| Tag | Content |
|---|
EnhancerAtlas ID | HS060-21883 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr20:46096970-46097880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr20:46097771-46097792 | TTTTTGTTTCTTTTTCTTTCT | + | 6.25 | | SPI1 | MA0080.4 | chr20:46097234-46097248 | TGCTTCCTCTTTTT | - | 6.41 | | SPIC | MA0687.1 | chr20:46097234-46097248 | TGCTTCCTCTTTTT | - | 6.59 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_10904 | chr20:46096117-46098495 | CD20 | | SE_32514 | chr20:46095700-46099108 | GM12878 | | SE_44071 | chr20:46096399-46098309 | MM1S | | SE_58317 | chr20:46012297-46142322 | Ly1 | | SE_58975 | chr20:46096568-46153547 | Ly3 | | SE_59709 | chr20:46094742-46170079 | Ly4 | | SE_60400 | chr20:46012252-46151621 | DHL6 | | SE_62944 | chr20:46096399-46137613 | Tonsil |
|
| | 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 |
| GH20I047466 | chr20 | 46094991 | 46098703 |
|
Enhancer Sequence | AAGGCCTTCA TTTGGGGAGA GGCCTTAAAT GTGCCAACTG CCAGCTGCAA GAACCAAGTG 60
GCCAGAACAT CGAGGTTTTG AAGTCTCGCA AAACAGATGT GTAAAAGTCA ACTGCACAGG 120
CAGGACCTTA GAGTGGCACC CGGAACCCAA GGCCTTGAAA GATCCCAGCT TGTTTCTTTA 180
CAGAAAGCTT GGCTTTGTTG ACCAGGCTGA TAGAAACCGC GCCCAGCTGT AGAAAGGTTG 240
CGTGTGTATA TATGTGCGTG TTTCTGCTTC CTCTTTTTTT ATCTCATACG ATTACAAACA 300
CATAATCTCA AGGGTCTGCA GCACATGTCA CCTTGGAGTT ATTTTAGATT TACCCCCGGA 360
ACATCAAACG TTCATTCCAG AAGGGTTTGA CAGGGCATAG AGAGTGCCGA CTAAACCCAG 420
AGGGGGCAAG TTCAAGCATG TTTTTCGCTA CCCCAATTTG CATCAGTGCC TCCCCACCCC 480
CCCAAAACAC ATGCCTCTTT TGCATTACTC AGTGAAAAGT GAAAACTGAT AAAGAAAAGG 540
CATGTTTTGT TAATTAAAAA CATCTTTATT TAATAGCATG GCTGCTAAAT CTGGTAAATA 600
GCAGCATGCT GCTAGATCTG AATAATGGGG TCGTTTTTTT CTTTGACACA GGGTCTCACT 660
CTGTCACTCA AACTGGAGTG CAGTGGTGCA GTCATGGCTC ACTGCAGCCT GGAACTCCTG 720
GGCTCAAGTG ATCCTCCTGC CTCAGCCTCC TGAGTAGCTG AGACTACAGG CACGTGCAAG 780
CATGCCCAGG TAATGGGGTC ATTTTTGTTT CTTTTTCTTT CTTCTTATTT CAACCCTATT 840
ATCTGACCTT TTTTTTTCCC TTGCAAATAT TCTTGTTCTG TCTCCTATGT CTGGAGATGG 900
AAGATAAGGA 910
|
