Tag | Content |
---|
EnhancerAtlas ID | HS108-10991 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:132485410-132486420 |
Target genes | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF3 | MA0522.2 | chr12:132486182-132486192 | AGCAGGTGTT | - | 6.02 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 132485686 | 132485800 | chr12 | 132485800 | 132486262 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I132001 | chr12 | 132486121 | 132486270 |
|
Enhancer Sequence | CTCTGTATTC AGACTTTCAG TCATCTCTTT TATTTCTTCA AATATGAAAT TTTATAATCT 60 CTGCCTAATA ATTGCATGGG TGATGTTTTT GCAGGTCTGA TTCTGCTGTC GTTTATGAAT 120 CCTGGTTTCT GCTGATGGTA CATTGTTTCC TAGCGTACTT TGTGATTTTT GACAATTTAT 180 TGGTGTAGGG ACCAGCCCCA CAGGGTCGGT GGGTTTCTTC CCACCGTGTG TGGAGACGAG 240 AGATTGTGGA AATAAAGACA CGAGACAAAG AGATAAAAGA AAAGACAGCT GGGCCCAGGG 300 GACCACTCCC ACCAAGACGC GGAGACTGGT AGTGGCCCCG AATGTCTGGC TGCGCTATTA 360 TTTATTGGAT ACAAAGCAAA AGGGGCAGGG TAAATAGTGT GAGTCATCTC CAATGATAGG 420 TAGGGTCACG TGGGTTACGT GTCCACTGGA CAGGGGGCCC TCCCCTGCCT GGCAGCCGAG 480 GCAGAGAGAG AGAGACAGCT TACGCCATTA TTTCTGCATA TCAGAGACTT TTAGTACTTT 540 CACTAATTTT GCTACTGTTA TCTAAAAGGC AGAGCCACGT GTACAGGATG GAACATGAAA 600 GCAGACTAGG AGTGTGACCA CTGAAGCACA GCATCACAGG GAGACGGTTA GGCCTCCGGA 660 TAACTGTGCG TGGGCCTGAC TGATGTCAGG GCCTCCACAA GAGGTGGAGG AGTAGAGTCT 720 TCTCTAAACT CCCCACAAGG AAAGGGAGAC TCCCTTTCCC GGTCCGCTAA GTAGCAGGTG 780 TTTTTCCTTG ACACTGAGGC TACAACAGGC GTCTTCCCAG ATCCTGGCGT TACCGCTAGA 840 CCCAGGAGCC CTCTGGTGGC CCTGTCCGGG CATAACAGAA GGCTCGCACT CTTGTCTTCT 900 GGTCACTCCT CACTATGTCT CCTCAGCTCC TATCTCTGTA TGGGCTGGCT TTTCCTAGGT 960 TATGATTATA GAGCGAGGAT TATTATAATA TTGGAATAAA GAGTAATTGC 1010
|