Tag | Content |
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EnhancerAtlas ID | HS118-01522 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:202075870-202078470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr1:202076050-202076061 | ACAGGGTGTGG | - | 6.14 | KLF5 | MA0599.1 | chr1:202076522-202076532 | GCCCCGCCCC | + | 6.02 | Klf1 | MA0493.1 | chr1:202077105-202077116 | AGCCACACCCA | + | 6.14 | Klf1 | MA0493.1 | chr1:202077514-202077525 | AGGGTGTGGCC | - | 6.32 | LBX2 | MA0699.1 | chr1:202077694-202077704 | GCCAATTAGC | + | 6.02 | RFX1 | MA0509.2 | chr1:202077284-202077300 | GGTTACCATGGCAACA | - | 7.85 | RFX1 | MA0509.2 | chr1:202077284-202077300 | GGTTACCATGGCAACA | + | 7.89 | RFX2 | MA0600.2 | chr1:202077284-202077300 | GGTTACCATGGCAACA | - | 8.01 | RFX2 | MA0600.2 | chr1:202077284-202077300 | GGTTACCATGGCAACA | + | 8.05 | RFX5 | MA0510.2 | chr1:202077284-202077300 | GGTTACCATGGCAACA | - | 8.14 | RFX5 | MA0510.2 | chr1:202077284-202077300 | GGTTACCATGGCAACA | + | 8 | ZNF263 | MA0528.1 | chr1:202076060-202076081 | GAAGGAGGGGTTGGAGTGGGA | + | 6.1 | ZNF263 | MA0528.1 | chr1:202076784-202076805 | GGAGGAGGAGGATGGGGAAAT | + | 7.16 | Zfx | MA0146.2 | chr1:202076012-202076026 | CAGGCCTAGGCCCA | - | 6.22 |
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| Number of super-enhancer constituents: 19 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:202074351-202079442 | Colon_Crypt_1 | SE_23723 | chr1:202074370-202077777 | Colon_Crypt_2 | SE_23723 | chr1:202077856-202079457 | Colon_Crypt_2 | SE_24689 | chr1:202074418-202077795 | Colon_Crypt_3 | SE_24689 | chr1:202077814-202079438 | Colon_Crypt_3 | SE_27253 | chr1:202074329-202078395 | Esophagus | SE_27872 | chr1:202072821-202079531 | Fetal_Intestine | SE_28794 | chr1:202072812-202079552 | Fetal_Intestine_Large | SE_32199 | chr1:202074329-202079443 | Gastric | SE_33417 | chr1:202074259-202079545 | H2171 | SE_34936 | chr1:202073327-202079210 | HeLa | SE_47709 | chr1:202074443-202079432 | Pancreas | SE_50637 | chr1:202074313-202079465 | Sigmoid_Colon | SE_52669 | chr1:202074270-202079462 | Small_Intestine | SE_57667 | chr1:202074454-202077840 | VACO_503 | SE_57667 | chr1:202077859-202079020 | VACO_503 | SE_58006 | chr1:202076961-202077719 | VACO_9m | SE_65583 | chr1:202074401-202078965 | Pancreatic_islets | SE_67005 | chr1:202074259-202079545 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 202076459 | 202076551 | chr1 | 202077636 | 202077876 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I202103 | chr1 | 202072772 | 202079378 |
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Enhancer Sequence | CCCACTGCCC CTAGAGCAGC CCAGGCCCCG CCCTCAGCCT GAGGACCCTG TGCAGAGCTC 60 AGCCAGTTCC AGGAGGGGAG GGCCTCTTGA AGGCAGTCGG GGGCCAGGGG AGCTGGTGCT 120 CACATTGAGG AGCTGTGGAA GGCAGGCCTA GGCCCACACA TCCTGTGCTA AGAAGAGAGG 180 ACAGGGTGTG GAAGGAGGGG TTGGAGTGGG AGACCCATAG CCTGATTCAG CCCCGAATGG 240 AAAAGTGAAG TTATGGGGGG ACTGAAAGGT TTGGTGACAG ATACTGGGAT GTGAGTCTGG 300 AAAGCGGCTT TGAGTCATGG CTTGGCATCT ACCCTCCCTT TGTGACCTTG GCCATGTCCA 360 TTGCCCTCTT ATCCCCATCT GTACAAGGCA GGCGCCTCAG TGTTCCCATC TGTACAAGGT 420 AGGGGCTCAG CTGGATAAGC CTAGGCTCCT TCTAACCCTG GCACTCTGTG GTTACCCAGG 480 TGGGCATCCC CACCCCAGTG CCCAACCTTC CCCTATCCCC ACTAGCTCCC GCATCTCCCC 540 CATGGAGAAA AAGAAACCTC GCTGGGTCAT GGAACATGGG AAGGGTTGGC AATTCCTGTG 600 TGAGGCAGCC CAAGGCAACC TCGGAGCCCT CCTGCAGATA CCCAGGGGGC CTGCCCCGCC 660 CCTGGCCCAG GCTCCAGACC ACAGAGCAGA CAACAAAGGC AGGCAGGTGG AAAATTCCCT 720 CTGGCTCTCC GCCCAGGCAC CCTGGATGGC AACTGTGCCA GCCTGGGCGG GCAAGAGCCG 780 GGAGTCCAGG ATACCAACAG GCAGCCTGGC AGCCCCAGGG AGCTGATAAG GGGCCTGTCA 840 AGGTCTCCCC AGTTCAATTG CCCCCCACTG CTCAGACACA GAAATTGTAT TCTACTCAGG 900 TGGACAAACA GGTGGGAGGA GGAGGATGGG GAAATATGTG GTTGTTTGAA CTTCTCAGAA 960 GTTGTAGCCC TGAGCCAAGA AGATTATGCC AACTCCTCCC ACTACCCTGA GCTGAGTGGT 1020 CCCTGGGACT CTTAATGGAG GACCGGGGGC TGCAGCTAGT TTGGCGGACA GACAGAAAAC 1080 GGATTTCGTC AAGTGTTCCT GTGCCTGCTG GGCTCCTGCT GGCTGCTGGT CTCTGCCCTG 1140 TGACCTTGGG CAGTGTGTAT GCTCCTGGAG GGCTTGCTTT GCCCATCTCT CACCCTGGAA 1200 TAACTGTCTG GGTCCTGCTC CCTGGAAGGG CATGAAGCCA CACCCATGTA AGGCCTAGGA 1260 GAAGTGAAAA GCCCTGTGTG TACATGTGAC TTGAGGCCGG GAGGCAGACC ACTCCCAGAG 1320 CCTGCATGTT CAAGGATTCC TTGCATCTGG AAAGCCAAGA CAGGGACCCC TCCTGCCTGC 1380 CTCTCTTCTG CTTTCTGCTC CGACCCCCTG AGCTGGTTAC CATGGCAACA GTTCCCTGCC 1440 TATCTCTCCA GAGGCCTTTC ACAGAATCCA GAGTTGGTTT CTACAATGTT TACCCACAAA 1500 CACTTTCTTG TTGCCAGTCA GTTCGGATGG CACTTCCAGA ACTGAGGAAA TACCTTTGTG 1560 ACTTCGCCAG GTCACAGCCA GCTGGCCCCT GGAATCACTC CCCAGTAGGG TGCCATCCTT 1620 CGGGCTCTGG AGAGCTGAGG AGTCAGGGTG TGGCCAGGTC AAGGTGAACC ACATGCTGCT 1680 GGGAAAACTA CCCAAAGGGC ACGTCCCACT GACCCGCAGT CAGCAGCCTG CAAGCGTCAT 1740 TGCCTCTACA GGGAACATTG TCCGTCTAGG CTGGCAGAAG AAGGCCCTAA AGATAAGGCA 1800 GGGCATGAAC CCAACTCCAT GACAGCCAAT TAGCTCCACT CCAAGAACCC AACCGCTGTG 1860 ACTCACTGAC AGCCAATCAG GAGGCCCAGG GCCAGATACT TTTTTCAGCT AGACACACCT 1920 GTAACCTGCT AGCCATCTGT TGAACCACAC CCCTGCCCCA ACCATTCTAG AAAGAAATAT 1980 AAATCTCTTT TACAGCTGTA AATGGAGAGC TCTGTAACTC TAATATGGAG GGAGATACAC 2040 GCTGATCTAT ATTGAGCTCA GAGACAGACA CAAATGCATA AACATGCACC TGCACAGATG 2100 AAAATCTAGC TATCAGCCCT GCTCCTTCCT GCCTCCACCA AGGTCACCAC CATCTCTATT 2160 CTCCTCCACC CTCCTGGGTC AGAAATTGGC AAAAGAGAAA AGGACATTGC AAGAGACCTA 2220 AATATACCTT TCCAGTGCAC AGTGGCAGCT TTCTGTGAAC TGTTAGGCCA ACAGTGGTCC 2280 AGACATTTTC CCTCATCCTC TGCAAAAAAC AACAAAACCA AACAAAAACA TTGACTGGGC 2340 ATCATTCGTA GGTTTACCTG GGAATACTAG TGCTTGGAGG GGACTGAGAG TACCCCTAGC 2400 AAAGCCCCAT TTTACGGATG AGGGCTAGGC CCAGAGGGAG GGTTTCTCCT TCCAGAGGAG 2460 GGCTCAGTGC TCGTGATTGT TGGCAAGGGC ATCTTGCCAA AGTTCCAGGA TCCAGGTCAG 2520 ATATTGGCCC CATGGTCCCA CCCTGGAGGA TTTCCTGTAG GGGGGTGCCC CCCAGCTGGC 2580 CACAGTGGAT CAGGCATGTC 2600
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