| Tag | Content |
|---|
EnhancerAtlas ID | HS180-32359 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr22:50825530-50826760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr22:50826145-50826166 | GAAGGTGGAAGAGGGAAGAGA | + | 6.13 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 50825738 | 50826544 | | chr22 | 50825613 | 50825663 |
| Enhancer Sequence | CGAGGCTGGA GTGAAGGGGT ACGATCATAG CTCAGGGCAG CCTCAACCTC CTGGGCTCAA 60
GCGATCCCCC TGCCTCAGGC TCCCGGAGTA GCTGAGATGA TAGTCCCACA CCACCATGCC 120
CAGCTAGTTT TTAAAACTTT TTTTGTAGAG CTGGGGTCTT GCTGTGTTGC CCAGGCTTGT 180
CTTGAACTCT GGGCTCAAGT GACCCTCAGC CTCAGCCTCG GCCTCCCGAA TTGTTGGGAT 240
TACAAGCATG AGCCATGTGC CTCTTTTCAC TTCTGATTTT GGATTTTTAC TTAACTTGTT 300
TGTCCCACTC CACCCCCTTT TTAAAGTTAG ACTCTTTTTC CTGGTCTTTT TTCCCCGGTG 360
GACTATGCTC AGGATCGACA TAGTCTTGTT TGTTCCTTGG TTGTACAAAT AGTCATTGTG 420
CTTCATGTGC TCACGTTGCC ATTTTTTTCC GGGCCAAATG GAAATCAAGC ATTCAGCCTA 480
TCCAGTGGTA TGTTGGTAAA TGTTTAACAA CGGGCTTTCT GGGGAGGAAA AAACCTCCTG 540
GTTTGTAACA CTTGCTGATT TCCATGGCGT TAATACTCCC ACCACGTTGG AGTTGAGCTG 600
CCAGGGTGAT GTCCTGAAGG TGGAAGAGGG AAGAGAGGTA TGAGGGCTCA GGTTGGGCCA 660
CCGCGGCGCA CGCCCTCTGT GGGCACAGTG ACTTTATCTC TGTTTCCGTC TCTTTACGCT 720
GAGGGTCTTT GAGAATGAAA CGTGCTGGGA ACTGTTCTAG AGCCTTTATG TGGAATAACT 780
TAGTAATCCT CCCCACAGGG GATGTCGATG CTGCATTTTA CGGGTGAGGA AATCAAGGCA 840
TGAGAGATCA TGTGAGTGGC CTCAGCTCAC ACCGCAGAGC TAGGACTTTG ATCATAAATC 900
TTTAAAAGAA CAAAACAGTG GCTGGGCGCC AGTGGCTCAT GCTGTAATCC CAGTGCTCAT 960
GCTGTAATCC CAGCACCTTG GGAGGCTGAG GCAGGTGGCT CGCTTGAGCC CAGGTGTTCA 1020
AGACCAGCCT GGGCAACATG GCAAGATGTG GTCTCTATAA AAAATTTTTT TAGGATTAAA 1080
AAAAAAAAAC AGTCAGCTTG GGTAACATGG CAAAACCTTG TCTCTACAAA AAAAGTACAA 1140
AAATTAGCTG GGTGTGGTGG CGCATGCCTG TAGTCCCAGC TACTTGGGAG GCTGAGGAGG 1200
GAGGATCACT TAAGCCTGGG AGGTTGAGGC 1230
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