Tag | Content |
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EnhancerAtlas ID | HS074-09919 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr21:44829310-44832540 |
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 | Klf1 | MA0493.1 | chr21:44831578-44831589 | TGGGTGTGGCC | - | 6.62 | 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: 8 | 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_52671 | chr21:44831925-44832753 | Small_Intestine | 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: 3 | Chromosome | Start | End |
chr21 | 44830426 | 44830842 | chr21 | 44831891 | 44832268 | chr21 | 44832284 | 44832425 |
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| Number: 3 | ID | Chromosome | Start | End |
GH21I043409 | chr21 | 44828944 | 44832920 | GH21I006127 | chr21 | 44829746 | 44831137 | GH21I006125 | chr21 | 44831738 | 44832739 |
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Enhancer Sequence | CGCGGCACGT GGAGGAAGCC ACGTTTAATT ATGCTGAGTG AGAGAAGCCA GCCCATCAGG 60 AGCACACGCT GTCTGATTCC ATTCCTAGGA ATTCTGGAAA ATGCAAACGC ATGCCCAGTG 120 ACAGGAAGCA GGTCATCCGT TGCCTGGGGC CGGGAACACG GCAAGGGCAC GGAGCGGAGA 180 GCCCAGGGGA GCTTTCTGGG TGACAGGCGT GTTCTGTGCG TCAATTCTGA TGGTGGTGAC 240 CCAGGTCGGT GCCCGGCAGA ACTCCTTGAA GTTCGCACCA AAGACGACGC ATTTGGTTCA 300 GGTCACTGGG AGCTCGGTGG AGCTGATTTG TTCTGGGGCA CATTTCTGCT GAGACGGATT 360 TGCGTTCTCC CCTGAGCCTC ACAGTCTTCC GGCCCCCCGC TCTGGAACCC AGGGCCCCGG 420 GCTTTCCACT TAACCTCTTG GCTGGAAGGG AACATGCTCT GTGATCATAG GAAGGTACCT 480 TCCCCTTCAA ATTTCAAAGA AAAGCCCCTA AAATCTGCTG GGGAAGCCCA TTCATTCCAG 540 ACCAGAACAC TGCAAAGGAC AAAAGGGGAA TGGAGCATTT CTGGCCACCT GGGTTCCCTG 600 AGTACTTTTT CTAAGTCCTT TCTTGTTTCT TGTTTCTTTC TTTCTTTCTT TTTTTTTTTT 660 AACAGAAATC ACATTCAAAT AAGTGAAATA ATAATAATTA GAAAAAAGTG AGTCAGACTG 720 AGACCCCAGC AGTTCCCCTG AGGAAAGAAA CTGAACATTC CCTACCTCCT CCCTCCCTCC 780 CTCCTATCTC CCTCCTCCCT CCCTCGTCTC CCTCCTCCTT CCCTCCTCTC TCCTTCCCTC 840 CCTCTTCTCT CCCTCTCTCC CTCCTCTCTC TCCTTCCCTC CCTCCTCTCT CCTCCCTCCT 900 CTCTCTCCTC TCTTCTCTCC CTCCTCTCTC CTCCCTCCCT CCTCTTTCTC CTCTCTTCTC 960 TCCCTCCCTC CCTCTCTGCC TCCCTCTCTT CTCCCTCTCT GCCTCCCTCC TCTCTCTCTC 1020 CTTTCCTCTT CTGTCCTCCC CTCTCCCCTC CCTCTCCCCC TCTCTCTTCT CTGCCAGGCG 1080 CCACACCAGC TGCACAGGCA GGACCCGGAG CCCAGCCCTC CTGGTCTCTG AAGAGCCAGA 1140 CCTGGACACC TTCCTCAGGA CCCGCCCGCC TCCGAACAGC AGACTCCTCC CAAGATCAGA 1200 GGTGGGGCCA CAGGCAGGGC GGCTGTGCTC ACCCAAGCCC TCACCAGCAT GCCGCCTCAA 1260 CACCCCGGTG TTATTCCGGA AGAAACACGA AGAGGCCAAC TCTGTTTCTT CCACCCCAAG 1320 AGAGTCGGTT CCTCTTAGGT CAGATTCAGT TCCTGCCTCC GAGGGAGGCG AGCACGTGCA 1380 GAAACAGGTG GATCTTGCCT CGGCTCCCTC CAGGCTGGGC CCAGGGACCT CCCTCTGGCT 1440 GGGGCATCCC CTCTCTCCCC ACCCCCACCC CGAGAGGCCA GTCCTGCTCC TGGGAGCCAG 1500 TATTTCTGGA CTGCCGGAAA GCCTTCTTCT TATCCCGCGG CCCAGCGAGG AGAGCGCCAG 1560 CCGTTCAGGG TGACAGAAAA GCACAGAGGC AGGGCCCAGG CGCCTCCAGG CGAAGGCCTC 1620 CGCTCCCACC GCTGCGAGAG GAGGCGCGTC CACGACGGAA TAAGCAGGCG GTCAGGTCGC 1680 CAACAATCCG GTCAACCACG GTGCTTCTTC CCTGGTGGGT GTCTGGCCCC GTTCTTGCTG 1740 GGGATGGCGC TCGGGGATGC CACCGTGTTT CCCCAGGGCC CACTGTGCAC CCTGCATGTC 1800 GCGCCCTTGT CACGGGAGCG GCCTGCTGAC CCGGAGCACG CGTGGCCGTC ACAAAGGGCT 1860 GCAAAGCTGC AGCACCAGAA CGCAAACTCA GGCGTGCGGC AACGGAGGCC ACGTTCTCAG 1920 CCACCGTGCC ACTCTGCATG TCAGCTGGCT GGGCGTGCCT CCGTCTTGTG TTAGCAAGGA 1980 CATGGCAATC ACCTGATTTG CTTTGGTTGA AGCTCCAGGC AGTACCTGGC CCCTCACCAG 2040 ACTGAAAAAG AAAGTCCCAG AACCCCAGAA CCCCGTATGG CTCAGAAGTG CCATCGAGTA 2100 CTAGGGGTGC GCCAGGGCCC GGCTCAGCCC GGCCAAGCCC CAGCAGGAAG GAACATGTCC 2160 TCAACGAGAA CATCCTGCAA AATGCCCGGG GTGGGTGGGG GATGCTCACG GTGCCAGACG 2220 TGGGCTAGGG GCCATAAAGG ACCCTCAGGC AAGGGGCAAA CACACCCATG GGTGTGGCCA 2280 GCTCCCTCTA CCCATCAGGA CCTCCCCAGT GGAGGGACTG AAATGACTCA GGAGCAGATC 2340 AAGGGGCCCA GGGCAGAATT CTGGAGTCCT ACAAGGCCTG TGGGAGGCTC CCCAAGGGGG 2400 GCTCCAACTT TCAACCTGAG AAGTCTAAGC CTCTATCACC ATCATCATCG CCATCGTCTT 2460 CGCCACCATC AGGAGTTCTG GAAGAAGCGC CCAAGCATGG GAGACACAGG GATGGTTTTG 2520 CCAGTGCTGT GTGTTAAGGA GCTGCTACCT GCTGGGGCTG CTTCAGTACC CTGGAGCACC 2580 ATGAGACACA TCTGTCCCCA CGAGGAGCTG ACCACTAGGT CGGGGAGCTG AGACATGGGC 2640 AGGTCACACC CTGAATTCGC ATGCACGACA CGACAAGAGG TTCCGACTCG AGGTTCCTGG 2700 TTTCTAAGGC TCCCAAACAA TAAACACAGG TGCCCTCAGC ACAGCCGCCC GGCTCCTTGT 2760 TCAGCAGATG CCACACAGCC CAACCTTGGT GTCCTGAGGC GGCCCCACTC TAAGCGGGGT 2820 GGAGCGACGA GGCTGCCTGG AGACAGAGCA GCTCCGTGGG CCCCCAGCTC CCCTGCCAGA 2880 TTCCCCCACA CAGGCATGGC CCAAGCAGGC ACCTCCGCTC ACTCAGGAGT GCTCAGCCCT 2940 GGTTTGGCCT CCCTGTCAGA CAGCCTCAAG CCACTAAGCC AGCGGCAGCC ACAGCCAGGA 3000 CCTCGGAGGC TACTGCTTTG TTCTTAGAGA CAGCAAAACC GCAGAGATGA CTCAGAAGAC 3060 AAAGAGCCCC CTCCCCGGCC TCTCCCACCA TCCAGCTGCC TGAGGGGCCG TCGCAGTGCA 3120 GGCTCTCCCG AGGGCCAGGA CGCCCTGTCT GAGCAGGGCT CCAGGAACAA TGAGGCTGGC 3180 CCCGGCCACA CTTATGCCCA GCCAACCTCA GCACCGACAG TGGCCTGCCC 3230
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