Tag | Content |
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EnhancerAtlas ID | HS191-23138 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr20:30180860-30183080 |
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 |
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| 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 |
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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 |
GH20I031590 | chr20 | 30178404 | 30186899 |
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Enhancer Sequence | CTGTCTAATT TTTTATATGT TTTTAGTAGA GACGGGGTTT CACCATGCTA GCCAGGATGG 60 TCTTGATCTC CTGACGTCGT GATCCGCCCG CCTCGGCCTC CCAAAGTGCT GGGATTACAG 120 GCATGAGCCA CTGCACCCGG CCTTTTTTTG TATTTTCAGT AGAGACAGAG TTTCACCATG 180 TTGGCCAGGC TGGTCTTGAA CTCCTGAACT CAAAGCCTGC CTTGGCCTCC CAAAATGCTG 240 GGATCACAGG CATGAGTCAC CGCACCTGGC CTATAGCTTC CTTTTAAACA GCACATCGTT 300 GCTTTTGCAT CAGCCAGAAA AAAAAAATAC TTTTTAGAAG AAAACGTACA TTATCATGAG 360 TCATAGTATT TGAGGAGTAC AGCTCTGAAG CGGCCTGAGG TGAGGGTGCA GCTGGAGGCG 420 CCGCCCCCTG GTGACTGGGT ACTCAGGGTT GGGTTGAGCC AGGAGGGTGG TGGTTGCCTC 480 AGGCTCTGTG AGGTGGGCAG GGAGCTGGGC AGGGAGCTGG GCGGGGTCCT GAGACATTCA 540 ACCTCAGCTG GTTCCTGGGT TCCGGGCCCT GGAGCAGTGA GGGAAGCCAG TTATATGGGA 600 GGCAGGTGAG TCAAAGGAGG GTCAGGCTGG GTGCCAGAGA GGAGGGCCAC TGCTTCTGTG 660 AGGGGGCCTC TGGGGCCTTC CGTCCATCAC CCAGTGGGCA TATGGGGACA CCACCGAGGC 720 CCAGAGACCT CTTGCCCAGT CTCCCCACTC TCACCTCAGA GGTCCTTGCA GCTAGGGGCA 780 GTGGCCTCTG CTGAGCTTTG CCCAGGGTGT AGCCAGTTGG CCTCAGGGCA CTCCTGACTG 840 GTGGCATGAG CCTCCCAGGC TGCCAGGGTC AGGTCAGCTC CCACGCCTCC ACCCTGGGCA 900 GGGCCCAGGC CTGCATTCAT GGGTGCAAGA GGAGAGAGAG GCCTGAGCCC TGGATGGGTG 960 TGGTTGTGTG TCCTTGGGGC TGATGCAGGA TTTTTTTTTT TTTTTTGAGA CGATGTCTTG 1020 CTCTGTTGCC CAGGCTGCAG TGCAGTGGCA CGATCTCGTC TCACTGCAAC CTCCATCTCC 1080 TGGGTTCAAG CAATTATCCT GCCTCAGCCT CCCGAGCAGA TGGAGTTACA GGCGTGCACC 1140 ACCACGCCTG GCTAATTTTC GTATTTTTAG TAGAGAGGGA GTTTCACCAT GTGGGCCAGG 1200 CTGGTCTCGA ACTTCCGACC TCATATAATC TGCCTGCCTT GGCCTCCCAA AGTGCCGGGA 1260 TTACAGGCGT GAGCCACCGC ACCTGGCCTT TCTGCAGGAT TCTGAATTGT GTATGTGTGG 1320 AGAGTAAGGG GACTGTGTGC TCTAGAAGGG CTGTGGTGGG AGGTCTCTGG CCTGGTGCAG 1380 GTGGGTGTTG GTTGGGTCTG TGCACTGTGG GAGTGGGTGC CTGCAGGAAG CCAGTTTATC 1440 CTTTTGCAGG CAGTGGACTT CTCTAAGGCT GCGGGCATGT GTGTTGGCAT CTTGGAGTCC 1500 CAGGTGTTTT GGCGTGAGTA ATACTGTATA GATGTAAGTG TGTGTAGTGT TTGCAATGTT 1560 GTAGTGTGGG TGCATGTGTC TGTGTGTCCT GTTTGTTGAG AGGATTCATT GCATGTGGTT 1620 CTGTTAGGAG TGATAATGGG GTGTTTTGAG ACATTTCCTC CTTGGTCTCT ATTTTTTGGT 1680 GTGTTGGTTA TGCAGATTTG GTGTTTCGGT AGTGTGCGCG GAGGTCAGTG TGTTGGTTGT 1740 ATATTATGGT GTACTGTTGT GCGTTGTGCA TTTGGCAGGT TGTGTCTATT GGTGTGTGGC 1800 TGTTGGGTTT GTCTGTTGTG TCAGTCGTAC ATATAAATGC CACGTTGGGC GTGTGGGTGT 1860 GTGCATTTGT ATATTGCTCT GTGGGTGTGC GAAGCAGTGT GTTTGTGTAA CCCTGCAGGT 1920 TTGGCCTATG CTGAGTAACC TAAGATGGGA GCTCCCTGAG CCTTGGCTCT GCCCTTGCCT 1980 TTGGCTGCTG GAGACCCTGG GCAGCAATGG CCCTTTGTCC AGCCACAGGA AAACCCCACC 2040 CCCCTCCATC GGCAGGGGAC TTGGGAGGGG CCCAGACTGG TAGGCTCCAG CCTCCCGTCC 2100 ATTGTTCTGG GGCCTCTCTG GAAAACAGGA TGGGAGGTGA AAGGTGGACA CAGGCCTGGA 2160 CCCCCACACT CCCTGAAACA ACCCAGGGGC ACAGCACAGA ATCCTTAGGA GGGAGGGCCT 2220
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