| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08997 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr13:33664540-33665850 |
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 | TCAATCACCT CCCACGAGTT CCCTCCCCCA ACACATGGGG ATTACAATTA CAATTACAAT 60
TCAAGATGAG ATTTGGGTGG GGACACAGAG CCAGAGCATG TCAGCATGGA ATTGTTGCTG 120
TCTGCTCACT TTTTCCTTAA TGGAGATTTT GTTCCATGTA TGGTAGGTAA TGATCTGAGG 180
CAGGAAGACA AAGAGCAGAT AGCATTCAGG GCCTCAAAAG ATTCCCCTAA TGTGTACAAA 240
CATACTAGAT CTGAAGTTCT GGTTCACCAT GGTTCTTCCT CATTAAGCCG CAGATTTCCA 300
CTTGGAAAAT TCATTGGTAA AGTGCCATGC CTGCTTGCTG CTGATAGGAT TTTCTTATTG 360
TCCAGCAGTA TGCAAGTATT CAGCCCTCAG TCTCTCAGAA GAGGGGTCTG AATTCCCTTG 420
TTCCGGGGTT GTGACCTTAA CCTTGTCCTG AGATTTATAG CCCCAGAGAG GCTCTCCTCC 480
TGATTTACAT AGTTCCTGAT GTCACTTTGA GCAGTTTAGT TCCAATCTCT GCAGAACATC 540
TTGACTATGG AATGTGGGAA CACGACGAGC TGTTTGTTTT ATACTCCCAA ATCCTTGAAC 600
AAAAGTTACA GAGTGTTTTT CTATCTTCTC AGAGGAAGAA GGCCCCTCTC CCATTCCCAT 660
TCAGTTCTAC CAAGCAGCAG CTGTTGCTGT GTGTACTGTG TTTAAAATCC CTTTGTTTTA 720
TGCAAAAGTA TTCTGCTTGA TGCCTGCTTT GCAATAATCT GAGCCCTGTA CAGTAATCTA 780
GTTATGAGGA CTAGAGGACT TAAAAGTATG AACTTTGAGA TGTATGGGGA AGATTAGGAC 840
AGCCACAAGC CTTCTGAAAA TTGAGCAATG CAGTCAAATA ATGGCTGTAT TTTGTTTGAA 900
ATGCTGCATA GCTGGTTTGA TGTTTGCATT GGGTTGGCTG ATGTCTTTTG TGTTGTGTGC 960
ATACCCTAGT GGGCTTATAC TGGAATCCCT GAAAACTGGC AGAAAACGAA ATAAAAATGT 1020
GCCCTCCTTT GCCATTTCCA ATTTCTTTTG AGTTGGGCAT TCTGTTTTTT GTGGTTCTAG 1080
AAGAGAAACA TGGTTCTGGA ACCTGTGGTT CTTTTGTGTG CCGCCCCAGG CTCAGCCTCA 1140
CAGACAGAGG CTCCAGCAGG GGCCGGTGAT GGATGATGGT GTTTCCCGCT AGTGGCTGCT 1200
CTTTAGAGAA CATATTTAAT TTCGGATGAC TGGATAGTGT ATTTCTCCCA AGTGATTTTG 1260
AATTGCCCAT CTCCAGGAAA GACAGGACTC TTTATCTGTG GCTTCTAACT 1310
|
