| Tag | Content |
|---|
EnhancerAtlas ID | HS081-00475 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:44047090-44049250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr1:44048046-44048064 | AGCAGGCCCAGGCATGCT | - | 6.03 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_05962 | chr1:44045982-44048063 | Brain_Hippocampus_Middle | | SE_23829 | chr1:44046994-44048030 | Colon_Crypt_2 | | SE_23829 | chr1:44048164-44048638 | Colon_Crypt_2 | | SE_26649 | chr1:44045820-44048922 | Esophagus | | SE_27645 | chr1:44047195-44049958 | Fetal_Intestine | | SE_28595 | chr1:44047280-44048969 | Fetal_Intestine_Large | | SE_33537 | chr1:44045757-44056755 | H2171 | | SE_52524 | chr1:44047044-44048792 | Small_Intestine | | SE_65452 | chr1:44047303-44047936 | Pancreatic_islets | | SE_65452 | chr1:44048025-44048999 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 44047816 | 44048271 | | chr1 | 44047550 | 44048400 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I043581 | chr1 | 44046992 | 44049104 |
|
Enhancer Sequence | AGGACCTGCC TCATGTAGAC CCTAATTGAA TCTACACCAC CCTGCTTTGC CAAGAGCAAC 60
CTGCCCCATA GGCCCTACTG TCCTACTGAC AGGACTTAGG CACACCTGAA AGGCCCTGCT 120
CCCTGGGTGC CTTGCCTCTG GTGCCCCCAC TGCTCGTCAT CTCATGGTTG GCAAAACCCC 180
TGCCTTCTGC CCTCAGCAGT ACTAGGGGCC CTTCAGCCCC AGCGCCTGGG GACAGCCTGT 240
ACTGGGCTGA CCACCAGCTC TGCATCCTGA GCCCTGCTTG TGGGTGGATG GCCGTGGAGG 300
AGTCCCCAGT GCCAGCCTGC TTTCTGGCCT GCACCCCGTC CCATCTCCCA GCAGAGAGGC 360
TTCGAGGTTT CCTCCCACAG CAGGCTCCTG AGCCTCAGAC GGCTTGATGT GGGCTCTAGC 420
CCTGAACTTC TCAGCCGCAG CACTGTTGAC ATTTTGGGCT GGACGATTCT TAGTTGTGAG 480
GGGCCATCCT GTGCATTGGA GGGTGTTTAG CAGCATCTCT AGCTCACTAG ATGCCAGTGG 540
CACCCCTCAG TCAAAACAAA CGTTGCAACG TGTCACCTGG GGGAAATTAC TGATGGCTTC 600
CCACTGCCAT TGTCTCCACC CATCTGACTC TCTTCACCTG TGTCCACTGG CCGCAAGGCT 660
TCGTCTCCTC ATCAGACTTG GCTTCGGTGT CTACCTCACA TCTCCCTTCT GTCCCCCAAA 720
TTCTCAGGGC TCCCAGTGTC GCTCTCTGAG GCCACGCGAC TGCTACATTT AATGGGACAG 780
TACACGTGAA GCACCAGGCA CATTGCCAGG CACACAGGAA GCACTTGCTA GTCAGTAGCC 840
TCTGCAGCTA GCACTCGGCT ACTAGTCAGT AGCCTCTCGG ATAGCACTGT GGGGGGATGT 900
GTCATCCAGT TACATCTGAC TTTGTTCACA GTTGCCTGCA GCTCCACCCA CAGTCTAGCA 960
GGCCCAGGCA TGCTGGGTGG GCCAGAGCCT TTCTCCTTCA CCACCTGACT CTCCCTGAGT 1020
GACTCATTCT CTCCTTCCAT CTACAGCTCT CTGGGTGTAC AGCTGCTGGG GCCAGGGTGG 1080
AGCCCTGCCC TCCTCAGAGC CTGGCCTACC TGTGCCAGGA CTACCAGCCT TCCCCCTTTC 1140
TCTAGGGACC TGGCTGCGGG CCACAGCTGT CTAAAACAGG GACAGTGCCT TTTTCCCCAC 1200
AGGTGCCCAG ACATGCTCCT TACACCGGTG GTGTGTGTGG GGGTGGCTTC TAGTGGCTCC 1260
TGTACCTTGG CAGGTTTGTG GGCTGGGTGG GCCTTGACCC CAGAGCCCGG TCCACAGGGT 1320
CTGTCTGAGC TGTGGGGTGC GTGTGAGGCA TGGGGGCCTG CCTGTGCCCC ATTTTCACCT 1380
GCCCCGGCCC CACCCTCGGC CTCCCTGGCG CCTGCTGGCG GGCCTCAGCC CTGTCCACCA 1440
TGTCCTCCAT GAGTCCTGAG TCTTTTGTGA GTGATGTGGT TCGTGTGCAC CTGTGTGCAT 1500
GTGTGTGTGC GAGGGGGCAC AGGAGTCTCG TCTCGTCTCC GTGCTGTGTG GGCAGATGAA 1560
GGTTGGCCTG TTTTTACTCT CTCTGTGTTT CTCCTTGTCT TTTTTTTATT CCCTCCTCAT 1620
CTTCATCGCA CTCTGCCATC AACCCAAACT CTCATCTCTC AGATCAGCGA GAAGGTTGGT 1680
CCTTTTCACT TCTTATCCAT CTACAGTTCG CCCATCGATG GGACACGCCT GTCAGTAGGG 1740
CCCAGCGGGC TCGGTCAGCT CCCTCAGGCT CACTGCGCCG TGCCTGCCTG CCAGTCTCTG 1800
TTGTTTGGGC CGGCGGGCAG GCAGGACCAG GGATGGGTGG GCAGACCCCT GACCTGCATG 1860
TTCCTGCTGC TTGGGTCCCT GGTGCACCAC GTGTCTGCAT GTCCCCTTAG CCTGGTTCCC 1920
CTGCAAGGGT GGTGGGGTGG GCATGCTGCA TGGCATGAAA CTGTACCCCA CCTTTGCACC 1980
CAGGCCGGGC CAGCTGTCTG ATCCAGGCGG TGCTCAGGAA TGGTTGTGGG GGGCTGTGGT 2040
CAGAGAGAGG TGTAAGACCT GTAGCGCTTT GTGTGCACCT GTGGGACCTT TCACCGCCCT 2100
CCTCGCCTAG AGACCCAGGC TCAGCCGAAA CTACTGGAAC ATTAAGGCGA GAGGCTAGAG 2160
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