| Tag | Content |
|---|
EnhancerAtlas ID | HS076-00958 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:20799410-20800520 |
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 | AGCAGCGCCT CCCCAAGGAC TGCTCCAAAG GTCAGACTTG AGGATGGAGC CCCAGGAGGC 60
TCAGGGAAAG AATCTGCTAT TTATTGAGCA CCTACTAGGT GCTGGGTAAT AGGTCATTTT 120
ACCACCTTTC CAGCACTCCT CTGAGGCCTT GATTCGTGGC CCCATTTCAC AGATGAGGGT 180
CAGAGAAGTA AAGGAATCGT GCGCTGAGCA TTCAGGTTAA CGTAGCCATC AGAGAGACCA 240
GGCTGAATCA CTGGTCTGCA GCTTCCCCGT TGGTGCCCTT GAACGAAATT ACCGCTTCTC 300
TAGACCTCAA TGGGGTAACA ACAGTGCTGC TGCTTCTGCG GGCTACTATG GGGCTTCACC 360
GAGATGGGGA CTCAGAGCAT GACGCATGCG CATTCGGACC ACGCAGCAGC TGCAACGATA 420
GACCACGCCC ACCTCTCCCA TGTGCCCTGC AGAGTCCCAC TTTCCTGAGG TCAAGACCAG 480
GACTGAGTTA AATCTGAAAT CTCTCCGCAT TCATCCAGGG AGTCGACCAG TCCAGTCCGA 540
GGCGCTAGTC ACGTTGTTGT GCCGTCTTAA CTCCCCAGTT TGGTCGCTTC AAAATGCTAA 600
TGCTTTCCAC CTCAGCTAGG ATTGCAGGGA AACCCAGGGC CCGCCCACCC CCCGCCCTCT 660
GACCATCTCA GAAATGCCCA GACACACATC AGCTTCTCTC TGCCAGTGAT AGGAACACAG 720
CCAGGTTCCA GTGGACCAAA GAAACTCTCC AGGAGCTTTC CCAAGACCTC CTCCCGAAAG 780
CAAGGGGAGA CGGCCCTGCT GCATGACTCC AGTCAAGACC CTCAAACTTT CTGTGCCCCA 840
GTTTCTTCAC AACTCCAGGA GATTGGTGGT CCCACTGAAG TCCATGGAGG GTTTATTTAT 900
TTCCTTCTTG ACAAATATTT ATTTAGACAC TGTTCTAGAG AGAGTAGCAG ACAAGGCATT 960
GCCCTCAGGA AGCTTCTGGC CTTTTGTGCC TGTTTCCCTG CCTGTTAAAT GGAGATTATA 1020
ATAGTGCCTA CCTCATACAG TTGTTGTGAA GATTAAATAA ATTAACATGT ATAAGAGCTT 1080
AGTGCAGCGC TGGGCGTGGT GGCTCACACC 1110
|
