Tag | Content |
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EnhancerAtlas ID | HS047-26755 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr5:38830070-38831520 |
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) |
RARA | MA0729.1 | chr5:38830392-38830410 | CCATGATCTTTTGGCCTT | - | 6.2 | RFX5 | MA0510.2 | chr5:38830524-38830540 | AGTTGCTATGGCAATA | - | 6.04 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_34224 | chr5:38829410-38833357 | HCC1954 | SE_36357 | chr5:38829625-38833381 | HMEC | SE_64916 | chr5:38830053-38832202 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I038829 | chr5 | 38829370 | 38833135 |
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Enhancer Sequence | GGAAAAGTTG TTTCTCCCTG AAAGACTATA CCCTAAATAA TACAAGGGTC ACAAGGCATA 60 TTGCTCTCCT TTATAACAAT GGCTGTGTGG TCCAGCTGCC ACACAATATC CAAGACTGGT 120 TCCACAATGA CAACTGCATC TTTCAGGAAC AGCTTCCATA ACTTGTTCTC TGCCTATTAG 180 AAGTCTCCTC TGACTAGAAC AACATCGAAA GATGTTTCTC TTCTATATCT CATGACATCT 240 GGAGAATTTG GGGCAAGAAT GAACAGCACC TTGTAGGATG CTCTTGGAAA CTTTGTCTTC 300 TTGGAAACAA TATACATATT CCCCATGATC TTTTGGCCTT GGAGTCAGCC AGCTTGCAAC 360 AAATTCAAGC TCTACCTACC ACTCAACAGC AATGCTACTG AGCTTTTCTC TGTCTCAGTT 420 ATAAAATGGG GTAATAATTG TACTTGTCTT CAAAAGTTGC TATGGCAATA TTTTTAGGTG 480 AAATTTTATG CAAGTTTACA TTATTATAAT TATACAGTTA AATTATCCTG CTTTTGCAAA 540 TGTTAGGACA AAACATGACC ATGTAAACCA ATCCTTGAGC CTCTCTCTGG GTCTATGGAA 600 AAGTCTGTGT CATTAGCTTC ACAGTAAATC CACTCTGACT ACCTCACAGG GGAATTAGAG 660 GATGACACAA CATACAGTCA GGGCCACTGG CACAAAGGTA ACTTTGTGCT TATTACACAA 720 GGGTGACCCC TCCAGATTGA CACAGGGCTC AGGGCCAGCA AAGCAAGGGC TAGATTTTAG 780 CTCTCACTAT TTTTCTTGGT TGGGGGCCTT TGGCATTGGC AAAACTGGAG GTTGCTGATA 840 TAGCTGGGGG TTGGTGCACT CCACCAAGGT CCTTGGCCAG CAGGGCGGAG GTGAGCAGGA 900 ACCACATTCA AGTCCCCTTT TCTTGCCAAG TTGTGTGTCT CGACATGCAG CTGCATATAC 960 CCAAGAATAG GGCATGTTTG GCTTCACACG AAATCTCTGT CTTTCTGCTA AACCCTGCAC 1020 CTACTTTTCT CTAATGTGTG CAGAGGTGCC TTAGAGCTTG TGGGTGGGCC AGCACATTGC 1080 ACCAGTATAG GTAGCAGCCC TGATCCCTGG CACGCAATAA GCACTTTACA AACCTAAACG 1140 TTCCTTTGTG TCCCTATCCC ACCCCCCATT CTTTCCTACC TATATAATGT TTTCCTTACT 1200 TGCTCAACCT TGTATAACTC GAGGTCATTA AAAAAGTTAG TTTGCATATT TTCAAGGAAG 1260 CAATTGGAAA CCTAAGTTGC TCCAGGGAAT TGCCTTACCA GTGTGTCCCT GTGCTTCCAG 1320 GGGATTCCAC ATAAGATAAC ATCTTTGGGG ATTTTGCCAG ATTCCTTGTC TGTATGCATT 1380 GGGGCACCGT GACAAAAATC CTTCGCTTGG CCAAACTTTA GTCAGAGTCC TGAACCCTCT 1440 CGTAGGCTCA 1450
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