| Tag | Content |
|---|
EnhancerAtlas ID | HS099-01466 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr1:157124350-157125420 |
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 | GAGAGCACTG CCACCTCCCA GCTGTGTGTG GGGACAGTGG GCCTGGCCAC CTGTCTCCTC 60
CTTCACCTCG GCCCCATCAG GGTCCCTTCC TTCTGGGCTG GCAGGGCCCA CTCTGTTCCT 120
GACAGACAAA TCAGCAGTCT TCCCTGTCTC CCACCACCCC TCTCCCTCTG CTTTGCCCCC 180
AGCCCTCACC CTCTCCCCTG AGCTGACTGA TAGGGATAAA ACCCTGATAC TCAGGAAGAA 240
TGGAGGGGGT GAATGCTCTC TTGGGTTTCT GGCTCCTCAG TCTCATCCCC TGGTATCCCC 300
CAGCCCCCTC CCTCACCTCC CAGCTCCTCC TCTTTGGTGG CCACAGCCCC AGCTCTTCCC 360
TTGACGCCCC TCAGGCCTGC CCTCCACCCC TACCCACCTC TGCCTGCAGG AGGGCACAGC 420
AGCACTCCTG CCCTGGCCTG GGCAGCCCTG TCCTTGGGGC AGGGCAGCTC AGCTTCTGGG 480
ATTTCCCCAG CCTACAGCCA GAAGGAAGTC TGACTTGGAG AGGGGAAACC TTACTCTTGG 540
CCTCTGTCCA GCTCCTGACA AGACCAAAGT TCAGGGGCGG AGCTGGTTTC CCTGGTCAGC 600
TGGGGACTCC CACTGACCTC TACTTATCAG GATTCGGGGT TTAGGTCTCT GGGCCTGGAG 660
AGCAGGTCAG GGGCAGGGAA ACGAGGGGCG GGGGAGGGTG AGAGCTGGAG GGCAGTGTGG 720
TGAAGGAGCT GCCGTGCCAA GGCCCCTGCC CACTTCCCCC AGGCCTGGCT TTTCCTGTCC 780
CTGAACCATG TTGAATGGTG GGGCGGGGGC TCTTGGGACT GTCTCCCTCT CCTGAGCTGG 840
GCATGTGTGC AGGTGGGCGT GGCTGGCTTC ACAGTGTCTG CATCCTCAGG GCTGATAAGG 900
GGCCTGCAGC AGCACCACCC TCTCCAGCCC TCTGGGGAAC CCCAGCTGTG GCTCCAGAGA 960
AGAGTGGGTT TGGGGCACAA TGCACCCGTG GTCTCATTTC GAGACATACA GGGGCTGGAA 1020
AGGCGGGGGG CTGGAGGCTG GTCTTCACTG GTGCCTCAGT TTCCCCTTCC 1070
|
