| Tag | Content |
|---|
EnhancerAtlas ID | HS116-35645 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr9:138998320-139001570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF16 | MA0741.1 | chr9:138998912-138998923 | GCCCCGCCCCC | + | 6.02 | | KLF4 | MA0039.3 | chr9:139000453-139000464 | CCACACCCTGC | + | 6.62 | | KLF5 | MA0599.1 | chr9:138998912-138998922 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr9:139000295-139000305 | GCCCCGCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr9:139001284-139001294 | GCCCCGCCCC | + | 6.02 | | Klf1 | MA0493.1 | chr9:139000451-139000462 | GGCCACACCCT | + | 6.32 | | TFAP2A | MA0003.3 | chr9:138998694-138998705 | TGCCTCAGGCA | + | 6.02 | | ZEB1 | MA0103.3 | chr9:139000779-139000790 | CCCACCTGCCC | + | 6.14 | | ZEB1 | MA0103.3 | chr9:139001291-139001302 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr9:139000862-139000883 | TGCCCCTGCTTCTCCTCCTCA | - | 6.07 | | ZNF263 | MA0528.1 | chr9:139000917-139000938 | TGCCCCTGCTTCTCCTCCTCA | - | 6.07 |
|
| | Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
| SE_06335 | chr9:138999308-139004425 | Brain_Hippocampus_Middle | | SE_24880 | chr9:138998517-139002637 | Colon_Crypt_3 | | SE_27238 | chr9:138998249-139002839 | Esophagus | | SE_34358 | chr9:138998996-139003846 | HCT-116 | | SE_41290 | chr9:138999650-139002647 | Left_Ventricle | | SE_42022 | chr9:139001070-139002421 | LNCaP | | SE_42851 | chr9:138998999-139002813 | Lung | | SE_47727 | chr9:139000981-139001614 | Pancreas | | SE_48413 | chr9:139000434-139002369 | Psoas_Muscle | | SE_49310 | chr9:139000245-139002578 | Right_Atrium | | SE_50914 | chr9:138998248-139002848 | Sigmoid_Colon | | SE_63238 | chr9:138991973-139023521 | GLC16 | | SE_65568 | chr9:138998988-139004881 | Pancreatic_islets | | SE_67042 | chr9:138998256-139002692 | H2171 | | SE_69162 | chr9:139000391-139003532 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGATTACAG GTGTGAGCCA CCGTGCCCAG CCTGGGAGTG GGGTTAGTTC TAAGTTGGTG 60
AGAGGCAAGC ACAGCTCTCG AGGGACATCC TGCCCGGAAG ACGTACTCGT GGGGGCCTCA 120
GCTGGCCCTT GGCACAGTCA TTCAGAAAGT GAATGTGAAG GCTTGCTCTG CACCCAGCCC 180
CAGGAACCCG TGGGGCAGCA ACCTGTTCTT TTGTTTGTTC GTGTTAGGCT CGGAGCTCCC 240
AGAGAGGGTC TAGCATCCTT CTACAGACCG ACCCCTGGAG ACAGCCCCCA CCAGGATACA 300
TCCTTGAGAA TAAGCCCCAG GAAAGGGTTT GGGCCACAAA TGGCCTTGTC TTCCTGGCCC 360
AAGGTCATCA GATCTGCCTC AGGCAGGGCC TGCAGCCAGC CCCCGGCACC TTCCCTTGAG 420
GAGAGGGTCT GCCCAGTTTT GGTGGAAGGA ACAGGGCACC AGCCTCCAGT GCTGCTTCTG 480
CAATCCCATG GCCCCGACCC AGGCCCCAAC CCAGGCCCTG GTAAGACGGT GACCCAGGGA 540
ATCTGGAGCT CCCTGGCCCA CTGCGGCAGC CGTGCCACAG GTGACATCGT GAGCCCCGCC 600
CCCCCGCCCC CCGCCCTGAG TCCAACCCCA GCCCTGGTTC CTTCTCCCTG AACTTCCCAC 660
CTGGGGACAG AATGCGGGCC TAGGGCTTTC CCTGGGGGTG ACCTGAGAAC AGCTAGTCCA 720
GCACCTCACC TCACTGCACG CTGTAGGCCC AGCCTCCCTG GGTTCCCGCC CCCTTATCTC 780
ACAGGAAGAG CTGGGCCTGG AGAGGGGCAG ATGGCTGCAC AGCCTCACGA GGGGCCGGGG 840
AGCCGCACCT CTTCCTGCCA ATCAGCCCAG CAACCGGCGA CCCCAAGCGC GGCGACCGCA 900
AAGGGAGTGC TTGCCCATCC GCGTTTGAAA GCAGACTTTT TCTCGGCAGG AACACAGGAC 960
TCACCTGCCA GTGGCTACCC AGGCAGGGGC TTCCCTGTTC CTCAAGGGGC CGGAGTCCCT 1020
CCGTTCTTTG GGGGACCATC TGAGGGAGCA CGGGAAGGAG CCATGGATGT GGAGGGCGGC 1080
AGAGCCAGGA CGTGAGACAC GACAGCAGAA AACACTTGGG CACACAAATG CCACACCCCC 1140
ACACGCACAT ACGTGCACAC ATACATGTGC CAGGCACGCA CCCCAGCCAG GTGGAGGAGG 1200
GTGGGGGTCA AACCAGGCTG CACCGAGCAC AGGTGGTGGC TGAGTTCCGG TTGGCCCAGC 1260
TCCAGGCTGT GGGGAGAAGA GAGATGGCGG CATTCTTTCG GACGCTTTTA TCCACTATGG 1320
GAGCAGGAAG ACAGCCAGGG TTATCACAGC ACAATTTGAA AAACATACAA ATAATTCATG 1380
TCAGCATAAC GTCATGGTGT TGTCAATAAT GAATCCACAC TTAAAACCCA GATTGATAGC 1440
TTCAAAGGGC AGCCCCCACC CCTGGACAGG TAGGCAGGGC GCAGAGCCAG CCCCTCTTGG 1500
TTCTGAGAAG CAAACTCGGA AGCAGTTCAG GTCAGAGGAG TCCAGGGACC GCCCTTGCTG 1560
GGAGGAAATG GGTGCAGTGC GGCCCAGCGC AGTGAGCGGG GCCAAGGGTC TAGCAGCACT 1620
CGAGTTCTGC CCAAAGACGA GAGAGAGGGT GCCGGCCTAC GTGCGCCCGC TGGGAAGAAC 1680
TGGAAATCCA TGTGCTCCCG TTCTGCGAAT CCCTTCACCA GGGCGTCGGC CACCGGAGTG 1740
GGAAAAAACC TCTCCCGGCG TGAGAGCTGG GGGCAGGCCC AAGGTGCTAG GGGCTCCCGG 1800
GAGGACTGGC CATGGCCACC CAGCATCCCT GTGCCTGGCC TGGGCCTCGG TGGCCAGTCC 1860
TCCTCGGCTG CAGACCCCAG TGAGGACAGG GACCTCACCA CCCACTGCCT GGCTTCTGAG 1920
GCAGCAGTGC CCCCATTAAA CCTGAGATGA ACTTCTCTGG GTCTTTCAGG AAGGAGCCCC 1980
GCCCCAGCAT CTGGGCTCCC AGGACGAGGG CAGTCACTAA GTGGTGATGT CATGTCACTC 2040
ATCGGCCTCT TCTGCCTGTG GCCATACAAC AGGCCCAGGC CTGTCCCATC CCGAGGGAGG 2100
CAGATCCTGG CTGGAGCTGG CGGAGACTTA CGGCCACACC CTGCCAAGGT GTGCCCACTG 2160
GGACCCGGGC CCAGCCTGTC ACGGCGCCTC TCCCTGTGCC ATCCGCCAGC CCAGGCTTGA 2220
TTGAGCTCCA TATGAATATT CATACAGCAT TCTGCTGGGA CCGTCGTTAA TATTCTGAGG 2280
AAGCGGCAAG AATGCCCGTC CCCATGTCGT GAGCCATGGT CAACGTGCTG CTGACACGAT 2340
GGTGGCTGTG GATTTTTCGG ATGCAATTGT CAGGCCTCCA GGCTCAGGAG GGTGGAGGCA 2400
GCACCGCCAT CTCCAGGCCC CACCAGCACC CATCCTCTGA CCACGGACCT CCCAGGCACC 2460
CCACCTGCCC CCTGGCCTTT GCCTACCACC GTGTCCTTAC CTGACCCAAC CTCGACCAAA 2520
TGCCCCTCTT CCTCACCGCT CCTGCCCCTG CTTCTCCTCC TCAGCCCTGA CCCCTCTGCC 2580
CTCCCCGCCC TGCCTCCTGC CCCTGCTTCT CCTCCTCAGC CCTGACCCCT CTCCCCTCCC 2640
CGCCCTGCAT TTACCCCACG CCCACAGCCC TCACAGGGCG GGGACACCGA GGTTCTCCCA 2700
TAAATTAACC AAGCCCCTTT ACGAAGCCCC TTCCCAAATA GAGCCGGCGC CCTCCTCCCC 2760
TGGGCCCGGG TCACCGCTGG GTCAGCGCCT ACCGGCTCCC CAGGCCTGCC CCATGCCCTC 2820
AGCTAGAGGC AAACCCAAGC TCATGGGCGC AGCGAAGCTG GCAGGAGGGG CCCTGGGGGC 2880
TGTGGCTCAC CCCTGCATGG CCCTCCTGCT GCCCTGAGAG CCCCTTGGCT CCGGCTGTCC 2940
CCATTAGTCG GGTAGGACTC TTGGGCCCCG CCCCACCTGC CCCTTCCAGT CTCCGCCCAG 3000
GTCAGGACGG CAGGTGGCCC CAGCAGGGCT GGCCTGAGAT GGAGGAACGC GGCCCCGACC 3060
CGGGCTATGG GGAGACTCTG GATGTGGCGG TGGATCCGCT GACGGGGCTT TGGGATGTGA 3120
TTATTTCCTG GGGGCTGACG GTAGCCCAGG AGCACCAAGA CCCAGCTCTG CCTTCCGCCT 3180
CCCACGGGGC CTCTCCTCTG CAGGAGGCCA TACAAGGACT GCACGGAAGG GGAGCGGCCC 3240
CGCAGGGAGG 3250
|
