| Tag | Content |
|---|
EnhancerAtlas ID | HS048-14064 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:21271200-21272570 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr16:21271260-21271275 | AGGGCTGGCTGACCT | - | 6.52 | | EWSR1-FLI1 | MA0149.1 | chr16:21272098-21272116 | GGAAGGAGGGAATGAACA | + | 6.02 | | FOS | MA0476.1 | chr16:21272491-21272502 | GGTGACTCATT | + | 6.02 | | Pou2f3 | MA0627.1 | chr16:21272270-21272286 | TTATATGCAAATCCCA | + | 6.03 | | ZNF263 | MA0528.1 | chr16:21272200-21272221 | TCCCCTGCCCCCTCCACCTCT | - | 6.07 |
|
| | 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 |
| GH16I021260 | chr16 | 21271914 | 21273767 |
|
Enhancer Sequence | AAAGCAAAAA TTGCCAAAAA GGACAGAACA AGTTTCTGCA GCATTTTGGC TCCTTAAGTA 60
AGGGCTGGCT GACCTCTGAT CTGCCATGAC CTTTGAAGTT TTCAGACAAA ACTGGATCCA 120
TGTGATGTCT TTGAACCAGG CTCCAGATAA AATTGTATTG CCTTTGTCTT CCAGTGCATG 180
AGAGATTTTA AAGACATTTA CCAACCTGCA AGGCATGGAT ACTTAACCAA TGGCATGGGC 240
TCTGGGTGGC CAGAGCGCTC CTGATGCTCT GCCAGGCATT TACTCTTTTG CTGCTTGATC 300
ACGAAGTATG GAAGGTCATG AGAGGGGGAC AGAGGGCACT CTCGAGGGGC TCAGGATAGC 360
AACTGTTTAC CAACCAGTTT GGGAGTATTT CAGTGTTTTA GGTGTATCAG CTCTGTTCCC 420
ATGTACTTTA TTTATTTATT TTTTGAGATG GAGTCTTGCT CTGTTGCCCA GGCTGGAGTG 480
CACGATGTCA GCTCACTACA ACCTCCACCT TCCGGGTTCA AGTGATTCTC CTGCCTCAAC 540
CTCCCAAGTA GCTGGGATTG CAGATGTGCA CCACCACGCC TGGCTAATTT TTGTATTTTT 600
AGTAGAGATG GAGTTTCACC ATGTTGGCCA GGCTGGTCTC AAACTCCTTA GCTCAAGTGA 660
TCTGCCCACC TTGGCCTCCC AAAGTGTTGG GATTACAGGC GTGAGCCACC GAGCTCAGCC 720
TGTTCCCATG TACTTCTGTT TCCTTCAATC TCATAGGGTG GAAGAGGACC TGGGGCAAGG 780
GACAGACTGG CCACTGGGAG CCCACCCTTT GTTGGGCTTC TATAAGGTAC CCCATACAAC 840
TCAGGTGGTA GGGGGCTCCC CATGGAAGCC CTCCTCAAAG CAGCAAGTGG GAGAGTAGGG 900
AAGGAGGGAA TGAACAGGGC TTAGGCTATA CTTTCCATCT GACTCTTTCA GGTTGGGTCT 960
CTGCCATTTC CCTTAAGGTT CCTGTCTTTT AACATCTTTG TCCCCTGCCC CCTCCACCTC 1020
TGAAGGGTAC CTTCTGAATT TCATCAAGAT CTGCACCGAA CTGATTCATT TTATATGCAA 1080
ATCCCACCTA ATCCTCAATG GTAACAGGTG GTGAGGAAAC TGAGGCCTAC AGAGGTCAGA 1140
TCACTTGCCT AAGGACACCT GCCTTTGAGT GGCGGGGAAG GGACTCTGAC CCAGGACTGC 1200
TCAGTTCCAG AGTTCATGGG CTTAGCACTA GGCTAAACCA TGTAAATAAT TGACCTGAAT 1260
GATGGAGCAC AATGATTCAG CTGCAGAGTC TGGTGACTCA TTGCTCTTTC CACCAATGGG 1320
TGAACCTGCC TTGTGCGCTA GTTGGATTTG TGCCCAGGGA GCAATGGATC 1370
|
