| Tag | Content |
|---|
EnhancerAtlas ID | HS042-41959 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr7:2915190-2917030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr7:2916059-2916072 | GGGGGCAGCTGCT | - | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2915365 | 2915542 | | chr7 | 2915575 | 2916141 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I002875 | chr7 | 2915376 | 2916288 |
|
Enhancer Sequence | CCTGCCTCAG CCTCCTGAGT AGCTGGGATT ACAAGCATGT GCCACCATGT CTGGCTAATT 60
TTTATATTTT TAGTAGAGAC AGGGTTTCAC CATGTTGGTC AGGCTGGTCT CAAACTCCTG 120
GCCTCAAGTG ATCCGCCTGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 180
TGTGCCCGGT CAAGTTCCTT CTTCTGATAA GGACTCCATT CACCGGGCTA GGGCCCTTCC 240
TACTCCAGTG TATCCTCATC TAACTAATTA CATCTGCAAT GATGCTATTT CCAAATAAAG 300
TGATGTTTGC AGTTACCAAT GGTTAGGACT TGCGCATATC TTTTGGGGAA TATAATTCAA 360
CTCACAAGAG AAGGTTGTAG CTGCAGGCAC TTGGGGCTCA GTCTTGGTGG CACCCCTCCC 420
TCCAAGAGGC TGTGTGGAAT GTGCTTGAGA ATTGCCCCCG TGAGGCGTGA GGAGCTGCGG 480
CATTGACCCG CCCCCTCCTG CCTGGAGGTG TCTCGGAGCC CTGGGATTTT CCTCCCAATG 540
TGGCATTCAC AGGCATCACA TCACTATCTG GCCATCAGCC ACGGTGGGAG TATTGACACC 600
ACAGACATCA GCGGATGTTA CAAATCAGGC TTCTTTTTCC CCGTGAATCA GCCTCCTGTA 660
CCACTCCGGC CCCTCCCTGG TGCAGGAGCA GTGCAGTGAG CTGATTCATG CGGAGAAAGA 720
TTGGTCTGGC CTGCCCCGTG AACGGTCTGT GTGTGGTCCT GGCCTGAGGA CACCCCAGCG 780
GGCTCATGTG GGGACTGCCT GCAGGTAACC TCTAGACTTG GCTGAGCACC AAGAGTGTTG 840
GCCATAGGGG ACCAGGCAGG TGGACGCCTG GGGGCAGCTG CTGGCTTCCC AGCGGGGCGC 900
TGCCTGAGGC CCGGTTTGCC CAGAGAAGTG AGCAGCCAGC TGTGGCCCGG CAGAGTCCCA 960
GGCCGTGCTG ACAGGTGTGG CCAAAGGGCA AAGGGTGTTA TTATAAAAGA GAATTTACGG 1020
CAGCGGCAGC TTGGGCTGGC TGAGCCCACG GGCAGCAGGA GGATGGAGTG GGGCTGGCAG 1080
GATGCTGGCA GGATGAAGGA TCTGCATTTC ATTGAGACAG TGGGTTGGAG TCCACGCGGC 1140
TGAGATTAAA TAGCCCGTCC CCGGAATGCA GAGAGCCAGA GATAAATCAG ACTTTACTGC 1200
AAGTGGGGTG GCAGGGAGTT AATTAGGAAA GAGAAAAAAA AATACATTTC AACTCACAAA 1260
GAAGCCCAGT GAGCCAGCAG AGAATAGCCC GGCCCCTCCA GGGGTCACTT TGGGGAGGGG 1320
CTGGCATCCC TGGTCCCACC AAAGGGCACA CAGGACTGGG AAGGATGTCA CCTTGGAAGT 1380
GTCAGGGCCC AGTGCAAGAG GGTGAGAATG CTGGCTGCCC CGTGGAGCTG TGCCCGGGCT 1440
GTGCCCCGGC TGGTCTTGGC CTGGGCCCTG CCAGTGAGGT GAGCTGGGTC CTGAACTTCC 1500
AGGTTGGGGA CCAGGTCCTG GAATTGCATC CTGGTGCAGG AGCAGGCATC GCAGGTCACA 1560
TTCAATGAGT GCTCAGAAAT ACTCACGGAG GACCGGGCGC GGTGGCTCAC GCCTGTAATC 1620
CCAGCACTAT GGGAAGTTGA GGTGAGTGGA TCACTTGAGG TCAGGAGTTC CAGACCAGCC 1680
TGGCCAACAT GGTGAAACCC CATCTCTACC AAAACCAGAA AAATTAGCTG GGTGTGGTGG 1740
TGGGCACCTG TAATCCCACC TACTTGGGAG GCTGAGTGGG GAGGATTGCT TGAGTCCAGG 1800
AGGCAGAGGT TGCAGTGAGC CAAGTCATAC CACTGCACTC 1840
|
