| Tag | Content |
|---|
EnhancerAtlas ID | HS113-08564 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr12:52816430-52817850 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:52817050-52817068 | CTCTCCTTCCTGCCGTCC | - | 6.05 | | EWSR1-FLI1 | MA0149.1 | chr12:52817054-52817072 | CCTTCCTGCCGTCCTCCC | - | 7.11 | | ZNF263 | MA0528.1 | chr12:52817050-52817071 | CTCTCCTTCCTGCCGTCCTCC | - | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 52816696 | 52816803 | | chr12 | 52816908 | 52817337 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052422 | chr12 | 52816160 | 52818832 |
|
Enhancer Sequence | TGGACACTCC TGTAGCCTCT CATCTGAACT CCCTTCTCTA TTCCCAGGTC TTGGGCTCTG 60
AACCCAAAGT CACTAAATTA TGCTCCTCCC ATTCTGTTCA CTTATGATTT CTAAAAATTC 120
ATTTATTGGA GATTCAGTCT GTGCCACACC ACACGACAGG TCAGCCGCAA GCATGATTTC 180
ATTTAATTCT CATAATAACT TTGTGAGGGT GGATGATAAA AATAAGGACA ATTTTGAATA 240
TCTTTTGAGC AGCCACTATG GGTAGCTGGT TTCCATGTAT CTTCTTTAAT CTGAAATAGC 300
ACTACAGGGG TTGCCGTTAA GATCCTTGTT TGACAAAGGA GGCCGATTGA GACACAGTGT 360
AGTTAGGCAC CTTTGTTGAG GTCACATAGC TAGTGAGCAC TGGGGCCATT GTCAGAACCC 420
GGACTCCTGG TCCCATGCCC TGAATCATTG CACCCCACAC AGTTGGGAAG ATCAGGCTCA 480
GAGATGAGAG CCAGCTTGGC CAGTGGAGAA AGCCTGAGGA TGTCACTGCA AATTCCTGTC 540
CCTCCACTTC TCTCCTCTCT TGGTCTGAAC TCGCCCTCAC CCCAACACCA GGGATTTCAC 600
AATTGTTCTC AGTGTCATTT CTCTCCTTCC TGCCGTCCTC CCTCTCCCGT CCACTCCAAA 660
TTTTAGCCCC TGGTTTTACA CTCATCTTCC CTCCTGATTC ACGGCCTCCC TCTCCCCCGA 720
CTTCACTTCC TGCTCCTTCA CCCTGGACAA GGGTGTTTTA GAACCCTGTC CCAAGTAGCT 780
CACATCAGTT CCTGAGCATT GAACTCACTC CCTCCAAGCC CACATCGACT GCCCCACTCT 840
GGGTGAGCCC ACTGGGCTAT GCCCCAGCTC AGGCCTGATG GGAGGGGTCC AGGAGACTGT 900
AAACTCAGGA ATGTGGGAGC TTACTGGATA TCTCACTGCT GCCTGCAATT ATGGGCTAAA 960
TGGCTCCTCT CCTTGGTGAA AGCGTTGCTC CCAGGGCTGC CTTTTAACTC CTCTTCGTGG 1020
CCTGTTATTT CTCTGCTGGG TCTGCAAGTT TGAAACTGTC AGGGAAAAAT CAGCCCCTCT 1080
GCTGGGCCGC CCACCCGGCG TCAGTATTCT GGAACACTGG TTTGGAATGG GGACGGCACT 1140
AACAGAGCAG GGAGGCCGGT CTGGGCTTCT CCCAACAGCT CCGGCTTCCC AAACAAGGCA 1200
TGCCAAGGAG AGGGAAAAGG AAGTCTGGCC AGCCCTGCAC TCCCTGCACC TCTGCAGCCC 1260
GCCCTCCCTT CCTCCCAGCC AGCTTTCTTA GCTCAGAGGG AAGGGGCAAG GGCTGATGCC 1320
TCTGAGCACT GGTTGTGTGA TCCCCATGCT GGGAGCAGGC CTGGGAGAGG AGGAGAATTG 1380
CTTTGGGTCA GTCACCATTC CAAACAGAGG GCCAGACACC 1420
|
