| Tag | Content |
|---|
EnhancerAtlas ID | HS131-09128 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr8:106580960-106582450 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr8:106581530-106581548 | TTTTTCCTTTCACTTTTC | - | 6.97 | | Myod1 | MA0499.1 | chr8:106581556-106581569 | AGGAACAGCTGCA | - | 7.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 106581035 | 106582017 | | chr8 | 106581834 | 106582267 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I105569 | chr8 | 106581341 | 106581490 |
|
Enhancer Sequence | CTTAACTCCT GTGCTTTAAA ATCATTCTAA AGGGCACGAG AATACCCCAA GGTTTTGGTA 60
AAGCCTAAAA AAGGCCTTCC TGTTACTCAC CTCCCCAGGT GATGCTCACC TCCCCAGTTC 120
TGACCCCTTT TCCACTCTCT TATAGACTTT AGGCATTCTG AACTACATGC AGTGCCCTGA 180
ATGTCCATTT TTTTTCCACA TCCGTACATT TGGTCATGCT GTTTTATCCT CCTGGAAACC 240
CCTATTCCCC CCTCCCCACC TATCTCTCTT CATCTCACTA AGTCCAATAC TTATTTAAAG 300
ACTCTGCTCA AAGTCACTTC CAAGGTAGAC CTTCTCTGAA GCCTCCTGTC TGGAATAGAT 360
AACCACTCTT GGAGTATTTC CCTGGTGCTC TAGGTTTACT AGGATAAGAG CACTGATCAC 420
ATAACTGTGA GCTCCTGTTT GCTTGTCTAT CTCCCCTGCA GACCATATGC TTATTATCTA 480
TTTTTTATCT TTCTATCCTT CCCACTTAGA ACAATGTCTA GCTTATACTA AGAGCTCAAT 540
GAATAACATT GAATGAATCA GCACATTAAT TTTTTCCTTT CACTTTTCTC CATATCAGGA 600
ACAGCTGCAC ACCCCTCCTT ATTCAAGACC CTGCATCCTT CCTGAGGCTT TACATCCATG 660
TCTGTTTCGT CTGTGATCTT GCTTCATCTG CCTAACTCAG CAGAGCAATT ACCACAGGAA 720
ATGCTATCTT GTACCTGTTT TATTTGTTTA TAGACTTGCA CTTTTATTTT AGTCTCGTTT 780
GAGAGGAAAC TTCAGTAGGA CAAGATAACT ATGTCTATTT CTTCAGTTTT TATCTCATAA 840
GGAGATATGC CCATGATGGT TTCTTGAGAA AAGTTGACTA ATTTCGGTGT AAGATTTGCA 900
ACCCTTGGAT GCAGCTAGGA GGATGAGGTG TTGCGCCTAG TGAGGCAATT ATGATTTGTT 960
TACAACAGAC TCAGTTTTAG ATCCCTCACT ATGACATGGG TGAAGGCCAA GAAGGTGTTC 1020
TGCTCTACCA TGCTTTCTGT GAAGTCTCAT CCAGCCTCAC ACGTTCCAGT GACAAACCAT 1080
CTGGGAAATT CCATCTGTCT CTGCTTGGAA ACTGAGGTGG CAGTCGCCCA CTGTGAGCAA 1140
TTTTCTATTA ACTTCTTGGA TAAGATCAGT CAGATTTATA CTGAATTGAT GGGAACCGTA 1200
AGAGCAAGAT TGTTCCAAGA GAAGACAAAT GTACTGATTC CTCTAATTGG GCTTAAGCCA 1260
GTTTCATTCA CAGACGCCCT TAGGTTCTAG TAGTGCAAGG ACTTATAACC TTTTTAATTG 1320
TACCCTGTTC CTCTTGGGAA ACATTGGTGA AATTCATTAT TGATGGAGGT TGTAGATTTG 1380
TCCCTTAGGG AGGGCAAGAT CCTGGCTTCT CTTATACTCT ATCTGCTATG TGGAGAATTA 1440
ATGGAAACTG AGTGGACAGA AAAGCTGCTC AAAGAAGACT TGAAGGCAAG 1490
|
