Tag | Content |
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EnhancerAtlas ID | HS129-19321 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:33383340-33384550 |
Target genes | |
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 | AGATTGAGAG ACTATCAAAC CCAAATATCC AGGGATTAAG TAGTTACATA GAAGTAAGTA 60 GTTACATAGA AGAAATATTC TATGTAACTG GGGCACTGAC AGGCCCTCCC ATCCCAGACA 120 CAGAAGGCTA CTTACTGCCC ACCGGAGCTT CTGCAGGGCC TGATAATGAT GGACATCACA 180 GTTCTGTGCC ACTTTTTGGA ATTAATCTAG AGAAAGAATT GAGACAGGGC ATCCCAGATG 240 AAGCCAAATA GGGGTGACTT ATAGTTCCCT GGTTAATTCC TGGAGGGGGT CCTGAATAAC 300 AGGCTCTTGG ATCATGCAAA GGAAGTAGAG TAATAAAGGA CCTATGAGAT TCATTGACAT 360 TGTGGTTGTC GAAGGAGGCA CCTTCTAGCC AGAAAATGGA AGATTTCTTT CCAGTGATTC 420 ATATGTATTA CCCAGAACAC TTTGACTTCC TGGAATTTAA AATATAAACT CAAGTCTCTT 480 GGCAATAACT TTTAAACACT GCAGATCACT GGCTTCTCCA CTCCTCTCCC TTTTCCCCTA 540 ACCCCGATCC TTTAAATAGA TAGCAGTATA CGTACATGTT AGGTAGCTGT GATGACAAAA 600 AAGTTCAAAA TGATGCACAG AGTGTACCTT CTTTCTTTTC TGTGATACTG TTGACACATT 660 CTCAGTCCAG CACAGTATAA CCATGCAATA GGAAACACAG TTCTTTGGAG AGCTCAGTTA 720 AGTGAGATGA AAATACCTAT CGTGATTCTG TGTCTCATGG CCAGGCAGGA TGCAATGACA 780 TGGGAATGCA GGGGGCCTAG GGTCTGCCTA ATCTCAGCCC TGTATGTGCT TCTGTGAGTG 840 AGGGAACAAA GTACCTGCCT AGCAAGCTGT GGCCTGGGTG GTGACAGCTA CATTTTGCTT 900 GCTTCCCTCT CCTAAGTGAG CAGTATACTT GCTGCTGTGG CTCCGCAACT CAAGGGCGTC 960 CTATCACAAA TAATGAAAAA TATGGGTCCT TTCAGCATAC AGATGACTTA GTGGTAATAG 1020 TCCCTTCGAA CCTTGAGTGC TTGCTTATAA AGTCAAGGCC CAGCCAATCC AGCAGCCACT 1080 TCACTGAGCT CTGGAGTTTG AGTTATCAAA AAGCTGTCAC CTCTTACACT TCCTGTCTAG 1140 CACCTTTTAA AGGTAACATC ACTGCCTCCA CTTCCAAAAA AGAATTTCTG TTCTCCATCT 1200 CTTCTATTTC 1210
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