Tag | Content |
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EnhancerAtlas ID | HS034-18531 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr20:30180850-30183080 |
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 | GCCACCACGC CTGTCTAATT TTTTATATGT TTTTAGTAGA GACGGGGTTT CACCATGCTA 60 GCCAGGATGG TCTTGATCTC CTGACGTCGT GATCCGCCCG CCTCGGCCTC CCAAAGTGCT 120 GGGATTACAG GCATGAGCCA CTGCACCCGG CCTTTTTTTG TATTTTCAGT AGAGACAGAG 180 TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGAACT CAAAGCCTGC CTTGGCCTCC 240 CAAAATGCTG GGATCACAGG CATGAGTCAC CGCACCTGGC CTATAGCTTC CTTTTAAACA 300 GCACATCGTT GCTTTTGCAT CAGCCAGAAA AAAAAAATAC TTTTTAGAAG AAAACGTACA 360 TTATCATGAG TCATAGTATT TGAGGAGTAC AGCTCTGAAG CGGCCTGAGG TGAGGGTGCA 420 GCTGGAGGCG CCGCCCCCTG GTGACTGGGT ACTCAGGGTT GGGTTGAGCC AGGAGGGTGG 480 TGGTTGCCTC AGGCTCTGTG AGGTGGGCAG GGAGCTGGGC AGGGAGCTGG GCGGGGTCCT 540 GAGACATTCA ACCTCAGCTG GTTCCTGGGT TCCGGGCCCT GGAGCAGTGA GGGAAGCCAG 600 TTATATGGGA GGCAGGTGAG TCAAAGGAGG GTCAGGCTGG GTGCCAGAGA GGAGGGCCAC 660 TGCTTCTGTG AGGGGGCCTC TGGGGCCTTC CGTCCATCAC CCAGTGGGCA TATGGGGACA 720 CCACCGAGGC CCAGAGACCT CTTGCCCAGT CTCCCCACTC TCACCTCAGA GGTCCTTGCA 780 GCTAGGGGCA GTGGCCTCTG CTGAGCTTTG CCCAGGGTGT AGCCAGTTGG CCTCAGGGCA 840 CTCCTGACTG GTGGCATGAG CCTCCCAGGC TGCCAGGGTC AGGTCAGCTC CCACGCCTCC 900 ACCCTGGGCA GGGCCCAGGC CTGCATTCAT GGGTGCAAGA GGAGAGAGAG GCCTGAGCCC 960 TGGATGGGTG TGGTTGTGTG TCCTTGGGGC TGATGCAGGA TTTTTTTTTT TTTTTTGAGA 1020 CGATGTCTTG CTCTGTTGCC CAGGCTGCAG TGCAGTGGCA CGATCTCGTC TCACTGCAAC 1080 CTCCATCTCC TGGGTTCAAG CAATTATCCT GCCTCAGCCT CCCGAGCAGA TGGAGTTACA 1140 GGCGTGCACC ACCACGCCTG GCTAATTTTC GTATTTTTAG TAGAGAGGGA GTTTCACCAT 1200 GTGGGCCAGG CTGGTCTCGA ACTTCCGACC TCATATAATC TGCCTGCCTT GGCCTCCCAA 1260 AGTGCCGGGA TTACAGGCGT GAGCCACCGC ACCTGGCCTT TCTGCAGGAT TCTGAATTGT 1320 GTATGTGTGG AGAGTAAGGG GACTGTGTGC TCTAGAAGGG CTGTGGTGGG AGGTCTCTGG 1380 CCTGGTGCAG GTGGGTGTTG GTTGGGTCTG TGCACTGTGG GAGTGGGTGC CTGCAGGAAG 1440 CCAGTTTATC CTTTTGCAGG CAGTGGACTT CTCTAAGGCT GCGGGCATGT GTGTTGGCAT 1500 CTTGGAGTCC CAGGTGTTTT GGCGTGAGTA ATACTGTATA GATGTAAGTG TGTGTAGTGT 1560 TTGCAATGTT GTAGTGTGGG TGCATGTGTC TGTGTGTCCT GTTTGTTGAG AGGATTCATT 1620 GCATGTGGTT CTGTTAGGAG TGATAATGGG GTGTTTTGAG ACATTTCCTC CTTGGTCTCT 1680 ATTTTTTGGT GTGTTGGTTA TGCAGATTTG GTGTTTCGGT AGTGTGCGCG GAGGTCAGTG 1740 TGTTGGTTGT ATATTATGGT GTACTGTTGT GCGTTGTGCA TTTGGCAGGT TGTGTCTATT 1800 GGTGTGTGGC TGTTGGGTTT GTCTGTTGTG TCAGTCGTAC ATATAAATGC CACGTTGGGC 1860 GTGTGGGTGT GTGCATTTGT ATATTGCTCT GTGGGTGTGC GAAGCAGTGT GTTTGTGTAA 1920 CCCTGCAGGT TTGGCCTATG CTGAGTAACC TAAGATGGGA GCTCCCTGAG CCTTGGCTCT 1980 GCCCTTGCCT TTGGCTGCTG GAGACCCTGG GCAGCAATGG CCCTTTGTCC AGCCACAGGA 2040 AAACCCCACC CCCCTCCATC GGCAGGGGAC TTGGGAGGGG CCCAGACTGG TAGGCTCCAG 2100 CCTCCCGTCC ATTGTTCTGG GGCCTCTCTG GAAAACAGGA TGGGAGGTGA AAGGTGGACA 2160 CAGGCCTGGA CCCCCACACT CCCTGAAACA ACCCAGGGGC ACAGCACAGA ATCCTTAGGA 2220 GGGAGGGCCT 2230
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