| Tag | Content |
|---|
EnhancerAtlas ID | HS039-02083 | Organism | Homo sapiens | Tissue/cell | ESC_NPC | Coordinate | chr13:21285420-21286270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RFX1 | MA0509.2 | chr13:21285625-21285641 | TGTTACCATGGCAACT | - | 7.32 | | RFX1 | MA0509.2 | chr13:21285625-21285641 | TGTTACCATGGCAACT | + | 7.33 | | RFX2 | MA0600.2 | chr13:21285625-21285641 | TGTTACCATGGCAACT | + | 7.44 | | RFX2 | MA0600.2 | chr13:21285625-21285641 | TGTTACCATGGCAACT | - | 7.47 | | RFX5 | MA0510.2 | chr13:21285625-21285641 | TGTTACCATGGCAACT | + | 7.54 | | RFX5 | MA0510.2 | chr13:21285625-21285641 | TGTTACCATGGCAACT | - | 7.54 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTACAAGTT GATTTGGCTC ATGGCTCTGG AGGCTGGAAA GCCCAAGGGT CTGGTGCTGG 60
CATCTGGTGA GAGTCGTCCC ACGCTGGAAG GTGGAAGCAA GTGACAGAGA GGGAAGGGCG 120
GAACTCATCC TTTTACCAGG AACCCCTCCA AGGATGGCAG AGCCCTCCTG ACCCAGTCAC 180
CTCTTCAAGG CCCCGCCTCC CACACTGTTA CCATGGCAAC TGAGTTTTTA ACACATGAGC 240
TGTTGGAGGG ACACAGACCA TAGCAGAGAG TAAAGGAGAG TAGGGAGAAC AGGGGACAGG 300
AGGTCAAGTA ACTTTCAAAT AGACACCCTA GGTCACCAAC GGCATTCGAA GAGGCCATGA 360
GACCCTCCCC AGCAGCCCAG TGCAGGTACG GTTCAGGTAC CCCGGCTGAA GGAAGCCGGT 420
ATTTTCCTGT GGAGAACCCA AGTACCAGAA TTTCAGCAGA TGACATTGGG GAAGAGGGGA 480
AATCACAAGA AAATAAATTC CCTTCAGGGA TTTCATTTGA AAAGCGCCAC CTTGGGATAC 540
AGATGTGGGA TACAGACTGG AAGTCACCTG AATGACCGCC TATAGGCAGC TAGTCAGATA 600
AAATGCTATA CAGCTGTGAA GACTGGCGGC TCTCAGTGTA CCTAAGGATA TCCCCTACTT 660
ACTAAATGTG CCCAAGTTCA GCTTCCAGTT ACCTGTGGGC AGTTCAGCAA TGGCCCATTC 720
ACTGCGACCT GTTTCCCATG TGGGCTGTCC ATTAATTATT CCACTTGACC GATATTGAAA 780
CCCAGGGTCA CATTCATTCA TCAAATATTG TCTAGGGGCT GGTGGGCAGG CCCCCTGGAA 840
TACAGCCAGG 850
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