Tag | Content |
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EnhancerAtlas ID | HS095-19181 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr21:40329490-40331820 |
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) |
Gata1 | MA0035.3 | chr21:40329680-40329691 | ACAGATAAGGA | - | 6.14 | SP4 | MA0685.1 | chr21:40330764-40330781 | GATGTGGGCGTAGCTTT | - | 6 | SRF | MA0083.3 | chr21:40331234-40331250 | TGACCTTATTTGGAAA | - | 6.01 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_25426 | chr21:40329363-40332454 | DND41 | SE_29427 | chr21:40325876-40332838 | Fetal_Intestine_Large | SE_39442 | chr21:40329593-40330913 | Jurkat | SE_39442 | chr21:40330986-40331666 | Jurkat | SE_50281 | chr21:40326133-40332526 | Sigmoid_Colon | SE_53397 | chr21:40330663-40331115 | Spleen | SE_53397 | chr21:40331130-40332045 | Spleen | SE_66408 | chr21:40329593-40330913 | Jurkat | SE_66408 | chr21:40330986-40331666 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I038954 | chr21 | 40326184 | 40332528 |
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Enhancer Sequence | GGACACTTAG CAAATGCTGC TTTTAATTCT TTCTTGCACT CATTCATTCA TTCAACAAAT 60 ATTCCCCCAG GCTTATGGAG CATGGGGCAC CACTGTAGGC ACTGGGGAAG TAGCTGCCAA 120 ATACAAAATA AAACCCAAAA AATCCCTTCT TCCCTGGAGC TTCCACTCTA CAGGTGGAGA 180 CAGAGAGGAA ACAGATAAGG AAACTCTAAG AGTTATGGGG TAAAGACAGC TGGGGGGGCG 240 GTGCGGGTGG AGGGGTTGCC TTGGTGGAAA GGTGATCTTA GAGCAAACAG GGAGAGAAGG 300 TGCAGAGGGA GCTCTGTGGT TACCTGGGGG GAAAATGGTC CTTCTACGCA GAGGGAGTGG 360 GAAGGGCCTA GGGGGAAGTA GGGCCAGCTT GATCCTGGGA GCCGTGTGGC TGTGGGCATG 420 GAGTAAATGG GGACGAGCAG GTGAGAGGTG AGGCAGGTAC ACTGAGGCCA GGTGGCCACC 480 AGGAGCACCT TGACTTTGCC TCTGAGTGGG ATGGCACTCA CTGCTCTGTG CAAAGGAAAG 540 TCATGACTGG ACTTGCTTTT TGCCAGACAC ACTTTGAGGC CAAGAGGGAG CAGGGAGAGG 600 AATGTTGACA TCATTGAGGT GTAGGATGAT GGAGTAAGAG ATGGACATGG TGGAGTGGGA 660 GCAGAGGCCA GGGTCTAGCT AGGTGTCAAT GGGGATGTTA CTGACAGAAA GACTCTACGA 720 TTCCTCCAGG TGGGGCATAC CCTCAACATC AGCCCATGGA TGGATGTTCC CAGACCCCAG 780 GAGTCTCACC ATAAATTCTC CCTGGGACAG ACTGTGGGTG GCAGTGGTCG CCATCTGTCC 840 TTGGCTGACA GGTGCCCAGA GCTGTGGCAG TGTCATTCCC AGCAGCCCCA GGATTAGGCT 900 GTTATCTCTG TTTACCAACA GGAAGAGACA CTCGGTGGAG GATTCAAGCT GATACAGGAG 960 CCGTGGATTG CCACCTGCCT CTTCTCCTAT GCCTGTCATG AGTACACACA CCAGTCCTGT 1020 CTGCTGGCCA AGCCCCCTTG CTCCCAGGTG GGAGAACAAT GTGTAGAAGC ACAAATTATA 1080 AACTGATTCT TGTGTTCTCT AAAGACAGTC TGTTTTTCAG ATCATGATTA GGAATGAGTA 1140 AACGGTAAGT CTCAAAGTTT TCAGGGGCTT ATTATACAGG GCCTATCAGA GTAAAAATAG 1200 AAATTACAAC AGCCCAACAT GGAAGAAAGT TTTCCTTCCT CACTCCCAAA CTTCAAACAG 1260 AGTCCGAGGG TTAGGATGTG GGCGTAGCTT TTTGGGGGGC CACAATTCAA CCCATTCCAG 1320 CTAACTTGAT TGAGTATTGA TGCCTTTTAA ACAAGCAATG GAGTGATCAT CGGAGATGAA 1380 GAAGCAATTT AAGCTCAACC CTCAAATGCA AACCCTTCCA AAGCAAACAT CCTAGGAGGT 1440 GCTACTTGAG TTAACCTCGG AGATGATTAA CCTGGGTTTT GCACCACTGC CCTGAGCCAT 1500 TTTCCACAGA ACAGAACAGA ACAGAATTCT TTATTATGTT TCTCAAGATG CTACTTTTCT 1560 ACACTGCAGT TATTTCAGGC ATGACTCATG TTAAAATGAG TGTGATAAGA TTTCTTGGTA 1620 AAACCCCTGG GAGGCTTTGA GTAGAGAGTT TTTAACAGTA GCTACCCCAA GCAAGGCAGC 1680 TGGAGTGGGT TGAATGGTTC CTCCCCAAAA GATCATCCCT GTCCTAACCC TTGGACTCTG 1740 ACTGTGACCT TATTTGGAAA AAGAGAGTTT ACAGATGTAA CTAAGTTTGA GATCTCAAAA 1800 TGAGGTCACC CTGGATTACA CAATGGGCCC TAAAGTCAAT TACAGGCATC CTTATAAGAG 1860 ACAGCAGAGA AGACACAGAC ACAGAGGGGA AGGCCATGTG AAGGCAGAGA ATGGAGTGAC 1920 GCAGCCACAA ACCAAGCAAT GCCTGGAGCC ACCAGAAGCT GGAAGAGGCA AGGAAGGGAC 1980 TCTTCTTCAG AGGGAGCAGG GCCCTGCCCA CACCTTAGCT TCAGACTTCT AGCCTCCAGA 2040 ACTGGGAGAG AAGAAATGTC TGTTGTTTGA AGCCACCCAG CTGTGGCACT TTATTACGGC 2100 AGCACGGGAA ATGCATACAG CCTCCAAAAG AGAACGAAGC CCTTCTGAGA GCTTGATTCC 2160 AGACATGCAA GACCCTGAGC CCACCGCGCC TGGGTTTCTG CCTACAGAAC TGTGAGATAA 2220 TCCATGGTTG TTTTACGCCA CTCCAATTGC AATAAGACAG TGAGGATGTC ATGTGAGTGA 2280 CCAGCAAGGC ATGTGGCCCA ACCAGACAGC CAGGGAAGGC CTTTAACGAG 2330
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