| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07870 | Organism | Homo sapiens | Tissue/cell | Fetal_kidney | Coordinate | chr2:237848190-237849360 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr2:237848546-237848556 | GTCACGTGAT | - | 6.02 | | TFEB | MA0692.1 | chr2:237848546-237848556 | GTCACGTGAT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGGTTTAGA CCTGGGAGGT GGCCATGGAG AGGAGAATAT GTAGATGAGA TAAATTTTAG 60
ACACAGAGCT ATGGATTTGA ATTACATTTT TGAAGTAAGT ACAAAGATGT CCCAGAGGGA 120
GCATCTCTCT CCATTAAATG TCCTGAAACC AGAAGTCTTC ACCCTCCTCT TCCCAGCCCC 180
CATGACACTG GGTAGGAGGA ATCCTTAATT GTGACATCAC CATACCCCAA AGAACCACGC 240
CTACTAGCAA GCACATCATT ACTTATGTGG ATCTCATCTT TCAGTGCGGG TGGATTGGGT 300
TGTCTAATCA TCACGGGCGC CGGTCATAAA TACTGCTGTC TGGGCTGTTT TCAACAGTCA 360
CGTGATGTGG GAAACACTGT CACTCACCTA AGCCATCTGC TCAGAACCAG GAGCAGCTGA 420
GCTAGGCCTG GCAAACGGGA CAATATATAC ACATTCTGCT CCTTTGATAG ATTTGTTTGG 480
GGAAAATGTT CTAGTGATTA ATGGGCCATT TCCTTGCTGA TACGCTGCAC GTGTAGCCAT 540
TAACAAATGA TTCCAGTGCA GCCTTGGCAA AGTCCCTCCT GTGTCATCTC AGGATGCGGC 600
TGGCAGGGCA GGCGGGAGGG GCTGGTGTCT GGGATGAGGT CAAGGCCCAG GGAAAACAGC 660
CTTCCTTTGT GTTCTGGCTG AGGAGGTGGG TCTGGTGGGG GCTGCAGGGA GCCCACAGAA 720
GGACCAGGGT GGGGGTCCAG GCTGCCGGAC CCAGCCCTTC ACTCCCATTA CTCCCAATAA 780
TATTCCTGCT GATGGCCCTG CAGGCACGTG CTCCTTCTTT AAGGATGGGC GGGCTTTTCT 840
TCAACTCATG ATCATATGTT TTGCTTCTCG GGGAACTTCT CGTTGGTTTT ACTGGCACTG 900
TCACGGGCCC TGGGTAGCAC CTGGGGACTC TGTCTTACGA TTAGGGACAA AGAGACAGAG 960
AACTGACAGC CCTAAAGAGG TTTGTCCCTG GGCTCAGTGT CACCCAGCAA CCAGAAGGGA 1020
CCCCTCATGT GGTGGCTTGT CCCTGGACTC AGTGTCACCC AGCAAGCAGA AGGGACTCCC 1080
TCATGTGGTT ATTGGTGAAG GTGAGCATTC TCAGAGTCCC TGCTGGGACA GTCCCCAAAG 1140
AGGCCTCTGC TCATGGGGGG CTCATGGCTC 1170
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