Variant report

Variant	rs57749415
Chromosome Location	chr11:67274621-67274622
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5)
CpG islands
(count:0)
Chromatin interactive
region (count:35)
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	CHD1	chr11:67271489-67275717	IMR90	lung:	n/a	chr11:67272871-67272881
2	HCFC1	chr11:67274349-67276814	Hela-S3	cervix:	n/a	n/a
3	CTCF	chr11:67272561-67275214	A549	lung:	n/a	chr11:67273761-67273770 chr11:67273757-67273770 chr11:67273750-67273771 chr11:67273760-67273773 chr11:67273758-67273768 chr11:67274999-67275012 chr11:67273211-67273224 chr11:67273756-67273772 chr11:67273755-67273773
4	RCOR1	chr11:67274557-67276938	IMR90	lung:	n/a	n/a
5	JUN	chr11:67274578-67276903	K562	blood:	n/a	chr11:67275627-67275636 chr11:67276199-67276208

No data

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67118066..67122624-chr11:67272137..67276691,11	MCF-7	breast:
2	chr11:67247191..67252288-chr11:67270350..67277699,12	MCF-7	breast:
3	chr11:67234460..67237754-chr11:67271882..67275850,7	MCF-7	breast:
4	chr11:67206947..67211030-chr11:67273670..67277577,4	MCF-7	breast:
5	chr11:67157498..67160851-chr11:67271704..67276538,6	K562	blood:
6	chr11:67230107..67238941-chr11:67268499..67277838,23	MCF-7	breast:
7	chr11:67274110..67276658-chr11:67374314..67376513,2	K562	blood:
8	chr11:67164456..67171429-chr11:67268926..67279263,19	K562	blood:
9	chr11:67172030..67174041-chr11:67273255..67275268,2	MCF-7	breast:
10	chr11:67232230..67234303-chr11:67273494..67275304,2	K562	blood:
11	chr11:67052872..67055062-chr11:67273802..67275420,2	K562	blood:
12	chr11:67186666..67191064-chr11:67273296..67275634,4	K562	blood:
13	chr11:67175295..67177468-chr11:67274003..67276174,2	MCF-7	breast:
14	chr11:67234712..67238016-chr11:67274176..67276331,3	K562	blood:
15	chr11:67274528..67277767-chr11:67349958..67353064,4	K562	blood:
16	chr11:67172672..67175218-chr11:67274575..67276166,2	K562	blood:
17	chr11:67182567..67190511-chr11:67270739..67276166,13	MCF-7	breast:
18	chr11:67139414..67143301-chr11:67273275..67276817,6	MCF-7	breast:
19	chr11:67140485..67142430-chr11:67273527..67275502,2	K562	blood:
20	chr11:67272696..67275492-chr11:67373280..67375901,2	MCF-7	breast:
21	chr11:67255717..67258681-chr11:67274499..67276548,2	K562	blood:
22	chr11:67166559..67171272-chr11:67271633..67274655,6	MCF-7	breast:
23	chr11:67140165..67142541-chr11:67273740..67276217,2	MCF-7	breast:
24	chr11:67256017..67258793-chr11:67272672..67274747,2	MCF-7	breast:
25	chr11:67271788..67274805-chr11:67372108..67375948,3	K562	blood:
26	chr11:67194364..67200337-chr11:67272800..67277654,9	MCF-7	breast:
27	chr11:67201204..67205243-chr11:67272634..67278205,5	MCF-7	breast:
28	chr11:67270685..67273123-chr11:67274247..67277444,3	K562	blood:
29	chr11:67272994..67275730-chr6:26029475..26032362,2	K562	blood:
30	chr11:67164491..67170697-chr11:67268115..67277759,17	MCF-7	breast:
31	chr11:67232230..67238185-chr11:67272105..67277120,9	K562	blood:
32	chr11:67156232..67161608-chr11:67271298..67276147,11	MCF-7	breast:
33	chr11:67201617..67208575-chr11:67270788..67277143,13	K562	blood:
34	chr11:67186666..67189529-chr11:67272076..67275550,4	K562	blood:
35	chr11:67156605..67157522-chr11:67274230..67274911,2	K562	blood:

No data

Variant related genes	Relation type
PITPNM1	TF binding region
ENSG00000084207	Chromatin interaction
ENSG00000255949	Chromatin interaction
ENSG00000172508	Chromatin interaction
ENSG00000172531	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000172613	Chromatin interaction
ENSG00000167792	Chromatin interaction
ENSG00000175505	Chromatin interaction
ENSG00000256514	Chromatin interaction
ENSG00000172725	Chromatin interaction
ENSG00000255119	Chromatin interaction
ENSG00000172663	Chromatin interaction
ENSG00000110697	Chromatin interaction
ENSG00000175482	Chromatin interaction
ENSG00000175634	Chromatin interaction
ENSG00000175463	Chromatin interaction
ENSG00000184224	Chromatin interaction
ENSG00000213402	Chromatin interaction
ENSG00000110711	Chromatin interaction

Extended variants
information (count: 134 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10896175	1.00[EUR][1000 genomes]
rs11227796	1.00[EUR][1000 genomes]
rs11227804	1.00[EUR][1000 genomes]
rs11821703	1.00[EUR][1000 genomes]
rs12288316	1.00[EUR][1000 genomes]
rs12293606	1.00[EUR][1000 genomes]
rs1382089	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1618605	1.00[EUR][1000 genomes]
rs1620333	1.00[EUR][1000 genomes]
rs1624189	1.00[EUR][1000 genomes]
rs1625032	1.00[EUR][1000 genomes]
rs1625892	1.00[EUR][1000 genomes]
rs1630068	1.00[EUR][1000 genomes]
rs1632616	1.00[EUR][1000 genomes]
rs1638558	1.00[EUR][1000 genomes]
rs1638559	1.00[EUR][1000 genomes]
rs1638560	1.00[EUR][1000 genomes]
rs1638561	1.00[EUR][1000 genomes]
rs1638562	1.00[EUR][1000 genomes]
rs1638563	1.00[EUR][1000 genomes]
rs1638570	1.00[EUR][1000 genomes]
rs1638572	1.00[EUR][1000 genomes]
rs1638575	1.00[EUR][1000 genomes]
rs1638576	1.00[EUR][1000 genomes]
rs1638577	1.00[EUR][1000 genomes]
rs1638581	1.00[EUR][1000 genomes]
rs1638584	1.00[EUR][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	1.00[EUR][1000 genomes]
rs1790741	1.00[EUR][1000 genomes]
rs1790743	1.00[EUR][1000 genomes]
rs1790744	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	1.00[EUR][1000 genomes]
rs1790763	1.00[EUR][1000 genomes]
rs1790764	1.00[EUR][1000 genomes]
rs1790765	1.00[EUR][1000 genomes]
rs1824712	0.85[AMR][1000 genomes];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	1.00[EUR][1000 genomes]
rs2511059	1.00[EUR][1000 genomes]
rs2514013	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514014	1.00[EUR][1000 genomes]
rs2514015	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514018	0.85[AMR][1000 genomes]
rs2514024	1.00[EUR][1000 genomes]
rs2514045	1.00[EUR][1000 genomes]
rs2514064	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2514262	1.00[EUR][1000 genomes]
rs2514263	1.00[EUR][1000 genomes]
rs2885171	1.00[EUR][1000 genomes]
rs3016861	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35363135	1.00[EUR][1000 genomes]
rs36052107	1.00[EUR][1000 genomes]
rs5019164	1.00[EUR][1000 genomes]
rs56050553	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56102510	1.00[EUR][1000 genomes]
rs56405884	1.00[EUR][1000 genomes]
rs57047868	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57134963	1.00[EUR][1000 genomes]
rs57748654	1.00[EUR][1000 genomes]
rs57757103	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57955602	1.00[EUR][1000 genomes]
rs58999825	1.00[EUR][1000 genomes]
rs59500232	1.00[EUR][1000 genomes]
rs596431	1.00[EUR][1000 genomes]
rs596944	1.00[EUR][1000 genomes]
rs601363	1.00[EUR][1000 genomes]
rs60136955	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60251934	1.00[EUR][1000 genomes]
rs602720	1.00[EUR][1000 genomes]
rs604540	1.00[EUR][1000 genomes]
rs60521870	1.00[EUR][1000 genomes]
rs611697	1.00[EUR][1000 genomes]
rs61282424	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61429992	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61610719	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs618633	1.00[EUR][1000 genomes]
rs641081	1.00[EUR][1000 genomes]
rs6591267	1.00[EUR][1000 genomes]
rs7104627	1.00[EUR][1000 genomes]
rs7121803	1.00[EUR][1000 genomes]
rs7124630	1.00[EUR][1000 genomes]
rs73490545	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73490554	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506004	1.00[EUR][1000 genomes]
rs73506015	1.00[EUR][1000 genomes]
rs73506048	1.00[AMR][1000 genomes]
rs73506054	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506056	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506069	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73506074	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs743679	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7934566	1.00[EUR][1000 genomes]
rs7947114	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8191436	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8191446	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8191449	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs949250	1.00[EUR][1000 genomes]
rs949251	1.00[EUR][1000 genomes]
rs949252	1.00[EUR][1000 genomes]
rs949253	1.00[EUR][1000 genomes]
rs949254	1.00[EUR][1000 genomes]
rs949255	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	esv2422195	chr11:67234322-67626901	Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	146 gene(s)	inside rSNPs	diseases
19	nsv1052919	chr11:67252337-67306030	Active TSS Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
20	nsv541078	chr11:67252337-67306030	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	70 gene(s)	inside rSNPs	diseases
21	esv3407558	chr11:67274456-67274781	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67270600-67276600	Enhancers	Fetal Heart	heart
2	chr11:67271000-67276800	Active TSS	Pancreatic Islets	Pancreatic Islet
3	chr11:67271200-67275400	Flanking Active TSS	Pancreas	Pancrea
4	chr11:67271200-67275600	Flanking Active TSS	Colonic Mucosa	Colon
5	chr11:67272600-67274800	Weak transcription	Fetal Kidney	kidney
6	chr11:67272600-67276400	Enhancers	Fetal Brain Male	brain
7	chr11:67272800-67274800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr11:67272800-67274800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr11:67272800-67274800	Enhancers	Spleen	Spleen
10	chr11:67272800-67275000	Weak transcription	Small Intestine	intestine
11	chr11:67272800-67275200	Weak transcription	Ovary	ovary
12	chr11:67273000-67274800	Enhancers	H1 Cell Line	embryonic stem cell
13	chr11:67273000-67274800	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr11:67273000-67275000	Flanking Active TSS	GM12878-XiMat	blood
15	chr11:67273000-67275000	Flanking Active TSS	HepG2	liver
16	chr11:67273000-67275400	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
17	chr11:67273000-67275400	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
18	chr11:67273200-67274800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr11:67273200-67275000	Enhancers	Primary hematopoietic stem cells	blood
20	chr11:67273200-67275000	Enhancers	Fetal Muscle Trunk	muscle
21	chr11:67273400-67274800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:67273400-67275400	Enhancers	Placenta Amnion	Placenta Amnion
23	chr11:67273400-67276600	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr11:67273600-67274800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr11:67273600-67274800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr11:67273600-67274800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr11:67273600-67274800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:67273600-67274800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr11:67273600-67274800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
30	chr11:67273600-67274800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr11:67273600-67274800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr11:67273600-67274800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr11:67273600-67274800	Weak transcription	Aorta	Aorta
34	chr11:67273600-67274800	Enhancers	Brain Germinal Matrix	brain
35	chr11:67273600-67274800	Enhancers	Brain Substantia Nigra	brain
36	chr11:67273600-67274800	Enhancers	Esophagus	oesophagus
37	chr11:67273600-67274800	Active TSS	Psoas Muscle	Psoas
38	chr11:67273600-67274800	Weak transcription	Right Atrium	heart
39	chr11:67273600-67274800	Enhancers	NHDF-Ad	bronchial
40	chr11:67273600-67274800	Active TSS	Osteobl	bone
41	chr11:67273600-67275000	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr11:67273600-67275400	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
43	chr11:67273600-67276800	Active TSS	HUES64 Cell Line	embryonic stem cell
44	chr11:67273800-67274800	Enhancers	Primary neutrophils fromperipheralblood	blood
45	chr11:67273800-67274800	Genic enhancers	Primary B cells from peripheral blood	blood
46	chr11:67273800-67274800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
47	chr11:67273800-67274800	Enhancers	Primary T killer memory cells from peripheral blood	blood
48	chr11:67273800-67274800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:67273800-67274800	Enhancers	Adipose Nuclei	Adipose
50	chr11:67273800-67274800	Enhancers	Colon Smooth Muscle	Colon

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