| Tag | Content |
|---|
EnhancerAtlas ID | HS110-01128 |
Organism | Homo sapiens |
Tissue/cell | KATO3 |
Coordinate | chr13:45941120-45942440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr13:45941300-45941310 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr13:45941300-45941310 | GGCACGTGCC | - | 6.02 | | NFAT5 | MA0606.1 | chr13:45942407-45942417 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr13:45942407-45942417 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr13:45942407-45942417 | AATGGAAAAT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr13:45942203-45942218 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr13:45941218-45941233 | GAGGTCAAGAGTTCG | + | 6.24 |
|
| | 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 |
| GH13I045366 | chr13 | 45940916 | 45943622 |
|
Enhancer Sequence | AAGCATTCAA AAGAGATGTG AAGGAAAAAA ATTTGGCCGG GAGCAGTGGC TCACGCCTGT 60
AATCCCAGCA CTCTGGGAGG CCAAGGTGTG CGGATCACGA GGTCAAGAGT TCGAGACCAG 120
CCTGACCAAC ATGGTCAAAC CTGGTCTCTA CTAAAAATAC AAAAATTAGC TGGGCATGGT 180
GGCACGTGCC TGTAATCCCA GCTACTCAGG AGTCTGAGGC AGGAGAATCG CTTGAACCTG 240
GGAGGCAGAG GTTTCAGGGA GCCGAGATCA CACCACTGCA CTCCAGCCTG GGCAACAGAG 300
GGAGACTGTC TCAAAAAAAA AAAAAAATAA ATAAATCAGC ATAGTAATTG ATGAGGACAA 360
GGACATTTTA TTATCATGGG ATTATGGGGA CAAATGATTG CTGAAATCAT AATTAGCTTT 420
CTGGCGGGGG AAGATAGTAA GGTAGAAAGA GGAGAAATGG GTGTAATCAA AGGAAGTGGC 480
AGAGAGAGAT TAAAAAAAAA AAACAGGAAA TGAGAACAAG AATATGACTA ACAATGCCTG 540
AGCCCCACCC ACCCATCCTC AGAGTGGACT CCCTCTCTCA AAGGCTTGTG GGCACCTGCC 600
CCCGAGCTGA CTCACCCTGT TCAGTCATCA CAGCTCACTG CAGTGATGAA GGCTCAGGTG 660
ATCCTTTCAC ATCAGCCTCT CCAGTAGCTG GGACTAAAGG CATGTGCCAC CATACCTGGC 720
TAATTTTTTG TTTTTGTTTT TGTTTTGAGA TGGAGTCTTG CTCTGTCACC CAGGCTGCAG 780
TGCAGTGGCA TGATCTAGGC TCACTGCAAC CTCCACCACC TGGATTCAAG CAATTCTCTG 840
CCTCAGCTTC CTGAGTAGCT GGGACTACAG GTGCCTGCCA TGACGCCCAG CTAATTTTTT 900
TGTGTATTTA GTAGAGATGG GGTTTCACCA TGTTAGCCAG GATGGTCTCG ATCTCCTGAT 960
CTCGTGATCC ACCTGCCTCA GCCTCCCAAA GTACTGGGAT TACAGGTGTG AGCCACCGTG 1020
CCCGGCCGTA TTTTTTGTAT TTTTAGTAGA GACAGGGTTT CACTATCTTG GCTAGGCTGG 1080
TCTTGAACTC CTGACCTCAA GTGATCCACC CACCTCGGCC TCCCAAAGTT CTGGGATTAC 1140
AGGCATGAGC CACTGTGCCC AGCCACCCGT CACCTGCTAG TGTAGACAAA TGAATAAACT 1200
TAGACAAGCA CATGGGCTCC CTCTATACCA GCCTAGACTT TGACACTGAA ACTCCATGAG 1260
TCTGGGCCAC TTCCTGCCAC AAGTGTGAAT GGAAAATAAA TCATTTTCCA AGGAACCCAA 1320
|
