Tag | Content |
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EnhancerAtlas ID | HS133-00841 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:27164770-27166580 |
Target genes | Number: 28 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr1:27165379-27165394 | GGGTTATGGTGACCT | - | 6.2 | Myod1 | MA0499.1 | chr1:27165460-27165473 | TGCAGCTGTTTCC | + | 6.19 | Myog | MA0500.1 | chr1:27165459-27165470 | CTGCAGCTGTT | - | 6.02 | Nr5a2 | MA0505.1 | chr1:27165418-27165433 | GCTGACCTTGAGCTG | - | 6.95 | Tcf12 | MA0521.1 | chr1:27165459-27165470 | CTGCAGCTGTT | - | 6.62 | ZNF263 | MA0528.1 | chr1:27166293-27166314 | GGAGGAGCAGGTTGAGGAGGA | + | 7.33 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_11995 | chr1:27164883-27166629 | CD3 | SE_17155 | chr1:27164628-27166664 | CD4p_CD225int_CD127p_Tmem | SE_17869 | chr1:27164128-27167250 | CD4p_CD25-_CD45ROp_Memory | SE_20193 | chr1:27164684-27166462 | CD56 | SE_22451 | chr1:27164809-27166659 | CD8_primiary | SE_24351 | chr1:27165187-27165532 | Colon_Crypt_2 | SE_50491 | chr1:27164913-27166801 | Sigmoid_Colon | SE_53016 | chr1:27164679-27166873 | Small_Intestine |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I026838 | chr1 | 27164718 | 27166958 |
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Enhancer Sequence | CCACTGTGCC TGGCCCCTTG CTTTCTTTTT AAATTATTTT TTGTAGAAAC AGGGTCTTGC 60 TGTGTTGCCC AGGCTGATCT CTCAAACTCC TGGACTCAAG CAGTCCTCCA GCCTTACCCT 120 CCCAAAGTGT TGGGATTACA GTCACGAGCC ACTGCACTCG GCCTGTTGCT TTCTTGAATG 180 CTGCTTCCTG CCTCCACCCC ACATATTTCC CTCTGTGTTC TTGAGGCATT GAGTATAGGC 240 ACCAGTAATG TCATTAATTG AATAGCTATT TAGGTCAGAT CTTGATATTA TGTTATTTCT 300 GATTTGTGTA AAATTTTACA AGGTTGATGT CATCATTACC CATTCTACAG GTGAGGAAAG 360 TGAGGCTTAG AGATTGATCA GCTTCTTAAG TTTACAGGCT AACAATTGGC CATGCCAGGG 420 TTCAAAATAA GATTAGGCAG GCCCAGAGTC ACCACACAGA GGCACTGCCT TGTAGGAGGA 480 CTCTTAATTA TCCACTTCTG TCTGACTCTG CCCTCAGGCG GGCTCTTCCT GTATCCACAG 540 GCCTAGCACT AAGCCTGGTA TGTGGTGAAG GCCCCATGAA CCCCAGAGAT GGACAGAAGT 600 GGTCTGGGAG GGTTATGGTG ACCTAGCACT CGAGGCCTGG GAGCTGTGGC TGACCTTGAG 660 CTGGCCTTAG AGGCGGGGAG ACTGCAGTCC TGCAGCTGTT TCCTCTGCAG GTGACAACAG 720 TGGAAGGGCA GAGGGCAGTC AGGGCCTTCT CAGCAGCCCG CAGCCAGCCC TGGGGAACTT 780 CCACAGCCCC AGCCTTTCAG GCTCTGACCG CAGAAGGCCT GCCTGCTCCT CTCCGAGAGC 840 TGTCTTAGGG TGGGGAAATT CCTTTGCCCT CACAGCCATT CAGTGACGAG TAGCCTTGCT 900 TTTCGTCTCA TTTTCACATC CTCAGAGCTT TGGTTTCTGC CTGGAAGGCA GCAGGAGGGC 960 CTTGCTGGCA TAAGGGCACC TTTTTACTTG GGAAGAGCCT GGCATAGCAG AAACAGCCCT 1020 GGAGTAGATC TTAGATTCCC TGAGGGCAGG GATAGCATCA CTTACCATCA CTCCCTTCTT 1080 TCTTCTTTTC TACAACAAAT ATTTTTTGAA CATCCACAGT ATGTCAGGCA GGCACAGGGT 1140 GAACAAAACC AATATCTTTG ACTCATTTCT ATGAATTTGC CCCTTACCTT CCCTGCCACC 1200 CCCAGGCCTT GTACAGTAAC TTGCACATAG TAGGTGCTCA TGTGTGAAAG AGTGAACAAA 1260 TGAGTGCCCT GGAAGACAAG GGTCCTAGTT TCAGCCCCAC CTTCTATTAT TGGAGTGAAC 1320 TTGCTTTCCC ATCTGTAACT CACAGGCACG GATCCCCTTG CCTAGCCCAG AGCAGTCTCT 1380 GTGATTGAGT GAGACTAGGA ATGTCAGCAC ACTTTGTAAG TCACTTTTCT CTATTGAAAC 1440 TGAAGAGACT TGAGTCTTTT GGTCAGGAAT GGAGAGTGGA CTTGCTCCAG GTGCTAACAA 1500 GCTGCCATCG GTAGTGGCTG CCAGGAGGAG CAGGTTGAGG AGGATTCTGA GGCTGAGTTT 1560 GGGGCGGTGA TGGGTCAGCA CTGTCCGGTC TGAGAATCAG CAATGGGAGA GCTGCTTGTC 1620 TTCCCCCATG AAGGGTGCAG CCCCTGCAGA GCCTCCTTTG TCCCAACTCT GGCGACTTTG 1680 ATTTAGCACC AGGTGGACTC TTGCTCCAGC ATGACACAGC GCTCTGCCTC CCCTGGCTCC 1740 TGGCAGCCTC AGGAAGCCGG GGTACAGAGC TTCATTTGCT CTTCTGCAGA GTGCTGGAGA 1800 GAAAGAAGCC 1810
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