| Tag | Content |
|---|
EnhancerAtlas ID | HS187-00011 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:1014780-1015970 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:1015447-1015457 | GCCCCGCCCC | + | 6.02 | | MAX | MA0058.3 | chr1:1015690-1015700 | ACCACGTGCT | + | 6.02 | | NR2C2 | MA0504.1 | chr1:1015277-1015292 | TGACCCCTCACCTCC | - | 6.06 | | ZEB1 | MA0103.3 | chr1:1015721-1015732 | GCGCAGGTGGG | - | 6.62 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_24070 | chr1:1014747-1016073 | Colon_Crypt_2 | | SE_24817 | chr1:1014715-1016105 | Colon_Crypt_3 | | SE_27529 | chr1:1014709-1015893 | Esophagus | | SE_34539 | chr1:1014601-1016160 | HCT-116 | | SE_41944 | chr1:1014719-1016037 | LNCaP | | SE_58139 | chr1:1014749-1016027 | VACO_9m | | SE_65935 | chr1:1014576-1016194 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001077 | chr1 | 1013259 | 1018692 |
|
Enhancer Sequence | GGGGAGGCTG AGGCTATGGG GACTCTGTGC AGGGCCGCTG TGAGGCCCTG AAAGCACTCG 60
TCGGAGGCTC CTGCTTCCTG AGGTCCGTGA CTCGGGTCAC ATGCCGCCTC CAGGAAGCAC 120
CCTGGCCCCT GCAGCTCTGG GAACGTCCTC CCGACAGCTC CTGGGAATAT CCTGGCACTG 180
AGGTCACTCT GGGCTCCCGG CTGACACTCG TGCCGGAGGC AAAGGTGAGG AAAGGCCGGA 240
GGAATGTGTG GTCTCGGCGC CAGGCCAGGC CTCCCTGTGC AGGAGAGGAG CCAGCAGCTC 300
CCCTTCTCTC AGCTCAGACG GTCTCTCAGG GCTCTCGGGA GGCTCAGAGC AGCTTGGCTG 360
GCAGATTCCA GGGCAGGGGG TGGGCCCGCC TGGTCCCCTC CGTCGCAGCC AGTGGGCGGG 420
AGGCTGGGCT GGTGAGCGTG TGGGCGTGTG TGAGCACACG TGCCCATGCT TGAGACATGG 480
ATGCTGGTGT GAGCACCTGA CCCCTCACCT CCTTCACTCG GTCTCCTCAC GCCCTCTCAG 540
GGACTCCTTC CCCTCCAGGC CTCGGTTACG GGTCACACCT GGCACTGCCA GGCCTGGGGA 600
CGTGGTGCGG CCGGTGCGGG GAGGGGCCTT CCAGGCTGCT GTGGGGCCCC CGGCCTCGCC 660
CCACCCCGCC CCGCCCCGTG CTGGGCCATT GCCTCAAATG CAGCGGCTCT GTTGGCCGTG 720
GGACTGGAAT TCTTTCCCAA GGGCCCAGAT GTGCAGAGGG GAGGCCGGTG CGGGGGAGCA 780
GGGCTCCGGG ACGTGCACTT GGGTCTAGCT TTGCCCCTGA CGTGCTGGGG CCGCCCCTAG 840
GCCCAGCTCA GTGTGTCCCT CCTGTGCCCA GTGAGGAGGG CGTGCCCCTC GCTGCCACAG 900
GTCCTGGCTG ACCACGTGCT GCCCAAGGGC CAATCGCGAG TGCGCAGGTG GGGGACGTGG 960
GGAGCCAGCT GAGGGGGATA TGTGGAGGTG TCAGGATGAC CCTGGGTTTT TGGTTTGGGC 1020
CACTGGGTGG GAGGAGGAGG AGGGGACCCA GAATTGAGAG ATGGGGCCTG GGGGGCTGCT 1080
CAGAGGGTGG GCTGGGAGGT GCCTGTCTGT GTCTGGCCTG GCCTCCAGAC CCTGCCTGGC 1140
TGGACCTGCT GTTCGTGCCT GTTTCCGATT TTATCCTCCA AACCAGACGC 1190
|
