| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11369 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:40048070-40050300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:40048672-40048693 | CAGTACTTTCACTTTCAGATA | + | 6.71 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr19 | 40049753 | 40049944 | | chr19 | 40048143 | 40048260 | | chr19 | 40048106 | 40049200 | | chr19 | 40048579 | 40048977 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I039557 | chr19 | 40048021 | 40048260 | | GH19I039558 | chr19 | 40048261 | 40050106 |
|
Enhancer Sequence | ATTTTAAGAT GCAAAATCAC AAGTGTTGTG AGGATGTAGA GATACTGTAA CCCTTGAATG 60
TTGCTGTTGG GAGTGTAAAA TGGTGCAGCT GCTGTGGAAA ACTATATGGC AGTTCCTCAA 120
AAAGGTCACC ATGTGATCCA GCAACAGCAC TTCTGAGTAT ACACCCTAAA GAATTGAAGA 180
AAGAGACTCA CGCTGATATT TGCACAGCAA TGTTCATAGC AGCATGATTC ACAACAGGCA 240
AGAGATGGAA ACAACCCCAA TTTCCATCTA CAGATATACG TACGATGGAA GATTATTAGC 300
CTTAAAAGTG GATGACATTT TGACGCTTGC TATCACGTGA ATGAGTCTTT AAAACATGCT 360
AAGTGAAATA AGCCAGACTC CCCCTGAGGC TGTAGGTGCA GGCTGTGGGG AGAAGGTAAC 420
GGGGCAGGAG TAGGGGCTAT GGACATTTGG ACCCTTCCTC CTGCAGCTTT CTTGTGCCTT 480
CAGGACCTGT GTAAGCCTGA TCTCTCTGCC CAGTGAGTCC CCACTTCCAT CCTGAGGCTA 540
TTTGGTCAGT GTCAGGTTGC AAAAGACACA CAACCATGAA ATGTGACTTG ACAGATACTC 600
TGCAGTACTT TCACTTTCAG ATAGCTCTGG CTGAACTTGC AACCTAAATA CAAATAGGAT 660
TTTGTTTCCT TTTCACTGCT AGTTATGATT TTCAAGAAAT CCATGGTTTA GAGGAAAATG 720
ATTTTGTAAT TTGTGCTGAA TTCTGATGCA TGCTATCTTG TCAGTATTTC AGATGAAAGT 780
GATAGAAAAG ACACTTGTTT ATTGAGGGAG CAGTTAGCAA GCCACTCAGA GTAGATACAC 840
AATGGCCTGC CCTAAGTGAA CTGGTGGGAA ATAAGAGTTG CTTGATCGTT GATTTTTTAT 900
GAAAGTAGAG CCTAGGACTT TCCGTAGGTG TGAGAAAGTG TGTGATGGAA AGAGGAGGAT 960
CAGGGATGGT GTGGAGGTTT CTGACCTGAG AGAGGGGACT TGGGGACTTC AGTCCCCACA 1020
TCCATCTTGA GGTTATTCAC TCAGTGTCAG GTTGCATAGA ACACACAACC GTGAAAGGTG 1080
ACGTGACAGG TGCTCTGCAG CACTTTCACT TTTAGATAGT TCTGGCTGAA CTTGTGATCT 1140
CACTAAAGAT AGAAATAGAT TTTCAAGAAA TCCATGGTAC AGAGGAAAAT AATTTTGTAA 1200
TTTATTGCTG GATTCTGATG CATACTATCT CATTAGTATT TCAGACAGAA GTGATAGGAA 1260
GGACACTTAC TGAGGAAGCA GTTAGCAAGA CACTCAGAGT AGACACACAA TGGCCTGCCC 1320
TAGGTGAACT GGCAGGAAAT CAGAGTCACT CTATCCGTGG TTGGCTTACG AAAGTAGAAC 1380
CATAGGACTT TCCACAGGTG TGAGAAAGCG TGTGAGGGAA AGAGGAGGAT AATGGACGGC 1440
ATGGAGGTTT CTGGACTGAG AGAGGGGATT TGGGGCATGA ATAACTGAGA GAGTAGCAGG 1500
GTGGGAGGGG CTGTGTCGGA GCTGAGCAGG GCTGAGTGGG AGTCATGGTC TATACTGAAA 1560
GCAGAGTAGG GATCTCATGG GGACTCTCTT CCTTCTACCT GGACCCCAAA ACTCACAGGT 1620
CCCTCCACTC AACCAGGAAA AAGAAGAGGG AAGCTCATAT GCTCTTCGCC CTCAGTTCAG 1680
GAATGGGGGG TGAACCATTT CATTTCTGGA AATGCTGAGA CCCAGATTTA GCAAAGACCA 1740
ATTTCCTCAT TTAAAGGGTG CACCCACATG ACCATGCCCT CCTCCTATCC TCCTTCCTGA 1800
CTTAATGGGA GAAGTCGTGT CACAGAGGAG GGGCTGAAGC CTCAAATAAT GGACAGGGCA 1860
GTCAGTACTT TTCAGAGCGT AAGTCTTGGT CAGAGATAAA TAGAAGGCAA ACCCTTTGAT 1920
CAGGATACAC AATGACATGG CTTCATGACA GGCATGCCAA ATACATTTCT GTTTGTGATA 1980
AATCATGGAG TCTGTTATAG CAGCACAACG TAGACTGAGG TGGAAGTGAA GTCCAGGAAG 2040
CTGGGCTGCA CAGCTCCTCA TCCTCATTCC ATCATTTCCA TCTGTGCATT TTCCTGGTGA 2100
TTCCCTGCCC CTGGCACATT CCTCACTGTC ATTTCTGCTG CATCACAGTC ACAGGCCTGC 2160
AAACAGAAAC TGAGTCTCTT CCTGTCACCC CCTGCTCACA CTGCTGGGAA ATCTTGCTAG 2220
GAAGGGCTTG 2230
|
