| Tag | Content |
|---|
EnhancerAtlas ID | HS082-02498 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:178499070-178500150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr1:178499984-178499995 | TCCTTATCTCT | + | 6.02 | | SOX10 | MA0442.2 | chr1:178499811-178499822 | TTCTTTGTTTT | - | 6.62 |
|
| | 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 |
| GH01I178530 | chr1 | 178498781 | 178499981 |
|
Enhancer Sequence | CTTACAGTTA TTTTGAGAGG AGGTAGGAAA TAAAATAATA GGAAAACGTG AGTGGGTGGG 60
GATCAGGACT GGCTATTCTA GAGGACAGGG GTGGGTCCCT TGTAACACAG CATCTCACTC 120
CTGTCAACCT GGTGGCCAAT GACAACAGAG TGAGGGGCAG TTGGCTCACC CCAGCCCTCC 180
CATAGGTAAC AGGTGCGGCA GCCCCAGGCC TTGACGCATG TGGTCATCAG AGAAACATGA 240
GGGTGAGTCA TCTGGGAGCA ATTAAGAGGG GAGGCCCAGG AGGAGGCCAG ACTGTGTCAT 300
CCATCCCATC ACTGCCACAG CACTGGCCCA GTGCCCACTC ACAACATTCC TTCTCCTGGG 360
TCACAGGCCA CAGGCCAGCC CAGAAGGTGG CTGAGGATGG GCTCAGGCAT CCAACACTTC 420
TGACTGGGGC CCAGATCCAT CTCTCTTAAA CTCAGCAGCT CTGAGGATCC CCCAATTCCA 480
TGGCAACGGG CTGCCTACCC ACCTTCCCAA GGGGTGCTAC TCTGACTTGC CACAGTCTAG 540
TCTCAGCAAA CTGAAGCTGT CCTTTAAAAA CATAAATTAG AACATGTCAC TCTTCAGCTC 600
AGAACTTTCC AGTGTTTTCC CACTTCTCTC AGAGCAAAAT GCAAAGTCAA TGGTTCACAA 660
AGCCCTACAG GATCCGCCCT GCTGCCTTCC CCATCCCTAA CCCTGTACAG TATTTCACTT 720
GCACTTTCTA GCCATGCTGG TTTCTTTGTT TTTCTTCAAA CACAACACAT ACCCTCTTGC 780
CTCAGGGCCT CTGCACTTGC AAACCCTACC CCCTCTCACC ACCCTGCCAC CACCATCACT 840
AGAATTCTCA GCCTTCCAGT CGGCCAGCTC CCTCGCCTCA AAGTTACCTT CTCAGTGGCC 900
CCCAGTCCCA GCATTCCTTA TCTCTCTTAC TGTCTGCTTT ATTTTTCTCT CCAGCACTCT 960
TGTCACCAAC TCACATACCA TACAGTTTAC TTATTTGTTT ATTGTCTGTC TTTTTCTACG 1020
AGAATCTAAG CTTTTTGAGT GTGGAGATTT TGTTTCTGTC ACTGCCATAT CCCAGGGCCC 1080
|
