| Tag | Content |
|---|
EnhancerAtlas ID | HS116-20806 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr20:30182940-30185340 |
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 | TAGGCTCCAG CCTCCCGTCC ATTGTTCTGG GGCCTCTCTG GAAAACAGGA TGGGAGGTGA 60
AAGGTGGACA CAGGCCTGGA CCCCCACACT CCCTGAAACA ACCCAGGGGC ACAGCACAGA 120
ATCCTTAGGA GGGAGGGCCT GGGGACAGTC CCCATTTTGT GGATGAGAAA ACTGAGGGGT 180
TTCATTCCTA TTAAAAGGGA GAGAGCCTGA AGCCCCACAC CCTTTATGTG CCCACCCACA 240
GCCTCCTGCC GGGTTTGGGG GATGGAAAAA TGACACCCCA GAATGGAAAC AAAACGGTCT 300
ATTGTGGTTT CCATTTCTGA ATGCTTACCA TGTGCTAAGT GCAGAAGTGT CATAACTCTG 360
CAGGTTAAGT TCATATTTTG TACCCATTTT GCACAGGAGT ACACTGAACC ATAAGGCAAC 420
AATTTATTCT TCAAAGGACA CTACTCTAAA CATTACTGTA TTTCAAGTAG TACGCTGTGT 480
GACCTTGAGC AAGTTGCTTA CCTTCTCTGG GCCAGGCCCT AGTTCAGCTC TGGGACACAG 540
CAGTGACCAA AGGAGCCGTG GTTCCTGCTC TCTTAGAGCC CATAGCCTGG GCAGGGAGGA 600
GGAGGCAAGG AATGGCAAAT ACACAAGAAA ACAAAGATCA TTTCTGATGG TAATGAATTC 660
AGTGAATAAG AGCAGGAGAA TGTAAAAGAA AGTAGCCTAG GGGGATCTGA GAAGGCCTCT 720
GGGGAGGCGA CATTTGACCT GAGACTTGAA GAATGAGGAG TCTGGCAAAG ACCTGGGGCT 780
GATCAGTGTT CTAGGAACAA GTAACAGCAA GGGCAAGGGC CCTGAGGCAG GACAGAGCTA 840
TTAATAGTTT AAGGAGGGAG GCCTCTGGGC TGGTGAGAGA AAGGGAAGGG GCCCAGTTGG 900
GTAGTGGGCA GGGGAGGAGT TTGGATCTTA TTCTCCGTGA GATGTGCTGG TTCTGGTGGT 960
AGTGGGGGGG CCTGTAGTCT CCTGTTACAA GGGTTGGGGG TGTGGGGACA GCCAGAGCCA 1020
AAGGTCTCTC CCCCACAGCT CCGGCAGTCC CAGCCCAGAG GCGCCGGCCT GGCGGCTGGA 1080
AGATTGCACT GTGGGCACAT CTGGGGAGCA GCTGCCGAGC CAGGGCCAGA GTGGGTCACG 1140
TGGCACAGGG CAGGACCGTC CTGGAGCCTA CAAGGCCAAG ACTCCTAGGA GGGGCAGTGG 1200
AGAACACTCT GGACGAGAAC AGTGCGTCAA CGAGGAGGAA CTGTGCACTG TAGACGTCCA 1260
GGCACACGGC CCCCTGCAGC CCCACACAGC CCCTGCCTCA GGACAGAGTG CCTGGGTTCA 1320
ATGCCACCTC CCAGCTTTGT GATCTGAAAC AAGTCACTCA ACCTCTCTGG GTCTCATGGC 1380
CTCAGCTGTG AAGGGGACAT GATATTACTA CCACAGTTCC ACAGGCTGTT CTTTTTTTTT 1440
TTTTTTTTTT TTTTTTTTTT TTAATTTTTT GAGACGCAGT CTCACTCTGT TGCCCAGGCT 1500
GGAATGCAGT GGCACCATCT CAGCTCACTG CAACCTCTGC CTCCCGGGTT CGAGCGATTC 1560
TCCTGCCTCA GCCTCCCTAG TAGCTGTAGT AGCTGGGACT ACAGGCTCCC GCCACCAGGC 1620
CTGGCTAATT TTTTCATATT TTTAGTGGAG ATGGGGTTTC ACCATGTTGG CCAGGCTGGT 1680
CTCAAACTCT TGACCTCAGG TGAACCACCC ACCTCAGCCT CCCAAAGTGC TCCCAGGCTG 1740
TTTATTTCTA ATTCAACAAA TATTCGTTGA GCACTTCCCA CATGCCAGGT GCTGCATGAG 1800
GCTCTGCGTG ACAGCAGGGA ACAGGACCTC CGTGGTCCCT TCCCTTCTAA GCACACAATT 1860
AATGCTTTAG AACCAGGCCT GGCATTGAGG AAACTCTTAG TAAATGTAAG CCATTTGCCT 1920
GGAGCTCTGG AGGCCAGAGG AGGCACCCTG GAAGGCAGAG AAGGAGGTGT GGTGACAGAA 1980
AAATCCTAAG GAAAGTGCAC TCCCTTTTAT CACCAGGTGC TGCAGTTGGC TCCTGGTATG 2040
GCTCATTTCA CTCTCACAAC CACCCTACGA AGAGGGATGA GCATTAGCTC CAATTTATGG 2100
ATGAGGAAAC TGAGGCCCAG TTTGTCAATG GCACAGCCAG GACTGGAGGC AGTGAAGGGC 2160
TGGTCCCTTT TTCTCTCTGG GGCTCAATAT TCCCATCTGT GAAATGGGGC ATTACAATAA 2220
TACAGCTGCA CCAGCTCCAG GGAGCAGTTG TGAAATCAGA TGTGCCAGGT ATGTGAAAAG 2280
GGCTTCCTGA GAGACTATGA CCATGAATGC TGGGTTGGGA ATATGGGGGT TCATTTAAGG 2340
AGCCCTCCGA ACTTCCTGGC CACCAGAAGT GTCGGTTTTC CTAAGGTGAC TCAGGAAAGG 2400
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