| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08088 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:133170090-133171040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr12:133170736-133170750 | AGGTGGGCGTGGCA | - | 7.14 | | SP3 | MA0746.2 | chr12:133170737-133170750 | GGTGGGCGTGGCA | - | 7.12 | | SP4 | MA0685.1 | chr12:133170735-133170752 | AAGGTGGGCGTGGCAAC | - | 6.33 | | SP8 | MA0747.1 | chr12:133170737-133170749 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr12:133170577-133170598 | GAAGGAAGAGGAAATGGGAAA | + | 6.12 |
|
| | 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 |
| GH12I132593 | chr12 | 133170057 | 133171053 |
|
Enhancer Sequence | ATTCTCTTGG GTTTGTCCCA GGAGTGAGCT TTGGGGTCAG ATGTCCAAGT TCACAGTCAC 60
ACTCGAGCCG TGACCTCGGC CGGGGCCTTG CCAGGTCCAG TCCTGGCCTC AAGATGCCCC 120
TTCAGGGTCA GCCCGCAGCC AGGGGTCCCA GAGCAGGCAA GGGCTTGAGG AGGGCCTCCC 180
GGGGCTGGGG CACCTGCCTT TCAGGTGAAA TATCAGAGTG TTCAACCCAG ACCATACCAA 240
TGGCACCCGC GCGGAGTGCA GTCACCAGGG AACCGCCCTG CGGCGATGGC CCCGGCGGGG 300
AGAGGGTGGG TGACGTGCGC TGCGGAGCAT CTGCCCTGGT GGAGGTGCAG CCCCACTCAA 360
AAAGGTTCAC CGTGTGAGTT AAAGATGTTT ACTGTGAACC CTGAAGCAAC CACTAAAACA 420
ACAAAACAAA ATTCTGGCTC ATAAGCCAAC AACTGCAATC AAACAGGATC ATCAAACAGA 480
ATCCAAGGAA GGAAGAGGAA ATGGGAAAGG GAGAGCCGGT GACAGCAGCG GGAGCAGAGA 540
GCAGGACGGC GGGCGTGGCC TCTACACAGT GAGACCAATG GGAGCAGAGA ACAGGATGGC 600
AGGCGTGGCC TCTGCATAGT GAGACCAAAG GGAGCAGAGA ACAGGAAGGT GGGCGTGGCA 660
ACTGCACACT GAGACCAATG GGAACAGAGC AGGACAGCAG GCGTGGCCTC CACGCAGCCA 720
CAGCCACACC GGAGCAAGTG GTCAGACAGC CCCAGTTAAG AGCAGAGATT GCCAGGGAGG 780
GTAGGACAGC AAAACCCAAC GCTAAACTGC TCATGAGAAA TGCACTTTAG ATATGGACAC 840
CAATAAGTCA AAAGGACAGG AAAAGCTATG CCATGCAAAC AAAAATTTTT AAAACCTGCA 900
GTGACTATGT CAATATCAAA GTAACTTCAG GGGCCGAGCA CGGTGGCTCA 950
|
