| Tag | Content |
|---|
EnhancerAtlas ID | HS048-25685 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:58518130-58519170 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:58518650-58518669 | GGCCGCCACCTGGTGGCCA | - | 8.59 |
|
| | 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 |
| GH03I058532 | chr3 | 58518328 | 58518928 |
|
Enhancer Sequence | TGAGACAGAG TCTCACTCTT TCGCCAGGCT GGAGTGCAAT GGCCTGAGCT CGGCTCATTG 60
CAGCCTCTGC CTCCCAGGTT CAAGCAATTC TCCTGTCTCA GCCTCCCGAG TAGGTGGGAC 120
TACAGATGCC CGCCACCACA CACGACTAAT TTTTGTATTT TTAGTAGAGA TGAGGTTTAA 180
TGATATTGGT CAGGCTGGTT CAAACTCCTG ACCTCAGGTG ATCCACTCAC CTCGGCATCC 240
CAAAGTGCTG GGATTATAGG CATGAGCCAC CGCACCCGGC TCATGTCTCT CTCTTATGTC 300
TCTGGTCTCT GCCTGTGTCT CCCTCTCTCT ATGTGTCTCT CATCTCTGTC ACTCTCCTGC 360
TTTAGTTGGG CTCAGCATAT TTGTTTTAAT TTTTTCCACA CAAGGTGTGG GTCCCCAAGT 420
GCCACAGATG TGTCCTTGGA GGTGAAATTC TCAAGTTTGA GGAAGGGGAA ATCCCTCGTT 480
GGGGCTTGGT AAATCACCAA GCCTCAGGGA CGCTTGATGT GGCCGCCACC TGGTGGCCAC 540
AGCAGGAGGT ACGGCGTTGG TGGCCTGATG GGGGCTGGTG ATGGGCGTGA GCCTTCCTGG 600
GTGTCTGCAG CAGGGGCAGG CAGGCGTATT CTTTCCACTG TGTCATCACA GGGCCTGTGC 660
TCTGGCTGGT GGCAAGCTCT GCCACTAACT CGGGAGATGA GAGGAACCGG GGTTGTGAGG 720
AGTGCCTAGG ACTAGACCAA GTGTGTGTGT TTGTGCGTGT GTGTGTGAGT GAGGCCTTGT 780
CTCTCATGGA TCGATTGTCT CCTCTACTTC AAAGTTCCTT TGGGGACTTT CCAGCCACTC 840
ACTAATGAAA TGTTTAATAT CCCACCTATT TTACAGAGTA AGAACCTGAG GCTCAGGTTG 900
GTGAACTGAC TTGCCCAAGG TCAGCAGCCT AGAACAGAAA ATCAATCTGA GGTCTGTTGG 960
ACCTCAAAGC CAGTGCTACT CTGCCCTCCA ACATTCTTCT ACTTGGGGAG AGTTAAGGAA 1020
GGGGGGTGGA TGTATACTCA 1040
|
