| Tag | Content |
|---|
EnhancerAtlas ID | HS086-06629 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr19:11028850-11030270 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr19:11029943-11029953 | TTTAATTAGA | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr19:11029117-11029132 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_51520 | chr19:11028973-11030901 | Skeletal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 11029194 | 11029387 | | chr19 | 11029622 | 11029688 | | chr19 | 11029693 | 11029743 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I010918 | chr19 | 11028974 | 11030901 |
|
Enhancer Sequence | AGTCCAGTGG TTAGCCTCAT TACCAATATG CTGCTGAACC ACCCGTTAGC TTTTATTGTT 60
TTTTGAAACA GGATCTCACT CTGTTCCCCA GGCTGGAGTA CAGTGGCTCA ATCACTTCAT 120
GGCTTACTTC AGCCTCGATC TCCCAGACGC AAGTGATCCT CCTGCCTCAG CTTCCCAAGT 180
AGCTGGAACT ATAGGAGTGT GCCACCATGC CCGGCTAATT TATTTTTTTG TAGATATGGG 240
GCCTCACTGT GTTACTCAGG CTGGTCTTGA ACTCCTGACC TCAGGTGATC CGTCCGCCTC 300
GGCCTCCCAA AGTGCTGGGA TTATAGGCAT AAGCCACTGC ACCTGGCGTT GAGCCTCTTA 360
TTAGCGGCTT TCTGCTTGGT GTCTTAGCCT CTGATGCCCT GCCTCGCTCA AAGCTCAGGA 420
GTTGGCCAAT TTCACAAGCG CACTGAGTGT GCACCGCCCA CCTTGCCCTC CTGCACTTAT 480
TTCCCTTTGC TTTGACATCA CAGCCCCTTG AATCCGAGCT GCCTTGGTAA CCCTGAGCTC 540
CCATTTTGCT TTCCCCACCC AAGGAAGCTG CTGAAAGGTC GAGGTGGCCG TTTTCTGCCC 600
TCCCCATGGG GAAAAGGTAG AGGCCAGAAA GGGCTCCCTC CAGAAAGGGC ATTTCCCTCC 660
TTTCCAGGAG CTTGATCCCC AAAATCCTGG CCGCTCTGGT TGGTCACCAG TGCTTCCAAC 720
AACTGGTTTA TTCTTTTCTT TGGATTTTAT TCGGTTTACA TAGTTCATGG CAGGTGTGTT 780
AGTCGGATAT AAACATTGCT GGGAGTGGAC AGCAGCACTA GTGTTGTTGT TGTTTTTAAG 840
AGACAGGGTC TCCCTGTGTT TCCCAGGCTT GATTCACACT CTCGGGCTTA AGCGATCCTC 900
CTGCCTCAGC CTCCTGAGTA GCTGGAGTTA CAGGCATACA ATTCCACACC CAGCTAGCAC 960
CTAGTTCTTT AACTTGCTTT TTTGGTTAAC TTGCTTAATG ATTTAGCTTG GAGATCTTTC 1020
CTCATCTGTT CATAAAGAGC CTCTTCATTC TTTCTCACGT CCGCATGGTC TTTGATGGGA 1080
GAGCCATCAC TGGTTTAATT AGATGGTTTC CAGTGTGTCG CTACCACGGA CAATCTAATT 1140
ATACATGTAA GTTTGTTGAT GTGTTCATGT ATCTGGAGGT TAAACTCCTG TAGTGCCAAA 1200
TCTTTTATGT GGATAAACAC TTGTCATTTG GAGAGCTGTC ACCTGATTGC CCTCGGTGGC 1260
GTTGTGCCGG TCCCCTCCTC ACGGCGTGTC TGGGAAGAGC AAGCTCGTTT TAGCTGCACA 1320
GCCTAGAAGC CGTGGGCAGA CCTGGGGGAA GGGGCAGGGC TCTCCCCTCC CATGCTGGCC 1380
CTGGCGTCAG ATGCCACGTC ACACCTGTGG TCTCTCCCAG 1420
|
