| Tag | Content |
|---|
EnhancerAtlas ID | HS041-05447 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr12:92946900-92947590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr12:92947411-92947428 | TGACCCCTACGTGTCCT | - | 6.2 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_20705 | chr12:92945282-92952214 | CD56 | | SE_29287 | chr12:92936425-92949133 | Fetal_Intestine_Large | | SE_32511 | chr12:92943906-92956751 | GM12878 | | SE_43617 | chr12:92943871-92947184 | MM1S | | SE_61802 | chr12:92927333-92988757 | Toledo | | SE_62925 | chr12:92932227-92990275 | 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 |
| GH12I092549 | chr12 | 92943353 | 92953871 |
|
Enhancer Sequence | CACACAACTC CTACACATGA TTACCCCTCC CGTTCACAAC ACGGCGATGC TGGAGAGCCC 60
TACATAGTCA GCAGACCCAT GCTACAGAGG GTTTGAGGAA CTCTTCCAAG GACACACAGC 120
CATTCCATGG TGGAACCAGA ACTCAAACAG GCATTCTGAT TTTAGAGCCT TTGCTCAATA 180
AATAGTTATA ACAGAAGAGA GAGTGGAGAC GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT 240
GTGTGTGTGT GTAGGGGTAG AAGATAGTGG TGGGGGAGCT TTCTGAGACC CTGCTACTCA 300
TGCCAGATTT TCTGGTCCTG ATTAGCTACT GCCTGGCTGC CAGAAGCTGT TATTATCACT 360
CACTCCCGTG CTCCTGTCAC TGGGCTTGTG GAAACTTGCC CTTCCTTCTG CTCTCGGTCT 420
CTGATGCTGA CAGCTATGCT GGAAAATCCC ATGCTGGCCA CTGCCACACT TACCAGAGGC 480
ATATTGTACG TGCTGGTCTG GACTTCCTGC CTGACCCCTA CGTGTCCTGT GCCTGCCCCT 540
TCACAGGAGG TCGGTCTACT TCCTGGCCAG GGCCTTTCCA GCCTGTCTCA CCCCTGTGCA 600
GGTAACAGAG CTCTTTTCTC TGCCACCACT TCCCCACGGA GTCTTTTCCA TGGTTCTCCC 660
TGACAGAATT CATGCTACAT AGTCTTTGTT 690
|
