| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01260 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:47943300-47944480 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr1:47943320-47943337 | GCAAGTCCCGCCCTCTT | + | 6.38 |
| | | 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 |
| GH01I047477 | chr1 | 47942901 | 47944366 |
| Enhancer Sequence | AGTTCTACAG CCAGTAACTG GCAAGTCCCG CCCTCTTTGG ATTTGAGCCT CCAGCTCTTA 60
ACCTCAAACA AGAAGACTGC TGGTGCAGGT GAACCTTGAA CTAGGTTTTG AAGAATGAAT 120
CAGAGTTAAA AAAAGGTGTG TCCAGTGGAG GAATGGTGTA TGCAAAAGCA AGCTGAGCAC 180
TGGGTGTGCT TTGGTACCAT AAAATGCTCA GATTCGCTGG GGGTGCAGGG AGGTGAGACA 240
AGACAGGTAG GCAGGGTCTG GATGGTGGAA AGCCGCCTAG AGCAGGCTAC AATGTTTGCA 300
GTTGAATTGA AAGATGTGAA AAACCATTGG AGGATTTCAC CTGTATGTCC TGGGTAATCC 360
CTTCCCCTTT CTGACCCTCA GTTTCCAGCT CCTCTGCCCT GATCTGCTTT TTCCCTCCCC 420
ACTGTCCCTT TGTCCCCTCC CTTCTCACCC CCTTGCTGCC AGGCCTGGTC CCATCCATCC 480
CTGGGCAGGA ATGAGGGCTG GGTGAACTGC CCCCTTCCCC CATCCCCAGG ACAGCGACGG 540
TTTCCAAATA TCTGTCTGTT GAAATAATGT TCTCTGGGCA CTGGGCCTCC CTCCCTCCCT 600
CACATTCCTG GGCGAGCCGG CCTGTTTGGC TTGCTCGGAC AAATATTGAC TTTCTCTGTC 660
CTTCTCACTC TGGGTCTGTT TAAAAGGCAT CAATCTTTGC CGGGGTGTGA GCTCCCTCTC 720
CGTAACCTGT GGCCTCTGCG GTCCTATTCG GGCAGGGAGT GGTAGGGGAG GGGCTCACAG 780
GCTCTGGGGA TACCCCTTTC TTGCTTGGCT GCACTATAGA GGCTTTTGGT GCAATGCTGT 840
TCCTTGTCAG CTGCTTTCCA CGCGGTCCTG CGTGGGGCCT AACAGCCCAC TTATGGAGCC 900
TCTACTTGAG GGTCAGGTCT ATGCCCGTGG CATGTGCACT GAGACCTTCA TACACATTTC 960
TCTAGACTCC TCAATAACCA GGCAGGAAAC CCTGCTGATT CTACCCTCAA ACAATTATTC 1020
ATCATCCAAC CACTTCTCAG CCTCCACCGC TACCCTCCAG GTCCCAGACA CCATCATCTC 1080
CTGGATCTGA CTCCTGGATT ATTAAGTTAA CTTCCTAAAT TCTGCCCCAC TTCCCTTCAG 1140
TCTGTTGTCA ATTTTGGAGC CAGAGGGATG GGTGAACATG 1180
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