Variant report

Variant	rs7941752
Chromosome Location	chr11:67229597-67229598
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:67201799..67203957-chr11:67229051..67231861,3	K562	blood:
2	chr11:67204954..67212426-chr11:67228820..67232211,6	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM134-1	chr11:67229181-67229791	ENSG00000270169.1

Variant related genes	Relation type
ENSG00000213402	Chromatin interaction
ENSG00000255949	Chromatin interaction
ENSG00000172725	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10896175	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227796	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11227804	0.86[AFR][1000 genomes]
rs12293606	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1618605	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1620333	0.90[AMR][1000 genomes]
rs1624189	0.90[AMR][1000 genomes]
rs1625032	0.90[AMR][1000 genomes]
rs1625892	0.90[AMR][1000 genomes]
rs1630068	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1632616	0.90[AMR][1000 genomes]
rs1638558	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1638559	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1638560	0.81[AMR][1000 genomes]
rs1638561	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs1638562	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1638563	0.90[AMR][1000 genomes]
rs1638575	0.90[AMR][1000 genomes]
rs1638576	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1638577	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1638581	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1638584	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1638585	0.90[AMR][1000 genomes]
rs1790736	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790741	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790743	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790744	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790756	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790763	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1790764	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes]
rs2511058	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2511059	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2514259	0.98[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2514262	0.90[AMR][1000 genomes]
rs35363135	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56405884	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs596431	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs596944	0.90[AMR][1000 genomes]
rs601363	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs602220	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs602720	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs604540	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs611697	0.90[AMR][1000 genomes]
rs641081	0.90[AMR][1000 genomes]
rs7121803	0.90[AMR][1000 genomes]
rs7124630	0.90[AMR][1000 genomes]
rs73506004	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs949250	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs949251	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs949252	0.90[AMR][1000 genomes]
rs949253	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs949254	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs949255	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 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	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	nsv983155	chr11:67220251-67251432	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67211800-67231200	Weak transcription	Right Atrium	heart
2	chr11:67211800-67232000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr11:67215800-67230600	Weak transcription	Fetal Intestine Small	intestine
4	chr11:67217200-67231400	Weak transcription	Thymus	Thymus
5	chr11:67219000-67231400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:67220400-67231400	Weak transcription	Gastric	stomach
7	chr11:67220400-67231400	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr11:67220400-67231400	Weak transcription	Right Ventricle	heart
9	chr11:67221400-67230800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr11:67223600-67231400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:67226200-67231000	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr11:67226400-67230600	Weak transcription	Spleen	Spleen
13	chr11:67227200-67231200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr11:67227400-67231400	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr11:67227400-67231800	Enhancers	Primary B cells from cord blood	blood
16	chr11:67227600-67230800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr11:67227600-67231200	Weak transcription	NHEK	skin
18	chr11:67227600-67231400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr11:67227600-67231400	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr11:67227600-67231400	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr11:67227600-67231400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr11:67227800-67230800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr11:67227800-67231000	Weak transcription	Fetal Thymus	thymus
24	chr11:67227800-67231200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr11:67228000-67230800	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr11:67228000-67230800	Enhancers	Primary B cells from peripheral blood	blood
27	chr11:67228000-67231600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr11:67228200-67231400	Weak transcription	Fetal Stomach	stomach
29	chr11:67228200-67231600	Weak transcription	Primary T cells from cord blood	blood
30	chr11:67228400-67231800	Weak transcription	Brain Germinal Matrix	brain
31	chr11:67228800-67230000	Weak transcription	Placenta	Placenta
32	chr11:67228800-67231200	Weak transcription	GM12878-XiMat	blood
33	chr11:67229200-67231200	Weak transcription	Fetal Muscle Leg	muscle
34	chr11:67229400-67229600	Enhancers	Skeletal Muscle Female	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links