| Tag | Content |
|---|
EnhancerAtlas ID | HS138-20594 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr2:70172460-70174330 |
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 | ATAAAAGTAA AGGACATTCA GCTTCCAGTG GCCAAGGGTC CCACAGGCAG GGTCTCTGCA 60
GGAAGTATTG TTCAGGGCTC AGCCCAAACT GGGTGGCGAG GCAGCTCCCT GCCCACTCTG 120
TTCCATGCAG AATTCTGGAG TCATTGCCTC TGCGAGTGTC CTTGTGGAGA CTAGATGAGG 180
TAGATGTGGC TGCTGGCTGC TGGCTGGGTT GAACATGTTG CCCAGAGGAA AGGGAAGCTT 240
TGTGTTGGGA CAGAGTGACT AACCCACTTT CAGGCAGACG GCAGGGCAGG CTCTAACTGG 300
CTGAAGCTTC CGGGAGCCTC CCCGGCTGTG GGTGAAGGCA GCGTGTCTGG TGAAGGCAGG 360
CTAGGGATGT AATGGGACAG GCGAACCATC TTATCCAAAG GGATGACCAC AGGAAGAGCC 420
AGGACGGAGG CCAAGGGCAT GCACCTGAGG CCAGGTCTGA GCGGGTGGAC TGGGGGTATT 480
GGAGCTAGAG AGGCCCACTC AGGCCCTGGA GAAAAGGGCA GGGGCTTTTC TAGGATGCTC 540
TTGGCCTTGC CTGGGGGCAG AGGTGAGGAA GACAGTCAAC GCAGGGAGCT CTGTGTCAGA 600
AATACGTCTG CCTTCAAAGA AAGCAGCCAT CCTGGAGGAG AAGGCACCTG GGAGGGCCTT 660
AGGGATAGGG GAAAGAGAGA AAGGCACTGG CCAACCAACA CCATTGGCCA GCCAGACAGC 720
CGGGCTGGGT GACACCTGGA GATAGCCCCC AGCCATGCAC AGGGACCAGT GGGCGTGGGA 780
GAACCAGTAT CTGTTTAGTT ACAAGCAGAA CATCCAACAC ACTCGCCTTG CCACGCTGAT 840
ACTGTCATCC CCCAGAAGGC GGAAAAAACC ATTGCTGTGA AGCATTCGAG CCAGTAATGA 900
CCAACAGAGA CCAATAGGCT GGCCAAGTGG AAATAGAAAC TCAGGGGGAG TGCCCATGTC 960
CCCTAGGTAC CCCGGAAGGT GGTCCTGGGT GATGGTCACG TGCACAGACT CTGGTCAAAT 1020
GGAGCTAAGG GTCGATGCCA ACTCCACCCT TAACACCCTC GGTGACCCCA GGCAAGTATC 1080
TGGGACTCTG CTGACCCGGT CTGTAGAGTG AGGATAATAA CAGCATGTAC TTCCCAGGGC 1140
TGCTAGGGGG ATTAAGTAAG GTAAAGTATG CAAACAGCTT TTCCCCATGC CTGACATGCA 1200
GAAAGCATTC AGTACATATG AGCAATTATA ATCATTTTCC CAGCCAAGGA GAGAACGTTC 1260
GAACACTGTC TGGCATGTGA CTTGGATTTT CAGAATACAA AATTCCAACA CTCAGAGAAG 1320
AAATAAGCTT GGAAGGGAAA ATTACATTAG AGGGTGGGGA AGTGTTCAAA TATGTCATTC 1380
TGACTGTGCT GTTTAGACAA CAAACAGTAG GCAGGAAGTG GTTAAACCGA AAGGGGGAGC 1440
AGAGGGTGAC TCAGGGACAG AATGTGGGCA TTGACAGTGG AGGGGTGGCT ATTTTCCAGG 1500
TAGTATCTCA CCTATGTGCT GTTCGGAAGG TCAAAACGAC CCTAAGACCC CGCCAGCCCT 1560
ACAGGGCAGT TCCTCTCATA GAGAGACCAG ATCATACAGA GGTGGCTCAG AGAGAGAGAC 1620
AGAGGGAAGC CCTTGCTAAA ATGCCCATAT GTTGCAAGTA TCTCATCAGA AGAGGCCAAA 1680
TGACTTCAGT TCCCGCATTC ACACGTACCT TTGCACTGCA AATTCAGAAC AACCGTAGGT 1740
AGAGCTCTAC CCAGACGGGG ACAACTCCAC ACTTCAAGTA TGACCTCTGA GCAACTGCAG 1800
AGGTTGTGAT GATTCTTGGC TACTTTGCAG TTAATAACTT TGGTCAAAGA AGCTACCAGT 1860
CAATGCAGAC 1870
|
