| Tag | Content |
|---|
EnhancerAtlas ID | HS080-02630 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:182631180-182632310 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:182632135-182632148 | GGGGACAGCTGCC | - | 6.29 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 182631234 | 182631600 | | chr1 | 182631943 | 182632000 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I182662 | chr1 | 182631801 | 182631970 |
| Enhancer Sequence | GACCTCCATG GGTGCTTCTT CCACTTTGTA TGGCATTTGT AAACAAATAT AATTGGAAAT 60
AAAATGGCTC CAAACATTTG CCCTCCAGAT TTTTTAAATT CTAAGGTTTA AAAAATAGCA 120
AAGTTGCTTT CTTTTGCCTG AGATTTCAGC CTATGAGGTG CTCAGCCAAG GAGAGGAGAA 180
GCTTTTTAAC ACAGGCACCA TAGTCCCTCT TCTGGTGCTG GAGCCATTTC AGCTCTGAAG 240
CAGTATTTTA CATAACCCTG CAGGCAGCGC TGAGTCAAAC TACCTGCCAA AGGTGATTGG 300
TTATTGCCCA GCCTCTCTGT TTGCTACAGA GAGCATCCTG GATCCAGCTT CTGACACCTC 360
CTCCTACTCC AGATGCTTCA TTGTATAGAT GAAGAAACAG AATTTCTAAG AGATTGAGAG 420
ATCCTATCCC GATCATCCAG ATATCCAGTA ATAGAGCTGG GTCAAAATCG AGAACACAGA 480
TCTGACTACC AGACAATGCT CTTCGCTTAA TTGTCCAAAA GCATGTTCCC CAATTAAGTG 540
GAAACCATGC TGTAAACCAA AAGCAGCCTC TGCCCCCAGA TCAGTTAGGT CTTCTAATAT 600
TGACAAGACG GAATTGAAGA GGAGCACTGA TGTCAGGATT CTATTTGGAA TCTTGAGGCC 660
ACCCAGCGTG TAGTCAGCAC ACTGCATTGT TTCCTGTGTT ATTGGTATGC ATGCCTGTTC 720
GCTCAGAGGC TGCATTCTCC ACCAGAGATG GACTGTGCCT TGTTCATCTT TGTGCTTCCC 780
CTCCTCCAGC TGCTTACCAT AGATTTTGCA CACCATGAGC ACTTGGTACA TCTTTTTAAA 840
CATAAATGAG TGCCCAAAAC ACCCAACGGA ACAGGGATGG CAAAGATGTC CTGTAGATTG 900
AGAATGGGGA GGGGGGGAAA TAATCATCTG TGTTTTCTGA AATAGAAATC TTAAGGGGGA 960
CAGCTGCCTA CATGTAGAGA ATTACCAGGG AGTGGGTTCT AGACTCCTGA ACATTTTTTT 1020
TGGAGCCCAG TCATTCAGGG ATTCTTCACT CTTTGCTTCT TAGGACATGT TATTGTCTTA 1080
ATTGCAAGCT CCACAAACCT CTGATCAACA CTGCCCCTCC TAAGAGACGA 1130
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