| Tag | Content |
|---|
EnhancerAtlas ID | HS044-10502 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr5:88247980-88249440 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Pou2f3 | MA0627.1 | chr5:88248594-88248610 | TTTTATGCAAATAATT | + | 6.16 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 88248349 | 88248499 | | chr5 | 88248701 | 88249400 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I088951 | chr5 | 88247774 | 88253330 |
| Enhancer Sequence | AGGTTGATAA CTGATTAGCA GAACGTGTAG TCTGTCATTT TTAAATATGT GCCCAATTTC 60
TTCACATAAA TCTTACCTTT AAAATCTTCA AGGGGAAAAT TTATTTTGGG CACATTGGCC 120
ATGAATATCA GTTGACATTT ATACAGCGCA TAGAATTTAT ACTGTGGGTT AGGATGTCGG 180
CCATAATTCT AGACTGATAG TTTGTAAAGG GAAGATTCCA TTTTGTACTG TTTATAAAAT 240
GTTACTCTGC AGTTCCGTGC TCCAAGACTA ACAAAGTCTA TCCAAGTATA GTCAAGCACT 300
GCAGTTTAAC TTATTGCATT CATTAAACTA GGCTTAGATT GTCCTAATTA TATGTTATCA 360
ACAATTAAGA AATGGATCAC ATGCCATAGA TTGGCTAAAA CATTCTGTAT TCTTGGCTGG 420
ATGCCAGTGG AGGTGTCAAG TTCCATTCTA CCTTGTCATC AGCTGCATCT CTGCTTTTGC 480
AGTACAAGCA GCAGCTGTGC TAGACAAAAT AATCTAAATT CTCACGTGTA CTTTTCCTTT 540
AGGAAACAGC TCACACTGAA TTGCATTTCT AGTGTGAATG GTACTACACC TGAGTGAGTT 600
TGTGCTGAAA CGTATTTTAT GCAAATAATT TTTAACTGAT ATAATCTTTC ATGACTTTTA 660
AATGTGTTTG TTCTATCAAA ATAATGGTCT TACTCTTCAT GCTGAAATTA TTACCAAATG 720
GATTCTGTGG GCAGCAAAGT ACTCTGCTCA TTCGGCAATG ATTTTCCTAT ACCTCAAATT 780
ACATAATTTT ATAGGTGCTC TGTTTCAAAG GAAAACAATC TTTATTGATC CAAGTAGTCA 840
AAATTAATCA TGGATCTCTG ATCTCAAAAC TCCTGGCAAA ATCCTTTTAT TCAGAACACC 900
CATATGCTAG ACGCTCAACA CTTCACAAAT CCTTGTGGGA GGATGGGTTT TTCAGTCTGA 960
TTGTTCAATC TAGTGCAGCT TCTGAAAGTG GAGATTCAGC AAGGCTTTCC CCTGAGCAGA 1020
GGCAGGCACA ACCAATTTTA TGAGTAGCTA AATTTGACCT GGCTTTTGCG TTACATTGTC 1080
ATCTTTGTTC TTGGTAATGT AAAAATGGGT TTTAGAAGTT GTTCTCCTTT CCATGTGTCT 1140
GACAGAGGGA AGATCCTCCC GCAGCAGCAG GTGTGTGTTG CAGCAGGATC TGAGAGTCAT 1200
GGTGCCAGAG CACCATGCTA AGTAAATAGA ACCCAACAGC TGGGTCTCCT TTGCTCCTGG 1260
AATAGATCCT GTACTACACA ATCATGGAAA GTTAGTCCGC ATGAGAGGCA GTGACTTTAA 1320
AGTTCACCAC AGAATTTACA TATGTGTTGA CATGCATTTT CAGGTCACCA ATTTACTTGG 1380
TTATTAAAAG CTTTACTGCA TCATATACGA ATCAAAGTGG AGGGGTCATG CCAAGTCCTT 1440
ACTCAGAAGG AGAAGATAAT 1460
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