| Tag | Content |
|---|
EnhancerAtlas ID | HS022-00048 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr1:2573340-2575470 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:2574921-2574932 | GCTTCCCGCCC | - | 6.02 | | INSM1 | MA0155.1 | chr1:2574927-2574939 | CGCCCCCTGCCA | - | 6.07 | | KLF5 | MA0599.1 | chr1:2574671-2574681 | GGGGCGGGGC | - | 6.02 | | NRF1 | MA0506.1 | chr1:2574631-2574642 | CGCGCAGGCGC | - | 6.14 | | PPARG | MA0066.1 | chr1:2575050-2575070 | CTAGGTCCCGATAACCCAAT | + | 6.2 | | ZNF740 | MA0753.2 | chr1:2573940-2573953 | CTGCCCCCCCCAC | + | 7.34 |
|
| | 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 |
| GH01I002640 | chr1 | 2572379 | 2575568 |
|
Enhancer Sequence | AGAGGACACA GAGAGAGGCA GGGAGAGTGG GGTCAGCCCC AAAAGCCCGG CCGCCCCTGC 60
CCTGCAGAGG TCCTCTGCAC AGCCAGCTTC TGCTGGCTCC CTGGGGATGG CGGGGCCCTG 120
GGCTGCACAG GAGCTGCCCG CTGCTTCTGG AGGGGCTGGC TGACCATGGG CAAGGGCAGG 180
AAGGGGGACC CAGGGTAGAG GACCCCTCCC TGCAATTCCC ACTGCCCTGG AACCTGCCAA 240
AGTGCTGTTC CGACCCTTGG CCCAAGGCCT GGCATCCTTG CCCACTGCTC TTCTCCCTGG 300
GCCTCGGATC AGGGACCTGG ATTTACCTCC TCATGGTCCC CTCCTGGCAG CCCTACCGCC 360
CCACCGGCTG GGCCCAGGTT CCCTTGACTG GGTGACCACA CCGGCCTCCT CCCTCGGTCC 420
CTCTGGGCCA AGTCACCTCT CCATCGGGCC CTCTGAGGGG GCTGCTGCCC AGCCCTTCCA 480
CTCTGCCCAC CTTCTGAAGG CTGCTCCAGG CCTCTGAGCA CGTGCACCCT AGCCCCTCTC 540
CCTGGGGCTG CTGGACGGAG GGCACAGCCT GTGCTGTGGG CTGCTGCTGG CCAGGCCTGC 600
CTGCCCCCCC CACTCCTCCC GGGCACTTTC CTGAGCCCAC CCAGGCCCAA TCGCCTCATC 660
TCTGACCCAG TTTTTTCACA GAGTCAACCA CGACCAGAAA TCCGCTCGCC TCGCTGGGCT 720
CCTCCTCCGC TCAAGAATCT GCAGGGGTTC CCCGCTGCCT GAGGAACACG CCAAGGTGCA 780
GGCCCCGCCT TTCTCGCTGG CGCTGCCTCT CTTCCAGCAG CCCGGCGGTC CTCGACGCTA 840
CCTCCCCCGG GGGGCGCAGC GCACCCAGGA CCCCGCCAGG CTTGGCCGCA CGGGGCGAAG 900
CCGAGGCCCA CGCCCGGGGT CCGTGCAGGG AGCGAGGGGG TCCCACGGCC CCGGCTTTGC 960
TGCTGGGCTC CCGCAGGGCA CAGTGTGGCC TCTTCTGCCA GCTGTGAGCG GCGCTGAGCA 1020
GGGCAGGGGC TCGAAACCCC GTCCCTCGCC TGCGGTGCGG CCCGCGGGAC CGCCCCTCTC 1080
CGGGCGGAGG CACCTGACCC CGACCCGTAG TTCACGGCCC GGGGTGGTAG TGAAGCCTCG 1140
GCCCGCGCAG GACCCGCACA TTTGGGCCGG GTCCATGGCA GCAGGAGGGC GAGGCCCCGA 1200
GCAGCTGTCG GACCCCGGGA GCCCCCAGGC CGCCCCAGTG GGGAAGGGCG CTCAATCCGA 1260
CCCCAGACTC CCCTGAGCCC GCGGCTCGGG CCGCGCAGGC GCAGTGCCAC CCGGAGGGGG 1320
CCGCCTGCCG AGGGGCGGGG CGCAGGAAGC GGGGCGAAAC CACTGTTGGC TCATTTCCGG 1380
GTGGGTCCCC GTCTCCAGGC AACCATTTCG CGTCCTGCAG ATTCTTGCCT GTGCCGGGAG 1440
CCGCCTCCTG GCGCCGCAGC CCAGCCGTAT TCTGCAGCCT CGGAGACCCG CGTCCAGCCC 1500
CGCCTCCGGG CTCGGTGACC CCCGTTCAGG AGACCCCATC TAGCCGCCTC CTCTGGGCTC 1560
CGGGACCATG GCCCCAGCCA GGCTTCCCGC CCCCTGCCAG GCCCTGCTCC CACCTCGAAG 1620
ACCCCAGCAC AGACCCCTCC TCCTGGCTTG GAAACGCCCA GTCCCTCTGG GAGCTCTGAG 1680
ACCCCACCCC GCCCAGCCCG GCCGCCTCCT CTAGGTCCCG ATAACCCAAT CTCAGCGTTG 1740
CTCTTCAGCT CGGGGGGGGC AGCGGCGCCC CCTCTGCAGC ACCGAACTGC CCCTTACACT 1800
GGTGTAGCCC CGACTCCGCC ATGAGCTCCC TGTTCTTCCT AGTGTGGTTT CTGTTTTCCT 1860
AAGTGGCCCC GGAGTGCTAG AACCCGCTGG TGTCAGGAAG CATTAAGGAG GTGAAATCCT 1920
GCCCAGGCCC CACTGGGGTG TAGTTCTGCC TCTGGGACCC CAAAGCCTGC TGTGCTCTTG 1980
GCCTCCCAGC CTGCCTTGTC CCCACGTGCC TTCTCCCGGC CTGCCATGGG TTTGGGGTGG 2040
GCTTCCTGCC GGGCAAGGTG CCCCTGGCTG GCTCAGTCTG GCCCTGAGGG CAAGGTCCTC 2100
TTCCCTCTCT TGCACCCAAG TCACCTGTGG 2130
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