| Tag | Content |
|---|
EnhancerAtlas ID | HS102-13536 | Organism | Homo sapiens | Tissue/cell | HuCCT1 | Coordinate | chr2:200093400-200095120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr2:200094096-200094110 | GAGGAATGAGTCAT | + | 6.13 |
| | | 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 |
| GH02I199228 | chr2 | 200093573 | 200094672 |
| Enhancer Sequence | AAGGCTCTAC ATTTCTGTCT GGCTGTAGCA AGTAGTCTAT GAGCTGGAGC GCCCAGGCAA 60
GACTGGGTCA CACAGCAATG TCCTTCTCCT CCTTGGGCAT TTTCTGGAAT TGCTGCTCTG 120
GAGACAATTG CCTCCACAAA GTTAATAGTA CTTCCGTGGG CTGCTTATCA ATTTTCTCTC 180
AGTCAACCCC AGCCAAGATT AAATCTTGGC TCACATCTGT GAGCGTGCCA CTCATTGGGG 240
TCCCCTTTTC TTCCATGGGG GAGCCCCCTG CAGGCAGGGC ATCTTCCCCT TCTTTAAGGT 300
GTGGACCCCT CAGTCCTGCT GACGGCCCTC TGCTTTCCCA AGAGCTACCA TACCAGTGGT 360
CATTTCATGT ATGTGGTGCC CTGTGTACAG GGTGAGGACA GCAGCTAGGG AGCCAAAGGC 420
ACTCAGAGGT ACAGAACCCA ACATGAGATC CCTCATTTGG GGCGTGAAAC ATTCATCATC 480
TGGCCCTTGG GTATTCAGGT CAAACAGCCT GCCGCATACC CATCACCCAG ATGACTTGCA 540
CCAAATCGAC ATACGACTGC CATTTACTCA CAATTTTGGG TATTTCCCTG GCATTGTTCC 600
ACACAGTCCA TATGGCTGCT CATAGCAGCC TGAATCAGGA TGTGGTCACC TTGCCCTGCT 660
GCTAACTGCC TGCTCACTTG CAACCGCTGA CTGAGGGAGG AATGAGTCAT GATAGAGGCC 720
AGCTTTTCCA TCTCAGAGGC AGAACAGGAG ATACTATCTA CTCCCTCGTC CCACAGACAA 780
AGCATCCAGG CGGGCAGGGG TTCCCCTAGA CGCTGGCGGC ACTGCTTGCC TAATTTCCGC 840
AACTCAGTTG GGGTATAGGC AATATATGAA GTGTGTTTTG TTACGATGGG GGGTCCTTGA 900
GCCCGCCCTT GGGATCCCAC AGGCTGTTCA TGGTCTACTT TCTGACAAAC CACTGGGTGA 960
GCCTGCAACA GGGGTTCTTC CTCCTCAGTA TCAGATTGAG TGCGGACCTC CAGCCAAGAC 1020
GGCGGACCCA GGCTTGCATT CATGTCAGAC TCTAATTTTT TCTCCAAGCT CTGTAGCGGG 1080
GACTCCATGC ACCCCGCCTG TGCCTGGAGG TCCCTTACCT GAGCTTTATC CCTCAGGGAC 1140
TGGGTATGCA CTTCTCGTAA CACAGTGAAA AATGCCCATC CAACTCTGCT GGCAAAGGTT 1200
CGCTCCTTCT CAGTGCTCTG TGCTTCCAGC TGCTTCAGCG CATTTTCCAC ACTCATGGGT 1260
GACCCATCGA CCACCACCCA GGTTTCCGCT AGGGCCCATC CTTGCAGCAT GGCTACCACC 1320
AGGTACCACA ACCCATGTTG TGGCCACATG GTCGACCCAG AATCAGTGGT GCCAAGGCTC 1380
ACTCACCTCG GGATCCTGCC AACTATGCCA AGTGTCAGGT TCTAGCCCAA GCTGAGGTCC 1440
AAGGAGAGTG GGTGTGTGAG TGGCAGGTAG CTGAAAGACC GCTTGAGGAA TCGTAGGCAG 1500
TTGCAACATG GCTTTATTCT CTTTCTGGGT GCAAGCTGTA GGTACAGCAT CAGCAGGATA 1560
GTTACACCTT TTACAGACAA TAGTGGCTCT GATCCAAGCA CAAGCTCTCA TGAGTGGTTA 1620
CATGTGCCTT ATGTGGTGTG GTTACATAAT GTGCACAATT GTGTGCCTGT GCTCCAAACC 1680
CACTGAGTCA TGCTGTGCCA GAAGGCCACC TAGGCCTACT 1720
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