Variant report

Variant	rs6565291
Chromosome Location	chr16:31880101-31880102
allele	C/T
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	CTCF	chr16:31880060-31880210	BJ	skin:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
2	CTCF	chr16:31880036-31880346	GM12892	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
3	CTCF	chr16:31880051-31880233	MCF-7	breast:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
4	CTCF	chr16:31880040-31880190	NHEK	skin:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
5	CTCF	chr16:31880001-31880420	GM10248	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
6	EP300	chr16:31879972-31880234	HepG2	liver:	n/a	n/a
7	YY1	chr16:31880008-31880325	GM12878	blood:	n/a	n/a
8	CTCF	chr16:31880020-31880170	HPF	lung:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
9	RUNX3	chr16:31879976-31880613	GM12878	blood:	n/a	n/a
10	MAX	chr16:31879952-31880515	GM12878	blood:	n/a	n/a
11	ARID3A	chr16:31879879-31880246	HepG2	liver:	n/a	n/a
12	SMC3	chr16:31879578-31880527	SK-N-SH	brain:	n/a	chr16:31880100-31880114 chr16:31880107-31880114 chr16:31880100-31880110
13	CTCF	chr16:31879927-31880323	HepG2	liver:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
14	CTCF	chr16:31880040-31880190	AG04449	skin:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
15	CTCF	chr16:31880040-31880190	HUVEC	blood vessel:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
16	CTCF	chr16:31879987-31880252	HUVEC	blood vessel:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
17	CTCF	chr16:31880002-31880257	LNCaP	prostate:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
18	CTCF	chr16:31880040-31880190	HFF-Myc	foreskin:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
19	CTCF	chr16:31879995-31880225	Kidney_OC	kidney:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
20	CTCF	chr16:31880020-31880170	SAEC	small airway:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
21	CTCF	chr16:31880040-31880190	HPAF	blood vessel:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
22	CTCF	chr16:31880036-31880297	GM19238	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
23	MAZ	chr16:31879910-31880110	HepG2	liver:	n/a	n/a
24	CTCF	chr16:31879995-31880246	Hela-S3	cervix:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
25	CTCF	chr16:31880080-31880230	GM12869	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
26	CTCF	chr16:31880020-31880170	GM12866	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
27	CTCF	chr16:31880020-31880170	RPTEC	kidney:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
28	CTCF	chr16:31879910-31880230	ECC-1	luminal epithelium:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
29	CTCF	chr16:31880100-31880250	NHEK	skin:	n/a	chr16:31880100-31880113 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
30	WRNIP1	chr16:31880077-31880478	GM12878	blood:	n/a	n/a
31	CTCF	chr16:31880040-31880190	Hela-S3	cervix:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
32	CTCF	chr16:31880020-31880170	GM12868	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
33	CTCF	chr16:31880040-31880190	AG04450	lung:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
34	CTCF	chr16:31879884-31880264	K562	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
35	ZNF143	chr16:31879981-31880226	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr16:31880060-31880210	GM12873	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
37	CTCF	chr16:31880020-31880170	GM12865	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
38	CTCF	chr16:31880019-31880252	NHEK	skin:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
39	JUND	chr16:31879950-31880202	K562	blood:	n/a	n/a
40	CTCF	chr16:31879970-31880275	T-47D	breast:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
41	CTCF	chr16:31879964-31880455	Spleen_OC	spleen:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
42	CTCF	chr16:31879972-31880260	Medullo	brain:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
43	CTCF	chr16:31880000-31880150	HRE	kidney:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
44	CTCF	chr16:31880040-31880190	AG09319	gingival:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
45	CTCF	chr16:31880005-31880234	HepG2	liver:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
46	CTCF	chr16:31880000-31880150	HA-sp	spinal cord:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
47	RAD21	chr16:31879790-31880314	HepG2	liver:	n/a	chr16:31880096-31880115 chr16:31880100-31880110 chr16:31880099-31880112 chr16:31880105-31880114 chr16:31880100-31880114
48	CTCF	chr16:31880020-31880170	A549	lung:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
49	CTCF	chr16:31880060-31880210	GM12866	blood:	n/a	chr16:31880099-31880115 chr16:31880093-31880114 chr16:31880100-31880113 chr16:31880098-31880116 chr16:31880100-31880113 chr16:31880104-31880113 chr16:31880101-31880111
50	RUNX3	chr16:31879971-31880583	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr16:31469205..31472299-chr16:31879583..31882157,3	MCF-7	breast:
2	chr16:31710665..31714360-chr16:31877425..31881145,4	MCF-7	breast:
3	chr16:31878665..31883270-chr16:31884134..31887533,7	K562	blood:
4	chr16:31870536..31871564-chr16:31879727..31880499,3	MCF-7	breast:
5	chr16:30996915..30997465-chr16:31879845..31880597,2	MCF-7	breast:
6	chr16:31198405..31200147-chr16:31878787..31881562,2	K562	blood:
7	chr16:31461549..31464190-chr16:31877877..31881538,3	MCF-7	breast:

Variant related genes	Relation type
ZNF267	TF binding region
ENSG00000089280	Chromatin interaction
ENSG00000260568	Chromatin interaction
ENSG00000140691	Chromatin interaction
ENSG00000131797	Chromatin interaction
ENSG00000260267	Chromatin interaction
ENSG00000185947	Chromatin interaction

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10871460	0.90[EUR][1000 genomes]
rs11150650	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11150651	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12444740	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12599066	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12919368	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12924931	0.96[EUR][1000 genomes]
rs1506907	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs1827959	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1828131	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1857943	0.81[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2358778	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3843960	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3843961	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3850114	1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3861268	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3861270	1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3913868	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3913870	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3913871	1.00[CEU][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4026652	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4026654	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4402587	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889517	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs4889518	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889563	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4889565	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889567	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889568	1.00[CEU][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889569	1.00[CEU][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6565290	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7197804	0.96[YRI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7200162	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7202831	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7203345	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7205034	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8048908	1.00[CEU][hapmap]
rs8056158	1.00[CEU][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs8058598	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8059500	1.00[CEU][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs8060276	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8062514	1.00[CEU][hapmap];1.00[YRI][hapmap]
rs9788838	1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9921760	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9928574	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9928704	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9929494	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv905747	chr16:31394179-31888684	Bivalent/Poised TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	123 gene(s)	inside rSNPs	diseases
2	nsv1067321	chr16:31652036-31959992	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv918074	chr16:31669781-31935033	ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
4	nsv1063037	chr16:31669981-31934894	Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv542903	chr16:31669981-31934894	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
6	esv3446880	chr16:31734687-31891223	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
7	nsv1066522	chr16:31831196-31959992	ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv1057300	chr16:31862900-31959992	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31877600-31880200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr16:31879400-31880200	Enhancers	HUVEC	blood vessel
3	chr16:31879600-31880200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr16:31879600-31880400	Enhancers	HepG2	liver
5	chr16:31879800-31880200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr16:31879800-31880200	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr16:31879800-31880200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr16:31879800-31880200	Enhancers	Brain Anterior Caudate	brain
9	chr16:31879800-31880200	Enhancers	Duodenum Mucosa	Duodenum
10	chr16:31879800-31880200	Enhancers	GM12878-XiMat	blood
11	chr16:31879800-31882200	Enhancers	Primary B cells from peripheral blood	blood
12	chr16:31880000-31880200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr16:31880000-31880200	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr16:31880000-31880200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr16:31880000-31880200	Active TSS	Primary T helper cells fromperipheralblood	blood
16	chr16:31880000-31880200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
17	chr16:31880000-31880200	Active TSS	Primary T killer memory cells from peripheral blood	blood
18	chr16:31880000-31880200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr16:31880000-31880200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr16:31880000-31880200	Enhancers	Adipose Nuclei	Adipose
21	chr16:31880000-31880200	Enhancers	Thymus	Thymus
22	chr16:31880000-31880200	Active TSS	Osteobl	bone
23	chr16:31880000-31880600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr16:31880000-31880600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
25	chr16:31880000-31880600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
26	chr16:31880000-31880600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
27	chr16:31880000-31880600	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr16:31880000-31880600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
29	chr16:31880000-31880600	Flanking Active TSS	Dnd41	blood
30	chr16:31880000-31880800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
31	chr16:31880000-31880800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
32	chr16:31880000-31881200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr16:31880000-31881400	Flanking Active TSS	Primary hematopoietic stem cells	blood
34	chr16:31880000-31881400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
35	chr16:31880000-31881400	Enhancers	HSMM	muscle
36	chr16:31880000-31881400	Enhancers	NHEK	skin
37	chr16:31880000-31881600	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr16:31880000-31881600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr16:31880000-31881800	Enhancers	Fetal Thymus	thymus
40	chr16:31880000-31882000	Flanking Active TSS	Primary B cells from cord blood	blood
41	chr16:31880000-31882000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr16:31880000-31882400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood

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