Tag | Content |
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EnhancerAtlas ID | HS101-02812 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:154904890-154906060 |
Target genes | Number: 32 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:154905910-154905931 | AAAATGAAAATAAAAATAAAA | - | 6.37 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_24423 | chr1:154904307-154905067 | Colon_Crypt_2 | SE_24423 | chr1:154905091-154905577 | Colon_Crypt_2 | SE_27195 | chr1:154904269-154905862 | Esophagus | SE_28280 | chr1:154903528-154905966 | Fetal_Intestine | SE_29277 | chr1:154903441-154905787 | Fetal_Intestine_Large | SE_35290 | chr1:154903493-154905818 | HeLa | SE_52835 | chr1:154903559-154905954 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I154931 | chr1 | 154903680 | 154905879 |
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Enhancer Sequence | TCTGCAGGAC AGGGAGATCA GAATCCAGTT AGCCTAGAAT TTCCAGGAGC TTCCATGTCC 60 CAGAAAGGGA GTCAAGAGGC CTGTGTTGAA GTCCCATTTC TACTACTGGT ATTATGTAAC 120 TTTGGTAGGT CTCAATGTCC CTGATCCTGT TTCCTCATCA GAAAATGGGG ATAACACTTT 180 CTGTTCTGTC TCCCACACAG GATTATTATG AAACTCTAAA GAATATAAAA GAGCCCTGAA 240 ACTAACAGGT AAAACCTATA AAGTGCTAAT TACAGTGTGA ACAGGCGCAC AATATTCTAG 300 CTGGATTAGG TTATTGCCCA GACCCTAAAC TAATTCTCTC ATAGCCAGAG GTATCTGTCT 360 CCACTGACTT GGTCACCATA ACATATATCA TTTATTAATT CACTGGTTGG GCATGGTGGC 420 TCACACCTGT AATCCCAATA CTTTGGGAGG CCAAGGCAGG AGGAGTGCTT GAGGCCAGGA 480 GTTCAAGACC AGCCTGGGCA ACACAATAAG ACCCAGAGAT ACCATCTCCA CCAAAAAATT 540 TAAAAATTAG CTGAGCATGG CAGCATGTGC CTGTACTCCC AGCTACTCCA GAGGCTGAGG 600 TGGGAGCATT CCTGAGCCCA GGAGTTCCAG GCTACAGTGA GCCATGATTG TACCACTGTA 660 TGCCAGCCTG GGAGACAGAG TGAGACCCTG TCTCATAAAA ATGAAATAAG AAAAGCAAAT 720 TTAAAAAACT GAAACAAAAG CCAGGTGTGG TGGCTCACGC CTGTAATCCC AGTACTTTGG 780 AAGGCTGAGG CAGCAGATCA CCTGAGGTCA GGAGTTTGAG ACCAGCCTGA CCAACACGGT 840 GAAACCCTGT CTCTACTAAA AGCATAAAAT TAGCCGGACA TGATGGCGCA TGCCTGTAAT 900 CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATCACCTGAA CCCAGGAGGT GGAAGTTGCA 960 GTGAGCCGAG ATCGCCCCAT TGCACTCCAG CCTGGGCAAC AAGAGTGAAA ATCCATCTCA 1020 AAAATGAAAA TAAAAATAAA AATAACTCAT TCGTTATTTA ATTTACTTAA CCAACCTTTT 1080 TTTTTTTTTT TTTTTTTGAG ACGGAGTCTT GCTCCACCAC CCAGGCTGGA GTGCAATGGC 1140 GCGATCTCGG CTCACTGCAA TCTCCGCCTC 1170
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