| Tag | Content |
|---|
EnhancerAtlas ID | HS182-12850 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:129165530-129167790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr2:129166381-129166395 | GTTGCGTGGGCGGC | - | 6.08 | | EGR2 | MA0472.2 | chr2:129166383-129166394 | TGCGTGGGCGG | - | 6.32 | | EGR3 | MA0732.1 | chr2:129166381-129166396 | GTTGCGTGGGCGGCG | - | 6.31 | | EGR4 | MA0733.1 | chr2:129166380-129166396 | AGTTGCGTGGGCGGCG | - | 6.21 | | Nr2f6(var.2) | MA0728.1 | chr2:129165561-129165576 | CGATCTCTTGACCTC | - | 6 | | REST | MA0138.2 | chr2:129166459-129166480 | GGTGCTGCCCACTGTGCTGCA | - | 6.25 |
|
| | 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 |
| GH02I128408 | chr2 | 129165774 | 129167269 |
|
Enhancer Sequence | GCCAGGCTGA TCACGTTGGC CAGGCTAGTC TCGATCTCTT GACCTCGTGA TCCACCCGCC 60
TTGGCCTCTC AAAGTGCTGG GATGACAGGC GTGAGCCACC GCGCCCGGCC TGTTTTGCTT 120
TTTCTATCCC ACAGACTGGA TGTGGGGACA GTATAAGACA ATGTTCTGGT GGCTGAATCC 180
CTTAGAAATT TCAGGGTTTT GTTTTATTGC GGGGAAGGAG GTTGGGACCA CAGAATTTGC 240
TTGCGAGAAT AAAGTTATTT TTTCCTGCAT GATTATTACC ACTACTAGTG TCATAATAGC 300
TATAAGTGTG TTTTGATGCA GCAAGCGAAA ATCATAGGGA TTCTAGAAAA CCCAAATAAA 360
TTGCAGCACG TTTACAGCAG CAACTACAAA CAAAGGTCTG GAAGTATCCT GAGCTCCCAG 420
CTGTGAGGAA GTTGGATGGG GGCGGGGGCG GCCTGCATGG GCCCCACGTG GGAGACACAG 480
GCCCTGTTAT ACCACATCTA GCCAGGGTCC TGCGTGGCAG GCATGTTGTG TCTAGTTTAA 540
GCATCCCATG GCATTTCATT CAGGTCTTGG GAACACACAC CTTGGGAACA AAGCCAGTCT 600
GTCTGCAGGC TGCAAAAGAG GATGCCTGGC CAGGAAGTTG GGGAGGATTT GGGGTAGAAT 660
GTGAAGGGCG ACTCCAGGGC ACAGCAGTTC CTGAGGCCTC TGGGAACGGG ATATCCATGT 720
GGTGGCTGAG AGAGTGCCCA GCCTTTCTGG GTGGAGCAGA GGCAGATGGG CAAGCTTCCC 780
TGTCCTACCC TGTTGCGTGG CTTTCCCTGG GCGTGTGTCT TTGTCTTGAG ATGATAATTC 840
CGGAGGATGC AGTTGCGTGG GCGGCGGGCA GGGGCCCTGT GGTTAGGGTG GGCGGCGGGC 900
AGGGACCCTG TGGTTAGGGT GGGCTGTGGG GTGCTGCCCA CTGTGCTGCA AACACAGGGG 960
ACTGATGGCA CATGAACAGG GAGAGGTCCT GGGAGGTCCT GATGCTCGTC ATGGTCAATG 1020
AAAAACTTCC TCCAAATACA GGCCTGCCAA GCTGCTTTTA TTTTATGAAT TCATGTTAAC 1080
ACATCACAGA AGTGAGTTTT TGTGGAATGT GCTTTGGGAA ATACGCTCAT GAGTGAGTCA 1140
GCTGCAAGAA ACCATCGAGC TGTCCCTGAT TTCCTGTGAG TTCCTTGGGC TGGGTCCTGG 1200
TCCTGGACAG TATGGATGGC CAGACACCAG GGAATTGGCT GGCCTCAGGG CTGACCCAGC 1260
CTCCTGGGCT CTTGCACTCA GGTCTCCTAA GGACCAGCAG GGCTAGGGAG CAGATATGTC 1320
AGGCCCTTTG TGATTGTGGT GTCCTGGTCT TTAGGCCTTC GGAGACCCAA GCAAGAGGGA 1380
AAGTGGGTAA TGGGGGAGAA ATAGAACATG GATTGGATGG ACTCAGAGCC CATCAGGATT 1440
GTGGGGCCAT GGGATTTTAG CCTCACAAAA CCTGAATCCA CTCTTGCGGT AGGACAGGGT 1500
CACTTGGGGG CTCATGGGGA GGAGGTAGGT GCAGTTGGTA AGTCAGAGGC GCTCTGCCCT 1560
GATATAGCCC CTCCCTAACT CCCTAAACCC ATGACCAGGC ACACGGCCGG CCCTGGGCTT 1620
TATTGCTCCT CTGAGACCCA CATGAGCAGC CCAGGTGGCC ACAGGGCTAG GGCAGTGTGA 1680
GCTCAAAGGT GAAATATCAG GTAGCAACAG GGCATCTCAA ACAGCCAATG AGCTGAAGAA 1740
AGCCGCTAAC CTCACCAGTC CTGAGAGGGA GGATGAGGCA CTGCTGCCTC ACACCCAGCA 1800
GGACTAGAGG CCTTGGCATG TCAAACGACA GTGGTGTTGG CCAAACTGTG GGGAGCAGGC 1860
CTCTCTCAAG GGGGTGCTCT TGGTGTAAGA GCAGCCCGGT GTGTTTAGAG ACATTTGGAC 1920
TGGGTGTGGC ACAGGCCTCC ATGGTCCTGC ACCTGCTCTG TACTGAGACA CTCCACACAG 1980
TCCCCAAAGA ACTGTGAGGG TGTTCATCCA GCATTCTCTG GATGAGTGGA TGAGTGACCC 2040
GTGGCAGTGC CATGGACCCC TACGCAGCAG GGAGGTGACA CCTGGGCTTC TGTGAGCAGC 2100
TCACATAGGC TGGGGCTGGG TGGCAAGGTC CAGCACGGGA AAGAAATGCA TGGTGCAATA 2160
CTCTTTAGGT AGATTAAACT ACATGGCCTG GAAGGACAGA TTCCAGGAAG CCTCCACATT 2220
GCAGGAAGTC TATCTGGCGT GTGGGAGTAG ATGCCTCTGA 2260
|
