| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00477 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:31627370-31628720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr1:31627810-31627821 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr1:31627811-31627821 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr1:31628027-31628047 | TGGGGGTGTGGGGGTTGGGG | - | 6.14 | | RREB1 | MA0073.1 | chr1:31628028-31628048 | GGGGGTGTGGGGGTTGGGGG | - | 6.38 | | RREB1 | MA0073.1 | chr1:31628035-31628055 | TGGGGGTTGGGGGTGTGGGG | - | 6.46 |
|
| | 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 |
| GH01I031151 | chr1 | 31624498 | 31629047 |
|
Enhancer Sequence | CTGCAGATAC TCTACATTTG TGTTTTGGCA TTTAATTTAA TTTCACAGCG ATCATTCGAC 60
GTCAGAATTT TGGTTCCCAT TCTACAAGTG AGAAAATTGA GGTTCAGGGA GGTCAAAGGA 120
CCCGTTGAAG GCCATGAAGT AGGATGCGCC AGAAGCCAGG CTTGAGAGCT GCATACTCGG 180
CGAGAGTTTC TCCAAGGCAA AGCCTGAAAC AGGAACCACA GGCTCTCCAG GTGGGGAGGC 240
TGGCGCTGAG GAATGTTCTC CTGAACAAAG GGCTCGGCTC GCGCGCCCGC ACACCCGCCT 300
CCCCCGGCGC CGGCCTTGGT CTCCAGAGAC AGTGGGGTGG GGGGTGGAGA CGCCCAGGTA 360
TGGCTCTCCT CCGTGGAATC AGCGATCCCA GGACCGAGGC CGGTTGACTC CGGAACAAAG 420
AGAGTCCTTG GGGCGGGGGC GGGGGCGGGG CCCGATCCGG GGACCGGAGG GAGCGGGGGG 480
GAGGGCGGGG CCGGAGTCGA GGGAGGGGCG GAGCCCGGGC CGGGGGACGA GGGCGGGGAG 540
CGGCCGGGCC CTGGGCGGGG CAGGGCGAGG CTGGATCTTC GGAACGAGTC CGTGAAGGAT 600
CGGGCGCGGG CGCGGGCGCG GGGCCGGAGG TGGGGACGAG GGGAGTTGGG AAGGGGCTGG 660
GGGTGTGGGG GTTGGGGGTG TGGGGGTCTG GCGGGACTTA TCTGGGGGAG GCTAAAGTGG 720
GTGCTGGAGG CGGGACCCGA GTCCCGGGAG AGGCGGGCGG GGAGTCGCCG CTAGAGCGGG 780
GCCCTTTTGG GGGCTGGAGA CCCGGAAGCT TAGAGGGCCC CCTGGCCCCG GAGAGGGGGA 840
GGGCGCAGGG CAGGAATGGA GGCGAGGCCT GGCCTCAGGA GCCGGGGGCG GCGGGTTCAG 900
GGCGCGATCC TCTCTGGGGG AATCCGCGGG TGGCCCGGGA GAGGCCGGGA GGGGGCGCAG 960
AGGGCGGCGC CGGGGCCACG TGGAGTCTGC GCGCCCCACC CGCTTTGGGC CGCGCTCCAC 1020
CCGCTTTGGG CCGCGCCCCA CTATCCCTGA GCGCCGCACT GTTGGCCCCG CCACACGTCT 1080
GTCCTGAGAA CCCGCAGGTC CCAGGCTGTG CGGCACCCCG CCGAGCCCTG GAGCAAGTCC 1140
TTCCCTGCGT GGGTCTTGTT TCCGCTTCTG TGAAATGACG ATGGCCCTTC TTGTTTTGCA 1200
GGGCCCTGGG AGAGTGGGTT GAGAGAATGG AAGTGAAGAG GAAGGCTTCA CCATCACCTT 1260
AACTAACATG TGTTTCCTAC CGTTAAATAA ACATTATAGG AGGCCACTGT TTTGGACTAA 1320
GTTTCTGCAC CAGGCCCCAG CCGACCAGAC 1350
|
