| Tag | Content |
|---|
EnhancerAtlas ID | HS073-00133 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr1:12125510-12126700 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:12126628-12126643 | TGAACTCCTGACCTC | - | 6.22 | | POU2F2 | MA0507.1 | chr1:12126175-12126188 | TTAATTTGCATTT | + | 6.25 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32538 | chr1:12122797-12131704 | GM12878 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 12125895 | 12126327 | | chr1 | 12126084 | 12126429 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I012067 | chr1 | 12126084 | 12126429 |
|
Enhancer Sequence | GCAAAACTGT AAACGCTACA GATAAAGCCA AGTCTTTTGA CACCGCCTCA TCCTGATCCC 60
TTCAAAGATA TAACCACCAT AATTGATTTG GTGTGTTTCC TTTGCAGACC TTTATAAATG 120
CATGTCCATA TTTATATTGT TTTAATAGAC ATATATATAG TTTTCCATAT ACTATACCCT 180
ACAGTACATA TGGTTCTTCA TTTGGCTTTA TAATGTCTAT GAGGCATCTT GGTGAGCTTT 240
CCATGCTGAA ACTTACAGAT CCTCTGCCTA TCTTTTAAAA TGCTATGTGA TCTTTTGCCA 300
AATGGGATGT TTCATAGTTT ATTTATGTCC TGGATGGATG GGTGCTAAGG TTGCCACCAT 360
TGTTCTTTCT TTCTTTCTTT GTTCTCTACT ACAGTGCACA GCCCTATATG GATGCTTTTG 420
GAAATAAATG TCTGTGATTC TTTCCTAGAC AAGAGACTGA GAAGAGAATA CTGAGGTTGC 480
AGGGCGAAAA TGCATTCAAA TTAAAAGACA CCACCGAACT GCCTTCCAGG GTGGCTGGAC 540
AATTTACCCT CCCGCTAGCA GTGCAAGAGA GTAGTAACTT TCCCACATCC TAACCGACAT 600
TTGATCTTAT CAGCATTTTA ATTTTTCTCA ATGTGATTAG TGAAAAGGGT TATATCCTTG 660
TTGCCTTAAT TTGCATTTCT CGCCTACCGG GGAAGCTGAG CATCTCTCTG GGCTCAGGCA 720
CTAGGTCATT TCTTGGCAGG AGTCAGGGAG TCCTTGGGGA AGGGACTACC TGCCCAACAC 780
AGTACTCCTT TTTGCCCCTC AAGCCTTCTC CCACTTCTGT TTTTTCCAGT AAAGGTTCGG 840
GAAGCTCGTT ATTTTAAAAA AAAAATCCCA AATTAGGGCT TGAATTTCCT TGAGTTTAAA 900
ATTTTTTTTT TTTTTTTTGA GATGAAGTCT CCCTCAGCTG CCCAGGCTGG AGTGCAGTGG 960
CACGATCTTG GCTCACTGCA ACCACCCTCT CCCAGGTTCA AGTGATTCTA CCGTCTCAGC 1020
CTCCCTAGTA GCTTGGATTA CAGGCACTTG CCATCATGCC TGGCTAATTT TTGTATTTTA 1080
GTAGAGATGG GGTTTCATAA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC CTCAGGAGAT 1140
CCATCCACCT CGGCATCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG 1190
|
