| Tag | Content |
|---|
EnhancerAtlas ID | HS118-18267 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:41426860-41428040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr8:41427220-41427231 | CATGAGTCACC | - | 6.62 | | FOSL2 | MA0478.1 | chr8:41427221-41427232 | ATGAGTCACCC | - | 6.14 | | IRF1 | MA0050.2 | chr8:41426937-41426958 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | JUNB | MA0490.1 | chr8:41427221-41427232 | ATGAGTCACCC | - | 6.32 | | JUND | MA0491.1 | chr8:41427220-41427231 | CATGAGTCACC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr8:41427869-41427884 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr8:41427159-41427174 | TGAACTCCTGACCTC | - | 6.22 | | SPI1 | MA0080.4 | chr8:41427659-41427673 | AGAAAGGGGAAGTG | + | 6.22 | | SPIB | MA0081.2 | chr8:41427661-41427673 | AAAGGGGAAGTG | + | 6.07 |
|
| | 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 |
| GH08I041569 | chr8 | 41426661 | 41427993 |
|
Enhancer Sequence | TTCTTGGACT ACATTTTTTA TGCCAATGGC AGGTATTGAG GTTGAACAAG CAACATTCAC 60
TTTATTTTTT CTTTCTTTCT TTCTTTCTTT TTTTTTTTTT GAGACAGAAT CTTGCTCTGT 120
CACCCAGGCT GGAGCGCAAT GGCACTATCC TGGCTCACTG CAACCTCTGC CTCACGGGTA 180
AGCGATTCTC CTCCCTCAGC CTCCCGAGTA GCAGGGATTA CAGGTGCCTG CCACCATGCC 240
CAGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTCACC ATGTTGGCCA GGCTGGTCAT 300
GAACTCCTGA CCTCAAGTGA TCCACCCAAC CTTGGCCTTC CAAAGTGCTG TGATTACAGG 360
CATGAGTCAC CCCAACCGGC CACTTCATTT TTTTCCCTAA AGGGCCTGCC CCACCTGACT 420
CTCGAACAAA ACAGCCAGGG TGCCCTGCCA GGTGGTTAAC AGGGTAAAGG CAGAAGCAGC 480
CAAACACACA GGCTTCCAGG AACAGTGTGG ACAGAGCTGC AGCTTCCTCA TCTGATAATG 540
GGAGCTATTG CAATCGCTAC TGTTTCCCCC TTGCCTTCTA GAAGGCCTGA CTCCATTAAG 600
GGTTGATCAT GAATAGGGCA GGTGGACTTA TAGAGCATGC TGTCAGAGTT GGGGGTTGCT 660
TTCAAATTCA AGCTAGTAAA AATCAACAGA AAAGATGAGT AGCCAGCTGT AGAAGTGACG 720
TACTCCTAAG ATGTGTGGTA ATGTATTTCT AATGACATTA GAGTTTCTGA AATCCATCTC 780
ATCATCATGG CCTAGCACTA GAAAGGGGAA GTGCTGGGAG ACCACGTGGA CCAGGCGTCA 840
CATTTAGAGA GGGTCTGGGA CCTAGACTTT TGATACTATC TCCAAATTAA GTTACACATA 900
CAACTACAGA GAGAACTAAC AGGATTGAAA AAAGATGCTG CTCAGCTGGG CTCAGTGGCT 960
CCTGCCTGTA ATCCCAGCAC CTTGGGAGGC AGAGGCAGGT GGATCACCTG AGGTCAGGAG 1020
TTCAAGATCA GCCTGGCCAA CATGGTGAAA CCCAGTCTCT ACTAAAAATA CAAAAATTAG 1080
CTGGACATGA TGGCAGGTGC CTGTAATCCA AGCTACTCGG GCAGCTGAGG TGGGAGAATC 1140
GCTTGAACCC AGGAGGTGGA GGTTGCAGTG AGCCGATATG 1180
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