| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06439 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:123430790-123432470 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:123432023-123432042 | CGGCACCACCTGGAGGCCG | - | 6.13 | | EWSR1-FLI1 | MA0149.1 | chr12:123431763-123431781 | GGAAGGCCGGAAGCAAGG | + | 6.67 | | RREB1 | MA0073.1 | chr12:123431574-123431594 | GCGGTGTGTGTGGTTTGTGG | - | 7.27 | | TP53 | MA0106.3 | chr12:123431489-123431507 | AGCATGCACTGGCATGTC | - | 6.6 | | TP53 | MA0106.3 | chr12:123431489-123431507 | AGCATGCACTGGCATGTC | + | 6.99 | | ZNF263 | MA0528.1 | chr12:123432191-123432212 | GAAGCAGGAGGAGGGTGAGGT | + | 6.45 |
|
| | 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 |
| GH12I122942 | chr12 | 123426680 | 123432837 |
|
Enhancer Sequence | GAAGGAGAAG ACCCCAAAAC AGCCTCACTA TGTACTGGAG CCCCCAGGCC TCTCTGGGTT 60
TTTCCACCCT TCGCTGGCAC CAGCTATATG CAAGAGGTTC CTAGGACAAA AAGACAAGAT 120
CTAGCCCTTT CTCCCCCATC CCCTTCTGGC TCAATTTGAC ACACTCAGGT AGTCAACTCC 180
AGAGAGGCTC TTGGGGCAAT GGTTTCAGCT CCTGAAGGAT AGGGCACGGT GCTGATCGTT 240
AAGTCATCCC CAGTATTCAA AAGAGGCTAT TCATGACTGG ACAGTTTTTG GTAATCCTTT 300
CAGAAAAGGG GCCTCAACAC CTGACCCTGT GCTGGAAGAG CAGGGGATGC CTTGGACGGT 360
TGTTCAGGTT GTACACTATT TAAGAAACAC CAACTATTAA AGGGGCACCA TTTACATCAT 420
CAACATAAAT TATGTTAGAG CCTGAGGGTT GATAAAGAGA TTCCAGAACT CCCAGCCAAG 480
TTCTACATGG TGGCAGGGGC CATGGGTTGT GAAATCTGCC CACACCATGT GCATGTCACC 540
ACAGGCAGAG CTGAAAAGTG GTCCCAAGTG TGCGGCCATC AGGCTGCTGT TCACCAGAGT 600
CCTGGAAGAG GCCCCTGGGT GGAGCTGTTC ACACTTTGCA GGAGTCACTA TGCTGATTCT 660
CAAGCCAGCC AGGAAGGCTG CCTGAGAGTC CAGGACAGGA GCATGCACTG GCATGTCCCA 720
TGACCATGTG TCACGCCCCA GCCGCAGGAA GCATGCAGGG TGCCTGAGTC ATGTTTGGCC 780
ATGGGCGGTG TGTGTGGTTT GTGGAGATGA CTCGCTGGCT ACACACAACA CATTCAGGCA 840
TGGGGTGGAA AACCCAAACA GAGCCTTCCT GAGGCCTCCC TTAGCTGAAC TAAAAGGCAG 900
GGCCTGCAGT GCACACAGAG GTGGGGGCTG AGGGGGAGCT CCAGGGTTTC TTGCTCCATC 960
CCAGGGGCTG GTGGGAAGGC CGGAAGCAAG GGGTGGGGAG CAGCGTGCCA GAAATGGCTC 1020
AGACTCTAAA GAATAGATTT ACTTTCTCAT CTCAGTGAGG ACGGTGGGGA GGCTCGTGAC 1080
CAGGAACTTC GGGAAGAGGT CCTACCTGTG TGGCTGGAGA AGACTGTGGG GAGTGGCCTC 1140
ACCGGGGGCT GGGTGGGAGA TGGCTTCCTT TGCTACCCTG GTCTCAGGTC ACCAACACCA 1200
AAGGCTCCAA TGGAGCTGCG ACAATGACTT ACCCGGCACC ACCTGGAGGC CGTCATGCAT 1260
CCAAGCCCCT GCTCTAGAAG TACCCCACGT GGGCCTGGGT GACTGTGAGG GGGTTGCCTG 1320
TACCTGTCAC AGGGTCACAG CCCTGCCTGT CTGAACCCAG CCTGTCTGTC CCTTAGGGCT 1380
CGGGGGCACC CGCCCATTCA GGAAGCAGGA GGAGGGTGAG GTCAAACCTG GCTCACGGCC 1440
CTAGCTCGGA AGCAGAAGCA GTGCCGTGGG GTGGCCAGAG GGGACAGCAG CCTGCCCATG 1500
ATGGCATCAC AGCGGGCCCG CGATGGCATC ACAGCGGGCC CGCACCACCC CCACATACAC 1560
ACCAGGCACG TTCCAACCCA GGGCCTTTTC ACTGGCTGTG CCCTCTGCTC AGCACATACC 1620
TCCCAAGATG CCCGCCTCCT TCAGACCCTT ATTCAGATGT CCCCTTCTCA GCAAGACCTA 1680
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