Tag | Content |
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EnhancerAtlas ID | HS007-07419 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr17:74655620-74656720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr17:74656111-74656122 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr17:74656111-74656122 | CTGAGTCACCC | - | 6.02 | Klf1 | MA0493.1 | chr17:74656316-74656327 | AGCCACACCCA | + | 6.14 | NFE2L1 | MA0089.2 | chr17:74656107-74656122 | TTTGCTGAGTCACCC | - | 6.88 | Nfe2l2 | MA0150.2 | chr17:74656109-74656124 | TGCTGAGTCACCCTA | - | 6.76 | ONECUT3 | MA0757.1 | chr17:74656201-74656215 | AGTAAATCAATAAT | + | 6.19 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_23442 | chr17:74655551-74657116 | Colon_Crypt_1 | SE_24491 | chr17:74655591-74656596 | Colon_Crypt_2 | SE_26767 | chr17:74655546-74657120 | Esophagus | SE_28083 | chr17:74655336-74656656 | Fetal_Intestine | SE_28742 | chr17:74655401-74656724 | Fetal_Intestine_Large | SE_50328 | chr17:74655302-74657159 | Sigmoid_Colon |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I076659 | chr17 | 74655144 | 74656944 |
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Enhancer Sequence | TACACTCCTG TCTGGATACA TTTCCCCCTC TCCTTTGATG TCCCCAGTCT GCCTCTTCTC 60 TGACACTGGC AGTTCTGCCC TGAGGCCCTC TTCTCAGACA GCCCTGCAGC ACTTTCTGCT 120 ACCCTTCTGT TTGGAACACT CAGAAGCCAA AGGTGCAACA ACCTGTTGTT GACCTTTTCC 180 TGCAGACTCC CCATTTCCTT GGGAGCTGTA GCCCAGGAAT CCCGTAGTGG TAGGAGTCTA 240 GCCCCAAGAC TGTAGATCAC TTAGGAGTTT CTTCTGTGAG AACATTCACA AAAATCAGAG 300 GGAGGATTTT GCCAGTGAGT GCAGCCATTC CCTGCGAGTC AGTAACCCTC TGCCCTGCAT 360 CCATCCCTGC AGGAAGGACC GGCCAAGAAC AATCGCCTCC ATGGATGAGC AGCCACCCGC 420 ACCGCCCGGG ACAGGGCAAG TCCTCTGCGG CACGGTGCAT TCACCATGTA ATTAGAGTCT 480 GAGTTGTTTT GCTGAGTCAC CCTATGTTTA TCACATATTT TGACACTTCC TTGACAGCAA 540 GCAGATGCCC CAAATTTTGT GTTTGCCCTG CTGGCGGTTA CAGTAAATCA ATAATAGTAG 600 ATAAGAAAAA CAAGTAAACA TCTCAAGCCC TAAAATGCAA TAAAATCTGT CATTAAAAAA 660 AACGGCTAGG AGGAAATTTG AGGGTTATCC TGCATGAGCC ACACCCAGAG CCATGCAGGG 720 AACGAAGTCT GCAGGTCCCC CGCTCTACCT TGGTGTCACC CAGGCATCTG AGAAACTCAT 780 CCACAGAGTC CAGCCCGAAG TTGCCATTCC CCAGAATGAG GAGTCTCCAG GGCTGGAGGA 840 GAGGCAGTCC CAGGATGCTC AGCTGGTTGC AACCCCTGTC CCCACTTGCA TCTCACCCCA 900 ATCAATAGCA CTATCATCAG GATTCACGTC CCTTTTTTTT TTTTTTTTAT TGAGACAGTG 960 TCTTGCTCTG TCACCCAGGC TGGAGTGCAG TGGTGTGATC TCAGCTCATT GCAACCTCAC 1020 CTCCCAGGTT CAAGCTATTC TCCAGCCTCA GCCTCCTGAG TGGCTGGGAT TACAGGTGCC 1080 TGCCACCACG CCCAGCTAGT 1100
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