Tag | Content |
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EnhancerAtlas ID | HS182-04841 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr12:13062890-13063510 |
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: 8 | 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 | chr12:13062902-13063968 | VACO_400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I012908 | chr12 | 13061782 | 13064421 |
|
Enhancer Sequence | AAAAAAGAAT CAAGTGATTT TGCTCTTATC TGGAGTTGAG ACAAGCCAGA TGTTCTCGTG 60 TTGTTTTCAT AAGCAAAAGA GGCTAAACTG ATGGCCAGAA AGTACTCCTG CTCATAGGGA 120 CCTATTCATT GGTCTCCAGG GTTTACACTG ACCTTTAAGT CTAATCACAG GGGGTGGGTG 180 GTTTTGGGAT AGGAATGAGG AACCTCCAAG GCCATGTTCT TAGCTCCAGC TAAAAATAGG 240 TCTTTCCTTT GCTCTTAAGC CTGAGGTGTG GAACTTCCTG GTGCTACTCA CTGCAGCTAT 300 GGTCCCTGTC TAGGGCACTT GGAAGTCTGA AGGGAGGCGG AGGAGGGCAG GAGGGGTTAT 360 TTAACCACCC AGCCCCTCCT GTCCGTTCCG TGGCTTCACT CCATCACCTC ACTCCTGTAC 420 TTCCTGTTCT CATTCACTGA TGAGTCTTCC TTCCTTCATT CATTTCAAGG GCCACTGTCA 480 GCTTTCTCCC TTAAAATGCT TCTCTGGCCT CCATGCTTTG CTGCTCACTT TCCTCCCTGG 540 GTCCCCTGAG CCACCCCATC CCATCAAATC CTTCCTGAGC CCTTCCACAG TTGGAACCAA 600 CAACCTCTGA AGCTTTGCTC 620
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