| Tag | Content |
|---|
EnhancerAtlas ID | HS110-02570 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr2:9276920-9278430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr2:9278185-9278198 | GAATGTTCCGGAA | - | 6.12 | | HSF1 | MA0486.2 | chr2:9277573-9277586 | GAACTTTCTAGAA | - | 6.41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 9277400 | 9278000 | | chr2 | 9277097 | 9277807 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I009136 | chr2 | 9276801 | 9278718 |
|
Enhancer Sequence | AGGCAGGAGA AGTGCTTGAA CCCAGGAAGC GGAGGTTGCA GTGAGCCGAG ATCGCGCCAC 60
TGCACTCCAG CCTGGGCAAC AAGAATGAAA CTCTGTCTCA AAAAAAAAAA AAAAAAAAGA 120
TAGCACAGTT TTACATGTTA AATGGTTAAG AAATACATAC ATACTAAAAT TAATATGGTG 180
TTTTCCTTTA AAAAGACTTG AGGCTTGTTT GAGGAAGTGG GCGTTGGGGT TGTGAGCTGG 240
GTGATCTGGA ATTGGGGGGG CATTCTAGCA CCAGAGCTGG ATGGATGTGG ATGTGACTCC 300
TAACACACCC TGTGAACGGA GGGCTGGAGG GTGCATGGGT GGGGTTGTGT GTTCCTAGGG 360
TGTGTGCGAG GGTGGGGTTG TGTGTTCCTA GGGTGCGTGC ACGGGTGTGG TTGTGTGTTC 420
CTAGGTTCTG GTCAGCCAGG TGCCATTCTC TGCATTCGCC TGGTGTTTCT GAGGACAAAA 480
TTGTGCAGAG CGAATGTGAA CTTTGAAACT CACGTTATGC TCCAATTGTT CCCTACTCTA 540
GCAATTGGGA ATTGCTATTG GAGCAATTGG AGCAATTTCA TTTTCAAAAC AAGCCGTACA 600
GCGGAACTGA AAGTATCACA TCCCTTGAGG ACTCCGGACA TGTTGGGGAA GGGGAACTTT 660
CTAGAAGGTG GCATCTGCAG ATGTCAACAT CGGCGGCGGT GCCAAGAGGG GCTTTGCAGG 720
GCCACAGGGC AGCAGCTCCA TGCAGCTGGC CCCATCCCAG GCCTGGTGAG CTCTCCTGGC 780
TGTGTACTCA GCCCTGAGCC TGATGACCAA CACCAGATGC ACAGCCTGCT GTTTACCAAG 840
CCCTCCCACC CACACCAGGG TGCCTCCTGA CAGCCTCACG GGGACAAAGT GCAGGCATCA 900
TTCGTCCACA TTTGACAGAG ATGGAAGGGG GGCTCAGAGA AGCTGATTAC TTACCCGAAG 960
ACACACAGCC TGCAAAGGGA GGTGGCACTT CCACATCCCA CGCTCTGGCT GACCCTCTGC 1020
CTGTCCTCCT GTGCAGTATG TGGGGTCTCG TCACCAAGCG CTGGGATAAA CTCGAGGGGC 1080
CAGGCTCAAG GCCACGCGTC CAGAGGCAAA TGCTGCAAGA AGAGAGGTGC AGGAAACCCA 1140
GGTAACCGAA AGGCACCTGC CTCGAGTGAG CTCCCTCCAG CCCTGACACC TGTTCCTTCT 1200
TTCAGTGGAA AGGACAAGCC GCCGTCCACA CTGCGCCTTT AACAGTTACA CCCAGCGAGG 1260
CTGAGGAATG TTCCGGAACA GCCAGGATGT GGGCTTCTTT GTAGCGGGAG TGTGCCACAT 1320
GTAGTTCAAT CCTGAGTCGG AGGCCTGAGC AAGCAGCTTG CAAGATGTTT GAGGAGCTTA 1380
GCATTGACTG TGGCAGGCGG GCCATTGCTT CTATGATTAA AAAGGCCCAA CTCCCCCCTA 1440
CATCTGCCCT CGACTCTCAG GGCACACCTG GGCCCTCAGG CCGGGTGTGC TCAGCTGAGC 1500
TTGGCCATTT 1510
|
