Input Chromosomal region, for example: chr1:1000-10000 to view the enhancers around this region



Chrom. Start End TF Name Source Predicted site? Tissue/Cell line id More
chr1 856539 856558 RFX2 JASPAR yes 118213233
chr1 856547 856562 TFAP2A JASPAR yes 118213234
chr1 856547 856562 TFAP2C JASPAR yes 118213235
chr1 856550 856561 TFAP2A JASPAR yes 118213236
chr1 856550 856561 TFAP2B JASPAR yes 118213237
chr1 856550 856561 TFAP2C JASPAR yes 118213238
chr1 856551 856560 TFAP2A JASPAR yes 118213239
chr1 856557 856572 MEF2A JASPAR yes 118213240
chr1 856558 856573 MEF2C JASPAR yes 118213241
chr1 856561 856565 YY1 TRANSFAC yes 118213242
chr1 856561 856571 HOXC10 JASPAR yes 118213243
chr1 856561 856571 HOXD11 JASPAR yes 118213244
chr1 856561 856572 HOXA10 JASPAR yes 118213245
chr1 856561 856572 HOXC11 JASPAR yes 118213246
chr1 856561 856572 HOXC12 JASPAR yes 118213247
chr1 856561 856572 HOXD12 JASPAR yes 118213248
chr1 856562 856571 CDX1 JASPAR yes 118213249
chr1 856562 856573 CDX2 JASPAR yes 118213250
chr1 856567 856582 NR2C2 JASPAR yes 118213251
chr1 856568 856587 CTCF JASPAR yes 118213252
chr1 856571 856590 CTCF JASPAR yes 118213253
chr1 856584 856595 E2F4 JASPAR yes 118213254
chr1 856584 856595 E2F6 JASPAR yes 118213255
chr1 856585 856590 SP1 TRANSFAC yes 118213256
chr1 856616 856626 SP1 JASPAR yes 118213257
chr1 856622 856627 SP1 TRANSFAC yes 118213258
chr1 856625 856644 CTCF JASPAR yes 118213259
chr1 856627 856641 ZIC1 JASPAR yes 118213260
chr1 856652 856672 PPARG JASPAR yes 118213261
chr1 856664 856683 PAX5 JASPAR yes 118213262
chr1 856674 856679 SP1 TRANSFAC yes 118213263
chr1 856675 856680 SP1 TRANSFAC yes 118213264
chr1 856675 856681 SP1 TRANSFAC yes 118213265
chr1 856678 856688 SP1 JASPAR yes 118213266
chr1 856685 856690 SP1 TRANSFAC yes 118213267
chr1 856693 856703 SP1 JASPAR yes 118213268
chr1 856694 856701 CEBPA TRANSFAC yes 118213269
chr1 856700 856705 SP1 TRANSFAC yes 118213270
chr1 856706 856717 FOXH1 JASPAR yes 118213271
chr1 856723 856727 H4TF2 TRANSFAC yes 118213272

chrom Position dbSNP ID Reference Allele Alternative Allele is SNP in TFBS id More
chr1 856557 rs147866846 A C 1051
chr1 856583 rs141671872 G A
1052
chr1 856620 rs558359928 G A
1053
chr1 856736 rs373919892 G A no 1054

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 between enhancer and TSS id More
chr1 818043 819983 + AL645608.2 ENSG00000269308.1 818043 0.0 0.0 4 61504
chr1 860260 879955 + SAMD11 ENSG00000187634.6 860260 0.92 1.0 5 96497
chr1 861264 866445 - AL645608.1 ENSG00000268179.1 866445 1.0 1.0 6 90312
chr1 879584 894689 - NOC2L ENSG00000188976.6 894689 0.69 1.0 7 62068
chr1 895967 901095 + KLHL17 ENSG00000187961.9 895967 0.67 1.0 8 60790
chr1 901877 911245 + PLEKHN1 ENSG00000187583.6 901877 0.96 1.0 9 54880
chr1 910579 917497 - C1orf170 ENSG00000187642.5 917497 0.99 1.0 10 39260
chr1 934342 935552 - HES4 ENSG00000188290.6 935552 0.71 1.0 11 21205
chr1 948803 949920 + ISG15 ENSG00000187608.5 948803 0.81 1.0 12 7954
chr1 955503 991496 + AGRN ENSG00000188157.9 955503 0.91 1.0 13 1254


Blank TSI value indicates lack of sufficient expression for calculation
Chrom Start End Strand miRNA Name miRBase ID TSS Score TSI of Normal tissues TSI of Cancer tissues id More

No results