| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07687 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:202774100-202775270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:202774236-202774248 | GTATGTTTATTT | + | 6.11 | | IRF1 | MA0050.2 | chr2:202774924-202774945 | TGTCACTTTCAGTTTTGCCTA | + | 6.24 | | JUN | MA0488.1 | chr2:202774334-202774347 | TTGATGAGGTCAT | + | 6.02 | | JUND(var.2) | MA0492.1 | chr2:202774333-202774348 | ATTGATGAGGTCATC | + | 6.54 | | RREB1 | MA0073.1 | chr2:202774962-202774982 | TCCCAAAGCACCCCCCGCCC | + | 6.14 |
|
| | 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 |
| GH02I201908 | chr2 | 202773308 | 202775456 |
|
Enhancer Sequence | ATCAAGATAC TCCATTCACT TCAGTGTCGA AAAAGAAACG ATCCAGAGTG TTTTTAACAG 60
CATCTTTGGA ATAAGTAATT CATCTTCCAG GGAGATTGCT TTGAAGGAGA GCCTCATGTG 120
GGATGCATAA GCTCTGGTAT GTTTATTTAA AACATACCTT AAATTTCCTT ACACATATTC 180
ACAAGTAACT TGCCTGGAAG CCCCAGACAC TCAGCTCTAC TAAGGCAGGA GAAATTGATG 240
AGGTCATCAA GTCCTTTTGA ATTGTATGTT CCTAGACTCT TAAACTTTTA TTCAGTGAAT 300
TGTAAACATG AGCAAAAGGT TTCACTGCGG GAAAGGACCC TGCCTAAACA GAGACGCTCA 360
CACACATGCA CCTCAACCCA CCTCTCCATT CTGCAATGTG GAGCCTTAAG CCATTGCTGG 420
CTTAGGGCTA GAGAGACTAT TTGGGGCTCT GAAGAGACAA ATCAGAATAG GCAGCTTTTT 480
TGATAGGAAG TCAGCAACTT CCATTCTTGC AACTACCCTG AGCTTAACTT AAATGCCTTC 540
CAGTTGCTAA AAACCTGCAG CTGTATCTGA GCCCAGACAG CCTTTTAACA AAAGTTGTCC 600
ATTTTTATGT GGCCAGCCAT TGGGTAATCA ATACACACGA GATCATCCTT CCACAACCTT 660
TTTCAGTCGC CAACACTTGA TGAGTCAGGG TAGTTAACCC AGCCCAAAGA CACTGTAGCT 720
GGGCTTCATC ACTACATTAG ACCCTACTTA AACCCTTCCT TGCTGATTTA CTTACAGCAC 780
AGCTCTTCTA CTTTTTGCAG TAACATAACT TTGGTTAAAG TTCTTGTCAC TTTCAGTTTT 840
GCCTACGCTG CCTCCCACTT CCTCCCAAAG CACCCCCCGC CCCCATCATG CTGTGCTCTC 900
CAGATGTTCA CAGTCCTGAA ATATCCCACA TGACAAAATA TATACATGTT GTAATTATCC 960
AAGTAAGTCC ATCTTTGCTT ACTTTGGTCT GGTTCCCATT TGTCTTATCA GTTAAATAGC 1020
AAAACTTTGA TTAGTGTGGT AGGCAGAACA CTGCCCACCC CCCAACCAAA GATCCCCACA 1080
TCCTAATCCC AGGAACCTAT ACCCATGCTA TGTTACATGG CAAGGGGGAA TTAAAGTTGC 1140
AAATGGAATT TAGGTAACTG ATTAGCTGAC 1170
|
