Tag | Content |
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EnhancerAtlas ID | HS180-15878 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr14:105723400-105724580 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TCF7L2 | MA0523.1 | chr14:105724035-105724049 | TGACATCAAAGGAA | + | 6.42 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_24921 | chr14:105722568-105724638 | Colon_Crypt_3 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I105257 | chr14 | 105723554 | 105724516 |
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Enhancer Sequence | CTGCAGGCGC CACTGGGGGC TGCGCTCGAG AGACAGGTGT GGGGACCCCG CACAGGACCT 60 GTCTTCGCTC AGATGAACAA ACAGGACCAA GAATGTGTCC TAAGTGATTC AAAACTCACA 120 TGGATACATA AGTTATCAAA CACAAGTCAC TGGTTAATAC ACTCTGCCAG ACAGCTGAAG 180 TGCACATCTC CCATGGGCCC ACTGTAGCTT CGAGAAGTCA CTAAGGACAC CTCCTGGAGC 240 TGGATCAGGA GTCCAGAGCA GGGGTCCAAA GGAAGATCCC CGGGACCAGA GCAGCAAAGC 300 CCCACCACGC AAGAACCTCG CAAGCAATCA GATGGTTAGG ACGCCAGCCC ACTCATCCAC 360 GCCCTGGGCT GGAGGCCCCT GACCTCTCTT GCAACTCCAT GCAGAACAGC AAGGCCTCCC 420 ACCCTAAGAA GGTGCCAGGG CTGGGTACAG GGGCATTCCG ACACAGAGCA GAACCCCCAG 480 GACGGCTGGG ACGTGAGCGG TGAGGCCCGT GAACAAAGGT GCATCTGAAG GCAGGCAGTC 540 CCAGAGGGCC GAGACAACGG GCAGGACCGA CTGCAGCACA GCCAACAGCC TCACAAGAGG 600 CACTATGAGA AGACCGGCGG CAGGGGTGGG GCCAGTGACA TCAAAGGAAA CCAAAGGAAA 660 GCAGTAAGAA CTACCTGGGG AAACGCCCGT GACAGCCAAC ACACACCAAC GGGAAAAGTG 720 AACGAGGCCA GAAGGCTACA CCCTGTGTGA CTCCAAGCAT ACACCTTCCG GAAAAGGCAA 780 AACTATGGAG ACAGCATTAG GTCAGTGGCC ACCAAGGGCT GGGGAAAGGC AGGGTGGGTG 840 GGCCGAGAGG AGGGTTCCAG GACGCTGCAG CTCTGCACCA CTCCGCACTG GTGGGTTCAC 900 ATATTGCATA TTTGTGAAAA CCCATAGAAG GCACAGCCCC AAGAGTGAAC CTCAATGTGA 960 ACTGTGGACT TTTCTTATCA ACAACTTGGC AAGACGGGCT CATCAACCAT AACAAATGGA 1020 CCAGCTAACA CAAGATGTTA ATAACATAGG GAAATTGGGG ATTGAAGGGG GTGTATGGGA 1080 ACTCTGTACT TTCTACACAA TTTTTCTGTA AACTAAGACT GCTCTAAGAA ATAAACTCTA 1140 CTGGGCTGGA CGCGGTGACT CACGCCTGTA ATCCCAGCAC 1180
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