| Tag | Content |
|---|
EnhancerAtlas ID | HS180-03012 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:150143680-150144710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr1:150144046-150144056 | ACCACTTGAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 150144008 | 150144455 | | chr1 | 150144303 | 150144629 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I150171 | chr1 | 150143827 | 150146084 |
| Enhancer Sequence | GATCTGCCAG CCTCAGCCTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCACGCCCAG 60
CCTGGAGTGT CTTCTTAAAG CAGTTCATGT CACTTGACTA CTTAAAACCA CCCTAATTTC 120
ATGTCACTCT TAAAAATCCA AATATTTTCT TTGGCAAATA AGGCCCTTCT CTGCCAAGCA 180
CAGTGGCTCA TGCCTGTAAT CCCAGCACTT TGGAAGGCTG AGGCAGGCAG ATAGCTTGAG 240
CCCAGGAATT TGAGACCAGC CTGCACAACA TGGCAAAACC TCATCTCTAC TAAAAATACA 300
AATAAATAGC CAGGCGTGGT GATGCATACC TATAGTCCCA GCTACTTGGG AGGCTGAGGT 360
GGGAGGACCA CTTGAGCCTG GGAGGTCAAG GATGCAGTGA ATCAAGATTG TCCCACTGCA 420
CTCCAGTCTG GGCGACAGAG TGAGAGCTTG TCTCAAAAAA GAAAAAGGGA AAAAAAAAAG 480
GTCCTTCTTC TTCTGACTCA TGCATATCTC CAACCTTATC CCCAGGCCAG ACACACAGAT 540
CTCTTTTCTG TTCTGTACAC ACGCCAAGCT CTTTCCCACC TCAGGACCTT TGCCCTTGCT 600
ATTCCTTCTG CCTAAAATAC CCTTGTTCTC TTTTTTAACT TCTTTATCCA AACATCAGTT 660
CTTATGAGCC TTCTCTGGCT GCTCTGTCTT GAGAGGCACC CCTTCCAACA GAATTGTTAC 720
CTTATCATTC TGCTTCCATC ACAACAATGA CCACAGTCTA ATTATTCTCC TCAGTTGCCT 780
CTTTATTTTC TCTCTCCCTG GGTAGAATAG AAGCCCGCAC AGGGTGGGGC CCTGACTTAT 840
CTCCCCACAC CTAAACTCAA TCTTTATTTG TGTAATGAAT GATTGAAGAA AGCCTTACCT 900
AACACATGTA CATCTCCACC ACATTATCCC CACCATTTAG TTCCATTGTA ATAAAAGTAA 960
TACCTTTTGA TGGTCCTTTA CAGTTTTAGA TAGCATGTTC TTGTTTGCCA TCAATAGCTC 1020
TCTCACACAC 1030
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