Variant report
Variant | rs1367043 |
---|---|
Chromosome Location | chr5:97006626-97006627 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:3)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
(count:3 , 50 per page) page:
1
No. | lncRNA name | Chromosome Location | lncRNA alias |
---|---|---|---|
1 | lnc-CTD-2215E18.1.1-2 | chr5:97006298-97006750 | XLOC_004483 |
2 | lnc-CTD-2215E18.1.1-2 | chr5:97006297-97006750 | NONHSAT102931 |
3 | lnc-CTD-2215E18.1.1-2 | chr5:97006298-97006755 | NR_105028 |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10041715 | 0.90[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10045335 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10045922 | 0.89[EUR][1000 genomes] |
rs10076476 | 0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10476720 | 0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10476723 | 0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10476724 | 0.96[EUR][1000 genomes] |
rs10476725 | 0.96[EUR][1000 genomes] |
rs10515257 | 0.88[ASN][1000 genomes] |
rs10515258 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs11135520 | 0.86[ASN][1000 genomes] |
rs11955062 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11957034 | 0.86[ASN][1000 genomes] |
rs11958000 | 0.86[ASN][1000 genomes] |
rs11958672 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11958735 | 0.86[ASN][1000 genomes] |
rs11958753 | 0.86[ASN][1000 genomes] |
rs11958897 | 0.86[ASN][1000 genomes] |
rs11959303 | 0.85[ASN][1000 genomes] |
rs11960434 | 0.86[ASN][1000 genomes] |
rs12153467 | 0.86[ASN][1000 genomes] |
rs12153708 | 0.84[ASN][1000 genomes] |
rs12186898 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12651707 | 0.86[ASN][1000 genomes] |
rs12652555 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12652654 | 0.87[ASN][1000 genomes] |
rs12653010 | 0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs12653049 | 0.86[ASN][1000 genomes] |
rs12653090 | 0.86[ASN][1000 genomes] |
rs12653530 | 0.83[ASN][1000 genomes] |
rs12653533 | 0.86[ASN][1000 genomes] |
rs12653710 | 0.85[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs12653789 | 0.87[ASN][1000 genomes] |
rs12654248 | 0.87[ASN][1000 genomes] |
rs12654249 | 0.87[ASN][1000 genomes] |
rs12654331 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12654570 | 0.87[ASN][1000 genomes] |
rs12654904 | 0.86[ASN][1000 genomes] |
rs12655451 | 0.87[ASN][1000 genomes] |
rs12655664 | 0.87[ASN][1000 genomes] |
rs12656115 | 0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs12656998 | 0.86[ASN][1000 genomes] |
rs12657000 | 0.86[ASN][1000 genomes] |
rs12657405 | 0.86[ASN][1000 genomes] |
rs12658079 | 0.88[ASN][1000 genomes] |
rs1560323 | 0.96[EUR][1000 genomes] |
rs1560325 | 0.82[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs1560327 | 0.96[EUR][1000 genomes] |
rs17087644 | 0.87[ASN][1000 genomes] |
rs17087647 | 0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs17087649 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs17087684 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17087722 | 0.85[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs2930824 | 0.85[ASN][1000 genomes] |
rs2930825 | 0.85[ASN][1000 genomes] |
rs2972980 | 0.87[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs2972982 | 0.83[ASN][1000 genomes] |
rs4280898 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4318808 | 0.96[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4370300 | 0.87[ASN][1000 genomes] |
rs4370301 | 0.87[ASN][1000 genomes] |
rs4371782 | 0.87[ASN][1000 genomes] |
rs4499855 | 0.87[ASN][1000 genomes] |
rs4565234 | 0.87[ASN][1000 genomes] |
rs4591774 | 0.87[ASN][1000 genomes] |
rs4869169 | 0.85[ASN][1000 genomes] |
rs4869170 | 0.85[ASN][1000 genomes] |
rs4869171 | 0.86[ASN][1000 genomes] |
rs4869172 | 0.86[ASN][1000 genomes] |
rs4869173 | 0.87[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4869175 | 0.87[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs4869176 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4869177 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4869178 | 0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4869362 | 0.87[ASN][1000 genomes] |
rs4869363 | 0.87[ASN][1000 genomes] |
rs4869364 | 0.90[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4869366 | 0.86[ASN][1000 genomes] |
rs4869367 | 0.86[ASN][1000 genomes] |
rs4869368 | 0.86[ASN][1000 genomes] |
rs4869369 | 0.86[ASN][1000 genomes] |
rs4869370 | 0.86[ASN][1000 genomes] |
rs4869380 | 0.87[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs4869381 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4869383 | 0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs4869384 | 0.85[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs4869385 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4869386 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs4869387 | 0.87[AMR][1000 genomes];0.80[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs5009275 | 0.86[ASN][1000 genomes] |
rs55869407 | 0.87[ASN][1000 genomes] |
rs55876261 | 0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs55930551 | 0.85[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs56159846 | 0.87[ASN][1000 genomes] |
rs56313483 | 0.87[ASN][1000 genomes] |
rs56691285 | 0.85[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs57093667 | 0.86[ASN][1000 genomes] |
rs58434977 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58789574 | 0.85[ASN][1000 genomes] |
rs58960401 | 0.86[ASN][1000 genomes] |
rs59482420 | 0.86[ASN][1000 genomes] |
rs59745660 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs60521916 | 0.86[ASN][1000 genomes] |
rs60859704 | 0.86[ASN][1000 genomes] |
rs61009572 | 0.87[ASN][1000 genomes] |
rs61120732 | 0.86[ASN][1000 genomes] |
rs61501692 | 0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs6556995 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6866014 | 0.86[ASN][1000 genomes] |
rs6876977 | 0.93[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs6879692 | 0.86[ASN][1000 genomes] |
rs6887204 | 0.96[EUR][1000 genomes] |
rs6898692 | 0.96[EUR][1000 genomes] |
rs72766393 | 0.80[ASN][1000 genomes] |
rs72766401 | 0.87[ASN][1000 genomes] |
rs72768203 | 0.86[EUR][1000 genomes] |
rs72768207 | 0.87[ASN][1000 genomes] |
rs72768209 | 0.87[ASN][1000 genomes] |
rs72768210 | 0.87[ASN][1000 genomes] |
rs72768213 | 0.86[ASN][1000 genomes] |
rs72768215 | 0.86[ASN][1000 genomes] |
rs72768216 | 0.86[ASN][1000 genomes] |
rs72768217 | 0.86[ASN][1000 genomes] |
rs72768218 | 0.86[ASN][1000 genomes] |
rs72768220 | 0.86[ASN][1000 genomes] |
rs72768222 | 0.86[ASN][1000 genomes] |
rs72768223 | 0.86[ASN][1000 genomes] |
rs72768233 | 0.87[ASN][1000 genomes] |
rs72768239 | 0.86[ASN][1000 genomes] |
rs72768240 | 0.87[ASN][1000 genomes] |
rs72768242 | 0.86[ASN][1000 genomes] |
rs72768248 | 0.87[ASN][1000 genomes] |
rs72768249 | 0.87[ASN][1000 genomes] |
rs72768250 | 0.87[ASN][1000 genomes] |
rs72774085 | 0.87[ASN][1000 genomes] |
rs72774086 | 0.87[ASN][1000 genomes] |
rs72774088 | 0.87[ASN][1000 genomes] |
rs72774094 | 0.87[ASN][1000 genomes] |
rs72775904 | 0.86[ASN][1000 genomes] |
rs72775906 | 0.86[ASN][1000 genomes] |
rs72775909 | 0.86[ASN][1000 genomes] |
rs72775911 | 0.85[ASN][1000 genomes] |
rs72775913 | 0.86[ASN][1000 genomes] |
rs72775914 | 0.86[ASN][1000 genomes] |
rs72775917 | 0.84[ASN][1000 genomes] |
rs72775919 | 0.84[ASN][1000 genomes] |
rs72775920 | 0.86[ASN][1000 genomes] |
rs72775921 | 0.87[ASN][1000 genomes] |
rs72775922 | 0.87[ASN][1000 genomes] |
rs72775924 | 0.87[ASN][1000 genomes] |
rs72775925 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs72775952 | 0.87[ASN][1000 genomes] |
rs72775953 | 0.88[ASN][1000 genomes] |
rs72775954 | 0.88[ASN][1000 genomes] |
rs72775955 | 0.87[ASN][1000 genomes] |
rs72775957 | 0.88[ASN][1000 genomes] |
rs72775958 | 0.87[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs72775963 | 0.87[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs72775966 | 0.87[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs72775977 | 0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs72775979 | 0.85[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs72775982 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72775984 | 0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs72775990 | 0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs72775991 | 0.85[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs72775992 | 0.87[AMR][1000 genomes];0.98[ASN][1000 genomes] |
rs72775998 | 0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7703706 | 0.96[EUR][1000 genomes] |
rs7709402 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7721614 | 0.96[EUR][1000 genomes] |
rs7722060 | 0.88[ASN][1000 genomes] |
rs9314213 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9314214 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9968766 | 0.91[EUR][1000 genomes];0.89[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534326 | chr5:96531217-97283481 | Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
2 | nsv882394 | chr5:96538585-97108559 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
3 | nsv1032548 | chr5:96565121-97046804 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv537813 | chr5:96565121-97046804 | Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
5 | nsv1022046 | chr5:96757900-97046804 | Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
6 | nsv1031429 | chr5:96777286-97269498 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
7 | nsv527650 | chr5:96783726-97260358 | Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
8 | nsv1028224 | chr5:96791214-97258383 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
9 | nsv537814 | chr5:96791214-97258383 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
10 | nsv882396 | chr5:96849023-97126520 | Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv882398 | chr5:96856849-97051163 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
12 | esv2422198 | chr5:96889331-97015454 | Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
13 | esv2422222 | chr5:96889331-97015454 | Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
14 | esv2422224 | chr5:96889331-97015454 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
15 | nsv1023404 | chr5:96889534-97071074 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Bivalent Enhancer Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
16 | nsv830417 | chr5:96915211-97129196 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
17 | nsv598965 | chr5:96934739-97101816 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
18 | nsv1020125 | chr5:96937248-97350644 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
19 | nsv462256 | chr5:96940843-97096042 | Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
20 | nsv598966 | chr5:96940843-97096042 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
21 | nsv598967 | chr5:96943871-97072819 | Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
22 | nsv4926 | chr5:96989823-97035011 | Enhancers Weak transcription Strong transcription | TF binding regionChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
23 | esv2755089 | chr5:96992975-97099320 | Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
24 | nsv598968 | chr5:97005141-97096042 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
25 | nsv462257 | chr5:97005141-97108559 | Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
26 | nsv598969 | chr5:97005141-97108559 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
27 | nsv432757 | chr5:97006304-97213768 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:97006000-97026800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |