| Tag | Content |
|---|
EnhancerAtlas ID | HS098-13639 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:69446100-69447610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr12:69447270-69447282 | TAAATCACTGCA | + | 6.92 | | GFI1 | MA0038.2 | chr12:69447059-69447071 | CAAATCACTGCA | + | 7.22 |
|
| | 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 |
| GH12I069052 | chr12 | 69445805 | 69447919 |
|
Enhancer Sequence | ACCGCGCCCG GCCAAAAAAA AGTTTTTTAA TTAAGTGCTA AGTGTTATAG GTGCACAAAA 60
ACGGGAGTGA TCTGTTTTAA AGCCTTTGGT AAAAGACGAC TTTTGAGCTG AGTTTTGTCA 120
GGTTAAGAAG ATAGCAAGAG CCTCTTGAAT AGAGAAAACA TCCCGTGAAC AATATTGAGG 180
TGCGAGACTA TGTTATATAC AAAGAACAAT GGATAATCCT ATGAAATTGG GGTGTTGATT 240
TTAAGGAGGG TGAGGTGGAA GTGAAAGCTA GAAAATGGAT TTGGGTCGGA TTTTCAAGGT 300
TTTTATATTT CAGGCTAAGT TTGGGGGTTT TACTCATAAA CAATAGTCGA GGATGCAAAA 360
GAGTAGAAAA TGTGGCAAAA CATGCGTGCT ATACAAGCTG TTTTTCATCA GTGAGGCCAA 420
GAATGTCCTG CGACTCAGAG CTTTGTCATC TTTGATGTTT TGCAAACCTC TTTTGGAGCC 480
AGACTCCAAC TGCAAATTTC AGACTTTCTC TTATGTTTAT GACCTTGTAT TTTTCAAAAG 540
GTTTAAAATT TCACATTGCT GCTATGTTCC ATCCAGTGAA GGCAAGGTTA CCTGCCAGAA 600
ATAATCTGAA AGGCAAACAG TACAGTTTTA CCAGTTTCTC TGTTATGTCA TTCATTTCCA 660
AGTAAAGAAT AGATCAACAA ACAGACAAAA TCCTTTTTGT CCCCAGACAG AATTTAAAAG 720
GTTAATTTTA TACATGTTGG TAGATTGTTT TCTCCTACAT GTGGTACAAA CCACCCGCTA 780
GAGGCAAATT ACTTAAATCA GCTCTCGTAA CCACACATAC ATATTTATGC AGCCAGCAGT 840
GGGAGGTGTG GAGGGCAGGG GGATTCCAGG TGACTCAGTA TGTCTGGCAT CTGGGTCAAG 900
AATTTCAACC GATGGCAGAG GGGTTGCCAC CATAATAGGT GCTGTGTATG AACTGCCACC 960
AAATCACTGC ATGTGATTTG TGCCGTGTGA GGTCCTTACA GATCTGTTTT GAGGCTAGGC 1020
AACCCTTAAT GTGAAGCAGC TTTGATTTTT TCCAGCTCAT TCAGCATGGA CGGCCTGGAG 1080
GACTTGCTTT CCTGCTAGCT TCTTAGGTGT CTAACTCCTA GTTAGTTGTG GTAAGTCTGT 1140
CCTGGAGTTT AAATTTTCCC AGTATTGACA TAAATCACTG CACATTGGAA AATTTCTAGG 1200
TGGCTCAACT ATATGCAGCA CATGGTGCCC AACGTGGGGG AACGTTCATT TTTCTCTCCC 1260
ATTTCTTTTA AGTGAAACTG CCATGAAAAG TAGACATTGA ACTGTATTTT AATCAGTATT 1320
ATTCCTCTTT CTTGCTGTGG AGATATCCAG TTACCTTGCA CTGACAGATC TTTGTCTTAG 1380
GAAGATCCAT CTGCTTAGCC CCTTTTAGCA AAGGGCCCAG ATGTTGCTGC AAATAAATTG 1440
CAAACTGGCA CAAAAGCCAA GGAGATTCAA AGGAGAAGGT TAGGAATGCC AAGCCCCTTC 1500
CTTCTTTGAG 1510
|
