| Tag | Content |
|---|
EnhancerAtlas ID | HS043-26577 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr21:43035680-43037150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr21:43036810-43036822 | GGCCACGTGCCT | + | 6.07 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_26552 | chr21:43032059-43037134 | Esophagus | | SE_36171 | chr21:43034932-43037302 | HMEC | | SE_37820 | chr21:43031929-43037606 | HSMMtube | | SE_45994 | chr21:43032241-43037876 | Osteoblasts | | SE_55708 | chr21:43032447-43038379 | u87 | | SE_67529 | chr21:43032447-43038379 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I041611 | chr21 | 43031961 | 43037514 |
|
Enhancer Sequence | GCACAATATC ATTTTGCACA TGTGCAAACA GAGCTGGAGG GCAGATTCCC AGAAGCATAA 60
GCGTCTGGTC AAAAGGTGGA TATGCATTCA TAGCTTTGCT GGAAATTGCC ACTTTGCCTC 120
CAATTTGTAC TCTGCCAGCA ATATGTGAAA GTATCTGTTT CCCCACTGCC TGCCTAAGGG 180
AGTGTATGTC TCACTTTTGT GTTGTTGCCA ATCCAGAAGA AGCATATTGC GTAGACTTTC 240
ATTTGAGACT CCATCTTTCT GTGTGGTTTG GCAGAAGACT GGGGGAACAT TCTTATACTG 300
GCTCTAAATG GAATGCAAGG ATACTGCATT AACTTATGAC TCAGTAAAGT AATTTATTTT 360
GGGGAGCTAA AATAATCAGT TTGCTGCTTT CTCATGATTT TTAACTTGAA GCAACATGAA 420
ACTGGGAAAA TAAAAATGGA TAGCAAGACT TTTAGACAAT GTCTGTTCAG TGATGTTTCA 480
AACATATTTT TGGCAGGAAC TAGAAATCAG TCCATGTAGC CCAAGAATGA TGCCAATTCC 540
ATATTCTGTG TTGCTGATTA TAAAGGAAGC AAAATGTTCC AGTAAGCAGA TGCAAAAGCA 600
GCCATCAGCT CTCAGATACA GGAGCAGATG AGCTGGAGAC GTCCTCACGC GAGCACCGGC 660
CGCTCTTCCC CATGCTGTGG GCAGCTTGCC TGTGGGAAAG GCCAAAGATT CCTTAAAAAG 720
AGATTCAAAT CTGCTCAAGT GCCAGGATAA GCATTTAATC AGGAGCCCAG CATCCTGCTC 780
CCCAATGAGT GGGGAAGATT TTCTAGGCCT GGAAAGTTTT TAAGAGGTAA TGTGCTATTC 840
TTAGTCATAA CAAATGAAAG ACAACCCACA TGTCCAGCCA GGCAGGATGG CCAATGGGCT 900
GTTCAGTTGC CAGCTGCCTT CCCAGCCCTC CGGGACAGAG TCTCCTGTGA TTCTGGCAGC 960
ATCCCCAGGA CAGAGCCCTC AGGACCAAGG TAGAAAGCGC TTGGGCAGGG CAGTGGTCTC 1020
CCAGTCAGCA GGCAGACCTC CTGGGACCAC GGGGTCAGAT GTGGGGCCTG AATGACTCCT 1080
GAGTCACAGC CCTGTCCCCT CTGACATCTC CCACTCCAAT GCCATGGTCT GGCCACGTGC 1140
CTTGGCTTCC CTTCCTACAC TTCAGTGGTC TAAGAGGATA ATTCCAAGAG CCCCTAATCT 1200
AGCTCTGGTC TGCCCCTCGT CTGAAGACTA GATTCCTCCA CTCACTGCCT AATACACCTG 1260
GGCTCCATCC TGTGAATGAA GTAAGTTGTT CAGAGCTACA GTCAAAGCTG CGAGCGGGAA 1320
TTCTCACAGC TCCTGGGATC TCTCACCAGT TCCAACAAAC TTCCCACCTC TCCAAGTCAG 1380
ACTAAGCCTG AGATGTGTAA CCTTCAGCTT AGTCTGCCTT AAACCAGCAT TTCCCAAGCT 1440
TACATTTAGA GATCCTCTTT TTAAAAAAAT 1470
|
