Tag | Content |
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EnhancerAtlas ID | HS098-04536 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:202002820-202005080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | + | 6.14 | CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | - | 6.14 | Foxq1 | MA0040.1 | chr1:202003046-202003057 | AATAAACAATT | - | 6.02 | NFAT5 | MA0606.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:202003070-202004639 | Colon_Crypt_1 | SE_23723 | chr1:202003133-202004433 | Colon_Crypt_2 | SE_24689 | chr1:202003019-202005179 | Colon_Crypt_3 | SE_25977 | chr1:202003098-202005224 | Duodenum_Smooth_Muscle | SE_26730 | chr1:202003201-202004852 | Esophagus | SE_27624 | chr1:202002753-202007729 | Fetal_Intestine | SE_28545 | chr1:202002635-202005490 | Fetal_Intestine_Large | SE_31432 | chr1:202003030-202004833 | Gastric | SE_33417 | chr1:202002752-202008344 | H2171 | SE_33792 | chr1:202002877-202005297 | HCC1954 | SE_34304 | chr1:202003057-202005125 | HCT-116 | SE_34741 | chr1:202002989-202005297 | HeLa | SE_41626 | chr1:202003359-202004353 | LNCaP | SE_43434 | chr1:202002760-202004009 | MCF-7 | SE_43434 | chr1:202004034-202004676 | MCF-7 | SE_50066 | chr1:202002922-202004883 | Sigmoid_Colon | SE_52354 | chr1:202003018-202004869 | Small_Intestine | SE_56834 | chr1:202002917-202004651 | VACO_400 | SE_57376 | chr1:202003233-202004124 | VACO_503 | SE_57376 | chr1:202004143-202004423 | VACO_503 | SE_57945 | chr1:202003251-202004112 | VACO_9m | SE_57945 | chr1:202004146-202004634 | VACO_9m | SE_65333 | chr1:202002930-202005541 | Pancreatic_islets | SE_67013 | chr1:202002752-202008344 | H2171 |
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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 |
GH01I202033 | chr1 | 202002815 | 202007566 |
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Enhancer Sequence | ACACAAAAAT AATTGTAACC CATTGCCCAC CCTAGCCCTG CCCGCCTTCC TATCTTCTTT 60 CTTGGTTTTA TTTTTCTCCA TAGCATTTAT CATGCTCAGA CACACAAAAT ATTTATCTAT 120 TTTTGCTGTT TGTAATTGTC TTTCTCCCCC CACTAAAATG AACACTCCGT GAGGGCATGG 180 CATTTTGCCT GCTTTGCTCA CAATGTGTAT CCCACTGAAG ACATCCAATA AACAATTTAT 240 CGAATAAATG AATGCATCTA CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA 300 TCTTTGAACC TCTGATTGGT GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG 360 GGCAAAAGGT TGACCTCTTT GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT 420 GGATGGGGAA GCTGTGTGAA TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT 480 CCAAGGAATT GGATATGAAA AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG 540 GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG 600 TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT 660 GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG 720 TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA 780 GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG 840 GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT 900 AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT 960 CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG 1020 TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC 1080 CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT 1140 GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA 1200 GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG 1260 ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC 1320 CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT 1380 GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA 1440 CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT 1500 CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC 1560 AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT 1620 TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC 1680 TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT 1740 TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA 1800 CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG 1860 TCTGTAATCT CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG 1920 AGGCTGCAGT GAGCTGAGAT TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC 1980 TGTCTCAAAA ACAAAAACAA AAACAAAACA AAAAAAATAA ACTTAGATGT ATATTTAAAA 2040 ATTGCTTTTT ACCCCTGAAG GTCTCAGCAT CCTACCTGCT CTATTCATTA GTGTTTAGAT 2100 TACCCATGAC ACCAGAAGGA CTTCCCAACC CAGAAAAAGA TCCAGGAGTT GATATAAAAT 2160 ATAGAACTAC TATAATATTA GCAACTTGGA GCAGCAAGTT CTTGACTTGG GAAAGTAGGA 2220 ATTCCTCTCA TTAAGAGATG TTTGCCCACA GGGAATGCTG 2260
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