| Tag | Content |
|---|
EnhancerAtlas ID | HS197-14053 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr22:46909760-46911950 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MITF | MA0620.2 | chr22:46911265-46911283 | CCAAGTCACATGACCCCC | + | 6.01 | | MITF | MA0620.2 | chr22:46911265-46911283 | CCAAGTCACATGACCCCC | - | 6.01 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26636 | chr22:46909700-46911877 | Esophagus | | SE_34191 | chr22:46909995-46911887 | HCC1954 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 46910107 | 46911726 | | chr22 | 46910355 | 46911003 | | chr22 | 46911084 | 46911930 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I046513 | chr22 | 46909817 | 46911837 |
|
Enhancer Sequence | TCACTGCAGC CTCTGCCTCC CGGGGTTCAC GCCATTCTCC TGCCTCAGCC CCCCCCGAGT 60
AGCTGGGACT ACAGGTGCAC GCATCCACAC CCAGCTAATT TTTGTATTCT TAGTAGAGAC 120
GGGGTCTCAC CTTGTTGGCC AGGATGGTCT CGATCTCCTG ACCTCATGAT CCACCCGCCT 180
CACCCTCCCA AAGTGCTGGT ATTACAGGCA CGAGCCACCG CACCCGGCCC TCATTTGTAA 240
TTTTTCACAG CTCTTTACTT GTCTTGTCTA CACTTTTCTC ACATCCCAGC ACCCACCTGG 300
GAAAGGTTCC TGGGGTCAGA ATCATCTGAC CTTGACTGTG GGTCTTTCCC ACCCAGGTAG 360
GCTCCAACAC CAGGGGAATC CCACCCAGTC CTCGAGATGA CAGTGTCAAA AACCCAGTAA 420
GCGAGACTAC TCACAATGGA GCCGGCATTT CTGAAGGGTG ATTATTTAAG CCACACCTCA 480
ACTGCGGGCC TATGTGATGC TGAAGCTCTT CCACCCAGAC GTTTCACCAG GCCCCGACGG 540
TCCATCCAGG TGAGGGCTGG AGTCAGGTCC ACCTGCACTC TGATCCCCGG GGGCCCAAGG 600
CCACACACCT CTGGCTGCCA GTCAGTCAGA ACCAGTCCTG GTGAGGTGGG GAGTGGGGGC 660
ATGAAGGATG TGGCCTGAGG ACACCCCAAC AGCATCTGTG TATCACCGCC AGACCCTTGC 720
TGAAAGTCAG GGATAATGCA ATGGCCCCTC TCAGCACCTC CCCAGACCTC CCCAGACTCT 780
GTGGTCCCTC CTCCCAGCAT CAAAGAGAAG AGTCACTCCC CGGAGGGAGC CGGGGCTGCA 840
GGGCCGAGGC TCACGGCTGG GCTCTGGAAT AAGAGGGGTG TTTCTGAATG AATTGCCCAG 900
CCCTGTCCTG CCTCGCTGAG TCATTCCCAA GTCAGCAAGC ACAAGTCACT GCGGGAAAAG 960
CTCTGGAGCT GCCACCCCTT CCCACCCCAG GGATGCCTGT CCGTACCCGC CGTCAATCCA 1020
GCCCTCAGGC CTGGGGGATG AGCACCTCAG ACGTGCTCTT TGCAGCTGGC ATCCGCTCCA 1080
AACTCCATGC CTCCCCACAA AAGTGGCTCT GTCCAAACCC CAGCCCTCTT GGGCCCTGGC 1140
AACCAGCCTA GTCCTCGCCA GCCCCTTCTA GAAAGCACCC CCAGCACCCC CTCAGCTTCA 1200
GCCTGGGCTG AGAAAAGGCT GTCTGGCAGC GTGGACCCCC CTCAGCGTCC CAGCAGAGCC 1260
AACCCCCCCC GGGGACACTC ATGGGACACA GCATGGGCAG TAGGAGCCAT TCCACCCGTG 1320
CATCAGCCCT CTGGCCACAC TCTGGGACCT CATGGCCCTG CCCACCACTC CCAGCCCACA 1380
GCCAGGCAAG TGACCCCCAC CTGGGCCCTC CTGGGGAGAG CTGCACAGCT GTCGGCAGCA 1440
CAGCTGGAAC CACAGCCCAG CGGTCTCAGT GCGTATCACA AAGGCTAGCT TGTGAGTGGA 1500
TGCTCCCAAG TCACATGACC CCCAGGTAGG AAGGTTTGCA CATGTTTCAT CAGGGTAAAG 1560
GGAAAGAGGC TCACCTTAAA CACAAACTCT ATGAAGGCCT TAGACAGAAA ATAGGAAAGC 1620
ATGACAGTCT GTGTCTCCAT GGTGAAGTCA GCTCTGGGAG GGCTGAGCCT GATGCAGAGT 1680
GGGTGTGCAC AAGCTGCAGG GCACCCCGGG GGCTGGAGGT GGAGGACACA GCCAATAGGA 1740
CGGGCCTCAG TCACACAGTG CTCAGGGCTG GGGACTCAAA GGCACAGAGG CTGAGGCTTT 1800
GTAAGTCCTG CTGGGGGATC AGGGGATGAC TAAGTCACTG GGGCCTCCCC AGCCTGGCAG 1860
GCTCCTATCT GTGTAACAGG CTCCCAGCAG CCAGTGTAGG AAGGCAGCCC CGGCAGGAGG 1920
ATACACCAGG ACATTCCGCC CATCCTGCAG ATCTCCAGCA CTGACCAGCA TCCACAGCAC 1980
AGTCGACTGG GGTTAAGAAA GTAGGAATGA GTTCAGAGAA ATGCAAATCA AAACCACAAT 2040
GAGATATCAT CTCACACCAG TTACAATGGC GATCATTAAA AAGTCAGGAA ACAACAGGTA 2100
CTGGAGAGAA TGTGGAGAAA CAGGAACACT TTTACACTGT TGGTGGGACT GCAAACTAGT 2160
TGAACCATTG TGGAAGACAG TGTGGCGATT 2190
|
