Tag | Content |
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EnhancerAtlas ID | HS148-01538 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:206939280-206940320 |
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) |
PBX1 | MA0070.1 | chr1:206939368-206939380 | ACATCAATCAAT | + | 6.44 | TCF7L2 | MA0523.1 | chr1:206939770-206939784 | TCGCTTTGATGTTT | - | 6.54 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_18640 | chr1:206938558-206940480 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19631 | chr1:206939257-206940450 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_61266 | chr1:206939355-206991151 | HBL1 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I206765 | chr1 | 206939241 | 206940345 |
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Enhancer Sequence | TTGTCACACA GCCTCAGGAA GTTCTGATGA CATGTGCCCA AGGTGGTTGG GGCACAGTTT 60 GGTTTTATAC ATTTTAGGGA GACATGAGAC ATCAATCAAT ATATGTAAGA AGTACATTGG 120 TTCCATCCAG AAAGATGGGG ACAACTCAAA GCAGGGAAGG GGCTTCCAGG TCACAGGTAG 180 GTAAGAGACA AATGGTTGCA TTCTTTTGAG TTTCTGATTC TTTTCCAAAG GAGGCTATCA 240 GATATGCATC TATCTCAGTG AACAGAGGGA TGACTTTGAA TAGAATGGGA GGCAGGTTTG 300 CCCTGAGTAG TTCCCAGCTT GACTTTTCCC TTTAGCTTGG TGATTTTGAG GCCCCAAGAT 360 TTTCCTTTCA CAGACTCAGG ATGTCTTCTT CAGTTCAGGA TGGACAGCCT CAGAGTAGAG 420 AGCTTCAGGC CCCCTCTCCT TATCTTCTGC TAACCTCCAT TCTTACTCCT ACCCTTTCAT 480 CTCAGAATTT TCGCTTTGAT GTTTCCCACT TCCTTCCTAT GGTTACTTTA ACCGAAGTGA 540 GTCAGGTCTT ACTGAAAAAC TGACCACAGC CTGTCCGCTC CCAGCCTTCC CCAGACCAGG 600 GCTGCCCAGG CAGAGCGTGA GGGGGACTAG TGTTTACTCA GCTCATTTTT TTCCTCCTCT 660 CTCCTCTAAG TCACGGGGCT TTGAGTAGGG CTTCCCCAGC CACCGTGCCC CTCCCAGCAG 720 ACCGCAGTCA GAAGCCAATC TCACATTTGT CTGGTGGCTC AGAGAGGGGA CAGAAAGAGC 780 AGCAGCTTAT GTCCTTGGCT ATCCTCTCAA GTGGGCTAAT TTGCTTATTT TCAACTCTGT 840 TGGGTCCAGC CCTGTTGCCT CTGATCTCAG CTCAAAGAGG ATTTGGCGGG AGTTTTTGGT 900 TGTGATAACC AATAACAACC AACTATACGC ACTGCGAACA TCTCCTAGTG CCAGAAGCCC 960 TGTTAGCTCA TTATCTTAAT CCTCAGGATA ACCCAGGCAA TTTGTATTCA CCCTAAAAAC 1020 TTCCCCTGGC CGGGTGTGGT 1040
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