| Tag | Content |
|---|
EnhancerAtlas ID | HS110-01984 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr17:48967460-48971530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr17:48967722-48967740 | TATAGGCTTTCAATTTCC | - | 6.04 | | ONECUT1 | MA0679.1 | chr17:48968379-48968393 | GAAAAATCAATAAT | + | 7.06 | | ONECUT2 | MA0756.1 | chr17:48968379-48968393 | GAAAAATCAATAAT | + | 7.22 | | ONECUT3 | MA0757.1 | chr17:48968379-48968393 | GAAAAATCAATAAT | + | 7.73 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_04178 | chr17:48969563-48971530 | Brain_Anterior_Caudate | | SE_05235 | chr17:48969922-48971855 | Brain_Cingulate_Gyrus | | SE_06067 | chr17:48970189-48971869 | Brain_Hippocampus_Middle | | SE_07466 | chr17:48969924-48971841 | Brain_Hippocampus_Middle_150 | | SE_26011 | chr17:48970082-48971402 | Duodenum_Smooth_Muscle | | SE_26691 | chr17:48970142-48971557 | Esophagus | | SE_27621 | chr17:48966641-48968102 | Fetal_Intestine | | SE_27621 | chr17:48968124-48969142 | Fetal_Intestine | | SE_27621 | chr17:48970259-48971523 | Fetal_Intestine | | SE_28540 | chr17:48966458-48968560 | Fetal_Intestine_Large | | SE_28540 | chr17:48970225-48971565 | Fetal_Intestine_Large | | SE_31399 | chr17:48967913-48968417 | Gastric | | SE_31399 | chr17:48968453-48969298 | Gastric | | SE_35686 | chr17:48966449-48971499 | HepG2 | | SE_36690 | chr17:48968026-48971625 | HMEC | | SE_47468 | chr17:48970340-48971027 | Pancreas | | SE_50311 | chr17:48970273-48971485 | Sigmoid_Colon | | SE_52502 | chr17:48966782-48967912 | Small_Intestine | | SE_52502 | chr17:48970105-48971475 | Small_Intestine | | SE_54634 | chr17:48970181-48971848 | Stomach_Smooth_Muscle | | SE_57199 | chr17:48968021-48971444 | VACO_400 | | SE_65373 | chr17:48968684-48969310 | Pancreatic_islets | | SE_65373 | chr17:48969594-48972024 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr17 | 48968400 | 48969252 | | chr17 | 48968000 | 48968400 | | chr17 | 48970603 | 48971400 | | chr17 | 48968904 | 48968954 | | chr17 | 48968980 | 48969503 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I050889 | chr17 | 48966685 | 48971524 |
|
Enhancer Sequence | ATGGTGTATG AGATTTAAAG AAGGTGTGAT TTTAAAAAAA GTGTGATTTG AGGGACGCTA 60
TTTATTTTAT TTTACATAAA AAAGAAGAAC CAGGATGCTG AAAATGATGC TATTGATTAT 120
AAATAGGAAG AAAACGCTAG TCGGTTGAAA TAGCCAGTAT GGTCTTGGTC ATTCATAAGG 180
AAAGAATGGC CCCTGTCCTG GGAGCTGGCT TTAGAAGAAC CCACTGTGGC AGAACTGGTC 240
AAATCCTCCA CCACCTAGTA CCTATAGGCT TTCAATTTCC TGCCAATAAG GCACCAAGGT 300
CTGCCTGAGA CTTGACATCT AAAAAACTCC TAATTGGCCA GGTGCGGTGG CTCATGCCTG 360
TAATCCCAAC ACTTTGGGAG GCTGAGGCAG GCAGATCACT TGAGGCCAGA AGTTCAAAAC 420
CAGCCTGGCC AACATGGAGA AACCCATCTC TACTAAAAAT ACAAAAATTA TCCAGGCATG 480
GTGGCTGGCG CCCATAATCC CAGCTACTCA GGTGGCTGAG GCTCAAGAAT CCCTCGAACC 540
CGGGAGGCGG AGGTTGCAGT GAGCCGAGAT TGAGCCACTG TACTCCAGCC TAGGCGACAG 600
AGTGAGACTC CGTCTCAATA AATAAATAAA TACATCAATA GCCCACGATT AAGCCAGGCA 660
TGCTGGCCCA TGCCTGTTGT CCCAGCTACT CAGGAGACTG AGGCAGGGTA ATCCCTCGCG 720
CCCAGGAGTT CAAGGCTGCA GTGCACAATG ATTATGCCTG TAAACAGCCC CGGCACTCCA 780
GCCTGTGCAA ATAGCAAGAC CTCATCTCTA AAAAAATAAG ATAAAAGCCA AAATGCCCAC 840
TATCTGACTC ACCAAAAGGT GTGTATTTAA GGCGTTGTCT GCAGTGCCTG GCTGAACCTA 900
CTGAAGCCTG AGGAAAAAGG AAAAATCAAT AATACAGGTT CTGTCTTCAT TGAAAAGTTT 960
GATATTTTGC GTCTCATGGA TTTTTTGCAC TAATTTGGAT GTTGAAAATA TTGCATTAAA 1020
ATATTATTTA TCTAGAGTAT TGGGTGTTTT AGGCACTCCC TTAAATTTTG TGCCTAAGGT 1080
GAGTGCCTCA CTCTCCTGGT CATAGTCCTG GCGCAGTGAT GTCTACAAAG ACTAATAAGA 1140
TTTACCTGTT ACCAAGCTCC TACTCTAATA AACATACTTA GCTCATTAGA TTAGCTAGTT 1200
GATACCAGCC CGATCAGCTC ACATAATTGC TTCCCTGGCC CTTGTTTATC CAGAAAGTAG 1260
AGTCCTGCCT CAAATTTCCT AGCCAGTGGT CATGTCTGTA CTCTTTGCTG CCAAACCCTT 1320
TCCAGACCCT CATACTGACT GCCTGGTTGG GCCCCTACCG ACACTGTCGA CCCTCTGAAC 1380
ATTGTGCACA ACCCTAGGAA GGAGCACTAG GTGCTGCCTA ACTCTGGATC CCCGACACTA 1440
ACTCCCTGGC CCAACTGGAC TCTTTCTCAT TTATCTGTGT CTGAGTCTCC TGGGCCTCAT 1500
TCCACCCTCC CAGAAGTTCT TCCTTTACTG CTTGCCTCCT GGTCAGGTCT TCCCTGAAAA 1560
AATACCCCAC CTGTGTGTGA ATCTTTCTGG TTTCTGGGTC TCGTGCCTCC CCTAAGCAAT 1620
GCAAACCTTG AGTCAAGTAC TACGCTCTTG CCCCAGGCCT GGCATTGTTA CGTTAATAAC 1680
CATTGAGAGC ATACCATGTG CCACTGACCC ATGCTTTCCT TGTGTTAACC CACATGCACC 1740
TCATCGTAAC CTTATGAGTA GATACTATTG TCATCTCCAT TTTACAAATG AGCAAACCAA 1800
AGCCCAGAGA GGCAAAGTTA TTTGCCCAAG GTCACACAGC TAAGAAGTGG CAGAAATGGG 1860
CTACAAACAC AGTTTCTAGA GCCCAACTCT TAACTATCAT GTTACCTAGC TTCTGCTTAC 1920
AGTCTAAGAA GCCCTGCGTG GAAAGTTTGG AATCAGATGA GTCTCAAATT CAAATCCCAG 1980
ATGTTCAGTT TATGAGCTTC ATGGCTGTGG GGTGTCACTT TAGTTCTCCT GGTCTCAGCT 2040
CCCTCATCTT GCATGGCTTT GTAAGAAGTG ACATTAGGCC CTCAGTACAC AGTAGACACA 2100
ACCATCACCC CCAACCTTTC CTGCAGGATA ACCCTAGCAA CCACAAACAT GCTGTGAGCA 2160
GGGCCTAAGG CACTTAATTC CACACTCTGG AAATGTCAGT AACCGTTGAA AAGAATAAAG 2220
CCAGTTCTAT TTGTAAAGCA TTTTACTGCC GATGGAGGAG GTGAAGTGCA TGTTGCGTTT 2280
GAAGGTTTGC AGCATGAACT CTAGAGGTCA GCTACCGAAG CTGAAGCCTG GATTCCACAA 2340
TCGTGTGTGA CTTTGGGCAA GTTTCTTTCT CTTTTTTCTT CCTTTTTTTT TTTTTTTTTT 2400
TTTTTTTCGG AGACGGAGTC TTGCTCTGTC TCCCAGGCTG GAGTGCAGTG GCACAATCAT 2460
GGCTCACTGC AGCCTTGACC TCCCAGATTC AAGAGATCCT CCTACCTCAG CCTCCCAAGT 2520
AGGTGGGACT ATAGGCGTGC ACAATCACAC CTGGCTAAGT TTTTTTTTTT TTTTTTTCCA 2580
GCGATAGGGG TCTTGCTATG TTGCCAGGGT TGGTCTTAAA CTCCTGGGCT CAAGTGATCT 2640
CCCCAGCTCG GCTTCCCAAA GTGCTGGGAT TACAGGCATG AGCCAACGTG CCTGGCCTGG 2700
GCAAGTTTCT TAAATTCCCT ATAGCTTAGT TATCTCATCT TTAACCGAGG GACAATAATA 2760
ATAACAATAA TAATAATAAT AATAATAATC ATAGCACCTA CCTTGCATAG GGTTGTTGCT 2820
GATTATAGAG TTAATACACA TGTAACACCC TTAGAATAGT GCCCTGAACA CACCGTGAGC 2880
TCTTCAAAGT GTAAACCGAT TGGTCTCTAA GATAAGGGGA ACTGGTATGT CACCACCATT 2940
TTGCAGTCCA GGAAACAAAG ACACTGAGGG GTTGAAGGAT TTGCTCAATA GCCCTCAGCT 3000
TTTGCAGAGT GGACCCCAAA TTGAAATTCA GAACCTCTGG TTAGAGGGTT GCTGGCTCCT 3060
CCATTTCATC CAGGAGTTTC TTATTTCCAT TTCTGACATG ACTGCGATTG GCTCTGATTC 3120
CCAAGCCACG GGTTTCCAAC CTTATTAATG CGCTCCTGCA AAAGCCAGGC TCCTCCTCAC 3180
AGGCTCTGCT GCTGTTCGGA GCAGGCCCGG GCTGCTGTGT ACCTCACAGC TCCCCGACAG 3240
AGTGCTGCAC AATGACGACC TTCGGTGGGG CAGACATTCG CCTCCATCAG GCGCCTAATT 3300
ATGCAAACCC TGAACATGAG ACTGAAGAGG AGACTGGCCT GCCCAGGGAC GATTGATGAG 3360
GCTGGCTGGT TTCATCTTCC CCATTGTGTA GGCCAGAGGC TTCATGATGG GAGCGGCTCA 3420
GCTGCGGGAT CTCGGTTGCT TTGTTGCAGG CGCTGGGGCA ACGAAGGGTG AACTGGGTTA 3480
ATAAAATGTG CTGGTGACTC ACTCCTAGGA AAGAACCTGT GATGGATCAT TAAGCTGTCT 3540
CGGAACTTAT TTCAGGCCCA CACCCGCAAG ATGAACGCTC TCAATTTGTT TATTAGGTCT 3600
CCAACAATAG GCCACTGTTC TCCTTCCCCA CAACTCAGTT ACACAATCTT TCCCCTCGTG 3660
TCTTTCAGCC ACCTACTGAA AATCTGTCTG TGTGCCGAGC ACGCGCTCCC CATCCCTCTA 3720
CCAAATGCCT GGCTGGCGCG TCATCCCTGG CTTTGATGGG TACGTTCACT TCCCTAGCGC 3780
TGGCTTCCCC TAAGATGGGG GGACTTACCC TCCTGCCTGA GCCCTCATGC TGGCAGATTT 3840
GGTTCTTTCC ATCTCCCTCT CCGCTGAAGT CTTCTCACCC TCACTGACTC CATGCTGGAT 3900
CTAGACCTCT GAATGGTCCA TCCTAGTGCC TGTCCTGGCT CTCCCAATTC CCCTTTAATC 3960
CAAAGGTCTT GGGTTGATCC TTTTTAAAAA GAAATTATTT TATTCTTTAA AACTATATAT 4020
AAATAATTCA TGTTTTTTTT TTTTTTTTTT TTTTTTTTTT TTGTTTTTTG 4070
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