Variant report

Variant	rs4244822
Chromosome Location	chr11:67071584-67071585
allele	C/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	TFAP2A	chr11:67069663-67071991	Hela-S3	cervix:	n/a	chr11:67071564-67071575 chr11:67071268-67071276 chr11:67071663-67071671 chr11:67071564-67071575 chr11:67071907-67071919 chr11:67070800-67070815 chr11:67071564-67071575 chr11:67071268-67071276 chr11:67071269-67071277 chr11:67071564-67071575 chr11:67071229-67071240 chr11:67070833-67070845 chr11:67071663-67071671 chr11:67071269-67071277 chr11:67070302-67070314 chr11:67071269-67071277 chr11:67071268-67071276 chr11:67071663-67071671
2	TFAP2C	chr11:67069594-67071982	Hela-S3	cervix:	n/a	chr11:67070859-67070874 chr11:67071563-67071578
3	MYC	chr11:67071495-67071720	MCF-7	breast:	n/a	n/a
4	ZBTB7A	chr11:67071435-67071654	K562	blood:	n/a	chr11:67071630-67071639
5	TCF12	chr11:67069552-67071878	ECC-1	luminal epithelium:	n/a	chr11:67070822-67070829
6	MAZ	chr11:67069497-67072451	IMR90	lung:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67071385-67071395 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67071867-67071883 chr11:67070274-67070281 chr11:67071259-67071269 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
7	POLR2A	chr11:67069431-67072015	MCF-7	breast:	n/a	n/a
8	MAX	chr11:67071352-67072101	A549	lung:	n/a	chr11:67071385-67071395 chr11:67071867-67071883
9	EGR1	chr11:67070146-67071925	MCF-7	breast:	n/a	chr11:67071186-67071196 chr11:67071184-67071198 chr11:67071185-67071198 chr11:67071186-67071197 chr11:67071180-67071202 chr11:67070419-67070428 chr11:67071186-67071197 chr11:67071185-67071198 chr11:67070906-67070916 chr11:67071185-67071198 chr11:67071186-67071195 chr11:67071184-67071199 chr11:67070833-67070846 chr11:67071186-67071196 chr11:67071187-67071196
10	POLR2A	chr11:67069946-67071695	HepG2	liver:	n/a	n/a
11	GABPA	chr11:67071374-67071966	MCF-7	breast:	n/a	n/a
12	GATA2	chr11:67071364-67071687	SH-SY5Y	brain:	n/a	n/a
13	POLR2A	chr11:67071455-67071861	Hela-S3	cervix:	n/a	n/a
14	EP300	chr11:67070720-67071835	ECC-1	luminal epithelium:	n/a	chr11:67070815-67070831
15	HDAC2	chr11:67070344-67071975	MCF-7	breast:	n/a	n/a
16	SMARCC1	chr11:67069862-67071742	Hela-S3	cervix:	n/a	n/a
17	MAZ	chr11:67070280-67071746	Hela-S3	cervix:	n/a	chr11:67070837-67070847 chr11:67071385-67071395 chr11:67071259-67071269
18	POLR2A	chr11:67070582-67071906	ProgFib	skin:	n/a	n/a
19	GABPA	chr11:67071391-67071857	K562	blood:	n/a	n/a
20	EP300	chr11:67071363-67071840	T-47D	breast:	n/a	n/a
21	EGR1	chr11:67070389-67071783	HCT-116	colon:	n/a	chr11:67071186-67071196 chr11:67071184-67071198 chr11:67071185-67071198 chr11:67071186-67071197 chr11:67071180-67071202 chr11:67070419-67070428 chr11:67071186-67071197 chr11:67071185-67071198 chr11:67070906-67070916 chr11:67071185-67071198 chr11:67071186-67071195 chr11:67071184-67071199 chr11:67070833-67070846 chr11:67071186-67071196 chr11:67071187-67071196
22	CEBPB	chr11:67071580-67071739	Hela-S3	cervix:	n/a	n/a
23	SRF	chr11:67070435-67071853	MCF-7	breast:	n/a	chr11:67070953-67070968 chr11:67070954-67070968 chr11:67071770-67071780 chr11:67070896-67070906 chr11:67070929-67070939
24	HCFC1	chr11:67069197-67071946	Hela-S3	cervix:	n/a	n/a
25	MAX	chr11:67070574-67071980	MCF-7	breast:	n/a	chr11:67070837-67070847 chr11:67071385-67071395 chr11:67071867-67071883 chr11:67071259-67071269
26	NR2F2	chr11:67070007-67071947	MCF-7	breast:	n/a	n/a
27	SIN3AK20	chr11:67070450-67071964	MCF-7	breast:	n/a	n/a
28	MAX	chr11:67069587-67071781	ECC-1	luminal epithelium:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67071385-67071395 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67070273-67070283 chr11:67070274-67070281 chr11:67071259-67071269 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
29	MAX	chr11:67069993-67072149	A549	lung:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67071385-67071395 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67071867-67071883 chr11:67070273-67070283 chr11:67070274-67070281 chr11:67071259-67071269 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
30	GATA3	chr11:67071233-67071789	T-47D	breast:	n/a	n/a
31	MAX	chr11:67071426-67071724	Hela-S3	cervix:	n/a	n/a
32	ZBTB7A	chr11:67069664-67072102	ECC-1	luminal epithelium:	n/a	chr11:67071264-67071272 chr11:67070600-67070608 chr11:67071630-67071639 chr11:67071400-67071411
33	CREB1	chr11:67070142-67072156	HepG2	liver:	n/a	n/a
34	SIN3AK20	chr11:67069436-67072792	MCF-7	breast:	n/a	n/a
35	ZBTB7A	chr11:67069746-67072178	ECC-1	luminal epithelium:	n/a	chr11:67071264-67071272 chr11:67070600-67070608 chr11:67071630-67071639 chr11:67071400-67071411
36	HA-E2F1	chr11:67070601-67071735	Hela-S3	cervix:	n/a	chr11:67071547-67071559 chr11:67070832-67070841 chr11:67071380-67071389 chr11:67071487-67071498 chr11:67070612-67070626 chr11:67071346-67071355 chr11:67071491-67071498 chr11:67071484-67071501 chr11:67071484-67071501
37	MXI1	chr11:67071496-67071632	HepG2	liver:	n/a	n/a
38	MYC	chr11:67071444-67071816	MCF-7	breast:	n/a	n/a
39	MXI1	chr11:67070211-67071927	IMR90	lung:	n/a	n/a
40	GATA3	chr11:67070442-67071919	MCF-7	breast:	n/a	n/a
41	EGR1	chr11:67070525-67071771	HCT-116	colon:	n/a	chr11:67071186-67071196 chr11:67071184-67071198 chr11:67071185-67071198 chr11:67071186-67071197 chr11:67071180-67071202 chr11:67071186-67071197 chr11:67071185-67071198 chr11:67070906-67070916 chr11:67071185-67071198 chr11:67071186-67071195 chr11:67071184-67071199 chr11:67070833-67070846 chr11:67071186-67071196 chr11:67071187-67071196
42	POLR2A	chr11:67069898-67072555	MCF-7	breast:	n/a	n/a
43	MYC	chr11:67070790-67071671	MCF10A-Er-Src	breast:	n/a	chr11:67070837-67070847 chr11:67071385-67071395 chr11:67071259-67071269
44	MAX	chr11:67070084-67071838	HepG2	liver:	n/a	chr11:67070837-67070847 chr11:67070159-67070170 chr11:67070272-67070283 chr11:67070272-67070282 chr11:67070155-67070174 chr11:67070158-67070171 chr11:67071385-67071395 chr11:67070158-67070171 chr11:67070273-67070282 chr11:67070271-67070280 chr11:67070273-67070283 chr11:67070274-67070281 chr11:67071259-67071269 chr11:67070158-67070171 chr11:67070160-67070169 chr11:67070160-67070169
45	SIN3A	chr11:67069640-67071761	H1-hESC	embryonic stem cell:	n/a	chr11:67070866-67070879 chr11:67070866-67070877
46	MXI1	chr11:67071545-67071649	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr11:67071532-67071916	GM12878	blood:	n/a	n/a
48	PML	chr11:67069636-67072073	MCF-7	breast:	n/a	n/a
49	CTCF	chr11:67071580-67071730	HCPEpiC	choroid plexus:	n/a	n/a
50	TCF12	chr11:67070252-67072173	MCF-7	breast:	n/a	chr11:67070822-67070829

No.	Distal block	Cell Line	Cell type
1	chr11:67069460..67071861-chr11:67118830..67121727,4	MCF-7	breast:
2	chr11:67069246..67073295-chr11:67139634..67145393,8	MCF-7	breast:
3	chr11:67071359..67073756-chr16:3070064..3072908,2	MCF-7	breast:
4	chr11:67071096..67073778-chr17:56708400..56710426,2	MCF-7	breast:
5	chr11:67070027..67071819-chr11:67270841..67273414,2	MCF-7	breast:
6	chr11:67070778..67073065-chr11:67157993..67159732,2	MCF-7	breast:
7	chr11:67069872..67072644-chr11:67140515..67142125,2	K562	blood:
8	chr11:67070466..67072644-chr11:67139702..67142015,2	K562	blood:
9	chr11:67069155..67071597-chr11:67234852..67239277,5	MCF-7	breast:
10	chr11:67054455..67063331-chr11:67064649..67075279,24	K562	blood:
11	chr11:67070042..67072610-chr11:67159168..67161895,3	MCF-7	breast:
12	chr11:67070995..67072990-chr11:67129655..67131719,2	K562	blood:
13	chr11:67069948..67073118-chr11:67121673..67124639,3	MCF-7	breast:
14	chr11:67069839..67071996-chr11:67139740..67141397,2	MCF-7	breast:
15	chr11:67070870..67071665-chr4:185654651..185655570,2	Hela-S3	cervix:

Variant related genes	Relation type
SSH3	TF binding region
ENSG00000110697	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000212195	Chromatin interaction
ENSG00000172932	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000201684	Chromatin interaction
ENSG00000006327	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000151725	Chromatin interaction
ENSG00000184697	Chromatin interaction
ENSG00000256514	Chromatin interaction

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10736657	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs10896166	0.95[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs11819783	0.84[AMR][1000 genomes]
rs12788405	0.90[EUR][1000 genomes]
rs12790040	0.84[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12791853	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12805811	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1419861	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1638569	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs17878756	0.89[ASN][1000 genomes]
rs17883741	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1790731	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1790735	0.92[ASN][1000 genomes]
rs1790737	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1790738	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1790739	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1790762	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1894112	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1944096	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2286619	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2298815	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2429459	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2429463	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2511057	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2514257	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2532605	0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2852875	0.87[ASN][1000 genomes]
rs34000912	0.89[ASN][1000 genomes]
rs34087937	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35176549	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35821109	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35876769	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3737460	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61734600	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6591240	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs6591241	0.95[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs66466718	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71457775	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7394531	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7934433	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs867193	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9326373	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9734588	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv933183	chr11:67008447-67160993	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	nsv897796	chr11:67021518-67186000	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
4	nsv897797	chr11:67023040-67293234	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	206 gene(s)	inside rSNPs	diseases
5	nsv897799	chr11:67024534-67072623	Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv897800	chr11:67024534-67086298	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv1043037	chr11:67027193-67357425	Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
8	nsv468603	chr11:67033076-67164495	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
9	nsv555253	chr11:67033076-67164495	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
10	nsv897801	chr11:67033076-67432479	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
11	nsv897802	chr11:67051245-67075024	Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
12	nsv1047890	chr11:67058231-67184436	Flanking Active TSS Enhancers Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
13	nsv1048230	chr11:67058231-67252397	Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
14	nsv897803	chr11:67067075-67084761	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67067000-67072600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:67069200-67073600	Weak transcription	GM12878-XiMat	blood
3	chr11:67069200-67079200	Weak transcription	K562	blood
4	chr11:67069400-67071600	Active TSS	iPS-20b Cell Line	embryonic stem cell
5	chr11:67069400-67072400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:67069600-67071800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:67069600-67072200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:67069600-67072400	Active TSS	H9 Cell Line	embryonic stem cell
9	chr11:67069800-67071800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr11:67069800-67072000	Bivalent Enhancer	Fetal Brain Male	brain
11	chr11:67069800-67072200	Active TSS	Pancreatic Islets	Pancreatic Islet
12	chr11:67070000-67071600	Active TSS	Lung	lung
13	chr11:67070000-67072200	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr11:67070000-67072400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr11:67070000-67072400	Flanking Active TSS	Stomach Smooth Muscle	stomach
16	chr11:67070200-67071800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr11:67070200-67072000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
18	chr11:67070200-67072200	Active TSS	iPS-15b Cell Line	embryonic stem cell
19	chr11:67070200-67072200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
20	chr11:67070200-67084400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr11:67070400-67071600	Active TSS	H1 Cell Line	embryonic stem cell
22	chr11:67070400-67071600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:67070400-67071600	Active TSS	HUES48 Cell Line	embryonic stem cell
24	chr11:67070400-67071600	Active TSS	HUES6 Cell Line	embryonic stem cell
25	chr11:67070400-67071600	Active TSS	Gastric	stomach
26	chr11:67070400-67071800	Active TSS	Esophagus	oesophagus
27	chr11:67070400-67071800	Active TSS	Fetal Intestine Large	intestine
28	chr11:67070400-67071800	Active TSS	Fetal Kidney	kidney
29	chr11:67070400-67071800	Active TSS	Ovary	ovary
30	chr11:67070400-67071800	Active TSS	Psoas Muscle	Psoas
31	chr11:67070400-67071800	Active TSS	Small Intestine	intestine
32	chr11:67070400-67071800	Active TSS	Stomach Mucosa	stomach
33	chr11:67070400-67072200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr11:67070400-67083800	Weak transcription	Dnd41	blood
35	chr11:67070600-67071600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
36	chr11:67070600-67071600	Active TSS	Breast Myoepithelial Primary Cells	Breast
37	chr11:67070600-67071600	Active TSS	Primary T cells from cord blood	blood
38	chr11:67070600-67071600	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr11:67070600-67071600	Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr11:67070600-67071600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr11:67070600-67071600	Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr11:67070600-67071600	Active TSS	Brain Hippocampus Middle	brain
43	chr11:67070600-67071600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr11:67070600-67071600	Active TSS	Brain Substantia Nigra	brain
45	chr11:67070600-67071600	Active TSS	Colon Smooth Muscle	Colon
46	chr11:67070600-67071600	Active TSS	Duodenum Mucosa	Duodenum
47	chr11:67070600-67071600	Weak transcription	Fetal Heart	heart
48	chr11:67070600-67071600	Active TSS	Rectal Mucosa Donor 29	rectum
49	chr11:67070600-67071600	Active TSS	Right Ventricle	heart
50	chr11:67070600-67071600	Active TSS	Hela-S3	cervix

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