| Tag | Content |
|---|
EnhancerAtlas ID | HS007-16927 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr8:134387500-134388560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr8:134387924-134387939 | AGGTGACTCAGCAAC | + | 6.23 | | Nfe2l2 | MA0150.2 | chr8:134387922-134387937 | AGAGGTGACTCAGCA | + | 6.01 |
|
| | Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
| SE_04561 | chr8:134386587-134388362 | Brain_Anterior_Caudate | | SE_05389 | chr8:134385474-134388701 | Brain_Cingulate_Gyrus | | SE_06509 | chr8:134385902-134390148 | Brain_Hippocampus_Middle | | SE_08729 | chr8:134385518-134388732 | Brain_Inferior_Temporal_Lobe | | SE_24207 | chr8:134386695-134389946 | Colon_Crypt_2 | | SE_29358 | chr8:134385800-134391190 | Fetal_Intestine_Large | | SE_32098 | chr8:134386605-134387970 | Gastric | | SE_32098 | chr8:134387978-134388675 | Gastric | | SE_35585 | chr8:134386643-134390255 | HepG2 | | SE_56399 | chr8:134385500-134387956 | u87 | | SE_56399 | chr8:134387960-134389888 | u87 | | SE_67089 | chr8:134378971-134391832 | H2171 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I133373 | chr8 | 134386059 | 134390480 |
|
Enhancer Sequence | TTTTTCAGAC CTGCAAGCTG TGGCTCAGAG AGCAAAGAGT CCCACCCAGG GTTACCGTTG 60
CTGGTGGCAG GGCCTGGCAC CTCACATCCA TGCACCTTGG GGTAGAATTA TAGGCCTGTC 120
TCCTCCACTG AGCTGGGCTC CAGGAGGGCT GGGGCAGGGC CTGGGTTCAA CTCCTAAACC 180
CCAAGTGGGC CCTTAGCTGG GACCTGGGAA ACCAGGGTCT TTTCCCCGTC GGGGCTTGCC 240
CAGGCCATGG GTGCTTGTCA CTGCCTGGCA CAATCCCAAG GCCACTGTTC CAGGCTGGAG 300
AAGGGGAGGG CAGTGGGAAG GCTGAAGGCA AGGGAGGGCT GAGGCTGGAA GCCACCTCCC 360
ATCTTCCTCC CACATGGAGA CGTGCAGCAC CTCACGCCCC TCCCAGGAAT CCCTCAAGGC 420
CCAGAGGTGA CTCAGCAACA CGTGAGCTAA GCTGTCCGAG CTGTGCCCCA CCTCTTGCCA 480
GATGCAGAGC CCAGTGGGGG GAGGGAACGT GCCACCCGCC ACGTGCACCC CTGCAGCAGC 540
TCAGCCTGCA GCAACAGAGC CGCCCCTGCC TCTCCCTCCC AATCTCTCTC TTCTTCTTTG 600
TGGGGACCTC ACATGTTCCT TCTGCCTCCA TTCAACCCTC ACCTCGCTCT ACAGGCATTA 660
AACGCAGGAC TGGTAGTTTG CTGTGCTGAT GGTGCCACAA AAGCTACCTC CTGCAATCCT 720
CTCTGCAATC CTGCCAGGCC AAGTGGGGAA ACTGAGACTC AGAGACAGTT TGTGACTTAT 780
GCAAGGAACC GAGATTCAAA CCTAGCTCAG CCTAACCCTG AAGACTGTGT GATTTCTCTT 840
TCATGAGCCA TGCTGAGTGG GATCATTGAC AAACTCTACC CCCTTTTGCG CATTTTACAG 900
AGTGGGAGGG AAGACTGAGG CACAGGGAAG GGAGGTGACT GGTGGGGGAG GGAAGGGACC 960
AGCATAATGT TGTCCTAGGA CAGAACGGTG GCTCTCTGTG TCCCCAGGGC ACTGTGGCTG 1020
ACACTGGGAC AGACTCCCTG CCCTAGGAAT GTGTGGTGAA 1060
|
