| Tag | Content |
|---|
EnhancerAtlas ID | HS102-10294 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr17:44139740-44141110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr17:44139866-44139876 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr17:44139866-44139876 | GGCACGTGCC | - | 6.02 | | Zfx | MA0146.2 | chr17:44140175-44140189 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH17I046062 | chr17 | 44139914 | 44142081 |
|
Enhancer Sequence | TTTTAGATGG ACTCTCACTC TCTCACCAGG CTGGAGTGCT GTGGCGAGAT CTCAGCTCAC 60
TGCAACCTCT GACTTCTTGG TTCAAGCGAT TCTCCTGCCC CAGCCTCTCG AGTAGCTGGG 120
ATTACAGGCA CGTGCCACCA CGCCCAGCTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT 180
CATCATGTTG GCCAGGGTGG TCTTGATCTC CTGACCTCAT GATCTGCCCC ACCTTGGCCT 240
CCCAAAGTGC TGGGATTACA GGCATGAGCC ACTGTGCCTG GCCAGCCTTT TTAAGGGCAA 300
AAGAGTTACT GCACTAAACG TGCATCTCAA TTTTAAGATA TATTCCAGCC ATAATTCAAC 360
TAAGCTGATA GCCCTTTAAA AACACAGTAA TTGGGCTGGG TGTGGTGGCT CACGCCTGTA 420
ATCCCAGCAC TTTGGGAGGC CGAGGCGGGT GGATCACTTG AGGTCAGGAG TTCGAGACCA 480
GTCTGGCCAA CACGGTGAAA CCTCATCTCT ACTAAAAATA CAAAAAATAG CTGGGCGTGG 540
TGGCGTATGC CTGTAACCCC AGCTACTCGG GAGAATGAGG CAGGAGAATC GCTTGAACCC 600
GGGAGGAGGA GGTTGCAGTG AGCCGAGATC GCACCATTGC ACTCCAGCCT GAGCAACAGA 660
GCAAGACTCC ATCTCAAAGA AAAAACAAAA CAAAACAAAA CCTCAATGAG TTCCCTCAAG 720
TATGTTTTAT TTGGTTCTGG AATGCAGTAG AGATCATTTA AGATGCAGGT AAGGAAAAAA 780
TATTAATCAC TTGCTTTGTG TGTTCTGTAC TCTGTACTCA CAATAACTGT GAACTCACTG 840
TCATGTAACA ATATTAGAAC ATAATTTACC TGTTAACTTC TTTGCTGTCA TTAGAAAGTA 900
AGCTCCATGA AGATAAGGGC TTTGTTTTCC TTACCAATGC AACCTGGCTG CCCTGAATAA 960
TACGGTGGGC ATTCAAAAAT GCTGTTGAAT AAATCTGTCT GGAAAACCGA GCAATTCAAG 1020
ATGACAGAAG ACAAGATGCT TGCTCATCAG CAAATACCAC TGAGGTCATG TCATGAGTGA 1080
GGAGCCATGT GAGACACAGA AAGCAACCTA GACAGAAGGA ATGGGGTGTG TCTCTAACTC 1140
TGGAAGAACT CCAGCTTTCT GCTAGATCTA GTACATGGTA TATTTCCCAA AGTCAACTAA 1200
TTTCTCTGTC TTATTTTTCA TGCAGCTTAC TTTTGTGTCA GGATGATTCT GTTTTAGAAA 1260
GTGGCATTGG AACAAAAGGA TATTTAGTTT TATGCCTATC TCTTGCCTAA GCTACCTTTT 1320
ATAATTTTAT ATGTACATTC AAAACTACAT TCGTTCTTAG GCATGGATCA 1370
|
