| Tag | Content |
|---|
EnhancerAtlas ID | HS048-26175 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:124283640-124284360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:124283965-124283984 | CCTCCACTAGATGGCAGCA | + | 6.62 | | EWSR1-FLI1 | MA0149.1 | chr3:124283952-124283970 | CCTGACTTCCTTTCCTCC | - | 6.04 |
|
| | 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 |
| GH03I124564 | chr3 | 124283794 | 124284247 |
|
Enhancer Sequence | GGCTCTGATG CACATTTGAG TTTGAGATCC ACTGACTTGT GAAGTCCAAG TGGCAGAGGC 60
CTTGCAGCCA AGCATTTTAC ACTGAGGAAG CCAAAGCCAG GCCTTAGTTC TGGGCTTATT 120
TTTGTAACTG GCCAGATAAT CAGCAGCAGG CATGCCTTCT ATGCAGACCT GTGCTAGATA 180
TTTCTAGGAG AGGAAGATGG GGACGAGGGT CAGCATGGAG ACCTGCTGCA GGCTTCCTGA 240
TGGTTAACTG TGAACTCAGA ACATATTTAA AACACTCCGG TGTCTGGAGT GCCATCTGGT 300
CTACCTCCAA AGCCTGACTT CCTTTCCTCC ACTAGATGGC AGCAGCAGGC TGAATTGTTT 360
GTGCTGCATC CAGCCTTCCA GGGTTTTTTC CACCAGGAGA AAAATGTCAG CTAAGACCGA 420
CGTCCTAATT CTCCTCGTGC CCTCCACTCC CAATTTAATC ATTGCCTGCT TTCCCCCCTG 480
TCCTCTGAGG ACTAAGGAGG GACTGTGTCA GGAAGTTGTG TGGGAATTTG AAATTGCAGG 540
CACAAGAGGA AAATCAAGGA AACTCAGGAA TCTGGTTCCG CTTGAAGTCT AGCCAAGAGG 600
AGAAGAGGGT ACACAGAAGG TAGATTGTGA GGGTAAAATG AGGTAATGGA GACAAAACAC 660
AGCAGTGCCT GGCATTCAAT GCACTTTAGT TGTCATGATA AGTTTTTGCT ATTATATCAT 720
|
