| Tag | Content |
|---|
EnhancerAtlas ID | HS052-08144 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr12:6844670-6845630 |
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 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 6845064 | 6845600 | | chr12 | 6844802 | 6845450 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I006735 | chr12 | 6844441 | 6845586 |
|
Enhancer Sequence | GAAATGCATA ATTTGGGGAA TGGGGCAAGA TAGACAATCC TATACTTACT GTTCATTTAT 60
CAGTCAATTG GCAAATACAT CTTGTTTTTT GTTTTATTTT GCTTTTGAGA CCATGTCTTG 120
CTCTGTCACC CAGGCTGGAG TACAGTGGCA CGATCATATG GGAATGGAGA GGGAAGCCCC 180
AGGGGCCCAA AAAATGTCAG AGAGACACGG GAGGAAAATC AAGAGAACAA TCCCGTAAAA 240
GTTTATGAAC TCCTGGGCTA AGCTCTGAGC TGTGCAAGCG TAGATCTGTC CCTGAACAGC 300
CTACCTAAGG CTTTGTGAAC TGAATTACAG AATGGATCAC TGTCCAGGTC TGACTGGCCA 360
CTGGGTGGCA CCCGAGCCGG CCTGATCCAA ATAGCACTGC AAACACTTTT AAAATAAAAC 420
CGACATTGAA ACCACAGTGC CAAAAAGGCA GGTCAAAACT TGCTGCCTGA ACCTGATTAC 480
CTGCTAAAAC AAATTACCAT TCAACATGTT CAACATGCTC CTTAAGATTT TAACAAGACC 540
CAGAGCCTCA AACCATAATA TTCAAAATAT CCAGAGTATG ATTTAAGGTG ACTCAGCATA 600
CAAATAACTC TCCAGGGAAA AGACAGCCAA CCCCAAGGAG GCAGAAGTGT TGGAATTTAA 660
AGCAAATGCT GCAAGCAGTC TAACCATGCA GGAAGAAGAA AGGGAGAATG CTTTTGAAAC 720
AAATGTAAAG AAAGTCTTAG CAAAGAAATG GAAGATATAA AGAACCAAAC AGAAAATAGC 780
AATAACTAGG CCGGATGTGG TGGCTCACGC CTGTAATTCC AGCACTTTGG GAAGCTGAGC 840
TGGACCATTC ACCTGAGGTC AGGAGTTCGA GACTAGCCTG GCCAACATGG TGAAACCCCA 900
CCTTTACTAA AAATACAAAA ATTAGCCAGG CGTGGTGGCA GGCACCTGTA ATCTCAGCTA 960
|
