| Tag | Content |
|---|
EnhancerAtlas ID | HS150-11831 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chrX:76643350-76644150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chrX:76643878-76643898 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | | RREB1 | MA0073.1 | chrX:76643879-76643899 | GGGTGGGGGTGGGGGTGGGG | - | 6.27 | | RREB1 | MA0073.1 | chrX:76643884-76643904 | GGGGTGGGGGTGGGGGTGGG | - | 6.27 | | RREB1 | MA0073.1 | chrX:76643885-76643905 | GGGTGGGGGTGGGGGTGGGG | - | 6.27 |
|
| | 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 |
| GH0XI077422 | chrX | 76642563 | 76644589 |
|
Enhancer Sequence | TCCAGGCTAA TGGCTTTTCT GGGCCCCAGG TCTGATCTCC AAGCCTGGAA CAGAGCTCAT 60
CAGGCCCTGA CTCAAAACTC AGGAAGGAAG CAGGTAAATT GCTACAGACT GCTTCCTTGT 120
GCTATTGGAT CTCTTGCAAG ACAGAACCCC CCAATGTGGT CCTAGAGGCC TCAGGCACTT 180
CCTGCATGCA AATACACTGT GTGTGCTGCA TGACAAGCCT AATGTGGACA AAAAGTAGGT 240
GGCCCCCTAC CAGGGCAGCT TGAGAAATGG CTTAAGAGAT TCCCTAACAA CAACAACAAA 300
AACAAAAACC GAGCTCTCCC AAGCCCAAGC ACCTGGAATC CACTATTACT CATTCCTCCT 360
AAAGCTCAAA AACTCCCTGT TGAAATATAA ACATATCGTC CAATTAACAC CCATTAACAC 420
ATTAGCATGG ATTCCTTTTC CAGATTGGCT GATAAAATAG CCTACAGAAC AGAAAGTAGA 480
GTCCTAATGG GATGGTAAAT AGGTTTAGGT AAAGGTCAGC AAGGCTGTGG GGTGGGGGTG 540
GGGGTGGGGG TGGGGTGGTC CGGGGTGGAG GGGAAGAGGC CTGAAAGGCA ATAACAGTGA 600
TTCTTTTACT GGTTACAAAG TGCTTGAGCC TCACAATAAC ATTGGCGAGA CATCAGAGAA 660
GGGTTTCTTG TCTCCCTCTT ACAGTGCCTA AAGAGGTTAA TTGCTGAGCT CAGTAGTATA 720
TCAGTTCATC ATTTGAATTG AGCTCTACAA ACATTTCCTG AACATCTGCT CCACTCAGGC 780
AATATGTTCT TTGTCCAGGA 800
|
