Tag | Content |
---|
EnhancerAtlas ID | HS101-09135 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:119088560-119089930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr11:119089830-119089841 | AAATCTCAGCA | + | 6.32 | HSF1 | MA0486.2 | chr11:119089209-119089222 | GAAAATTCCAGAA | - | 6.17 | NFAT5 | MA0606.1 | chr11:119089205-119089215 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr11:119089205-119089215 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr11:119089205-119089215 | AATGGAAAAT | - | 6.02 | Six3 | MA0631.1 | chr11:119089902-119089919 | CATGGTGATACCCTGTC | - | 6.11 | TFAP4 | MA0691.1 | chr11:119088808-119088818 | AACAGCTGAT | + | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 119089168 | 119089648 | chr11 | 119088717 | 119089742 | chr11 | 119088927 | 119089063 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I119217 | chr11 | 119088031 | 119090057 |
|
Enhancer Sequence | GCTTGAAGCC AAGAGTTCAA GACCAGCCTA GTCGATGTAG TTAGAACCCC ATCTCTACAA 60 AATAAAAAAT AAAAAAATTA GTTGGCCGTG GTGGTGAGTT CCTTTAGTCC CAGATACTCA 120 GGAGGCTGAG GTGGGAAGAT CACCCAGGAG TTTGAGGCTG CAGTGAGCTA TGATCCTGCT 180 ACTGTGCATC AGCTTGGGCA ACAGAGTGAG ACCCTGTCTC TAAATAAAGG AAAGGAAAAA 240 GGAAAAGAAA CAGCTGATTC TTAGTTACCT CAAGTGAAAA TTATGTTGAC ACTTTTCCAC 300 AGTCCCACTT AACATAAATG TAGTAGTTGC TGGGGAGTTA AAGATGACCC GGCACTCACA 360 CTTACAATTT GTGTGATACA ACTGAAGGTA TGTAGAGGGC TCTGGGAACC CTCTATGCTA 420 TAGAGTCACT GGGGCTCATG AGGCAAACCA TTAATCTCTG AGGAGACAAA AAGGGGATGG 480 GGAGGAACTT TAGACCAGTC AGGCTCTTCT GTAATACCCT CATCCACAAT TGTGTCTTAA 540 TTAGTGTATG GCATCTAAAA GTGATACTAA AACATTTACA GTAGTCCCTT CATATCCATA 600 GTTTCGCTTC CTGCTGTTTC AGTTACCTGT GGTCTGAAAA TATTAAATGG AAAATTCCAG 660 AAATAATCCA TAAGTTTTAA ATTGTATGCT GTTCTGAGTA ACGAGGTGAA ATCTTGCAAT 720 CTTACGCTGC TTCTGTCCTG GGCATGAATC ATCCCTTTAT GCAGTGTAGA TACATACTGT 780 GGATATAGTA GTGTATCTAC ACCGTCTACA CTACCCACCG GTTAGTCACC TAGTAGTCAT 840 CTTGATTCTT AGATCAACTG TTGGCAGTCT TGCAGTGCCT GTATTTGAGT CACCCTTATT 900 TTGCTTAATG ACCCTCAAAG CATAAGAGTA ATGATGTCGG CATTTTAAAT ATCCAAAGAA 960 AAGCCAGAAA ATGCCTTCTT TAAGTGAACA GGTGAAAGCT GTTAAGAAAA GAAAAAACTC 1020 ATATTCCGAG GTTACTAAGA TGTACAGTAA GAATGAATCT TCTACTCATG AAATTCTGAA 1080 GAAAGGTCTG GGCTCAATGG CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCTAAGGTGG 1140 GTGTATCACT TGTGTCCAGG AGTTCGAGAC CACCCTGGGC ATGTGGTGAA ACCCTTCTTT 1200 ATTTTAAAAA AAAATTTTGA AGAAGCAAAA AGAAATTTAT ACTAGGGCCG GGCGTGGTGG 1260 CTTACACCTG AAATCTCAGC ACTGAGGGAG GCTGAGGCTG GTGGATCACT TGAGGTCAGA 1320 AGTTGGAGAC CAGCCTGGCC AACATGGTGA TACCCTGTCT CTACTAAAAA 1370
|