| Tag | Content |
|---|
EnhancerAtlas ID | HS108-28606 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr3:124295530-124296840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr3:124296713-124296725 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr3:124296717-124296729 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr3:124296721-124296733 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr3:124296725-124296737 | AAACAAACAAAC | - | 6.32 | | GATA2 | MA0036.3 | chr3:124296309-124296320 | AGAGATAAGAA | - | 6.32 | | Gata1 | MA0035.3 | chr3:124296309-124296320 | AGAGATAAGAA | - | 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 |
| GH03I124576 | chr3 | 124295821 | 124295970 |
|
Enhancer Sequence | ATCCACTTTC CATTTGACTC ATCAGAAACC TCTGCACTGT ACTCCGTGAA TGTACATGCT 60
GCTGCAGCTG CTATTTGTGC CTGTAGGAGG GAAGGTGGCG TTGGCAGAAT TAAAATGCCA 120
TCCCACATAG TGGACACTTA GCAATCATAA GTTTACCTTA ATTGAAACTC AGAGTGATAG 180
ACTGGCACTC TTATACTGCC CTACTTTGGG AACACTTTGA CCTACTTAGA GGTAAACGTT 240
TTTGGAAGTA GATAAAACCT GGAGTGGTTT GTTTTTAGCA ATTCCAGCTG CAGCCATCTT 300
TCACTTTGAT AAATAGCTCA TCTGCCCCTG AGCTCAGGCC AGCTCAGGCG GCTGCTCAGT 360
ACAGATATCC AGGAACCTGT CCTTGTTGCC AGCAGTTCTT CCTCTCTGTC CTCACAGAAG 420
AGGAATGTTG GCCATTCTGG GGAGACATCT GTGTCCTCTC AGTATGGCCT GAACCACCCC 480
CCTACCTTGA ACCTGGTTCA GACAAGACAG TGATCAGTAA TACTTCCTGG AAAAAAAAAA 540
AAGAGGGTGG CTGCAGGCTG AGCTGGGGCC TCTCTTAAGG ATAAGTGAGA CAGCTAGAAA 600
GAGGCAAACA GGTGTCAATT GGGCAAGTAC AGAGGAACAC ATTTAAAGGT CAGTAGGTGA 660
AGACATATGG ACTGAGCTCA GTAATGGTTC AGTCATTAGA GTCCAGGAGC TGTCTGTCAC 720
CAAGTGGATG ATGGTACCCA CAGGGCCAGC AGTGGTGCAG TGGTTAGACC ACACTAAACA 780
GAGATAAGAA GGAGAAGAGA TTACTATGCG TGATTCTGGC AAGCACACTT TTTCTGTACA 840
CCTTACTGTT AAAATAACGC ATATTACCTG GGAATGGTTA CCCACACAGA TATTATACAC 900
TTTTGAAAAA AAACATATTT GGGCTGGACA CAGTGGGTCA TGCCTGTAGT CTCAGCACTT 960
TGGGAGGCTG AGGTAGGATG ATTGCTTGAG GCCAAGAGTT CAAGACCAGC CTGGGCAATG 1020
TAGTGAGACC CCATCTCTAT AGGCAGGTGT GGTGATGCAT GCCTGTAGTC CCAGCTACTT 1080
GAGAGACTGA GGTGGGAGCC CATGATTTTG AGGTTACAGT GAGCTCTGAT TATGCCACTG 1140
CACTTCAGCC TGGATGACAG AGCAAGACCC TACCTCCAAA ACAAAACAAA CAAACAAACA 1200
AACAAACAAA ACCCCCCACC ATATTTGGAG TTCAAATTAA ATATAGAAGC AATGTACACA 1260
TTGTACCTCC TCTCTCTAAT TGAAGTGTTT CTGGTTACTG ATGACTATTG 1310
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