Tag | Content |
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EnhancerAtlas ID | HS095-29829 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr8:101483900-101484910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr8:101483909-101483920 | ACCAATAAAAC | + | 6.32 | IRF1 | MA0050.2 | chr8:101484400-101484421 | ATTTGGTTTCAGTTTGATTTA | + | 6.07 | ZNF740 | MA0753.2 | chr8:101484053-101484066 | GTGGGGGGGGTAA | - | 6.41 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_22743 | chr8:101483886-101485006 | CD8_primiary | SE_27991 | chr8:101483399-101488990 | Fetal_Intestine | SE_28830 | chr8:101483384-101489121 | Fetal_Intestine_Large | SE_32305 | chr8:101483709-101485077 | Gastric | SE_32533 | chr8:101483317-101490498 | GM12878 | SE_34085 | chr8:101482418-101486804 | HCC1954 | SE_36367 | chr8:101484099-101485072 | HMEC | SE_47999 | chr8:101483989-101484303 | Pancreas | SE_47999 | chr8:101484469-101485013 | Pancreas | SE_62291 | chr8:101421434-101542088 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I100471 | chr8 | 101483587 | 101489609 |
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Enhancer Sequence | AAACCAAGAA CCAATAAAAC CATTTCCACT TCTTTGCCAG AAGAGAAAGT CATCCCCAAA 60 TAGAGGATAT GGATGCTTAG GTTTCAAAGA AAGGCCAAGA AAGGGTAACC CAGCACAGCT 120 GAGGCAGGTT TTTTTTTGTT TGTTTTGTTT GTGGTGGGGG GGGTAAGGGG GGTGTGGGGT 180 GTGGAGTACT GACTTCTCAC ACTCCTAAGA GGTTGCTAAG CAGGGCATCT TATTAAATGC 240 CCGGCAATGG AAATCAGCCA AGTGTTCCCA GGGAGGGGGC CCTCTCCCAG TCCTGGGCTC 300 CCCTAGGAAA ACAGATCTTA ACAAAGCTCT TGATTATTTT GCCATGTCCA TGATTTAGCA 360 CTTTTTCCTG GCGTTGGAAA ACAGCTGAGA ACATTGAGCA AGTCCTTTTT GCTCATAGAT 420 AATTCCTTTA GTTTGGTTCT TACCACTTGT TTGAAACAGG GACTGGCTCC AGCCCGTTCC 480 TTATACGGAT GGCGCCTCTA ATTTGGTTTC AGTTTGATTT ATGCCAGGAT CTAACTCACT 540 ATGGAGTTCA ACTAAGAATT TTACAAACAC TTTTTGATGC TAATGATATG TGTCTCACAA 600 TCTAGACATC TGGACTTAAT GTCAAACAAA TATTACCCAC CACAAAAACC AGTTGGATCT 660 GTTTGTGGTT ACTTCAGCCC TGAGCAGTTC CTTCTTTAAA GGCTCTGACC TGATAAAGTA 720 GCTTTTGGCC CCATCAGCCT GCTGGCTAGG TGAGATAAAG CGATCCCTGA ACCATTTGCT 780 CCTTTTTCTC AGACCTACAC TCTGAAGCTG GATGGCCCAG CCCCTCCCCA GCACAAAAAC 840 ATTGTGTGAT CCTGTCTGTT GAGATGCTTT TCTCTGGGCC AGATTCTCCA CATAAGCAAT 900 GCAGGATTAG GATATGATGC TTGTTTGCTT GGAGATCCAG GTGGTATTTG GAAGTGGCTT 960 GCACAATCAC ATCCCTATGG GAACTTACCT CCCATGTGCT TTTGGGAAAG 1010
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