Tag | Content |
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EnhancerAtlas ID | HS182-10371 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr18:21549710-21551280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr18:21550429-21550439 | ACTTGGCACC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_62548 | chr18:21544867-21602342 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr18 | 21549736 | 21549922 | chr18 | 21550196 | 21550883 |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I023969 | chr18 | 21549715 | 21551318 |
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Enhancer Sequence | CAGATGAGAA CTGCTTTCCA CCTAGGAGAA TCAGGTATTG AAGGAGCACG CCTACCCTTC 60 TCCACGCTGT GCCATGAAAC AACTCTCGGA ACTTCCATGA GTGGCACTCA TGCTCCAGCC 120 ACTCACAAAT AGACCTTTGT GTCATTTATT CAGCACTTGG TAGGTCCAAG GCACTGTGCC 180 AACCCCTTAC CTATGCATCT CATTCAATCC CAACAATTAC TTTGAGAATC GGGTATGATT 240 ATTGCATTTA GCAGGGAGAA AAGAGAGAGG AAGCCCCAAG TAACCGGGCC AGTCCTTATG 300 GAACTATTAC CCTATATTAA TAATGCGTTC CTGATGCCTA GATGTCTGGG GCTTTGCTGA 360 CCCTGGAGGA ACTGCCTTTC TCAGGGTCAG CTAATTTCTA GAGAAAGTAA ATGACTTGCT 420 TGGGAGCACC TTTCAAATGC AAGCCACCCA ACCCAGAGCC CATACCCCGG GTGCCACCTC 480 TTCTATTAGC TCTCACACTC AGGACCATGT GCTCCCACTC TAATCACCCT AGGGACAGAT 540 GGCAGACAGC AAGAGGCAGC CCCTATGTCC CAGACTCCTG TGAAATTATT CAAACTAGCA 600 AATCATAAAC CTGCTTACCC TGCCTGGCGC CATTCCTTCC TGCAGAAACC ATGATAAAGA 660 CTCTTGCCTA CGTTTCCCCC TCACTCCCTC TGCTGCCTGA CTGGCCCTGG TACTTCCCCA 720 CTTGGCACCT GTGGCATGGT GTGGGCCCCT TTCTTGGAAT ATGTGAGTAT CACAGAGTAT 780 CTTTTCAACG GCAATTGTCT TCTGATCTGT TGGCCTCCCC ATACCAGAAA AAACAGACCC 840 ACATTCTAAT ACGCATGCCC AGTGTCGCCC CTGTGCTAAT CTGAGCCAAA AAAGCAGAAC 900 CACAAATGGA AACATCACAT CCTGTTTATC ACTAGTATTG GTGTTCTCAA AGACAAATTA 960 AGGCCTTTAG GGGTATATTC CAAGAGCATG AGAAAGAAGA GGGACTGCTA GTCTTACCCA 1020 CTAATTCTAT CCAAGATGCA GATAGCAGCC ATTCATTTCC TGCTTGGTTT TTTATTTGTT 1080 TTTGAGACAG GGTCTGGCTG TCACCCAAGC TGGAGTGCAG TGGCACCATC ATGGCTCATG 1140 TCAGACTTGA CTTCCCAGGC TCACACGATC CTCCCACCTC AGCCTCCTGA GTAGCTGGAG 1200 CTACTGGTGT ATGTCACCAT CTCCAGCTAA TTTTTTTTTT CATTGTAGAG ATAGGGTCTT 1260 GCTATGTTGC CCAGGCTGGT CTCAAATTTA TGGACTCAAG CCATCCTCCC ACCTTGGCCT 1320 CCCAAAGTGC TCAGATTACA GGCATGAGCC ACCACTCTTG GCCTCCTGCT TAGTTTTGAT 1380 AACACAATGA TGATGAAGAA GGAGAAATCA GTCTCTCTGG AGGATGATGA TTTTTGCACA 1440 TTCATCAAAA GGGGTTTAGA AACAGTTGGG AACAGCAGAC GAACATGGTC ATCCTTCCCC 1500 TCTGGTAGGC TGGCATTCTT ACTTCCTCCA GAAAGCATTC GTCCACCATA GATGAAAGCT 1560 TTTTTTTTTT 1570
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