| Tag | Content |
|---|
EnhancerAtlas ID | HS187-17175 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr3:53105860-53107770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:53106848-53106867 | TCCTGCCCTCTAGTGGCTG | - | 6.77 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr3 | 53107035 | 53107200 | | chr3 | 53105993 | 53106338 | | chr3 | 53107324 | 53107487 | | chr3 | 53106812 | 53106929 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH03I053071 | chr3 | 53105884 | 53108148 |
|
Enhancer Sequence | AGGTGAAGCC AAAGACTCAA AAGCAGGTCC TTGCCTCCCG TGACTGCAGG CACAGCCCAG 60
TGAGGGGCAG CAGGGCTGCC AATGGTCCCC TGAATTGGCA CCCACTTCCT GGGTTTAGCA 120
CCACTGTGGC CTCAAGAGGC CCTAAAGGAG GGTTGTCATG GCATGCACCA TGGGTTCCTC 180
ACATAGTTCC TCTGGCCCAG GGGAACACGT GTCCTAGAGG CAGCTGCTCC TGGCGTCACT 240
GTTGGTAGGT CCAGATGAAG GACAGGCCTC TGCCTGGGAG TGTCAGGATG CAGAGAGGCT 300
GCCTCATTCC TGCTGCGGCA GCCAGGGTCC CCACACACTC ACACTCATGT CAGCGAGGTC 360
ACAGGAGGTC GTCTCTACAT GAGGCTGTGA TAAGGCTGCG TGGGAGCCTG CATGCAGGCT 420
CAGCATCATC CTGCCCGGGC GGGAACCCTG GTCCACCCTT GCTGTAGGAC TTCAGTCAAA 480
TGACAGCCTC TCTTGACCCT CAGTTTCCCC AACTGCAAAA GTAGCACCCG ACAACATGCA 540
CTGACCCCCC AGGGCTGCTG GGCGTGCTTG GCTGATGGTT CACTCTCAGA AGTATCTGTC 600
CCTACCCACC TCGTAGGTGC GGTCAGGTGA GTTCTTCTCT GCCTCTGTTT CCACACTGCA 660
CCTGGAAGAA GCTGGAGGAC CTGCTCTCCT AATTGCTCCT CTACCACTGA TGTTGTAAGA 720
AGGGGACACT GACTTGTCAC TCTCTGCCAA TGTAGGAGCC AGGCACTGTC TCTGTTGGCT 780
CAGGGCTGGG CTCCCAGGAA GTAAAAGCCT AAAGGCTCAG GGAGGCCATT TAAGGTCTAG 840
GGTCCAGTGG ACTTTCGGAC GCATCGCAGC CTCCGCTGAG CCCTTCTAGC AGGCTTGTGG 900
TGACTGCACC CTGGGGCGGC TGCTCCATTG TTTCCTGTCA GTCCCGCTCA TCTGCTCAAC 960
AACCCTTTGG AGGAAACACA CAGGAGGGTC CTGCCCTCTA GTGGCTGCCG GCGGCCAGGT 1020
CTCTCCTCAC AGGGCTCCGC CCGCGACCTC AGAGGAGCCC ACCGCCCTCT CTGCCTGCTC 1080
TAGTGCCTGC CGCACAGCAA CAAGCAGGCA TTTCCTGGGG GTGAAGCCGA GGCTGGCCCC 1140
ATGAGCTGAC ACCCAGCAAT CTTCATCTCC GAGCACCTTT GAGTCCTGGG GGGCCCTGCT 1200
TCCAGATGTG AGCCCCCAGC CCGTGGGGCT GGGTGGTCCT GGGCTGTGCC ACAGGGTTTC 1260
AGCCCACCGC GAAGGAGGCC TGACGGTGTC CAGGTCGAGG GCACCTGTGG GCAATGATTG 1320
ACATAACACT GCAGAGAGAG AGCCTGGTGG GGCACCGGCC TCTGCCCAGG CTGGGTTCCG 1380
GGGCCTTCCC CCATGTGCCC ACATCCCATG CTTCCCCCGT TACAGCCTCT GCCGTCAGAC 1440
TGCGCACCAG CATCTGTGGG TGAGGAGAGA ACCTGGGCTG GGGCTTGACA CAAAAGGGGC 1500
TTTGCCTCTG GACACCCCCA CCTGTGCCGC AAGTGGAGGG GGCGGGGAAA CGGGGAGGAG 1560
GGAAAGTAAG CGGAAGTCCC GCCTCTGTGG AAGCGCCTCT GCACCCTTTG TCCCCCAAGG 1620
GAAGCACAAG TGTGTGGCCA GTCAGATAAA GCAGGCCTTT CCTTGCCTTT ATGGAGCCAC 1680
GGGCTGAGGC TGGACCAAGG GTCAGTGAGG GGTTCAGGAG GCCCCCTCTG CGCCTCTCTT 1740
CCAGGCCCTG AGCCCATCAT TCCCTTCGTT GTTAGAGTGA AACTGTGAAG AGCCGCAGCT 1800
CTGTGCCGGG CGAAGAGGAT TTGGCAGTGA AAAGGATGAG CTTGCCTTGC CCTGGGGGCA 1860
ACTGGCACCT GGGGTAAGAG GTGGCCGGTG AGAGCCTGAG CCCTCTGGAG 1910
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