| Tag | Content |
|---|
EnhancerAtlas ID | HS105-49620 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr20:30182590-30185200 |
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 |
|
| | 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 | TGTTGGTTGT ATATTATGGT GTACTGTTGT GCGTTGTGCA TTTGGCAGGT TGTGTCTATT 60
GGTGTGTGGC TGTTGGGTTT GTCTGTTGTG TCAGTCGTAC ATATAAATGC CACGTTGGGC 120
GTGTGGGTGT GTGCATTTGT ATATTGCTCT GTGGGTGTGC GAAGCAGTGT GTTTGTGTAA 180
CCCTGCAGGT TTGGCCTATG CTGAGTAACC TAAGATGGGA GCTCCCTGAG CCTTGGCTCT 240
GCCCTTGCCT TTGGCTGCTG GAGACCCTGG GCAGCAATGG CCCTTTGTCC AGCCACAGGA 300
AAACCCCACC CCCCTCCATC GGCAGGGGAC TTGGGAGGGG CCCAGACTGG TAGGCTCCAG 360
CCTCCCGTCC ATTGTTCTGG GGCCTCTCTG GAAAACAGGA TGGGAGGTGA AAGGTGGACA 420
CAGGCCTGGA CCCCCACACT CCCTGAAACA ACCCAGGGGC ACAGCACAGA ATCCTTAGGA 480
GGGAGGGCCT GGGGACAGTC CCCATTTTGT GGATGAGAAA ACTGAGGGGT TTCATTCCTA 540
TTAAAAGGGA GAGAGCCTGA AGCCCCACAC CCTTTATGTG CCCACCCACA GCCTCCTGCC 600
GGGTTTGGGG GATGGAAAAA TGACACCCCA GAATGGAAAC AAAACGGTCT ATTGTGGTTT 660
CCATTTCTGA ATGCTTACCA TGTGCTAAGT GCAGAAGTGT CATAACTCTG CAGGTTAAGT 720
TCATATTTTG TACCCATTTT GCACAGGAGT ACACTGAACC ATAAGGCAAC AATTTATTCT 780
TCAAAGGACA CTACTCTAAA CATTACTGTA TTTCAAGTAG TACGCTGTGT GACCTTGAGC 840
AAGTTGCTTA CCTTCTCTGG GCCAGGCCCT AGTTCAGCTC TGGGACACAG CAGTGACCAA 900
AGGAGCCGTG GTTCCTGCTC TCTTAGAGCC CATAGCCTGG GCAGGGAGGA GGAGGCAAGG 960
AATGGCAAAT ACACAAGAAA ACAAAGATCA TTTCTGATGG TAATGAATTC AGTGAATAAG 1020
AGCAGGAGAA TGTAAAAGAA AGTAGCCTAG GGGGATCTGA GAAGGCCTCT GGGGAGGCGA 1080
CATTTGACCT GAGACTTGAA GAATGAGGAG TCTGGCAAAG ACCTGGGGCT GATCAGTGTT 1140
CTAGGAACAA GTAACAGCAA GGGCAAGGGC CCTGAGGCAG GACAGAGCTA TTAATAGTTT 1200
AAGGAGGGAG GCCTCTGGGC TGGTGAGAGA AAGGGAAGGG GCCCAGTTGG GTAGTGGGCA 1260
GGGGAGGAGT TTGGATCTTA TTCTCCGTGA GATGTGCTGG TTCTGGTGGT AGTGGGGGGG 1320
CCTGTAGTCT CCTGTTACAA GGGTTGGGGG TGTGGGGACA GCCAGAGCCA AAGGTCTCTC 1380
CCCCACAGCT CCGGCAGTCC CAGCCCAGAG GCGCCGGCCT GGCGGCTGGA AGATTGCACT 1440
GTGGGCACAT CTGGGGAGCA GCTGCCGAGC CAGGGCCAGA GTGGGTCACG TGGCACAGGG 1500
CAGGACCGTC CTGGAGCCTA CAAGGCCAAG ACTCCTAGGA GGGGCAGTGG AGAACACTCT 1560
GGACGAGAAC AGTGCGTCAA CGAGGAGGAA CTGTGCACTG TAGACGTCCA GGCACACGGC 1620
CCCCTGCAGC CCCACACAGC CCCTGCCTCA GGACAGAGTG CCTGGGTTCA ATGCCACCTC 1680
CCAGCTTTGT GATCTGAAAC AAGTCACTCA ACCTCTCTGG GTCTCATGGC CTCAGCTGTG 1740
AAGGGGACAT GATATTACTA CCACAGTTCC ACAGGCTGTT CTTTTTTTTT TTTTTTTTTT 1800
TTTTTTTTTT TTAATTTTTT GAGACGCAGT CTCACTCTGT TGCCCAGGCT GGAATGCAGT 1860
GGCACCATCT CAGCTCACTG CAACCTCTGC CTCCCGGGTT CGAGCGATTC TCCTGCCTCA 1920
GCCTCCCTAG TAGCTGTAGT AGCTGGGACT ACAGGCTCCC GCCACCAGGC CTGGCTAATT 1980
TTTTCATATT TTTAGTGGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCAAACTCT 2040
TGACCTCAGG TGAACCACCC ACCTCAGCCT CCCAAAGTGC TCCCAGGCTG TTTATTTCTA 2100
ATTCAACAAA TATTCGTTGA GCACTTCCCA CATGCCAGGT GCTGCATGAG GCTCTGCGTG 2160
ACAGCAGGGA ACAGGACCTC CGTGGTCCCT TCCCTTCTAA GCACACAATT AATGCTTTAG 2220
AACCAGGCCT GGCATTGAGG AAACTCTTAG TAAATGTAAG CCATTTGCCT GGAGCTCTGG 2280
AGGCCAGAGG AGGCACCCTG GAAGGCAGAG AAGGAGGTGT GGTGACAGAA AAATCCTAAG 2340
GAAAGTGCAC TCCCTTTTAT CACCAGGTGC TGCAGTTGGC TCCTGGTATG GCTCATTTCA 2400
CTCTCACAAC CACCCTACGA AGAGGGATGA GCATTAGCTC CAATTTATGG ATGAGGAAAC 2460
TGAGGCCCAG TTTGTCAATG GCACAGCCAG GACTGGAGGC AGTGAAGGGC TGGTCCCTTT 2520
TTCTCTCTGG GGCTCAATAT TCCCATCTGT GAAATGGGGC ATTACAATAA TACAGCTGCA 2580
CCAGCTCCAG GGAGCAGTTG TGAAATCAGA 2610
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