| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10528 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:158336640-158337720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr2:158336766-158336777 | GGGTGACTCAG | + | 6.02 | | IRF1 | MA0050.2 | chr2:158336825-158336846 | AAAGTGAAAGGAAAAGCAAAG | - | 6.5 | | JUNB | MA0490.1 | chr2:158336766-158336777 | GGGTGACTCAG | + | 6.02 | | NFE2L1 | MA0089.2 | chr2:158336766-158336781 | GGGTGACTCAGCACA | + | 6.51 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09357 | chr2:158335840-158337753 | CD14 | | SE_44051 | chr2:158335330-158337627 | MM1S | | SE_56058 | chr2:158335817-158338247 | u87 | | SE_58338 | chr2:158259858-158366019 | Ly1 | | SE_59716 | chr2:158277372-158337629 | Ly4 | | SE_67887 | chr2:158335817-158338247 | u87 |
|
| | 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 |
| GH02I157479 | chr2 | 158335839 | 158337706 |
|
Enhancer Sequence | AAGGACGCTT TCCTGGCAGC ATTCATCACC TGCTAAGTGA AGAGCCCTTA GGTCCTGAAT 60
AACCAGCAGC AATATGCAGG TACTACATTG AGGGTCTTGG GGGAGACTCT GAAACTTGCT 120
GGCTTTGGGT GACTCAGCAC ATTCCCAGCC ATGATGGCTA TGGGTGAGAC TTCTTCTGCT 180
TGAAAAAAGT GAAAGGAAAA GCAAAGGGGA CTTTGTCATG CACCTTGGCC ACAGGGTTGT 240
AAAGCACAAA GCAGGCCTCT TGGGGTCCTC AATTCCAGGA CTTGGCTCTT GGATGGCATT 300
TCTGGACCTG CCCTGGGCCT GAAGGGAGCA CGCTGCCCTA AAGGGTGAGT CCCAACCCAG 360
GCAGCATTCA CCACAAGCTG ACTGAAGAGA CTTTGTACCT TAAGGGAACA TTGGTGGTAG 420
TCTGGTAGTA CTCCCTGTAG GCCTGTGGTG ACGGTGGCCA AGAGGTGAGG CTCCTCTGCC 480
TTTGAAAAGG TGAGAGAAGA GTGAGATGGA CTGTATCTTG TAGTTTGAAT GCCAGCTCAG 540
CTGCAGTATA ATAGACTTCT AAGGGTTTTG ACTCTAATCC CTGGCTGCTG GGTGGCACCT 600
CTGGGCCTTC CTGGAGCCTG GGGGAACTTG CTGCCCTGAA GGAAAGGACA CGGGCCTGGC 660
TGTCTTTGCC ACTTGCTGAT TGCAGAGAAC ATAGGCAGTA GCCAGGGAGT GGTTGCAACA 720
GGCCTTGGGT GAAATCCAGT ACTGTGCTGG CTTCAGGTCT GACTGAGAAC AGTCATAGTG 780
GTGATTGCCA CAAGGGAGCT TGTATCACTC CACCCCCAGC TTTGGGTGGC TCAGAATAGA 840
AAGAGAGGCT CCATTTGTTT AAGAGAAACT AAGGGAAGAG AAAAAGAGTC CCTGTCTGAT 900
AATACAAAAA ATTTTCCCAG ATCTTGTCTA AGACCATCAA GGCAGTACCT CTACAAGTAT 960
GCAATAACCA CAGTGTTACT GAGCTTGAGG TACCTCTTGA AGCAGATACA GCTTAGATCA 1020
CAACATCCAA GTCCTATCAA ATATCTGGAA AGCCTTCCCA AGAAGGACCA GTACAAACAC 1080
|
