| Tag | Content |
|---|
EnhancerAtlas ID | HS081-01277 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:157124530-157125440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:157124908-157124923 | CAAGACCAAAGTTCA | + | 6.29 | | KLF14 | MA0740.1 | chr1:157125200-157125214 | AGGTGGGCGTGGCT | - | 6.71 | | SP1 | MA0079.4 | chr1:157125201-157125216 | GGTGGGCGTGGCTGG | - | 6.27 | | SP3 | MA0746.2 | chr1:157125201-157125214 | GGTGGGCGTGGCT | - | 6.78 | | SP4 | MA0685.1 | chr1:157125199-157125216 | CAGGTGGGCGTGGCTGG | - | 6.22 | | SP8 | MA0747.1 | chr1:157125201-157125213 | GGTGGGCGTGGC | - | 6.62 | | ZNF263 | MA0528.1 | chr1:157124659-157124680 | CCCTCACCTCCCAGCTCCTCC | - | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_53221 | chr1:157123106-157125707 | Small_Intestine |
|
| | 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 |
| GH01I157153 | chr1 | 157123210 | 157126550 |
|
Enhancer Sequence | AGCCCTCACC CTCTCCCCTG AGCTGACTGA TAGGGATAAA ACCCTGATAC TCAGGAAGAA 60
TGGAGGGGGT GAATGCTCTC TTGGGTTTCT GGCTCCTCAG TCTCATCCCC TGGTATCCCC 120
CAGCCCCCTC CCTCACCTCC CAGCTCCTCC TCTTTGGTGG CCACAGCCCC AGCTCTTCCC 180
TTGACGCCCC TCAGGCCTGC CCTCCACCCC TACCCACCTC TGCCTGCAGG AGGGCACAGC 240
AGCACTCCTG CCCTGGCCTG GGCAGCCCTG TCCTTGGGGC AGGGCAGCTC AGCTTCTGGG 300
ATTTCCCCAG CCTACAGCCA GAAGGAAGTC TGACTTGGAG AGGGGAAACC TTACTCTTGG 360
CCTCTGTCCA GCTCCTGACA AGACCAAAGT TCAGGGGCGG AGCTGGTTTC CCTGGTCAGC 420
TGGGGACTCC CACTGACCTC TACTTATCAG GATTCGGGGT TTAGGTCTCT GGGCCTGGAG 480
AGCAGGTCAG GGGCAGGGAA ACGAGGGGCG GGGGAGGGTG AGAGCTGGAG GGCAGTGTGG 540
TGAAGGAGCT GCCGTGCCAA GGCCCCTGCC CACTTCCCCC AGGCCTGGCT TTTCCTGTCC 600
CTGAACCATG TTGAATGGTG GGGCGGGGGC TCTTGGGACT GTCTCCCTCT CCTGAGCTGG 660
GCATGTGTGC AGGTGGGCGT GGCTGGCTTC ACAGTGTCTG CATCCTCAGG GCTGATAAGG 720
GGCCTGCAGC AGCACCACCC TCTCCAGCCC TCTGGGGAAC CCCAGCTGTG GCTCCAGAGA 780
AGAGTGGGTT TGGGGCACAA TGCACCCGTG GTCTCATTTC GAGACATACA GGGGCTGGAA 840
AGGCGGGGGG CTGGAGGCTG GTCTTCACTG GTGCCTCAGT TTCCCCTTCC CTGGGGCCGT 900
TGCTGGGGGA 910
|
