| Tag | Content |
|---|
EnhancerAtlas ID | HS044-12484 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr7:156943230-156944740 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HOXA9 | MA0594.2 | chr7:156943904-156943914 | GTCGTAAACG | + | 6.02 | | RFX1 | MA0509.2 | chr7:156944496-156944512 | TGTCACCATGACAACC | + | 6.25 | | RFX1 | MA0509.2 | chr7:156944496-156944512 | TGTCACCATGACAACC | - | 6.25 | | RFX2 | MA0600.2 | chr7:156944496-156944512 | TGTCACCATGACAACC | + | 6.01 | | RFX2 | MA0600.2 | chr7:156944496-156944512 | TGTCACCATGACAACC | - | 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 |
| GH07I157150 | chr7 | 156943289 | 156944330 |
|
Enhancer Sequence | CTGAAACAGC CTACATGTCT AAATACAGGA CATTTGTTAA ATAACCGTTA ATATAACAAT 60
GCAGTGAAAT ACTGTGCAGC CATTTAAAAT GGTCATGATG CGTATTAATG TCTGTCATTA 120
ATTTATTAAC ATACTTGTAT TTATGAACAT GATTTATTGT TAATGGAAAT AAGTAGATTA 180
CAAAACAGGA TTGCAGTCTG CATTTAAATT ATGTTTATCT GAACAGTAAA GATAGCTAGT 240
TTCCCAGTTT CTTAATTTCC ATTGAATAAA AGAAAGATAC TAGTTGCTTA TTGCTGTGTA 300
ATAGAGCTTA AAGCAATACG TTTTTGTTAC CTTGGTCAGT TCTGTGGGGC AGGCATCTGG 360
ATCTACTTCT GCGCTGGCCT GTTCACAAGC CTGGAAGTTA GTGCTGGCCG TTGGCAGGAG 420
AGTCAGTTCT CGGCCGCTTG CGGGGCTTCT TAGGGATACC GTGTCCTCAT GGCAGCTGGC 480
CTCCCGCTAA GCTGCTGAGC AGACAGAGCA GGGAGGAAGG GCAAAGCCTG TGGTGACTTT 540
GGTCATGGTG TATTTGTCCA GCCCACTCTC GGGGTGAGGG GAGTCGGGCT CCACCCCCTA 600
AAGGGCAGCA GTAGCAAAGC GTCTGTGGAC ATAATCCTGA AGCCACCGTA GAAGGGAGCT 660
TCAGGTTTAG CTTAGTCGTA AACGCTGGCG CTGCAAAACA AATACGCTGT GTTTTCTGCC 720
TCAGCCTATT AGGAGTTAAA AATTGTGGTT TTCCTTCTTA CCTCTTACCT TCTGTATCAG 780
TAGTTATTGG CTACATAAAT AACAACACAG TGAGTTAAAA AGCAAGCATT GTCAACATAC 840
ATTTTGGTGA ATGTGAGTTC ACTCGGAGAA GATTGTATAG CTCTTTGGAA ATGTAACAAA 900
GAAATTGGCA AACTAGGAGC AGCTTAAAAA ACAAGTAAAT AGAGACCTGA CTTAAAATGC 960
TATTTTTCTA GATGTGCCCT CCTGATCATG TGCTGGCTTT TCTTGTGAAC TGTTACCTTC 1020
TCCCGTATGC TGCTTGGAAA TGCTTAGGTT CCTGCATTAT CCTGCCGGAA ATACTATCTA 1080
TTAAGCCGTT TAAGTGTCTT CCTCAAAAAA GCCCAGTAGA ACCATAAGGA GTAATTTTTT 1140
GTAACAATGC AAATTCACTG ATTTAGATCA TTTAGCTTTT TAATCCATTT GCCCTTGGAG 1200
AGAAGAGGGG GCTATGCAAT TGGACCAAGA GGAGTCAATG ATTTTGAAGT CAGTCAGCCC 1260
TTGGTTTGTC ACCATGACAA CCGTGGAGCA GGAGGTAGCC ACATCATGAC AGGGAGGAGA 1320
GGTGAGTGAA GTGAGAAGCA GGGGAGCATC ACAGTAAAGT GGCCGTCATC TGAGAACTCT 1380
TCTGCACAGC CTCGTACCCA GAAGTTTGTT CCCCTTCTGT TCTAGTACCA TGTGTGTATC 1440
CTATTTCCAG AACCCCAAGC AAGCATCAGT TTTTGTGTGC TGGACTGGGT AGGATTCTTA 1500
GGACTATTTA 1510
|
