| Tag | Content |
|---|
EnhancerAtlas ID | HS007-00198 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:20799440-20800620 |
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 | GTCAGACTTG AGGATGGAGC CCCAGGAGGC TCAGGGAAAG AATCTGCTAT TTATTGAGCA 60
CCTACTAGGT GCTGGGTAAT AGGTCATTTT ACCACCTTTC CAGCACTCCT CTGAGGCCTT 120
GATTCGTGGC CCCATTTCAC AGATGAGGGT CAGAGAAGTA AAGGAATCGT GCGCTGAGCA 180
TTCAGGTTAA CGTAGCCATC AGAGAGACCA GGCTGAATCA CTGGTCTGCA GCTTCCCCGT 240
TGGTGCCCTT GAACGAAATT ACCGCTTCTC TAGACCTCAA TGGGGTAACA ACAGTGCTGC 300
TGCTTCTGCG GGCTACTATG GGGCTTCACC GAGATGGGGA CTCAGAGCAT GACGCATGCG 360
CATTCGGACC ACGCAGCAGC TGCAACGATA GACCACGCCC ACCTCTCCCA TGTGCCCTGC 420
AGAGTCCCAC TTTCCTGAGG TCAAGACCAG GACTGAGTTA AATCTGAAAT CTCTCCGCAT 480
TCATCCAGGG AGTCGACCAG TCCAGTCCGA GGCGCTAGTC ACGTTGTTGT GCCGTCTTAA 540
CTCCCCAGTT TGGTCGCTTC AAAATGCTAA TGCTTTCCAC CTCAGCTAGG ATTGCAGGGA 600
AACCCAGGGC CCGCCCACCC CCCGCCCTCT GACCATCTCA GAAATGCCCA GACACACATC 660
AGCTTCTCTC TGCCAGTGAT AGGAACACAG CCAGGTTCCA GTGGACCAAA GAAACTCTCC 720
AGGAGCTTTC CCAAGACCTC CTCCCGAAAG CAAGGGGAGA CGGCCCTGCT GCATGACTCC 780
AGTCAAGACC CTCAAACTTT CTGTGCCCCA GTTTCTTCAC AACTCCAGGA GATTGGTGGT 840
CCCACTGAAG TCCATGGAGG GTTTATTTAT TTCCTTCTTG ACAAATATTT ATTTAGACAC 900
TGTTCTAGAG AGAGTAGCAG ACAAGGCATT GCCCTCAGGA AGCTTCTGGC CTTTTGTGCC 960
TGTTTCCCTG CCTGTTAAAT GGAGATTATA ATAGTGCCTA CCTCATACAG TTGTTGTGAA 1020
GATTAAATAA ATTAACATGT ATAAGAGCTT AGTGCAGCGC TGGGCGTGGT GGCTCACACC 1080
TGTGCTCAGC ACTTGTGAGA GGTCATGCCA AGAGGACTGA TTGAGTCCAG GAGTTGGAGA 1140
CCAGGCTGGG CAACATAGTG AGACCCCCAT CTCTACATAA 1180
|
