Tag | Content |
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EnhancerAtlas ID | HS182-22114 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:130773260-130774590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxq1 | MA0040.1 | chr9:130773286-130773297 | AATAAACAATA | - | 6.62 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_31463 | chr9:130773361-130773950 | Gastric | SE_47183 | chr9:130772538-130774752 | Panc1 | SE_62942 | chr9:130767703-130798071 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 130773312 | 130774385 | chr9 | 130773335 | 130774587 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I128010 | chr9 | 130772506 | 130774950 |
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Enhancer Sequence | TTAAATAAAT ACCTGTTTAC TGAAGTAATA AACAATAAAC AACAGAGCCC AACAGTTGGT 60 TTGTTCTCAT CCACATTTTT CTCAAAAGCA AAAATGGGCT CAGAGATCAG AGGTTTGTCC 120 AGGGTTACCA GGTGAGGCTG GAGGGTCCCC CTCTTTACAG GAGGCAGGGG CTGGGCTGGG 180 GCCCATCTGA GTCGAGGGTC ACTGTGAGTG GAGGTCAAGG CTGGAGGAAC TGGGCCCGTC 240 TAGGGGGCGG GTCAGCTGGG GAAGCACCTT AGAAAGGATG TGCTGAGCAC AGCTGCCCAG 300 GCAGAAGAGG AAGGAACCCA GGGCTCCTGT GGCTGCAGCC GATCTTCCCG AGTCTGGCCC 360 CACCCCCGAA CCCCGGCCAC TCTGTAACAC TTCCACACAC TCCCTCTGGC CAATGTTGCT 420 ACTTAAATGG CTTTTCAAGG TGGGTCACAC CAGGTACGGA CAAGGGTTGA AGGCCAGGCC 480 CACTTGCCCA CTGCCCACAG AAGTATAAAT CGGTCTGACC ATTTTAGAGG ATGGTTTGGC 540 AATATCTGTG AAAACATGCA AAGTGCAAAC CCTTTGACCC AGTAATTCCG CTTCTGGGAA 600 CTTATCCTAA AGAAACGCTA ACGTCCATGA AATTGGCAAT GTTATTCACA CAGGGGGTTA 660 TTTACTGTAG CACTGTTTGT CATGGCAAAG AACTGGAAGC CACCTAATGT CCATCAGGAG 720 GAAATGGATA AGTAAATTAT GCTTGCAGTT CCCATGGAAA ACTACAGTCA TTCAAAACAA 780 TGAGCCTGTC TATATGAAAT GCCAGAGGAG GATGTTCATG ATATATATAG GTATTGTTAA 840 GATTTCTTAA AGTTGCGGAA CAATATGTTT CAATTATCTA TTGCTGAATT GCAAAGTACC 900 CGGAAACTGG CCCTTCTTCA GCATCATGTG GCAGCAGGGG TCACTGATGC GGGTGCATTC 960 AACTGGGAGT TTGGCTGGGG CTCGAACTTC CAAGGATGAG AGGATGATGC CCTCTCATCC 1020 TCCAGCACCC ATCTCCACAT GGCCTTATCA TTCCACAGTC CTGCCTGAGC CTCCTTCCAG 1080 CACGGGGGTT TGATCCCAAG AGTGAGTAAT GTATTTCAAG AAAACAAGCC TCCAAGTGTA 1140 AACCCTTATT GAAACTCTGC AGCAGGCTTA CTAGTGTCCC TTTGACCCAA GTTTATCACA 1200 TGACCAGGCC CAAATTCAAC ATGTGACAAC CTACATCAGG GCCTAGATGC TGGAGGCAAG 1260 ATATACCAGG GCCATTATTA ACAATCTAGT ATAACATATG TAATAGGATC ATATTTTATT 1320 AAGAAACCAT 1330
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