Tag | Content |
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EnhancerAtlas ID | HS116-17970 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:33383270-33384430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr2:33384371-33384382 | CTTGAGTGCTT | - | 6.02 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_01563 | chr2:33383324-33383754 | Aorta | SE_01563 | chr2:33383791-33384605 | Aorta | SE_26207 | chr2:33382880-33385303 | Duodenum_Smooth_Muscle | SE_39053 | chr2:33383211-33383768 | IMR90 | SE_39053 | chr2:33383887-33384945 | IMR90 | SE_45294 | chr2:33382980-33384989 | NHLF | SE_46037 | chr2:33382498-33385105 | Osteoblasts | SE_54947 | chr2:33382858-33385126 | Stomach_Smooth_Muscle | SE_55978 | chr2:33380284-33386066 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 33383509 | 33383834 | chr2 | 33383497 | 33384405 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I033157 | chr2 | 33382278 | 33386062 |
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Enhancer Sequence | TCCTCAGTCA TTTTGTAAAC CTTTGTTCAA CAAAAGAATG AATACATTGT GTTGTGTAAA 60 CTTCAGATAG AGATTGAGAG ACTATCAAAC CCAAATATCC AGGGATTAAG TAGTTACATA 120 GAAGTAAGTA GTTACATAGA AGAAATATTC TATGTAACTG GGGCACTGAC AGGCCCTCCC 180 ATCCCAGACA CAGAAGGCTA CTTACTGCCC ACCGGAGCTT CTGCAGGGCC TGATAATGAT 240 GGACATCACA GTTCTGTGCC ACTTTTTGGA ATTAATCTAG AGAAAGAATT GAGACAGGGC 300 ATCCCAGATG AAGCCAAATA GGGGTGACTT ATAGTTCCCT GGTTAATTCC TGGAGGGGGT 360 CCTGAATAAC AGGCTCTTGG ATCATGCAAA GGAAGTAGAG TAATAAAGGA CCTATGAGAT 420 TCATTGACAT TGTGGTTGTC GAAGGAGGCA CCTTCTAGCC AGAAAATGGA AGATTTCTTT 480 CCAGTGATTC ATATGTATTA CCCAGAACAC TTTGACTTCC TGGAATTTAA AATATAAACT 540 CAAGTCTCTT GGCAATAACT TTTAAACACT GCAGATCACT GGCTTCTCCA CTCCTCTCCC 600 TTTTCCCCTA ACCCCGATCC TTTAAATAGA TAGCAGTATA CGTACATGTT AGGTAGCTGT 660 GATGACAAAA AAGTTCAAAA TGATGCACAG AGTGTACCTT CTTTCTTTTC TGTGATACTG 720 TTGACACATT CTCAGTCCAG CACAGTATAA CCATGCAATA GGAAACACAG TTCTTTGGAG 780 AGCTCAGTTA AGTGAGATGA AAATACCTAT CGTGATTCTG TGTCTCATGG CCAGGCAGGA 840 TGCAATGACA TGGGAATGCA GGGGGCCTAG GGTCTGCCTA ATCTCAGCCC TGTATGTGCT 900 TCTGTGAGTG AGGGAACAAA GTACCTGCCT AGCAAGCTGT GGCCTGGGTG GTGACAGCTA 960 CATTTTGCTT GCTTCCCTCT CCTAAGTGAG CAGTATACTT GCTGCTGTGG CTCCGCAACT 1020 CAAGGGCGTC CTATCACAAA TAATGAAAAA TATGGGTCCT TTCAGCATAC AGATGACTTA 1080 GTGGTAATAG TCCCTTCGAA CCTTGAGTGC TTGCTTATAA AGTCAAGGCC CAGCCAATCC 1140 AGCAGCCACT TCACTGAGCT 1160
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