| Tag | Content |
|---|
EnhancerAtlas ID | HS047-13279 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr16:70801320-70802740 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr16:70801354-70801367 | TTCTAGAACTTTC | + | 7.04 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26579 | chr16:70801754-70802858 | Esophagus | | SE_36921 | chr16:70799896-70804127 | HSMMtube | | SE_44141 | chr16:70801057-70803447 | NHDF-Ad | | SE_46350 | chr16:70801725-70802876 | Osteoblasts |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I070767 | chr16 | 70801362 | 70802754 |
|
Enhancer Sequence | AATCAGCAGA GGCTACAAGC TGGGAAATAC TGATTTCTAG AACTTTCTGC CTGCTTATTT 60
ACAGGGCAGC TAGCTACACC AGGAGAGCTG GTGTCACTGA AGACATCATG ACCCTTGGCA 120
ACAGCCTGAG CCTCATAGTG GGGACTTCAT ACAACACCTG TTTGAGAACT CCTAAATCAA 180
ATGAGTTAGG GAGGCCAACT GCAAAAGTGG AACTCTCCAA CTGCAACTAA TAAAGTTAAA 240
TGCACGGGCT CTGGAGTCAG ACAGATCTAG CTTGAATTCC AGCTTGGCTA CTAATTAGTT 300
GAGTGACTCT GGGCAAGAAG TTAACCTCTC TGGGTCTGTT TCCTCATTTG TAAGATGGGG 360
ATAATAACAA GGTTCTTGTA ATAACAATTG TAGCTAAAGT GTGTAAAGTG CTTTCTGCGG 420
CCCAGGCACC ATGCTATGTT CTTTACATAC TTAAAAAGCT TTTAAAAATT ATTATTATTA 480
TTATTGAGAC AGGGTCTTGC TCTGTCACCC AGGCTGGAGT GCAGTGGTAC AATCATGACT 540
CACTGCACCC TCAAGCTCCG GGGCTCAACT GATCCTTCCA ACTCAGCCTC CTAAGCAGTG 600
GGAACTACAG GAATGTGCCA CCACACCCAG CTCATTTTTG TATGTTTTGT AGAAACAGGT 660
TTTCACCATG TTGCCCTGGA CTGGTCTCTA ACTCCTGGGC TCAAGCAACC AGCCTGCCTT 720
GGCCTCCCAA AGTGCTGGGA CTACAGGCGT GAGCCACTGT GCCTGGCTGT TCTTTACATA 780
CTTTAACTCA CTGAAGCCCC ATATCCCTTT GAGGTCAGTA CTATCATTAT ACTGAGTTTA 840
AAGATGAGGA AACTGAGGCG GGGGAAATCA CGCTACTTGA CCAAGGCCAC AGCCAGGCAT 900
GCTGGAGTTA GGGCATGAAT CCAGGCAGTT GGCTCCACCA GGCAGAGCAG TCACGAGAGA 960
GAACACACCC AGTGGAGACA TTTCTCTCTT AACCCTTTCC TCAGCTGGCA AGCATGCTTC 1020
CTCCAACCGG GTTCCTTCAC GTTCCACCTC TCCCTGGGGA GTCCAATTTT CCACCTCCCA 1080
TGTATTTCCC ATGCTCTGGA GGGTGGAGGA ACCCAGACCT ACAGCCACCT CACCACCTGC 1140
TGCTTTTCCA GGTGGCATTC TTCCATGGCT AAGCCTGGGG CCACCAGGGG CTTCCCGAGT 1200
ATCGCAGGAA GAGGGGAGAT GAGGGAGGGG GAAGACAGCT TCTGCTCTCA GGTTTAGTCA 1260
GTTAATTCTC CCTGTGTTTC GGTCCAAGTG AGAAATCTTT CATAAAAAAT CTGGGATGCA 1320
AGGATTGCTT CCATGGTGAT CCTTGAACCC CTGAAAGTGA ATTCAGAATT TCATGTGGAT 1380
GTGCATTTTT TTGGTGTGTG TGTGACAGAG TCTCGCTCTG 1420
|
