| Tag | Content |
|---|
EnhancerAtlas ID | HS106-02380 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chrX:39675730-39677080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chrX:39676344-39676365 | AAGCTGAAAGCGAAAGGATGA | - | 6.08 | | RREB1 | MA0073.1 | chrX:39676228-39676248 | CCCCCACCCACCAACCTCCG | + | 7.04 | | STAT1 | MA0137.3 | chrX:39676811-39676822 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chrX:39676811-39676822 | TTTCCCAGAAA | - | 6.32 | | Stat4 | MA0518.1 | chrX:39676808-39676822 | TGGTTTCCCAGAAA | - | 6.04 |
|
| | 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 |
| GH0XI039815 | chrX | 39674539 | 39677704 |
|
Enhancer Sequence | AAACGTGATG TGGAGAGGGA TGTGTCTTAG CTACACCTAT GTCCAGAATT AAGCCTCTGC 60
ACAGGTGTGG ATTTTACCTC GAGGCTAATA AAGCTTAAAG TTCAGGGCCT TGACTCGCAC 120
AGTCCCCTTC CAAGGCCCTG GTAGGGTCCT AGCAGTTATC ATTTGTACCT CTGCACTGTT 180
TTTCTTCAAG AAGGCCCCAA AATTCACGTA ACTTTTAGGC CCCCAAACTT GGATCTGACC 240
CTGCAGCTGC ATTAAGAAGA GATTGGGCTG CTATTCTGGT TTCTCCTTCC AGGGGGTAAG 300
TTTATCCGCA GGGTACAGGA GGGCAGAAGG GACTGTACCT CCCCACAAGA GGGGTTTTGC 360
CTCCGCTCTG CTTCTCTTGG AGGAGCATTT CCCAAGCTCC TCCTCCTCAC CTCGTTCTGG 420
GAGAGGGTTA ATAGACGTGG GGGTAGGAGG CCTCTTGGGG CCAAATACTT CTGGAAAGAT 480
TGGCGGCCTC TCCACTGCCC CCCACCCACC AACCTCCGGA AGATTCACAA TGTACATTAG 540
CATAGTAAAG GCTCCAGATA AAGAAAACGT TTGGCTTTGT TTACTGTGGG GGTTGCCCAT 600
ACTTCCTGGA GCTTAAGCTG AAAGCGAAAG GATGAGTAGG AGTCAGATAG TTGTAGGAGT 660
CAGATAGTTT TAGGAGTCAG AGGGTTTTAG GCTTGAGGGT ACAGCCCCAG CAAAAGCCTC 720
GCAAAGCCCG GAGAACTGGA AGAAATTGCT GCTGGAAGGC AGAGTTTGAG GTGGTGGAGC 780
CGGGAGGGAT GGACTAGAGG AGCCCCCCAA GCAGGCCTTT CATCCTGAGG ACACCGGGCG 840
ACAACGCGCT CAGAGCTCTG AATCAGAGCT TCCCTGAATC ACAGGCAGAG CTCCCAGCTC 900
TCTGAAGGCT TGGCATGCTG CTGTTTGCAT CCTTCCATCT GTTAGCGATG TTTCAGGCTG 960
GGCAGGCATT GTCCTCATAG AGTTTCTCCC CCATTGTCTC TGCCTCTGCT CACCCCAAAG 1020
CTGGCAGAAC CACAGCGCCC AGTGGCCTCT GGCTGCAGAG GGCATGAGGA CTTCAGGCTG 1080
GTTTCCCAGA AACAGGAGGG TTTGTAGATA ACCCTGATAC CCTATGACCA AAGGCACCGT 1140
TCCCAAAACC CCTGCCCATG GAGCTATAGC CTAGTGCTGC CAAGTAAAGT TTGGTTCTGG 1200
AAAAAACAAT TAGCCTACAG GGGTAGCACT AGCTGTTTCT GAAGTTCTAC AGCCCAGGCC 1260
ACCACTGGGT GCTGGCCTCA GTCCCATGAA CCTTCAGCCC TGCCAATGAG AAGAATTCAC 1320
AGATTTATTG TCTTCTAGAA AGGTTGGGGG 1350
|
