| Tag | Content |
|---|
EnhancerAtlas ID | HS101-44214 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr8:134121260-134122660 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ETV6 | MA0645.1 | chr8:134122436-134122446 | CACTTCCGCT | - | 6.02 | | MAFK | MA0496.2 | chr8:134121528-134121547 | ACCTGCTGAGTCAGAATCT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I133110 | chr8 | 134122288 | 134122488 |
|
Enhancer Sequence | CCTTGTCTAA AGAAGGAAAC TGAGCTACAG AGAGAGGCAG CAATTTACTC GGGGTCCTGG 60
AACTACAAGG TAGTTCTGCC CTTTCAACCA TTATCTCTAG AGCCTGACCT TTCAACCATT 120
ATCTGTCCTG TTTCCTGGAG GAGGTGAGCC CTGAGCAAAA CCTGGATTTT CTATTATAAT 180
CTGATTGCTG ACTGTGAAGT TCCCAGGCCA ACGGCATCAG CATCACCTGG GAGCTTGTTA 240
AAATGCACGT TCCTGGGCTC CACTCTGGAC CTGCTGAGTC AGAATCTGTA TTTTATCAAG 300
ATTTCAGTCT ACTTTAACGC TTATTGGATT AAAAAGCATG TGTCTAGTTC AATAGCTGTT 360
ATCCAGGCAA ACTAGGGAAA GGTGTTTAGG CAGGAGGAAC AGCAGGCGCA AAGGCTTAAA 420
AGTACGAGAG AACATTTGGT GTTGAGGAAA CAGCACTCCT CACGTGGCCT GGGCATTTTG 480
GTAATATTTC AGCAGCCTAG TTCTCAGGAG TCACAGAAAT TGAAGGCCAA GTGGCAGCTC 540
GTCTGGGTGG CAAGGGCAAA GCACAGCTGG GTTTGTTCCC CACCTGTGTG ACTTACTCAG 600
CTGTGTAAGA CAGCACTTAG CCTCTCTGAG CCAGTTTCCT TGTCCACCCC CTCAGGATGG 660
TTATGGGAGC AAATGAGAAG AGGGTGCACC AGGGACCCAG CACAGCATCT GACACGCAAT 720
GGGTGCTTGG TGCGTGGCAC TTGTGCTGAC CTCGGCTACT CCCTTTGCCG ACATGACTCA 780
GGCAGCATCA TTCTCACCCC TTGGCAGTCT CCTCTAAGTT CCAGCAAATG GCATTGCACA 840
GGGAGGAGAC AGTTTATGAA CTTGTTTTAC TCCTCTGCAG CCCAGGAGGC ATTGGTATCT 900
TGGCTAGGGC TCTCACTATG ACCCCCTCAT GTTATGTATG AGAAAATGGT GCCCAGAGAG 960
AGAAAGCCAC TCTCTCAAGT TTGTACAGTG ATTGCCAGAT AGCGGGTGCT GGGACTTGGA 1020
GATCCTGGTG CCCAGACCTC AGTATAGCTC CCTCATGTTA AGATTTGAAG GCAGATTATG 1080
CCTGCCACGT AGCAAAGCAG CCTGGGGAGA ACCCACTTTA GTGCCACTGC ACCGTTGTCC 1140
TTGTACCCTC CTGGGCTCCC AGAACTGAGT TCTCCCCACT TCCGCTCCAG CCCGGGGCAT 1200
TAGACCCACC CAATATCTGA GGTGGGGGCA TCATGGATTC CTTCTTTATA AAGCATCTGT 1260
GAGCAGTACT TGGCCCTCGA ATTTGGCACC TTCTGCCTTC CCCACCTGCC TTCACTCATC 1320
GCCCAATCTC CTTGTTCACA GCTCAGAGCT GAGCAAACAG GCTGCAGCAT TGAGACAGCC 1380
ACTGGAACGA ACTATTATAT 1400
|
