| Tag | Content |
|---|
EnhancerAtlas ID | HS173-02414 |
Organism | Homo sapiens |
Tissue/cell | SH-SY5Y |
Coordinate | chr10:125971540-125973890 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr10:125971651-125971662 | TACTTCCTGGT | - | 6.02 | | INSM1 | MA0155.1 | chr10:125971937-125971949 | TGTAAGGGGGCA | + | 6.27 | | MEF2C | MA0497.1 | chr10:125973639-125973654 | AAATTAAAAATAGAA | + | 6.12 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09796 | chr10:125972568-125981551 | CD14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I124284 | chr10 | 125973498 | 125975690 |
|
Enhancer Sequence | GATAAGGAAA CTGAGTCATA GAGAGGGGCC AAGTACTTGC CCAAGGAACT CAGCAAGCCA 60
GGATTGTGCC CCCAGCAGTC AGAGCCTGTG AACTTAACAC CTGGGCTCTG GTACTTCCTG 120
GTGCCCTTAG AGATGAGCCA AGGAGGCTCA GAAAGAGATT GGCTGCCCGA CTTCTCCCAA 180
CTAGCCAGTG ACCACGCTGG ACCTGGGACC TGCGTTCCCT TCTAGATGAA GATCTGGGGA 240
GTACAAAGGA AGAATGAGGG GTACAAGGTC ATCAGCAACA CAGACCTGGC AAAGAACCTA 300
GTGTCCCATT TGTGAAGCCT CATAACAGCC CCATCAGAGG AAGCTGAAAA CTCAAAAGGC 360
ACCAGGTAAA CTCTAAGCCA GTACACCTTG GCTCATGTGT AAGGGGGCAA TTTGCAGAGG 420
CAAGGTCCTA TCACCAATGG GCTAACCTGC AGGGAGGCAG AGGATGTGAG AAGCTGCCTG 480
GACCCCTCCT TGCTCCATCT CGTCTTTGCG CAGATGGGGA AGCTGAGCCC CAGAGCATCC 540
AATGTCACAC AGCTGGTTAG GACATGGCCC ACTCTCTCCT GTCACCTAAT AAGGACGGCT 600
GAGGCAGGGC CTGAGGTGGA TGCGCTTGTC TGACTGCCCA GGGCTCTGGT CCCTGCTCAA 660
CCTTTAAATG GTTGCAGGGC CTCAGGACAC CCCCTCTCTC CTCCCCACCC TTCATTTCTC 720
CATTTGTAAA ATTATTCAGG TTAAACTAAA TATTATTGCA ACCTTCAGCC TCAGCACCCA 780
CGATTCCCTT TCAGTCTAAA AGGTTGCTGG CTCTGGACCC AATTAGGATA AATCAATTTC 840
AGACAGTGCC CATCTCCCTC GGGCTCCACT CTCCCCATCC CGCTCCCATT TGCCTGTCAG 900
CCTCCAGAGT AACCACTTAC TGAATTACCA AGAAGGCCAT CAGATCAAGA GCGGAGGAAA 960
TGGCAGAAAC CAATCTTAAC AAAATGTATT TGATCTGCAA ATAAGACGCC ATCCCCTTCC 1020
CGCCGCAGAG TTTATCATTT TTTATTTAAG CCCAGTGCAG CCGAGCATAT GGACAGCAGC 1080
TTGCTTCTGT CTTCGAGAGA GAATAACAGG GCCCAGACAC AGGCCGACCC CAGGACAATG 1140
GAGCACCCTC TACTCACTGT GATGGGGGCG CAGGCATAGG AGCCCCTTCT GCTCTCCTTC 1200
CTGCAGGACT TCCGTGATGT CTGAAAACTC TCTGTGGGAG TGAGACTTTG TGAAAATTAC 1260
ACTGAAGTCA TAGTAACGAC AGGAGCAGCT CCCAAGTCTT GCACACTCAT TATGTGCCCA 1320
AGGCAGTGCT AAGCATGTCA CATGCTATCG CATTTAATCT CTGGGCCATG GATGCCGTGG 1380
CTCTCTCCAT TGCACAGGTT AACAAACTGA GGCTCAAAAG GATAAGTACC TTGCCAAGGC 1440
CACCTAGCAG CCAATCAACA ACAGAACCAG GATTTAAATC TGATCTGACT GTGTGTCCTG 1500
TGCTCCCAAC CTCCCCGCCA CCTGTCTCGC GAAAGATTGA TGGAGTTAAG AGTCTTTGGG 1560
CTCAGACACA GATCTTCTAG AAGGCCCCTA TGAAAACTGA AACAATGCAT TTTCAAAACA 1620
ATCAGGGAGA TTTGATTATG GACTAGATAT TAGTGATACC AAAGAAACAC TTAGGCTGAT 1680
AGTGATGCTG GCGTGTAAGG AGATATCCAG GGTTTTAGAA ATGCTCATTG GATTCTGCGG 1740
CAATGAGACC TTGTGTCTGG GGCTTGCTAT GAAATCATTC AGGAGACAGA GAAAGGAAAT 1800
AGGGCAAAAA TCTTACTAAC TGTTGAATCT GGGTGGCGGC TCTATCTCTA CTTTTGAGTG 1860
TATTGAAAAT ATTCATAATT ATATCTTTTA AAACACACGC AAAACAAGAC TAGCCATTTA 1920
GGAAATGCAA ACCAAAACCA CATGAGATAC TACCTCACGC CCATCATTAT AGCTACTATC 1980
AAAAACCAGA AAATAACAAG CGTTGGCAAG GATGTGGAGG AATTAGAACC CTTGTCCACT 2040
GCTGGTGGGA ATGTAAAGCG GCGTGGCCAC TATGGAAAAC AGTACGGCAG TGCCTCCAAA 2100
AATTAAAAAT AGAACTACCA TATGATCCAG CAATTCCACT TCTAGGTACA CACCCAAGAA 2160
TTGAAAGCAG GGTCTAGAAG AGCTACTTGT CCACCCATGT TCATAGCAGC ACTATTCACA 2220
ATAGCCAAAA GGAGGGAGCA ACCCACATGT TCGCCCGCAG ATGAACAGAT AAACAAAAGG 2280
TGGCATATCC AAACAATACA ATATTATTCT GCCCTAAAAA GGAAGAAAGC ACCAGGCACA 2340
GTGGCTCACG 2350
|
