Tag | Content |
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EnhancerAtlas ID | HS101-12033 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr13:29281840-29283520 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr13:29282730-29282751 | ACTTTCTTTCTTTTTCTTTTC | + | 6.31 | IRF1 | MA0050.2 | chr13:29283473-29283494 | AGAGAGAAAGTAAAAGAAGAA | - | 6.5 | NFE2L1 | MA0089.2 | chr13:29282334-29282349 | ATTGCTGAGTCATAA | - | 7.37 | Nfe2l2 | MA0150.2 | chr13:29282336-29282351 | TGCTGAGTCATAAGG | - | 6.25 | RUNX1 | MA0002.2 | chr13:29282498-29282509 | CTCTGTGGTTT | + | 6.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_29169 | chr13:29281867-29282763 | Fetal_Intestine_Large | SE_29169 | chr13:29283310-29286591 | Fetal_Intestine_Large |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I028707 | chr13 | 29281779 | 29283144 |
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Enhancer Sequence | AAACCTCACC CTTTTAAAGT CTGCAATTCA GTGGTTCTTA GTATGTTGCA GATTTGTGCA 60 ACCATCACCA CTATCTGTGG AACATTTTCA TCACCCCGAA AAGAAACTGT ATACCCATAA 120 GTAGTCATTC CCCTTCCCCA GCCCCAGTCA AGCCCTAATC AAATTTCTGT CTCTATGGAT 180 TTGCCTATTC TGCACATTTC ACGTAAACAG AATCATATTT AAATGACAAT ATGTGGCCTT 240 TTGTGACTAG CTTCTTAAAT TTGGCATAAT CATTTCATAG TTCATCCATG TTATGGCATG 300 TAACAGAACG ATATTTCTTT TTATTGCAGA AGAGCAGTTT GCTGGATGGA TAAACCACAT 360 TTTGTTTACC CATTTGTCAG TTCATGAACA TTTGCATAGG TTTCACTTTT TGGCTATTAT 420 GAATAATGCT GCCATGAACA AGATTTTATG TGGACATATG CTTTCACTTC TCATGGTATG 480 TAAGTAGGGG AGGGATTGCT GAGTCATAAG GCAACTAACT TTCTGAGGAA CTGCCAAACT 540 GCTTTGTACA GCTGCTGCAC CATTTTATGT TCCCACTCGC AGTGTATGAG GGCTCCAATT 600 TCTCCACATC CTCATCAACA CTTGCTATGG CCTATTTTAT TTTGGCCACC CCAGCCCACT 660 CTGTGGTTTT GCTTTGCATT TCCCTGATGG CTAATGATAT CCAGCATTTT CATGCGCATA 720 TTGGTCACTT GTATATCTTC TATTCAAATC CTTTGCCCAT TTTTAAATTG AGTTGTCTTT 780 TTGTTGTTGA ATTTTAAGAG TTCTTAAATA TGCTGGATAC GAGTTCCTGC TCAGACAAAT 840 ATAATTTGCA AATATCTTCT CCCATTCTGT GGGTTGTCGG TTGTCATTTC ACTTTCTTTC 900 TTTTTCTTTT CTTTTTTTTT TTTTTTTTTG TATTTTTAGT AGAGACGGGG TTTCACCATG 960 TTGGTCAGGC TGGTCTCAAA CTCCTAACCT CGGGTCATCC ACCCGCTTTG GCCTCCCAAA 1020 GTGCTGGGAT TGCACATGTG AGCCACTGCG CCTGGCCTCA CTTTCTTGAT GTTGTCCTTT 1080 GAAACATAAA AATTTTTCAA AGGACAAACT TTGAATGAAG TTTTTGGATG AAGTCTAATC 1140 TATCAATTTT TCCTTTGTTC TTGTGCTTTT GGTGTCATAT CTAAGAAACT ATTGCATAGT 1200 CCAAAGAAGC AGATAGATTT TTACATAGTT TATATAAATT TTTCCATTTG TTATTGGTTT 1260 TCAAAGCAAT CATCATCACA TCATCTATAA ACAGATGTGT GAATATATAG CTACATCTTA 1320 TGAGTGAAAA ATAAGAGGCC GGGTGCGGTG GGTCACGCCT ATAATCCCAG CACTTTGGGA 1380 GGCTGAGGCG GGCTGATTAC CTGAGGTCAG GAGTTTGAGA CCAGCCTGGC CAACATGGTG 1440 AAACCCTGTC TCTGCTAAAA ACACAAAAAT TAGCCAGGCA TGGTGGCAGG AGCCTGTAAT 1500 TCCAGCTACT TGGGAGGCTG AGGCAGGAGA ATTGCTTGAA CCCAGGAGGC AGAGGTTGCA 1560 GTGAGCCGAG ATCACACCAT TGCACTCCAG CCTGGGCAGC AAGAGTGAAA CTCCGTCTCA 1620 AAAAAAAAAA AAAAGAGAGA AAGTAAAAGA AGAAATATAT TTTTAATTTA TTGAATTATG 1680
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