Tag | Content |
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EnhancerAtlas ID | HS183-00371 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr1:202002840-202004970 |
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 | CATTGCCCAC CCTAGCCCTG CCCGCCTTCC TATCTTCTTT CTTGGTTTTA TTTTTCTCCA 60 TAGCATTTAT CATGCTCAGA CACACAAAAT ATTTATCTAT TTTTGCTGTT TGTAATTGTC 120 TTTCTCCCCC CACTAAAATG AACACTCCGT GAGGGCATGG CATTTTGCCT GCTTTGCTCA 180 CAATGTGTAT CCCACTGAAG ACATCCAATA AACAATTTAT CGAATAAATG AATGCATCTA 240 CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA TCTTTGAACC TCTGATTGGT 300 GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG GGCAAAAGGT TGACCTCTTT 360 GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT GGATGGGGAA GCTGTGTGAA 420 TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT CCAAGGAATT GGATATGAAA 480 AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG GGAGGGTGGG GGGGACAGGT 540 CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC 600 AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC 660 CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC 720 TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA 780 CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG 840 CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA 900 ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC 960 ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC 1020 TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT 1080 TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC 1140 CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG 1200 CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA 1260 GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT 1320 CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT 1380 CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT 1440 CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA 1500 TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA 1560 TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT 1620 TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA 1680 GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT 1740 GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT 1800 ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG TCTGTAATCT CAGCTACTCG 1860 GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT 1920 TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC TGTCTCAAAA ACAAAAACAA 1980 AAACAAAACA AAAAAAATAA ACTTAGATGT ATATTTAAAA ATTGCTTTTT ACCCCTGAAG 2040 GTCTCAGCAT CCTACCTGCT CTATTCATTA GTGTTTAGAT TACCCATGAC ACCAGAAGGA 2100 CTTCCCAACC CAGAAAAAGA TCCAGGAGTT 2130
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