| Tag | Content |
|---|
EnhancerAtlas ID | HS044-03725 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr13:33664510-33665990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr13:33665215-33665228 | AGCAGCTGTTGCT | + | 6.59 | | Sox3 | MA0514.1 | chr13:33665249-33665259 | CCTTTGTTTT | + | 6.02 | | TEAD1 | MA0090.2 | chr13:33665086-33665096 | ATGGAATGTG | - | 6.02 | | Tcf12 | MA0521.1 | chr13:33665214-33665225 | CAGCAGCTGTT | - | 6.32 |
|
| | 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 |
| GH13I033090 | chr13 | 33664525 | 33667419 |
|
Enhancer Sequence | AGAACAGCAC AGGGAAACCA CCCCCATGAT TCAATCACCT CCCACGAGTT CCCTCCCCCA 60
ACACATGGGG ATTACAATTA CAATTACAAT TCAAGATGAG ATTTGGGTGG GGACACAGAG 120
CCAGAGCATG TCAGCATGGA ATTGTTGCTG TCTGCTCACT TTTTCCTTAA TGGAGATTTT 180
GTTCCATGTA TGGTAGGTAA TGATCTGAGG CAGGAAGACA AAGAGCAGAT AGCATTCAGG 240
GCCTCAAAAG ATTCCCCTAA TGTGTACAAA CATACTAGAT CTGAAGTTCT GGTTCACCAT 300
GGTTCTTCCT CATTAAGCCG CAGATTTCCA CTTGGAAAAT TCATTGGTAA AGTGCCATGC 360
CTGCTTGCTG CTGATAGGAT TTTCTTATTG TCCAGCAGTA TGCAAGTATT CAGCCCTCAG 420
TCTCTCAGAA GAGGGGTCTG AATTCCCTTG TTCCGGGGTT GTGACCTTAA CCTTGTCCTG 480
AGATTTATAG CCCCAGAGAG GCTCTCCTCC TGATTTACAT AGTTCCTGAT GTCACTTTGA 540
GCAGTTTAGT TCCAATCTCT GCAGAACATC TTGACTATGG AATGTGGGAA CACGACGAGC 600
TGTTTGTTTT ATACTCCCAA ATCCTTGAAC AAAAGTTACA GAGTGTTTTT CTATCTTCTC 660
AGAGGAAGAA GGCCCCTCTC CCATTCCCAT TCAGTTCTAC CAAGCAGCAG CTGTTGCTGT 720
GTGTACTGTG TTTAAAATCC CTTTGTTTTA TGCAAAAGTA TTCTGCTTGA TGCCTGCTTT 780
GCAATAATCT GAGCCCTGTA CAGTAATCTA GTTATGAGGA CTAGAGGACT TAAAAGTATG 840
AACTTTGAGA TGTATGGGGA AGATTAGGAC AGCCACAAGC CTTCTGAAAA TTGAGCAATG 900
CAGTCAAATA ATGGCTGTAT TTTGTTTGAA ATGCTGCATA GCTGGTTTGA TGTTTGCATT 960
GGGTTGGCTG ATGTCTTTTG TGTTGTGTGC ATACCCTAGT GGGCTTATAC TGGAATCCCT 1020
GAAAACTGGC AGAAAACGAA ATAAAAATGT GCCCTCCTTT GCCATTTCCA ATTTCTTTTG 1080
AGTTGGGCAT TCTGTTTTTT GTGGTTCTAG AAGAGAAACA TGGTTCTGGA ACCTGTGGTT 1140
CTTTTGTGTG CCGCCCCAGG CTCAGCCTCA CAGACAGAGG CTCCAGCAGG GGCCGGTGAT 1200
GGATGATGGT GTTTCCCGCT AGTGGCTGCT CTTTAGAGAA CATATTTAAT TTCGGATGAC 1260
TGGATAGTGT ATTTCTCCCA AGTGATTTTG AATTGCCCAT CTCCAGGAAA GACAGGACTC 1320
TTTATCTGTG GCTTCTAACT ACTCATCGTA GGATTGATTA TTAGGCCTGT TTCCTCTTAC 1380
TTTAATATGT AGATGAGGTA GCAACAGAGA AATTGGAGGA CCACAAGGAA AACCAAGCAA 1440
TAGCACAAAA ATCCAGTTGT TCTATATTTT GGTCCAGTGC 1480
|
