| Tag | Content |
|---|
EnhancerAtlas ID | HS038-11934 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr2:149573900-149575350 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:149574202-149574214 | GTTTGTTTGTTT | + | 6.32 | | ZNF263 | MA0528.1 | chr2:149575065-149575086 | GGGGGTGGAGGAGAGAGAAGA | + | 6.43 |
|
| | 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 |
| GH02I148817 | chr2 | 149574970 | 149575169 |
|
Enhancer Sequence | CTTGCTTTGT CGCCCACGCT GGAGCAGTGG CACAATCATA GCTCACTGCA GCTTCCACAT 60
CCTGGGCTCA AATGATCCTC CCACTTCAGC TTCCAAGTAG CTGAGACTAC AGGTGTGCCA 120
TCTCACCAGG TTGATTTTTA AAAATTCTTC GTCGAGACAG GATCTTGCTT TGTTGCCCAG 180
GCTGGTCTTG AGCTACTACT GGCTTTGAGC GTCCTCCTGC CTTAGCCTCC CAAAGTGCTG 240
GGATTATAGG TGTGAGCCAC CATACCTAGC CGTCTGTGTT GTTTTTCATT TGTTTGTTTT 300
TTGTTTGTTT GTTTTTGAGA CAAAGTCTCA CTCTTGTCCC CCAGGCTGGA GTGCAATGGC 360
ACGATCTCGG CTCACTGCAA CCTCCGCCTC CCAGGTTCAA GCGATTCTCC TGCCTCAGTC 420
TCCCGAGTAG CTGGGATTAC AGGTGCCTGC CACCACGCCC CGTTAATTTT TGTATTTTTA 480
GTAGAGACAG GGTTTCACCA TGTTGGCCAG GCTGGTCTCG AGCTCCTGAC CTCAGGTGAT 540
CCACCCTCCT TGGTCTCCCA AAGTGCTGGG ATTACAGGCA TCAGCCACCG TGCCTGGCCG 600
CTGTCTGTGT TTTTGACACT GAAGTGATGG TGGTAATTTT CAAAGCTCTA CAGAAATACT 660
CATTAAATTC CCCCTACCCT CAGCTGAGTG AGACTAGGGT TCTGATTCTA GGACAAATAA 720
GGATCTTTGG GGCTCATTGC TATGAGCTAT AAATGTCCCA GGGAGAAAAA TCAAGTAGGG 780
TCTTATTTTA GAGAAACCTA TCTCTGCCTG GCTCTCTCTC CTTTCCCACT TGATAAAGAT 840
ATTGGCTTTT CAGAACTCCC AGCTCAGCTT CTGAAAGCCA CAGTGGTATG AGTGGAGCAC 900
TGAAAAGAAA AGCAGGAACC CCTCCCCCAC TTGGTGCCAG CTTTCCTTGG AGAGCGGGGA 960
AGCATCATTA AATGACAGCA AGTTGAAAAT TGTCAGCGAG ATAGGCTATT TGCATGCGAC 1020
ATTGAAACCT CTATGCAATC GTCATTTCCG AGTTGTGACT GCCTGTCTGC AAGGACACAT 1080
TGGATGGTTC CCAGATCACT GCAGCCTCCA AAATTGGACC TGGTTTTATG AGCTGACGTC 1140
TGGATATGAT GTCTCCTGGG AAAGTGGGGG TGGAGGAGAG AGAAGATTTT AAAGAGCTCC 1200
TTAAATTAAA ACCCAAAGCA TCTCCAGTCT GCACAGTGAG AACTGCGTCA GCCAGGCACA 1260
CTTTCTCTTT GCACAGCCTG TAAATGATGC TGAGAGATGG TCTCCCGGAC TGCCTGTCAT 1320
TTAACTCTTT CTGCACTGGG GGACAGGGCA ATCTTCTGGA GCCAAACTGT ATGATGCAGC 1380
AGGGAGCTCA GAGCACATTT TGAATCAGAG TTTCTGATCC CTAGAATCAC TCGATGAACT 1440
TTTAATTTTT 1450
|
