| Tag | Content |
|---|
EnhancerAtlas ID | HS109-23916 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chrX:53316400-53317580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chrX:53316842-53316853 | AGTGACTCATC | + | 6.02 | | JUND | MA0491.1 | chrX:53316842-53316853 | AGTGACTCATC | + | 6.32 | | ZNF263 | MA0528.1 | chrX:53316896-53316917 | AGGGGAGGGGAAGAGAGAGAA | + | 6.22 | | ZNF263 | MA0528.1 | chrX:53317006-53317027 | AGAGGAAGGGGAGGAGAAGAG | + | 6.88 | | ZNF263 | MA0528.1 | chrX:53317486-53317507 | TCCTCCTCCCACTTCTCCTCC | - | 8.41 |
|
| | 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 |
| GH0XI053286 | chrX | 53315206 | 53318307 |
|
Enhancer Sequence | CCTCACAACA AAGTGTACCC AGACTAAGAC AAGTGAAAAT TGGGAATGTA AGTGCAGGGT 60
TTGTGTAAGC AAAATCGCAT AAAGAACACT TAGGTAGAGA GGGGTGAATG CAATTGTCCA 120
GCGTTTGTGT TTGTTCACCC AGAAGCTCCC TGGTTCCCTG ACACTTGCAA CCACAGCCAC 180
ACGCTCCAGC CACACGCTCA CACACACTGA CATTCAGTGG CACACAGCAA CAAACGCAGC 240
AGCAACCAGA TATGGTTCTC TGCAGACCCC CTGACATGCA GGGCCACGCG CCAGCATGCA 300
GTGTTGCACT TTGCTCTTCA CAGCCACGCT GCCATGCAGC AGTGCACACC CACATGCATA 360
AACACAGAGG TGCTGCCCGT AAGGCTCAGG GCAGGAGTCG AAGCTTCACT GAGCTCTGTG 420
CAGCCTCCCT CCCCAGCTGC CAAGTGACTC ATCCCCAGGG CTGCTAATTA AAGCCAGGAC 480
AGAGGGGACA GAGGCAAGGG GAGGGGAAGA GAGAGAAGGC AAGTTTATTT CGGTGCCAAC 540
CAGGCACTCA GCCAGCTTAG GGGTCACCCA CTTCCTGGGG CTGGGCCAGG CGGCGGCAGA 600
ACACAGAGAG GAAGGGGAGG AGAAGAGAAA CCTCTTACCC CTTCTTGCCC TTCTTTAGCT 660
TCCTGGAAAG TTACCTCCTC CTCTCTCCCA CTGTCAAAAT CCAGCTCTGA CTCCTCTAGA 720
CTTCTGTCCT CACAAACTGG CTGTCTACAC CATCATCACG CTCCCATTTG GGCTGGCCCG 780
AGCTGGCTCA TCTGTGTCTG CAGCAACCCC AGACTGTGAA GCAGTAAGTG GCAAGGTTCC 840
AGGCAAAGGA AGTGGTAGGA ACAGGGCAGG GTGGGCAACC GGGCTGAGCC AAATGGGAGG 900
CATCATGGGA GGTGATGCAG CTGGATGGCT CTGGGGATGG GTAGTGTCTT GGACATGTGG 960
ATGGGGGAGC CACAGACGGT TCATGAGGTC TTGGCCATCC CAGATTGCCA AGAGGTGAAA 1020
ACAAGAGATT ATCTAATCCA AACTCCTGTA GGACAGATTG GAGCACTGAG GCCCACAGTG 1080
GGAGGCTCCT CCTCCCACTT CTCCTCCAAC TGCAGTGGCT CCCGTTGCCA TAGGGACGTC 1140
CCTGTCTCCG CGGGTGTCAG CGGCTCCCCC ACCCCCTCCC 1180
|
