| Tag | Content |
|---|
EnhancerAtlas ID | HS110-00889 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr12:12111340-12112820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxa2 | MA0047.2 | chr12:12112138-12112150 | TGTTTACTTTGT | + | 6.18 | | NKX2-3 | MA0672.1 | chr12:12112739-12112749 | TTCAAGTGGT | - | 6.02 |
|
| | 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 |
| GH12I011958 | chr12 | 12110940 | 12112751 |
|
Enhancer Sequence | GAATGAATAA GGGAACAGAT CATTTCTTCT GAGCTGTTTG CAGTCTGGCT AAGCCAATTG 60
AAAGAATGCC TTCTCTTGCA ATCTACAAAT TGAAAAGCCT GTGAGACCCT CAGGACACTC 120
AGGCAAGTTT TCCAGCATAT GTGACAATAC CAAGCCTTAG TGCATTTGCC TCTCACGTGG 180
AGGAGTCTCT TCTAAAAATG AAACAGAGAT GAAGGGTGAG ACTCTTACAG TGGTTCAACT 240
CCCCTAAGAT CCTCTTGTGA TTTAGAAGCA TCTTGGAAAG AAATCCTTGA CACTCGCCTC 300
GCCCACCCTG AGCTATAAGG TAAAGCTCTC GGTGGTAAAC GTGGCTCCCT GGTAGGGAGA 360
CTTCTTTTAT CCTCATTGTT TCTGGAGGGG GAAGTGTTAG CACAGAGACT CCCTGGGAAA 420
CCCGAGGATG CCTCACCACC TCACCATAAC AGCAGGAAAC CCAGAAATGA TTCACAGCTG 480
AAACCTCTGG CCCACATCGA CACATCACAT CACATGGTTG TTTCAACTGG AAACCAAACA 540
GCCATCTGGG CATGATTATC TGTATTTTTG TGAAGGTGTA AATACACAGT GAGTAGGAAG 600
AGTCCAATAA AACCTATTAT AATGTTGGTG GTGGGCACCA CAAAGAGAGC ACCCCTTAAT 660
AGACATTCCC TGGTCCAGTG AAAGACATAC TTTGTACTGA GTCCCGCGCC TGGGAGACCT 720
TCCAGGAAAG TAAATCCCCA GGAGAGAGAG GCATTTCCCA GTAGGTGCTT TGCTTTTTGG 780
TTGTTTTCTT TTCTTGGTTG TTTACTTTGT TCTACTTTGT TTTTACTACA GTTCTGTCCT 840
ACTGGTGGCG GAGTGGGACT CCTTCATGAT GTGGCACAGT TTCCTTGAGT TTTAGGAAGA 900
AACGGCCCAT GTGGCAGATT CAGAAACAAT GAATCAGCAC CTAAACAAAC AGGAAGGTAA 960
GCGGCCCTCC CAAGGTCACC TGGGTAGTGG CAGGGTGTGA ACCAGAGTCC AGGTGTCCTG 1020
ACCACCCACC ACCGCCTGTC CTCCTCCCTC ATACAAGATC CCTTCTAGGC CAGCGCTGAG 1080
AATAAAGGCA GCGGCATCAT GGGGAGGGGG TGAGGACAGA AGGGTCAGGG AAGGCACTGG 1140
GAGGGAGAGG CAATCCCAAC CCAACTCCAA CAGCCTAGGG TCAAAGCCCA GCTCCACTCC 1200
TGGCAGCTGT GAGACTTTGG TGCATTTAAT GTCCTTGAGC CTCTATTTCT TCACCTGGAA 1260
AATGGGATTG ATGACAATAT GCGTCCCTCC AACAACTAAA TGGCACATCA AAGCTTTGGT 1320
TAAAGGGGTT GGCACATCGT GAGGACCACG TCAGCTCTTA ATACTCCAAT GATGGCTTCC 1380
CTATAAGTGC AGAGTCTTCT TCAAGTGGTG GTTAGCACGG GTTTTGCCTG TTCCTTTAAT 1440
CATGGCTGTG AATTTGCTCC GGCACCATTG TTCCCAAAGT 1480
|
