Tag | Content |
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EnhancerAtlas ID | HS046-02737 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:202003400-202005230 |
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 | IRF1 | MA0050.2 | chr1:202005141-202005162 | GTTTCCTTTTACTTTTCTTTT | + | 6.23 | IRF1 | MA0050.2 | chr1:202005162-202005183 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | 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 | ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC 60 CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT 120 TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG 180 AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC 240 GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT 300 GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG 360 ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC 420 CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT 480 TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG 540 GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC 600 CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC 660 ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA 720 CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA 780 TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG 840 GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT 900 GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG 960 TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT 1020 GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT 1080 TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT 1140 TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG 1200 TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA 1260 GCTGGGTGTG GTGGCAGGCG TCTGTAATCT CAGCTACTCG GGAGGCTGAG GCAGGAGAAT 1320 CACTTGAACC TGGGAGGCGG AGGCTGCAGT GAGCTGAGAT TGCACCATTG CACTCCAGCC 1380 TGGGCAACAG AGTGACATTC TGTCTCAAAA ACAAAAACAA AAACAAAACA AAAAAAATAA 1440 ACTTAGATGT ATATTTAAAA ATTGCTTTTT ACCCCTGAAG GTCTCAGCAT CCTACCTGCT 1500 CTATTCATTA GTGTTTAGAT TACCCATGAC ACCAGAAGGA CTTCCCAACC CAGAAAAAGA 1560 TCCAGGAGTT GATATAAAAT ATAGAACTAC TATAATATTA GCAACTTGGA GCAGCAAGTT 1620 CTTGACTTGG GAAAGTAGGA ATTCCTCTCA TTAAGAGATG TTTGCCCACA GGGAATGCTG 1680 CATAGAAAAG AATTTGGCTG GAACTCTTTT TTTCCACTAT GACTCCATTC ACACTTGAAT 1740 TGTTTCCTTT TACTTTTCTT TTTCTTTCTT TCTTTTTTTT TTTTTTTTTT GAGACAGAGT 1800 CTCGCTCTGT CACCCAGGCT GGAGTGCAGT 1830
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