Tag | Content |
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EnhancerAtlas ID | HS073-09552 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr21:44829360-44831090 |
Target genes | |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:44830181-44830199 | CCTTCCCTCCCTCCTCTC | - | 6.02 | EWSR1-FLI1 | MA0149.1 | chr21:44830177-44830195 | CTCTCCTTCCCTCCCTCC | - | 6.44 | IRF1 | MA0050.2 | chr21:44829948-44829969 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | ZNF263 | MA0528.1 | chr21:44830159-44830180 | TCCCTCTCTCCCTCCTCTCTC | - | 6.01 | ZNF263 | MA0528.1 | chr21:44830129-44830150 | TCCCTCCTCTCTCCTTCCCTC | - | 6.07 | ZNF263 | MA0528.1 | chr21:44830212-44830233 | CTCTCCTCTCTTCTCTCCCTC | - | 6.08 | ZNF263 | MA0528.1 | chr21:44830152-44830173 | TCTTCTCTCCCTCTCTCCCTC | - | 6.15 | ZNF263 | MA0528.1 | chr21:44830255-44830276 | TTCTCCTCTCTTCTCTCCCTC | - | 6.16 | ZNF263 | MA0528.1 | chr21:44830068-44830089 | TCCCTACCTCCTCCCTCCCTC | - | 6.23 | ZNF263 | MA0528.1 | chr21:44830110-44830131 | CCCTCGTCTCCCTCCTCCTTC | - | 6.23 | ZNF263 | MA0528.1 | chr21:44830137-44830158 | CTCTCCTTCCCTCCCTCTTCT | - | 6.25 | ZNF263 | MA0528.1 | chr21:44830355-44830376 | CCCTCCCTCTCCCCCTCTCTC | - | 6.25 | ZNF263 | MA0528.1 | chr21:44830168-44830189 | CCCTCCTCTCTCTCCTTCCCT | - | 6.27 | ZNF263 | MA0528.1 | chr21:44830090-44830111 | CTCCTATCTCCCTCCTCCCTC | - | 6.32 | ZNF263 | MA0528.1 | chr21:44830173-44830194 | CTCTCTCTCCTTCCCTCCCTC | - | 6.33 | ZNF263 | MA0528.1 | chr21:44830240-44830261 | CTCCCTCCCTCCTCTTTCTCC | - | 6.33 | ZNF263 | MA0528.1 | chr21:44830272-44830293 | CCTCCCTCCCTCTCTGCCTCC | - | 6.33 | ZNF263 | MA0528.1 | chr21:44830302-44830323 | CCCTCTCTGCCTCCCTCCTCT | - | 6.34 | ZNF263 | MA0528.1 | chr21:44830347-44830368 | CCCCTCTCCCCTCCCTCTCCC | - | 6.36 | ZNF263 | MA0528.1 | chr21:44830187-44830208 | CTCCCTCCTCTCTCCTCCCTC | - | 6.53 | ZNF263 | MA0528.1 | chr21:44830226-44830247 | CTCCCTCCTCTCTCCTCCCTC | - | 6.53 | ZNF263 | MA0528.1 | chr21:44830298-44830319 | TTCTCCCTCTCTGCCTCCCTC | - | 6.56 | ZNF263 | MA0528.1 | chr21:44830349-44830370 | CCTCTCCCCTCCCTCTCCCCC | - | 6.68 | ZNF263 | MA0528.1 | chr21:44830230-44830251 | CTCCTCTCTCCTCCCTCCCTC | - | 6.82 | ZNF263 | MA0528.1 | chr21:44830118-44830139 | TCCCTCCTCCTTCCCTCCTCT | - | 6.86 | ZNF263 | MA0528.1 | chr21:44830133-44830154 | TCCTCTCTCCTTCCCTCCCTC | - | 6.86 | ZNF263 | MA0528.1 | chr21:44830223-44830244 | TCTCTCCCTCCTCTCTCCTCC | - | 6.94 | ZNF263 | MA0528.1 | chr21:44830275-44830296 | CCCTCCCTCTCTGCCTCCCTC | - | 6.94 | ZNF263 | MA0528.1 | chr21:44830125-44830146 | TCCTTCCCTCCTCTCTCCTTC | - | 6.96 | ZNF263 | MA0528.1 | chr21:44830259-44830280 | CCTCTCTTCTCTCCCTCCCTC | - | 6.97 | ZNF263 | MA0528.1 | chr21:44830234-44830255 | TCTCTCCTCCCTCCCTCCTCT | - | 7.17 | ZNF263 | MA0528.1 | chr21:44830263-44830284 | TCTTCTCTCCCTCCCTCCCTC | - | 7.18 | ZNF263 | MA0528.1 | chr21:44830191-44830212 | CTCCTCTCTCCTCCCTCCTCT | - | 7.19 | ZNF263 | MA0528.1 | chr21:44830184-44830205 | TCCCTCCCTCCTCTCTCCTCC | - | 7.24 | ZNF263 | MA0528.1 | chr21:44830087-44830108 | TCCCTCCTATCTCCCTCCTCC | - | 7.35 | ZNF263 | MA0528.1 | chr21:44830216-44830237 | CCTCTCTTCTCTCCCTCCTCT | - | 7.36 | ZNF263 | MA0528.1 | chr21:44830200-44830221 | CCTCCCTCCTCTCTCTCCTCT | - | 7.41 | ZNF263 | MA0528.1 | chr21:44830343-44830364 | TCCTCCCCTCTCCCCTCCCTC | - | 7.61 | ZNF263 | MA0528.1 | chr21:44830243-44830264 | CCTCCCTCCTCTTTCTCCTCT | - | 7.65 | ZNF263 | MA0528.1 | chr21:44830156-44830177 | CTCTCCCTCTCTCCCTCCTCT | - | 7.83 | ZNF263 | MA0528.1 | chr21:44830165-44830186 | TCTCCCTCCTCTCTCTCCTTC | - | 7.94 | ZNF263 | MA0528.1 | chr21:44830107-44830128 | CCTCCCTCGTCTCCCTCCTCC | - | 7.97 | ZNF263 | MA0528.1 | chr21:44830177-44830198 | CTCTCCTTCCCTCCCTCCTCT | - | 8.18 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_10405 | chr21:44828872-44832961 | CD19_Primary | SE_11196 | chr21:44827821-44836466 | CD20 | SE_20443 | chr21:44829157-44832861 | CD56 | SE_34640 | chr21:44829674-44836743 | HeLa | SE_58455 | chr21:44763901-44850830 | Ly1 | SE_59568 | chr21:44816711-44859975 | Ly3 | SE_62541 | chr21:44767678-44851140 | Tonsil |
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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: 2 | ID | Chromosome | Start | End |
GH21I043409 | chr21 | 44828944 | 44832920 | GH21I006127 | chr21 | 44829746 | 44831137 |
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Enhancer Sequence | GCCCATCAGG AGCACACGCT GTCTGATTCC ATTCCTAGGA ATTCTGGAAA ATGCAAACGC 60 ATGCCCAGTG ACAGGAAGCA GGTCATCCGT TGCCTGGGGC CGGGAACACG GCAAGGGCAC 120 GGAGCGGAGA GCCCAGGGGA GCTTTCTGGG TGACAGGCGT GTTCTGTGCG TCAATTCTGA 180 TGGTGGTGAC CCAGGTCGGT GCCCGGCAGA ACTCCTTGAA GTTCGCACCA AAGACGACGC 240 ATTTGGTTCA GGTCACTGGG AGCTCGGTGG AGCTGATTTG TTCTGGGGCA CATTTCTGCT 300 GAGACGGATT TGCGTTCTCC CCTGAGCCTC ACAGTCTTCC GGCCCCCCGC TCTGGAACCC 360 AGGGCCCCGG GCTTTCCACT TAACCTCTTG GCTGGAAGGG AACATGCTCT GTGATCATAG 420 GAAGGTACCT TCCCCTTCAA ATTTCAAAGA AAAGCCCCTA AAATCTGCTG GGGAAGCCCA 480 TTCATTCCAG ACCAGAACAC TGCAAAGGAC AAAAGGGGAA TGGAGCATTT CTGGCCACCT 540 GGGTTCCCTG AGTACTTTTT CTAAGTCCTT TCTTGTTTCT TGTTTCTTTC TTTCTTTCTT 600 TTTTTTTTTT AACAGAAATC ACATTCAAAT AAGTGAAATA ATAATAATTA GAAAAAAGTG 660 AGTCAGACTG AGACCCCAGC AGTTCCCCTG AGGAAAGAAA CTGAACATTC CCTACCTCCT 720 CCCTCCCTCC CTCCTATCTC CCTCCTCCCT CCCTCGTCTC CCTCCTCCTT CCCTCCTCTC 780 TCCTTCCCTC CCTCTTCTCT CCCTCTCTCC CTCCTCTCTC TCCTTCCCTC CCTCCTCTCT 840 CCTCCCTCCT CTCTCTCCTC TCTTCTCTCC CTCCTCTCTC CTCCCTCCCT CCTCTTTCTC 900 CTCTCTTCTC TCCCTCCCTC CCTCTCTGCC TCCCTCTCTT CTCCCTCTCT GCCTCCCTCC 960 TCTCTCTCTC CTTTCCTCTT CTGTCCTCCC CTCTCCCCTC CCTCTCCCCC TCTCTCTTCT 1020 CTGCCAGGCG CCACACCAGC TGCACAGGCA GGACCCGGAG CCCAGCCCTC CTGGTCTCTG 1080 AAGAGCCAGA CCTGGACACC TTCCTCAGGA CCCGCCCGCC TCCGAACAGC AGACTCCTCC 1140 CAAGATCAGA GGTGGGGCCA CAGGCAGGGC GGCTGTGCTC ACCCAAGCCC TCACCAGCAT 1200 GCCGCCTCAA CACCCCGGTG TTATTCCGGA AGAAACACGA AGAGGCCAAC TCTGTTTCTT 1260 CCACCCCAAG AGAGTCGGTT CCTCTTAGGT CAGATTCAGT TCCTGCCTCC GAGGGAGGCG 1320 AGCACGTGCA GAAACAGGTG GATCTTGCCT CGGCTCCCTC CAGGCTGGGC CCAGGGACCT 1380 CCCTCTGGCT GGGGCATCCC CTCTCTCCCC ACCCCCACCC CGAGAGGCCA GTCCTGCTCC 1440 TGGGAGCCAG TATTTCTGGA CTGCCGGAAA GCCTTCTTCT TATCCCGCGG CCCAGCGAGG 1500 AGAGCGCCAG CCGTTCAGGG TGACAGAAAA GCACAGAGGC AGGGCCCAGG CGCCTCCAGG 1560 CGAAGGCCTC CGCTCCCACC GCTGCGAGAG GAGGCGCGTC CACGACGGAA TAAGCAGGCG 1620 GTCAGGTCGC CAACAATCCG GTCAACCACG GTGCTTCTTC CCTGGTGGGT GTCTGGCCCC 1680 GTTCTTGCTG GGGATGGCGC TCGGGGATGC CACCGTGTTT CCCCAGGGCC 1730
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