| Tag | Content |
|---|
EnhancerAtlas ID | HS060-04765 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:115742420-115743890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SCRT1 | MA0743.1 | chr10:115743788-115743803 | GAGCACCTGTTGCTT | - | 6.62 | | SCRT2 | MA0744.1 | chr10:115743790-115743803 | GCACCTGTTGCTT | - | 6.82 |
|
| | 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 |
| GH10I113981 | chr10 | 115741347 | 115744110 |
|
Enhancer Sequence | GGATCTGGCT GGCAATGCTT TTGCCTTTTC ACTGCCTGAA CTGAGTCCAC AGGACCAGGT 60
GCTCCAGCCC CTCCCACTCT GGCTCCTTCT TGGCTCAGCC CCCTGAAGTC AGAAGGGCCC 120
TTCCTTCCCA TCCTTTCAGA AGGAAGAGAG AAGAGGAAGG CAAGGTCCCA GTGACAGGGG 180
AAGGGCCCAA GATGACCTTG GAGGCACAGA GAAAGCTGCC TGGAACTCAA CTGCCCTCAG 240
AGCCCACTGG TTCACCCCCC CTCACCTCTC TTGGTTTCTG AAGCTTAAAA TAGCCTGAAC 300
CGGTGTGGCC ACATTTCACT GTGCCACTCG GAGAGAACCC CTAGGGTGTT TTCAAAGCTA 360
GTGCTGAGCT CCTCGGGGCA GGCTCCAGCT ATAAGTTATT CATACACACC CTAGCTCCAC 420
CAGGTCTGCT GCAAAAATGT GTTCTGAGCG CTTTTCTGCT AAGGCCCCAT CTACAGGCAG 480
CTCCACTTGC TGGGAGGGGT CAGATCAGTC AGCTACTTTA TTTAATAAAG AGGGATTCTG 540
AAACCCTTCC GTGGCTGCTA GGAGTGCTGC TGACCAGAGC AAAGCGACCA CAGGTTCTAA 600
GCAGAGGCAG GGGCTGCATG GTGGGGAAAG GCATAGCCTG GGAGTCAGGC AATTGGTGTT 660
CTAGATCCAC CTCCGCCCAC ACCGTTAGAT GATCTGAAAT AAGTCACCTC CCCTCTCTTT 720
GCCTCTGTAG GTCTCTCAAA CTGGTTCTGT CCTCTGCTAC GTACTAGTCT CATTCTTAGA 780
CCTTATATGA TGTCAAGATG GCTTCCAGCA GCTCCAAACC TACTTCCTCT CATGTTCACA 840
TCCAGCAGGA AACAAAGAGG GCTTCCCTTC CCCTCGTTAG CCAGACCAAA GTCCTGCCCT 900
GACCCCTGTA GCTTGAGTTG GGCTATGTGC CCATCTAGGG TAGGGGACAT GGTGAGCTGG 960
CCCACAGAGC CCACTCTGAC CTCCTTCTGG GGCTTCCGTA TACTGCAAAG GCTGGAAAAC 1020
TGAAATATAC ATCCACAGCC TCCCTCTAAG CTGGGGTTCT GCAAGCACAT CAGGTCCCAG 1080
CCACAGGATG TGGTAGGGTG AGATTTGAAA GACAGCCGTG AGAGAGGCAC TCTTTTCTTG 1140
CTGTGGCTCC TGGCCCAGGA CGGTTGTTTC AGTGTCCAGT CTCTAGCTTC TCAGATGTTG 1200
AAAAGCTTCA GAACCCTAGC CTGTAGCAAC TGGATGTATT CTTGAATACA GGGGTTCTAG 1260
TGGGGGCCTC CTCACTCTCT GCCTTCTTGT TTGATCACTG GTGGGCAATG GGCATCTTTC 1320
AGGAAACCCA GCCAGAGCCT GCTCCTTCAG TCCTTCCAGT GATTTCATGA GCACCTGTTG 1380
CTTTGTGTTG AATACCTTTC TGATTAAAAA CTGCCAGAGT AATTCCTTGT ATCTGACTGC 1440
TGGCCAAGGC ACCATCCCTG AACCAGTCAC 1470
|
