| Tag | Content |
|---|
EnhancerAtlas ID | HS048-37636 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr9:104240580-104242120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:104240993-104241012 | CAGCCACCAGATGGCAGAA | + | 6.95 |
| | | 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 |
| GH09I101478 | chr9 | 104240578 | 104244329 |
| Enhancer Sequence | CAAAGCCAGT ATAAAATAAT AATTGCTAGT AAGGTCAATG CAAAACTAAA TGGTGTCTGC 60
AGTACAGAAA GTAAATCTGT TGCCTCAGAC GCATCATAAG GTTTACACAC ATTTGGAGGA 120
AAACTGTATA GTTTGTGAGT TATTGCAAAG GGAGGATTGC CCAGGAACCA TACGAGGCTG 180
CTGTGGAGCA GACTCAGCCA GTGCTCTCAT ATCCATGGTC TCCCCTTGGG CACACAGAAA 240
GACCTCATTT CCTAGTTTGC CTTCTCCAGG TGGAGTCATG TGACTAGGGC TTGTCAGCAA 300
AGTGACAGGT GTCACACCTG GGACAAGGTA GTTGAGAACA GATGTGCCAT CTCGACTTTC 360
TCTTTCCCCA TCTGCCAGCT GAATGGAGAG CCCTGGTGGA TCTAGAGGAG GTACAGCCAC 420
CAGATGGCAG AAGCCTGGGT CCTTGAATCC TTTACATACA TATCCCAGTG TTGGGACGGC 480
ATGGAACAGA TGTCCCTTCC GCTGCCCACC TCCCAGTACC CTCCCAAACT AGAGTGGACT 540
GTGTTGTGAG CAATACATAA ACCACTGTGT CTAGACACCA ATAATTTTTG GACTTTATTA 600
CAGCAGTTAG CCTACTCTGC CCTCTACAGT TGTGTAGAAT ACCAAATGTA CAGTGACATG 660
GTTAATTTCT CAAGTAGAGA AACAAGTTTC ATTTCAGCCA CAGAAGCAGA TTGTACTATG 720
GGACTCCAAA GGTGAGACAG ACTATCCTAG TACTAAGAGA TCTGGATAGT ACCCAAAGAG 780
GGAACAAAGC AAGGAGAGGT TTGAATTATG CAACCCCAGT CTTGCTGGTT TGTGAACATC 840
CAGCATATTG CAGACTGGTT GCTTCTTCCT CTGCTCTGCT CAGCGCAATG GAGTTAACAA 900
ACCATGTGGT TGAACGTGAT TGAACGTGGC CTCACCACTT CCACATCACT GCTGATGGAA 960
GCCAATACTA GAATTGGGCT GAACTCCCAC TCCTGCAGTA TTGGCCTTGG AAAAGGAGGC 1020
ATTCGAGTGG ATTTCTGCTC ATACTATTAT CCCTGCCTTT GTTATTACCA CAAGGGAGCT 1080
GGATCAATCT AGAGGAGGGA ACTAGAGACA ATGAGATAGG GCAGGCAGTT TGGAAAATGC 1140
CAGGCACATA GTAAAGGCTA TCACTTACTA TGATATGTCA GGGGGGAAAG AAATGGAAAC 1200
ACCTAGAACT GACATCAGGA GAACCTTTGG TCCCAGGGAA TTTATCCTAC TGGGGACAAT 1260
AAAATCATTA ACATCTCACA TAGTCCTTTA CTTTAAAACT ACGTCTGTGA GACTGCTGTT 1320
CTACTGACAA TCAGGAAAAG AGAGGGATTT GGTTCAGAGG ACACATGGTC CCTACCTATA 1380
TTGATCAGCT TTGCTGGGGT GATTAACAGC CTCAAATCTT TATAACTTAA AGTGATAACA 1440
TGTATTTCTT GCATACGGGT TTGTGGATAG CTGTGGCTCA GTTGGGGTCA GCTCCAGAAT 1500
GTAGGTCAGA ATTAGCTCAT GCCACATGCC CCTCCTTCTA 1540
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