Variant report

Variant	rs4262761
Chromosome Location	chr12:72652175-72652176
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TPH2-3	chr12:72652079-72654128	NONHSAT029464

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10506650	0.92[CEU][hapmap];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10506652	0.92[CEU][hapmap];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10784960	0.89[CEU][hapmap];0.89[EUR][1000 genomes]
rs10879387	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10879391	0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10879392	0.92[CEU][hapmap];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10879394	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs10879398	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11179146	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11609294	0.87[EUR][1000 genomes]
rs12229324	0.91[CEU][hapmap];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3803030	1.00[CEU][hapmap];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4237861	0.88[CEU][hapmap];0.89[EUR][1000 genomes]
rs4254109	1.00[CEU][hapmap];0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4360737	0.87[EUR][1000 genomes]
rs4423229	0.87[EUR][1000 genomes]
rs4584622	0.88[CEU][hapmap];0.88[EUR][1000 genomes]
rs4587772	0.88[EUR][1000 genomes]
rs4639975	0.87[EUR][1000 genomes]
rs4760827	0.87[EUR][1000 genomes]
rs4760829	0.92[CEU][hapmap];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6421234	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7135786	1.00[CEU][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7295741	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs7307765	1.00[CEU][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7963246	0.88[EUR][1000 genomes]
rs7974998	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422452	chr12:72485933-73175581	Flanking Bivalent TSS/Enh Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv899257	chr12:72569746-73145896	ZNF genes & repeats Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
3	nsv832452	chr12:72584971-72764495	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv770	chr12:72615837-72660510	Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv899258	chr12:72624088-72957899	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv559362	chr12:72641784-72694691	Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
7	nsv1044083	chr12:72647640-73275526	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:72630400-72663200	Weak transcription	NH-A	brain
2	chr12:72646600-72663400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr12:72647600-72663000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr12:72647800-72663200	Weak transcription	Fetal Intestine Small	intestine
5	chr12:72648000-72663200	Weak transcription	NHLF	lung
6	chr12:72648400-72652600	Weak transcription	HMEC	breast
7	chr12:72648600-72653800	Weak transcription	Brain Angular Gyrus	brain
8	chr12:72649000-72652600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:72649600-72663400	Weak transcription	Pancreas	Pancrea
10	chr12:72649800-72653200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:72650800-72653000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr12:72650800-72653400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr12:72651600-72663400	Weak transcription	Fetal Kidney	kidney
14	chr12:72651800-72655400	Strong transcription	Adipose Nuclei	Adipose
15	chr12:72651800-72655800	Strong transcription	Fetal Intestine Large	intestine

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