| Tag | Content |
|---|
EnhancerAtlas ID | HS108-01687 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:46973710-46975660 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:46974605-46974616 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr1:46974605-46974616 | GGATGACTCAG | + | 6.14 | | NFE2L1 | MA0089.2 | chr1:46974605-46974620 | GGATGACTCAGCTCA | + | 6.1 | | Nfe2l2 | MA0150.2 | chr1:46974603-46974618 | CAGGATGACTCAGCT | + | 6.44 | | RREB1 | MA0073.1 | chr1:46974488-46974508 | CCCCCACCCCCCACCACCCC | + | 6.51 | | RREB1 | MA0073.1 | chr1:46974487-46974507 | CCCCCCACCCCCCACCACCC | + | 6.57 | | RREB1 | MA0073.1 | chr1:46974481-46974501 | CCCCCACCCCCCACCCCCCA | + | 6.63 | | RREB1 | MA0073.1 | chr1:46974480-46974500 | CCCCCCACCCCCCACCCCCC | + | 6.69 | | RREB1 | MA0073.1 | chr1:46974484-46974504 | CCACCCCCCACCCCCCACCA | + | 7.47 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCTCGGTGG GTGAGAAAAG GATTCAGTGG CATGGATGGG GAGTTTGATG TCCTGGGAGG 60
TGGTGCCACC CACCCCATCC TGTCCCAGGT CCAGCCTTGA GCAGCTGGTA AACCCACATG 120
GGCTCAGCCC TGTGCCAGGC AGGCCTCAGA AAACTTCAGG GAACTCCTAG GGAGAACAGG 180
TGCCCATGAC CCATGAGAGG GCACAACAGG AGGGTATCCA AGGTCAAATG CTGGGGCAGC 240
TCAGAGCAGC AGGATCAGCT GGGGTAGTCA GGAAGAGCTT TCTGAAATCC ACAGGGGCAG 300
GAACCAGGCC TCAAAAAGGC CAACATGAGC AAAGGCACAG AAATGGGATG GGATCTCCAC 360
CTGGGTAGCA GCACTGGCCT GGCAGGGAGG GCATGGCCAG TCTCACTCCT TTAGACCCTG 420
CCAGGCCTCT GGGCAGAACT CAGTGGATAA AGGTTCTCTG GACCAGTGTG GAGGCATTAG 480
TTTCTAGTGT GGGGATGTTG GATACAGTCC TATGCACAAC CTGGTGGTGA CATCAGCTCC 540
TGACAGTATT CCAGGACCCA AGGACCAGAG CACAGAGAGG AGTCAGGGAC AGGGGGCTCA 600
TGTCCGCTGG TGGGGGCAGA GGAACTGGGG TGTTCAGCCC ACCCCCAACT CTCTAATTCT 660
TAGGAAGGAA GGACATGAAC TCCAAGTGAG CCTTTGTATG GAGGCCTTGC CTTCCAGCAG 720
AGGCTCTGCC GGCGGTTTAG AGAGCCTGGC TTCCCTGTGA CACCTACACG CCCCCCACCC 780
CCCACCCCCC ACCACCCCTG CAGTCCCTGG AGCCAGCAGT AGGATGCTGA GCTGTTGCTC 840
CTTCCCCAAC CAGAGTGGGG CTGACAGAGC GGTCCCCACT CCTTCCCCTG CCCCAGGATG 900
ACTCAGCTCA GGGCTGAGTC AGGCCTAGGA TTAAGGTCAG TCTGTGAGGG GTTCAGGACT 960
CTCTTTTTAA ACTGAAGAAG AAGTATCTCA AAGTCTGGGG CTTCCTGGAT ACCCAGTTGC 1020
CTCTTCCTAT TCTTTTTTTT TTTGCGGAGG GGGGATGGAG TTTTGCTCTT GTTGCCCAGG 1080
CTGGAGTGCA ATGGTGCCAT CTTGGCTCAC TGCAACCTCC GCCTCCTGGG TTCAAGCGGT 1140
TCTCCTGCCT CAGCCTCCTG AGTAGCTGGG ATTACAGGGG CCCACCACCA CGCTCAGCTA 1200
ATTTTTTGTA TTTTTAGTAG TGACAGTGTT TCATAATGTT GGCCAGGCTG GTCTCGAACT 1260
CCTGACCTCA GGTAATCCAC CCGCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACTGTGC 1320
CGGGCCTCCT CTTCCTATTT AGGGTGCTGT GGATGACTTC CCATTCCCTG GAGGGCGGGG 1380
GAAGGACTCT GGCACCCCTT TGCAGAGGCT GAGATGACTC AAGTTCCCTT CAGCACAAAC 1440
AGGGCAGGAT CCACTTATGA CATGATGGGA GGCAGTGAGG AGAGCGGTTA CTGTCTATCC 1500
TTCAGGGGCT AGTCAAGTGA AAGGGCTGAA GGCTATACCC CAGGATGGAG GCTAGACCTC 1560
GGCCCTAGGT AGACACCTAT CCTGGGTGGT TATCATGTTA CCAGACATGT GGACAGGACT 1620
GTGGAATCAA TGGTCCATAG TCCTGTCTCC CCTACAAACC CACAGTGGTT GGAACCAGGT 1680
CTCTTTGTCC TTCTGTTCTT GGGGAGGCAG CCACAAGGGT CAAGACTGAG TGCAACAAGC 1740
CTTACCTGAG ACGTGAGCCC TGCCACCCCC ACCCTCCCCG CTCCACTCTT ACCCCTTAGC 1800
CAGGCTCTCT GTTCAGGAAA CAGAAGAGTA GGAGCCTGAG GCCCTGCCAT CAGAGACTCT 1860
AGGCCAGCTG GGATGAGGGG GTTTACATGC AGAGGACAGA GAATCAAGTG CTGGTGAATT 1920
CTGTCTGCCT AGTCAGTCCT CCCTTGACTA 1950
|
| |
|
|
|
