| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00553 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:20904410-20905850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr1:20905477-20905488 | TTCTTGGCAGA | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_56034 | chr1:20905232-20906226 | u87 |
|
| | 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 |
| GH01I020578 | chr1 | 20905233 | 20906226 |
|
Enhancer Sequence | ACTCTGTCAC TCAGGCTGGA GTGCACTGGC ACAATCAAGG CTCACTGCAG CCTTGGCCTC 60
TCAGGTTCAA CGATCCTCCT GCCTCAGCCT CCTGAGTAGC TGGGACTTCA GGTGCACGCC 120
ACCACACCAG TTAGTTTTTA AATTTTTTGT AGAGACAGGG TCTCCCTCTG TTGCCAAGGC 180
CAGTCTTGAA CTCTTGGGCT CAGGTGATTC TTCTGCCTTG GCCTCCCAGA GTGCTAGGAT 240
TACAGGCATG AGCCACCACA CCTGGCCAGC ACAATTTTTT AAAGAGGTAA AAGTATGAGT 300
TAGGAATGAT TCACTTCCAG TTCTTGACAA TACCACAAAC CAGCAAGGTC ACTGCCTCCC 360
TCCCTGCCTC GTCAGCCCTT TCCCTGGGAG CACCACAGAA AACCTACTTG GTAGTAGAGC 420
GGCAGGGGCC AGAGGAAGTG AGAATATTCT AAGGTGCTGT CTTGTTGAGA AAGAAAGTAT 480
ATATGTCGAT AAACTTGATA AATTGACAGG GGAAATTAAC ATAAATACAA ACAATAATTA 540
TGGCTAACCA CTAAAGAAAG AAAAAGAAAA GGAATAATTT TCAAATGAGT AGAAGGAAAA 600
GTGTCAATGT AATAAAAGGC AGAAAAAGAG GGGGTAAGGG AGAAAAAAAT ATATAGTGAT 660
TGGTCAGGGT TCCATTGCAG ACAACAGCGT CCACCCAGCA GGCCCAATAG GAATGGGTTG 720
ACGAGGGTGA TCGGGTTGGT TTCAGACACG TTGGAAGGGT TGAGAGGCCA ACTCTAGGCT 780
GAGCTTCCAG GAATAACCCT TGAATCTCAC TGTAAAATGA GCCTAGCTGG AGAGCTTCTG 840
CCACTGCTGC TGACTCAAGA CCCTCGCTAC CCATGTTGCA GTGCAGGAGG CTCCACGTCA 900
CAAAGCTGCT GACACCCGCT TAGCACCAAG AAGCCAGAAG TTGATCTGGA ATTAGGGCCT 960
CCGCTGCAGC CACCTCAGAA CAACCGAAAC GCTTCCACCA CGATGCAGCC AGAAGAACCG 1020
TGTGGCCACT TCCTCCCAGT ACCTTCCCTT TCTGGTTTGT TTGCATTTTC TTGGCAGAAG 1080
CCAGGTGACA CGTGGAAATC CTAGCTGCAT GAGAGTCTGG AAATGTCCTC TCTAGCCGTC 1140
CAGCCTCTAA AGTACAAGAA GTCATGATGG AAAGAAGGAG GTTTGGAGAG GGGCTGAGTT 1200
GGGTCGGTCT TTGGCCCTTG CCACAGTCCA CTCACTCTTA GTCACTCAAC CTCCATTTCC 1260
AAGCTGCATT CCCTTCTTAA ACTTCCATGA AACAACCACA ACGTGTCACC ACCCACAGTA 1320
ATGCAAACGT ACCTCAATCA GACAAGAAAC ACTCTTATTC TTTGCTCAGA CAGGAACATC 1380
CAAAGCCCCA GCAGTTACTG CTTCCATCTC CCACTCCAGG GAACTTGGGT GATGTTCACT 1440
|
