| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10493 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:68882840-68884250 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr11:68883711-68883721 | GACATATGTT | - | 6.02 | | RUNX1 | MA0002.2 | chr11:68883821-68883832 | AAACCACAGAA | - | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32040 | chr11:68881672-68884306 | Gastric |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I069114 | chr11 | 68881970 | 68883960 |
|
Enhancer Sequence | ATTCCAGGAT TTATAATCTC AGAGGTGGGA TTTAAAGCCA CGACCCTCTA ATCCTTCCCA 60
AGCAACAGAA GGCACGGAGT GTGTTCGCGG TGTCAGGGAG GGTGGTGGGA AGGCAGGGGC 120
GGAGGTCCCT TCGGAGGCCT GACCTTCCCA GGACCCCTCA CCAGCGGTCA GCAGCCGGGG 180
TCCCGGGAAG AATTCTGCCG AGAGAGAGCT TTTTCCCCTT CAAGGAATAA AAAGCACACA 240
CACACATTCC TCCGAATCAA AGGTGTGTCC AGAGAGAGGG AGGGCAAGGC CCCTTGACCA 300
GCAGCTGCCA GCAGCCTGGG CACATGACAG CCCCTGAAGG CTGCTGGCAC CGACTCTGGC 360
CAGGCATTTG CAGTGGACGG CGGTGCCAGG ACAGGGAGGG CGGCCTTTCA CCAGCTTGGC 420
ACCTCTGCCA TGTGACGGCC GCCTCCCCTG GGGGAGGGCG GGGCCGCTCC TCTCCCAGCA 480
GGCGGGTGCA GCCCCAGGGG TGCTGCAGGC CACTGCGGGA CCTTCAGCGT CCGGCTCCCG 540
GCACTGGCCT CTGTGCCCTG GCCGTTCCTG GGGTGGGGCA TGGGTCAGGA ACTCGCACTC 600
TCACTCTCGG GAGATAGGAA CTCAGTCCCA TTCATAACCC CACCGTGTAA CCTGGAAGGC 660
ACTTTGCAGT TTACAAAGGC CGTCATAGCC AGGGTCCTTG AAGGAGGCGT GTCACCGTCC 720
ACTCTCCAGA GAGCAGCCTG CGGCCTGGGA GGTGGGCTTC GCCTCCTCGA CGTCACATGT 780
TGGGGGCTGT TTCCTCGTTG ACTTCCAGTG CAGGGCTGTG ATCTGGAGTC CAGGCCTTGC 840
TGGCCGGGAC CCCCAGGACA AGGGTGGCCG TGACATATGT TCTGGCGCCT TCAGTACTAG 900
TGAAAGAAAC GAGCCGGCCG TGTCAGCTGG GAGATTTCTT GCGGCTGCCG TAACAAAAGA 960
TCACAAACTG GTGGGGGCTG GAAACCACAG AAATGCCTTC TCTCCCAGTG CTGGGGCCGA 1020
AGCCCGATAT CTAGATGTAG GCAGGGCTGC GCTCCCTCCG ACTGCTCCAG GGAGGGACCC 1080
CGGCCTCTGT CTGCCCTGGT GCCTCCAGGT GCCCTGTGGC TTGTGGCTGC CCCGCTCCAG 1140
TCTCCGCCTT GTTTTCATGT GGCCCCCATC TCTTCTCCCT GTGTCTCTCC TCTGAGCCTT 1200
CAGGAGGAGG CTGGTCATTG GATTTTGGGT TCTCCAGGAT GATCTCACCT CAAGGTCCTT 1260
AATTGCATCT GCAGATGCCT GTTTCCAAAT AGGGCCACAT TTGGTTAGGA CGTGGACACG 1320
TCTTTCGAAG CCACCATGCA GGCCGCTACA GGAGGTTTCA TGAATTCATC TCAATTTCCA 1380
GAGGACCTGG TGTTGCTTGG CCGGCCCCCT 1410
|
