| Tag | Content |
|---|
EnhancerAtlas ID | HS158-37447 | Organism | Homo sapiens | Tissue/cell | Pancreas | Coordinate | chr22:46299030-46300220 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr22:46299881-46299902 | TGCTCTGTCCACGGTTGTGAA | - | 6.57 |
| | | 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 |
| GH22I045903 | chr22 | 46298882 | 46299909 |
| Enhancer Sequence | TCTTGGAAGG ATGTTCTCCT GGCTCAGGAA GCGCCCCCTC GATGCCACTG CAGCCTGGCC 60
CAGAAGCCAG GGGGACTCGG TTCCTGCTGC TGAGGGGGTC CCAGGTTGGT GGCCCAGCCT 120
TTGGAAGGCA TGGAGGGGCA GGGACGCCCA CAGCCTGTGC TAGGACAGGC ACCTGAGTCC 180
CCTCCTGGTG CCCCATCCCA GCATCTCTGA GCTACCCCAG GGTACCCTGC GTCCTCCCAG 240
AGGTGGTGGC GGGGCTGGGG CTGGGTGGTG ACATCATGGG TTGAGCTGTG CCAGTTCTTT 300
CCCGACCTCG GAAACCCCAA CATCCCGCTC CAGGAACTGG CCTGCGGCGT TGGCTTTGGC 360
TGGGCGCCCC AGGAGTGTGG CAGGGAGGCC CGGGGCCCCC ATCCCCCCAG CAGTCAGCCC 420
TGAGGCCCCC CCCTTCCCTT CGGGGGCTCC CAGGGAGCCT GGGCCAAGTG TGAGAACCAG 480
CAGGGTCAGC TCCTCAGGTC CTGCCCCCGC CCCTGCCCCT CCTCTACTGC AAGAAAAATA 540
AACAGCTGTC CCGTCTCTCT GAGACTGGAA ACACCACCGC AGCCGCAGCC TCGGCCGAGC 600
TATGGGGCTG ACTCACTGCC CGCCCTGGGC GGGGGCAGCG AGAAGGGGCC GGGGCTGCCC 660
TGAGGAGCCC TGTGGTGACC CTTCTTTCCA CTGTGCCAGG GGGACGGGAG GACACGTCCA 720
TCTCAGGACT CCTGAGCTCG GCCACGTCAC CCTGCTCTCC CTCTGGCCAC TCTGTGACCT 780
TTGTCAGCCA GGCCTTGACC TCTCCTGGCC CCAGGGTCCT CATCGGCCCA AACGCAGGCT 840
GGAGCATCTC TTGCTCTGTC CACGGTTGTG AACAGGGAGG AGCATGGTGG CTGGGTTCAG 900
GGGTCCACCC TGGGGCCTCA TGTAGTAGAG CAGGAAAATA AATGTGTCGG AGTGACTTTC 960
ATCAAGGGTG GAAATGGAAA CCTGTGTTCC TGGGCGCCTC GATCATTCGG GAATCTGATG 1020
ATCCTGAAGT CACCATCGGT CTCCCACGCC TCCTGCGCTC GTCCTTCAAG CCTTCTTTCT 1080
TTTCCACGGA TACCTTCCAG TGTTCCCAGG CCAGCTCCCT CCTGTGGGTG GAGGGCGTGG 1140
GCAGGAGGGC AGTCCCTTTT CTCCGAGACC CTTGGTTGAA GCTCCAGGCA 1190
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