Tag | Content |
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EnhancerAtlas ID | HS147-02696 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:115627320-115628500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SRF | MA0083.3 | chr1:115627533-115627549 | TTGCCATATATGGAAT | + | 6.25 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_01910 | chr1:115626841-115628711 | Aorta | SE_12264 | chr1:115627545-115628557 | CD3 | SE_12941 | chr1:115627135-115628701 | CD34_Primary_RO01480 | SE_13473 | chr1:115626884-115629213 | CD34_Primary_RO01536 | SE_14129 | chr1:115626971-115629195 | CD34_Primary_RO01549 | SE_14940 | chr1:115627159-115628548 | CD4_Memory_Primary_7pool | SE_16535 | chr1:115627461-115628280 | CD4_Naive_Primary_8pool | SE_20532 | chr1:115626812-115629663 | CD56 | SE_54685 | chr1:115624380-115634175 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I115084 | chr1 | 115626914 | 115629662 |
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Enhancer Sequence | TGTCTCTGAC AGGTGATTGC TCTGAAGTTA CTGTTTGAAA TAAGTTTGGG AAAGAGTGGA 60 AGGTGACCTC TATGAGATTC ATGTGAGTCA AACTTCTTTG ACTCCCAAGC CTGCAAGACA 120 CTGTCTTTCT TAAATGTACC TGTTAGGCAT CCCCAAGTGA AAACCCAAAG CTGTATTAAT 180 AATGGTGAGA AGGAAAGGAG GGCAACTTCA GACTTGCCAT ATATGGAATC TGCTTTTCAA 240 CAATGAACAG CTCTGCTTCC TGTGGGTCAG TAACGCTGAG CAGCTAGTGC AGCACAATGA 300 TAGGAAAACA CTGACCATAC AACAATAAAC CAAGGAATAA ACAGCGCCCA GGTTTTCCTT 360 TAAGCCAACA TATGCGGCTT GGTGGGGGTG TAGTGTTTTA TTTATATTGC TATGCAACGT 420 AGGAAAAAAA AAGGTGATTT CAATGAAAGG CACAGGAATA TGCTGTGCTA TCTGATCGCA 480 GGTCTGAATT TAGACATGAC AGATGTTGGG AGGGGTTTCA CATTTGACAT CAACCACGAT 540 AAGAGAAATT AATGTAGTGG GGTTAATGGC TAGGCTTTAT TTTGTTTTTA AAAATTCAGT 600 GGTGAGTACA GTCAGCGGCC CTGGGCCAGG GAATACTGTG CTGGCTCTGG CAGGGCCTGG 660 TTGTATGTTT ATGAAACCAG GAGCACAGCC TAGGGAAACT TAAAGCAAGC TGCCAGAGGA 720 GGCTGCAAAT TGATCTGTTA AATCGCAGAT CACCAAACAG AACCTGTCCC ACCTCTATGC 780 TTACTTCTGG CGAGGTTCTG ATTGGAAGGA AGTGCTGTCA CCCAAGGAAC CCCGTAACTC 840 CGAGGGGCAG GCACATGAGC TTCTAAGGGT GTGTGTAAAT TTATACTTCA GTCACAGCTA 900 AAGTCTGGCC TTCTAGGAAA ACTATCCCCC ACCCCTTTCC CAAACTTCCC ACGAAGCCCT 960 CCAACCACAA AAAAACAACT TTAGAAACTT GAGTGGGGCT TTTCTGGAAT CAGGTTCCCT 1020 CAGTTACAGT GAAGGCAGAT ATCTAGATAC TTTATCCCAC ACTTTCCCTT AAGTCATGAG 1080 GTGCCTGTTT CAGTTGCCTC TTCGCTCTAG TTGCTGCCTC CACCCCCACC CCCCATGAAA 1140 CTGGGGGAGA GGAAGGTCCT TCATGTCCTA CTGCATGCCT 1180
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