Tag | Content |
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EnhancerAtlas ID | HS187-11364 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr18:21549730-21551440 |
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 | CCTAGGAGAA TCAGGTATTG AAGGAGCACG CCTACCCTTC TCCACGCTGT GCCATGAAAC 60 AACTCTCGGA ACTTCCATGA GTGGCACTCA TGCTCCAGCC ACTCACAAAT AGACCTTTGT 120 GTCATTTATT CAGCACTTGG TAGGTCCAAG GCACTGTGCC AACCCCTTAC CTATGCATCT 180 CATTCAATCC CAACAATTAC TTTGAGAATC GGGTATGATT ATTGCATTTA GCAGGGAGAA 240 AAGAGAGAGG AAGCCCCAAG TAACCGGGCC AGTCCTTATG GAACTATTAC CCTATATTAA 300 TAATGCGTTC CTGATGCCTA GATGTCTGGG GCTTTGCTGA CCCTGGAGGA ACTGCCTTTC 360 TCAGGGTCAG CTAATTTCTA GAGAAAGTAA ATGACTTGCT TGGGAGCACC TTTCAAATGC 420 AAGCCACCCA ACCCAGAGCC CATACCCCGG GTGCCACCTC TTCTATTAGC TCTCACACTC 480 AGGACCATGT GCTCCCACTC TAATCACCCT AGGGACAGAT GGCAGACAGC AAGAGGCAGC 540 CCCTATGTCC CAGACTCCTG TGAAATTATT CAAACTAGCA AATCATAAAC CTGCTTACCC 600 TGCCTGGCGC CATTCCTTCC TGCAGAAACC ATGATAAAGA CTCTTGCCTA CGTTTCCCCC 660 TCACTCCCTC TGCTGCCTGA CTGGCCCTGG TACTTCCCCA CTTGGCACCT GTGGCATGGT 720 GTGGGCCCCT TTCTTGGAAT ATGTGAGTAT CACAGAGTAT CTTTTCAACG GCAATTGTCT 780 TCTGATCTGT TGGCCTCCCC ATACCAGAAA AAACAGACCC ACATTCTAAT ACGCATGCCC 840 AGTGTCGCCC CTGTGCTAAT CTGAGCCAAA AAAGCAGAAC CACAAATGGA AACATCACAT 900 CCTGTTTATC ACTAGTATTG GTGTTCTCAA AGACAAATTA AGGCCTTTAG GGGTATATTC 960 CAAGAGCATG AGAAAGAAGA GGGACTGCTA GTCTTACCCA CTAATTCTAT CCAAGATGCA 1020 GATAGCAGCC ATTCATTTCC TGCTTGGTTT TTTATTTGTT TTTGAGACAG GGTCTGGCTG 1080 TCACCCAAGC TGGAGTGCAG TGGCACCATC ATGGCTCATG TCAGACTTGA CTTCCCAGGC 1140 TCACACGATC CTCCCACCTC AGCCTCCTGA GTAGCTGGAG CTACTGGTGT ATGTCACCAT 1200 CTCCAGCTAA TTTTTTTTTT CATTGTAGAG ATAGGGTCTT GCTATGTTGC CCAGGCTGGT 1260 CTCAAATTTA TGGACTCAAG CCATCCTCCC ACCTTGGCCT CCCAAAGTGC TCAGATTACA 1320 GGCATGAGCC ACCACTCTTG GCCTCCTGCT TAGTTTTGAT AACACAATGA TGATGAAGAA 1380 GGAGAAATCA GTCTCTCTGG AGGATGATGA TTTTTGCACA TTCATCAAAA GGGGTTTAGA 1440 AACAGTTGGG AACAGCAGAC GAACATGGTC ATCCTTCCCC TCTGGTAGGC TGGCATTCTT 1500 ACTTCCTCCA GAAAGCATTC GTCCACCATA GATGAAAGCT TTTTTTTTTT TTTTTTTTTT 1560 TTTTAGACGG AGCCTCACTC TGTTTCCCAG GCTGGAGTGC AGTGGCACAA TCTCGGCTCA 1620 CTGCAACCTC CGCCTCCCAG GTTCAAGTGA TTCTCTGGCC TCAGCCTCCC AAGTAGCTGA 1680 GATTACAGGC ACATACCACC ATGCCTGGCT 1710
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