Tag | Content |
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EnhancerAtlas ID | HS048-00485 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:20073750-20075000 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:20073810-20073830 | CCCCACCACACCAACCCTCA | + | 6.56 | ZNF263 | MA0528.1 | chr1:20074114-20074135 | TCCTCCCCTCCCTTCTTCCCC | - | 6.43 | ZNF263 | MA0528.1 | chr1:20074099-20074120 | ACTCCATCACCTCCCTCCTCC | - | 6.45 | ZNF263 | MA0528.1 | chr1:20074115-20074136 | CCTCCCCTCCCTTCTTCCCCA | - | 6 | ZNF263 | MA0528.1 | chr1:20074111-20074132 | CCCTCCTCCCCTCCCTTCTTC | - | 8.09 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_52839 | chr1:20073346-20075121 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I019747 | chr1 | 20074401 | 20074550 |
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Enhancer Sequence | ATTCTGAGGG AAAAGAGGCT GGTCTTTAGG GCCAGCTGTG CCCAGGATCC CTTGAGACAT 60 CCCCACCACA CCAACCCTCA AACAGGGGCC AATGCTGGGT AGCTACTCTG CCACTCAGAG 120 TAAGGCACCA AAGTCACCTT GAGCCCACTG ATGGTTTAAA AAGCTGAAAA CATTCTAAAA 180 CCCAGCCGGG GAATCTCAGT GTATGGGATG TACTACTTAC CCAATGGATC CATCCTAACA 240 GGGTTGCAAT TTGAATAATA AAAAGACAAA AAATAATAAT AGCAAGAGAA GCACAAAAAA 300 GATCTTTAAA CAGATGGACC CAGAAGAAGC ACAAAATAGA TAATCACAGA CTCCATCACC 360 TCCCTCCTCC CCTCCCTTCT TCCCCAACCT GCCATCTGAT CCCACCTCCC TCTGGGATAT 420 TTGGAAACCA ATTTCCTCCA AAATGATCAT TTTGAAGATG GGAGACCTTG GCCTTGGAGC 480 AGTAGCTAGA CTTGTTCAGA CTTGAAATGG AAATGCTAGA AAATCTAGCA AAAGGAAAAC 540 ATTTAGAGTG AATTGGGGTC AGGTGTGCCC TGAGAACTGC TGTTGTGAGC ACTCAAGAGT 600 CAGGAAGCCC AATTTTCCTA TTGGACATTC AGCCCTGAGC CCCTTTGCTG CGGCTGGGAT 660 GGAGAGGTTA TTAAGTAGGA ACTCTGAACT GAGGTTGGAG TCTGAACAAT AACTCAGTGT 720 GGAGTGATAG CAAAGCATGG TGATAATCAA AGAAGAAAAA TGGTTAATCT TTACCAAGGG 780 CTTCTTATAT CTCAGCCACT GGGCTTTGCA CTTCACAGGA TTAATCTTAT CCTAAGAAGC 840 AGTATGGTTA TTGTACCCAT ATTATAGATG AATTAAGGGA TAACAGTCAC TACCTCCCCA 900 TGAACTGTGA GGATCCAGAA ATAGATTATC TGTAAAGCAT TTAGCATGGC GGCGGGCACA 960 CTGCAAGTGC TCAGCGCAAC TGGGGCTGAT GTCATCACGA TGCTGCATCT CCCCAAGCCT 1020 CAGTTTCCTC TTTTGTCAAA AGGCGGACAC TAATTTCTAC CTCATAAAGT TGTTGGCTTG 1080 TAAGGATTAA ATTCATTCGT TCTTCGTCCA TTCAGTCAAT AAAGTTATAT TGAGAATGGA 1140 TGGCATGCTG TGCTTTCCCA TCTCCTTGAG CAGAAAAATG TATGTGCTCA ACCAGTACCT 1200 GTTTCCTTCC CATCTCCCTC CTTGTGAACC ATACATTTTA TTGAGAAATA 1250
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