Tag | Content |
---|
EnhancerAtlas ID | HS111-03127 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr20:30180780-30183080 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr20:30181278-30181297 | CGCCGCCCCCTGGTGACTG | - | 6.36 | FOSL1 | MA0477.1 | chr20:30181110-30181121 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr20:30181110-30181121 | CATGAGTCACC | - | 6.02 | Zfx | MA0146.2 | chr20:30180946-30180960 | CCCGCCTCGGCCTC | + | 6.01 |
|
| Number of super-enhancer constituents: 37 | ID | Coordinate | Tissue/cell |
SE_02970 | chr20:30181389-30181892 | Bladder | SE_02970 | chr20:30181992-30185401 | Bladder | SE_23092 | chr20:30180932-30185504 | Colon_Crypt_1 | SE_23905 | chr20:30180954-30181864 | Colon_Crypt_2 | SE_23905 | chr20:30182067-30184386 | Colon_Crypt_2 | SE_24856 | chr20:30180918-30182002 | Colon_Crypt_3 | SE_24856 | chr20:30182053-30184543 | Colon_Crypt_3 | SE_27857 | chr20:30180854-30185380 | Fetal_Intestine | SE_28873 | chr20:30180831-30185610 | Fetal_Intestine_Large | SE_31829 | chr20:30180412-30185861 | Gastric | SE_33158 | chr20:30181452-30181850 | H1 | SE_33158 | chr20:30182756-30183557 | H1 | SE_33920 | chr20:30180844-30185589 | HCC1954 | SE_34238 | chr20:30180059-30185985 | HCT-116 | SE_34774 | chr20:30178236-30186156 | HeLa | SE_35318 | chr20:30180823-30185856 | HepG2 | SE_38269 | chr20:30180858-30184814 | HUVEC | SE_41187 | chr20:30180928-30185594 | Left_Ventricle | SE_42444 | chr20:30180946-30185866 | Lung | SE_44319 | chr20:30181009-30181986 | NHDF-Ad | SE_44319 | chr20:30182026-30185793 | NHDF-Ad | SE_44941 | chr20:30181086-30185438 | NHLF | SE_47160 | chr20:30178251-30187234 | Panc1 | SE_48882 | chr20:30181003-30181958 | Right_Atrium | SE_48882 | chr20:30181969-30185515 | Right_Atrium | SE_50279 | chr20:30180885-30185736 | Sigmoid_Colon | SE_52484 | chr20:30180829-30185715 | Small_Intestine | SE_54437 | chr20:30181089-30181806 | Spleen | SE_54437 | chr20:30182461-30185240 | Spleen | SE_55719 | chr20:30180277-30185711 | u87 | SE_57184 | chr20:30181330-30184438 | VACO_400 | SE_57391 | chr20:30181275-30181985 | VACO_503 | SE_64122 | chr20:30180984-30181864 | HSMM | SE_64122 | chr20:30182475-30185373 | HSMM | SE_67492 | chr20:30180277-30185711 | u87 | SE_68887 | chr20:30181002-30181975 | H9 | SE_68887 | chr20:30182050-30185155 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I031590 | chr20 | 30178404 | 30186899 |
|
Enhancer Sequence | AAGCTCCGCC TCCTGGGTTC ACGCCATTCT CCTGTCTCAG CCTCCTGAGT AGCTGGGACT 60 ACAGGCGCCC GCCACCACGC CTGTCTAATT TTTTATATGT TTTTAGTAGA GACGGGGTTT 120 CACCATGCTA GCCAGGATGG TCTTGATCTC CTGACGTCGT GATCCGCCCG CCTCGGCCTC 180 CCAAAGTGCT GGGATTACAG GCATGAGCCA CTGCACCCGG CCTTTTTTTG TATTTTCAGT 240 AGAGACAGAG TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGAACT CAAAGCCTGC 300 CTTGGCCTCC CAAAATGCTG GGATCACAGG CATGAGTCAC CGCACCTGGC CTATAGCTTC 360 CTTTTAAACA GCACATCGTT GCTTTTGCAT CAGCCAGAAA AAAAAAATAC TTTTTAGAAG 420 AAAACGTACA TTATCATGAG TCATAGTATT TGAGGAGTAC AGCTCTGAAG CGGCCTGAGG 480 TGAGGGTGCA GCTGGAGGCG CCGCCCCCTG GTGACTGGGT ACTCAGGGTT GGGTTGAGCC 540 AGGAGGGTGG TGGTTGCCTC AGGCTCTGTG AGGTGGGCAG GGAGCTGGGC AGGGAGCTGG 600 GCGGGGTCCT GAGACATTCA ACCTCAGCTG GTTCCTGGGT TCCGGGCCCT GGAGCAGTGA 660 GGGAAGCCAG TTATATGGGA GGCAGGTGAG TCAAAGGAGG GTCAGGCTGG GTGCCAGAGA 720 GGAGGGCCAC TGCTTCTGTG AGGGGGCCTC TGGGGCCTTC CGTCCATCAC CCAGTGGGCA 780 TATGGGGACA CCACCGAGGC CCAGAGACCT CTTGCCCAGT CTCCCCACTC TCACCTCAGA 840 GGTCCTTGCA GCTAGGGGCA GTGGCCTCTG CTGAGCTTTG CCCAGGGTGT AGCCAGTTGG 900 CCTCAGGGCA CTCCTGACTG GTGGCATGAG CCTCCCAGGC TGCCAGGGTC AGGTCAGCTC 960 CCACGCCTCC ACCCTGGGCA GGGCCCAGGC CTGCATTCAT GGGTGCAAGA GGAGAGAGAG 1020 GCCTGAGCCC TGGATGGGTG TGGTTGTGTG TCCTTGGGGC TGATGCAGGA TTTTTTTTTT 1080 TTTTTTGAGA CGATGTCTTG CTCTGTTGCC CAGGCTGCAG TGCAGTGGCA CGATCTCGTC 1140 TCACTGCAAC CTCCATCTCC TGGGTTCAAG CAATTATCCT GCCTCAGCCT CCCGAGCAGA 1200 TGGAGTTACA GGCGTGCACC ACCACGCCTG GCTAATTTTC GTATTTTTAG TAGAGAGGGA 1260 GTTTCACCAT GTGGGCCAGG CTGGTCTCGA ACTTCCGACC TCATATAATC TGCCTGCCTT 1320 GGCCTCCCAA AGTGCCGGGA TTACAGGCGT GAGCCACCGC ACCTGGCCTT TCTGCAGGAT 1380 TCTGAATTGT GTATGTGTGG AGAGTAAGGG GACTGTGTGC TCTAGAAGGG CTGTGGTGGG 1440 AGGTCTCTGG CCTGGTGCAG GTGGGTGTTG GTTGGGTCTG TGCACTGTGG GAGTGGGTGC 1500 CTGCAGGAAG CCAGTTTATC CTTTTGCAGG CAGTGGACTT CTCTAAGGCT GCGGGCATGT 1560 GTGTTGGCAT CTTGGAGTCC CAGGTGTTTT GGCGTGAGTA ATACTGTATA GATGTAAGTG 1620 TGTGTAGTGT TTGCAATGTT GTAGTGTGGG TGCATGTGTC TGTGTGTCCT GTTTGTTGAG 1680 AGGATTCATT GCATGTGGTT CTGTTAGGAG TGATAATGGG GTGTTTTGAG ACATTTCCTC 1740 CTTGGTCTCT ATTTTTTGGT GTGTTGGTTA TGCAGATTTG GTGTTTCGGT AGTGTGCGCG 1800 GAGGTCAGTG TGTTGGTTGT ATATTATGGT GTACTGTTGT GCGTTGTGCA TTTGGCAGGT 1860 TGTGTCTATT GGTGTGTGGC TGTTGGGTTT GTCTGTTGTG TCAGTCGTAC ATATAAATGC 1920 CACGTTGGGC GTGTGGGTGT GTGCATTTGT ATATTGCTCT GTGGGTGTGC GAAGCAGTGT 1980 GTTTGTGTAA CCCTGCAGGT TTGGCCTATG CTGAGTAACC TAAGATGGGA GCTCCCTGAG 2040 CCTTGGCTCT GCCCTTGCCT TTGGCTGCTG GAGACCCTGG GCAGCAATGG CCCTTTGTCC 2100 AGCCACAGGA AAACCCCACC CCCCTCCATC GGCAGGGGAC TTGGGAGGGG CCCAGACTGG 2160 TAGGCTCCAG CCTCCCGTCC ATTGTTCTGG GGCCTCTCTG GAAAACAGGA TGGGAGGTGA 2220 AAGGTGGACA CAGGCCTGGA CCCCCACACT CCCTGAAACA ACCCAGGGGC ACAGCACAGA 2280 ATCCTTAGGA GGGAGGGCCT 2300
|