| Tag | Content |
|---|
EnhancerAtlas ID | HS105-53751 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr22:44523020-44525230 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr22:44523980-44523993 | GAAGATTCTGGAA | - | 6.16 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65916 | chr22:44524774-44525565 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTTTTCTTGT GGAGTAGCTG CTGTTCCATC TTGTTTGAAT AATCACATAA GCACTTGAGA 60
AGGCAATTCT AAAATCTCTT GAGTGTCAAG TGGTTTGACA TATTAAAACC ACTTTTTTTT 120
TTTGTACTGA AAAAAAGAAC AGTGGACTAG AATATTCAGA TAGTAACACA GCATCAGAAT 180
GTCTTGCCTC ATTTTGTGAA TGTTGTTACA CTGAAATGAC ATAATATACT GTTGATGTGA 240
GATCCTCTTG ATGTGATACT ACTGATGTGA TCACCTGATC CTTGAGCTCC AGGATGCCAG 300
GAATGACACT GATGTAGGCA TTCAGCTCTT TGGCTTTCCA AAGGCAGAAG CCCAAACCAA 360
ATAGGAGATT TTAGCTGAAT ACCAAGGTCA AAGCCAACTT CTGTGCATCC GTAGTAGAGA 420
AGAGGTCTGA GGACTGGGTC TGGGCTGTCA GCCATTAGTG GTCAGGAAGA GGAAGTTCTG 480
GCAAAGGTCA GTCACAAGGG AGGGGGAGCC AGAGGAGTGT TGCATTCAGG AAGGGTAAAG 540
GAGGTGTTTC TAGGAGGTGA GAGGAGGAAA GAGAACAGAC TTCTGGTTTG GCCATGTGGA 600
AATTGCCCAG AGTGAACCAG CAGGACCCCT GAGGAGTCCC TCTTCTTTTT TTTTTTTTCT 660
CTTGAGATAG TGTCTCACTC TGTTGCCCAG GCTGGAGTGC AGTGGCGTGA TCACAGCTCA 720
CTGCAGCCTT GACCCCTAGG CTTGGATGAT CTTCCCACCT CAGCTTCCCC GGGAAGCTGG 780
GATCACAGAT GCATACCACC ATGCCCAGAT AATTTTTGTA TTTTCTGTAG TGCTGAGGTT 840
TTGCCATGTT GCCCAGGCTA GTCTTGAACT GGGCTCAAAC GATCCTCCCA CCTTGGCCTC 900
CCAAAGTGCA GGGATCACAG GGATGAGCCA CTACACCCAG CCGAATCCCT CTTCTTGAGA 960
GAAGATTCTG GAAGCAGCTG CCGGGTTCTC TGCCACATGC CAGGTTTCTG GGGGTGTAGC 1020
TCCCCTGTGT TTGCAGTGCA GCCCTCAAGG TAGACTGCAT ATGGCCAGAG TGAGGTGCCC 1080
GTGCTGTGGG AGCTCCTGGC TGTCGTCCTG CTGGTCACTC ACGGGCACAC CCTCTCCTTG 1140
TGAAGGTGAA GTTCTTCATC ACATGTGTAC TCAACCCCCA TGTGGCCATC ACTCAGGGTC 1200
ACCTGCTACA TGGGAGAATC CTCCCCAGTT TTCTCTCTTT CTGTGCTAGG AAGATAGGGG 1260
TCCTGGCCAC AACAGAGCCC TGAGCTGCTC CTGCGGCCCC CGCCAGTGGG CACAGTGATG 1320
TCTGATGATG CAAGTGATCA TGTGCCGTAT TCTCTGTTGC ACAGGAGTCA CCCAAGACCC 1380
AGCCTAAGGC AGCACACAGG CATGGCCAGT CTCTTTGGTC TCTGTTGCCT GCTGTTTCCA 1440
CCACCAAATT CATATTTTCA AGTCCTACAT GCAGGGCCCA CCCATGTGAC CTCATTTTAC 1500
CTTAACTGCC TCTTTAAATA CAGGCACATT GCAAGGTATG AGAGCCTCGC CCACTAGGAG 1560
AGATGGGTAG CCTGGCAGCC TCCCACTGTC CCTGCTACCA GCCAGCCCTG CAGGTTGAAC 1620
CTCGGAATGT GACTGTATTT ATAGAGATAA TAATAGGCTG GGTGTGATGG CTCACACCTG 1680
TAATCCCAGC ACTTCCGGAG GCTGAGGTGG GCAGATCACT TGAGGTCAGG AATTCGAGAC 1740
CAGCCTGATC AACATGGTGA AACCCTGCCT CTACTAAAAA TACAAAAATT ACCTGGGCGT 1800
GGTGGCACAT GCCTGTAATC CCAGCTACTC GGGAGGCTGA GGCAGGAGGA TCGCTTGAAC 1860
CTGGGAGGCA GAGGTTGCAG TGAGCTGAGA TGGTGCCATT GCACTCCAGC CTGGGTGACG 1920
AGAGTGAAAC TCCATCTCAA AAAAATAAAA AAATTAAAAG AGGTAATGAA AGTAAAATGA 1980
GGCCATACGA GTGGGTGGGC CCTAATTCAA TATGTCTAGG GTTCCTATAA AAAGAGGAGA 2040
TTAGGACACA GACATGCACA GAGGGAGACC AAGTAAGGAC ACAGGAAGGA GAGGGCAGCC 2100
ATCTACAAGC CAGGAGAGGG GCCTCAGAAG GGTCTACCCT GCCGGTGCCT TGATCTTGGA 2160
CTTCTGGCCT CCAGAGCTGT GACATAAATC TCCGTTGTTT AAGCCGCACG 2210
|
