Tag | Content |
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EnhancerAtlas ID | HS012-00887 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr1:202003020-202004800 |
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: 25 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:202003070-202004639 | Colon_Crypt_1 | SE_23723 | chr1:202003133-202004433 | Colon_Crypt_2 | SE_23723 | chr1:202004446-202004634 | 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 | CAATGTGTAT CCCACTGAAG ACATCCAATA AACAATTTAT CGAATAAATG AATGCATCTA 60 CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA TCTTTGAACC TCTGATTGGT 120 GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG GGCAAAAGGT TGACCTCTTT 180 GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT GGATGGGGAA GCTGTGTGAA 240 TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT CCAAGGAATT GGATATGAAA 300 AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG GGAGGGTGGG GGGGACAGGT 360 CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC 420 AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC 480 CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC 540 TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA 600 CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG 660 CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA 720 ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC 780 ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC 840 TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT 900 TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC 960 CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG 1020 CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA 1080 GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT 1140 CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT 1200 CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT 1260 CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA 1320 TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA 1380 TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT 1440 TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA 1500 GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT 1560 GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT 1620 ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG TCTGTAATCT CAGCTACTCG 1680 GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT 1740 TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC 1780
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