Tag | Content |
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EnhancerAtlas ID | HS133-00944 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:28213200-28214510 |
Target genes | Number: 30 | Name | Ensembl ID |
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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) |
Nr2f6(var.2) | MA0728.1 | chr1:28214492-28214507 | GAGGTCAAGAGATCA | + | 7.23 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09233 | chr1:28207973-28222018 | CD14 | SE_20343 | chr1:28208587-28215125 | CD56 | SE_50884 | chr1:28208283-28214544 | Sigmoid_Colon | SE_53500 | chr1:28208262-28214990 | Spleen | SE_62491 | chr1:28184415-28220281 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 28213825 | 28214033 | chr1 | 28213479 | 28214114 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027881 | chr1 | 28208477 | 28220166 |
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Enhancer Sequence | ATCATTTATT AAATTCTGAC TGCGTGCCAG GCACTTACAA ACCATATCCA AATCCTCAAC 60 TTTCCAGAAT GCCTGATTTT AAAGATTAGG GAACAGGCTG CATGGTCAAG TACCTTAGGA 120 CGCTGACAAG TTGCAGTTAA GGGTGAGGAC CTGGAAAGTA TGAGACTGGG TTAGGATCCC 180 AGCTTGCTAC CTACCAGCCA GGGCTATGAG CAAGTTATTT TAACCTAAGT TTCAGTTTTT 240 TGACATGTCA GATGAAACTA TAGTTACTAC CCCAGAAGAC TGACTGTTTT AAGGATCAAA 300 TGAGATAATC TTTGTAAACC ATTTAGTACA GTGCCTAGCA CATAGTAAAC ATTCAACAAA 360 CATGCATCAT TATTGAGCAA GATCGTGTAG CTGTTCTGTC TCCAAAGCCT ATACTCTTTC 420 CACCCCTCCA CAATGTTTCC TAGTCACGGA ATACATCCCA GTGTTAAAAA TATACCATAT 480 CCCTAGACTG TGGAGATAGA GTATACTGAC TGGTTGGTGG GCCTCCCTGT CTTTAGTGGA 540 GATAATACAA GCCTTTGTCC GTGCAGAGAC TAACCCAGTT TTCAGAGGCA GTCAAGGCCC 600 GTTCAGTGAG ACAAGACCAC AGGCCACATT TCCTCTAAGT AGTGGGACTT TGGTTTATGG 660 ACTGATGCGG TCACAGACAG CAAAGGCAGG AAACAGACAA AGAGATGAAC TGAGACTCCA 720 GCTGAGATGG GAGCCTAAAG AGGGTGAGAT GCCCACTTCC TGGTTTCTAG GCATCGCCCC 780 TGGGTGTGTC CTTCCTTTGC TTAACATCTC CCTGGGCTGC CTGGACTCGC TGCACTTTTT 840 AGCCTCCAGG CCTCCATACT CCAGCATGGA GTTCTCCAGG TGACTACTGA GTGGCTCCTA 900 CAGGCTGCTG GGCCAGTCAC CAGGATCTGA CATCCCATCC TCATCTGCCC ACCAGCTCCC 960 ATGCCCTTCT CCAGAGAAGT CAACCTGCGC TGCAAAGGAG GACCCTGAGG AAGAGAGTAC 1020 CATAGGGAGA AGCAACAGGC AAGAAAGTCA GACAGAAAGT TCCTCCTTGG CACAGAATCC 1080 GGAGGGGCTA GGGTGATGCA CAAAATGCCA ATAGTTTTCA TTTCCACATT TGCATTTACT 1140 CTTGGCACAA AATTGAGCAA GATGAGTAAC AAAGCCACAA AAGCAGGGGT AAAAGAGGGC 1200 TACCAGTTCC TATAAAATGG GCTGAGTAGG CCAGGTGCAG TGGCTCACAC CTATAATCTC 1260 AGCACTTTGG GAGGCCGAGG CAGGTGGATC ATGAGGTCAA GAGATCAAGA 1310
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