| Tag | Content |
|---|
EnhancerAtlas ID | HS176-24731 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr21:40211110-40212360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr21:40212202-40212212 | GGGGATTTCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_26886 | chr21:40211585-40212348 | Esophagus | | SE_28570 | chr21:40210940-40212412 | Fetal_Intestine_Large | | SE_32351 | chr21:40210969-40211390 | Gastric | | SE_34978 | chr21:40209649-40213598 | HeLa | | SE_36155 | chr21:40210493-40213751 | HMEC | | SE_50186 | chr21:40210363-40211552 | Sigmoid_Colon | | SE_50186 | chr21:40211703-40212366 | Sigmoid_Colon | | SE_52374 | chr21:40210777-40211475 | Small_Intestine | | SE_52374 | chr21:40211703-40212315 | Small_Intestine | | SE_64260 | chr21:40210447-40214043 | NHEK |
|
| | 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 |
| GH21I038837 | chr21 | 40209875 | 40213675 |
|
Enhancer Sequence | CCTGCATGCG GTGAGTGTGC AGCAGCCCTT GACCTTGGTC CTTGTCTCCT ACCTCGGGTC 60
ATGAACAGCA AAGGTGAGCA CACATCCCTG AGTGCCCTGG ACGGGCCTGG CTGGGGCCAG 120
CGTATCATGC TGTGCCCAGT ATATTATTCA TAGCTCCCTT TCACTCTTAA AATTGCTTCA 180
GTTACGACAA TAAATTATAT GATCACAGAA TGAATGGGTC ACTTGCATTC AAACTTTTCA 240
AAGAGAACTG CAACATTCCT AAAATATAGA AGCTCATGAG AAAATAGACA ACATGAGTCA 300
AATCAAACTC TAAATACAGC CGTGGACAGT CAAAGAAACG CCACTGCTTT GCCAAGTTAG 360
CCCATGTGGG AACATCACGT TTTTGGTTAA GACAATTCTA TATTCTTAAA GGCCAAATGT 420
AAGCCACCTC AGTTTTGGGA AGGTCCCAAT AAAAGCTGAA TAATGTGTAA GCATAGTTTA 480
AAGTTAAGGC CCCTCTAATT TATTGTGGAC CTGAAGATAT TATGCTTGAA AATCATTTCA 540
CAGGAGTCCA TTCTAAAGTT TGTATGATGC AACGTTCTTG TGAATTATAG ACAAATGATT 600
CATCTGTTTG ACTCAGATTC AAGGACATTT TTTGTGGTGA AGTAAGGCAC TGAGTCTCAA 660
GATATAATGT AAAGATATGG AGTTGCTATG CCAGGAAAAG AACTATAGAA AGGGCAGCTA 720
GGAAGTCAAT GCAATAGTCA GCACACCTCT GGGGCCCTCC CTGGGAGCCT CTGATTCCAT 780
TACTCTTGGG TGGGCCCTGG ACATCTATAT TTTCTCCAAG TTCCATTCAT GATTCTAATG 840
CTCAGCAAAG CTGGGGAACC ACTGCAATAA GGCATGATCT TGAGAGTTAT GGCGCAGAGA 900
CATGCATCTG CCTCTGACTC AGCACAAGGG GCACCCCGCT TCTCACGTCT CATGACTGCA 960
TGGTGTACAG TGTGGTCAGT TCAGCCTTTA TGTCTAACCT CTGTCCTTCT CCACCCTGTG 1020
GGGTGCCGCT GACCTGTGGG GTGTTGACCA CAAACAGATT CCTACCCCAT GTTTCTTGGG 1080
GGTTCATCCC ATGGGGATTT CCAGAAGGAG ACTGGAGTTT CACTCTCCTG CCTCCCCTGA 1140
TCCCTGCTTT TTTTTTTTTT TTTTGAGACA GGGTCTCACT CTAACACTCA GGCTGGAGTG 1200
CCGTGGTATG ATCTCGGCTG ACTAGCAACC TCCACCTCCT GGGTTCAAGC 1250
|
