Tag | Content |
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EnhancerAtlas ID | HS182-14565 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr21:45302740-45305230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr21:45303995-45304006 | GATGAGTCACC | - | 6.32 | FOSL2 | MA0478.1 | chr21:45303996-45304007 | ATGAGTCACCC | - | 6.14 | JUNB | MA0490.1 | chr21:45303996-45304007 | ATGAGTCACCC | - | 6.32 | JUND | MA0491.1 | chr21:45303995-45304006 | GATGAGTCACC | - | 6.62 | Sox3 | MA0514.1 | chr21:45304843-45304853 | CCTTTGTTTT | + | 6.02 | TCF7L2 | MA0523.1 | chr21:45304087-45304101 | GCCCTTTGATCTCT | - | 6.25 | TFAP2A | MA0003.3 | chr21:45303585-45303596 | TGCCTCAGGCA | + | 6.02 | ZNF263 | MA0528.1 | chr21:45304145-45304166 | CTTCCCCCTCCTCCTTCCCCC | - | 6.37 | ZNF263 | MA0528.1 | chr21:45304118-45304139 | CCACCCGCTTCCCCCTCCTTC | - | 6.52 | ZNF263 | MA0528.1 | chr21:45304131-45304152 | CCTCCTTCCCCCTCCTTCCCC | - | 7.1 | ZNF263 | MA0528.1 | chr21:45304157-45304178 | CCTTCCCCCTCCTCCTTCTCT | - | 7.44 | ZNF263 | MA0528.1 | chr21:45304144-45304165 | CCTTCCCCCTCCTCCTTCCCC | - | 7.53 | ZNF263 | MA0528.1 | chr21:45304128-45304149 | CCCCCTCCTTCCCCCTCCTTC | - | 8.27 | ZNF263 | MA0528.1 | chr21:45304151-45304172 | CCTCCTCCTTCCCCCTCCTCC | - | 8.48 | ZNF263 | MA0528.1 | chr21:45304138-45304159 | CCCCCTCCTTCCCCCTCCTCC | - | 8.88 | ZNF263 | MA0528.1 | chr21:45304141-45304162 | CCTCCTTCCCCCTCCTCCTTC | - | 9.11 | ZNF263 | MA0528.1 | chr21:45304154-45304175 | CCTCCTTCCCCCTCCTCCTTC | - | 9.11 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_24414 | chr21:45302931-45303346 | Colon_Crypt_2 | SE_24414 | chr21:45303855-45305193 | Colon_Crypt_2 | SE_28487 | chr21:45301529-45305495 | Fetal_Intestine | SE_31723 | chr21:45303707-45305281 | Gastric | SE_40549 | chr21:45301909-45305917 | K562 | SE_43150 | chr21:45303798-45305196 | Lung |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I043882 | chr21 | 45301737 | 45305874 |
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Enhancer Sequence | CCTCAGGGGC CTGGGGCAAC TGCTGGCCAC CAAGCAGTGT CCAGTGTCAT AGCCGCTCAC 60 TTGTCCTGTG GGGCCACCCA TGAGATGCAG GATTCCTGGT CAGCCCCAAC ACCAGGCCCA 120 CACCTCCACG CAGGCCTGGA AGGCAGGAGA GAGCAAGCTT TCTTCTCCTT TATTTGTGAA 180 TTATCAGCAC CTAGAAACTT AAGCGGGCAA ATGCTGAATT GCTGGAGACT GTGAAGCTGT 240 GATACACACA GAGTTGCTCC TTCCCTTCCT GGCTGGGGTG CTGGCCTGGG GAGCCTCCTG 300 CCCGGGTCAC TCCACTGCGC ATGCTCTGTG GCTACCGTGA GACTGACCTG CCTCAGACAC 360 CCTTCTCCTT GAGCCTCAAG GGCCTCATGG CCTGGACCTC CGTGATCAGC CAGAGGAGCC 420 CAGAGTCCAT GGTGCTGTGG CCTCCTGCCC ACTCTGGGAC CCCAGGGAGA GGGCCTGTCC 480 TCGCTGAGCC TCCGACACCG GTTCTGAGCC TCTTGGACAA CATTTTCTCT CCAGTTTACA 540 AGTAGGAGCC CCTTGCATAA ATAAGATGGG GAAAATCCCT GCAGATGACA TGGCCGGGGC 600 CCTGGGCCCC GGGAGCCATT TCTGTTCCTT GTCACTCAGC CTGGCCAGTC CTTGAGTTTT 660 TCCCCAGAGT GTCCTCAATA AGGAATAGCA AGCCTGGGTA TTTTCTTCTG GTCAGTATTC 720 CGTTTTTTTG TTTTGTTTTG TTTTTTGTTT TGGAGATGGA GTTTCGCTCT GTTGCCCAGG 780 CTGGAGTACA GTGGTATAAT CTCGGCTCAC TGCAGCCTCT GCCTCTTGGG TTCAAGCGAT 840 TCTCCTGCCT CAGGCACCCA AGTAGCTGAG GTTACAGGTG CCCACTGCCA CACCTGGCTA 900 ATTTTTGTAT TTTTAGTAGA GATGGGGTTT TGCCATGTTG GCCAGGCTGG TCTCAAACTT 960 CTGACCTCAG GCAATCCACC TGCCTTGGCC TCCCAAAGTG CTGGGATTAC AGGTGAGAGC 1020 CACTGTGCCT AGCTAATTTT GTATTTTTAG TAGAGAGACG GGGTTTCTCC ATGTTGGTCG 1080 GGCTGGTCTT GAACTCCTGA GCTCAAGTAA TCCGCTTGCC TCAGCCTCCC AAAGTGCTGG 1140 GATTACAGGT GTGAGCCACC ACGCCTGGCC AGTGTTCTGG TCTGTTTGTG ATGGGTGTAA 1200 GAATCTGTCT CTTTAAAGAG GTGCCTCTGG CCAGGTGGTT ACCTCTGTCA CCAGAGATGA 1260 GTCACCCAGT CTCAGCTCGC AGGCCTTCCT GGACGTTCCC AGATAGTCCC CAGTGCTGGA 1320 GGCCTGTCGA AAGTGTAGCT CCACCACGCC CTTTGATCTC TTCCTCCTCT CCTCTTCCCC 1380 ACCCGCTTCC CCCTCCTTCC CCCTCCTTCC CCCTCCTCCT TCCCCCTCCT CCTTCTCTCC 1440 TGCTGAGGGC ATTTGGCCTC ATAGATAAGC GGTTTCTAAT GAGCTCACTG GTTTCCGATG 1500 GTGGGTGGGG AGTGACTCTG GGCTTTCTGT GCTGCCTCTT CGACCTCGTC CCTGTTTTCT 1560 GCTGTGCGGA GCATGGCCCT TTCCTAATCC GAAAGAGCCG CACAGTCCCT TCCAGTGCTG 1620 CCTGTGGTCT CGCCCAGCTG GCTGTGCTAT TGCGGGACAT GGGGCCCAGC CTCCTGCTCC 1680 TTCAGAGGCC TGGGGTGGGT GAGGCTGGGG TGCCCTGGTG CTGGATGCAG GGGTGCTGTG 1740 GTGCTGAATG CTGGGGTGCC CTGGTGCTGG ACGTTGGGTG CCCAGGCACT GGATGCTGGG 1800 GTGGCCTGGT GCTGGATGCT GGGTGGCCTG GTGCTGGGTG GCCTGATGCT GGGTGCTGGG 1860 TGGTCTGGTG CTGGATGCTG GGTGGCCTGG TGCTGGGTGC TGGGTGGCCT GGTGCTGGGT 1920 ACTGGGTGCT CTGGTGGTGG ATGCAGAGGC AGGGCTATCT GTGGGTCTGC CCTTGGGTGT 1980 GGGGCAAGCC AGGTCAGCAT ATTGCAAAGC ACACGTTGGG CTGCTGCTTG TGTAATTGTC 2040 TCCTTGTCTC TGCTCTCTCC CTTCTCCCAC CTCACATGGG ATAGATCGGA GTTAACAGTG 2100 ATGCCTTTGT TTTTTGTCAA AAGCATCATA CTCATGCCCC GTGGCATTCT CTTTAAGGGA 2160 AGAGCTGGTT TTACTAAAGA TGTGCTTCAA TGCAGTGACG TGCGGTGCTG AGCAAGGCCG 2220 GGAACCTGGC CCCTGACCTG TGTACACTGG CCGGCCGTGC TCCCCTCACC CTGCGGCTAG 2280 ACCTCAAATG GCATCCCCAC CTCCCTCAGC CAACTGCAGC CCCTCTGGTA GCATGGAGCT 2340 CGCAGACGCT GGGTGCAGGA GGCCTGGGCC TGGGCCAGAC GGGTTCCCTG CACAGCTGCT 2400 TTTGCGTCAT TGATGCAGAC GCGGAGACTC ACTTCTCTGC TTCGTGTGTT CCTAGTTGGT 2460 CTCCAGTTCT TGAACAAATA ACTTTCAATT 2490
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