| Tag | Content |
|---|
EnhancerAtlas ID | HS042-05028 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr10:29758330-29759200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EHF | MA0598.2 | chr10:29758680-29758692 | AACCCGGAAGTG | + | 6.74 | | ELF1 | MA0473.2 | chr10:29758680-29758692 | AACCCGGAAGTG | + | 7.22 | | ELF3 | MA0640.1 | chr10:29758680-29758693 | AACCCGGAAGTGC | + | 6.39 | | ELF4 | MA0641.1 | chr10:29758680-29758692 | AACCCGGAAGTG | + | 7.22 | | ELF5 | MA0136.2 | chr10:29758681-29758692 | ACCCGGAAGTG | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_54688 | chr10:29757749-29763499 | Stomach_Smooth_Muscle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I029469 | chr10 | 29758574 | 29762281 |
|
Enhancer Sequence | TGGGGTTCAC CAAATCAAAC TCTGGGGACA TGTGACCCTA GGAAGCTCTT CACTTTTCCT 60
CACTGAGGTC CTCACAGGTC TCAGTTGCCT CCTGAATGCC TGGGCGACAC TGGGCTTCTC 120
TGGCAGCTTG CAATGCTTAT TTTGCCTGGG CTGCTAGGAA GTGCAGAGCC ACAGAGGCAG 180
ACCACCTTAC CGGGGGGGCC GGCCACCACA GCGTCCTCCC TGGGCTGTGG CCTTCACTGC 240
CCTTCCGGTT CCCCTCTTCC CCAAGGTCCC CACTCAGTGC TATCTCACAG TGTGCTGAGT 300
CTTTGCAAGT GGCCAACGGC AGGTGCCTGC CTGGGAGGGG AACAAAACCC AACCCGGAAG 360
TGCTGTACCC GGGAAGTGCC CGGAGAGTCC GATCCCTCTC CATCGGGGGC TGCTCTCCAG 420
AATGGGGGAT ATCTTATCGT CTGACACAGA TGGCGGTTTC CCACACTCTT CTTTAGCTTT 480
TTAACACTCT GCTGTTCTGG CAAACGAAAA CTCCACAAAT TTGAAATGTG CTCCCTTTAA 540
ATATCAAAGG CCCCCAGGCT TCTCATCCAA AAGCTGAACG GCAACTATGA AGAAAGAACC 600
CAGAGTGCTT CCAAGAGTCA CTCCCTGGCT CCTCACCAGC CTCTCACCCA GCCAGATAAA 660
TCCTCAGAGC GGCCCCCAAG TCGGAGGTCT GGACTGAGAT GTGTGTCCTC TCTGCTCGGA 720
ATGTCAGAGG CCCCTGACCA CGTTCCCAGC CATCCTTTGC TGCAGTCACT TTCAGCACCC 780
TGGGATCTGC TGGGAGTCTT GGTACCCCTG AGCCTGCCCC GTCCCTCTGG GAAGCCCGGT 840
GTGTGGGGGG ACTCGCCGCA GACACAACAC 870
|
