| Tag | Content |
|---|
EnhancerAtlas ID | HS042-00950 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr1:26101360-26102490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:26102379-26102391 | GTTTGTTTGTTT | + | 6.32 | | GFI1 | MA0038.2 | chr1:26101366-26101378 | TGCTGTGATTTA | - | 6.27 | | Gfi1b | MA0483.1 | chr1:26101366-26101377 | TGCTGTGATTT | - | 6.62 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_33518 | chr1:26100201-26102442 | H2171 | | SE_55546 | chr1:26100284-26102505 | Thymus | | SE_65420 | chr1:26095438-26102418 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 26101558 | 26101680 | | chr1 | 26102135 | 26102200 | | chr1 | 26101389 | 26101767 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I025770 | chr1 | 26096535 | 26102593 |
|
Enhancer Sequence | GCTGCTTGCT GTGATTTAAA CCTTTTACCA GTCGTCTGCC AGCCTGCACT GTCTTGTGTT 60
TTGTTTTAGA AAGCCTTGTT TTTTATCTTT GCATCTGCGT GTCTCAGTTG TGTCTTCAAA 120
GAGGCAGTGG TTTATAATTT CCTCTTGACT GCAATTACTT AGCTTGGGGC CAACCCCCAG 180
TGGAAATAAT GTGTGGGAGG CGGTCTGGAA GGTGCAGGTG CCAGGTCTGG TGCGCAGCAT 240
CCTGAGGTCT CCCTCAGATG TCTGTGTTCT CTCCAAAGTG TTGACAACTG GTGACTCGGA 300
CCCAGGTTTC TGAGCCCTGA CACTCCTCCC CTGCACCGCA GGCTTAGTGA CGCCGAGCAG 360
CTGCCAGGGA CATGGCTCTG CCCGGGAGCC AGGCCGGGCC CAGAGCAGAC CCCTGCCTGC 420
AGCCCGGCTG CTCTGCAGGT GTCCTCAGCA CTCCCCCATG TGGAGCAGGT GCCCTGGCAT 480
GTCACATTGT CAGCGCTTTT CCATCTGCCA CTCAGTGTGG GTCCTGCAGC CAGCCCACCA 540
GCCCTGGGCC CTGACAGGAG AGAAAAAAGG AAAAAACAGA CCCAGGAGTG AGCGAGTGTT 600
CCTTGAGCAT CTTCTGTGTG TCGGGCACTG GCTGGAGGCT GCTGCTGGTG GCTTCTGCTG 660
TCACACGGCA CTCAGAGTCT GAGAGAGAGA CAGATATACA ACAGAAACAG ATGCCAAGTA 720
GGAATGGCAC CATGTAGAAG GGTGACAGGG GCCCATAGGT AATGGCAGTG GCAGTGCTGG 780
TTTAAATTGG GGCATTCTCT CCAAGGAAGT GACATTCTGG AGGAGGTGGG GTTAGCAGAG 840
TCAGGGCTGG AGCATGCAGG AAGGAGGCGC AGCACCAGCT AAGCCCCGAA GCAGGAAGAA 900
AAATGCAGCT TTCAAGAATG TCACCTTTGC AGAGAGATTT TCCCTGACCT CCCTCTGCAA 960
AGTACAGCAC TGCCCCCACC CCAGTTTTTT TTGTTTTGTT TTGTTTTCTT GGGTTTTTTG 1020
TTTGTTTGTT TTTTTATGAC AGAGTCTCAC TCTATTGCCC AGAGTGGAGT GCAGTGGTGC 1080
AATCTTGGCT CACCGCAACT TCTGCCTCCT GGATTCAAGT GATTCTCCCA 1130
|
