| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15195 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr19:11009300-11010450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:11010387-11010408 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | | Klf1 | MA0493.1 | chr19:11010306-11010317 | TGGGTGTGGCC | - | 6.62 | | TFAP2A | MA0003.3 | chr19:11009971-11009982 | CGCCTCAGGCA | + | 6.62 | | ZNF263 | MA0528.1 | chr19:11009517-11009538 | GAGGGAGGGGAGAGGAAGGGA | + | 6.22 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23673 | chr19:11008924-11010460 | Colon_Crypt_1 | | SE_24532 | chr19:11008947-11010425 | Colon_Crypt_2 | | SE_30825 | chr19:11008999-11010458 | Fetal_Muscle | | SE_48197 | chr19:11008793-11011250 | Psoas_Muscle | | SE_51520 | chr19:11008746-11011610 | Skeletal_Muscle | | SE_68858 | chr19:11008941-11010261 | H9 |
|
| | 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 |
| GH19I010898 | chr19 | 11009109 | 11010781 |
|
Enhancer Sequence | TGCCACAGTG AGTTTCCTGC GGGCAGGGCT GCATCTGTGG CGAGCACTGA ATCGCCACTG 60
CTGGATCCAG ATGCCTGTGC GTCCCGGGCC CCAAGGCTCC CTTCTACCCT CCTCCTGGGG 120
TGCTGTTCGC AAGCCAGGAG ACAGGCTGTG CATTCCCTGC CTACTCAGAG GTGACCCTGG 180
GCCAGGTGTG CGATGGCCCA CTGGACCCAT AGTAGCAGAG GGAGGGGAGA GGAAGGGAGA 240
AAGTGGGAAC AGCATGTGCA GAGGCCTGGG GCCTGGCCCA TGTAGGGACT AGAGGGTTGA 300
GTGTGTCCAT GGGGAGGGGC CAAGACGGGG AGAGCCATGA GGAATGATGG GCACAGAGCT 360
CAGAGGCTCG GGAGTCTCCT GAACAAAGAG AGGAACACGG CTTAGCTTGT TTTTTTTTTT 420
TTTTTTTTTG GTTTGTCAGT ATTTCCCAGG TGTCTTCTGT GTGCCAGGGA CTAACTTGGG 480
GATAAAGCTG TGACTTTGAG AAGCTGCCGG CTCCGCGGGC TTTAGCAGCT GCTGCTGTGA 540
TGAAGCGATC CACTTGCCCT CAGCCCCGGC ATCTTTGGCC CAAGCCCAGC CCTAGCCCTG 600
GCTGGGCACA GCCAGGCTTC ACTTGGCCAC AGGTCCTGTA GTTGCCTGCC TGGCGCCAGG 660
TCAGAGAGGG ACGCCTCAGG CAACATCGGG TTGCCAGGCT GCTTGGTAAA CAGGCCTCCC 720
TGGGCCCACT TGCTGTCGCC CAGGTGTGGC TAACAGATCG ACAGTATCTC CTGCCCCAGG 780
ACGGGTATGA GTGTGGGCAC CATGCCAAGG TTGGATGTCC CTTCCTGGGA CCCACCCACA 840
GCTGGGAGCA CTTTATCTTG GGCCTCTGTG GGTGTAGTGA GGCTGTGAGT CTGGGGCAGT 900
GGCCTGCTGA CACCCTCCTG GCAGGGCTCA GGAGGTTCCT CCATGCCCTG CCCTCAGGAG 960
GGCGGCACCT GGCTCCTGGG GTGGGAGAGA GTCTGGCAGG ACTGGCTGGG TGTGGCCGGG 1020
GAGCTGCCCT TCAGGTCTCA TATCTGTAGG CCCTCATACC TGGACTCGTC AGTTAGGAAC 1080
AGTTTTCTTT TTCTTTTTCT TTTTTTTTTT TTTTGAGACG GAGTCTCACT CTGTCGTCCA 1140
GGCTGGAGTG 1150
|
