Variant report

Variant	rs1638559
Chromosome Location	chr11:67219247-67219248
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:67218830-67219280	GM12878	blood:	n/a	n/a
2	POLR2A	chr11:67218683-67220346	GM12878	blood:	n/a	n/a
3	POLR2A	chr11:67217429-67220463	GM12892	blood:	n/a	n/a
4	POLR2A	chr11:67218444-67219731	GM12878	blood:	n/a	n/a
5	POLR2A	chr11:67218681-67219298	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67219241-67219291	HCT-116	colon:	n/a
2	chr11:67219241-67219291	BJ	skin:	n/a
3	chr11:67219241-67219291	T-47D	breast:	n/a
4	chr11:67219241-67219291	HepG2	liver:	n/a
5	chr11:67219241-67219291	HNPCEpiC	eye:	n/a
6	chr11:67219241-67219291	HAEpiC	amniotic membrane:	n/a
7	chr11:67219241-67219291	PrEC	prostate:	n/a
8	chr11:67219241-67219291	HRPEpiC	eye:	n/a
9	chr11:67219241-67219291	Hepatocyte	liver:	n/a
10	chr11:67219241-67219291	HEEpiC	esophagus:	n/a
11	chr11:67219241-67219291	MCF-7	breast:	n/a
12	chr11:67219241-67219291	IMR90	lung:	fetal
13	chr11:67219241-67219291	NHBE	bronchial:	n/a
14	chr11:67219241-67219291	CMK	blood:	n/a
15	chr11:67219241-67219291	ECC-1	luminal epithelium:	n/a
16	chr11:67219241-67219291	HUVEC	blood vessel:	n/a
17	chr11:67219241-67219291	AG04449	skin:	fetal
18	chr11:67219241-67219291	ProgFib	skin:	n/a
19	chr11:67219241-67219291	GM19239	blood:	n/a
20	chr11:67219241-67219291	U87	brain:	n/a
21	chr11:67219241-67219291	GM06990	blood:	n/a
22	chr11:67219241-67219291	BE2_C	brain:	n/a
23	chr11:67219241-67219291	Hela-S3	cervix:	n/a
24	chr11:67219241-67219291	NB4	blood:	n/a
25	chr11:67219241-67219291	MCF10A-Er-Src	breast:	n/a
26	chr11:67219241-67219291	SK-N-SH_RA	brain:	n/a
27	chr11:67219241-67219291	HCM	heart:	n/a
28	chr11:67219241-67219291	AG09309	skin:	n/a
29	chr11:67219241-67219291	NHDF-neo	bronchial:	n/a
30	chr11:67219241-67219291	AG10803	skin:	n/a
31	chr11:67219241-67219291	PANC-1	pancreas:	n/a
32	chr11:67219241-67219291	GM12891	blood:	n/a
33	chr11:67219241-67219291	Jurkat	blood:	n/a
34	chr11:67219241-67219291	RPTEC	kidney:	n/a
35	chr11:67219241-67219291	Caco-2	colon:	n/a
36	chr11:67219241-67219291	GM12892	blood:	n/a
37	chr11:67219241-67219291	PFSK-1	brain:	n/a
38	chr11:67219241-67219291	SKMC	muscle:	n/a
39	chr11:67219241-67219291	HEK293	kidney:	embryo
40	chr11:67219241-67219291	HIPEpiC	eye:	n/a
41	chr11:67219241-67219291	A549	lung:	n/a
42	chr11:67219241-67219291	ovcar-3	ovarian:	n/a
43	chr11:67219241-67219291	NH-A	brain:	n/a
44	chr11:67219241-67219291	HRE	kidney:	n/a
45	chr11:67219241-67219291	HMEC	breast:	n/a
46	chr11:67219241-67219291	NT2-D1	testis:	n/a
47	chr11:67219241-67219291	SK-N-SH	brain:	n/a
48	chr11:67219241-67219291	HL-60	blood:	n/a
49	chr11:67219241-67219291	SK-N-MC	brain:	n/a
50	chr11:67219241-67219291	HPAEpiC	pulmonary alveolar:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:67218019..67220766-chr11:67230531..67233882,3	K562	blood:
2	chr11:67215208..67219901-chr11:67230573..67236211,5	K562	blood:

No data

Variant related genes	Relation type
CABP4	TF binding region
CABP4	CpG island
ENSG00000172663	Chromatin interaction

Extended variants
information (count: 136 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:112)

rs_ID	r²[population]
rs10896175	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227796	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11227804	0.83[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs12293606	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1382089	1.00[EUR][1000 genomes]
rs1618605	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1620333	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1624189	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625032	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1625892	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1630068	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1632616	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638558	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638560	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638561	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638562	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638563	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638570	1.00[EUR][1000 genomes]
rs1638572	1.00[EUR][1000 genomes]
rs1638575	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638576	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638577	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638581	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638584	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1638585	0.90[AMR][1000 genomes]
rs1638587	1.00[EUR][1000 genomes]
rs1790729	1.00[EUR][1000 genomes]
rs1790730	1.00[EUR][1000 genomes]
rs1790734	1.00[EUR][1000 genomes]
rs1790736	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790741	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790743	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790744	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790745	1.00[EUR][1000 genomes]
rs1790749	1.00[EUR][1000 genomes]
rs1790750	1.00[EUR][1000 genomes]
rs1790754	1.00[EUR][1000 genomes]
rs1790756	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790763	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790764	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1790765	1.00[EUR][1000 genomes]
rs1824712	1.00[EUR][1000 genomes]
rs2054409	1.00[EUR][1000 genomes]
rs2447590	1.00[EUR][1000 genomes]
rs2447591	1.00[EUR][1000 genomes]
rs2447597	1.00[EUR][1000 genomes]
rs2511058	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2511059	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514013	1.00[EUR][1000 genomes]
rs2514014	1.00[EUR][1000 genomes]
rs2514015	1.00[EUR][1000 genomes]
rs2514024	1.00[EUR][1000 genomes]
rs2514045	1.00[EUR][1000 genomes]
rs2514064	1.00[EUR][1000 genomes]
rs2514259	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2514262	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514263	1.00[EUR][1000 genomes]
rs2885171	1.00[EUR][1000 genomes]
rs3016861	1.00[EUR][1000 genomes]
rs35363135	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56050553	1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56405884	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57047868	1.00[EUR][1000 genomes]
rs57748654	1.00[EUR][1000 genomes]
rs57749415	1.00[EUR][1000 genomes]
rs57757103	1.00[EUR][1000 genomes]
rs57955602	1.00[EUR][1000 genomes]
rs58999825	1.00[EUR][1000 genomes]
rs59500232	1.00[EUR][1000 genomes]
rs596431	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs596944	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs601363	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60136955	1.00[EUR][1000 genomes]
rs602220	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs604540	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs60751057	1.00[EUR][1000 genomes]
rs611697	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61282424	1.00[EUR][1000 genomes]
rs61429992	1.00[EUR][1000 genomes]
rs61610719	1.00[EUR][1000 genomes]
rs618633	1.00[EUR][1000 genomes]
rs641081	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6591267	1.00[EUR][1000 genomes]
rs7104627	1.00[EUR][1000 genomes]
rs7121803	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7124630	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73490545	1.00[EUR][1000 genomes]
rs73490554	1.00[EUR][1000 genomes]
rs73501797	1.00[EUR][1000 genomes]
rs73501800	1.00[EUR][1000 genomes]
rs73506004	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506015	1.00[EUR][1000 genomes]
rs73506054	1.00[EUR][1000 genomes]
rs73506056	1.00[EUR][1000 genomes]
rs73506069	1.00[EUR][1000 genomes]
rs73506074	1.00[EUR][1000 genomes]
rs743679	1.00[EUR][1000 genomes]
rs7941752	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7947114	1.00[EUR][1000 genomes]
rs8191436	1.00[EUR][1000 genomes]
rs8191446	1.00[EUR][1000 genomes]
rs8191449	1.00[EUR][1000 genomes]
rs949250	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949251	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949252	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949253	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949254	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949255	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 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	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
3	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
4	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
5	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
6	nsv897804	chr11:67090571-67224278	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
7	nsv1039205	chr11:67135246-67252397	Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Weak transcription 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	122 gene(s)	inside rSNPs	diseases
8	esv1818769	chr11:67138811-67300457	Flanking Active TSS Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	167 gene(s)	inside rSNPs	diseases
9	esv1798859	chr11:67139954-67272983	Active TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
10	nsv897805	chr11:67155210-67283891	ZNF genes & repeats Flanking Active TSS Genic enhancers Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
11	nsv897806	chr11:67155210-67294308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Enhancers 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	148 gene(s)	inside rSNPs	diseases
12	nsv897807	chr11:67155210-67414492	Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Active TSS Enhancers Weak transcription 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 miRNA target site	176 gene(s)	inside rSNPs	diseases
13	nsv897808	chr11:67155210-67419855	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	176 gene(s)	inside rSNPs	diseases
14	nsv897809	chr11:67156875-67276235	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	148 gene(s)	inside rSNPs	diseases
15	nsv555254	chr11:67164495-67288594	Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
16	nsv534229	chr11:67164667-67411909	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
17	nsv897813	chr11:67175692-67283891	Bivalent Enhancer Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Strong transcription 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	132 gene(s)	inside rSNPs	diseases
18	nsv521723	chr11:67175692-67311258	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
19	esv1847460	chr11:67182600-67219337	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
20	nsv524096	chr11:67186000-67224988	Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
21	nsv468604	chr11:67186000-67283891	Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
22	nsv555256	chr11:67186000-67283891	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	132 gene(s)	inside rSNPs	diseases
23	nsv527056	chr11:67207426-67294308	Genic enhancers Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	115 gene(s)	inside rSNPs	diseases
24	esv1813337	chr11:67217703-67235815	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67211800-67220000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr11:67211800-67231200	Weak transcription	Right Atrium	heart
3	chr11:67211800-67232000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr11:67212000-67219400	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr11:67212000-67219600	Weak transcription	Pancreas	Pancrea
6	chr11:67212000-67219800	Weak transcription	Esophagus	oesophagus
7	chr11:67212200-67219600	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr11:67212400-67219400	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr11:67212400-67226800	Enhancers	Primary B cells from peripheral blood	blood
10	chr11:67212600-67219800	Enhancers	Primary T helper cells fromperipheralblood	blood
11	chr11:67212800-67219600	Weak transcription	Lung	lung
12	chr11:67213000-67220000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:67213600-67219800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr11:67213600-67220000	Weak transcription	Rectal Mucosa Donor 29	rectum
15	chr11:67215400-67227200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:67215800-67230600	Weak transcription	Fetal Intestine Small	intestine
17	chr11:67216000-67219800	Weak transcription	Colonic Mucosa	Colon
18	chr11:67216400-67219600	Weak transcription	HUVEC	blood vessel
19	chr11:67216400-67219800	Enhancers	Primary B cells from cord blood	blood
20	chr11:67216600-67219400	Enhancers	Fetal Thymus	thymus
21	chr11:67217000-67219400	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr11:67217200-67231400	Weak transcription	Thymus	Thymus
23	chr11:67217800-67219400	Weak transcription	Adipose Nuclei	Adipose
24	chr11:67217800-67220400	Enhancers	Fetal Muscle Leg	muscle
25	chr11:67218000-67219600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr11:67218000-67221400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:67218200-67219400	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr11:67218200-67220200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
29	chr11:67218200-67221600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:67218400-67219400	Weak transcription	Placenta	Placenta
31	chr11:67218400-67220000	Weak transcription	Brain Hippocampus Middle	brain
32	chr11:67218600-67221800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr11:67218600-67227000	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr11:67219000-67220400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr11:67219000-67231400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr11:67219200-67219400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
37	chr11:67219200-67219400	Flanking Active TSS	Spleen	Spleen
38	chr11:67219200-67219800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr11:67219200-67219800	Enhancers	Gastric	stomach
40	chr11:67219200-67220000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:67219200-67225800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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