| Tag | Content |
|---|
EnhancerAtlas ID | HS191-07914 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr11:115398170-115399480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:115398947-115398968 | TTTTGTTTTCTTTTTCATTTT | + | 6.38 | | SOX10 | MA0442.2 | chr11:115398284-115398295 | TGCTTTGTTTT | - | 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 |
| GH11I115527 | chr11 | 115398192 | 115399439 |
|
Enhancer Sequence | TTAAATACTC CTGCCAGAAT GTAAGCCACC TGAGAGCAGG GATTTTCACA AAGCAGCAAT 60
AGCAGTGCCA CACACTGGCC CTGTGTTTGA GTGTGAGCTA ACTAATGGCT ATCCTGCTTT 120
GTTTTTTGTG TGTTTTGTGT TTTTGTTTTT TTCTCCAGAA ATATGGAGTA TGCAGATCCC 180
AGCACAGACT CACAGGATCT GGTTCATGCA TAAATTGGCA AGGTTTAAGT CAGCCTGGTT 240
CTCCTGGGAT TCTTAATCAA AGTTTTGCTG AGCCCAGGGT AGGGAGGATG AGTTGGGAAA 300
ACCTACCCCT TCCATATTGT TTCCTTTTTA ACAGCTTGAA GTGAGAGAAA AATAGTCAAT 360
TGTAGAAAGA AGGAAGTGGA AGGCTCAATG CCCCCTCTGC CTCCCACAGG CTGCCATCAA 420
ACCTGTTTAT CCTGTTTCAC TTTTAAAGCC CTGTTCCAAA GAGAGCTCTG TCATTGGCTC 480
TTTCCCCTGT GGAATCACAG CTGCTATGTT TTCAAATACC ACCCTGGTTT TCTGAATGGC 540
TTAAAGCTCA TTAAGAGATA GAGAAAGAGT TTCTGATTCT CTCTAAAGGA GTACTTCCCT 600
ACTCCATGCC TAGCTCTGAA GGCTAGTGGG CTCCCCGCTG TCACTCCACT AATGCCAGTA 660
ATCTGCTCGT AAATTCCAAA AACCTAGATC CAGGAACCCT GAAACTTGTG TTCATATTAT 720
AAAAATACAC TTTATATATT TTAGAGTTGC TTTATCTCTA GCTATACAAT TATACTTTTT 780
TGTTTTCTTT TTCATTTTCC ACCAATGGTA GGACAGTTCT CCAGGTGGCC TCAGACTGAC 840
CCAGTTCTTC TCCTTTCTTC CTTGCAGTTC TCAAGACTAA CTGTAGGATG TTCTGGGACT 900
GCAACATCCT GAGATAAGGA AGGAATGACA AGAGCAGCCT GGGCCCTGTT CCAGTTCCCC 960
CTTAGAAACA GGACGTCCTT CAGTGCTTTA GCCCAGCATG TCATGCGGCC TCTGGGAATA 1020
AAACCCAGGG TAGGCTGCTT TCTGGAATCT CTTAGCTGCC GTGCAAGTGG GGCACGTGCT 1080
GATGAGACTC CATCCATCCA CGGCAGCTTT CCTGAGCCTG GAGGGACCAG CTGGCAATGA 1140
ATCGTAGGCT TTTGTTGTTC CTTGCTGTCT GTCTGGAAGT CATAAATCCA CTTCATATAA 1200
CTCGCTGCAT ATGAGCGTTT TCTGTCTCAC TGGACTCAGA AAAGTTGGTA ACCAGTGCAC 1260
AGTGAGCCTG CTTTACATCA ACCACTGGAC ACTCCATGAG AACCTGAAAC 1310
|
