Tag | Content |
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EnhancerAtlas ID | HS105-17701 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:13062560-13063700 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:13063334-13063352 | TCTTCCTTCCTTCATTCA | - | 6.78 | EWSR1-FLI1 | MA0149.1 | chr12:13063338-13063356 | CCTTCCTTCATTCATTTC | - | 6.84 | RREB1 | MA0073.1 | chr12:13063058-13063078 | AGGGGGTGGGTGGTTTTGGG | - | 7.2 | ZBTB18 | MA0698.1 | chr12:13062932-13062945 | AAGCCAGATGTTC | + | 6.19 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_02173 | chr12:13062824-13063862 | Aorta | SE_23547 | chr12:13062912-13063768 | Colon_Crypt_1 | SE_24533 | chr12:13063058-13063688 | Colon_Crypt_2 | SE_28138 | chr12:13062026-13064517 | Fetal_Intestine | SE_28922 | chr12:13061553-13064754 | Fetal_Intestine_Large | SE_34394 | chr12:13062863-13063891 | HCT-116 | SE_38847 | chr12:13061711-13063715 | HUVEC | SE_57272 | chr12:13060420-13062872 | VACO_400 | SE_57272 | chr12:13062902-13063968 | VACO_400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012908 | chr12 | 13061782 | 13064421 |
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Enhancer Sequence | CAAGCCATGA TTTCCTGCAG TGATCACAGA GCAGAGAAGG GAGAAAGCCC TTTTATCACA 60 AACCAGCAGG AAGTCTCTGT AAAATTGGTA AGGATTCTGG TTTAGTGTGA AGAACCACAT 120 TTTTTGTGTA TGTTTCTGGG CCCATGGGAA GGAACAGATC ATATTTGACA TACAAGAATC 180 AAATGATTCA GGCCAGGCAT GGTGGCTCAC TCCTGTAATC CTAGCCCTCT GGGAGGCTGA 240 GGTGGGAGGA TTGCTTGAGC CCAGAAGTTT GAGACCAGCT TGGGCAAAAT AGCAAGACTT 300 CATCTCTATT TAAAAAAAAA AAAAAAAAAA AAAAAAGAAT CAAGTGATTT TGCTCTTATC 360 TGGAGTTGAG ACAAGCCAGA TGTTCTCGTG TTGTTTTCAT AAGCAAAAGA GGCTAAACTG 420 ATGGCCAGAA AGTACTCCTG CTCATAGGGA CCTATTCATT GGTCTCCAGG GTTTACACTG 480 ACCTTTAAGT CTAATCACAG GGGGTGGGTG GTTTTGGGAT AGGAATGAGG AACCTCCAAG 540 GCCATGTTCT TAGCTCCAGC TAAAAATAGG TCTTTCCTTT GCTCTTAAGC CTGAGGTGTG 600 GAACTTCCTG GTGCTACTCA CTGCAGCTAT GGTCCCTGTC TAGGGCACTT GGAAGTCTGA 660 AGGGAGGCGG AGGAGGGCAG GAGGGGTTAT TTAACCACCC AGCCCCTCCT GTCCGTTCCG 720 TGGCTTCACT CCATCACCTC ACTCCTGTAC TTCCTGTTCT CATTCACTGA TGAGTCTTCC 780 TTCCTTCATT CATTTCAAGG GCCACTGTCA GCTTTCTCCC TTAAAATGCT TCTCTGGCCT 840 CCATGCTTTG CTGCTCACTT TCCTCCCTGG GTCCCCTGAG CCACCCCATC CCATCAAATC 900 CTTCCTGAGC CCTTCCACAG TTGGAACCAA CAACCTCTGA AGCTTTGCTC GCAGTCCAGA 960 TGAACCAAGT CGCTGTGCTT TCCTGCCTGT GCCTGTGCTC CAGGTGTGTC TGTCCTCTGC 1020 CTGGTGTGAC CATCTCCCTC TTCTGCCCTT CTCCAGGATC AGGCATTCCC CAGTTTCCCC 1080 TGGTAATCAC TCCACCCTGT GCATCTGTAG GACTTTGAAA TGCTCTTATC AGGGTCTGTC 1140
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