| Tag | Content |
|---|
EnhancerAtlas ID | HS148-14367 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr5:76060880-76061950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA | MA0729.1 | chr5:76061291-76061309 | AAGGTCATTCGTTCAAGT | + | 6.27 | | SOX10 | MA0442.2 | chr5:76061013-76061024 | AAAACAAAGAA | + | 6.62 | | Stat6 | MA0520.1 | chr5:76061523-76061538 | GGTTCTCAGGAAGGG | - | 6.34 |
|
| | 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 |
| GH05I076765 | chr5 | 76060955 | 76062039 |
|
Enhancer Sequence | TTTTCTTTCA TGGGAGATTT TTATTACTGA TTTAATCTCC TTACTTATTA TTGGTCTGTT 60
CTATAAGTTT AGTTTTATGT AACACTTCAC ATACTTTGTA CTTGGTAAAC TCTCATGGTG 120
TCTATTTCTT TGTAAAACAA AGAAATAACA AAGCATCAAA AGAATGTAAG ATCAGATCCA 180
CTTTGTGACA TCCACAAGGA GTACTATGTC TGGCTATTGT TTAGATTCGT TTGGAACTGA 240
TCTCTTGAGT TCTCAGTCAC TCTCTACCTG ATTTGTAACA GGATAAGGAA TGTTTCAAGC 300
TGCACGTCTT ACAGACTCAG GCCAAGCAAA AATACTGTTA ACACAGAAAA CTCTGCCAAG 360
ATTCATTTTT AAAGCCATGA GTTTCCATCC CACAAAGTGC ATATTATTCA GAAGGTCATT 420
CGTTCAAGTC AGAGTTCACA TGGTTTTCAA TAAACCACTC TTCAGATGAC CTAACTTAGG 480
AAAGAATCTC ATTCTTGGGG TCAGTTTCTT TTAGGGAATA TTTAGTTAGC ATTTGAATGA 540
GCTGGCTTGC TCTGGAGAAG CAGTGGCTTG ACTTTGGCCC CTGATATGGC ATGGACTTGA 600
GGTTGTGCAG GGTGTGAGTC TAACCTTTTG GAGACCTCTG TCAGGTTCTC AGGAAGGGGG 660
TACAGAGTCC TGGGTCTCTA TCTTCTTCAA GCACAAATTG CATCCCCATC CAACTACCAG 720
TTGAAAAGAC AGGACACAGG CCAGGTGCAG TGGCTCACGC CTGTAATCTC AACACTTTGG 780
GAGGCCGAGC CGGGTGGATC ACCTGAGGTC AGGAGCTCAA GACTAGCCTG GCCTACGTGG 840
TGAAACCTTG TCTCTACTAA AAATACAAAA AAGTATCCGG GTATGGTGGC ATGTGCCTGT 900
AATCTCAGCT ACTCTGGAGG CTGAGGCAGG AGAATTGCTT GAACCGGGAG GCAGAGGTTG 960
TGGTGAGCTG AGATCGCGCC ATGGCACTCC AGCCTGGGCA ACAAGAGTGA AACTCTGTTT 1020
CAAACATACA ACATATATAT TATCAACATG AAACACGATA TTCAGATATT 1070
|
