Chrom. | Start | End | Enhancer ID | TSS of gene | Distance between enhancer and TSS | Tissues that enhancer appears | More |
---|---|---|---|---|---|---|---|
chr11 | 2082720 | 2083054 | vista9390 | 2182439 | 99385 |
|
|
chr11 | 2094981 | 2101122 | enh28559 | 2182439 | 81317 |
|
|
chr11 | 2111841 | 2126075 | enh13690 | 2182439 | 56364 |
|
|
chr11 | 2126698 | 2133125 | enh13691 | 2182439 | 49314 |
|
|
chr11 | 2140548 | 2144672 | enh94865 | 2182439 | 37767 |
|
|
chr11 | 2163004 | 2168086 | enh13692 | 2182439 | 14353 |
|
|
chr11 | 2164154 | 2164440 | vista9391 | 2182439 | 17999 |
|
|
chr11 | 2166198 | 2166337 | vista9392 | 2182439 | 16102 |
|
|
chr11 | 2176984 | 2177085 | vista9393 | 2182439 | 5354 |
|
|
chr11 | 2197020 | 2197182 | vista9394 | 2182439 | 14581 |
|
|
chr11 | 2198165 | 2204510 | enh79778 | 2182439 | 15726 |
|
|
chr11 | 2198525 | 2198662 | vista9395 | 2182439 | 16086 |
|
|
chr11 | 2200082 | 2200579 | vista9396 | 2182439 | 17643 |
|
|
chr11 | 2206004 | 2210212 | enh89599 | 2182439 | 23565 |
|
|
chr11 | 2210565 | 2239175 | enh13693 | 2182439 | 28126 |
|
|
chr11 | 2212480 | 2212615 | vista9397 | 2182439 | 30041 |
|
|
chr11 | 2213244 | 2213359 | vista9398 | 2182439 | 30805 |
|
|
chr11 | 2223798 | 2223980 | vista9399 | 2182439 | 41359 |
|
|
chr11 | 2226111 | 2226485 | vista9400 | 2182439 | 43672 |
|
|
chr11 | 2234751 | 2234909 | vista9401 | 2182439 | 52312 |
|
|
chr11 | 2238005 | 2238048 | vista9402 | 2182439 | 55566 |
|
|
chr11 | 2238430 | 2238670 | vista9403 | 2182439 | 55991 |
|
|
chr11 | 2241825 | 2245975 | enh98772 | 2182439 | 59386 |
|
|
chr11 | 2253365 | 2258975 | enh13694 | 2182439 | 70926 |
|
|
chr11 | 2275525 | 2280875 | enh13695 | 2182439 | 93086 |
|
|
chr11 | 2282365 | 2289515 | enh13696 | 2182439 | 99926 |
|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | TSS of gene | Distance between TFBS and gene | id | More |
---|---|---|---|---|---|---|---|---|---|---|
chr11 | 2176775 | 2177820 | TCF7L2 | GTRD | no | Colon (HCT116) | 2182439 | 4619 | 107952639 | |
chr11 | 2176805 | 2177668 | TCF7L2 | GTRD | no | Colon (HCT116) | 2182439 | 4771 | 107952640 | |
chr11 | 2176960 | 2177699 | TCF7L2 | GTRD | no | Colon (HCT116) | 2182439 | 4740 | 107952642 |
Chrom. | Position | dbSNP ID | Reference Allele | Alternative Allele | Distance between TSS and SNP | Tissue | q Value | id | More |
---|---|---|---|---|---|---|---|---|---|
chr11 | 1868169 | rs35085249 | C | G | 285599 | Liver | 0.342316 | 1797285 |
Genomic Location | chr11:2153768-2182439[-] |
TSS | 2182439 |
Gene Name | INS-IGF2 |
Ensembl ID | ENSG00000129965.9 |
ENTREZID | 723961 |
Uniprot | |
F8WCM5 | |
Protein Name | |
isoform 2 | |
Insulin |