| Tag | Content |
|---|
EnhancerAtlas ID | HS048-11578 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr14:67885070-67886420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr14:67885839-67885860 | GCCCCTTCCCTCGCCTCCTTC | - | 6.29 | | Zfx | MA0146.2 | chr14:67886339-67886353 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 67885961 | 67886126 | | chr14 | 67885134 | 67885269 | | chr14 | 67885295 | 67885950 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I067417 | chr14 | 67884418 | 67887196 |
|
Enhancer Sequence | GAAATCCTTT CAGCCTAAGT CAGGGGTCCA TGGCAGTAGA TTGCATTACT ATTCCCAATT 60
ATTCATTCCC CTATCCCCTG TGATAGAATT ACACATCCCT GTCCCATTGA CTCAGGTTTG 120
GTCTTGTGAC TCGATTTGGA CAATGCAACC TCAGATGCAT ATCTCAGCAG AAGCTTTGAG 180
CACCATTGCT TGGTGCCACA AGCCCCGCGC GGCCCAGATA GGGGCTGCTC CTACTCTGGG 240
TCCAGGAATG AAGGTGACTT GGAGAGAGAG CTGCAGCCAA TGTGAGTGCG AAGTCAGCCT 300
CTGTTGTAAA CACTGAGATC TGGGGTGGAG TGAGGGGGTA GAGGATACTG TCACCACCAT 360
GGAAGTTAGT CAAAGCTGAT CGACACACTT GTCACACTGT GATGCTACAA AGCAATGCCA 420
GAGGGACTAC GTGACTTGGA GCCTCTCCCT GCCATGGAGG GGTGGGTGCC CTCTCCCTGT 480
CATTAACACC CTGAAACCTA CCTCCCTGTT CCACTGAAAA AGCTGGAACG CCTTGAGAGG 540
TCAGTCACTC TCCCCAGGGC GCTCTGCAAG GCTTTGCTGG GGATGAGAGC CCAGACCCAT 600
TGCTTCCCCA CCAGTGCCAT CCACCTTGCC ACCCCCTAGA ACTCAGCCTG GAAGGAGAAA 660
TGCCCCTTGG CAGATGTCTC AGGGCCATCA GGGCTGGGGT GGAGCAGGAT GTGAGGTGTG 720
ACTCAGCTGT GTGCACGGGC AGGGCTGGAC CTGCTGGATA TAGATAAGAG CCCCTTCCCT 780
CGCCTCCTTC CATTCTGCTT TCCTCACTGC TTTCCCTAAA TGTTATTCCT GGAGGCTAGG 840
CTTTTGGTTT TGCTTATTTT GAGTGGGTAA ACAAGAGAGG GGCAGAACCT TGGCCTAGGG 900
ATGTCTGAGG ACCCCCCAGC ACAGGAAGGG AGTAGCCATG GTGTTATGCT CACCCCTGCG 960
GAGCCCCTGT AGTTACAGCT GCTCTCCAGG CCTCAGGGGC TCCCACCTGG CTGGTCATCA 1020
AAATCACCTG CACGGTTTTT CCCAGCCCTA CCTAAGAGCA CCATTTACAA CAATGCAGGG 1080
TATTTACTGC ACAAAAGGAA CCTGGCTAAG AAGGCAAATG GGGGCCGGAG GTGCAGTCTG 1140
CGTTCAACTA CCAAAGGCAT GCCTCCACGC AGGGCTGCCT TCCCCAAAGA AAGCAGGGGG 1200
GTTCTCATCT CATAAAGGCT GCATCCAGGC GGGGGGCGGT GGCTCACGCC TATAATCCCA 1260
GCACTTTGGG AGGCCGAGGC GGGCGGATCA TGAGGTCAGG AGATCGTGAC CACGGTGAAA 1320
CCCCGTCTCT ACTAAAGATA CAAAAATTAG 1350
|
