Tag | Content |
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EnhancerAtlas ID | HS095-06448 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:130778540-130779910 |
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) |
Myod1 | MA0499.1 | chr11:130779702-130779715 | AGCAGCTGTTTCC | + | 6.14 | TP53 | MA0106.3 | chr11:130779373-130779391 | TACAAGCTCTGACATGTT | + | 6.35 | TP63 | MA0525.2 | chr11:130779373-130779391 | TACAAGCTCTGACATGTT | - | 6.18 | Tcf12 | MA0521.1 | chr11:130779701-130779712 | CAGCAGCTGTT | - | 6.32 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_01768 | chr11:130778682-130780252 | Aorta | SE_37154 | chr11:130777760-130780914 | HSMMtube | SE_41512 | chr11:130778629-130779587 | Left_Ventricle | SE_46237 | chr11:130777645-130780693 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I130908 | chr11 | 130778051 | 130780341 |
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Enhancer Sequence | CAAAGATCAC TCAGGTCAAA ACTAAGATAT CTGGAGTTGA GTTGTTATAA CTTATCTACT 60 CATACAAGAC CAAATAAAAT AATCCTCACT AAAGATTAAC TCCATTTCTT CAGAATGGCA 120 AAATGACATA CAGATATTTG CTAAAAAGGA CAATGTACAA ACAAAACCTT AAACTATCAA 180 AGAAACAGAA CGAAACATTT ACTCTTCCTC TGGTGCTTCT TGCTAACTAA CACTGCTGGC 240 TCAGAGCAGC ACCATGCCTT CTTTGACTCA TTCTTGTGGT ATTCCTCCAT AAGGAGTAAG 300 CTAGCATAGC CAAGACAAGG CTGAAGAGAG TGGTCAGCAG ACTACAGTAA AGACTGGGGG 360 AGAACAAACC AGGGAAAGAA CACTTGAGGA TGCATGCATT TAGATAATGC AGCTTAGAAA 420 ATACAACTTG TTCTCCAGGA TCACAGAACT GTAGTCTGTG AGGGTGGGGA GGTCCTCATC 480 TGTCTCATTC ACTGATGTAT GAACAGCAGC TGGTAGAGTG TCTGGCTGAA AACAGGCATC 540 CAGTAAGTAG ATGTGGAAAT AATGGATGAA TGATATCTGC ATGGAACTCT GGGCATTTAC 600 CCAGTTGATC CCTTTTTAGT TTGTAGTTTT TTCCATAGCA GTGGATATCC CCTAACACCT 660 ACTACATGAA ATTCTATTTT ATTTGTTGCT CCAAGCCTAG ATGAGAAGAG GGAGGCTACT 720 CTTCCGCCAA TGTGTCAGTG TTTCCCAACC CTATAAAACA CACATCACTT TTGATAAACA 780 TAAGCCTCAG ACTTCTGCCC CAGAGATGCT CATATCAGTT GGTAATCACT GCTTACAAGC 840 TCTGACATGT TACACAAATG TCCTTCTTCC ACCATCTCCA TAGGTGCTGA GATAACCTCT 900 TGAAAAAGAT ACAATTCTCT CCATACTCTG TTCTCTAGCG GAGAACCATG ACACCACTCT 960 AAATCCAGCC TCAGGTCGTC TTAGGCTCTC TTTCCTGGGT GACCCAACAC TGGAAATGAA 1020 CTTTACCCTC TGAAAGACCA CCCCTCATGC CAGCTATCTG TGAAGACACA GATCAATCTT 1080 CACATGCCTC CAACAGTACA ACAATATAAT GATACCCCCA GGAGATATGT GTACACTTAA 1140 GAGTGTTGGG GTACTGTTTC CCAGCAGCTG TTTCCTGTGA TTCAGCAAGC TGATGATTCA 1200 ACCAATATTT GGCAACAGGT CTTGACAATT TAAGTCCATG TTCTATTGAC GGCTCTGTGC 1260 TGCCCCTTCC CACACCCTAC TGCTCTTATT TTTCAAGGAC TGCCTCCATT CTGATGAATC 1320 CTCCCCATTT ATAGATCAAA ACTAAAGCTG AGCACAGTGG CCCTGCTGGT 1370
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