Tag | Content |
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EnhancerAtlas ID | HS155-06023 |
Organism | Homo sapiens |
Tissue/cell | Ovary |
Coordinate | chr17:39948820-39950940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr17:39950148-39950167 | CGACCAGCGGATGGCACCA | + | 6.09 | FOSL2 | MA0478.1 | chr17:39949567-39949578 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr17:39949567-39949578 | CTGAGTCACCC | - | 6.02 | TCFL5 | MA0632.2 | chr17:39949732-39949742 | TCACGCGCAC | + | 6.02 | ZEB1 | MA0103.3 | chr17:39949631-39949642 | CCCACCTGCCC | + | 6.14 | ZNF263 | MA0528.1 | chr17:39949364-39949385 | GGTGGAGGGAGAGGCTGGAGG | + | 6.14 | ZNF263 | MA0528.1 | chr17:39950879-39950900 | TGCCCCTTCCCAGCCTCCTCC | - | 6.26 | ZNF263 | MA0528.1 | chr17:39950882-39950903 | CCCTTCCCAGCCTCCTCCTCC | - | 6.96 | Zfx | MA0146.2 | chr17:39948825-39948839 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_23177 | chr17:39948805-39950762 | Colon_Crypt_1 | SE_23845 | chr17:39948823-39950568 | Colon_Crypt_2 | SE_24826 | chr17:39948792-39950552 | Colon_Crypt_3 | SE_26576 | chr17:39947886-39951114 | Esophagus | SE_27684 | chr17:39947694-39953126 | Fetal_Intestine | SE_28604 | chr17:39947659-39953352 | Fetal_Intestine_Large | SE_31640 | chr17:39948788-39951021 | Gastric | SE_35990 | chr17:39948033-39951096 | HMEC | SE_40900 | chr17:39947989-39951264 | Left_Ventricle | SE_42558 | chr17:39948749-39951297 | Lung | SE_47748 | chr17:39948821-39950630 | Pancreas | SE_48895 | chr17:39948755-39951241 | Right_Atrium | SE_49575 | chr17:39948820-39950509 | Right_Ventricle | SE_50269 | chr17:39948758-39951244 | Sigmoid_Colon | SE_52578 | chr17:39948765-39951219 | Small_Intestine | SE_56909 | chr17:39948805-39950751 | VACO_400 | SE_57643 | chr17:39948796-39950605 | VACO_503 | SE_58007 | chr17:39948820-39950619 | VACO_9m | SE_64699 | chr17:39948561-39950841 | 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 | 39949116 | 39949497 | chr17 | 39949517 | 39949745 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I041791 | chr17 | 39947888 | 39953024 |
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Enhancer Sequence | ATCCACCCGC CTCGGCCTCC CAAAGTGCTG GGATTACAGG TGTGAGTCAC CACAACTGGC 60 CTGGGAGTGT GCTCTGTAAC TTACCTAGAT CTATGGCATG TAGGCCTCAT TTGTGCTCTT 120 GGCCCTGCCC ACTGGCTTTG GGGGTGGGGG CTTACTCAGA AGGCCCCCTT CAGGGCTCGG 180 GGAGGACACA GCTGCAGAAG AGCCTGCAGG CTCCCAAACT CTGCTGGCTG GAGTGGGCCC 240 AAGCATGGCC AGAAGCTGGG AAGGGAGCAG GAGGCTGCAG GGCTCTGGAG GGAGGCTGTG 300 GGGAGATGGA CTCCTGCCTT TTTTCCTGCC TTGTGTCCAG GGGAGGGGCC TTGAGGCCAG 360 AGGCTGCCCA CAGCCTGGTC CTGTGGGCGT GTGTCTTTTA ATTACAGATG TAGCTCCAGC 420 GACACTTCAC TGCAAGGCGT GTGGGTGGGG ATGGAATGTC AGAAGGAAAA CAGGAGACAA 480 GAAAACAGAG ATAGGACGGG CCAGAAATAG TACAGGCCAG GGTGAGATAG CAGCGGCCAG 540 TGGTGGTGGA GGGAGAGGCT GGAGGAGGGT CTGTCGAAAC CTCTCCAGAG AATGCCTGTC 600 CCAGGCTGCC CCTCCTTATT CACCCCAAGC CCCGCAAGTT GAAACTCCAG GACCGGTGGC 660 ATCTAGATCG GGCTCCAGAG CTGGTTCACC AACTCCCTAA GCAACACCCT CCTCCTGAGT 720 GGGGAGGGGT AGCCGAGCCT TTGCGACCTG AGTCACCCGC TTCCTGCTCC TGGTCTGGGC 780 GACTCCATGC ACAGGCTGAC ACAGCTGGGG CCCCACCTGC CCTGCCAGCC TGTCCCGCTC 840 CTCCCTCTTT CCACAAGCCA GGAGAGATGC CTGCCCTGAC AAGGCATGCT TCCCACGGAG 900 AGGCCATCCC TCTCACGCGC ACACACGGCT GGAGGCAGCC ATTTCTCCCT GACCTGTGGA 960 GAGCCTTGGG AAGAGGAAGA AGGCATAGTC TAAGCGGAGC CCCCTTTTCC CTGCATCTAT 1020 GAAGAAACTG CGGCTGGAGC CAGGAGAGGG ACTTCCCCAA GATCACACAA GAAAATTCCT 1080 GGCAGGGCTG GGACTTGAAC CTTGGTCTTC TGCCAGCCAG TTCACCTCCC CCACCAATGT 1140 AGGTCTCTTT CCACCCCAAG GAAGGCAAAG ACGGGCTGCA GTCAGGGAGG AGACGAGAAC 1200 CAATTTTGCC AGCTTGATTT TGTCAGCTCA GAGGTGTGAC CCCAGGAAAA CCTTGGAGTT 1260 AGACAGCCAG GGCTGGGGGA GGGGGTGGCT CTGGGTGGTC CCAGACTCAG GCCTTACTTC 1320 CCCTAAGCCG ACCAGCGGAT GGCACCACCT AGAGCCTCTA GCCATCAATT ATGCAAACAG 1380 ACCCTTCCCC ACCCCCGCCT CTCGCCCTCC GGCCCTCTCT GCTTCCCAGG TCTTTAAGCG 1440 CTGGACTCCA CCTGGCTGAG AACTGGGACA GGACTCAGCG GCCCCTGGCC TTGTACTTTC 1500 ATCCCATCTT TCCCAGTCCC ATCCCACGGC CCCCAGGGAA TTTGAGAGTT GAGATCCTTG 1560 AATATTTCAT CAGCACTTCA GCCTCCAGTG GAAGCAGCAG CCAACTTACA TCTCCTGGAG 1620 CATTTATGGC CCCAACAGAG AACCTGGAAG TAGCCAGGGG GAGGGGTGGG TGCATGGGGG 1680 AGGGTGAAGC TTGGGCCAGG CTGCCAATAA GGGTTGATGG AGAAGAAGGC TGCCGGGTCC 1740 AAAGTGTGTG TGAGCTGGGG GAAAGGGGCT CCAAAGCCGG GAACATTTCC GTGTTTGAGG 1800 ATACAGATGT ATTTTAAAAT AAATAAACAA AATGGAGTTA TCAAAACAAT TATACGCAAG 1860 GTTAAAGTCA TATGACAGGG TTTTCTGACT TCAGTCCTGC CCCTGTCTCG TGACTGGGTT 1920 TATAACCTCA TCCGGAGATA AGGTAAAAAA TTTTAATGGG AGCTTTTTTT TTTTTAGGGC 1980 TGTGAGGCCC TCAAATGACC CCCTACTGCC TGGGGCCAGG GAGGAAAGGC CAAATTCTCC 2040 AGCTACATTG GCTGAAACTT GCCCCTTCCC AGCCTCCTCC TCCAGGAAGG TCAGGAGGAT 2100 TTAGCCCAGT AGTCAAGGAA 2120
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