| Tag | Content |
|---|
EnhancerAtlas ID | HS108-36522 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr7:17846140-17847510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr7:17846158-17846175 | GAGGTCAACATGACCTT | - | 6.31 | | ESR1 | MA0112.3 | chr7:17846158-17846175 | GAGGTCAACATGACCTT | + | 7.85 | | ESR2 | MA0258.2 | chr7:17846159-17846174 | AGGTCAACATGACCT | - | 6.12 | | ESR2 | MA0258.2 | chr7:17846159-17846174 | AGGTCAACATGACCT | + | 6.26 | | PPARG | MA0066.1 | chr7:17846156-17846176 | AAGAGGTCAACATGACCTTG | - | 6.29 |
|
| | 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 |
| GH07I017807 | chr7 | 17846841 | 17847256 |
|
Enhancer Sequence | TTATTCTGAC ATTCTAAAGA GGTCAACATG ACCTTGGTTA TCACCAATAT GGTTTATGAA 60
AAATGTGTGT TATTGTGGAT TGCCAGAAAT GAATCAGAAA GATAGGTAGA CGCCATTATT 120
AATTAAAAAA AAAAAGTGAG TGGCTGGCAA GACAGCCAAA TAGGAACAGT TCCGGTCTGC 180
AGCTCCCAGC GAGATCAACG CAGAAGGTGG GTGATTTTTC CATTTCCAAC TGAGGTACCC 240
AGCTCATCTC ACTGGGACTA GTTAGAAAGT GGGTGCAGTC CACAGAGGGC GAGCTGAAGC 300
AGGGTGGGGC GTCGCGTCAC GCGGGAAGTG GAAGGGGTCA GGGAACTCCT TCCCTAGCCA 360
AGGGAAGCCA TGAAGGACTG TGCCTTGAGG AATGGTGATT TTTGGTCCAG ATACTACGCT 420
TTTCCCACAG TCTTTGCAAC CCACAGACCA GCAGATTTCC TCCGGTGCCT CCGCCACCAC 480
GGGCCTGGGT TTCAAGCACA AAACTGGGCG GCCGTTTGGA CAGACACCAA GCTAGCTGCA 540
GGAGTTTTTT TCATACCCCA GAGGTGCCTG GAATGCCACC GACACAGAAC CGTTCACTCC 600
CCTGGAAAGA GGGCTGAAGC CAGGAAGCCA AGTGGTCTAG CTCAGCAGAT CCCACCCCCA 660
CGGAGCCCAG CAAGCTATAA GATCCACTAG CTTGAAATTC TTGCTGCCAG CACAGCAGTA 720
TGAAGTCCAC CTGGGACACT CGAGCTTGGT GGGGGGAGGG GCGCCCAGCT AGGTGGGGGG 780
AGGGGCCCCC ACTAAGGCTT GAGGAGGTGG TTTTCTCCTT ATAGTGTAAA CAAAGCCTCA 840
AGGAAGGTCG AACTGGGCGG AGCCCACCAC AACTCAGCAA AGCCACTGTA GCCACACTGC 900
CTCACTAGAT TCCTCCTCTG GGCAGGAAAG AAAGGCAGCA ACCCCAGACA GGGGCTTATA 960
GATAAAACTC CAATCTCCCT GGGACAGAGC ACCTGGTGAA AGGTGCGGTT GTGGGCGCAG 1020
TTGCAGCATG CTTAAACGTT CCTGCCTGCT GGCTCTGAAG AGAGAGGCAG ATCTCCCAGC 1080
ACAGCGATCG AGCTCTGCTA AAGGACAGAC TGCCTCCTCA TGTGGGTCCC TGAGCCCCAT 1140
GCCTCCTGAC TGGGAGACAC CTCCCATCAG GGGTCGACAG ACACCTCATA CAGGAGAGCT 1200
CCAGCTGGCA TCTGGAGAGT GCCCCTCTGG GATGAAGCAT CCAGAGGAAG GAACAGGCAG 1260
CAATCTTGGC TGCTCTGCAG CCTCTGCTGG TGATACTCGG GCAAACAGGG TCTGGAGTGG 1320
GCCTCCAGCA AACCTGCCAC AGAGGGGCCT GATTGTTAGA AGGAAAACTA 1370
|
