Tag | Content |
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EnhancerAtlas ID | HS010-01464 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr14:68942790-68944240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ETV6 | MA0645.1 | chr14:68944188-68944198 | CACTTCCGCT | - | 6.02 | Nfe2l2 | MA0150.2 | chr14:68943104-68943119 | TGTTGAGTCATGCTG | - | 6 | PPARG | MA0066.1 | chr14:68943271-68943291 | AGTAAGTCATCTTGACCCAT | - | 6.72 | ZBTB18 | MA0698.1 | chr14:68943650-68943663 | TGTCCAGATGTTT | + | 6.07 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_10790 | chr14:68941587-68945700 | CD19_Primary | SE_11720 | chr14:68935880-68946652 | CD20 | SE_26831 | chr14:68943045-68944312 | Esophagus | SE_28965 | chr14:68942020-68944405 | Fetal_Intestine_Large | SE_34136 | chr14:68942695-68944042 | HCC1954 | SE_36586 | chr14:68941854-68944765 | HMEC | SE_55269 | chr14:68943617-68944052 | Thymus | SE_62722 | chr14:68925713-68995876 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I068474 | chr14 | 68941597 | 68945422 |
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Enhancer Sequence | TTAGTAGCCC AGAATCTAGT TAGGAGAGAT GTAGTTAAAT AAGTTTAATC AAAAGCCAAC 60 TGTGATACCT ATTACCAAGG TTCAAACAGT GGAATATAGA AGGATAAAGG GAATAGACTT 120 ATTCCAAGTA GGATGACTGA GGTAGGTTCT TGAGAGTACG TGGGACTTGG ACTGGATTTC 180 AGCTTGTGAA TACTGACAAA AACCGCATTC CATTGTCTCT TGACAGAAGC CAATTTCTTT 240 TGCTATTTGA GGATAGATTC AGGGACACTG GGGAATGCTG ATTAGTTCCA TCACTAATGC 300 TGATTAGTAG TGAATGTTGA GTCATGCTGA CTAATGTGTT CTAAATGGAT TGACTCAACA 360 ATAAAGGCAA CGTTGAGAGT CAAGAGTTCA GATCCTGAAT TTCACCGATG AAGTGTAAAT 420 CATTTCGCCA CTTAGTGCTT AATTTTTTTG TCAATTAAAA TGTGCTCGTG GGTGAGAATC 480 CAGTAAGTCA TCTTGACCCA TGAGGGCTTT ACAAACTTCA AGGATAACAG ACAGCTTAAC 540 AGCAACTACC AGGACAGGCT TATGCAACCT CAGGTTATTC ATAGCTCACA CAGAGTCAGA 600 ACACCCATCA CATGCTGCTC GCCAGCCATG CGAAACTTCT GTTTCCTCAC ACATGCCATG 660 AGAACTGACA AACAGTGCAC TGAACTCACA AAACCCGACA AATAGAGGAG CTTTTGAAAA 720 ATCTTCCTAT CTACCTACTG GGGTGTCTGT GTCTTTCTAC AACAAATGTC GCCACAGAAC 780 TAAGGGCTTG CATTGCAGAC ACAGCTCTTT CTCTCTTTTG ACATCTCCCC AGCTAGACTG 840 CTTGAGAACC TGGCCTTCCA TGTCCAGATG TTTACTGAAT TCTGAAGCCC TCCCAGAGAG 900 CCCAGGTTCT TTTGTTGCTC TCCAAATCAT TTCCCACAGA GGCTGACCAG TGTCCTGAAG 960 GAGCCCTTCA ATAGGGAGGA TAAATGAAGG CAGATGAAGA CATGACCCCC TGAGGCTTGC 1020 CCACATCCAC TGGAACAAAG GGTGTGAGGC ACAACCTTGT AAGGAGTGTT TTGGTCAGCC 1080 GCGTCCCTAT GCGAGGCCAA GTCTCCCCCA CAGGGCTGCT TTCAATGGCT ACCATCATAG 1140 TGGAAGTATT GGGCATTTGT TAAGGACTGT GGTGTGCTAG ATATAGCACA AAACATCTAA 1200 ATCATGGTCC CCTGCCTTTG TGAGGGCTTC CTGGCTACAG ATGGCAGCTG GCTTTCTCAG 1260 GGGAAACTTG GGGGTCATAG AGAAAGCTGA AGAGGGGTGC TTGCTTCTGT GGATGACCTC 1320 TTCCCACCCA GTGCAGCGAC ACTCCCCTTT TGTCTATAGC TATCCTTAGT CAAGCCAGGG 1380 CTGCGGGACC CTAACCCACA CTTCCGCTGT GTTTCTGGAT CTCTGGTTTG CAAGGCCAGT 1440 GGCTCTGTGG 1450
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