Variant report

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11155311	0.82[ASN][1000 genomes]
rs12192270	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12193494	0.84[ASN][1000 genomes]
rs12193892	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12197980	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12199447	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13191026	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13195900	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13199178	0.80[AMR][1000 genomes]
rs13199393	0.84[ASN][1000 genomes]
rs1338535	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1539333	0.91[EUR][1000 genomes]
rs17291151	0.80[AMR][1000 genomes]
rs2328507	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34196129	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35286147	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35296418	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4424099	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs56392216	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67470559	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6911970	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6937798	0.84[ASN][1000 genomes]
rs7745970	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7757372	0.88[EUR][1000 genomes]
rs9496699	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758084	chr6:143916621-144079976	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759476	chr6:143916621-144079976	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1032369	chr6:143925374-144007513	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv604805	chr6:143930404-144005949	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143917000-143973600	Weak transcription	Fetal Intestine Small	intestine
2	chr6:143930400-143949400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr6:143930800-143946600	Weak transcription	Primary T cells from cord blood	blood
4	chr6:143935600-143946600	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr6:143936400-143946200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:143937000-143946600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:143937000-143947000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr6:143939000-143955800	Weak transcription	Stomach Mucosa	stomach
9	chr6:143939600-143946200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr6:143942200-143950600	Weak transcription	Esophagus	oesophagus
11	chr6:143942200-143955600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr6:143942400-143947400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr6:143943000-143946200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
14	chr6:143943600-143950400	Weak transcription	Fetal Stomach	stomach
15	chr6:143943800-143945400	Weak transcription	Aorta	Aorta
16	chr6:143943800-143950600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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