Variant report
Variant | rs4550961 |
---|---|
Chromosome Location | chr4:76978693-76978694 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10002099 | 0.81[EUR][1000 genomes] |
rs10003240 | 0.80[EUR][1000 genomes] |
rs10003382 | 0.80[EUR][1000 genomes] |
rs10010920 | 0.86[EUR][1000 genomes] |
rs10014049 | 0.80[EUR][1000 genomes] |
rs10014837 | 0.80[EUR][1000 genomes] |
rs10017431 | 0.80[EUR][1000 genomes] |
rs10021768 | 0.80[EUR][1000 genomes] |
rs10025102 | 0.80[EUR][1000 genomes] |
rs10025181 | 0.86[EUR][1000 genomes] |
rs10033061 | 0.82[EUR][1000 genomes] |
rs10034055 | 0.83[EUR][1000 genomes] |
rs10856873 | 0.85[EUR][1000 genomes] |
rs11097212 | 0.80[EUR][1000 genomes] |
rs11097219 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs12502834 | 0.85[EUR][1000 genomes] |
rs12510335 | 0.82[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs12647111 | 0.81[EUR][1000 genomes] |
rs13105341 | 0.83[EUR][1000 genomes] |
rs13111790 | 0.85[EUR][1000 genomes] |
rs13113455 | 0.86[EUR][1000 genomes] |
rs13113632 | 0.85[EUR][1000 genomes] |
rs13128319 | 0.86[EUR][1000 genomes] |
rs13130018 | 0.80[EUR][1000 genomes] |
rs13130221 | 0.80[EUR][1000 genomes] |
rs13133745 | 0.81[EUR][1000 genomes] |
rs28433437 | 0.85[EUR][1000 genomes] |
rs28505472 | 0.84[EUR][1000 genomes] |
rs28548768 | 0.85[EUR][1000 genomes] |
rs28642977 | 0.82[EUR][1000 genomes] |
rs28681066 | 0.83[EUR][1000 genomes] |
rs28681694 | 0.85[EUR][1000 genomes] |
rs28757394 | 0.82[EUR][1000 genomes] |
rs28848839 | 0.82[EUR][1000 genomes] |
rs28868672 | 0.84[EUR][1000 genomes] |
rs28896243 | 0.82[EUR][1000 genomes] |
rs3921 | 0.80[EUR][1000 genomes] |
rs4129781 | 0.82[EUR][1000 genomes] |
rs4241578 | 0.80[EUR][1000 genomes] |
rs4241580 | 0.80[EUR][1000 genomes] |
rs4241581 | 0.82[EUR][1000 genomes] |
rs4257674 | 0.80[EUR][1000 genomes] |
rs4276310 | 0.82[EUR][1000 genomes] |
rs4302486 | 0.80[EUR][1000 genomes] |
rs4304003 | 0.85[EUR][1000 genomes] |
rs4309862 | 0.80[EUR][1000 genomes] |
rs4331799 | 0.80[EUR][1000 genomes] |
rs4345214 | 0.80[EUR][1000 genomes] |
rs4356932 | 0.80[EUR][1000 genomes] |
rs4359936 | 0.85[EUR][1000 genomes] |
rs4359937 | 0.82[EUR][1000 genomes] |
rs4373188 | 0.84[EUR][1000 genomes] |
rs4380549 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs4386624 | 0.80[EUR][1000 genomes] |
rs4394024 | 0.81[EUR][1000 genomes] |
rs4401475 | 0.86[EUR][1000 genomes] |
rs4406046 | 0.81[EUR][1000 genomes] |
rs4417995 | 0.80[EUR][1000 genomes] |
rs4422436 | 0.86[EUR][1000 genomes] |
rs4432767 | 0.86[EUR][1000 genomes] |
rs4435768 | 0.85[EUR][1000 genomes] |
rs4456983 | 0.82[EUR][1000 genomes] |
rs4478212 | 0.82[EUR][1000 genomes] |
rs4524415 | 0.82[EUR][1000 genomes] |
rs4529084 | 0.81[EUR][1000 genomes] |
rs4532263 | 0.83[EUR][1000 genomes] |
rs4532264 | 0.84[EUR][1000 genomes] |
rs4535358 | 0.85[EUR][1000 genomes] |
rs4541535 | 0.83[EUR][1000 genomes] |
rs4543142 | 0.82[EUR][1000 genomes] |
rs4543147 | 0.86[EUR][1000 genomes] |
rs4547819 | 0.86[EUR][1000 genomes] |
rs4580676 | 0.80[EUR][1000 genomes] |
rs4583787 | 0.80[EUR][1000 genomes] |
rs4593163 | 0.86[EUR][1000 genomes] |
rs4605683 | 0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4610366 | 0.83[EUR][1000 genomes] |
rs4616778 | 0.86[EUR][1000 genomes] |
rs4637430 | 0.82[EUR][1000 genomes] |
rs4643846 | 0.84[EUR][1000 genomes] |
rs4859414 | 0.80[EUR][1000 genomes] |
rs4859415 | 0.81[EUR][1000 genomes] |
rs4859584 | 0.80[EUR][1000 genomes] |
rs4859586 | 0.80[EUR][1000 genomes] |
rs4859587 | 0.80[EUR][1000 genomes] |
rs4859588 | 0.80[EUR][1000 genomes] |
rs4859589 | 0.81[EUR][1000 genomes] |
rs4859590 | 0.80[EUR][1000 genomes] |
rs4859591 | 0.80[EUR][1000 genomes] |
rs4859595 | 0.80[EUR][1000 genomes] |
rs4859597 | 0.81[EUR][1000 genomes] |
rs4859598 | 0.82[EUR][1000 genomes] |
rs4859599 | 0.82[EUR][1000 genomes] |
rs4859600 | 0.81[EUR][1000 genomes] |
rs4859601 | 0.83[EUR][1000 genomes] |
rs4859602 | 0.83[EUR][1000 genomes] |
rs4859603 | 0.82[EUR][1000 genomes] |
rs4859604 | 0.81[EUR][1000 genomes] |
rs4859605 | 0.81[EUR][1000 genomes] |
rs6532093 | 0.80[EUR][1000 genomes] |
rs6532111 | 0.80[EUR][1000 genomes] |
rs6532114 | 0.81[EUR][1000 genomes] |
rs6532121 | 0.82[EUR][1000 genomes] |
rs6532130 | 0.83[EUR][1000 genomes] |
rs6532142 | 0.83[EUR][1000 genomes] |
rs6532143 | 0.82[EUR][1000 genomes] |
rs6532152 | 0.80[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs6532153 | 0.80[AFR][1000 genomes];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs6532155 | 0.85[EUR][1000 genomes] |
rs6532156 | 0.85[EUR][1000 genomes] |
rs6532157 | 0.85[EUR][1000 genomes] |
rs6532158 | 0.80[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs6532159 | 0.86[EUR][1000 genomes] |
rs6532160 | 0.86[EUR][1000 genomes] |
rs6532161 | 0.86[EUR][1000 genomes] |
rs6532163 | 0.86[EUR][1000 genomes] |
rs6532164 | 0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs6532165 | 0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs6532166 | 0.83[EUR][1000 genomes] |
rs6532172 | 0.85[EUR][1000 genomes] |
rs6811252 | 0.83[EUR][1000 genomes] |
rs6811301 | 0.83[EUR][1000 genomes] |
rs6811469 | 0.87[EUR][1000 genomes] |
rs6814012 | 0.80[EUR][1000 genomes] |
rs6814817 | 0.80[EUR][1000 genomes] |
rs6816898 | 0.80[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs6819597 | 0.81[EUR][1000 genomes] |
rs6825045 | 0.80[EUR][1000 genomes] |
rs6826163 | 0.85[EUR][1000 genomes] |
rs6826398 | 0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6826406 | 0.88[EUR][1000 genomes] |
rs6827767 | 0.83[EUR][1000 genomes] |
rs6828596 | 0.81[EUR][1000 genomes] |
rs6829896 | 0.83[EUR][1000 genomes] |
rs6835736 | 0.82[EUR][1000 genomes] |
rs6837830 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs6844097 | 0.80[EUR][1000 genomes] |
rs6845396 | 0.80[EUR][1000 genomes] |
rs6848603 | 0.89[EUR][1000 genomes] |
rs6848620 | 0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6850515 | 0.84[EUR][1000 genomes] |
rs6850760 | 0.80[EUR][1000 genomes] |
rs6852075 | 0.80[EUR][1000 genomes] |
rs6856681 | 0.86[EUR][1000 genomes] |
rs6856958 | 0.80[EUR][1000 genomes] |
rs6857372 | 0.86[EUR][1000 genomes] |
rs7375677 | 0.81[EUR][1000 genomes] |
rs7376624 | 0.84[EUR][1000 genomes] |
rs7376863 | 0.80[EUR][1000 genomes] |
rs7376943 | 0.86[EUR][1000 genomes] |
rs7377856 | 0.80[EUR][1000 genomes] |
rs7436646 | 0.80[EUR][1000 genomes] |
rs7655350 | 0.86[EUR][1000 genomes] |
rs7664354 | 0.86[EUR][1000 genomes] |
rs7665152 | 0.82[EUR][1000 genomes] |
rs7674409 | 0.82[EUR][1000 genomes] |
rs7676265 | 0.84[EUR][1000 genomes] |
rs7683657 | 0.82[EUR][1000 genomes] |
rs7684461 | 0.82[EUR][1000 genomes] |
rs7684889 | 0.82[EUR][1000 genomes] |
rs7688306 | 0.86[EUR][1000 genomes] |
rs7689664 | 0.82[EUR][1000 genomes] |
rs7699624 | 0.82[EUR][1000 genomes] |
rs8878 | 0.80[EUR][1000 genomes] |
rs9884374 | 0.80[EUR][1000 genomes] |
rs9990733 | 0.82[EUR][1000 genomes] |
rs9999755 | 0.82[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3353539 | chr4:76530136-76993859 | Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 51 gene(s) | inside rSNPs | diseases |
2 | nsv529613 | chr4:76654941-77081576 | Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 38 gene(s) | inside rSNPs | diseases |
3 | nsv1004627 | chr4:76793910-76999584 | Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs4550961 | NAAA | cis | Whole Blood | GTEx |
rs4550961 | NAAA | cis | Skin Sun Exposed Lower leg | GTEx |
rs4550961 | NAAA | cis | Heart Left Ventricle | GTEx |
rs4550961 | NAAA | cis | Artery Aorta | GTEx |
rs4550961 | CXCL10 | Cis_1M | lymphoblastoid | RTeQTL |
rs4550961 | NAAA | cis | Esophagus Muscularis | GTEx |
rs4550961 | NAAA | cis | Nerve Tibial | GTEx |
rs4550961 | ART3 | cis | Nerve Tibial | GTEx |
rs4550961 | NAAA | cis | Esophagus Mucosa | GTEx |
rs4550961 | ASAHL | Cis_1M | lymphoblastoid | RTeQTL |
rs4550961 | NAAA | cis | lung | GTEx |
rs4550961 | ASAHL | cis | multi-tissue | Pritchard |
rs4550961 | NAAA | cis | Adipose Subcutaneous | GTEx |
rs4550961 | NAAA | cis | Muscle Skeletal | GTEx |
rs4550961 | NAAA | cis | Artery Tibial | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:76975400-76979200 | Weak transcription | HMEC | breast |
2 | chr4:76976000-76979800 | Weak transcription | Fetal Intestine Small | intestine |
3 | chr4:76976000-76980800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
4 | chr4:76976200-76979800 | Weak transcription | Fetal Intestine Large | intestine |
5 | chr4:76976200-76980000 | Weak transcription | Primary monocytes fromperipheralblood | blood |
6 | chr4:76976400-76980200 | Weak transcription | Rectal Mucosa Donor 31 | rectum |
7 | chr4:76976600-76979400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
8 | chr4:76976600-76979400 | Weak transcription | Stomach Mucosa | stomach |
9 | chr4:76976600-76980600 | Weak transcription | Primary B cells from cord blood | blood |
10 | chr4:76977000-76979400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
11 | chr4:76977200-76979400 | Weak transcription | NHEK | skin |
12 | chr4:76977200-76980000 | Weak transcription | K562 | blood |
13 | chr4:76977400-76981600 | Weak transcription | Primary B cells from peripheral blood | blood |
14 | chr4:76977800-76978800 | Weak transcription | GM12878-XiMat | blood |
15 | chr4:76978000-76982800 | Weak transcription | HUES48 Cell Line | embryonic stem cell |