| Tag | Content |
|---|
EnhancerAtlas ID | HS059-25279 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:61934600-61936030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr2:61935243-61935255 | GTCTGTTTACTT | - | 6.52 | | FOXP2 | MA0593.1 | chr2:61935244-61935255 | TCTGTTTACTT | - | 6.32 |
|
| | 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 |
| GH02I061707 | chr2 | 61934598 | 61936653 |
|
Enhancer Sequence | AGCTCACTGC AACCTCTTAC CTCCTGGGCT CAAGCAATCC TCCCATCTGA GTCTCCTGAG 60
TAGCTGGGAT TACAGGTGAA TGCTATCATG CCTGGCTAAT TTTTGCATTT TTAGTAGAGA 120
TGGGGTTTTA CCATGTTGCC CAGGCTGGTC TCGAACCCCT GGACTCAAAC AATCCCTCTG 180
CCTCAGCCTC TCAAAGTACT GGGATGACAG GTGTGAGCCA CCCCGGTGGC CAACAAACTA 240
TTAACAAGGG GCAGGATTAT GGAGACTTTT CTGTTTTGTT AAATGTTCAT TTAAAAGTAA 300
TAAACACATT ACACAAGAAA AATAACAAAC GTAACAACAA AAAGAATAAT ACAAAATGAA 360
AGGCAAGAAA TTAAGTAATA CATTTTACAA ATATTTTCAT GGGGAACTAT TGAAAATTTA 420
TTGAAAACAA CATGTTTTCC AAGAATTTAG AATGGAAAAG TTGTTCCACC TGCAGCTTTC 480
TGATTGAGTA GCTGGATGCT GTGATCTTTC ACTCAGTTAC CCCCTCTTCA TCCTGGTTGA 540
TTTCCAGCTT TCAATAAAGC TTTTCACCTG ACGCAGGATA ATAGCGAGTG CATGTGTGCT 600
GGTTTGTTTA CTGTGAGTCT CTCAGAGGAA ATCATGTGCA TCTGTCTGTT TACTTTTCCG 660
TGGAACCTAG AAGGTCACCT CTAAAAATAA TCTTGCTCGG TGTTAGAGTT TCTGTGACAC 720
AGAGGTACAT ACCTCACATG CTCTCCACAG TTAGTGCGCT AAGCCAGGCA TATCTAGTTC 780
CCAAATGACT CAGATCAGAG AAGGAGGGGA AGGCAGCTGC CAGCTAAGAT GTCTAGTGAC 840
TGATTTAAGA GCAGATGCAG AGGAAGCCCT TTACAAAATG GGACACACTC ATGGCTGCCT 900
TTCTAGATCA GTGATGTTGA ACTTTTAAAT ATGTTTATTG GCTTTTTGTA TTTCTTCTTT 960
GTAAGTTTCC AAAGGAAATA TTAGGAGAAT TTCTGAACCA GAGCCCATGC TATGGCTATT 1020
TGACTTTGCA GTAGACACAT TTGGATGCCT TTTCACTACC TCCTTTGGCC CCGAAGCTCT 1080
TGTTAAAACA GGTGCGCCTG AGGAACTGCG TTTATGCGTG AAGAACACTC TCCATTTGCC 1140
CCTGACGTCT GCCTCACTCT TCCCAGATTG AACCTTTATT ATCCCATGCT GGGCTGGGAC 1200
CTCATTATGG AAGGCCTCGA AAGCCAGCCT GCGGAGGTTG AACAAGGGAG TAGGATGATG 1260
AGAGTTCTGC TGTAAGAGAT TAACCCAGCA TCAGTGTAAG AGACTTGAGA GGGAAGAATG 1320
GGTAGAGAAA GAGATCAGTT AGAAGTCTTT TATTGGCTGG GCATGATGGC TCACACCTGT 1380
AATCCCAGCA CTTTGGGAGG CCAAGGCGGG CGGATCACCT GAGGTCAGGA 1430
|
