Tag | Content |
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EnhancerAtlas ID | HS101-01610 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:54762880-54765160 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF3 | MA0640.1 | chr1:54763481-54763494 | TCACTTCCTGGTT | - | 6 | KLF4 | MA0039.3 | chr1:54764892-54764903 | CCACACCCTCT | + | 6.02 | RUNX1 | MA0002.2 | chr1:54764137-54764148 | AAACCACAGAG | - | 6.14 | Sox3 | MA0514.1 | chr1:54763463-54763473 | AAAACAAAGG | - | 6.02 | TCF3 | MA0522.2 | chr1:54764328-54764338 | AACACCTGCT | + | 6.02 | ZNF263 | MA0528.1 | chr1:54763699-54763720 | TCTTCTGCCCCCTCATGCTCC | - | 6.24 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_01019 | chr1:54763385-54764722 | Adrenal_Gland | SE_01595 | chr1:54759882-54763142 | Aorta | SE_01595 | chr1:54763205-54766233 | Aorta | SE_03451 | chr1:54763335-54764813 | Brain_Angular_Gyrus | SE_04187 | chr1:54762347-54767014 | Brain_Anterior_Caudate | SE_04901 | chr1:54759648-54768125 | Brain_Cingulate_Gyrus | SE_05919 | chr1:54759767-54771349 | Brain_Hippocampus_Middle | SE_07802 | chr1:54760466-54768146 | Brain_Inferior_Temporal_Lobe | SE_08904 | chr1:54763438-54764392 | Brain_Mid_Frontal_Lobe | SE_24580 | chr1:54763280-54765674 | Colon_Crypt_2 | SE_25961 | chr1:54763062-54766000 | Duodenum_Smooth_Muscle | SE_26701 | chr1:54761810-54766205 | Esophagus | SE_28122 | chr1:54763260-54766102 | Fetal_Intestine | SE_29698 | chr1:54763517-54764671 | Fetal_Muscle | SE_31383 | chr1:54762143-54763114 | Gastric | SE_31383 | chr1:54763224-54766540 | Gastric | SE_33414 | chr1:54760874-54771052 | H2171 | SE_41585 | chr1:54763231-54765192 | LNCaP | SE_42582 | chr1:54763182-54765442 | Lung | SE_46626 | chr1:54763560-54764562 | Ovary | SE_46626 | chr1:54764577-54765151 | Ovary | SE_47967 | chr1:54763774-54764522 | Pancreas | SE_50141 | chr1:54761833-54763128 | Sigmoid_Colon | SE_50141 | chr1:54763195-54766115 | Sigmoid_Colon | SE_52383 | chr1:54763209-54766161 | Small_Intestine | SE_54182 | chr1:54763572-54764609 | Spleen | SE_54942 | chr1:54761882-54766050 | Stomach_Smooth_Muscle | SE_63284 | chr1:54754699-54809827 | NCI-H82 | SE_65414 | chr1:54763199-54766030 | Pancreatic_islets | SE_66951 | chr1:54760874-54771052 | H2171 | SE_68686 | chr1:54763342-54765795 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I054297 | chr1 | 54762821 | 54766370 |
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Enhancer Sequence | GGGTCTGGTA CCAATTTGGG ACAGGAGTCC AACCTGAATT TGCCTATCTG TAAAAAGAGA 60 AGTCACCATT CCCTGCCTGG CCTACCTCAC AACAGTGGCA TGAAGCACAA ATGAAGAAAC 120 AGACATAAAA ACTGTCTCAA GGCTGGGTGT GGTGGCTCAC GCCTGTAATC CCGGCACTTT 180 GGGAGGCCAA GGCGGGCGGA TCACTTGAGG TCAGGAATTC GAGACCAGCC TGGCCAACAT 240 GGTGAAACCC CCCTCTCTAC TAAAAATACA AAAATTAGCC GGGCGTGGTG GTGCCTGCCT 300 GTAATCTCAG CTCCTTGGGA AGCTGAGGCA GGAGAATCGC TTGAACTTGG GAGGCAGAGG 360 TTGCAGTGAG CCGAGATCAT GCCACTGCAC TCCAGCCTGG GAGACAGAGT GAGACTTTGT 420 CTCAAAAAAC AAACAAAAAA CTGTCTGAGA ACAGAAGGGC AACGCCACCA TCCCCATCAC 480 CCTGGATAAT CAAAGGAGCT GGGAACAAAG ATGCCACACA AGAGCACTGG GTGAGGAGTC 540 AGGCTTGGCT GGCTGCCCCC AGAAGGCCCT TCCCTGTACC CATAAAACAA AGGGAATGGA 600 TTCACTTCCT GGTTTCCAAG CCTGGTTGCA CATCAAAATC ATGTAGTGAG CTTTGCAACA 660 ACTAAGCTGC CTGTCTTCCT GAGGGGGCAG GGATCCAGCT TCTGGGAGCT CCTGGACCAG 720 ATGTTCCATC AGATCCCTCC TCAGTTCTGT CTCTACCCTG ACCCCAGCAG GGGAAACAGA 780 TCCCAGGTTC TGGGGATGGC TGGGCCAGAT GCGCAGGCCT CTTCTGCCCC CTCATGCTCC 840 CCAACCAGTC TCCTAGGAGG CCTGCAGGAA GCCTCCGGGT GCAGGTCAGG GCTTCAACAG 900 CTGCCCAAAC AGGTATGGGC CCAGATTTAA TTGGCCTCTT GGTTAAGCTT TCTAATCTCA 960 TTAAAGCTGC CTCCATCAAG CAGACCGAGG CTCTGAATTG AATCACAGAA GAGCGCTGCC 1020 CTGCCCCACT GTAAGCTGAT TAGGTCTGGG GAGGCCTAGC TCGGACCCCT CTCTGCACTA 1080 CCATGCCGTA CGGTCACACG GAAGGCACGA ACCCAGACTC ACGAAGAGGG GCACACTGAC 1140 GAGGGGGCAG CAGGAAGGAA GTTCAGCGAA GCAGTCCCAG CAAGGGTGTG GTACCAGACC 1200 TGCCTACTCC CACCACTCTG GGGAGCCAGT GCTGTCCCCA GGATTTTCAG TAAATACAAA 1260 CCACAGAGTA ATCTGATTTC CTATCTTATC AGTGTGCAGT GCCAGAGGCC ACCCGGCTCC 1320 AGGAGAAAGC TGCCCTTCTA GGCAGAGCGT GGGACTCACA ATTACCTCTC CAACTTCTTT 1380 TCGTAGCTTT AGAGCTCTAC TTCATTCAGA TGGAAAGGAG GCAGCAGAGG GGTGTGGTGT 1440 GGGGCCCAAA CACCTGCTTT CCATCTCTAG AAGAGAGGAC TTGTCTTGCC ACTCACTCTC 1500 TCCCTGACCC CTTCCACCTC CACAAGGAGC TACACTGCGG CTCTTCTCCG ATCCAGCTCC 1560 TGGACGTCAG CTTCAAAAAC ACCATGGTCA GCGTGTGCAA ACAGCCCTGA GCAAATACGC 1620 GTCGCCCACT TCTCCATCAT CTCGCTTTAT CTAAATATAT CCCAAGGAAA TAACTTGGCA 1680 GTGGTGAGAA ATTCTGCAGA GGCTCCAAAG TAACAAAAAC AAAACACACA CACACACACA 1740 CACACACACA CACGAGCTCT GTTCAAGGTG CCACGCTGAG CTGAGGATAG GCATGGAGAT 1800 ACAAACACTC ACAAGGAACA GCCACCCAGG GTGTGCTGGG GGTTCAGTCC CACTGAGGGT 1860 TCGTGCTTGG TTGTTATTAA TATTTAATAG GGAAGACAAT ATTTTAGAAG AGACAGGACT 1920 CTGTGCAGGT TGCAGGCCAG GCTAGCATAG ATGCCCTGTC CAAGGGAGAT GTTAAGGGGG 1980 CACGCCTAGC CAAGTACACA CACACACCCA TCCCACACCC TCTGGGACTT GCTGCAAGAC 2040 ACTGGTATTT TCCGCTCCAC TTGCCAAGAA TGGAGCCACC CTGCCCTGCA TGCTTGATCC 2100 TCAAACTCCT GGAAACAAAG GCGGCAGTCA CGGGGGCGTG CTAGCACACC TCAGGCACTG 2160 GTCCGATGTT CCCCTACCCT CTGCCATTTT CACTAAAGGG GAAACTAAGG CCCAAAGCAG 2220 AAGACAGACA TGCCCAGAAC CTGGCCAGGG TCCCTCTTAC TCCACCACGC TGTCGATAAT 2280
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