| Tag | Content |
|---|
EnhancerAtlas ID | HS108-24873 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr20:30183080-30185270 |
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 | GGGGACAGTC CCCATTTTGT GGATGAGAAA ACTGAGGGGT TTCATTCCTA TTAAAAGGGA 60
GAGAGCCTGA AGCCCCACAC CCTTTATGTG CCCACCCACA GCCTCCTGCC GGGTTTGGGG 120
GATGGAAAAA TGACACCCCA GAATGGAAAC AAAACGGTCT ATTGTGGTTT CCATTTCTGA 180
ATGCTTACCA TGTGCTAAGT GCAGAAGTGT CATAACTCTG CAGGTTAAGT TCATATTTTG 240
TACCCATTTT GCACAGGAGT ACACTGAACC ATAAGGCAAC AATTTATTCT TCAAAGGACA 300
CTACTCTAAA CATTACTGTA TTTCAAGTAG TACGCTGTGT GACCTTGAGC AAGTTGCTTA 360
CCTTCTCTGG GCCAGGCCCT AGTTCAGCTC TGGGACACAG CAGTGACCAA AGGAGCCGTG 420
GTTCCTGCTC TCTTAGAGCC CATAGCCTGG GCAGGGAGGA GGAGGCAAGG AATGGCAAAT 480
ACACAAGAAA ACAAAGATCA TTTCTGATGG TAATGAATTC AGTGAATAAG AGCAGGAGAA 540
TGTAAAAGAA AGTAGCCTAG GGGGATCTGA GAAGGCCTCT GGGGAGGCGA CATTTGACCT 600
GAGACTTGAA GAATGAGGAG TCTGGCAAAG ACCTGGGGCT GATCAGTGTT CTAGGAACAA 660
GTAACAGCAA GGGCAAGGGC CCTGAGGCAG GACAGAGCTA TTAATAGTTT AAGGAGGGAG 720
GCCTCTGGGC TGGTGAGAGA AAGGGAAGGG GCCCAGTTGG GTAGTGGGCA GGGGAGGAGT 780
TTGGATCTTA TTCTCCGTGA GATGTGCTGG TTCTGGTGGT AGTGGGGGGG CCTGTAGTCT 840
CCTGTTACAA GGGTTGGGGG TGTGGGGACA GCCAGAGCCA AAGGTCTCTC CCCCACAGCT 900
CCGGCAGTCC CAGCCCAGAG GCGCCGGCCT GGCGGCTGGA AGATTGCACT GTGGGCACAT 960
CTGGGGAGCA GCTGCCGAGC CAGGGCCAGA GTGGGTCACG TGGCACAGGG CAGGACCGTC 1020
CTGGAGCCTA CAAGGCCAAG ACTCCTAGGA GGGGCAGTGG AGAACACTCT GGACGAGAAC 1080
AGTGCGTCAA CGAGGAGGAA CTGTGCACTG TAGACGTCCA GGCACACGGC CCCCTGCAGC 1140
CCCACACAGC CCCTGCCTCA GGACAGAGTG CCTGGGTTCA ATGCCACCTC CCAGCTTTGT 1200
GATCTGAAAC AAGTCACTCA ACCTCTCTGG GTCTCATGGC CTCAGCTGTG AAGGGGACAT 1260
GATATTACTA CCACAGTTCC ACAGGCTGTT CTTTTTTTTT TTTTTTTTTT TTTTTTTTTT 1320
TTAATTTTTT GAGACGCAGT CTCACTCTGT TGCCCAGGCT GGAATGCAGT GGCACCATCT 1380
CAGCTCACTG CAACCTCTGC CTCCCGGGTT CGAGCGATTC TCCTGCCTCA GCCTCCCTAG 1440
TAGCTGTAGT AGCTGGGACT ACAGGCTCCC GCCACCAGGC CTGGCTAATT TTTTCATATT 1500
TTTAGTGGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT CTCAAACTCT TGACCTCAGG 1560
TGAACCACCC ACCTCAGCCT CCCAAAGTGC TCCCAGGCTG TTTATTTCTA ATTCAACAAA 1620
TATTCGTTGA GCACTTCCCA CATGCCAGGT GCTGCATGAG GCTCTGCGTG ACAGCAGGGA 1680
ACAGGACCTC CGTGGTCCCT TCCCTTCTAA GCACACAATT AATGCTTTAG AACCAGGCCT 1740
GGCATTGAGG AAACTCTTAG TAAATGTAAG CCATTTGCCT GGAGCTCTGG AGGCCAGAGG 1800
AGGCACCCTG GAAGGCAGAG AAGGAGGTGT GGTGACAGAA AAATCCTAAG GAAAGTGCAC 1860
TCCCTTTTAT CACCAGGTGC TGCAGTTGGC TCCTGGTATG GCTCATTTCA CTCTCACAAC 1920
CACCCTACGA AGAGGGATGA GCATTAGCTC CAATTTATGG ATGAGGAAAC TGAGGCCCAG 1980
TTTGTCAATG GCACAGCCAG GACTGGAGGC AGTGAAGGGC TGGTCCCTTT TTCTCTCTGG 2040
GGCTCAATAT TCCCATCTGT GAAATGGGGC ATTACAATAA TACAGCTGCA CCAGCTCCAG 2100
GGAGCAGTTG TGAAATCAGA TGTGCCAGGT ATGTGAAAAG GGCTTCCTGA GAGACTATGA 2160
CCATGAATGC TGGGTTGGGA ATATGGGGGT 2190
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