| Tag | Content |
|---|
EnhancerAtlas ID | HS060-19905 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:113058170-113059230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PAX6 | MA0069.1 | chr2:113058785-113058799 | TTCATGCATGAATG | + | 6.22 | | TEAD1 | MA0090.2 | chr2:113059141-113059151 | CACATTCCAT | + | 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 |
| GH02I112300 | chr2 | 113058301 | 113060147 |
|
Enhancer Sequence | AGTTTCATTC TCTACAGATA CAGATTAGCA GCATTGGCAT TGTCCATCTA TTTATTATTC 60
ATTTAGGTAT ATGATCGAGT GCTTACTATG GAAACCTTTA TGCTGTATGC TGAGGGTTAT 120
AGTAGTGAGT GAAATAGTTG GCTCTTAAAG AGTTTACATT GCAATGGGAA AGCTATGAAA 180
AAAACAACAA GGTACTGGAT AGAGAATTAT GTGGATTTGG GGTAGGGAAG AAGGGGAACC 240
TATGCTGACT GAGAAATCAT GGACAAGTTG GCAGCAATGT AGGAGCAGGT TTTGAAACTC 300
CCTGAATTTC CTCCATTAAA ATCACATCAA TTAGGATAAC ACAACCAAAA CCCATTGACA 360
ACATCTACAA AAAAAGGAAG AAACAAGTTA TCTCTAATAA ACCTAAAAAG TACAAATGAC 420
TGGAGCCAAA CGATAGACAG CAACAAGAGC AGTGTAACAA CAGCATCAGT ACAAATGAAG 480
CAGAGGGAAA ATAAAGGGAC TTCCAGAAAC CAAGTTGCCA ACAGATATTC ACCTCAAATG 540
GTCAGTGCCC AGCACGGAAA CCTCATGGGC CTGAGAACAG CAACAGAAAC TGGGAGGGGG 600
CTGTGCTATC ACCAGTTCAT GCATGAATGT AAGGTGACCA CAGAAATTGG ATGGTGCTGA 660
AAAGATCTGG ACCTGATGAA CCCCAAATAT GAATCAACCA AATTCCTTTT TATGACAGAG 720
TCCCACACTG AGGAGGTAAC TGCTGGAAGT AAAGTCTACA TTGAGAAACA GGCATATAGG 780
GCCAAGGAAA GAAATAGTCA GATAACAAAT GGGGGAAGGA AGCAGAAGAG GCATAGCTCA 840
GAAAATAGCC ATATTTTTGA ATACTTCATG CTAACAACAG AAGAGATAAC CCTAGAGCTA 900
TGAAGCTAGG AAAGCTTTAT TGGCCCATTC CATCCATTTT TTTCACATGA GAAGCAAGAT 960
AAGACTATGG TCACATTCCA TAGTTGTTAT TGTAAGATAA AAGAGAATAA TGGAGAGTAA 1020
GTCTTCCAGA AAAGAAAGCA TGCCCACAAA GCATATGAAA 1060
|
