| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00454 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:20799190-20800590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr1:20799830-20799844 | GACCACGCCCACCT | + | 6.87 | | Klf12 | MA0742.1 | chr1:20799830-20799845 | GACCACGCCCACCTC | + | 6.65 | | SP1 | MA0079.4 | chr1:20799828-20799843 | TAGACCACGCCCACC | + | 7 | | SP3 | MA0746.2 | chr1:20799830-20799843 | GACCACGCCCACC | + | 6.48 | | SP4 | MA0685.1 | chr1:20799828-20799845 | TAGACCACGCCCACCTC | + | 6.71 | | SP8 | MA0747.1 | chr1:20799831-20799843 | ACCACGCCCACC | + | 6.32 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_05163 | chr1:20797832-20802020 | Brain_Cingulate_Gyrus | | SE_06168 | chr1:20798872-20800261 | Brain_Hippocampus_Middle | | SE_06941 | chr1:20798775-20800441 | Brain_Hippocampus_Middle_150 | | SE_27987 | chr1:20799763-20800544 | Fetal_Intestine | | SE_28809 | chr1:20799528-20814863 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I020472 | chr1 | 20799241 | 20800347 |
|
Enhancer Sequence | TCCCCAGAAA AACAGCATCC CCGGGCACAC CTGTGGGTGA CAGGGCAGCA TGGCCCACTG 60
TAGAGCCTAA GGGTGGGGCA GCATAACGGG AAGGGGCCCA CCGAGACAGT CAGGACCCTG 120
CTTCATAGAG CAGGGCAGAG CAGTCATTAG AGACCTTCCC CTTCCTTCTG CGCCCCTGAT 180
ATTAGAGGAA GGCTCCCCCT TCCTCTAATA TCAACTCCAC AGCAGCGCCT CCCCAAGGAC 240
TGCTCCAAAG GTCAGACTTG AGGATGGAGC CCCAGGAGGC TCAGGGAAAG AATCTGCTAT 300
TTATTGAGCA CCTACTAGGT GCTGGGTAAT AGGTCATTTT ACCACCTTTC CAGCACTCCT 360
CTGAGGCCTT GATTCGTGGC CCCATTTCAC AGATGAGGGT CAGAGAAGTA AAGGAATCGT 420
GCGCTGAGCA TTCAGGTTAA CGTAGCCATC AGAGAGACCA GGCTGAATCA CTGGTCTGCA 480
GCTTCCCCGT TGGTGCCCTT GAACGAAATT ACCGCTTCTC TAGACCTCAA TGGGGTAACA 540
ACAGTGCTGC TGCTTCTGCG GGCTACTATG GGGCTTCACC GAGATGGGGA CTCAGAGCAT 600
GACGCATGCG CATTCGGACC ACGCAGCAGC TGCAACGATA GACCACGCCC ACCTCTCCCA 660
TGTGCCCTGC AGAGTCCCAC TTTCCTGAGG TCAAGACCAG GACTGAGTTA AATCTGAAAT 720
CTCTCCGCAT TCATCCAGGG AGTCGACCAG TCCAGTCCGA GGCGCTAGTC ACGTTGTTGT 780
GCCGTCTTAA CTCCCCAGTT TGGTCGCTTC AAAATGCTAA TGCTTTCCAC CTCAGCTAGG 840
ATTGCAGGGA AACCCAGGGC CCGCCCACCC CCCGCCCTCT GACCATCTCA GAAATGCCCA 900
GACACACATC AGCTTCTCTC TGCCAGTGAT AGGAACACAG CCAGGTTCCA GTGGACCAAA 960
GAAACTCTCC AGGAGCTTTC CCAAGACCTC CTCCCGAAAG CAAGGGGAGA CGGCCCTGCT 1020
GCATGACTCC AGTCAAGACC CTCAAACTTT CTGTGCCCCA GTTTCTTCAC AACTCCAGGA 1080
GATTGGTGGT CCCACTGAAG TCCATGGAGG GTTTATTTAT TTCCTTCTTG ACAAATATTT 1140
ATTTAGACAC TGTTCTAGAG AGAGTAGCAG ACAAGGCATT GCCCTCAGGA AGCTTCTGGC 1200
CTTTTGTGCC TGTTTCCCTG CCTGTTAAAT GGAGATTATA ATAGTGCCTA CCTCATACAG 1260
TTGTTGTGAA GATTAAATAA ATTAACATGT ATAAGAGCTT AGTGCAGCGC TGGGCGTGGT 1320
GGCTCACACC TGTGCTCAGC ACTTGTGAGA GGTCATGCCA AGAGGACTGA TTGAGTCCAG 1380
GAGTTGGAGA CCAGGCTGGG 1400
|
