Tag | Content |
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EnhancerAtlas ID | HS135-00774 |
Organism | Homo sapiens |
Tissue/cell | MM1S |
Coordinate | chr15:31726910-31728030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr15:31726949-31726960 | TGTGGATTGGG | - | 6.14 | FOXP1 | MA0481.2 | chr15:31727837-31727849 | AAGTAAACAGAA | + | 7.22 | FOXP2 | MA0593.1 | chr15:31727837-31727848 | AAGTAAACAGA | + | 6.32 | IRF1 | MA0050.2 | chr15:31727816-31727837 | TGTTACTTTTTCTTTCTCTTG | + | 6.34 | KLF16 | MA0741.1 | chr15:31727377-31727388 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr15:31727378-31727388 | GGGGCGGGGC | - | 6.02 | Stat6 | MA0520.1 | chr15:31727785-31727800 | TGTTTCCTGAGAAGC | + | 6.01 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_12339 | chr15:31725499-31731468 | CD3 | SE_20602 | chr15:31725156-31731134 | CD56 | SE_24087 | chr15:31726373-31727926 | Colon_Crypt_2 | SE_50542 | chr15:31725268-31731125 | Sigmoid_Colon | SE_52936 | chr15:31725341-31731061 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH15I031433 | chr15 | 31725389 | 31731119 |
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Enhancer Sequence | GGAAGCAGGC TTCTTGGAGC TCCCCTTCAT CCTCAGCCCT GTGGATTGGG CAGCAGCCCA 60 CGCCTCCCTG CCCCAGCCAC AGCCCCCCGT CAATGCCGGC GCGCAGCAGC TTTTGCTCAT 120 CCTGCCCTGG TTCCAACCCC AAGGCCATGG GGCAGCCCAC TGGGCGCCTT CCTGCATGGG 180 TGTCCCCCTT TGCTGCTGTG TCTAGACTGC AGACACAAGT GCTGGCGGGG GCCGGGGGAC 240 TGGCCAAAAC TAGGGCTGAA ATCATGTTCA AAACCACAGT CAAGGCGGAC TTGTCAGAAA 300 TATTCCTTTC CTTGAGCCGT CGCAGCTCAG CCTCCTTGAA TCACCCTGGC CACTTCCTTC 360 CTGTGTATAT CTTATGCACG CTAAGGGACG GGGCGGGTGC AACGTGTGTG TTTTTACTTC 420 TTTTAAGTTT TGTCTATGTT TTGTCCTTTC AATGTGTTGT AGGCTGTGGG GGCGGGGCTG 480 TTCCGAGGGG CCTTTGTCAC AGTAAGGGAC ACTGGGGACA GCTCGGGCTT TCTCTTCAAG 540 CTGAAAACCT TTGGTTGTGA GAATGACTAG GAGAAGGGTC TCGCTAGGGT CATGCTTAGG 600 ACCCTTCGCA GGTGGTGTGT TTAATCTCAA AACGGCCTCA AGAGGCTCTC GATCTTTTAC 660 AGGTGACAAA GAAGACAAGG AAGACAAGGA AGGTGATCCG GGAGGCTGGA GAGCTTGTCA 720 AGGTCACAGA CCCACGGTTT TCCGCCCCCT AGGGTCCAAG CTCTTTCCTG GACATCTGCA 780 GGCAATGTCG ACACGCCCTC CAGTGTCTGT GGCGGGCAAA GGATGTGTCT CCACCCCCAG 840 ACCTTCCGAT CCTGTGCTGA AAGTGTCCCT CAGCCTGTTT CCTGAGAAGC CCAGGGGCTT 900 TTGGCTTGTT ACTTTTTCTT TCTCTTGAAG TAAACAGAAT AAAAGAGAGT TGCTCAGACG 960 TCTTTGGCTG TGACCCACAG GAGATGATGC AATCTCCACG GCACCCCCAC ATGCATGTGT 1020 ATGCACAGGC GTGTACAGAT ATCTAAAACT GGCACCAATT TCACAAAAAC ACTCACCCTT 1080 ATGCGAGACA CATTCACCCT ACACTCATCC CCCATCTCTA 1120
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