Tag | Content |
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EnhancerAtlas ID | HS078-07212 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr17:4756430-4758550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr17:4756435-4756455 | TGGGGGAGTGTGGTTGGTGG | - | 6.39 | RREB1 | MA0073.1 | chr17:4756486-4756506 | GGGGGGAGTGTGGTTGGTGG | - | 6.39 | RREB1 | MA0073.1 | chr17:4756590-4756610 | TGGGGGAGTGTGGTTGGTGG | - | 6.39 | RREB1 | MA0073.1 | chr17:4756625-4756645 | TGGGGGAGTGTGGTTGGTGG | - | 6.39 | RREB1 | MA0073.1 | chr17:4756658-4756678 | GGGGGGAGTGTGGTTGGTGG | - | 6.39 | RREB1 | MA0073.1 | chr17:4756690-4756710 | TGGGGGAGTGTGGTTGGTGG | - | 6.39 | RREB1 | MA0073.1 | chr17:4756738-4756758 | GGGGGGAGTGTGGTTGGTGG | - | 6.39 | RREB1 | MA0073.1 | chr17:4756543-4756563 | AGAGTGTGGTTGGTGGGGGG | - | 6.51 | RREB1 | MA0073.1 | chr17:4756472-4756492 | GGAGTGTGGTTGGTGGGGGG | - | 7.14 | RREB1 | MA0073.1 | chr17:4756490-4756510 | GGAGTGTGGTTGGTGGGGGG | - | 7.14 | RREB1 | MA0073.1 | chr17:4756724-4756744 | GGAGTGTGGTTGGTGGGGGG | - | 7.14 | TP53 | MA0106.3 | chr17:4757814-4757832 | GTCATGTCCTGACTTGTT | + | 6.27 | TP63 | MA0525.2 | chr17:4757814-4757832 | GTCATGTCCTGACTTGTT | - | 7.04 | ZNF263 | MA0528.1 | chr17:4757506-4757527 | TTCTCCCTCACTCCCTCCCCC | - | 7.08 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_03584 | chr17:4756706-4757302 | Brain_Angular_Gyrus | SE_03584 | chr17:4757345-4757957 | Brain_Angular_Gyrus | SE_04067 | chr17:4756396-4758269 | Brain_Anterior_Caudate | SE_05001 | chr17:4756396-4758456 | Brain_Cingulate_Gyrus | SE_05952 | chr17:4747417-4758504 | Brain_Hippocampus_Middle | SE_06909 | chr17:4756558-4758487 | Brain_Hippocampus_Middle_150 | SE_07984 | chr17:4752070-4758516 | Brain_Inferior_Temporal_Lobe | SE_26876 | chr17:4751864-4758585 | Esophagus | SE_36518 | chr17:4756417-4758646 | HMEC | SE_64738 | chr17:4756410-4758656 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 4756821 | 4757222 | chr17 | 4757217 | 4758141 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I004852 | chr17 | 4755295 | 4758565 |
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Enhancer Sequence | GTTGGTGGGG GAGTGTGGTT GGTGGGGGAG TGTGGTTGAG GGGGAGTGTG GTTGGTGGGG 60 GGAGTGTGGT TGGTGGGGGG AGTGTGGTTG GTGAGGGAGT GTGGTTGGTG GGAAGAGTGT 120 GGTTGGTGGG GGGAATGTGG TTGGTAGGTA GAGTGGTTGG TGGGGGAGTG TGGTTGGTGG 180 GAAGAGTGTG GTTGGTGGGG GAGTGTGGTT GGTGGGAAGA GTGTGGTTGG GGGGAGTGTG 240 GTTGGTGGGA AGAGTGTGGT TGGGGGAGTG TGGTTGGTGG AGTGTGGTTG AGGGGGAGTG 300 TGGTTGGTGG GGGGAGTGTG GTTGGTGGGA AGAGTGTGGT TGGTGGGGGA GTGTGGTTGT 360 TGCTGTGTGC CATCGGAAGG CTATGCAAGT TTGAGCGCTT GCTTCACCTT GACAAACATT 420 TCACTTGTTA GAGCCCTGGC TTTCTCATCT GTGCTCTGAG CTAGTCATTC CTGCCAAGCT 480 TCCCTGCAGG TTTAAGTGCA GATGCAGTCA TGACTGTGAA AGCACCCTGT GAACTGTAAA 540 GTCTGGGCAG TTGGGTGGTG GTAGGAGAGG CAGCAACTGT GAGAGGATGA ACTTGATTCT 600 GCTGATCTCG GACGGAAACT GATTCTTGGG AGAGAGACAG AATCAAACGG CTCTGACATT 660 TGAAAAGCCA TGGCCTCGCT TACCTACAGT GAGACTTGAG AAGAAGTGCT GGGGAGGTAA 720 AGGCTGAGAT ACCACCTCCG CTGCCTGAAA GACTTTGCAA GATACTCCAG CTGGGGATAG 780 GAGATGGCTA GAATGACCTC CAACTATCTT CACACCCGAG GCTGGGGCTG CCCTTCCAGG 840 CCTGCAGTTC TGTATTTTCC CTTAGAAGGT TCTGGAGGCA GACGGAACCT CAGAAGCAAA 900 CGGTTTATTT TTTAGGTTTT TCAGTTTATT TTTAAATTTC TGACTGTGAT GGTGTTTATT 960 TTTTCCTTTT CCCTTTCCCC ACTTCCCCGG CTCAGCATCA GAAAGGGACC ATCTGTCCGT 1020 TGCCTTGCTG TGGCCATTTT AGAACCAGCG CAAGGCTGCT TGAATCTGGT CCCCTCTTCT 1080 CCCTCACTCC CTCCCCCACC ACCTGGCTTT CTCTACTCTG CACTGCCTGC TTTCATCCAG 1140 CTCCCTCCAG GTGTCAGCTG CCACCTCTTA TAGGCCTCCA TCTGTGAAGA CCTCCAGGCT 1200 GAGTCCAGCC ACCAGACCAG GGCCCCTGTC TGAGGCAGCC AGATCTGTGG GGAACCTAGA 1260 CATGGAGGCA GCAAAATTAC CCTTTGAGAG GAGGAGGGGA ATAAATTCCA GTCTCCTTGC 1320 TCCAGGCAGG GCCCCTCTGC TCTGACTGGT TTCTGATGAG AATGGTATGT GTATTCATGT 1380 ATGTGTCATG TCCTGACTTG TTTCTGCCTC TGCATGTACC TGCAAGTCAG TGTGTGTGTG 1440 CATGCGTGTG TCTCACACAT CCCTCTGGCA TAGAGATCCA TGAGTGATTT ATAAACTGCC 1500 TTTCCTCCCA TCACATAAAT ATTTTTCCTG GTTTCTTCGC CTTCCTTCTA CTTCTAGAAC 1560 TGGCCTGATT TCCTCCCCTC CAGTGCTTCA TTCCCATAAA AACACTTCAA AACACAGGTA 1620 GCCATCGATA GACAGAGGAC AAGTACTTCA CGTTGTGGAT TCAGAATAAA AAGATCCGGT 1680 TGAGTTCCAC AGTGTGAGAG GCAGGGTTAG CAGAGTGGAG AGTCTGTTTC AGAGAGTAAG 1740 AAGCGCTGAG AAAAGGAGTT TTTTTGAAGG CTTCATTAAA AAGAGTCCAG GCTGGGCGCG 1800 GTGGCTCCCG CCTATAGTCC CAGCACTTTG GGAGGCCCAG GTGGGCAGAT CACTTGAGGT 1860 CAGCAATTCG AGACCAGCCT GGCCAACATG GTGAAACCCC ATCTCTACTA AAAATACAAA 1920 AGATTAGCCG GGCGTGGTGG TGGGCGCCTA TAGTCCCAGC TATTACTATA CTTAGGAAGC 1980 TGAGGCAGGA GAATTGCTTG AACCTAGAAG GGGAGGTTGC AGTGAGCTGA GATTGTGCCA 2040 CCACACTCCT GTCTTAAAAA AAAAAAAAAG GCCAGGCATG GTGGCTCACA CCTGTAATCC 2100 CAGCACTTTG GGAGGCTGAG 2120
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