Variant report

Variant	rs2156349
Chromosome Location	chr11:58668565-58668566
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	SMC3	chr11:58668274-58668629	GM12878	blood:	n/a	chr11:58668444-58668458
2	ELF1	chr11:58668232-58668654	HepG2	liver:	n/a	chr11:58668476-58668489
3	CTCF	chr11:58668216-58668643	HCT-116	colon:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
4	ZNF143	chr11:58668258-58668632	GM12878	blood:	n/a	n/a
5	CTCF	chr11:58668348-58668573	GM19239	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
6	TEAD4	chr11:58668259-58668677	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr11:58668352-58668594	MCF-7	breast:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
8	CTCF	chr11:58668328-58668590	LNCaP	prostate:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
9	CTCF	chr11:58668220-58668663	K562	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
10	CTCF	chr11:58668314-58668608	GM19238	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
11	ELF1	chr11:58668259-58668630	A549	lung:	n/a	chr11:58668476-58668489
12	CTCF	chr11:58668079-58668775	HCT-116	colon:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
13	PBX3	chr11:58668191-58668617	SK-N-SH	brain:	n/a	n/a
14	RAD21	chr11:58668203-58668614	ECC-1	luminal epithelium:	n/a	chr11:58668440-58668459 chr11:58668444-58668458
15	FOXA1	chr11:58668385-58668715	HepG2	liver:	n/a	n/a
16	CTCF	chr11:58668420-58668570	GM12871	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
17	EP300	chr11:58668167-58668596	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr11:58668420-58668570	AoAF	blood vessel:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
19	CTCF	chr11:58668330-58668613	GM12892	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
20	MAX	chr11:58668255-58668632	NB4	blood:	n/a	n/a
21	CTCF	chr11:58668420-58668570	WERI-Rb-1	eye:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
22	RAD21	chr11:58668187-58668703	ECC-1	luminal epithelium:	n/a	chr11:58668440-58668459 chr11:58668444-58668458
23	SP1	chr11:58668018-58668585	H1-hESC	embryonic stem cell:	n/a	chr11:58668210-58668220
24	CTCF	chr11:58668381-58668576	GM20000	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
25	ELF1	chr11:58668240-58668714	K562	blood:	n/a	chr11:58668476-58668489
26	CTCF	chr11:58668420-58668570	GM06990	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
27	ELF1	chr11:58668244-58668717	MCF-7	breast:	n/a	chr11:58668476-58668489
28	CTCF	chr11:58668290-58668655	A549	lung:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
29	SMC3	chr11:58668244-58668634	HepG2	liver:	n/a	chr11:58668444-58668458
30	BHLHE40	chr11:58668390-58668584	HepG2	liver:	n/a	n/a
31	ZNF143	chr11:58668278-58668604	K562	blood:	n/a	n/a
32	RAD21	chr11:58668200-58668654	A549	lung:	n/a	chr11:58668440-58668459 chr11:58668444-58668458
33	CTCF	chr11:58668460-58668610	WI-38	lung:	n/a	n/a
34	FOXA1	chr11:58668327-58668644	T-47D	breast:	n/a	n/a
35	HA-E2F1	chr11:58668158-58668787	MCF-7	breast:	n/a	n/a
36	SIN3A	chr11:58667873-58668660	H1-hESC	embryonic stem cell:	n/a	chr11:58667980-58667994
37	CTCF	chr11:58668312-58668607	K562	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
38	MXI1	chr11:58667989-58668660	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr11:58668420-58668570	GM12872	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
40	MAX	chr11:58667976-58668712	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr11:58668330-58668597	Fibrobl	skin:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
42	MYC	chr11:58668002-58668619	H1-hESC	embryonic stem cell:	n/a	n/a
43	GTF2F1	chr11:58668280-58668648	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAFK	chr11:58668289-58668587	HepG2	liver:	n/a	n/a
45	ELF1	chr11:58668298-58668594	A549	lung:	n/a	chr11:58668476-58668489
46	CTCF	chr11:58668312-58668606	GM12878	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
47	RAD21	chr11:58668148-58668730	H1-hESC	embryonic stem cell:	n/a	chr11:58668440-58668459 chr11:58668444-58668458
48	CTCF	chr11:58668353-58668601	GM12891	blood:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458
49	NANOG	chr11:58668130-58668673	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr11:58668339-58668583	Medullo	brain:	n/a	chr11:58668444-58668457 chr11:58668442-58668460 chr11:58668437-58668458

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:58667985..58668808-chr11:58825960..58826578,4	MCF-7	breast:
2	chr11:58668032..58668917-chr11:58825619..58826508,3	K562	blood:

Variant related genes	Relation type
ENSG00000224130	TF binding region
GLYATL1	TF binding region
ENSG00000255240	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10792206	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792207	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10896872	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896873	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896874	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896875	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896876	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896877	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896878	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10896879	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10896880	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10896882	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10896883	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10896884	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11229687	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11229688	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11229689	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11229692	0.83[ASN][1000 genomes]
rs11229693	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11229694	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11229695	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11229701	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11229704	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11229705	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11229708	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11229711	0.96[ASN][1000 genomes]
rs12222588	0.82[JPT][hapmap]
rs12222597	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12272494	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12277628	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12278662	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12281983	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12292314	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1808064	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1815856	0.94[CEU][hapmap];0.85[CHB][hapmap];0.87[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1893627	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1893628	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1893629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1938786	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1943264	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2156344	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2156345	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3740950	0.81[ASN][1000 genomes]
rs4271397	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4547111	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4573693	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4939243	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56155456	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58848038	0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61889804	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61889805	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61892604	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7108461	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7118637	0.94[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7126489	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7129011	1.00[CEU][hapmap];0.85[CHB][hapmap];0.92[JPT][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73483072	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7930111	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7939049	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs948818	0.84[ASN][1000 genomes]
rs948819	1.00[CEU][hapmap];0.90[CHB][hapmap];0.93[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9787921	0.80[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[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	nsv1050013	chr11:58394598-59221090	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv948365	chr11:58515163-59156405	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
3	nsv1048605	chr11:58534660-58672438	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1045858	chr11:58547772-58674568	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1052173	chr11:58553516-58678496	Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	esv3444895	chr11:58614102-58779384	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	esv1824025	chr11:58626835-58669877	Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv1831269	chr11:58626835-58669877	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	esv3445007	chr11:58638330-58709867	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	esv3502182	chr11:58668199-58731237	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	esv3502181	chr11:58668236-58731215	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
12	esv3478019	chr11:58668282-58731214	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
13	esv3478030	chr11:58668282-58731214	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	esv3502183	chr11:58668353-58731177	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2156349	GLYATL2	cis	brain	BrainEAC

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58651000-58671200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr11:58659400-58671000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:58665000-58668800	Enhancers	Primary hematopoietic stem cells	blood
4	chr11:58665200-58671600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr11:58667400-58668600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
6	chr11:58667600-58668800	Active TSS	Fetal Brain Female	brain
7	chr11:58667800-58668600	Active TSS	iPS-18 Cell Line	embryonic stem cell
8	chr11:58667800-58668600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:58667800-58668600	Enhancers	Fetal Muscle Trunk	muscle
10	chr11:58667800-58668800	Active TSS	ES-I3 Cell Line	embryonic stem cell
11	chr11:58667800-58668800	Active TSS	H1 Cell Line	embryonic stem cell
12	chr11:58667800-58668800	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr11:58667800-58669000	Active TSS	HUES6 Cell Line	embryonic stem cell
14	chr11:58668000-58668600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:58668000-58668600	Active TSS	Fetal Intestine Large	intestine
16	chr11:58668000-58668600	Active TSS	Fetal Kidney	kidney
17	chr11:58668000-58668600	Active TSS	NH-A	brain
18	chr11:58668000-58668800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:58668000-58668800	Active TSS	H9 Cell Line	embryonic stem cell
20	chr11:58668000-58668800	Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr11:58668000-58668800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:58668000-58668800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr11:58668000-58668800	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr11:58668000-58669000	Active TSS	HUES64 Cell Line	embryonic stem cell
25	chr11:58668200-58668600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr11:58668200-58668600	ZNF genes & repeats	Brain Germinal Matrix	brain
27	chr11:58668200-58668600	Enhancers	Spleen	Spleen
28	chr11:58668200-58668800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
29	chr11:58668200-58668800	Enhancers	Fetal Intestine Small	intestine
30	chr11:58668200-58668800	Bivalent Enhancer	Fetal Muscle Leg	muscle
31	chr11:58668200-58668800	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
32	chr11:58668200-58669200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr11:58668400-58668600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr11:58668400-58668800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr11:58668400-58668800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:58668400-58668800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr11:58668400-58668800	Enhancers	Liver	Liver
38	chr11:58668400-58668800	Enhancers	Fetal Brain Male	brain
39	chr11:58668400-58668800	Enhancers	Pancreas	Pancrea
40	chr11:58668400-58668800	Enhancers	A549	lung
41	chr11:58668400-58668800	Enhancers	NHEK	skin
42	chr11:58668400-58668800	Active TSS	Osteobl	bone
43	chr11:58668400-58669200	Enhancers	HMEC	breast
44	chr11:58668400-58669400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr11:58668400-58670600	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr11:58668400-58670600	Weak transcription	NHDF-Ad	bronchial
47	chr11:58668400-58670800	Weak transcription	NHLF	lung
48	chr11:58668400-58672000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr11:58668400-58672400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:58668400-58672400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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