Tag | Content |
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EnhancerAtlas ID | HS092-32219 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr5:133364200-133365630 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr5:133364974-133364985 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr5:133364974-133364985 | CTGAGTCACCC | - | 6.02 | NFIL3 | MA0025.1 | chr5:133365377-133365388 | TTATGTAACAT | + | 6.32 | YY1 | MA0095.2 | chr5:133364637-133364649 | AAAGATGGCGGC | + | 6.22 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_23722 | chr5:133364159-133365420 | Colon_Crypt_1 | SE_28305 | chr5:133364047-133365635 | Fetal_Intestine | SE_29210 | chr5:133363953-133365850 | Fetal_Intestine_Large | SE_52852 | chr5:133364324-133365142 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I134028 | chr5 | 133364133 | 133365610 |
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Enhancer Sequence | TTCAATGTTT CATTGCACTG AGGATTTTCT AAATGGTTCT CTAACTGTTG TTCATTTCTT 60 CTGTGGGAGG GAACATCCAG TCATCTAACA ATGCTCAGCT CACTAATTCC TCTGGCCTGG 120 CATTGCTCTT CCTCCTCCTT CCCTCCCGTG AATGCCTCCT GAGGTAGGTG GGATGACCGT 180 CATTTCACAG TGGGAAGGGA CCTTGCGGCC AGCCAAACCA CTGGTAGGCA AATGTGACTG 240 TACATCAGGG ATCATTGATC CCTCAGCCAA GTACAGATTC CTAGGCCCTG TATCATCTGC 300 CCAATCAGAT GGGACAGTAT GGAAGGTTTA AAATATGTCC ACATATTCTT TGACAATCCT 360 CCCTTCAGAA GGCAGTTGCT AATTCCCCTG TCCTTGAATG TGGACCACAG CACTCTCCTG 420 GATCCCTCAT CCTAGGAAAA GATGGCGGCC ATGTCATAAG GACACTCAAG CAGCCCTGGA 480 AGAGGCCCAT GTTGGGTGGA ACTGAGCCCT CCTAGCAGCA GTAGGGTGAC CAATCGTTCT 540 GGTTTGTCTA GGACAGTTCC AGTTTTCACA CTGAAAGTCC CACATCCTAG GGAACCTCTT 600 AGTCCTAGGC AAACAGAAGT GGGTGCCCAT CTAACATCTA GCACCAACTG GCCAGCCATG 660 TGAGTGAGCC ACCTTGGAGG AGGCTCCTTC TGCCCCAGCG AAGCCTTCAG ATGGCTGCCC 720 CTGACCAACC TCTTGATTGC AGCTTCATGA GAGACTCTGT GCCTAACAGC ACAGCTGAGT 780 CACCCAAGAA CTCCTGACCT ACAGAAAATA TGTGGGGTAA TAAAGGTTGA TCATTGTTTT 840 AAGCCACTGC ACTTTGGGGT AATTTATTAT GCCACAATAT ATAAGTAATA CACTCAGGAA 900 TCTGTATTTT GTCACACTGT TGGGTAATTG GGCTTATGAA TCAGCATTTG TGAACCACAG 960 ATCTGGTCTT ATTCCCTAAA GCAGCACTTT CCAATAGAAC TTTCTGCAAT GATAGAACAG 1020 CCGTGCATCT GTGCTGTGCA ATTTGATGGT CACTAGGCAA ACGTGGCTAT TGAGCATTCA 1080 AAATGTGGCT GATATGACTG AGGAACTAAC TTTTTAATTT GATTTAATTT TAATAAATTA 1140 AACTTGACAT TTAAATAGCA CATGTGTAGG ATTCCATTTA TGTAACATTC TTGAAATGAC 1200 AAAAGTAGGG AGATAGAAAA CAGATTAGTG GTTACCAAGG GTTAGGGATG GTGGGAAAAG 1260 GGCGGTGGGA GTGACTATAA AAGGATAGCC TGTGGGAGGT CTTTGAGATG CTGGGATAGT 1320 TCTGTATCAC GATTAGGTGG TAGTTACATA AATCTACACA TGTGAGAAAA TGGCACAGAA 1380 CTATACACAC ACATTGTACT AACATCAACT TCCTGGTTTT GATATTGCGC 1430
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