| Tag | Content |
|---|
EnhancerAtlas ID | HS180-50662 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chrX:10586680-10588320 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chrX:10587577-10587598 | ATCCACTTTTTCTTTCCTTTT | + | 6.52 | | ZNF263 | MA0528.1 | chrX:10586961-10586982 | TCTCCTTCCTTTTCCTCATCC | - | 7.06 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGGGCTGTTT TCCAACTTCA CGTAAATGCC ACAACAAACT AGGCATGGGA AAAACCATTC 60
CAAGCTGGGG GAAGCAAACC TTAGGCATAA GGCACGGAGA CTGCCATGGT TCCTGAGGAA 120
TTGTGTGGGA ACAGGGATTC TGGAAATTGA GCTCAGACAC CACCGAGGAG AGGACAGGTG 180
GCTCTGCACA GGATCAAATA ACTTCTTTGT TCCAGCTAAG GACCTTTGTC AAAAATGTTT 240
TGCGTTCCTC TTTTTCCTTT TCAATCCTTT CCAATTACCC TTCTCCTTCC TTTTCCTCAT 300
CCCACTTTAG TAGACATTAA AAGTATGAGG TTGGACTGTG AGTTTGCAGA ACTTAAAGAC 360
GTCCTCCCCA CAGTCCCTAC CAAGGCAAGG GCAATTCATT GCAAGCAGAC GGCACTTGCT 420
CCTCCGCAAG TGTTTTTCTG CACTCACTGA AACTTGCCAA GCCTGCTTGC TGAGCGAACA 480
AGCGAGGGGG CAAGAAGGCG GAGGGTTTGC GCTGACCATT CGAAGGGGGC TCTGCTTCAT 540
CTCCCAAGGC TGTGGGAAAG GGACAGAAAG TTCGAAACCC CTCCCCTGCG CTCTTAAATG 600
GAAAGCTCAC TTCCCCCAAA GTGTGCAGGG TGGCGAGCAC CCAACCCACT TAGAAGAAAA 660
AGTGAAGAGC TTTTCCGGTT GCGATACAGA TGCTAACTTT CCCATCCAGA TTTATTCAGA 720
GCTGGTAAAA GCAATAGCAT TCCTCTTGAA ATCCCTGCCC TTCCAAGCCT ATTGGCATGT 780
TTTTCCAGCC TTGTTTTCTC CTTATATGAG TATTGTTCTT GATATTTAAA TATTGACATA 840
AAATTCTTCC ATAACTTTGA TTGAGTTGTA AATCACACCC TCTCCTTGGC TTCCTACATC 900
CACTTTTTCT TTCCTTTTCT TGCTTAACAG CAAAGCTATA AACCTCTTCC TGGACTGATA 960
AGGAATTTTA TCATCATGCC CCAGAGCCAC AGAAGAAGCT GTTGGTTTAG AATTCTTTTC 1020
AAAGACTCAT TTAAGTAATC CCCCAGCCCT TTCTCCGCTC ACTACTTTCA GGGCTGCCTT 1080
CTCACGTCCA GAAGCAATAC AGTTTCCAAA CTGCTAGAAC AGAAAAACAA ATTTGCATTT 1140
TTCTGGAAGG ACTGTCTGTG CTCATTTCAA GCTGGTTCCG CCTTCTCCGC CAGAAACACA 1200
GTAAGTGCTC AGAATGCGAA ACCAAAATGA GATAAGAGGC CCCGTGAAAT TCTTTTTCAG 1260
GACATTCAGC TGTCTTTATT CTAGCCCAAA GCATAGGGTA GAGGCACTAA AAGCTCGAGA 1320
TACATCCTGC ACGATACATT CCAGCGGCCG CAAACTGGAA TTGATTTACA TATATTCTAC 1380
AAACTGCTTG TAAGCCCTTT ACAACGACTG CCTGACATCA ACCACAATTA GAGGCAAAAG 1440
TGGGGGCGGG TGGCGAGGAC CAGACCGGGG TGGCTCAGGT AAAATGTGCT TCTTTGGTTG 1500
TCTTAGGAAA ATGCAGCCCC GTCTTTCCGC CAAACGCATC GACTACGGCC AGGCGCCTGC 1560
TAACCCAGCA AGCTCTCCGC AGTAACACGT CGCAGGGGTC CCGGGCGGCG CCCGCCCCCT 1620
CCGCCGCCAG CGCAACCGCC 1640
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