Tag | Content |
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EnhancerAtlas ID | HS180-01568 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:46287650-46288790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr1:46287702-46287712 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr1:46287702-46287712 | GGCACGTGCC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:46287779-46287794 | TGAACTCCTGACCTC | - | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I045822 | chr1 | 46288006 | 46288840 |
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Enhancer Sequence | CCCAGGTTCA CGCGATTCCT GTGCCTCAGC CTCCCAAGTA GCTGGGATTA CAGGCACGTG 60 CCATCACGCC CAGCTAATTT TTGTATTTTT AGTAGAGATG GGGTTTTGCC ATGTTGGCCA 120 GGCTGGTCTT GAACTCCTGA CCTCAAATGA TCCACCCACC TCAGCCTCCC AAAGTTCTGG 180 GATTACAGGC ATGAGCCACC GTGCCTGGCT ATTTTCAGTG TTTTAATCTT GATGCTGCTT 240 AGTGGGTCTG TTCAATTTGT GAAAATTCAT TGAGTTCTAT GCTTAGGTAT GTGTACTTTT 300 CTAAAATGAG TAATGTACTT CAGTAAAAGT TAAAAATCCT AGCTTAAAAG TTCAAATTTC 360 ATATTTAATT TATATTTCCT TTCCTTTGCC AGGTTTTGAC TCGAAGAGAC TTGCAGTAAG 420 AAGGGGTGTG ATCCTCTCTT TCTTTTCTCC TCTCCTCTGT TATCTGGTTT CTTTACTTTG 480 GTGTCTTGTG GGAAGGAATA GGGAAATTGA AAAGTGTATG TGTTTCTCTT AATTGGTACT 540 GATCAAATTC TTTCTTGATT GTTCTTTCTC TGGCTAAGAC GGATTATTCA TCCATACAGT 600 GTAGCAGGCA TCCAAATGCT GGTTCTCCCA TGCAGCTGGT TGTAAGTTTT TTTGAGATAG 660 GATCTTTCCC TCTCCACATT GTCTTCATAG AGGATATCCA CTTTAGCTTG ATGTCTTCCA 720 AGGCCTCCTC AGTTCTCTCT ACCTAGAGCT TCTTGCTGTG CTTGTCACCT TTGTGAGTGG 780 CCAACCCTCT TTAATGGATT ACCAGCATTA GTCCAAAGTC TGCTTCCTTC CCTGGTTTCT 840 CCTTGATCCA TAGGTACTGT TTCATCCTTG ACATGCCAAA TAGTGCAAAT ACAAGCTGTT 900 CCCTTGCTAC CTTCTGTTTT TGCATTAAGT TCTATTTCCT GTTCCCCGTC TCACTGCTCA 960 GTCCTGCTAC AGTTAGGTGC CTGGACACAT CAATTGTTTG ATTCAGTGCC ACAATATCCT 1020 CCTTTATCCT TTTATTCACT TACCACCATG TTTTGAAATT GTCTTTTTCT TCTTTTCAGG 1080 TATTTTTCTT CACCAACTTC ACTCTTCTTT TTATGTTTGG GCATTTGTAA ATCATGTTTT 1140
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