| Tag | Content |
|---|
EnhancerAtlas ID | HS106-00637 |
Organism | Homo sapiens |
Tissue/cell | iPSC |
Coordinate | chr13:101162140-101163470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Lhx3 | MA0135.1 | chr13:101162377-101162390 | AAATTAATTTTTC | + | 6.11 | | PHOX2A | MA0713.1 | chr13:101162752-101162763 | TAATCTAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr13:101162752-101162763 | TAATCTAATTA | + | 6.14 | | Phox2b | MA0681.1 | chr13:101162752-101162763 | TAATCTAATTA | + | 6.32 | | TEAD1 | MA0090.2 | chr13:101162265-101162275 | CACATTCCAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_63392 | chr13:101157984-101186963 | NCI-H69 |
|
| | 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 |
| GH13I100508 | chr13 | 101160878 | 101163962 |
|
Enhancer Sequence | GGGAAAGAAT TTGTTTTTGC CCTGTGGATG GGTCAGAAAC ATCTGCTTCA GGTATAGTTT 60
ACAAGCGTTA TTTATTAACC CATGAGCCGA AAACCCAGAT GAGGAGCTCT GACTATTGAA 120
AACTACACAT TCCATGTTTT TATAAATGTA TATTAAGATG AATTCCACAT ACCTATTATT 180
TGGATTTCTG GCAGCCGGAA CTTCTACAAG GAATTTGTGT TTTTAAAAAG GAATGTAAAA 240
TTAATTTTTC TTGTATCAGA GTTTTGCTGT ATATGAAGAA ATCCTGCTCA TGGGCAGAAA 300
GCAAAGGTTT CAAAGGAACC TCATCTCCAT ATGGTTTTAC TCGATAATCC TTTATCCACC 360
ATCTTCAGCT CTCATTCCTT TGCTTTCTCG CCTGTGGCTA CATTTCTATC TCTGCATCAA 420
TTAGCACAGT GATTTATACA ACAAGCAAGC AGTTTAGAGG TAATGGTACA CAATTAACAT 480
CTCATTCCAC CATAAAGGGT ATGCTAAATA CCCCAGTCAT TGCTTTCTCT GCCTGGAATT 540
GAAATAAGTG TTTGTCCTAA TTCATATGCT ATCTGATGTG AAGTGGGCCT GCTTTGTACC 600
GCACTACACC ATTAATCTAA TTATAGATAG CTGCAAATGA AGTGCTGTCT GAGCTGGGAG 660
ATTGAAGAAA ATAGCCTTTT GTCATTTAGC ATGACTCTGT GAAGCAAGAT CACACTTTAC 720
AGGGCAATAC TACAAAATGG AAATCTCAAT AATATTGCTG CCTGTTGCAT CTTTTCTAAT 780
TACAACAATA TTGTAAACAC AACTGGGCGC TGATATAAAT AGAGCTGTAG ATATGCTGTC 840
ATGTGGGTTG TAGGAGAAAG TCCTCCGAGT GCTGTTGGAT TAAATGATGC ATCCTGATTG 900
ACAGCTACCT TGAGACTGCA CTGATGGAGT TGTCACAGCA TTATGCTAAC AGGCTGCTCC 960
AGCGACTGCA GCTGTAGGAG GCTGTGGTTC GCCCTGCGCC TTAGCTGCTG CCTGTCCATG 1020
TCCGCTCCTT TGCCTGGGCT GCACCTCCAA AGGAAGGACG GCCGTAGGCT TCAATTCTGT 1080
GTATTGTCAC TGTTGTGTCT TGGAGATTTG TGGTGGTGGT GGTGTAGCTC AGATATCAGG 1140
CGATTGGGCC CTGTGCAGAA GTAGAGGGAA ATTATTTTGT ATGGCTCCTA ACCTTGCTCT 1200
GCTTTTCCTC AAGTGATAAT TGTGTACCCT ACAAAGAATT TAGGAGAGTA GAACGTGGTT 1260
GAATTTCAAG TCTCATTCCA CTGAACTGTT TTAACTCATA TCTAGTTTTT CTCTGCTTTT 1320
CAGCCACGCC 1330
|
