Tag | Content |
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EnhancerAtlas ID | HS182-09506 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:45004840-45006880 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr17:45005600-45005612 | TGCCCGAGGGCA | - | 6.27 | TFAP2C | MA0524.2 | chr17:45005600-45005612 | TGCCCGAGGGCA | + | 6.52 | ZNF263 | MA0528.1 | chr17:45005163-45005184 | CATTCCTCCCCCTCCTTCTTC | - | 6.66 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28004 | chr17:44999703-45009235 | Fetal_Intestine | SE_29222 | chr17:44999726-45009313 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr17 | 45005056 | 45005106 | chr17 | 45006024 | 45006228 | chr17 | 45005698 | 45005789 | chr17 | 45005565 | 45005619 |
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Enhancer Sequence | TCATTTATGC ACACCTGTAT TTTCTTCAGA AAGTTTGAAA GCTGCTCTGC TTTTTCCATT 60 TGGGTTTTAA GTGAGCTTGA GTTTATTTTT ATGTGTTACC TGAGGTGGCC TTTTTCTGTA 120 CGGGTAACAA ACCGGAGCTG TTGGCATTTA TTGTAGTCCC TTCTTTCAAA AGCTCCCAAA 180 TAACGTGGGG CTGTGTCTAG GCTGTTTCTT TCCTCTTGGG CCAGCTGTAG GGTTTGCCTT 240 TCCTTGTCTG TCTGCACCTG CACTGCCGCC ATATTGTTTC CATTGTTACT GCTTTGTAAG 300 TCATAATGGC AGGTGGGACA AGTCATTCCT CCCCCTCCTT CTTCAGAGTG GTCTTGGCTA 360 TTCTTTACCT CCCCCCTTTT TATTATGTCA CTGTTCGTGT TGATCATATT ACCAACTTTC 420 AGATTTTTCT GTTAAATCAG CATTGAAAAT TTACCTCACA GCCTGCGTCA GGACTTCCTT 480 AGAGTCCTAA TTCTCCTTTC TGTCCCCGTT ACCCTCCGGT CCCCTGTACC TGTTCCCTTG 540 GTTGCCCTGC TTCAGGTGTC GGCTACCTCA GGCTGCATTC CTACATCAGC CCCCATACCT 600 CCACACCCCC GCATCATCCC ACAATATCCC AGACTTACTT TCCGGAAGCA ACGGCCTGGT 660 CTCGGACTCT AGCAGTGATT TCTAGTTGCT TCTCAGGGCC ACAGGTCTTG CCTAGGAGCA 720 CCCTGGGGAG TCATTTGACA GCTCACCCAG CTTCTTTTGG TGCCCGAGGG CATATCTGGA 780 GGCCATAGGG AAGCCCTGGA AAAGACTGGG CACAAGCTGA AGCCAAAGTT GGGTGCCTGG 840 CTGGCATTGG TAGATTTGGG GTCCTGGTTT GCATTGCTCA CGATGCAGAA TGGTTGCTGA 900 CCTTTCCTCC AGCGTTGGGG ATGATGTGAG AGTCCAGCAG GCCCCCTTCA TGTGGGCCCT 960 AACTTGGGGA AATCTCCACC GTGAGCACCG GGAAGTGGAT GGTGGGGCCA GCATAAGCAG 1020 TATCCCGAGG ACTGATCATG GAGGACCATT AGGAAGGGGG TCTTAAGGAT GACCTTGGCC 1080 AGACCGTGGG AAGCCTCCAG AGAGTGTTAC CCAGATCCAG GGTACAGTGT TGCATTTCCA 1140 AATGAGATGG CAGTTCCTTC GTTCCTTGAT ATTGTCGGAG AAGGATGTTT ACCAAACAGA 1200 AGGTCCCTGT CTCAGGGTCT TCCTCTGAAT GGTTTCCTCC AGTGAGTCAC TTCAGCATCC 1260 TCTCCCCCAA CCCGATTCCC TTTCAAGCAG CCCACCCTAC TTGTAATCCA CATGTCTTGA 1320 ATGAATTTTT GCATATCATT TTCTTCTATC TTCCTTCACC AAATGATGTC TCCCTTCTTC 1380 ACAGCGATGC TCAGAACTCT TTCCATCCAC ATAACTTACC TGGTTTCTCT TTCTCAGCCC 1440 CACCCCTCTG TCTGCTTGCC TGTGACACCA CTGTGCAGAG CTGCCCCTCT TTCTGTTTGT 1500 TTATACTTAT GTGTATTGCT TTTCTCGTGA ATCTTCCCAG GGCTTGTTCA TGTCTGTTTA 1560 GCCTGTCATT CCTCATTATG TTGTTTCTCA AGGACAAGGA TTATATCTCC CTCGCCCTTT 1620 GACTCTTCCT GGTACAGGCC AGTGCTTAGC ACATTAGGTC GTAGAACAGA AAGTAGGATT 1680 GGCCGGGTTC AGTTTGAGGT TTATCACTTG CTGTGTGATC TTGAACAAGT TACATAACCT 1740 TTCTGGGCTT CAGTTTTTAT AAAATGAGGA TGATAATGGT ACTTTCCTCA TAGGGTTATT 1800 GATTTGGCAG AGTATCTTGG ATATGGTAAG CACCCATAAT CTGCCTATCA GTGTTATTGT 1860 TAGTAGTTAA GATATTAGAA ACCATGCCAA AACGTGGGAC CTAAAGTGCC ACATACAAAT 1920 TTTACAGTTC AGTGATGCTG TCGATTTAAA TCAGTTACAT GTTGGCATCA GAAAAATTGT 1980 CTTTCCTGAC TGAAGCGCTG TTGATTACTC CTGTCTCACT CATTTCCTCC CTCTTCCTTT 2040
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