Tag | Content |
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EnhancerAtlas ID | HS051-08643 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr14:100613240-100614720 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr14:100613695-100613706 | GCGCCTGCGCA | + | 6.62 | TP63 | MA0525.2 | chr14:100613348-100613366 | TTCATGTACGAACATGTT | - | 6.04 | ZNF740 | MA0753.2 | chr14:100613992-100614005 | CTGCCCCCCCCCC | + | 6.33 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_17314 | chr14:100612171-100614800 | CD4p_CD25-_CD45RAp_Naive | SE_23614 | chr14:100610526-100615265 | Colon_Crypt_1 | SE_23822 | chr14:100610367-100618738 | Colon_Crypt_2 | SE_24776 | chr14:100606794-100618712 | Colon_Crypt_3 | SE_31785 | chr14:100606840-100615721 | Gastric | SE_52768 | chr14:100610298-100615730 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I100140 | chr14 | 100606368 | 100615136 |
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Enhancer Sequence | GCACCTGTAG AGAGGAGGGC GGGGCTCAGG GGCTGGTTCT CCTCGGGGCC GCACCCGCGA 60 GCACACACGC AGACACCTGA GCACACGCGG TGGGCATGCA CATGCATATT CATGTACGAA 120 CATGTTTGCG CGCGCGCACA CCCACACACA CACATGGGTG TACATAATGC AAACACACCG 180 TCGCCTCTGG GGTGCCCATG TCCAGCTTGG CCAAACACAA GGCCACCCCT CTGGTCCTCC 240 CTGCCAACCA CCACTTCCTG GGTGCCTGGA AGCGTGGCGC TGGCTGCTGG AGGGCCTGGT 300 GGCCTGAACT GCGCCCAGGA CGCTGTGGCA GAGGCACCCA CGGGCTCAGC TCAGAGCGCC 360 TGCCCCAAGT GGTAGTTGCA GAATTCATTG CACCACTCCA CTCGGCCCCG CCTTCTGACC 420 CGGCAGACCC CACTGCTCGG GGGAGTTCTC CCGCAGCGCC TGCGCAGTGC TGAGTGCCCG 480 CCTGAGTCCT ACCAGGCCAC AGTGTCACAC CCATGCATCT CAGCCCTGTG ATCCGCCAAC 540 CTTGGCCTCA GCCAGCCTCA CTGCTTGTCA TGTTCCAAGG GCCTCTTGAG CACCTGCTGT 600 CCCCTCCAGC CTTTGCTCTA CACAGACACC CCCACCAACT TCCTCCAGGA AGTGCTCCCA 660 GCTTCAGCGC CCGCAACTGC GCCACCACCA CGCCGCCCCA CTGCTCAACG GCATGCAGCC 720 TTGGCCCAGC TCCCATCACA GGGATGCCCT CCCTGCCCCC CCCCCCCAGG ATGCCTTTCC 780 TGCCCCCTCT TTGCCCTGTC ACCTCCTAAG GATGCTCTCA GGACGCAGGG AGCCTGGCCG 840 CAAAACCAGG ACAGCGGGGC CAGCACCAGG CACCCAGAGC CTCTCACTTT GCTCAGGAAA 900 GGTAAAGGCT CATGGCTCAC GGCAGGCACT CTTGCCAACT TGCTCTGCCA TCTCCTGAGG 960 CGGGCACCTC TCCCCTCCGC CCCGTCACCT CCTGAGGCGG GCACCTCTCC CCCGTGCCTC 1020 TGCCTTATCT ATACAACAGG GATAATGGAT GAGGAGGCAG CTGCCTCCTG GGCTGTGGTG 1080 AAGTTCAAGT GAGATGGTCC CTGGTGCAGA GCACCGCCTT GGTACTGCCA GCCGGAATGG 1140 AGGGCACAGG CCACGGCCCA GGCTTGGAAT TTGGTCTGAT TCCAGAGTCA CACGGGCCAC 1200 AGTGCACACG CATACAGGGA CGTGTGCACA AACACCTGCA CAACCAGGTA AATACATAAC 1260 CACACACAGA TGCGTGTGCG CACGCCCAGG CACACATGCA AATGCCTGCG CACGTGGGCA 1320 GGCACCCACA CATAATCACA GGGCAAACAT GCTCACACAC AGACACGTGC ACACCCCGGT 1380 GCACACAGAG GCGTGCGCTC AGGCGCTCGA ACACCTCCCC AGTGCCACCT CCTCCCGCCC 1440 CCTTTGCCAC AGGTAACTCC AGCTCTTTCC AGGCAGCCAG 1480
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