 miRNA target site	29 gene(s)	inside rSNPs	diseases
2	nsv1047025	chr11:3750969-4017601	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv1046065	chr11:3808818-4049150	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv540909	chr11:3808818-4049150	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs4910869	RRM1	cis	Artery Tibial	GTEx
rs4910869	STIM1	cis	lung	GTEx
rs4910869	RRM1	cis	Thyroid	GTEx

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:3973200-4008400	Weak transcription	Fetal Lung	lung
2	chr11:3984000-4010400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr11:3986000-4008000	Weak transcription	HepG2	liver
4	chr11:3987000-4010400	Weak transcription	Fetal Intestine Small	intestine
5	chr11:3989400-4010600	Weak transcription	Spleen	Spleen
6	chr11:3989400-4031000	Weak transcription	Aorta	Aorta
7	chr11:3989800-4006600	Weak transcription	Liver	Liver
8	chr11:3994400-4016600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:3998600-4008800	Enhancers	Primary T helper cells PMA-I stimulated	--
10	chr11:4000600-4010800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr11:4001400-4011800	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr11:4002200-4008600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr11:4002200-4008600	Weak transcription	Gastric	stomach
14	chr11:4002600-4007200	Enhancers	Thymus	Thymus
15	chr11:4002600-4009600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr11:4003000-4007200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr11:4003000-4010600	Weak transcription	Esophagus	oesophagus
18	chr11:4003200-4016600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr11:4003600-4007600	Enhancers	Primary T killer memory cells from peripheral blood	blood
20	chr11:4003800-4007000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr11:4003800-4007200	Enhancers	Primary hematopoietic stem cells	blood
22	chr11:4003800-4007200	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr11:4004400-4009400	Enhancers	Psoas Muscle	Psoas
24	chr11:4004400-4009600	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr11:4004600-4010600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr11:4004800-4010000	Enhancers	Skeletal Muscle Male	skeletal muscle
27	chr11:4005000-4006800	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr11:4005000-4010200	Weak transcription	Dnd41	blood
29	chr11:4005400-4006800	Enhancers	Colon Smooth Muscle	Colon
30	chr11:4005400-4007000	Enhancers	Ovary	ovary
31	chr11:4005400-4011800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:4005600-4006600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr11:4005600-4007000	Enhancers	K562	blood
34	chr11:4005600-4008000	Enhancers	Fetal Brain Male	brain
35	chr11:4005800-4007000	Enhancers	Primary B cells from peripheral blood	blood
36	chr11:4005800-4007000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
37	chr11:4005800-4007200	Enhancers	Fetal Stomach	stomach
38	chr11:4005800-4010800	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr11:4006000-4006600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:4006000-4006600	Enhancers	Fetal Heart	heart
41	chr11:4006000-4006800	Genic enhancers	Primary T helper naive cells from peripheral blood	blood
42	chr11:4006000-4006800	Enhancers	Duodenum Mucosa	Duodenum
43	chr11:4006000-4006800	Enhancers	Right Ventricle	heart
44	chr11:4006000-4007000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:4006000-4007000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr11:4006000-4007000	Enhancers	Fetal Thymus	thymus
47	chr11:4006000-4007000	Enhancers	Left Ventricle	heart
48	chr11:4006000-4007600	Enhancers	Fetal Brain Female	brain
49	chr11:4006000-4007600	Enhancers	Stomach Smooth Muscle	stomach
50	chr11:4006000-4007800	Enhancers	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links