Tag | Content |
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EnhancerAtlas ID | HS110-00012 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr1:1079630-1081000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:1080703-1080721 | GGAAGGAAGGCAAGGAGG | + | 6.93 | Nr2f6(var.2) | MA0728.1 | chr1:1080757-1080772 | TGACCTCATGACCCC | - | 6.63 | ZEB1 | MA0103.3 | chr1:1080366-1080377 | CGCACCTGCGC | + | 6.32 | ZNF263 | MA0528.1 | chr1:1080701-1080722 | GGGGAAGGAAGGCAAGGAGGG | + | 6.1 | ZNF263 | MA0528.1 | chr1:1080311-1080332 | CTCCCCTCCCTTCCCACCCCC | - | 6.23 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_10678 | chr1:1078154-1080826 | CD19_Primary | SE_24482 | chr1:1077845-1081465 | Colon_Crypt_2 | SE_24970 | chr1:1077814-1082618 | Colon_Crypt_3 | SE_27531 | chr1:1078709-1080956 | Esophagus | SE_28002 | chr1:1078456-1081135 | Fetal_Intestine | SE_29232 | chr1:1078835-1080697 | Fetal_Intestine_Large | SE_34473 | chr1:1079431-1080895 | HCT-116 | SE_41856 | chr1:1079979-1080636 | LNCaP | SE_52392 | chr1:1077928-1081420 | Small_Intestine | SE_56870 | chr1:1078454-1081111 | VACO_400 | SE_57937 | chr1:1079709-1080662 | VACO_9m |
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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 |
GH01I001142 | chr1 | 1077792 | 1081590 |
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Enhancer Sequence | TCCGGTGCCT CTGAGAGACA AGCCTACTCC CCCCGGGCTG GGTGGCCCAG GGCACAGTTA 60 GACCCGGGAG TGGAAAAGGC GGTGGCGGTT TTCTTGCTGT TGTCCCGGCA GCGTCTTTGG 120 TGACACTTTC CCGCCTTTGG AGACCAATTA CCCGGCAGAG GCCCAGTGGC CTCATTAACT 180 CTGCTGCGGC GTCGAGAAAG GGGGAAGGAG CCAGCCCACG GGCAGGGCAG GGCGGCTGCA 240 GACTCTCCCG CAGCTCAGGG GCCTGGAGAA ACCTGGCCAC ACCTGGCCCA GCTGGGTCAG 300 GCCTCTGCCA ACAGGAGCCC AGGGCCCCAG CGCTCCCCTC CCTGCCAGGG AAACAGCCCA 360 TAACGACAGC CTTTCCTGGA GCCTGGGTTG CATCAGCCGA GCCGCCAGCC ACAGGGCCCC 420 AGCAACGGCA CCTGGGCCCG GGGCCTGGCC TGCCGGGGAC ACTCGGCTGT GCGCACCTCG 480 AGGGGCTCTA CAGCCTGTGG GGCCGCGCCT GCCTCTCGGG GCTTCCGGGC GATTCCTCCT 540 TCTCCTCCGT GGTGTGTGCT GTGCAGACGG GGACCGGGCC AGGCCAGACG CCGGATCCAG 600 AGCAGCTTCC CAGACAGGCC ACCCACCCCT CCGAGGCCTC CCTCAGTCCC CTGGCGGGAG 660 TCCCCGGCCT TCCGGGCCTC TCTCCCCTCC CTTCCCACCC CCAGGAGGGG AGAGGACTGA 720 GGCCTGGGGT CACTGCCGCA CCTGCGCTCT GAGACCTGCA CTCGCCCAGG CCGGAGTCCC 780 CACGAGGCAG GAACCCTGGC ATGCGGCCGG CAGTGCCCAC AGCACCCAGT CAGCCGGGAG 840 GGGTCTCACC CCACAGCCCC CCGCTCCTCC CCTCCACACC CAACCACAGT CCCTCCTGGC 900 TGACACCGTG GCCCCTCCTG GCCTGTGCTC CCCGGGAACC TCAGTCAGTG TCACTTGAAC 960 TCCAGCACCG GACCTGGCCC CGTCCATCCA GCCTCTGCCC CGAGAGCCCC GCCCGTATCT 1020 CCAGAGGACA CGCCCTGCCA GGGGACAGGC GGGAGCAGCT GAGGGCCGCC CGGGGAAGGA 1080 AGGCAAGGAG GGCATGTAAT CGCCTGACCA CATGGCCGAC CCCCTTGTGA CCTCATGACC 1140 CCCACCACCT TCATGGCCGA CCCCACCTGA CCTCATGGCC GACCTGACCT GACCGCACGG 1200 CTGACCCAAC CCCATCTCAT GACTGACCCC ACCTGACTTT ATGGCTCACC CCAGTGACCC 1260 CATGGCCAAC CCCACCTGAC CTCATGGCCG ACCCGATCTG ACCTCATGGC TGATCCTCAT 1320 GACCTCACTG ACCCCCCTGA CCTCATGGCT GACCCCCCAG GAGGGCTCCC 1370
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