Tag | Content |
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EnhancerAtlas ID | HS105-06360 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:202003340-202004670 |
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 | 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 | GATATGAGAT GCCAGACGGG GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG 60 ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC 120 CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT 180 TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG 240 AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC 300 GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT 360 GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG 420 ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC 480 CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT 540 TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG 600 GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC 660 CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC 720 ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA 780 CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA 840 TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG 900 GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT 960 GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG 1020 TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT 1080 GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT 1140 TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT 1200 TGCCTGTAAT CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG 1260 TTCAAGACCA GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA 1320 GCTGGGTGTG 1330
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