Tag | Content |
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EnhancerAtlas ID | HS048-11703 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr14:70471570-70472880 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr14:70471973-70471983 | GGGGATTAGC | - | 6.02 | HNF4G | MA0484.1 | chr14:70472205-70472220 | TGGACTTTGGTCCTT | - | 6.73 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34800 | chr14:70458321-70472832 | HeLa |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I070004 | chr14 | 70471439 | 70472899 |
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Enhancer Sequence | TGAGTGACAC AGACCTTCTC TGTCTACTGT CTGCTCTCTC CACCCGTCTC CCCCTTTGAC 60 CTCCACTTCC TCCATCACCA TGAGGTTCCC ATGTTCTTTC TCCAAAAAGC TTACAGCATA 120 GCTGGTCTAC CAATAACTGC TGACTGCATG TGCAGAAGGT GCTTTGGTGT TGGGTTACCC 180 AGGATCTCAG CTTTTCTGTC TGCTCCTTTC TTCAGCAGTT CCTCCTCTGG AAGGCAGTGT 240 CTAGAAAGAA AGGCCAGCCC AAAGATCTGA AACTCAAATC TTGTAATGTT TATGTTTTTT 300 GGCCATTTTT GCTTTAAACA AAAAAAGAAG AGAAAGGAAA AAGATGATGA AGAAGAAAAG 360 GTTTCTGGGA TAAAAGACTA AACTCTGGGC TAAAATCAAG TCTGGGGATT AGCTGAGGAT 420 TTAGGTTATC CATGCTTTCC TTTGTTCCTA ATCACCATGA GTAATTGAGA GGCACAGAGG 480 CCTGGGCTAG TCCTAGCCGA CAGAGCTGTG CTCCAGGCTT ATCCTCTCTT GGTGGGATGT 540 GAAAGAACCC GTGCCCTGGG CCTGGAGACA GGGTTCATGT TTGTCTGGTC CAACCTCTTT 600 TTTCCTCTCC TGTCTCCTGC CCTGCCCACT CCTGCTGGAC TTTGGTCCTT CTTTGCTATG 660 TGCAATTAGT GGTGGACAGG GTTGTGTGCC TTCTGGTGAC AAGGGGTGGA CATGGTTTCA 720 CTTCTATCTG AGTATTTACC ATGTGCCAGA CTAGGTACTG GACAGTTTGC TTGGATGTTT 780 TTTCTATTGT GTTTCTTCTC TTAGGCAGTC AGAGGTTTGT CAGTGAAACT TTAACCACTC 840 ATTGCCAAGT GCGGAATGAC CTGACTCTCA CTTCTTCTCT GCACCATCTG AGGGACAGGA 900 TTATAGGGGC GGGCGTGTGA GTGTGTATGT GTGGCCATGC ATTTCCATGC CCCCCTGGAC 960 AGCCCTGATT GTTCCCTCTC CCCTTCCGTT TATGGCTTCC AGGTGTTTAC AGATGGTCCT 1020 GGCCCATTCT CATAGATACC TGGCCAGACC TTCTAATCTT GTCATCTTTC CCTGAGTGTT 1080 CCTGAGCACA GATTATTTTA GAATAGTGTG TGTTCACTTC TGGGGAGCTC CCTCTCTGAA 1140 CCCATGATCA TGAAGAGACC CACAAAATAG GCCCCCTGTC TTGCATTCTG GAAGGGGACT 1200 TCTTGGTACC TAAGAAAACT GATAGATGTG AATTTTAAGA CCCATTTGGG ATTTAGGTAA 1260 CTGAGAAGGA AAGAGGATGA TAGTGGCCCC ATGGGTGGTC TGGCTTTTTG 1310
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