| Tag | Content |
|---|
EnhancerAtlas ID | HS073-08247 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr2:61934430-61936070 |
Target genes | |
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 | | IRF1 | MA0050.2 | chr2:61934525-61934546 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | | IRF1 | MA0050.2 | chr2:61934519-61934540 | TTTTTCTTTTTCTTTTTCTTT | + | 6.17 | | 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 | AAAGAAAGTT GTAAGACTGT ATCTTTTATT TTGTTGATAT ATAGATATGA GTATTTGTAT 60
ACAATATCTG GAGACATATA CAATAATTTT TTTTCTTTTT CTTTTTCTTT TTTTTTTTTG 120
AGAAAGGGTC TGGCTTTGTT GCCCAGGCTG GAGTGCAGTG GTACGATCTT AGCTCACTGC 180
AACCTCTTAC CTCCTGGGCT CAAGCAATCC TCCCATCTGA GTCTCCTGAG TAGCTGGGAT 240
TACAGGTGAA TGCTATCATG CCTGGCTAAT TTTTGCATTT TTAGTAGAGA TGGGGTTTTA 300
CCATGTTGCC CAGGCTGGTC TCGAACCCCT GGACTCAAAC AATCCCTCTG CCTCAGCCTC 360
TCAAAGTACT GGGATGACAG GTGTGAGCCA CCCCGGTGGC CAACAAACTA TTAACAAGGG 420
GCAGGATTAT GGAGACTTTT CTGTTTTGTT AAATGTTCAT TTAAAAGTAA TAAACACATT 480
ACACAAGAAA AATAACAAAC GTAACAACAA AAAGAATAAT ACAAAATGAA AGGCAAGAAA 540
TTAAGTAATA CATTTTACAA ATATTTTCAT GGGGAACTAT TGAAAATTTA TTGAAAACAA 600
CATGTTTTCC AAGAATTTAG AATGGAAAAG TTGTTCCACC TGCAGCTTTC TGATTGAGTA 660
GCTGGATGCT GTGATCTTTC ACTCAGTTAC CCCCTCTTCA TCCTGGTTGA TTTCCAGCTT 720
TCAATAAAGC TTTTCACCTG ACGCAGGATA ATAGCGAGTG CATGTGTGCT GGTTTGTTTA 780
CTGTGAGTCT CTCAGAGGAA ATCATGTGCA TCTGTCTGTT TACTTTTCCG TGGAACCTAG 840
AAGGTCACCT CTAAAAATAA TCTTGCTCGG TGTTAGAGTT TCTGTGACAC AGAGGTACAT 900
ACCTCACATG CTCTCCACAG TTAGTGCGCT AAGCCAGGCA TATCTAGTTC CCAAATGACT 960
CAGATCAGAG AAGGAGGGGA AGGCAGCTGC CAGCTAAGAT GTCTAGTGAC TGATTTAAGA 1020
GCAGATGCAG AGGAAGCCCT TTACAAAATG GGACACACTC ATGGCTGCCT TTCTAGATCA 1080
GTGATGTTGA ACTTTTAAAT ATGTTTATTG GCTTTTTGTA TTTCTTCTTT GTAAGTTTCC 1140
AAAGGAAATA TTAGGAGAAT TTCTGAACCA GAGCCCATGC TATGGCTATT TGACTTTGCA 1200
GTAGACACAT TTGGATGCCT TTTCACTACC TCCTTTGGCC CCGAAGCTCT TGTTAAAACA 1260
GGTGCGCCTG AGGAACTGCG TTTATGCGTG AAGAACACTC TCCATTTGCC CCTGACGTCT 1320
GCCTCACTCT TCCCAGATTG AACCTTTATT ATCCCATGCT GGGCTGGGAC CTCATTATGG 1380
AAGGCCTCGA AAGCCAGCCT GCGGAGGTTG AACAAGGGAG TAGGATGATG AGAGTTCTGC 1440
TGTAAGAGAT TAACCCAGCA TCAGTGTAAG AGACTTGAGA GGGAAGAATG GGTAGAGAAA 1500
GAGATCAGTT AGAAGTCTTT TATTGGCTGG GCATGATGGC TCACACCTGT AATCCCAGCA 1560
CTTTGGGAGG CCAAGGCGGG CGGATCACCT GAGGTCAGGA GTTCAAGACC ATCCTGGCCA 1620
ACATGGTGGA ACCCCGTCTC 1640
|
