| Tag | Content |
|---|
EnhancerAtlas ID | HS044-05501 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr17:5597530-5598700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr17:5597565-5597580 | AGGTCTGTCTGACCT | - | 6.53 | | EWSR1-FLI1 | MA0149.1 | chr17:5597898-5597916 | GGAAGGGAGGAAGGGAAG | + | 7.41 | | TFAP2C | MA0524.2 | chr17:5598042-5598054 | TGCCCCGGGGCA | + | 6.74 | | TFAP2C | MA0524.2 | chr17:5598042-5598054 | TGCCCCGGGGCA | - | 6.74 | | ZNF263 | MA0528.1 | chr17:5597892-5597913 | AGAGGCGGAAGGGAGGAAGGG | + | 6.09 |
|
| | 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 |
| GH17I005694 | chr17 | 5597901 | 5598070 |
|
Enhancer Sequence | GGAGAAGCTC CCATCTGTGA GTAAGTGTTG GAGCCAGGTC TGTCTGACCT CGAAGTTGAA 60
CTTCCACTCT CCACTCTGAG AAGAAGCGTG CTTAGGGAGG CGCTGCTTGT AGAAAAGGAT 120
CCTGGAGAAC TATTCATTTG TCATCACTCA GGCCAAGAGA GTAACAGAAG AAATGATCAA 180
TGAAAAACCC TCCAAAAGTT GTCATCGGCT TGGGTTTATC CTGCTTTAAA TCATAACTTA 240
AGCAGCCTGA AATGGTATTT CCCAAAGATG GGAATGAAAT TCTGGTTATT CAAGGAAGAA 300
GCCAAGGGCT GGGGGTTTGC AGGAGCAGTT TCCAGACTCC CAGGAGTGCA GGTAAGCTCT 360
GAAGAGGCGG AAGGGAGGAA GGGAAGAGCA GGGGAGGAGG AGGGGCTGGA GCCCAACGAG 420
AGAGGGAGGG GCCTGTCTAA GCCCATACTG CACTGGGGAC AGCTCTTCCC CTGGGGCAAC 480
GACAGGCTCT TACCATCAGC CTTTTCCCAA GATGCCCCGG GGCACAGTTA AGTGCTTTAA 540
GTGGCAGCTC CGCAAAAGGC CATCTCCCGC CAAGACTATA AAATGGAAAA ATGGTGATGC 600
TATATTCACG GCAAAGAATC AAGCGAGCAG AGCCTTAACA AGGAATTTAT AAATCAGTTA 660
CTAGGAACAT TAAAATGCCT CTTGCTGCAC TTAATCTCCA GCTTCCTTTC TTCTTCCAAA 720
TACCTAACAC ATCAGTCTTT TTTACTGGCT CTGGTGGACC CTTCAAGGAA GTCTGTTCCT 780
TTTTCAGAAT AAATATATGT GTATTCTCTT GTCTGACTCA ACTCGACTGT AAAACAAATA 840
ATGATACGTG CTTACTCTGG TTCTTCAGAT AAATATGAGA GGAGGCAGTT TTGTCTTTCT 900
TTGGTCTGGG ACATCCCTGG GAGCAGGAAT CATGGCTGTG CCAAGCACAG TTTCTGTAGC 960
TGCATCCCAT GCGATCCTGT AAGTAGGCAC ACTTGGAATG TAACGCCAGC AACGCGTGGT 1020
CTAGACATAG TCAAGCTTGG CCCAATAAAA ACAGGAGAAC CAAACTGCAC TCCAAGGCAT 1080
TCCCCAAGAC TCTTGTATAA TAAGAACAGC CAACGCTTCC ATGAGCCTAC CTTAGGCCAA 1140
CTGCTGTCCT AAGCACATTG CGTTTATCAA 1170
|
