| Tag | Content |
|---|
EnhancerAtlas ID | HS053-08692 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr12:6844510-6845920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:6845024-6845043 | TGGCCACTGGGTGGCACCC | + | 6.48 | | NFE2L1 | MA0089.2 | chr12:6845255-6845270 | AGGTGACTCAGCATA | + | 6.56 | | Nfe2l2 | MA0150.2 | chr12:6845253-6845268 | TAAGGTGACTCAGCA | + | 6.29 | | Rxra | MA0512.2 | chr12:6844526-6844540 | TGACCTTTAAACTG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr12 | 6845064 | 6845600 | | chr12 | 6845776 | 6845871 | | chr12 | 6844802 | 6845450 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I006735 | chr12 | 6844441 | 6845586 |
|
Enhancer Sequence | AAAGCCTCCA AGGACATGAC CTTTAAACTG AAACTAGAAG CCCAAGTAGG AATTAGCCTG 60
ATGAAAGAGA GGGCGAGCAT CTTGGATGGG AAGAATAGTG GGATAAAGGC CTGCAGGCAG 120
AAAGGCTTCA TTCTGTGACC CGCTGCCTGT CCCTCAATAG GAAATGCATA ATTTGGGGAA 180
TGGGGCAAGA TAGACAATCC TATACTTACT GTTCATTTAT CAGTCAATTG GCAAATACAT 240
CTTGTTTTTT GTTTTATTTT GCTTTTGAGA CCATGTCTTG CTCTGTCACC CAGGCTGGAG 300
TACAGTGGCA CGATCATATG GGAATGGAGA GGGAAGCCCC AGGGGCCCAA AAAATGTCAG 360
AGAGACACGG GAGGAAAATC AAGAGAACAA TCCCGTAAAA GTTTATGAAC TCCTGGGCTA 420
AGCTCTGAGC TGTGCAAGCG TAGATCTGTC CCTGAACAGC CTACCTAAGG CTTTGTGAAC 480
TGAATTACAG AATGGATCAC TGTCCAGGTC TGACTGGCCA CTGGGTGGCA CCCGAGCCGG 540
CCTGATCCAA ATAGCACTGC AAACACTTTT AAAATAAAAC CGACATTGAA ACCACAGTGC 600
CAAAAAGGCA GGTCAAAACT TGCTGCCTGA ACCTGATTAC CTGCTAAAAC AAATTACCAT 660
TCAACATGTT CAACATGCTC CTTAAGATTT TAACAAGACC CAGAGCCTCA AACCATAATA 720
TTCAAAATAT CCAGAGTATG ATTTAAGGTG ACTCAGCATA CAAATAACTC TCCAGGGAAA 780
AGACAGCCAA CCCCAAGGAG GCAGAAGTGT TGGAATTTAA AGCAAATGCT GCAAGCAGTC 840
TAACCATGCA GGAAGAAGAA AGGGAGAATG CTTTTGAAAC AAATGTAAAG AAAGTCTTAG 900
CAAAGAAATG GAAGATATAA AGAACCAAAC AGAAAATAGC AATAACTAGG CCGGATGTGG 960
TGGCTCACGC CTGTAATTCC AGCACTTTGG GAAGCTGAGC TGGACCATTC ACCTGAGGTC 1020
AGGAGTTCGA GACTAGCCTG GCCAACATGG TGAAACCCCA CCTTTACTAA AAATACAAAA 1080
ATTAGCCAGG CGTGGTGGCA GGCACCTGTA ATCTCAGCTA CTTGGGAGGC TGAGGCAGGA 1140
GAATCGCTTC AACCTGGGAG GTGGAGGTTA CAGTGAGCTG AGATTGTGCC ATTGCACTCC 1200
CCCAGCCTGG GTGACAACAG CGAGACTCTG TCTCAAAAAC AAAAACAAAA ACAAAAACTT 1260
CCCAAACCTG GCAAAAGACA AAGACAGATT CAAAAAGTTT GGTGGATAGC AAACAAGATA 1320
TACTCAAATC CATGTCCATA GCCAGCGTGG TGGCACATGC CTGTAGTCCG AGCTACTTGG 1380
AAGACTGAGG CAGGAGAATC ACTTGAACCT 1410
|
