| Tag | Content |
|---|
EnhancerAtlas ID | HS148-04646 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:105650820-105651960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-3 | MA0672.1 | chr12:105651316-105651326 | ACCACTTGAA | + | 6.02 |
|
| | 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 |
| GH12I105253 | chr12 | 105647044 | 105652164 |
|
Enhancer Sequence | CCATCCCTGG ACCCATCAAC CTTCTGCCTT CATGTAATTT CAAAGTGTTC TCCAGTAGAG 60
AAGAATGTCA CGAAGGCCTC CTTTATAGAA GTACATTACT CATACATAGT TTATTTTTCA 120
CTAGCGTTCT CCCGGCTAGG ATGAAATTTT TCAGGCTTAA TCATGTCTAA AAGAAGAAAT 180
ATTTTGGAAA GTTTGAGCAA ACTCACTTCA GAAACTATTG AGGATTTAGA AAATCAAGTT 240
GTAGATGTGT TTTAGGTGAA GAAGTTTCAT GAGGGTCATC ATTACTTTCG GCAAGCCTCT 300
GTTAAGTCCT AGGCACTGTG GAATAGCTTG GACTCCATGA AGATCCCTTT GTTGAATAGT 360
TTGGGTCCCT CCAGGGTATG TTAGAGGCTA GACTGGCCAT GTCTACAGCC TCAGCCACTC 420
ACTGCACTTC ATTAATTTAA ACGACTCCCA TGAGCTCTGA CATATTGGAA GTGAGAGTAG 480
GTTGCTGGAT CTAATGACCA CTTGAAATCA TTCCCAACCC ACAAATAAGT TTTCACGGAA 540
TTCTCATTCC TGAATAAAGT TAAATCATGA TTTTGACACA CCGTGGAGGA CTTGGCTCTT 600
AGTCATAGCT CTGTGAGTCA CTCTGCTCAC CCAGAAGGTC ACTGAAGATT CAAATGAGGC 660
AGATAGGATT GTCCATCTCT GCTGGAAAAT TGTTCTATAG CAATTTTGCC TATCTAGTAC 720
AACATTTTGG AATGCTTGGA ATAGAGTAAC AGCAACAGCA ACACAATCAT AGACCATGAT 780
AACTGCCATA CATTGAGGCC TAATGTATGT TAGATGTTGT GTTAGGTGCT TATATAATTG 840
AGGTCGACAA CCACGCAAGG CATGTATCAT TATTCTTATT GTGTGTATTA GGAAACAGAG 900
GCTTACATGA CAAGTTTGGA GGTGGCGTTG GGATTTGGGC TCAGATCTAG CTGACTCTGA 960
TGCCTGTGCT TTGCCCACCA CACTGAACTG CCCTGAAAAT GTGATTCTAT ACCTGAATCT 1020
TGCTTTCTGG GATGCTATGT AATTGAAGAA AAGTCTTTGA TACCCCAATT ACCCTGATGT 1080
GATTATTACA CATTGTATGC CTGAATCAGA ACATCACATG TACCCCATGA ATACATATAC 1140
|
