Tag | Content |
---|
EnhancerAtlas ID | HS092-08318 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:3395810-3397190 |
Target genes | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr11:3397034-3397045 | GGTGACTCATT | + | 6.02 | FOSL2 | MA0478.1 | chr11:3397033-3397044 | GGGTGACTCAT | + | 6.14 | JUNB | MA0490.1 | chr11:3397033-3397044 | GGGTGACTCAT | + | 6.32 | MEF2A | MA0052.3 | chr11:3396637-3396649 | TTTATTTTTAGC | - | 6.04 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGACAGCACT GTGCTGGGCA CCTCACGTCA TGTGAGTTAA TCCTCACCAC ACCCTGGGTG 60 ATGGAACCAA GTGTCCTGCA ACTCTCAAGA TATAGATGAA GGGACCAGGC TTTGTGGTTC 120 CTCTTCTATT TTCCTATCAT TAACGTTTTA AAAGTGTAGT GATAAAAGCT CCAGATAGAC 180 CAATGGAAGG GATACAGAGG GGATGAAGTG TAGTGCAAAG GCACTTTCCA TTGTTGTGTT 240 TATCTTCACT TTCTTGTGGC TTGTGAAGCA ACTATTAGAC CCACAGGACT GAGAAAGAGC 300 TTGCTGGATA CGATGTCTCT AACAGCGCTG GTGTTAGTAA AAAAGAAAAA TTAAGGCTCC 360 AAAATAGAGA GTCCTTTGAT CCCATTTATC TGCTTTGGGG TTTCCGAAAA TTCTGTGTAT 420 CAGTTCCGGA GAGGCAGCAG GAGTCAAACT CTGATTTAAC TCTGTAGTTA AACTCCAAAC 480 TGATTTAACT CTGTAGCTAA ACCCAAAACT CTGATTTAAT TCTGTAGTTA ACTCTGTCGG 540 AGGAGAGTCC AGGGTGAAGC CAGACCTGGA TGAGACTCAG AGAAGGAGAG TCTGGGCATG 600 TCTGGGCAGG GAGAGGGCCC TACGCAGGAT TCTGCTCTCT ATGCTACTAG AGTATTTACA 660 ATTCTGTTTT TCCTAAAACT GCCCCCCACC CCAAAATTTA AATCCCAGGG TTTGTATAAT 720 TTTAATCTAT TTTGGCCACT TCCTTGTCTA TTTTATAACA TAAAATAACA AGCAATTTAA 780 CCGAAACCTT TAGGATTTTC TAGGACAGAT ATGGTAGAAG CTAAATATTT ATTTTTAGCC 840 GGGCAAAAGC AACAGAAATA ATACCACCAC CACCTTGTCT GTCTGAATAT CCCTTCAATA 900 TGACATCAGA ACTCACAACA ACCACATCAG GAAAATGGCC CAAATGAAGC AGAAGTCCCT 960 TTGACCACTC CCTTCTTCAT GCTGACCCCA AGACGCTGAA TTCAATGATT TATCCAGTTA 1020 CTGGAAATGG AAAAGTTTCT GGCTTGCGGG GACCATGGCT GCCTTCTCTG TTTTCCTAAT 1080 GGCTACACAG GATGGAATCA ATTAGTTTAT CAGTTTGAAT CTCCAGATCT CATTTTTGTT 1140 TTTTACTGAA GTACCAGAAA AACTGGAGTA ATTCCCATGT GGATACCAAT GAGGTTTCTT 1200 CTCTGAGGGG AGGAACAAAC CCTGGGTGAC TCATTTCTCT TATTCTACAA CAGAAGCACA 1260 GATAGACCGT TTTGTCAGCC TGAGCCCCGT CTGCACAGTG CACTCCTGAA TGTCCAAAAG 1320 ACTCCAGGTG CTGGTGAGAG AGTTCCTGGT GACCCTGCAC AGATGCCCTC TATGGCCATG 1380
|