Tag | Content |
---|
EnhancerAtlas ID | HS098-34454 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr20:30182480-30185500 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2B | MA0660.1 | chr20:30183776-30183788 | GCTATTAATAGT | - | 6.02 | USF1 | MA0093.2 | chr20:30184073-30184084 | GGTCACGTGGC | - | 6.62 | USF2 | MA0526.2 | chr20:30184070-30184086 | GTGGGTCACGTGGCAC | + | 6.53 | ZNF263 | MA0528.1 | chr20:30185335-30185356 | AAAGGAGGACTGGGAAGAAAA | + | 6 |
|
| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_02970 | chr20:30181992-30185401 | Bladder | SE_23092 | chr20:30180932-30185504 | Colon_Crypt_1 | SE_23905 | chr20:30182067-30184386 | Colon_Crypt_2 | SE_23905 | chr20:30184613-30185129 | Colon_Crypt_2 | SE_24856 | chr20:30182053-30184543 | Colon_Crypt_3 | SE_24856 | chr20:30184583-30185563 | 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 | chr20:30182756-30183557 | H1 | SE_33158 | chr20:30183782-30184386 | 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 | chr20:30182026-30185793 | NHDF-Ad | SE_44941 | chr20:30181086-30185438 | NHLF | SE_47160 | chr20:30178251-30187234 | Panc1 | SE_48882 | chr20:30181969-30185515 | Right_Atrium | SE_50279 | chr20:30180885-30185736 | Sigmoid_Colon | SE_52484 | chr20:30180829-30185715 | Small_Intestine | SE_54437 | chr20:30182461-30185240 | Spleen | SE_55719 | chr20:30180277-30185711 | u87 | SE_57184 | chr20:30181330-30184438 | VACO_400 | SE_57184 | chr20:30184515-30185473 | VACO_400 | SE_64122 | chr20:30182475-30185373 | HSMM | SE_67492 | chr20:30180277-30185711 | u87 | SE_68887 | chr20:30182050-30185155 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr20 | 30183118 | 30184366 | chr20 | 30183712 | 30184220 | chr20 | 30184650 | 30185068 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH20I031590 | chr20 | 30178404 | 30186899 |
|
Enhancer Sequence | CTGTTAGGAG TGATAATGGG GTGTTTTGAG ACATTTCCTC CTTGGTCTCT ATTTTTTGGT 60 GTGTTGGTTA TGCAGATTTG GTGTTTCGGT AGTGTGCGCG GAGGTCAGTG TGTTGGTTGT 120 ATATTATGGT GTACTGTTGT GCGTTGTGCA TTTGGCAGGT TGTGTCTATT GGTGTGTGGC 180 TGTTGGGTTT GTCTGTTGTG TCAGTCGTAC ATATAAATGC CACGTTGGGC GTGTGGGTGT 240 GTGCATTTGT ATATTGCTCT GTGGGTGTGC GAAGCAGTGT GTTTGTGTAA CCCTGCAGGT 300 TTGGCCTATG CTGAGTAACC TAAGATGGGA GCTCCCTGAG CCTTGGCTCT GCCCTTGCCT 360 TTGGCTGCTG GAGACCCTGG GCAGCAATGG CCCTTTGTCC AGCCACAGGA AAACCCCACC 420 CCCCTCCATC GGCAGGGGAC TTGGGAGGGG CCCAGACTGG TAGGCTCCAG CCTCCCGTCC 480 ATTGTTCTGG GGCCTCTCTG GAAAACAGGA TGGGAGGTGA AAGGTGGACA CAGGCCTGGA 540 CCCCCACACT CCCTGAAACA ACCCAGGGGC ACAGCACAGA ATCCTTAGGA GGGAGGGCCT 600 GGGGACAGTC CCCATTTTGT GGATGAGAAA ACTGAGGGGT TTCATTCCTA TTAAAAGGGA 660 GAGAGCCTGA AGCCCCACAC CCTTTATGTG CCCACCCACA GCCTCCTGCC GGGTTTGGGG 720 GATGGAAAAA TGACACCCCA GAATGGAAAC AAAACGGTCT ATTGTGGTTT CCATTTCTGA 780 ATGCTTACCA TGTGCTAAGT GCAGAAGTGT CATAACTCTG CAGGTTAAGT TCATATTTTG 840 TACCCATTTT GCACAGGAGT ACACTGAACC ATAAGGCAAC AATTTATTCT TCAAAGGACA 900 CTACTCTAAA CATTACTGTA TTTCAAGTAG TACGCTGTGT GACCTTGAGC AAGTTGCTTA 960 CCTTCTCTGG GCCAGGCCCT AGTTCAGCTC TGGGACACAG CAGTGACCAA AGGAGCCGTG 1020 GTTCCTGCTC TCTTAGAGCC CATAGCCTGG GCAGGGAGGA GGAGGCAAGG AATGGCAAAT 1080 ACACAAGAAA ACAAAGATCA TTTCTGATGG TAATGAATTC AGTGAATAAG AGCAGGAGAA 1140 TGTAAAAGAA AGTAGCCTAG GGGGATCTGA GAAGGCCTCT GGGGAGGCGA CATTTGACCT 1200 GAGACTTGAA GAATGAGGAG TCTGGCAAAG ACCTGGGGCT GATCAGTGTT CTAGGAACAA 1260 GTAACAGCAA GGGCAAGGGC CCTGAGGCAG GACAGAGCTA TTAATAGTTT AAGGAGGGAG 1320 GCCTCTGGGC TGGTGAGAGA AAGGGAAGGG GCCCAGTTGG GTAGTGGGCA GGGGAGGAGT 1380 TTGGATCTTA TTCTCCGTGA GATGTGCTGG TTCTGGTGGT AGTGGGGGGG CCTGTAGTCT 1440 CCTGTTACAA GGGTTGGGGG TGTGGGGACA GCCAGAGCCA AAGGTCTCTC CCCCACAGCT 1500 CCGGCAGTCC CAGCCCAGAG GCGCCGGCCT GGCGGCTGGA AGATTGCACT GTGGGCACAT 1560 CTGGGGAGCA GCTGCCGAGC CAGGGCCAGA GTGGGTCACG TGGCACAGGG CAGGACCGTC 1620 CTGGAGCCTA CAAGGCCAAG ACTCCTAGGA GGGGCAGTGG AGAACACTCT GGACGAGAAC 1680 AGTGCGTCAA CGAGGAGGAA CTGTGCACTG TAGACGTCCA GGCACACGGC CCCCTGCAGC 1740 CCCACACAGC CCCTGCCTCA GGACAGAGTG CCTGGGTTCA ATGCCACCTC CCAGCTTTGT 1800 GATCTGAAAC AAGTCACTCA ACCTCTCTGG GTCTCATGGC CTCAGCTGTG AAGGGGACAT 1860 GATATTACTA CCACAGTTCC ACAGGCTGTT CTTTTTTTTT TTTTTTTTTT TTTTTTTTTT 1920 TTAATTTTTT GAGACGCAGT CTCACTCTGT TGCCCAGGCT GGAATGCAGT GGCACCATCT 1980 CAGCTCACTG CAACCTCTGC CTCCCGGGTT CGAGCGATTC TCCTGCCTCA GCCTCCCTAG 2040 TAGCTGTAGT AGCTGGGACT ACAGGCTCCC GCCACCAGGC CTGGCTAATT TTTTCATATT 2100 TTTAGTGGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCAAACTCT TGACCTCAGG 2160 TGAACCACCC ACCTCAGCCT CCCAAAGTGC TCCCAGGCTG TTTATTTCTA ATTCAACAAA 2220 TATTCGTTGA GCACTTCCCA CATGCCAGGT GCTGCATGAG GCTCTGCGTG ACAGCAGGGA 2280 ACAGGACCTC CGTGGTCCCT TCCCTTCTAA GCACACAATT AATGCTTTAG AACCAGGCCT 2340 GGCATTGAGG AAACTCTTAG TAAATGTAAG CCATTTGCCT GGAGCTCTGG AGGCCAGAGG 2400 AGGCACCCTG GAAGGCAGAG AAGGAGGTGT GGTGACAGAA AAATCCTAAG GAAAGTGCAC 2460 TCCCTTTTAT CACCAGGTGC TGCAGTTGGC TCCTGGTATG GCTCATTTCA CTCTCACAAC 2520 CACCCTACGA AGAGGGATGA GCATTAGCTC CAATTTATGG ATGAGGAAAC TGAGGCCCAG 2580 TTTGTCAATG GCACAGCCAG GACTGGAGGC AGTGAAGGGC TGGTCCCTTT TTCTCTCTGG 2640 GGCTCAATAT TCCCATCTGT GAAATGGGGC ATTACAATAA TACAGCTGCA CCAGCTCCAG 2700 GGAGCAGTTG TGAAATCAGA TGTGCCAGGT ATGTGAAAAG GGCTTCCTGA GAGACTATGA 2760 CCATGAATGC TGGGTTGGGA ATATGGGGGT TCATTTAAGG AGCCCTCCGA ACTTCCTGGC 2820 CACCAGAAGT GTCGGTTTTC CTAAGGTGAC TCAGGAAAGG AGGACTGGGA AGAAAATGCA 2880 CACTCAATTC ACACTACCAA CAAGGCCAGA AAAATGCCCA TCTGACAACA AGATAAGCAG 2940 GCAATCTTTA TTTAAACTCC TTGTCAGGCC TTAAACATGT AAAAGATAAG GCCAGGTGTG 3000 GTGGCTCATG CCTGTAAATC 3020
|