Tag | Content |
---|
EnhancerAtlas ID | HS076-27411 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr19:740990-742350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr19:741990-742001 | CATGAGTCACT | - | 6.14 | IRF1 | MA0050.2 | chr19:741827-741848 | TCTCTCTTTCTTTTTCTTTTT | + | 6.65 |
|
| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23277 | chr19:741551-741999 | Colon_Crypt_1 | SE_23981 | chr19:741541-741822 | Colon_Crypt_2 | SE_24804 | chr19:741479-742153 | Colon_Crypt_3 | SE_27769 | chr19:736895-745751 | Fetal_Intestine | SE_28712 | chr19:736989-741165 | Fetal_Intestine_Large | SE_28712 | chr19:741257-742194 | Fetal_Intestine_Large | SE_52481 | chr19:736969-741424 | Small_Intestine | SE_52481 | chr19:741469-744219 | Small_Intestine |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I000737 | chr19 | 737127 | 744196 |
|
Enhancer Sequence | TACCCTGGCA TGGTGGTGCG TGCCTGTGGT CCCAGCTACT TGGGAGGCTG AGATGGGAGG 60 ATCACTTGGG CCCAGGAGGT TGAGGCTGTA GTGAGCCGTG ATCGCACCAC TGCACTCCAA 120 CCTGGGCAAC AGAGTGAGAC CCTGTCTCTT AAGAATAAAA AATAATAATA AAGAATTGCT 180 AGCGTGACAG AAGCCACAGA AAATGCACAT CCAGGGGGCT GTGAGAAGTC TCACAGGGTG 240 AGGATGGGGC CGGGGGAGGC TTCCCAGAGG AGGCAAGCAG GGGCTCATCA GAGACACGCA 300 GTGCATGGGA ACCACACCTG GCAGAGCCGC AGCCCCTGCA AAGGCCCTGA GGTAGGATGG 360 AGTCAGCTGG GCTGGAGGGC TGAGGGGAGT TGGGCTGCAG GAGTGAGGGG AGACGGGCTG 420 CAGGGGTGAG GGGAGACGGG CTGCAGGGGT GAGGGGAGAC GGGCTGCAGG GGTGAGGGGA 480 GACGGGCTGC AGGGGTGAGG GGAGCTGGGC TGCAGGGGTG AGGGGAGACG GGGTGAGGGG 540 AGACGGGCTG CAGGGGTGAG GGGAGACGGG CTGCAGGGGT GAGGGGGAAC CAGGTTGGTC 600 AGGGAGTTGA GGAGCTGGGC TCACGCAGGG AGGAGAAGGG TGCTTTGCCT GGAGGCAGGG 660 GGACAGGCGG GGCCGTGTCC TGAGGGCTTT GGGAAGCCTT GGGTGCGTTG GGTCCTGACG 720 GTGCTGAGGT CTAATTTGGT TTTAAGGGCT CCTCCTAGAG GTCAAGAGGC AAACAGGCTG 780 TGGGAGATGC CAGGGACCCC AGGAGGAGGA GGGAAGCTCC ACACTGAAGC CCCACTCTCT 840 CTCTTTCTTT TTCTTTTTAT TTATTTACTT TCTGAAGAAA GAGTTTCACT CTGTCGCCCG 900 GCCCGCAGTG CAGCGATGCC ATCACAGCTC ACTGCAGCCT CCAGCTCCTG GGCTCAGGCG 960 ATCCTCCTGC CTCGGCCTCC CGAAATGCTG AGACCACAGG CATGAGTCAC TGCACCCGGC 1020 CTCTTTTTCT TTTATGAGAT ATAATTCGCA GACCATAAAA TTCCGCCTTA ATGGGAGGCT 1080 CATCTGGGCC CGGGACATTG AGGCTGCAAT GAGCTATGAT GGCACCCCTG CACTCCAGCC 1140 TGGGCCACAG ACCAAGACCC TGTCTCAAAA ACAAGAAAGA GGAGAGAAGC CCCATCCCCA 1200 TCAGCTGTCA CTTCCTGTCC CCTCCCCAGT CAGCGTCACT CCCTATCCCC TCCCCAGCTC 1260 TGGCACCCAC GCATCCCCTC CTGTCTCTCT GGATTGGCCT GTCCTGGACA TTTCATAGAA 1320 ATGAGATCAC ACGGCCGGGT GCGGTGGCTC ACACCTGTAA 1360
|