| Tag | Content |
|---|
EnhancerAtlas ID | HS117-04141 |
Organism | Homo sapiens |
Tissue/cell | LHCN-M2 |
Coordinate | chr2:235913630-235915020 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr2:235914665-235914676 | CTGCAGCTGTC | - | 6.62 | | Tcf12 | MA0521.1 | chr2:235914665-235914676 | CTGCAGCTGTC | - | 6.14 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_05140 | chr2:235913446-235915518 | Brain_Cingulate_Gyrus | | SE_05986 | chr2:235912983-235917339 | Brain_Hippocampus_Middle | | SE_29217 | chr2:235906866-235919843 | Fetal_Intestine_Large | | SE_31459 | chr2:235913090-235921057 | Gastric | | SE_38006 | chr2:235913397-235915616 | HUVEC | | SE_41684 | chr2:235913476-235915044 | LNCaP | | SE_47485 | chr2:235913482-235917291 | Pancreas | | SE_65336 | chr2:235913309-235920314 | Pancreatic_islets | | SE_69100 | chr2:235913434-235917126 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I234998 | chr2 | 235906788 | 235921345 |
|
Enhancer Sequence | TGTTGAACTC ACTGTTGGCA TGGACCAGCA AGGGTCGCTG TCACATAAAG GCCTGTGTTA 60
GGTGCCATCC GCCTGCAGAT CCCCCTGGGT GTTAACACAG GACTGCGAGG AAGCACTGCT 120
TGTGGAGAGC AGGATAGTCA ACAACAGACC TAGGCCAGGT GTTTGCCCAG GTGTCACACA 180
GGAGGCTTGC TGTGGAAAGG CAGCTTCCTG GGCATGCCCT GTGCTGGCCA TGTCTGTCTG 240
TCTGTCTGTC TGTCCCTCCC AGCCCTGCTG TGCTGTTGGC CCAGGGAGTG GTCTGAATTG 300
GCTGTACCCC AGGGGGCTCC CCTGACTTCT GGCTTGCGGT GGAGAGGGAG GTGTCAGGGG 360
AGCCCCTCGC CTGGGGCTCA CTCCGGCTCC CCTGACTGGG GGTCCCTGTC TCCCCCAGGT 420
TCCAGTGGAG GCTTCCCCCT TCCCCACTTC CCTGGCGTCA CTTCCCCCAG GGGTCCCTTC 480
ACTGTTGTAA ATTGTCCCTT TCCTGTTGGG GCCTTGAGTG ATGTCTCAGC CCTACTGAGT 540
GAAGATCTCC AAGGCAGGCC CAGAACCTGC ATTTTAACAA ATCTTCCCCT GACACCTTGA 600
GCCCCTCAGA GCTGCTGAAC CCCCGCCTCC GCCACCCTGC TTAGTTGTTG ATCTTGGCTT 660
CCTCGTGTCC AGGCTACAGG CTGACCTCTC TTGTGCTTCT GCCTTTCAGA GCTTCAAAGG 720
AAGCACATGT TTGCTGAACC CTCCCAGGGA TCCAGGCTTT GCAGGTTTCA CACACATCTT 780
ACAAAATGCA GTGGGGGCAG AACGAGAGGA GAGCCAGAGC ATGCTGGCTT TGGGAGGGGT 840
GGCCCATTGT AAACAAGCCA GCCCTGGCCG TCCCAGGGTC CCAGGCAGGC TGGCTTGGTT 900
GGGTCTACAC ACAGCCAAGC ACTCTTAGCT CCTGCAATTG GAATCCCGCT CTTGCGTGCC 960
CGCCTGTGTT CCTGGCTGTG GGAGGCGCCA GAGGGAGGTT TTGATCCCTG GGGGAGTAGG 1020
AAGCCGGCCC AGCCCCTGCA GCTGTCTGGC CCCAGCCACT AATCCTGGGC AGGAGCCGCC 1080
TGTCCTGGCA TGGTGCTGGG CTGGCTGGAG TGGAGTGACC TGAGAATGGG GCCTGCTTTG 1140
TACCCAGAGC ACACGCCGGC CACGGCTTTT ACGACCTAGC GAGCAGGACG GGAAAAGGCC 1200
AGCAGGTGGG AGATGGGAGT CAGCCTTGGT CTCCTTTGTC TTTGCGGGCT TTGTTCCGCG 1260
AGGATTTTTT CTTTCCTGCC CTTTTCCTTT GGGCTGAGCG TGAGTGTGTT CAGAAAATCT 1320
CAGAGCGGCC ACTTGCTGCC CCAGGGGGTA TCATACGCAT CATGGGTTTG GTCAAGAGTG 1380
GATCCATCAA 1390
|
