Variant report

Variant	rs71514835
Chromosome Location	chr1:175886613-175886614
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFWD2-4	chr1:175886432-175887024	NONHSAT007762

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10913093	0.85[EUR][1000 genomes]
rs10913100	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11805196	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11807032	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12239742	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12406237	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12409939	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12724711	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12726210	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12726737	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12728682	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12730153	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12730725	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12735431	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12736942	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12738956	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12740514	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12745657	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12752542	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12752829	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12753832	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12754330	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12755734	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12757152	0.85[EUR][1000 genomes]
rs12758770	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12759426	0.83[EUR][1000 genomes]
rs12759478	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12759736	0.86[EUR][1000 genomes]
rs1303987	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57385190	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6687954	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7525623	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7528198	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7534440	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7551283	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7555561	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33328	chr1:175446583-175910001	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	esv1823794	chr1:175869554-176311778	Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
3	esv3344055	chr1:175873040-175887908	Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr1:175863200-175906400	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr1:175874400-175945600	Weak transcription	A549	lung
3	chr1:175877400-175894600	Weak transcription	HSMM	muscle
4	chr1:175877800-175902400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:175879800-175896000	Weak transcription	Fetal Stomach	stomach
6	chr1:175880000-175897200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr1:175880000-175897400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:175880000-175937800	Weak transcription	HSMMtube	muscle
9	chr1:175880400-175891800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:175880400-175904400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr1:175880600-175896200	Weak transcription	Placenta	Placenta
12	chr1:175880600-175896400	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr1:175881000-175897200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr1:175881000-175905200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr1:175881000-175924200	Weak transcription	Brain Angular Gyrus	brain
16	chr1:175881200-175894800	Weak transcription	Primary T cells from cord blood	blood
17	chr1:175881400-175889400	Weak transcription	Brain Germinal Matrix	brain
18	chr1:175881400-175893400	Weak transcription	GM12878-XiMat	blood
19	chr1:175881400-175894800	Weak transcription	Fetal Muscle Leg	muscle
20	chr1:175881400-175896600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr1:175881400-175897400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr1:175882000-175895000	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr1:175882600-175894600	Weak transcription	Fetal Brain Female	brain
24	chr1:175882600-175895600	Weak transcription	Lung	lung
25	chr1:175882600-175902200	Weak transcription	Aorta	Aorta
26	chr1:175882600-175910200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr1:175883200-175895000	Weak transcription	Adipose Nuclei	Adipose
28	chr1:175883200-175908200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:175883400-175886800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr1:175883400-175886800	Weak transcription	Brain Anterior Caudate	brain
31	chr1:175884200-175897400	Weak transcription	Pancreas	Pancrea
32	chr1:175884400-175886800	Bivalent Enhancer	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:175884400-175889200	Weak transcription	Right Atrium	heart
34	chr1:175885800-175896400	Weak transcription	Stomach Smooth Muscle	stomach
35	chr1:175885800-175897200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:175885800-175897400	Weak transcription	Left Ventricle	heart
37	chr1:175886000-175888600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:175886000-175895000	Weak transcription	Ovary	ovary
39	chr1:175886200-175896200	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr1:175886400-175886800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
41	chr1:175886400-175929400	Weak transcription	Brain Inferior Temporal Lobe	brain

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