| Tag | Content |
|---|
EnhancerAtlas ID | HS050-05376 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:203333140-203334290 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr1:203334187-203334200 | AGGGGGTTCCCCC | - | 6.04 | | NFKB1 | MA0105.4 | chr1:203334187-203334200 | AGGGGGTTCCCCC | + | 6 |
|
| | 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 |
| GH01I203363 | chr1 | 203333037 | 203334981 |
|
Enhancer Sequence | TTCCCCATGG GCTTAGAGAT CTAACCCACT CTGGCTTAAG GAAAACAGAC AGGACAACTG 60
AGCAGAGATA GCTTTTGCAT CCAGTCCTGT AATGATCTCG CCTTTTTCCA GTGCCTTGGC 120
TGCTGCAGGC CTGCCAGCAC ATAGAGAGTG GCATTGATTG TAATCGACAT CTGTTGAGCT 180
GTCACTTCCC CCAGCTCCTG TCCTCCCTCC AGAGACCCTC ACTTTCCTGC CTTGTGGGTG 240
CATCTGCAGA AGTAGCTGCA TTGAGTCTCC ACTGAGGCAG CCAGGGGCGG TGTGAGCTGG 300
AGGCTTGCCA CTACAAAAGG ATCCTTCTGT TTTTCTCTCT TCATCTGGGA ACCTGGGGAG 360
CATCTTATGT CTGCATCAGT GTTGCCACAG GGACTTGACC CGTTGCCCTC GCTTCAGAGG 420
GCAGGATCTG CAGCCCAGAG GCGTTAAGTG ACTTTCCAGA AGTCAGGCAA GGGAATGATG 480
GCTCAATATC CTGGCTGGAG CCTTCTGACT AGCCCCTGTT TTCTTACTCT CCCCTGTTCC 540
TGCCTTATCT ATCCTCTGAT ACTGACAGCA GGCGCGCAGA CTCCTGGCGA AGAGAGGGAT 600
CACAAACTCA GACAGGAAGG CGCGACAAGA AGCCACGTGG CTTGCGCCTG CCTCTAGGCA 660
AGATTAGACT AAACTCCTGT GGGTCTTGCT TACCCCTGCT GGTATAGCAG AGATGTCTCT 720
GGTAGGAGGA AGGGAGGGGG ATGTGGTGGA CAGGCTATTC TCAGGGACTT GATAATTATT 780
GCTTTGTTTC CTTAACCATC CATGATCCCA GCCCTGGGGT CTACCTTCTG ATCTCCTCCC 840
TCCCTTCTTG TTCAAAGTCT ATGGTTTTAC TGCTTAAAAA AAAAAAAAAT GTGTCAGCCA 900
CTCCCAGCTT TTACAATTCT GAAAGTGTCA AGACCAGTGA AGAGTTGTGT GTTGTGTTTT 960
GTTTTGACGT CTCTAAAGAA AGCGATGGGG AAGAGCCCTA GAGAGGCTTA GCTTCAGGGA 1020
AATCCTGAGC CTTAAAGGAA GGAGAGCAGG GGGTTCCCCC AGTACATATA CAGGCTTCCA 1080
TCTTTTTACT GCTGCCTCCA ATGATTCTTA GTGACACAGA GGTTGAAATG GGATGCGTCG 1140
TCCAATCACT 1150
|
