| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00011 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:1014700-1016130 |
Target genes | | Number: 29 | 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 | AGGCTATGGG GACTCCGTGC CGGGAGGCTG AGGCTATGGG GACTCCGTGG GGGGAGGCTG 60
AGGCTATGGG GACTCCGTGG GGGGAGGCTG AGGCTATGGG GACTCTGTGC AGGGCCGCTG 120
TGAGGCCCTG AAAGCACTCG TCGGAGGCTC CTGCTTCCTG AGGTCCGTGA CTCGGGTCAC 180
ATGCCGCCTC CAGGAAGCAC CCTGGCCCCT GCAGCTCTGG GAACGTCCTC CCGACAGCTC 240
CTGGGAATAT CCTGGCACTG AGGTCACTCT GGGCTCCCGG CTGACACTCG TGCCGGAGGC 300
AAAGGTGAGG AAAGGCCGGA GGAATGTGTG GTCTCGGCGC CAGGCCAGGC CTCCCTGTGC 360
AGGAGAGGAG CCAGCAGCTC CCCTTCTCTC AGCTCAGACG GTCTCTCAGG GCTCTCGGGA 420
GGCTCAGAGC AGCTTGGCTG GCAGATTCCA GGGCAGGGGG TGGGCCCGCC TGGTCCCCTC 480
CGTCGCAGCC AGTGGGCGGG AGGCTGGGCT GGTGAGCGTG TGGGCGTGTG TGAGCACACG 540
TGCCCATGCT TGAGACATGG ATGCTGGTGT GAGCACCTGA CCCCTCACCT CCTTCACTCG 600
GTCTCCTCAC GCCCTCTCAG GGACTCCTTC CCCTCCAGGC CTCGGTTACG GGTCACACCT 660
GGCACTGCCA GGCCTGGGGA CGTGGTGCGG CCGGTGCGGG GAGGGGCCTT CCAGGCTGCT 720
GTGGGGCCCC CGGCCTCGCC CCACCCCGCC CCGCCCCGTG CTGGGCCATT GCCTCAAATG 780
CAGCGGCTCT GTTGGCCGTG GGACTGGAAT TCTTTCCCAA GGGCCCAGAT GTGCAGAGGG 840
GAGGCCGGTG CGGGGGAGCA GGGCTCCGGG ACGTGCACTT GGGTCTAGCT TTGCCCCTGA 900
CGTGCTGGGG CCGCCCCTAG GCCCAGCTCA GTGTGTCCCT CCTGTGCCCA GTGAGGAGGG 960
CGTGCCCCTC GCTGCCACAG GTCCTGGCTG ACCACGTGCT GCCCAAGGGC CAATCGCGAG 1020
TGCGCAGGTG GGGGACGTGG GGAGCCAGCT GAGGGGGATA TGTGGAGGTG TCAGGATGAC 1080
CCTGGGTTTT TGGTTTGGGC CACTGGGTGG GAGGAGGAGG AGGGGACCCA GAATTGAGAG 1140
ATGGGGCCTG GGGGGCTGCT CAGAGGGTGG GCTGGGAGGT GCCTGTCTGT GTCTGGCCTG 1200
GCCTCCAGAC CCTGCCTGGC TGGACCTGCT GTTCGTGCCT GTTTCCGATT TTATCCTCCA 1260
AACCAGACGC CCAGCCTGGT GCAAATGCAG GAGTGGAGTT TCCAGGGGGA TGTGGACTCC 1320
TTCCCTCCAC CCCCACCTCG GTCCCTGTCT CCTTCCCTCC GCCCCCACCT CGGTCCCTGT 1380
CTCCTTCCCT CCGCCCCCAC CTCGGTCCCT GTCTCCTTCC CTCCGCCCCC 1430
|
