Tag | Content |
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EnhancerAtlas ID | HS030-10269 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr2:216697430-216699830 |
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) |
Foxd3 | MA0041.1 | chr2:216699508-216699520 | GTTTGTTTGTTT | + | 6.32 | Sox3 | MA0514.1 | chr2:216697702-216697712 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38160 | chr2:216695686-216701569 | HUVEC |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I215830 | chr2 | 216694725 | 216700091 |
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Enhancer Sequence | CTGGAGTGCA GTGGCACGAT CTCAGCTCAC TGCAACCTCC ACCTCCCAGC TTCAAGTGAA 60 TCTCCTGCCT CAGCCTTCCA AGTAGCTGAG ACTACAAGCA CGTACCACCA CATCCAGCTT 120 ATTTTTATAT TTTTAGTAGA GAGAGGTGAG GTTTCGCCAC GTTGGCCAGG CTGAGCTCGA 180 ACTCCTGACC TCAGTTGATC CACCTGCCTC GGCCTCCCAA AGTGCTGGGG TTACAGGCAT 240 AAGGATTTTA ATTGACATAA GCAAATGAGA GAAAAACAAA GGTAGATTTG TGAAATAAAA 300 GATGACTTTA TGCCAAATGA AAGCGAAGGA GGTTCAGGTG CCAAGGTCTC TATAGTTCAA 360 ATGGAGAAGT GGTGGAGAAA TTGGGGCCAC TCCAATGCCT TGTGCAACAG CATAAGCATG 420 CCAAATTCCA AAACCTGTAC CATGACAGCC AGTAATACAT TCACACTGTG AGTAGCAGTT 480 TAAATTTCTC AAAACTTCAT CTGTCACACC AAATTTATGT TGTTAATTTG AGTTTTACTG 540 GTTTTAGAGT TTTTTTCTTC AGTTTGTAAA TTTATTTCAG TTTTATAATT AGAAGAGCTA 600 TAAGCATCAG CCTTTACACC CAGCTTTATG TTTGCACTTA TGTAAGTAAC ATTGTCATTA 660 AATTAACAAT GACACTGAGG AAAACTGTTC CTCATGTTCA CATAAGCTTT GGAAACTAAT 720 CTTTTACATT AACAGTGGTT GTTCCTAGCC ATGGAGTTAT CATTCCAGCT CCTATTGATG 780 GAATCAGCCC TGTTTTCAAT TTTTTAGTTG ATCAGAGATG AAAGAAACGG TCCCTTTTTG 840 TTTTCTAGAG GCTTGAGGGG ACACTTCTGG CCTTCTATGT GCAGGGACTA TAATTTCCCT 900 CAAATTTATC GGTGAAAGAA AATGGTCAGT TGAGAGTTGG CAAACATGTG AAAACAATAA 960 AGCAGAAAGG AAAACCCAAT TCAGTCCATT GCCTCAAAGA ATAGGGAAAA GGCTGTGTTT 1020 TCTGATAACA TATCTCATGG GAGACACCAA GGGACTACTG CAGTCTGCAT AGGCATGGGG 1080 AGAAGCCATG TTTTACATTA CAGGTCTAGA AAGTGAAATT GAACATTGCA ATCTATACCT 1140 ACCCATTTGT CTCCCTATCT CTAAAAAACA CATATGAGGA AAACAGTTTT GTTCTACATG 1200 GTGTCCAAAG GTTTGTCTTC AGACCTGCGC TGGTCTATGG AAAAATTTTC ACTGGTCTTC 1260 AACAAAACGA GGAAGATAAG GTCAACACAG TGTTTATATA AGTATGTTGG TGTAAGGTTA 1320 CCAGCTGTTC CCAGGAAGAA CTGTTCTTTG TTCTAAGATG TGATGTAACC CTAGCCACAC 1380 ACATGCTTAA AGCAAGCGTT TCCTCCAGGT TAGGAATCAA ACACATTCAT GGACTTCTGG 1440 CCTTCCAAAA TCACAAAGTA CTGCAAAATA ATGTTACATG CTAGCATTTT ATAATATAAT 1500 AAAATTATTA TATTATAAAA TTAAATTTAT TTTATAAAAT TATGTTGAGT AGAGTTCCTT 1560 TTATTTTTTA TTTATTTGGA CATGTAAAAA AATTACTTTT CTGTTTTGTT TTTGCTTTTT 1620 GCAGTTTTAC TGGTTCGTGA AAGTTCAAGA ACCATAGAGT AACGACAAGA GCTGTGACTT 1680 AGAGGTAAAG AAAATGGGGT TCTAACCTGA GCTTCACTAC CTCGGGAAAG CTGCTTAGCC 1740 TTTCACAGTC TCAGGGCCCT CATACAAAAA AGAGACGATA GCATCATCCT TCATAGAGCC 1800 ACATGTGAGG ATTCATGAAA CATACATAAA GCATCTGAGC ACTTAATAAA TGGACGTTAT 1860 CATCATTGGT AGCTATCAGC TCTTGGTTTT CTTTCTTTCT TTTCTTTTTC TTTTTTTTTT 1920 TTTTTTTTTT TTTTTTTGAG ACAGTCACTC TATCACCCAG CAGTGGCACA ATCTCGACTC 1980 ACTGCAATCT CCATCTCCCA GGTTCAAGCG ATTCTTGTGC CTCAGCCTCC CAAGTACCTG 2040 GGATTACAGG TATATGCCAT CATATCCAGC TAATTTTTGT TTGTTTGTTT TTGTTTTTGT 2100 TTTTTTTTTT AGATTGAGTC TCACAGTGTT GCCCAGGCTG GAGTGCAGTG GTGCAATCTT 2160 GGCTCACTGC AACCTCCGCC TCCCAGGTTC AAGTGATTCT CCTGCCTCAG CCTCCCAAGT 2220 ACACACCTAG CTAATTTTCG TATTTTTAGT AGAGATGGGG TTTCACCATG TTGGCCAGGC 2280 TGGTCTCAAA CTCCTGACCT CAGGTGATAT GCCCGCCTCA GCCTCCCAAA GTGCTGGGAT 2340 TATAGGCATG AGCCACTGTG CATGGCCCAG CCCTTGGTTT TTCATACATT CGATATAAAT 2400
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