Variant report
Variant | rs7079325 |
---|---|
Chromosome Location | chr10:18860469-18860470 |
allele | C/T |
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] |
---|---|
rs10400076 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10430567 | 0.87[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs1055116 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10734063 | 0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10741091 | 0.84[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10741111 | 0.90[ASN][1000 genomes] |
rs10741115 | 0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10741129 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs10741132 | 0.88[AMR][1000 genomes] |
rs10764582 | 0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10764583 | 0.89[AFR][1000 genomes];0.88[AMR][1000 genomes] |
rs10764600 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10764601 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10764602 | 0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs10764603 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10764604 | 0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs10764605 | 0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes] |
rs10764625 | 0.93[ASN][1000 genomes] |
rs10764640 | 0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10764691 | 0.87[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs10828851 | 0.86[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs10828870 | 0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs10828871 | 0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs10828872 | 0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs10828896 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10828911 | 0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs10828965 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10828967 | 0.85[AFR][1000 genomes];0.83[AMR][1000 genomes] |
rs10828975 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs10828983 | 0.95[ASN][1000 genomes] |
rs10828991 | 0.93[ASN][1000 genomes] |
rs10829009 | 0.93[ASN][1000 genomes] |
rs10829022 | 0.81[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10829037 | 0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs10829039 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10829040 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs10829058 | 0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10829060 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs10829070 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10829148 | 0.83[EUR][1000 genomes] |
rs10829151 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs10829213 | 0.87[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11014892 | 0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11015048 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11015077 | 0.95[ASN][1000 genomes] |
rs11015196 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11015255 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs11015312 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs11015421 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs11525266 | 0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11593617 | 0.88[ASN][1000 genomes] |
rs11812341 | 0.86[ASN][1000 genomes] |
rs11815228 | 0.88[ASN][1000 genomes] |
rs12219183 | 0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs12359758 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs12569474 | 0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs12569487 | 0.88[AFR][1000 genomes] |
rs12570792 | 0.81[AFR][1000 genomes] |
rs12766105 | 0.88[ASN][1000 genomes] |
rs12785031 | 0.84[ASN][1000 genomes] |
rs2272274 | 0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs3740102 | 0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs3817494 | 0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs4445544 | 0.88[ASN][1000 genomes] |
rs4747349 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs4747350 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs4747355 | 0.81[ASN][1000 genomes] |
rs4748488 | 0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4748492 | 0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs4748509 | 0.86[AMR][1000 genomes] |
rs5022622 | 0.93[ASN][1000 genomes] |
rs56410858 | 0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs57066269 | 0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs57579336 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62634837 | 0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs62634838 | 0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs62636218 | 0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6482533 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs6482597 | 0.91[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7077722 | 0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7081461 | 0.90[ASN][1000 genomes] |
rs7081690 | 0.92[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs7081977 | 0.95[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7085318 | 0.88[ASN][1000 genomes] |
rs7087030 | 0.91[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs7088091 | 0.81[AMR][1000 genomes] |
rs7093454 | 0.88[ASN][1000 genomes] |
rs7099260 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7100880 | 0.84[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs72787951 | 0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[ASN][1000 genomes] |
rs72787963 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7477076 | 0.92[ASN][1000 genomes] |
rs7894016 | 0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7895784 | 0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs7898781 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7899017 | 0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs7901598 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7904263 | 0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs7907891 | 0.88[ASN][1000 genomes] |
rs7909570 | 0.87[AMR][1000 genomes] |
rs7909845 | 0.88[AMR][1000 genomes];0.81[EUR][1000 genomes] |
rs7917584 | 0.91[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs7919487 | 0.88[ASN][1000 genomes] |
rs7922550 | 0.87[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7922829 | 0.87[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 | nsv550042 | chr10:18683267-18994583 | ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 16 gene(s) | inside rSNPs | diseases |
2 | esv34545 | chr10:18821185-18908294 | Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 5 gene(s) | inside rSNPs | diseases |
3 | esv1793653 | chr10:18827828-18888369 | Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
4 | esv1794817 | chr10:18827828-18888369 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
5 | esv1811259 | chr10:18827828-18888369 | ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
6 | esv1840241 | chr10:18827828-18888369 | Enhancers Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
7 | esv1841068 | chr10:18827828-18888369 | Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
8 | esv1851495 | chr10:18827828-18888369 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
9 | esv1835982 | chr10:18833550-18872699 | Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | esv2757371 | chr10:18835325-18906507 | Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
11 | esv2759736 | chr10:18835325-18906507 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
12 | esv1814421 | chr10:18839350-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | TF binding region | 2 gene(s) | inside rSNPs | diseases |
13 | nsv466760 | chr10:18839350-18905935 | Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
14 | nsv550044 | chr10:18839350-18905935 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 4 gene(s) | inside rSNPs | diseases |
15 | esv18824 | chr10:18841137-18862749 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
16 | nsv550052 | chr10:18841795-18860469 | ZNF genes & repeats Strong transcription Weak transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
17 | nsv550053 | chr10:18841795-18861203 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
18 | nsv550054 | chr10:18841795-18862122 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
19 | esv1802087 | chr10:18841795-18862211 | ZNF genes & repeats Strong transcription Weak transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
20 | esv1805552 | chr10:18841795-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
21 | esv1807060 | chr10:18841795-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
22 | esv1812459 | chr10:18841795-18862211 | ZNF genes & repeats Strong transcription Weak transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
23 | esv1834849 | chr10:18841795-18862211 | ZNF genes & repeats Strong transcription Weak transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
24 | esv1836472 | chr10:18841795-18862211 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
25 | esv1842030 | chr10:18841795-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
26 | esv1850544 | chr10:18841795-18862211 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
27 | nsv550055 | chr10:18841795-18862211 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
28 | nsv550056 | chr10:18841795-18862728 | ZNF genes & repeats Strong transcription Weak transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
29 | esv1845973 | chr10:18841795-18872699 | Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Enhancers Flanking Active TSS | TF binding regionChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
30 | esv1793359 | chr10:18841795-18872872 | ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS | TF binding regionChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
31 | nsv550061 | chr10:18843332-18860469 | Strong transcription Weak transcription ZNF genes & repeats Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
32 | nsv550062 | chr10:18843332-18861203 | Weak transcription Strong transcription ZNF genes & repeats Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
33 | nsv550063 | chr10:18843332-18862122 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
34 | nsv550064 | chr10:18843332-18862211 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
35 | nsv550066 | chr10:18844621-18860594 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | TF binding region | 1 gene(s) | inside rSNPs | diseases |
36 | nsv550073 | chr10:18846155-18860469 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
37 | nsv550074 | chr10:18846155-18860594 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
38 | nsv550075 | chr10:18846155-18861203 | Weak transcription Strong transcription ZNF genes & repeats Enhancers | n/a | n/a | inside rSNPs | diseases |
39 | nsv550076 | chr10:18846155-18862122 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
40 | esv1809399 | chr10:18846155-18862211 | Weak transcription Strong transcription ZNF genes & repeats Enhancers | n/a | n/a | inside rSNPs | diseases |
41 | esv1815913 | chr10:18846155-18862211 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
42 | esv1838942 | chr10:18846155-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
43 | esv1838957 | chr10:18846155-18862211 | Weak transcription Strong transcription ZNF genes & repeats Enhancers | n/a | n/a | inside rSNPs | diseases |
44 | esv1841381 | chr10:18846155-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
45 | nsv550077 | chr10:18846155-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
46 | nsv550082 | chr10:18846206-18861203 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
47 | esv1807864 | chr10:18846206-18862211 | ZNF genes & repeats Weak transcription Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
48 | nsv550083 | chr10:18846206-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
49 | nsv550086 | chr10:18846312-18862211 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
50 | nsv550093 | chr10:18847555-18860594 | Weak transcription ZNF genes & repeats Strong transcription Enhancers | n/a | n/a | inside rSNPs | diseases |
SNP | Gene | Cis/trans | Tissue | Source |
---|---|---|---|---|
rs7079325 | NSUN6 | Cis_1M | lymphoblastoid | RTeQTL |
rs7079325 | NSUN6 | cis | lung | GTEx |
rs7079325 | ARL5B | cis | multi-tissue | Pritchard |
rs7079325 | ARL5B | Cis_1M | lymphoblastoid | RTeQTL |
rs7079325 | ARL5B | cis | Whole Blood | GTEx |
rs7079325 | RP11-499P20.2 | cis | Esophagus Mucosa | GTEx |
rs7079325 | CACNB2 | Cis_1M | lymphoblastoid | RTeQTL |
rs7079325 | RP11-499P20.2 | cis | Thyroid | GTEx |
rs7079325 | RP11-499P20.2 | cis | Skin Sun Exposed Lower leg | GTEx |
rs7079325 | RP11-499P20.2 | cis | lung | GTEx |
rs7079325 | RP11-499P20.2 | cis | Whole Blood | GTEx |
rs7079325 | RP11-499P20.2 | cis | Nerve Tibial | GTEx |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr10:18840800-18867200 | Weak transcription | Fetal Thymus | thymus |
2 | chr10:18842000-18866800 | Weak transcription | Left Ventricle | heart |
3 | chr10:18842000-18868400 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
4 | chr10:18842000-18869200 | Weak transcription | Stomach Smooth Muscle | stomach |
5 | chr10:18842000-18886400 | Weak transcription | Colon Smooth Muscle | Colon |
6 | chr10:18844000-18871000 | Weak transcription | Fetal Heart | heart |
7 | chr10:18846200-18899200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
8 | chr10:18846400-18866600 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
9 | chr10:18846600-18866600 | Weak transcription | Pancreas | Pancrea |
10 | chr10:18848400-18915800 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
11 | chr10:18848800-18866800 | Weak transcription | Aorta | Aorta |
12 | chr10:18849000-18868600 | Weak transcription | Gastric | stomach |
13 | chr10:18849400-18866200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
14 | chr10:18849800-18910800 | Weak transcription | Brain Inferior Temporal Lobe | brain |
15 | chr10:18850000-18865600 | Weak transcription | Primary T helper cells PMA-I stimulated | -- |
16 | chr10:18852600-18864800 | Weak transcription | Ovary | ovary |
17 | chr10:18853200-18866800 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
18 | chr10:18855000-18862200 | ZNF genes & repeats | iPS-20b Cell Line | embryonic stem cell |
19 | chr10:18858000-18863200 | ZNF genes & repeats | HUES64 Cell Line | embryonic stem cell |
20 | chr10:18858200-18861200 | ZNF genes & repeats | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
21 | chr10:18858400-18861200 | ZNF genes & repeats | Fetal Lung | lung |
22 | chr10:18859600-18868600 | Weak transcription | K562 | blood |
23 | chr10:18860000-18863200 | ZNF genes & repeats | H1 Cell Line | embryonic stem cell |
24 | chr10:18860400-18863200 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |