Tag | Content |
---|
EnhancerAtlas ID | HS048-20472 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:63285250-63286130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr2:63285846-63285857 | GGGCGGGAAGG | + | 6.62 | EWSR1-FLI1 | MA0149.1 | chr2:63285851-63285869 | GGAAGGAAACAAGGAAAC | + | 6.4 | IRF1 | MA0050.2 | chr2:63285403-63285424 | AAAAAGGAAAAGAAAGCAAAA | - | 6.12 | ZNF263 | MA0528.1 | chr2:63285330-63285351 | GAAAGAAGAGGGGGAGGGGAA | + | 6.28 |
|
| 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 |
GH02I063058 | chr2 | 63285480 | 63285937 |
|
Enhancer Sequence | GACTCAATTC CCGAAGCAAT TCCTTTCTCT TCAGAGGCAG GAGCCTGGCA CTGATTTCTT 60 CACCCTAATT GCCTGCACCA GAAAGAAGAG GGGGAGGGGA AGAGGGTCGG GAGGCGGGAA 120 AGGATAGCTC TGTAATGCTC TCAGAGCTGA GCCAAAAAGG AAAAGAAAGC AAAACGACAA 180 AAAACTGATC CGTGTCCTGC ATGTTGGCAG CAGACAACCT TCCTTGCTGC TGAGCTGTCC 240 CGGGTGGCTT CACCGCGGCT GGGGAATCCG AGCCATTCCT TCCACGTGCT AAGATGTCCC 300 TCTAAGCCCT CAGCTCCTGC CAGAAGTAGC CAAATTACCT TTCTTCGTAC TGTAAACTTC 360 CTTTAAAACA TACAAACTCA TAACCTGGAA AAGTCGACAA GGACGCCTTT CACTTTGGCA 420 GGGGAAGAAG ACGACTGGCT TGCATCTGGG GGTCAGGAAG GACAGTTCCA TCTCCCTCTG 480 AGGGAAGACG GGGTTGAGGG GTAATCCTCC CCCAGAAAAT GCAGAGCCTG GAACTGTCCA 540 GACTCTGGCC TGAAACCTCC TGGGTGTAAG GCCATGAATC TGCTCGACTT GCTCACGGGC 600 GGGAAGGAAA CAAGGAAACA ACGAAAAGTT TCCTGCGAAG TGACCAACAT CCCCTATTTT 660 TTAAAAATTC CGTGTGAGAC CTGAGAACAC ACTGTGAAGC GGGGTTCGGA GAACGACCCC 720 TCCCGCGTTC CGCGCCCAGC GGGGTCGCAG GGCTGCGAGC CCGGCTGTAG CAAAGCTTTC 780 TCGGCCGCGT CCTCCCTCCG GATTCGGTAG GCCAGGCTCG GGCGCGCCCT TCCCACACCA 840 ACAAACCATC TTTCCCGACT CAGCAGAGGC CCACAGGGGC 880
|