| Tag | Content |
|---|
EnhancerAtlas ID | HS042-27413 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr2:237848080-237849600 | 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 | TGAAGGCTTG TTGCATTGGG TGCCTTGCTC ATGCACTCTC TGGCTACTGT GATGTGGAGA 60
GACTTCAGTG AGTCAAGACA GAAGACAGGC ACCAACACTG CACCTGGCGA GAGGTTTAGA 120
CCTGGGAGGT GGCCATGGAG AGGAGAATAT GTAGATGAGA TAAATTTTAG ACACAGAGCT 180
ATGGATTTGA ATTACATTTT TGAAGTAAGT ACAAAGATGT CCCAGAGGGA GCATCTCTCT 240
CCATTAAATG TCCTGAAACC AGAAGTCTTC ACCCTCCTCT TCCCAGCCCC CATGACACTG 300
GGTAGGAGGA ATCCTTAATT GTGACATCAC CATACCCCAA AGAACCACGC CTACTAGCAA 360
GCACATCATT ACTTATGTGG ATCTCATCTT TCAGTGCGGG TGGATTGGGT TGTCTAATCA 420
TCACGGGCGC CGGTCATAAA TACTGCTGTC TGGGCTGTTT TCAACAGTCA CGTGATGTGG 480
GAAACACTGT CACTCACCTA AGCCATCTGC TCAGAACCAG GAGCAGCTGA GCTAGGCCTG 540
GCAAACGGGA CAATATATAC ACATTCTGCT CCTTTGATAG ATTTGTTTGG GGAAAATGTT 600
CTAGTGATTA ATGGGCCATT TCCTTGCTGA TACGCTGCAC GTGTAGCCAT TAACAAATGA 660
TTCCAGTGCA GCCTTGGCAA AGTCCCTCCT GTGTCATCTC AGGATGCGGC TGGCAGGGCA 720
GGCGGGAGGG GCTGGTGTCT GGGATGAGGT CAAGGCCCAG GGAAAACAGC CTTCCTTTGT 780
GTTCTGGCTG AGGAGGTGGG TCTGGTGGGG GCTGCAGGGA GCCCACAGAA GGACCAGGGT 840
GGGGGTCCAG GCTGCCGGAC CCAGCCCTTC ACTCCCATTA CTCCCAATAA TATTCCTGCT 900
GATGGCCCTG CAGGCACGTG CTCCTTCTTT AAGGATGGGC GGGCTTTTCT TCAACTCATG 960
ATCATATGTT TTGCTTCTCG GGGAACTTCT CGTTGGTTTT ACTGGCACTG TCACGGGCCC 1020
TGGGTAGCAC CTGGGGACTC TGTCTTACGA TTAGGGACAA AGAGACAGAG AACTGACAGC 1080
CCTAAAGAGG TTTGTCCCTG GGCTCAGTGT CACCCAGCAA CCAGAAGGGA CCCCTCATGT 1140
GGTGGCTTGT CCCTGGACTC AGTGTCACCC AGCAAGCAGA AGGGACTCCC TCATGTGGTT 1200
ATTGGTGAAG GTGAGCATTC TCAGAGTCCC TGCTGGGACA GTCCCCAAAG AGGCCTCTGC 1260
TCATGGGGGG CTCATGGCTC ACTGGGGCTT ACTCCACTGA GAAGGGAGGT AAGAGAGTCA 1320
GGGTGGAGCT CCCACCAGCT CAGTCTCTTA ACTTGGACTC TGCAGAGCCT CAAGGAGCAC 1380
CTCACAAGCC TGCTTCGAAT GCAGGCTCCC AGGCCTGGGA GAGGTGCACC CCATCCCTAT 1440
TGTACCCCCT TCCTGATGAA AGGAGAGAAA TGATTCCAGG GTTCCAGAGA CTCAAGCAGC 1500
TTAGAAATCT CTGCACTGAG 1520
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