Tag | Content |
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EnhancerAtlas ID | HS182-10137 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:79023010-79024770 |
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) |
TFAP2A | MA0003.3 | chr17:79023912-79023923 | TGCCTGAGGCA | - | 6.02 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_25200 | chr17:79022511-79025155 | Colon_Crypt_3 | SE_26560 | chr17:79022179-79025369 | Esophagus | SE_31420 | chr17:79022257-79025350 | Gastric | SE_34261 | chr17:79015484-79025415 | HCT-116 | SE_36440 | chr17:79022176-79025537 | HMEC | SE_41709 | chr17:79023438-79025169 | LNCaP | SE_42160 | chr17:79015988-79025385 | Lung | SE_47416 | chr17:79021645-79027438 | Panc1 | SE_47964 | chr17:79023284-79024545 | Pancreas | SE_57453 | chr17:79022161-79025209 | VACO_503 | SE_65309 | chr17:79022165-79025391 | Pancreatic_islets | SE_69007 | chr17:79022537-79023808 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr17 | 79023098 | 79024730 | chr17 | 79024187 | 79024380 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I081048 | chr17 | 79022188 | 79027464 |
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Enhancer Sequence | GATTTCTGTC CTGGCAGGGG GGCATGGGGT CACAGAACGT GGGCCCCTGG GGAGCTCTCT 60 CTGTGCCTGT GGCCCCCCAG GAGTCTCTCA GTTTTGCTGT GGTCTTGAGG ATGGCACAGC 120 GTGTCCCTGA GCGCCCTCAG TGTGGACAGC TGGGCTTCAA ACTCACTTCA GAGCCGCCGT 180 GTGGGGGTGG CGCCTCTGAG GGCTTGAGGT TATTTTCTTG TGCGGTTTCT CTCTCCTGGC 240 CTAGGTTTTT CTGGGTTTTT TGCACCTCTT GGTGTTGATA AGAAACAAGC TCCCTTCCCC 300 TTTTAAAGCC CACAGACTTT CCCGATCTCC TCCCCATCCC CTGCCCCAGC ACTGTCAGGG 360 CGTCTGGGCG TCTGAGCTCA GCTCCTTCCT GGTGGCATCC TGCAAAAAGA TACACTCGCT 420 CAGTGACTCG GAAAAGCCAC GTCGGTGTGG CTGAGAACAG AGTTCTTTCC ACCTGGGGCC 480 GCTGCTGTTG GTTTTCATTC CGGAAGAGCT GGAGCTGCCT GTCACTGGCT CCCCTGCCCC 540 CACCTGGGGA CCCCCAGGCA CTGCAAAGTG CCTGTTGGCT ATGGGCCCCC GGACCAGGAC 600 CTTGGCCTGA TTAGGGGAGC CGGAGGTGGA AGTGGAGGCG GGACTGGAGT GTATGCCCCA 660 CAGTGGGCTC TCCTCAGGCT GGGGACTTCC ACACGGGCCC ACTGGGTCAG GATGGCCCGT 720 GCCTGTGTTC TAGGATAATG GGATGGACTG GTTCGGAGGC TCAGAGAGAC GCCTGACCAG 780 ACGCCTGACT GGAGATGGTC TCCCAGCAGA GGGGCTGGGC TCTTCAGGGG CCACTGGGCT 840 CCTCCCGTGG TTCCTGGGAG AGGGAGGAAC CCGGAGGAGG GGTGGGTGGC ACCTACAGTG 900 CGTGCCTGAG GCAGGGCTCC ACAGAAGGCC TCTCTGCTGG CCCAGCGGCT GGATGCAGAT 960 GCAGAAGGAG GAACTGGCCC TTCCGCCCGC CCGGGAAGGG GAGTCCCCCC TTACAATGTT 1020 GGCTCAGTGG GATCGATGCC TCTGCCATTG CCTTCGGGCC AGGACAGCAG CACTTGCGTG 1080 TCCCGGCCGC CGCCCCTCTC TTGCAGATGG AGGCAGGGCC GTGCCCAGGT GTCCTGGTGG 1140 CTGTTCCCTG CCCGCTGTCT CCTGCATTCC TTCCGTGTGA GCTCAGCTGC TGCACTAAGG 1200 AAGCGAAACC TTGGTGCTGC CCCGTGCGTC ATGCGGTAGG CATGGCCGCC GTGCTGACCC 1260 GCCGTGGTTG GCCCTGGGTG GCTCCTGGCC TGTTTCTCCT GCTGCTCAGG ATGTTAGTGG 1320 AGCTCACAGG GCTCAGGTTG AGCCTCTTCC ACCCGGGGGC CTGTGGGGGT CATGGTCCTG 1380 GAGCCAAGCG CGTGGGGCTC TTGTGAGCAA GGGGTCTGCT CTGGCACGCC CACCTCCGTG 1440 GTAGTGTTTT CATACCTGTG TCACACAGGG TGAGAAACAT GCTTGATGCT GCAGCTCAGC 1500 ACACACACGC ACACAAATGT GCACATGCAC ACGTGGACAC ACATGCACAC ATGCATGTGT 1560 GTATGCACAC ATGGGCACAG ATGTGCATGC AGACATGAGC ACACGCACAC CAGAACACTA 1620 GAGTCGGCCG CATCCTCCTC ACTTGGCTGA TGCCCCCTTC TGCTTGATTT CATCACAAGA 1680 AACGCGCATC CGGCAGCATT TCCCGACCGC CTTCACCGCC AGTCCCGGTC TGCATGGTCA 1740 GTTTGAACCA GGCTGCCGAG 1760
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