Tag | Content |
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EnhancerAtlas ID | HS040-00325 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:9356800-9357740 |
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) |
NKX2-5 | MA0063.2 | chr1:9357553-9357563 | ACCACTTGAG | + | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00563 | chr1:9348992-9359362 | Adipose_Nuclei | SE_23490 | chr1:9356949-9357472 | Colon_Crypt_1 | SE_23818 | chr1:9356989-9357261 | Colon_Crypt_2 | SE_26667 | chr1:9356517-9358284 | Esophagus | SE_52461 | chr1:9351595-9357776 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I009296 | chr1 | 9356950 | 9357472 |
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Enhancer Sequence | TCTATGCGGG GCAAGAGTCG GGAGATGTAC GTCCTTTCTG ACTTGGGCTT GAGGCTCCTT 60 CCTTGCTTGG ACAAAGGGAG GATGGCAAAA CCCAACAGCA CATTGGGGGA TCTGTCCTGC 120 TGCCAACCCC CTGAAACCTT TGGGAAGCTG CCTGTTTGCT TTGTGTTTTA AAAGTTCTGT 180 TCATTGCCCA ACGTTAAAAA TAAATGAGTC CAGTGGTCAT GAGACAGACC ACATCAACAA 240 CAGGCTTAGG CTCTCGGGGC CTTTCTTGGA GATGGGGAAG AGAATCCGCC AAGGCACAGC 300 CCAGCCTTGC CTGCCATTGA GGTCCAGACC TTGTGCAATG CAGGCATGGG ATTTGTGGCA 360 GGGCTGGGTG TCAGGAGATG TGACTGTGAG AATGGTTTGT CAACAAGCTC TGAATCTGAC 420 CTGAAGCTTA GCCTGACCCT CTTGAGTTTA CTGCGTAGGC GATGGGTGGA GGAATCCAAG 480 AACCTCTGCC ACCCTTGGGC GTCTCTTGGA AAACTAGGGA GGCATTGGGT GATTTGAGCA 540 CAAGATGAAG AAAATATCAG GATGCAAACT CCACACTTGA GAAATGACTG CTGAGTAGGA 600 ATATAGGATT CCAGGGTTGG AAAAACCTAC CTGTGACAAG GGCTTGACGG GTGCCCCAGT 660 TGTGAACACA CCTTGCCAGA CAGTCAGAGT GTGGCCAATC TGGTCACACC CTTTCCAAGG 720 TCAGAGTGAG GAGCTGCACT CCACACCAAG AGAACCACTT GAGTTTTCTA ATTTATACAA 780 GCAGACACCA AGGGAGCATG TGTGGGAGTG GATATTAGGA TGTGGAACGA ACATGAAGTT 840 GGATCTGGCC GAATTTATGG ATATGGGCCC ACTAAGCGGA GATTCTGCAC TTGATGTTGT 900 AGCTCAGGGG GTTAAGAAGA GATCTGTTTG GTTGGCTGAC 940
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