| Tag | Content |
|---|
EnhancerAtlas ID | HS048-21309 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:137180790-137181410 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:137181190-137181209 | TGTCCACAAGGTGGCAGGC | + | 6 |
| | | 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 |
| GH02I136423 | chr2 | 137180771 | 137181582 |
| Enhancer Sequence | AGCTAGTCGG GAGGCTGAGG CAGGAAAATT GCTTGAACCC AGGAAATGGA GGTTGAAATG 60
AGCCAAGATC GCGCCATTGC ACTCCAGCCT AGGCGACAAG AGCGAAAACT CCCTCTCAAA 120
GAAAAAGGAA AAAAACTCTT AGTTAACACT AGCGTTAACC CCAAAGTTAA AGGTGAGTCT 180
GGTTTGGATT TGGGGCATTT AAAACTTGCA TCACCCCTGA CATAAAAAGT CTGAATTATG 240
CGGAGAAAAA ATGCTCCCCA AATCCTCCTC ACGAGCTAAT TTTGCCGAAC GAATCCGCTT 300
CTCACCTGCA TTCGCGCCTC TCGCCGCCTT TCTTTCAGGC GCACAGAGAT AAGGTGGGCA 360
GAGGGCACTG GAGCCAGCCC ACCGGCGGTT TTACTCCTGG TGTCCACAAG GTGGCAGGCC 420
AGGCACTTGG ATTTGCGCAG CCAAGGGCGT GCGCAGCCCG CGGCCGGAAG CGTCCCGGCA 480
GATCGCAGAC GGGGTGTTGA GGGACCCCGC GCTTTTGCTT TCTTATGATT TGGGGGCTGG 540
TACCTGGGCT AGAGCTGAAG CCGGCAGGTC AGTTTCCTGG GAGCAGGGGT GTGTCTGTTC 600
TCAGAGAAGG GTTTAAGCCG 620
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