| Tag | Content |
|---|
EnhancerAtlas ID | HS034-04717 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:3028190-3029610 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr11:3028494-3028508 | CTTCCAGGAAAGGG | + | 7.25 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_05033 | chr11:3028560-3032548 | Brain_Cingulate_Gyrus | | SE_06002 | chr11:3027566-3032629 | Brain_Hippocampus_Middle | | SE_27418 | chr11:3027685-3028401 | Esophagus | | SE_32090 | chr11:3027688-3028617 | Gastric |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I003006 | chr11 | 3027567 | 3032629 |
|
Enhancer Sequence | TGTAGGAGAA GCAGAGCAGT TCCCTCAGAC ATGGAGGAGC CAGGGCCCAC ACAACCAGTG 60
CCTCCTCCAG TGCTGGGGAA GGAGGGGCCG TGGCCCACAG AACAAGTGCC TCCTCCAGTG 120
CTCAGGAGGG AGGGGCCCCG GCCCACAGAA CGAGTACCTC CTCCAGTGCT TGGGAGGGAG 180
GGCCCAGCAG CTTGATTGGC TGCAGAAGCC CAGAGACTAG TGTCTCCCGT AAGCCCAGGG 240
GCTGTTCTGG GGGTGCAGGG CAGAGCCAGG AGGAAGCATA GCACACTGGC CGCCGGAAGC 300
AGTTCTTCCA GGAAAGGGAC ACAAGTTGGG CCGACAGCAG GGGTGGGAGG GTCAGGACAG 360
GCCTGGGGGT CCCTTCGGGT GCTAACACTC TTCATCTGAG GCAGCCTCTC TGTTGGTGCC 420
AGAATCAGCT TTCTTACAGA AGGACCATTT ACACTCAAGC CCCAAGGACT TGGTTCCCAA 480
ATGCACACGG GACTGCGATG GGGGTCCTGA CCGGCACCCA GGAGAGCTGA GTCCCAGGAC 540
CACCAAGGAG CTCGAGCTCT GTGAGAATCA GCCCTCCCAG GGCTGAAGCG CACGCAGCTG 600
TAAAGGCGGG GCTGAGCGGT GGGGGTGGAC CGCAGGTTGC TTCCCAAGAC TGTGCTCACC 660
TCTGCCTCTG ACTGGGGACC TGACCCAGCT GGGAGGGTGA AAGGAGGCAT GACAGGGAGG 720
GCGACTGTGA CCTCCATCAC ATGGGGAGGG AGCTTCGCTT GGAAACCCAT GTGTCTGTGG 780
CTGACTTCAG AGCGCAGCAG TGCAGACTTG CCCGGCATCC CACGGTTCTC CTAGTGGGCT 840
CCTCACGCAG TCTCTAGCAG GCGCCCCCTC TGTGTCTCTG CTCTGCCCGA GTTTTCCCGT 900
TCCCAGCCCA CGCACAACGC CCAGGTAGAG AACAGGACAT AAGAAGTTTT GGGTGTTACA 960
GGGTAAATGG GATGCCAACC TATCTCAGAA AGACTCCAGA GTATCAGGTG ATGTGACAGC 1020
ATCTCCTAGA CTACATCAAC AGGACAGATG CTTGCTGCTC TCCAAGTGAC AACTTTCTGC 1080
TCTGAAATCT GACCTTGGGT TTGCTGGAAT CACCACACCC TTTAGTTTTC TTCTGGCCCC 1140
TCAGCTTGCT GCGCCCAACT GTGCTAGGCG GGCAGGTGCC CTGCCCCCCA GCCTGCTGGG 1200
ACCCCCACCA TCCCACCCCA TCCTCCTGCC TGCCCTGCCT TTGGGCAGCA CTGACCATGC 1260
ACATGCTGCC ATTCTCGTCT GTCCTTTTCC TGCTGTGTCC TCATAACTGA GACCCCTAGA 1320
GCTCCTTGCT GGGCACCCCA CACCTTCATT CACTGCTAGA TAAAATATTC ACATATCCGG 1380
GCAGGCACGG TGGCTCATGA CTGTAATCCC AGCACTTTTG 1420
|
