Tag | Content |
---|
EnhancerAtlas ID | HS187-15903 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr21:44829990-44832730 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | 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 |
|
| 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 |
|
| 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 |
|
| Number: 3 | ID | Chromosome | Start | End |
GH21I043409 | chr21 | 44828944 | 44832920 | GH21I006127 | chr21 | 44829746 | 44831137 | GH21I006125 | chr21 | 44831738 | 44832739 |
|
Enhancer Sequence | AAGTGAAATA ATAATAATTA GAAAAAAGTG AGTCAGACTG AGACCCCAGC AGTTCCCCTG 60 AGGAAAGAAA CTGAACATTC CCTACCTCCT CCCTCCCTCC CTCCTATCTC CCTCCTCCCT 120 CCCTCGTCTC CCTCCTCCTT CCCTCCTCTC TCCTTCCCTC CCTCTTCTCT CCCTCTCTCC 180 CTCCTCTCTC TCCTTCCCTC CCTCCTCTCT CCTCCCTCCT CTCTCTCCTC TCTTCTCTCC 240 CTCCTCTCTC CTCCCTCCCT CCTCTTTCTC CTCTCTTCTC TCCCTCCCTC CCTCTCTGCC 300 TCCCTCTCTT CTCCCTCTCT GCCTCCCTCC TCTCTCTCTC CTTTCCTCTT CTGTCCTCCC 360 CTCTCCCCTC CCTCTCCCCC TCTCTCTTCT CTGCCAGGCG CCACACCAGC TGCACAGGCA 420 GGACCCGGAG CCCAGCCCTC CTGGTCTCTG AAGAGCCAGA CCTGGACACC TTCCTCAGGA 480 CCCGCCCGCC TCCGAACAGC AGACTCCTCC CAAGATCAGA GGTGGGGCCA CAGGCAGGGC 540 GGCTGTGCTC ACCCAAGCCC TCACCAGCAT GCCGCCTCAA CACCCCGGTG TTATTCCGGA 600 AGAAACACGA AGAGGCCAAC TCTGTTTCTT CCACCCCAAG AGAGTCGGTT CCTCTTAGGT 660 CAGATTCAGT TCCTGCCTCC GAGGGAGGCG AGCACGTGCA GAAACAGGTG GATCTTGCCT 720 CGGCTCCCTC CAGGCTGGGC CCAGGGACCT CCCTCTGGCT GGGGCATCCC CTCTCTCCCC 780 ACCCCCACCC CGAGAGGCCA GTCCTGCTCC TGGGAGCCAG TATTTCTGGA CTGCCGGAAA 840 GCCTTCTTCT TATCCCGCGG CCCAGCGAGG AGAGCGCCAG CCGTTCAGGG TGACAGAAAA 900 GCACAGAGGC AGGGCCCAGG CGCCTCCAGG CGAAGGCCTC CGCTCCCACC GCTGCGAGAG 960 GAGGCGCGTC CACGACGGAA TAAGCAGGCG GTCAGGTCGC CAACAATCCG GTCAACCACG 1020 GTGCTTCTTC CCTGGTGGGT GTCTGGCCCC GTTCTTGCTG GGGATGGCGC TCGGGGATGC 1080 CACCGTGTTT CCCCAGGGCC CACTGTGCAC CCTGCATGTC GCGCCCTTGT CACGGGAGCG 1140 GCCTGCTGAC CCGGAGCACG CGTGGCCGTC ACAAAGGGCT GCAAAGCTGC AGCACCAGAA 1200 CGCAAACTCA GGCGTGCGGC AACGGAGGCC ACGTTCTCAG CCACCGTGCC ACTCTGCATG 1260 TCAGCTGGCT GGGCGTGCCT CCGTCTTGTG TTAGCAAGGA CATGGCAATC ACCTGATTTG 1320 CTTTGGTTGA AGCTCCAGGC AGTACCTGGC CCCTCACCAG ACTGAAAAAG AAAGTCCCAG 1380 AACCCCAGAA CCCCGTATGG CTCAGAAGTG CCATCGAGTA CTAGGGGTGC GCCAGGGCCC 1440 GGCTCAGCCC GGCCAAGCCC CAGCAGGAAG GAACATGTCC TCAACGAGAA CATCCTGCAA 1500 AATGCCCGGG GTGGGTGGGG GATGCTCACG GTGCCAGACG TGGGCTAGGG GCCATAAAGG 1560 ACCCTCAGGC AAGGGGCAAA CACACCCATG GGTGTGGCCA GCTCCCTCTA CCCATCAGGA 1620 CCTCCCCAGT GGAGGGACTG AAATGACTCA GGAGCAGATC AAGGGGCCCA GGGCAGAATT 1680 CTGGAGTCCT ACAAGGCCTG TGGGAGGCTC CCCAAGGGGG GCTCCAACTT TCAACCTGAG 1740 AAGTCTAAGC CTCTATCACC ATCATCATCG CCATCGTCTT CGCCACCATC AGGAGTTCTG 1800 GAAGAAGCGC CCAAGCATGG GAGACACAGG GATGGTTTTG CCAGTGCTGT GTGTTAAGGA 1860 GCTGCTACCT GCTGGGGCTG CTTCAGTACC CTGGAGCACC ATGAGACACA TCTGTCCCCA 1920 CGAGGAGCTG ACCACTAGGT CGGGGAGCTG AGACATGGGC AGGTCACACC CTGAATTCGC 1980 ATGCACGACA CGACAAGAGG TTCCGACTCG AGGTTCCTGG TTTCTAAGGC TCCCAAACAA 2040 TAAACACAGG TGCCCTCAGC ACAGCCGCCC GGCTCCTTGT TCAGCAGATG CCACACAGCC 2100 CAACCTTGGT GTCCTGAGGC GGCCCCACTC TAAGCGGGGT GGAGCGACGA GGCTGCCTGG 2160 AGACAGAGCA GCTCCGTGGG CCCCCAGCTC CCCTGCCAGA TTCCCCCACA CAGGCATGGC 2220 CCAAGCAGGC ACCTCCGCTC ACTCAGGAGT GCTCAGCCCT GGTTTGGCCT CCCTGTCAGA 2280 CAGCCTCAAG CCACTAAGCC AGCGGCAGCC ACAGCCAGGA CCTCGGAGGC TACTGCTTTG 2340 TTCTTAGAGA CAGCAAAACC GCAGAGATGA CTCAGAAGAC AAAGAGCCCC CTCCCCGGCC 2400 TCTCCCACCA TCCAGCTGCC TGAGGGGCCG TCGCAGTGCA GGCTCTCCCG AGGGCCAGGA 2460 CGCCCTGTCT GAGCAGGGCT CCAGGAACAA TGAGGCTGGC CCCGGCCACA CTTATGCCCA 2520 GCCAACCTCA GCACCGACAG TGGCCTGCCC TGTGCCTGCC CCTGCCCATG GCTCCTGCCT 2580 GCTCTCCTCA TGGGAACTGC TGCGCACTCA CTGAGCATCT GCCTCCTTGA GAAAAAACTT 2640 TGTTTTCTTC TTAAAAACAT TGTGGTCCCG GCGCAGTGGC TCACGCTTGT AATCTCCACA 2700 CTTTGGGGGG CTGAGGTGGG CGGACCTCAA GTGTGAGGTC 2740
|