Chrom Start End Enhancer ID Tissues that enhancer appears More
chr16 89480385 89484641 enh86227
chr16 89486618 89495835 enh32030
chr16 89488709 89489334 vista23573

Chrom Position dbSNP ID Reference Allele Alternative Allele id More
chr16 89483872 rs185274639 C T 4676344
chr16 89483994 rs7195636 C A 4676345
chr16 89484134 rs2911257 C G 4676346
chr16 89484199 rs11642483 G A 4676347
chr16 89484259 rs150636221 G A 4676348
chr16 89484287 rs139706998 G C 4676349
chr16 89484412 rs149777484 G T 4676350
chr16 89484495 rs116308914 T G 4676351
chr16 89484769 rs75012888 T C 4676352
chr16 89484809 rs144505103 A G 4676353
chr16 89485096 rs2911256 G C 4676354
chr16 89485170 rs563552422 A C 4676355
chr16 89485187 rs530972277 T C 4676356
chr16 89485209 rs549271421 G C 4676357
chr16 89485313 rs528116980 G T 4676358
chr16 89485323 rs111813377 G A 4676359
chr16 89485330 rs116810273 A C 4676360
chr16 89485339 rs192177820 C G,T 4676361
chr16 89485412 rs112606596 C G 4676362
chr16 89485430 rs573075340 T A 4676363
chr16 89485501 rs188667921 G C 4676364
chr16 89485519 rs193184142 T A 4676365
chr16 89485549 rs184474160 C T 4676366
chr16 89485628 rs188838840 G A 4676367
chr16 89485663 rs143095537 C A 4676368
chr16 89485698 rs35325035 G GA 4676369
chr16 89485698 rs397855925 G GA 4676370
chr16 89485786 rs115168300 G C,T 4676371
chr16 89485787 rs62068635 C T 4676372
chr16 89485796 rs151175807 G C 4676373
chr16 89485951 rs183983386 G A 4676374
chr16 89485955 rs112155730 A G 4676375
chr16 89486020 rs140160928 C T 4676376
chr16 89486026 rs150300059 C T 4676377
chr16 89486064 rs557074981 A T 4676378
chr16 89486166 rs114449952 C T 4676379
chr16 89486240 rs76982362 C G 4676380
chr16 89486325 rs187504824 T C 4676381
chr16 89486441 rs562598230 G A 4676382
chr16 89486503 rs116619480 T C 4676383
chr16 89486506 rs376819773 A G 4676384
chr16 89486589 rs566666286 C G 4676385
chr16 89486644 rs143777101 G T 4676386
chr16 89486702 rs370685699 G A 4676387
chr16 89486708 rs146125310 C G 4676388
chr16 89486872 rs12597443 T C 4676389
chr16 89486890 rs138859496 T C 4676390
chr16 89486925 rs573430322 G A 4676391
chr16 89486992 rs115031568 A G 4676392
chr16 89487123 rs79225559 C A 4676393
chr16 89487137 rs2911255 C T 4676394
chr16 89487146 rs141446404 C T 4676395
chr16 89487166 rs552073002 A C 4676396
chr16 89487341 rs17702309 T C 4676397
chr16 89487429 rs574534247 G C 4676398
chr16 89487474 rs568388611 CGGAGTCAG C 4676399
chr16 89487479 rs2965936 T C 4676400
chr16 89487582 rs527376550 C T 4676401
chr16 89487673 rs545857084 T C 4676402
chr16 89487824 rs549667554 G A 4676403
chr16 89487995 rs534047911 G A 4676404
chr16 89488091 rs144545094 G C 4676405
chr16 89488220 rs190325606 A G 4676406
chr16 89488261 rs72803358 C A 4676407
chr16 89488299 rs182571627 C T 4676408
chr16 89488318 rs571974445 C T 4676409
chr16 89488329 rs139960931 G A,T 4676410
chr16 89488342 rs77664881 G C 4676411
chr16 89488375 rs575880916 C G,T 4676412
chr16 89488428 rs375564827 G A 4676413
chr16 89488587 rs2911253 T G 4676414
chr16 89488643 rs116225393 G A 4676415
chr16 89488699 rs146955894 C T 4676416
chr16 89488735 rs115111264 A G 4676417
chr16 89488779 rs2965937 A T 4676418
chr16 89488792 rs193084180 T C 4676419
chr16 89488794 rs183194820 G A 4676420
chr16 89488795 rs114294407 G A 4676421
chr16 89488859 rs147572608 G A 4676422
chr16 89488935 rs527725336 A G 4676423
chr16 89488978 rs146208760 C T 4676424
chr16 89489061 rs75300484 C T 4676425
chr16 89489175 rs74946980 T C 4676426
chr16 89489226 rs553023786 G A 4676427
chr16 89489580 rs115336679 A G 4676428
chr16 89489694 rs116728578 G A 4676429
chr16 89489695 rs114660630 G A 4676430

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand Gene Name Ensembl ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More

No results

Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End strand miRNA Name miRBase ID TSS TSI of Normal tissues TSI of Cancer tissues Distance to TFBS id More

No results