Tag | Content |
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EnhancerAtlas ID | HS180-04117 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:202003040-202005110 |
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 | ACATCCAATA AACAATTTAT CGAATAAATG AATGCATCTA CCTGATACCT CATCAAGAAA 60 TTGATGACCA CTAATTATCA TCTTTGAACC TCTGATTGGT GACCTCTGGC AAGGCTGAGG 120 ACCTTTAGCT CTAATCAATG GGCAAAAGGT TGACCTCTTT GCTACTGATT GGCTTTTCCT 180 TTTCATTATA CCCTTGGGCT GGATGGGGAA GCTGTGTGAA TCAACGCTTC ATAAGCCTTC 240 CTCTCTGAGA ACTAGGGCTT CCAAGGAATT GGATATGAAA AGGCAGAGAG GAAGGAGGAG 300 GATATGAGAT GCCAGACGGG GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG 360 ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC 420 CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT 480 TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG 540 AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC 600 GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT 660 GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG 720 ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC 780 CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT 840 TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG 900 GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC 960 CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC 1020 ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA 1080 CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA 1140 TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG 1200 GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT 1260 GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG 1320 TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT 1380 GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT 1440 TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT 1500 TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG 1560 TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA 1620 GCTGGGTGTG GTGGCAGGCG TCTGTAATCT CAGCTACTCG GGAGGCTGAG GCAGGAGAAT 1680 CACTTGAACC TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT TGCACCATTG CACTCCAGCC 1740 TGGGCAACAG AGTGACATTC TGTCTCAAAA ACAAAAACAA AAACAAAACA AAAAAAATAA 1800 ACTTAGATGT ATATTTAAAA ATTGCTTTTT ACCCCTGAAG GTCTCAGCAT CCTACCTGCT 1860 CTATTCATTA GTGTTTAGAT TACCCATGAC ACCAGAAGGA CTTCCCAACC CAGAAAAAGA 1920 TCCAGGAGTT GATATAAAAT ATAGAACTAC TATAATATTA GCAACTTGGA GCAGCAAGTT 1980 CTTGACTTGG GAAAGTAGGA ATTCCTCTCA TTAAGAGATG TTTGCCCACA GGGAATGCTG 2040 CATAGAAAAG AATTTGGCTG GAACTCTTTT 2070
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