Variant report

Variant	rs11570181
Chromosome Location	chr11:57555770-57555771
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	EBF1	chr11:57555566-57556394	GM12878	blood:	n/a	n/a
2	WRNIP1	chr11:57555717-57556132	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:57555711-57556150	GM12878	blood:	n/a	n/a
4	POLR2A	chr11:57555675-57556203	HUVEC	blood vessel:	n/a	n/a
5	POLR2A	chr11:57555711-57556161	H1-hESC	embryonic stem cell:	n/a	n/a
6	HNF4G	chr11:57555265-57555927	HepG2	liver:	n/a	chr11:57555619-57555634 chr11:57555620-57555633 chr11:57555545-57555560 chr11:57555620-57555634 chr11:57555621-57555633 chr11:57555620-57555634
7	CHD2	chr11:57555678-57556263	GM12878	blood:	n/a	n/a
8	HNF4G	chr11:57555416-57555887	HepG2	liver:	n/a	chr11:57555619-57555634 chr11:57555620-57555633 chr11:57555545-57555560 chr11:57555620-57555634 chr11:57555621-57555633 chr11:57555620-57555634
9	ATF2	chr11:57555724-57556352	GM12878	blood:	n/a	n/a
10	EP300	chr11:57555286-57555789	HepG2	liver:	n/a	n/a
11	CUX1	chr11:57555762-57556314	GM12878	blood:	n/a	n/a
12	HNF4A	chr11:57555424-57555800	HepG2	liver:	n/a	chr11:57555619-57555634 chr11:57555594-57555609 chr11:57555620-57555633 chr11:57555545-57555560 chr11:57555620-57555634 chr11:57555621-57555633 chr11:57555619-57555634 chr11:57555620-57555634
13	BCL3	chr11:57555765-57556222	GM12878	blood:	n/a	chr11:57555914-57555921
14	MAZ	chr11:57555752-57556251	GM12878	blood:	n/a	n/a
15	SPI1	chr11:57555765-57556326	HL-60	blood:	n/a	chr11:57556141-57556154 chr11:57555916-57555925 chr11:57556013-57556026 chr11:57556152-57556165
16	TCF7L2	chr11:57555572-57555785	HepG2	liver:	n/a	chr11:57555670-57555684 chr11:57555672-57555681
17	MTA3	chr11:57555721-57556288	GM12878	blood:	n/a	n/a
18	TEAD4	chr11:57555271-57555840	HepG2	liver:	n/a	n/a
19	EP300	chr11:57555429-57555787	HepG2	liver:	n/a	n/a
20	POLR2A	chr11:57555757-57556340	HL-60	blood:	n/a	n/a
21	FOXA1	chr11:57555337-57555804	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:57554543..57556933-chr11:57559268..57561458,2	MCF-7	breast:
2	chr11:57548343..57550815-chr11:57555382..57557117,2	MCF-7	breast:
3	chr11:57548996..57550773-chr11:57554255..57556606,2	MCF-7	breast:
4	chr11:57555253..57557894-chr11:57565432..57567473,2	MCF-7	breast:

Variant related genes	Relation type
CTNND1	TF binding region
ENSG00000198561	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10750870	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10792110	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10896644	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10896649	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10896653	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11229109	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11229119	0.85[AMR][1000 genomes]
rs11570176	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12270209	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12274865	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12363024	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12801694	0.84[ASW][hapmap];0.85[LWK][hapmap];0.95[MKK][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs12805343	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1424753	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1613592	0.84[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.85[ASN][1000 genomes]
rs1624389	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1631684	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs1647394	0.82[ASN][1000 genomes]
rs1647403	0.88[JPT][hapmap];0.85[ASN][1000 genomes]
rs17455422	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17455626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783818	0.85[CEU][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1783824	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1783826	1.00[JPT][hapmap]
rs1783827	1.00[JPT][hapmap]
rs1783828	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs1783976	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783977	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1783978	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783979	1.00[ASW][hapmap];0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783980	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783981	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1783983	0.84[CEU][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap]
rs1783985	0.85[ASN][1000 genomes]
rs1785498	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1785499	0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1786438	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1798172	0.84[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.85[ASN][1000 genomes]
rs1798173	0.81[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.85[ASN][1000 genomes]
rs1798177	1.00[JPT][hapmap];0.81[MEX][hapmap]
rs2156638	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2911728	0.82[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2956981	0.85[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2956982	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3017889	0.85[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs36036499	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4611222	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs471398	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs547118	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56392705	0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs585337	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs585761	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs588612	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs593239	0.81[ASN][1000 genomes]
rs606499	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs615133	0.85[ASW][hapmap];0.81[LWK][hapmap];0.82[MEX][hapmap];0.84[YRI][hapmap]
rs623541	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs627145	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs633129	0.85[ASW][hapmap];0.82[MEX][hapmap];0.84[YRI][hapmap]
rs639158	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs644219	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs645145	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs652191	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs652908	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs653889	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs658936	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs659165	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs665058	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.90[MEX][hapmap];0.95[TSI][hapmap];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs666021	0.86[JPT][hapmap]
rs671508	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs682258	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs686489	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7105506	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7115528	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7117020	0.85[CEU][hapmap];0.85[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7120868	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7479922	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7947357	1.00[JPT][hapmap]
rs7948571	0.93[ASN][1000 genomes]
rs929934	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044030	chr11:57073395-58035564	Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	nsv541047	chr11:57073395-58035564	Active TSS Enhancers Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
3	nsv530621	chr11:57139699-57703639	Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
4	nsv1040913	chr11:57315006-57696122	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers 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	93 gene(s)	inside rSNPs	diseases
5	nsv832164	chr11:57407617-57578825	Enhancers Strong transcription Genic enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
6	nsv508633	chr11:57419585-57560045	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
7	nsv1054205	chr11:57544264-58358509	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs11570181	SLC43A3	cis	cerebellum	SCAN
rs11570181	TIMM10	cis	parietal	SCAN
rs11570181	MS4A7	cis	parietal	SCAN
rs11570181	YPEL4	cis	lung	GTEx

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:57546400-57559000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr11:57546400-57559200	Enhancers	Stomach Mucosa	stomach
3	chr11:57546800-57564000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr11:57547000-57558600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr11:57547000-57558600	Enhancers	Liver	Liver
6	chr11:57547200-57555800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr11:57547400-57558600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr11:57547400-57558800	Weak transcription	Aorta	Aorta
9	chr11:57547800-57558600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr11:57549200-57557200	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr11:57549400-57555800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr11:57549400-57558400	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr11:57549400-57559600	Weak transcription	Hela-S3	cervix
14	chr11:57550000-57555800	Weak transcription	HUVEC	blood vessel
15	chr11:57550400-57557200	Enhancers	Fetal Intestine Large	intestine
16	chr11:57550400-57559200	Weak transcription	Fetal Kidney	kidney
17	chr11:57550600-57558400	Weak transcription	K562	blood
18	chr11:57550800-57556400	Enhancers	HepG2	liver
19	chr11:57551400-57556200	Enhancers	Colonic Mucosa	Colon
20	chr11:57551600-57556400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr11:57552000-57555800	Weak transcription	Lung	lung
22	chr11:57552000-57559400	Weak transcription	Brain Angular Gyrus	brain
23	chr11:57552200-57557600	Enhancers	Placenta Amnion	Placenta Amnion
24	chr11:57552200-57560000	Enhancers	Primary monocytes fromperipheralblood	blood
25	chr11:57552400-57556600	Enhancers	Placenta	Placenta
26	chr11:57552400-57557600	Enhancers	Duodenum Smooth Muscle	Duodenum
27	chr11:57552800-57558800	Enhancers	Dnd41	blood
28	chr11:57553200-57556600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:57553200-57557000	Enhancers	Primary B cells from peripheral blood	blood
30	chr11:57553400-57556600	Enhancers	Fetal Lung	lung
31	chr11:57553400-57556800	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr11:57553600-57556200	Enhancers	Right Atrium	heart
33	chr11:57553600-57557800	Enhancers	Adipose Nuclei	Adipose
34	chr11:57553800-57556600	Enhancers	Stomach Smooth Muscle	stomach
35	chr11:57554000-57556000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr11:57554000-57556400	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr11:57554000-57556600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr11:57554000-57556600	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr11:57554000-57556800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr11:57554000-57557200	Enhancers	Fetal Intestine Small	intestine
41	chr11:57554000-57557800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr11:57554200-57556200	Enhancers	NHDF-Ad	bronchial
43	chr11:57554200-57556400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr11:57554200-57556600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr11:57554200-57556600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr11:57554200-57556600	Enhancers	HSMMtube	muscle
47	chr11:57554200-57557000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr11:57554200-57557600	Enhancers	Colon Smooth Muscle	Colon
49	chr11:57554200-57558800	Enhancers	Primary hematopoietic stem cells short term culture	blood
50	chr11:57554400-57556400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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