Variant report
Variant | rs2421575 |
---|---|
Chromosome Location | chr2:73919522-73919523 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10172044 | 0.82[EUR][1000 genomes] |
rs10191988 | 0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10200762 | 0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10208995 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs11126414 | 1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs11126415 | 0.96[CEU][hapmap];0.93[CHB][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs11126416 | 0.88[CEU][hapmap];0.83[EUR][1000 genomes] |
rs11126417 | 0.87[CEU][hapmap];0.82[EUR][1000 genomes] |
rs11891140 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs11892172 | 0.87[CEU][hapmap];0.84[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs11894953 | 0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12052539 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12053242 | 0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12233112 | 1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs12233115 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs12611487 | 0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs12612423 | 0.82[AMR][1000 genomes] |
rs12615807 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12619258 | 1.00[CEU][hapmap];0.93[CHB][hapmap];0.92[YRI][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12620091 | 0.84[CHB][hapmap] |
rs12624267 | 0.87[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12713788 | 0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12713789 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12713790 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12713791 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12713793 | 0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs12713794 | 0.83[EUR][1000 genomes] |
rs12713795 | 0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs12713797 | 0.82[EUR][1000 genomes] |
rs12713798 | 0.87[CEU][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs12992607 | 0.88[CEU][hapmap];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12997018 | 0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12997568 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs12998980 | 1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs13000788 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs13003035 | 0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs13005729 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs13006448 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13006598 | 0.83[AMR][1000 genomes] |
rs13013228 | 0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13014700 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13015885 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13020517 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs13022837 | 0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13026192 | 0.93[EUR][1000 genomes] |
rs13031853 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13031866 | 0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17350056 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17350125 | 0.96[CEU][hapmap];0.93[CHB][hapmap];0.82[YRI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17350188 | 0.87[CEU][hapmap];0.88[YRI][hapmap];0.92[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs17434634 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17434655 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1806683 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs1815028 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs2001436 | 1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2001490 | 1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2006997 | 0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs2012574 | 0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs2116367 | 0.88[CEU][hapmap] |
rs2272051 | 0.83[CEU][hapmap];0.80[AMR][1000 genomes] |
rs2272178 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs2421557 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2421558 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs2421559 | 0.83[CEU][hapmap];0.84[AMR][1000 genomes] |
rs2421574 | 0.83[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2421582 | 0.82[CHB][hapmap] |
rs2421672 | 0.83[CEU][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs2421674 | 0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs2421675 | 0.88[CEU][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs2421676 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes] |
rs2421677 | 0.83[EUR][1000 genomes] |
rs35421685 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs35498419 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs35767294 | 0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35791379 | 0.87[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs3813228 | 0.83[CEU][hapmap] |
rs3980695 | 0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs4241257 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4358149 | 0.87[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4513320 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4530394 | 0.82[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs4852316 | 0.91[EUR][1000 genomes] |
rs4852938 | 0.87[AFR][1000 genomes] |
rs4852966 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4852967 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4852972 | 0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4852975 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs4852976 | 0.96[CEU][hapmap];0.92[CHB][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4852977 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4852978 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs6732812 | 0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs6748233 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6749841 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6750494 | 0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6750515 | 0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6750877 | 0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs6755500 | 0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs7210 | 0.87[CEU][hapmap];0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs7368570 | 0.84[AMR][1000 genomes] |
rs7370393 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs7558546 | 0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7591112 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs7597302 | 0.80[AMR][1000 genomes] |
rs7599453 | 0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7606947 | 0.83[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7608328 | 0.85[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs891695 | 0.81[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs891696 | 0.82[AMR][1000 genomes] |
rs9309475 | 0.87[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs9309476 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv428051 | chr2:73717032-74030067 | ZNF genes & repeats Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | esv2757806 | chr2:73717032-74078592 | Active TSS Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 36 gene(s) | inside rSNPs | diseases |
3 | esv2759060 | chr2:73717032-74078592 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 36 gene(s) | inside rSNPs | diseases |
4 | nsv1013385 | chr2:73822056-74041441 | Strong transcription Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
5 | nsv874274 | chr2:73847024-73922475 | Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv874275 | chr2:73847024-73931971 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv874276 | chr2:73847024-73964214 | Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 9 gene(s) | inside rSNPs | diseases |
8 | nsv1008311 | chr2:73854911-73923089 | Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
9 | esv3334222 | chr2:73867401-73923991 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv874277 | chr2:73870010-73931971 | Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
11 | nsv874278 | chr2:73870010-73931971 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
12 | esv3340115 | chr2:73870416-73930142 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
13 | nsv874280 | chr2:73870573-73927764 | Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
14 | esv2762675 | chr2:73875799-73928886 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
15 | nsv441760 | chr2:73875799-73928886 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
16 | esv3426494 | chr2:73876125-73939153 | Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
17 | esv3460808 | chr2:73877074-73940302 | Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
18 | esv3460809 | chr2:73877074-73940302 | Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
19 | nsv829461 | chr2:73877427-73931225 | Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
20 | nsv874281 | chr2:73878352-73927764 | Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
21 | nsv874282 | chr2:73878827-73922475 | Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
22 | nsv874283 | chr2:73878827-73927764 | Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
23 | esv2753082 | chr2:73891045-73955545 | Weak transcription Bivalent Enhancer Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
24 | nsv979022 | chr2:73897805-73932073 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
25 | esv34157 | chr2:73901718-73949151 | Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
26 | nsv834260 | chr2:73906106-74076520 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 33 gene(s) | inside rSNPs | diseases |
27 | nsv998315 | chr2:73919185-74003998 | Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 11 gene(s) | inside rSNPs | diseases |
28 | nsv1000675 | chr2:73919185-74038946 | Active TSS Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:73900600-73954800 | Weak transcription | Brain Dorsolateral Prefrontal Cortex | brain |
2 | chr2:73902200-73931400 | Weak transcription | Brain Anterior Caudate | brain |
3 | chr2:73919200-73920000 | Weak transcription | Ovary | ovary |