| Tag | Content |
|---|
EnhancerAtlas ID | HS007-00819 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:110679140-110680280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr1:110680001-110680013 | TTCTGTTTACAT | - | 6.92 | | FOXP2 | MA0593.1 | chr1:110680002-110680013 | TCTGTTTACAT | - | 6.02 | | RFX1 | MA0509.2 | chr1:110679701-110679717 | GGTCACCATGGCGACG | - | 6.11 | | RFX1 | MA0509.2 | chr1:110679701-110679717 | GGTCACCATGGCGACG | + | 6.12 | | RFX2 | MA0600.2 | chr1:110679701-110679717 | GGTCACCATGGCGACG | + | 6.2 | | RFX2 | MA0600.2 | chr1:110679701-110679717 | GGTCACCATGGCGACG | - | 6.2 |
|
| | 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 |
| GH01I110136 | chr1 | 110679621 | 110679770 |
|
Enhancer Sequence | ACCTATGACT CCAGCTGTGT TGAATCACCT GGGTGCAAAG GTACCTAAAG TTCCACTCAT 60
CAGAGTCACA CTTAAATCTG TGGCCCACCA CAGACCCCAG CCCAGAGGCC CCAGTTAGAT 120
GGAGAGGAAT CTGACAATGA CAAATAGCCT GGTTCTTGCC CCAGTTTTGC AACTGACTTG 180
CTGTGTGACC TTGGAAGAGT TAGTCCACCT TTCTGAGTCT TCTTGTTTTC ATCTGTATAA 240
TCAAGGGTGG TGGCCTAGAG GATTGTTACG ATGCTTTCCA GGTCTAAACC TTTGATTCTC 300
TGACTCAAAG GCAAGGCTTC TTGAATAAAT ATATTCCTCT CCTGACAGCC AGCCTGGGGA 360
AATAGATAAT TCTGTCAGAG CATCCTTGCA CTAAACCTAG AGCTCTGCAG TCTCCCCCAA 420
GGCTGGAAAC TTTATCTTTA TTCATTGTTC ATCCTTGTTC TCCCTCTCTT TGGCTCTCCC 480
TCCAGCCGTG TTTTGCTACC CCACCCCCAA TCCAGGACAC TGCAACCTGT CATGAATGAA 540
GAGTGGCTGG TCACATGGCC CGGTCACCAT GGCGACGGAT CCCCGCAGAC GAGGTAGGCA 600
TCAAAGTCAC ATGAGAACCC CGGAAAACTG GCTGAGGTAT TTATAGAAGC AGTGGCTGGT 660
GCCTTTATGG AAATGGGTCT ATATTTGACT CTGGTACTGA AACCTCCATG CTGTCCCTGG 720
GGCAAGGCAG GTTTTGCATC TGATTCTCTC TCCTCATGCC TGGTGGGGCA AACATTCCCC 780
TCCCCTTCTT GTTGTCTCCT GGCAGAACCC CCCCACCCCT ACTCCCAGCT GATGCCGGTC 840
CTGCCAGAGC TGACTCCCCT ATTCTGTTTA CATTGAACGA TGCTTCCTTC CAGGCTGGAG 900
TTTGGGGCCC CAGGATGCTG GGTGTGTTGG GAATTTGGGA CCCCTTCTTC ACCCTTTTCC 960
CCATGTACAA ACTGGAGGAA TGTCCTTGCT GCTCTCTAAA TATTAGAGGG ATACTGCTTT 1020
CCTCAAAGAC TTTGCCACTT GTTTCTTCCT TAAGAGTTTG GAGGTTGCTG GTAAAGGGAG 1080
GGAGGATATT TCTGAGTCCA AGCCACAGAA AGGTTCAGCC ACCTCTGCCC TTCATGGGTA 1140
|
