| Tag | Content |
|---|
EnhancerAtlas ID | HS023-17312 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr22:40405150-40406870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:40405220-40405238 | GCTGCTTCCCTTCCTTCC | - | 6.31 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23648 | chr22:40404562-40406179 | Colon_Crypt_1 | | SE_24534 | chr22:40405289-40405850 | Colon_Crypt_2 | | SE_27100 | chr22:40400619-40406600 | Esophagus | | SE_33456 | chr22:40389950-40407904 | H2171 | | SE_34987 | chr22:40403092-40407658 | HeLa | | SE_65865 | chr22:40404750-40406808 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I040007 | chr22 | 40403673 | 40407125 |
|
Enhancer Sequence | CAGGGCAGGT GTGGGAGGCG ACTCGGCCCC AGGCGCACAT GGGTAGGTAA TCAGTGGGAA 60
AGTGTCCCTA GCTGCTTCCC TTCCTTCCCC AGGATAAGTG ACTGTCACCA AAAGGCCCCC 120
CCGAGATCAG CAAGCTTGGC CTGTGGCCTT TTGCTTTTTC ACACCCACAG AAGGGGTGAA 180
GCTGGGGCTC TTTGCAGGCA ACAGCAGCCG CACCCGCCCG AGTCCTGAGC TCCACGTCAG 240
CAGGGCAAGG GGACGGATGG TGTTGTCTTT CTCTGGCCAT GCATCTCAGT TTGCATCCTG 300
CTGTGCAGGA TGAATTGGAG GGCAGAGGTG AGTAGGAGAG AGCAGTTAGG AAGCTCATCA 360
AAGCATGGTA GGAAAGGAGG AGAGTCCGAG CTGGGGCGGT ACCAGTGGGG ACAGAAAGGA 420
TTAACCCTGA GAAGGTGCCC GGGGTGGGGC CTGCTGGATT CAGTGACTGA TGGGATTTGG 480
TCGGTGGGGA GGAGGAGGAG GCCTGGGCTT CTGGCCAGAG TGACTAGGAG GATGTTGATC 540
TGGGGAGTGC CTGTGTGGCT GAGGGACACG TCCAAGCTGC AGTCGGCTCT GTGGTTGTGG 600
ACACCTGGCA GAGCCATGCC TTCTCTAGTC TGGGTCATCC AAACACACGT GGGGTGCAGG 660
GGCCAGGTGG AGCCCTCTTG TCGTTTTTGT TATCTAACGG TAATTACGGA GTCCAGAAAG 720
AGAATTGGAA ATGCCGGCAG TTTAATTAAA GCTGAATGGC AGGAGAGGGG CATTTGGAGG 780
CTCCCTCCCT GCCTTCACTC CCCGTCCTGC CGCCCAGGCA GGATGTCAGA TGAGGAGACG 840
TTGAGCTCAT CAAACACCCA ATGAGAAGTC TTACAACATC AGAAGCTGTC TGCCAATGCG 900
CCTGCGACAG CTTATAGAAA CTGCTGCCGC CTCGAATCAA CCTCTCTCCC CAGGCATTGC 960
ACGTCAGTAG GTAACCAGGT AAAGGACGCC GGGGGTGGGC AGCCAGCTGG AGGGGGCGTG 1020
ATTTCCTCCC CCAACAAAAT CGGCTTCCCT GGGTTCTGAG CCCATGATAT CATGTTTTTA 1080
AACCCGATTT TCCATCTACA CTGGGAGCTT TGAAGTTCGC TCGGTGTGGG GAATCACGTG 1140
CTCAGTGAAA GACCCAAGCG GAGAGACTGG GGAGCTGGTT CCCCTGGGCC TGACACTGCG 1200
GAGCTGAATG TCAAAGCAGG GCCCTCAGAG ACCAAAGCGG AGGGTAATTA TCACTTCTCC 1260
ACAACTAGAT TGCAGGAGTC AGCCAGCAAT TGATTTTTTT TTCTACTTCA GATATTTCAT 1320
TGTTTAATTG GTAGTGACAC AGATGGCTGG CTCGCATCAG GGCGTCACAG TCCGACTCGC 1380
GAAAGCCAGG CTGTGGGGAC TGCTGCCTCT CCTGACATCC TTAGGCAGGT GGGGCTAGGA 1440
CAGGCCAGCT TCCCTGCTTA ATTTTTCAAC CACAAAGCAA AAGTAAGCTT GTGAACCTGA 1500
GACATGCTTC TGCAAACCGG TCAAGCTGTC CTCAGCGACA TGAGTCCACT CTAAACTGGA 1560
CACCTTGGAG TGTTCAGAAA TGAGAGGACA GTGAACTCTT GCCTAGACAG CTCGTGGGAG 1620
ATAAACTATC AGCACTAGGA GATGGCGATC AAGTATCAGA GCCCTGGAAA CTGCATTGCT 1680
GGTGGAATGA AGCCAGAACT CTGTACATTG TGTTCAAACC 1720
|
