| Tag | Content |
|---|
EnhancerAtlas ID | HS191-20655 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr2:70172500-70174310 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr2:70173453-70173463 | GGTCACGTGC | + | 6.02 | | ESR1 | MA0112.3 | chr2:70173986-70174003 | AAGGTCAAAACGACCCT | + | 6.27 | | FOSL2 | MA0478.1 | chr2:70173903-70173914 | GGGTGACTCAG | + | 6.02 | | INSM1 | MA0155.1 | chr2:70173007-70173019 | TGCCTGGGGGCA | + | 6.04 | | JUNB | MA0490.1 | chr2:70173903-70173914 | GGGTGACTCAG | + | 6.02 | | SP8 | MA0747.1 | chr2:70173227-70173239 | AGTGGGCGTGGG | - | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09668 | chr2:70170084-70175672 | CD14 | | SE_65154 | chr2:70171871-70174956 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 70173540 | 70174234 | | chr2 | 70172567 | 70172868 | | chr2 | 70172627 | 70172794 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I069945 | chr2 | 70171934 | 70176194 |
|
Enhancer Sequence | CCACAGGCAG GGTCTCTGCA GGAAGTATTG TTCAGGGCTC AGCCCAAACT GGGTGGCGAG 60
GCAGCTCCCT GCCCACTCTG TTCCATGCAG AATTCTGGAG TCATTGCCTC TGCGAGTGTC 120
CTTGTGGAGA CTAGATGAGG TAGATGTGGC TGCTGGCTGC TGGCTGGGTT GAACATGTTG 180
CCCAGAGGAA AGGGAAGCTT TGTGTTGGGA CAGAGTGACT AACCCACTTT CAGGCAGACG 240
GCAGGGCAGG CTCTAACTGG CTGAAGCTTC CGGGAGCCTC CCCGGCTGTG GGTGAAGGCA 300
GCGTGTCTGG TGAAGGCAGG CTAGGGATGT AATGGGACAG GCGAACCATC TTATCCAAAG 360
GGATGACCAC AGGAAGAGCC AGGACGGAGG CCAAGGGCAT GCACCTGAGG CCAGGTCTGA 420
GCGGGTGGAC TGGGGGTATT GGAGCTAGAG AGGCCCACTC AGGCCCTGGA GAAAAGGGCA 480
GGGGCTTTTC TAGGATGCTC TTGGCCTTGC CTGGGGGCAG AGGTGAGGAA GACAGTCAAC 540
GCAGGGAGCT CTGTGTCAGA AATACGTCTG CCTTCAAAGA AAGCAGCCAT CCTGGAGGAG 600
AAGGCACCTG GGAGGGCCTT AGGGATAGGG GAAAGAGAGA AAGGCACTGG CCAACCAACA 660
CCATTGGCCA GCCAGACAGC CGGGCTGGGT GACACCTGGA GATAGCCCCC AGCCATGCAC 720
AGGGACCAGT GGGCGTGGGA GAACCAGTAT CTGTTTAGTT ACAAGCAGAA CATCCAACAC 780
ACTCGCCTTG CCACGCTGAT ACTGTCATCC CCCAGAAGGC GGAAAAAACC ATTGCTGTGA 840
AGCATTCGAG CCAGTAATGA CCAACAGAGA CCAATAGGCT GGCCAAGTGG AAATAGAAAC 900
TCAGGGGGAG TGCCCATGTC CCCTAGGTAC CCCGGAAGGT GGTCCTGGGT GATGGTCACG 960
TGCACAGACT CTGGTCAAAT GGAGCTAAGG GTCGATGCCA ACTCCACCCT TAACACCCTC 1020
GGTGACCCCA GGCAAGTATC TGGGACTCTG CTGACCCGGT CTGTAGAGTG AGGATAATAA 1080
CAGCATGTAC TTCCCAGGGC TGCTAGGGGG ATTAAGTAAG GTAAAGTATG CAAACAGCTT 1140
TTCCCCATGC CTGACATGCA GAAAGCATTC AGTACATATG AGCAATTATA ATCATTTTCC 1200
CAGCCAAGGA GAGAACGTTC GAACACTGTC TGGCATGTGA CTTGGATTTT CAGAATACAA 1260
AATTCCAACA CTCAGAGAAG AAATAAGCTT GGAAGGGAAA ATTACATTAG AGGGTGGGGA 1320
AGTGTTCAAA TATGTCATTC TGACTGTGCT GTTTAGACAA CAAACAGTAG GCAGGAAGTG 1380
GTTAAACCGA AAGGGGGAGC AGAGGGTGAC TCAGGGACAG AATGTGGGCA TTGACAGTGG 1440
AGGGGTGGCT ATTTTCCAGG TAGTATCTCA CCTATGTGCT GTTCGGAAGG TCAAAACGAC 1500
CCTAAGACCC CGCCAGCCCT ACAGGGCAGT TCCTCTCATA GAGAGACCAG ATCATACAGA 1560
GGTGGCTCAG AGAGAGAGAC AGAGGGAAGC CCTTGCTAAA ATGCCCATAT GTTGCAAGTA 1620
TCTCATCAGA AGAGGCCAAA TGACTTCAGT TCCCGCATTC ACACGTACCT TTGCACTGCA 1680
AATTCAGAAC AACCGTAGGT AGAGCTCTAC CCAGACGGGG ACAACTCCAC ACTTCAAGTA 1740
TGACCTCTGA GCAACTGCAG AGGTTGTGAT GATTCTTGGC TACTTTGCAG TTAATAACTT 1800
TGGTCAAAGA 1810
|
