| Tag | Content |
|---|
EnhancerAtlas ID | HS189-01501 | Organism | Homo sapiens | Tissue/cell | Thymus | Coordinate | chr2:29266180-29267680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr2:29267019-29267030 | TGGGTGTGGCT | - | 6.14 | | SOX10 | MA0442.2 | chr2:29266245-29266256 | AAAACAAAGCA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATCCCTCAG GAGGACAGCA AGGGAAGCAG GGATGAGCTC TTAGATAAAC TTGTGCCTGA 60
TGAGAAAAAC AAAGCACTGA GTGCCCCTCT CCAGGAATGC AGGGGCTCTG TGCTGAGGTA 120
TTGAAGGAAC TTGGAAAAAG TGAGACTGGA AAGACTTCCT CGTGCAGAAC TCTAAAAACT 180
CTGTCCCCTG TAAAGAGAAG TCTGGCCTGG AGAAGGTCAG CTCCTGGGTC CCAGGATACA 240
CGTGCTGGGC TGCTGTGGTA ACACCACATA GGCCACCTGC CCTCACCTAC CTGACAGGTG 300
CAGGCAAGAC ACAAAGCCAC ATCTCTGAAA AATGCATTTT GTTACTTGCC CAACTTCCTA 360
CTGAATTAAG TTGTGACTAG TGTGGTTGCA AAATGCTGGG AGCTTGGCAT GCTGGTTTCT 420
CTGCAGTCCA CAAGGAGAAG GTTCTGATGA TGGTGTGTAT TTCTCAGCTT AGCACACCTT 480
TCTAGGACAG GCCCATTTTT CTCACGTTGT GTGTCTTTGT GAGAAATGCA TCTCTTCAAG 540
TTTAATAGTT TGAGAAACCA GGAGGTGTCA GCTAGAATGG AGAGGAACAA GCAGCTTCTA 600
AATTCAGTAG ATACGGAGTC CTGCTGCAGT CGACTTCGGG AATATGAAGG AGCCAGACAG 660
CCAATTTATT CCGGAAATGT CCCCACCCCA TTTGCTTGTG TTTTCACCAT TAGTGGCTCA 720
TCTCTGTAAT AAACACTCAT ACTATTTCAG TTCTTTCAAG ATACAAATGG GGTGGTGCTC 780
AGTCCCCAGA ACTTTACCCA TGGGCATGGC TGGGCAGCCA GGGAGCTGCG CCTCGCAGCT 840
GGGTGTGGCT GGATGGTTGG TGGAGCTGGG ATTGGGGGCG GGCACACTGG GACAATTTTT 900
TCAAAAAGGT TTAAAACACC TCTTTTCCCA AACCTCCCGA AAGGCATATT GGGGCATATA 960
GACGATAAAC TCAGCCATCT TTGCAAGTAC ATTCATGCTG GGTCTGAGAC TCAGACCACC 1020
TGGAGTTTAC AAGTAAGGAG AAAATCAGGC CAGGGCAGTG AGGTCATATA TAAACCATTG 1080
ATGATAATAT GTGCTCCTCA GCCCACAAAC TCCCTCCTCT GACCCTGCCA GAGCCAGCCG 1140
GGTGCTTCTG CTCTGGATAG GATGACCAAG CATCCTGGGT TCCCGGGACT CGGGACTGAC 1200
AGTGCTGAAA TGGGGAGAGC CCGGGCCCAC CAGGACCAGT CAGTCACCCT GGCCTCAGAC 1260
CTGCAGGCTT TTGGTTACAA GAGCACAGTG CTTCTCACCT GGTGTCAGGG TTCATGTCTA 1320
AGCGTCTGTC TGCTTGTCAG AGGAGCCTCT TGAGGGGGAT GGGAGTACTG GGTTTTACTT 1380
GGCTCCTAGC TCTATGCCTG TTACATAGAT GATATCAGTA TGTGTTCAGT GTAGAAATGA 1440
ACCACCACCA GCTGTGGGTA CATCTTGGTG GGTAGAGCAC AAATTCAGGC TTTGAGAAGA 1500
|
| |
|
|
|
