| Tag | Content |
|---|
EnhancerAtlas ID | HS078-09567 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr2:61934640-61936040 |
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 | | Nr2f6(var.2) | MA0728.1 | chr2:61936020-61936035 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 | TCCCATCTGA GTCTCCTGAG TAGCTGGGAT TACAGGTGAA TGCTATCATG CCTGGCTAAT 60
TTTTGCATTT TTAGTAGAGA TGGGGTTTTA CCATGTTGCC CAGGCTGGTC TCGAACCCCT 120
GGACTCAAAC AATCCCTCTG CCTCAGCCTC TCAAAGTACT GGGATGACAG GTGTGAGCCA 180
CCCCGGTGGC CAACAAACTA TTAACAAGGG GCAGGATTAT GGAGACTTTT CTGTTTTGTT 240
AAATGTTCAT TTAAAAGTAA TAAACACATT ACACAAGAAA AATAACAAAC GTAACAACAA 300
AAAGAATAAT ACAAAATGAA AGGCAAGAAA TTAAGTAATA CATTTTACAA ATATTTTCAT 360
GGGGAACTAT TGAAAATTTA TTGAAAACAA CATGTTTTCC AAGAATTTAG AATGGAAAAG 420
TTGTTCCACC TGCAGCTTTC TGATTGAGTA GCTGGATGCT GTGATCTTTC ACTCAGTTAC 480
CCCCTCTTCA TCCTGGTTGA TTTCCAGCTT TCAATAAAGC TTTTCACCTG ACGCAGGATA 540
ATAGCGAGTG CATGTGTGCT GGTTTGTTTA CTGTGAGTCT CTCAGAGGAA ATCATGTGCA 600
TCTGTCTGTT TACTTTTCCG TGGAACCTAG AAGGTCACCT CTAAAAATAA TCTTGCTCGG 660
TGTTAGAGTT TCTGTGACAC AGAGGTACAT ACCTCACATG CTCTCCACAG TTAGTGCGCT 720
AAGCCAGGCA TATCTAGTTC CCAAATGACT CAGATCAGAG AAGGAGGGGA AGGCAGCTGC 780
CAGCTAAGAT GTCTAGTGAC TGATTTAAGA GCAGATGCAG AGGAAGCCCT TTACAAAATG 840
GGACACACTC ATGGCTGCCT TTCTAGATCA GTGATGTTGA ACTTTTAAAT ATGTTTATTG 900
GCTTTTTGTA TTTCTTCTTT GTAAGTTTCC AAAGGAAATA TTAGGAGAAT TTCTGAACCA 960
GAGCCCATGC TATGGCTATT TGACTTTGCA GTAGACACAT TTGGATGCCT TTTCACTACC 1020
TCCTTTGGCC CCGAAGCTCT TGTTAAAACA GGTGCGCCTG AGGAACTGCG TTTATGCGTG 1080
AAGAACACTC TCCATTTGCC CCTGACGTCT GCCTCACTCT TCCCAGATTG AACCTTTATT 1140
ATCCCATGCT GGGCTGGGAC CTCATTATGG AAGGCCTCGA AAGCCAGCCT GCGGAGGTTG 1200
AACAAGGGAG TAGGATGATG AGAGTTCTGC TGTAAGAGAT TAACCCAGCA TCAGTGTAAG 1260
AGACTTGAGA GGGAAGAATG GGTAGAGAAA GAGATCAGTT AGAAGTCTTT TATTGGCTGG 1320
GCATGATGGC TCACACCTGT AATCCCAGCA CTTTGGGAGG CCAAGGCGGG CGGATCACCT 1380
GAGGTCAGGA GTTCAAGACC 1400
|
